Homestasis and Fluid Balance Flashcards

1
Q

Define homeostasis

A

Maintenance of the volume and composition of body fluids

Maintenance of a constant internal environment

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2
Q

Define negative feedback

A

Reverse a change in the controlled condition

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3
Q

What 4 elements does negative feedback require?

A

Sensor, ability to compare to reference, sufficient gain, effector mechanism.

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4
Q

What is gain?

A

Correction/Error
E.g Infusion of blood into someone caused SBP to rise from 100 to 175mmHg (no functional baroreceptors) and to 125mmHg in individual with functioning baroreceptors. Gain = -50/25 =-2

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5
Q

What would a Gain of -5 suggest?

A

A gain of -5 would suggest a more sensitive control system compared to a gain of -2.

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6
Q

Define positive feedback

A

Reinforce/amplifies the change in the controlled condition

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7
Q

How much of a 70Kg male is water?

A

60% (42L)

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8
Q

How much of a 70kg female is water?

A

50% (35L)

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9
Q

What proportion of the total body water is intracellular fluid?

A

60%

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10
Q

What proportion of the total body water is extracellular fluid?

A

40%

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11
Q

What is the extracellular fluid composed of?

A

Interstitial fluid
Plasma
Transcellular fluid

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12
Q

What proportion of the extracellular fluid is interstitial fluid?

A

75% of ECF

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13
Q

What proportion of the extracellular fluid is plasma fluid?

A

1/5 or 20%

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14
Q

What proportion of the extracellular fluid is transcellular fluid?

A

5%

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15
Q

There is more potassium/sodium within the cell than there is potassium/sodium

A

There is more potassium within the cell than there is sodium

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16
Q

There is more ——– outside the cell than there is ——-

A

There is more sodium outside the cell than there is potassium

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17
Q

what is the osmolarity of the intracellular fluid?

A

280 mOsm - 300 mOsm

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18
Q

what is the osmolarity of the extracellular fluid?

A

280 mOsm - 300 mOsm

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19
Q

Is chloride more extracellular or intracellular?

A

More extracellular - tends to be with sodium

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20
Q

Why is it important to have different concentrations of ions in the ICF and ECF?

A

Setting the membrane potential

Generating electrical activity

Muscle contraction

Nutrient uptake via secondary active transport

Generation of intracellular signaling cascades

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21
Q

How do solutes (ions) move?

A

Passive transport across a permeable membrane - Electrochemical gradient

Intrinsic membrane proteins
Pores - e.g. Aquaporins

Channels - voltage gated channels like Na/K ATPases for Ca2+

Carriers and Co Transporters - SGLT and GLUTs

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22
Q

Na+/K+ ATPase is a form of —— transport. It takes —- sodium ions —- of the cell and —- potassium ions —-. Therefore there is always a —— for —– to move passively —– the cell. These are located in the ———— membrane and are ubiquitous.

A

Na+/K+ ATPase is a form of active transport. It takes 3 sodium ions out of the cell and 2 potassium ions in. Therefore there is always a gradient for sodium to move passively into the cell. These are located in the basolateral membrane and are ubiquitous.

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23
Q

Define osmosis

A

Osmosis is net diffusion of water (across a semi-permeable membrane) from a region of high water concentration to one that has a lower water concentration

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24
Q

What is osmotic pressure?

A

The amount of pressure required to stop the flow of water through a semipermeable membrane

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25
Q

If you put red blood cells into solution that has the same number of osmotically active particles, there will be — net movement of water, there is – change in cell volume, so the solution is ———.

A

If you put red blood cells into solution that has the same number of osmotically active particles, there will be no net movement of water, there is no change in cell volume, so the solution is isotonic

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26
Q

If you put a cell (280mOsm) into a solution that is 180mOsm, water is going to move ——- the cell causing it to —–. This is a ——- solution

A

f you put a cell (280mOsm) into a solution that is 180mOsm, water is going to move into the cell causing it to burst. This is a hypotonic solution

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27
Q

If you put a cell (280mOsm) into a solution that is 400mOsm, water is going to move —– of the cell causing it to ——. This is a ——–solution

A

If you put a cell (280mOsm) into a solution that is 400mOsm, water is going to move out of the cell causing it to shrink. This is a hypertonic solution

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28
Q

If a patient has lost blood, what IV solution would you administer?

A

Isotonic IV solution because you don’t want to change the structure of the red blood cells

If the red blood cells swell they can’t move through arteries

If the red blood cells shrink can move through fenestrations in the glomerulus

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29
Q

What increases the surface area of the small intestine and therefore absorption?

A

Folds of kerckring
Microvilli
crypts of lieberkuhn
submicroscopic microvilli

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30
Q

The absorption of non-electrolyte nutrients (such as proteins, fats and carbohydrate, micronutrients and vitamins) occurs almost exclusively in the —– intestine

A

small intestine

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31
Q

small and large intestine (colon) absorb —– and ——

A

small and large intestine (colon) absorb water and electrolytes

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32
Q

what is the key function of the large intestine?

A

Absorption through micro villi and crypts

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33
Q

The large intestine doesn’t have —– but has __

A

villi

Semilunar folds
Crypts
Microvilli

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34
Q

How many litres of fluid is presented to the large intestine and how much is reabsorbed per day?

A

2L/day is presented to the large intestine and 1.9L/day is reabsorbed

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35
Q

How much fluid is presented and reabosrbed by the small intestine per day?

A

8.5L/day is presented to the small intestine and 6.5L/day is reabsorbed

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36
Q

how much fluid is lost as fecal fluid per day?

A

100mL

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37
Q

How much fluid is secreted by the small intestine?

A

1L/day

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38
Q

Does the small intestine actively absorb sodium?

A

yes

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39
Q

Does the large intestine actively absorb sodium?

A

yes

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40
Q

Does the small intestine actively secrete potassium?

A

No

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41
Q

Does the large intestine actively secrete potassium?

A

Yes

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42
Q

Does the large intestine absorb nutrients?

A

No

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43
Q

Absorption of non-electrolyte nutrients occurs mainly in the —– intestine

A

Small intestine

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44
Q

The —– intestine absorbs water, sodium, chloride and potassium and secretes bicarbonate.

A

Small intestine

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45
Q

The —– intestine absorbs water, sodium and chloride and secretes bicarbonate and potassium.

A

Large intestine

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46
Q

How is water absorbed?

A

Osmosis

Coupled to solute movement (glucose)

Transcellular or paracellular

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47
Q

where does sodium absorption occur (cells)?

A

In villus epithelial cells of the small intestine and the surface epithelial cells of the large intestine

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48
Q

Sodium potassium ATPases

There are Na+/K+ atpases in the ———– membrane pushing – sodium — of the cell and into the —– and bringing – potassium – the cell.

This maintains a high ——– sodium concentration and low —— sodium concentration.

There is always less Na in the —, so there is always a drive for Na —- the cell.

This provides a force for sodium diffusion from the ——- across the —– membrane.

The transport is mediated by sodium ——– transporters.

A

There are Na+/K+ atpases in the apical membrane pushing 3 sodium out of the cell and into the ECF and bringing 2 potassium into the cell.

This maintains a high extracellular sodium concentration and low intracellular sodium concentration.

There is always less Na in the cell, so there is always a drive for Na into the cell.

This provides a force for sodium diffusion from the lumen across the apical membrane.

The transport is mediated by sodium coupled transporters.

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49
Q

Na/glucose or Na/amino acid co transporters

The ———- ——– makes sure there is —— sodium within the cell.

There is a —- for sodium to move — the cell.

When sodium moves —- it co transports glucose via ——-.

The glucose moves out of the cell and into the blood via —–.

A

The Na/K ATPase makes sure there is low sodium within the cell.

There is a gradient for sodium to move into the cell.

When sodium moves in it co transports glucose via SGLT.

The glucose moves out of the cell and into the blood via GLUT2.

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50
Q

Na-H exchanger

The ———- ——– makes sure there is —— sodium within the cell.

There is a —- for sodium to move — the cell.

When sodium moves —- there is an exchange of hydrogen —— of the cell.

Theses exchangers are found on both the apical and basolateral membrane

A

The Na/K ATPase makes sure there is low sodium within the cell.

There is a gradient for sodium to move into the cell.

When sodium moves in there is an exchange of hydrogen out of the cell.

Theses exchangers are found on both the apical and basolateral membrane

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51
Q

Parallel Na-H and Cl-HCO3 exchangers

The ———- ——– makes sure there is —— sodium within the cell.

There is a —- for sodium to move — the cell.

When sodium moves —- there is an exchange of hydrogen —— of the cell.

Sodium is positively charged and chloride is negatively charged so when sodium moves — the cell via Na-H exchangers chloride also moves —- the cell via Cl - HCO3 exchangers.

When hydrogen and bicarbonate move into the —- they form ——– which is unstable and breaks into — and —-.

A

Parallel Na-H and Cl-HCO3 exchangers

The Na/P ATPase makes sure there is low sodium within the cell.

There is a gradient for sodium to move into the cell.

When sodium moves in there is an exchange of hydrogen out of the cell.

Sodium is positively charged and chloride is negatively charged so when sodium moves into the cell via Na-H exchangers chloride also moves into the cell via Cl - HCO3 exchangers.

When hydrogen and bicarbonate move into the lumen they form H2CO3 which is unstable and breaks into H2O and CO2.

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52
Q

Epithelial sodium channels

The ———- ——– makes sure there is —— sodium within the cell.

There is a —- for sodium to move — the cell.

Sodium moves —- the cell via specific sodium channels.

A

The Na/K ATPase makes sure there is low sodium within the cell.

There is a gradient for sodium to move into the cell.

Sodium moves into the cell via specific sodium channels.

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53
Q

How is chloride absorbed?

A

Linked to Na absorption (Na-H and Cl-HCO3 exchangers)

Paracellular across tight junctions- passive absorption

Cl-HCO3 transporter - active

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54
Q

How is potassium absorbed?

A

Passive paracellular

Active - hydrogen potassium exchangers

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55
Q

How is potassium secreted?

A

Passive - paracellular

Active (large intestine) - Via BK channels

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56
Q

What will happen if you have some disease in your large intestine causing active fluid loss?

A

BK channels will actively secrete potassium.

There is loss of water and potassium ions leading to hypokalemia

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57
Q

Chloride secretion

In the ——– membrane —— —— push – sodium —- of the cell and — potassium —- the cell.

Epthelial channels in the —– membrane move the —- —— ions back — of the cell.

The ——- channel in the ——– membrane brings —, — and —- into the cell.

In the —– membrane the —– secretes ——– into the lumen. Sodium and water enters the lumen via ——– transport.

It is driven by —- ions and —— (second messenger)

Results in fluid and ion loss from the —– due to increased activation of —-.

A

In the basolateral membrane Na/K ATPases push 3 sodium out of the cell and 2 potassium into the cell.

Epthelial channels in the basolateral membrane move the 2 potassium ions back out of the cell.

The NKCC1 channel in the basolateral membrane brings Na, 2Cl and K into the cell.

In the apical membrane the CFTR secretes chloride into the lumen. Sodium and water enters the lumen via paracellular transport.

It is driven by calcium ions and cAMP (second messenger - signals CFTR to be placed into the membrane)

Results in fluid and ion loss from the ECM due to increased activation of CFTR.

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58
Q

What happens during cystic fibrosis?

A

Lack of CFTR = no secretion of chloride and therefore no secretion of sodium

Results in dense secretion and respiratory problems

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59
Q

The —– intestine is a net absorber of water, sodium, chloride and potassium but it is a net secretor of bicarbonates

A

Small intestine

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60
Q

The —— intestine carries out net absorption of water, sodium and chloride with few exceptions, but it carries out net secretion of potassium and bicarbonate

A

Large intestine

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61
Q

The dysfunction of fluid absorption in the GI tract leads to ———-

A

Diarrhoea

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62
Q

Would the volume of diarrhoea be larger if a dysfunction in the GI tract occurred in the small or large intestine?

A

Small intestine

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63
Q

—— diarrhoea results from disturbances of absorption.

The amount of —– consumed is not able to be processed by the body.

—— is retained in the —– of the intestine causing an increase in ——- —— so —– is retained in the ———. This is due to ——- intolerance (lack of the enzyme —–).

Increased volume of ——– enters the colon and may overwhelm the ability of the colon to absorb ——- from it. Leads to pronounced diarrhoea.

An ——– reaction to gluten results in the destruction of the —— cells and if severe the —-. This causes nutrient malabsorption. There is an ——- in osmotic pressure in the ——– and water is —— in the lumen. This is due to coeliac disease.

A

Osmotic diarrhoea results from disturbances of absorption.

The amount of sugar consumed is not able to be processed by the body.

Sugar is retained in the lumen of the intestine causing an increase in osmotic pressure so water is retained in the lumen. This is due to lactose intolerance (lack of the enzyme lactase).

Increased volume of chyme enters the colon and may overwhelm the ability of the colon to absorb water from it. Leads to pronounced diarrhoea.

An autoimmune reaction to gluten results in the destruction of the epithelial cells and if severe the villi. This causes nutrient malabsorption. There is an increase in osmotic pressure in the lumen and water is retained in the lumen. This is due to Coeliac disease.

64
Q

——– diarrhoea results from disturbances in secretion.

Elevation of ———- activity of cells in unidirectional secretory flux may exceed unidirectional ——— flux and net secretion prevails.

Cholera toxin permanently activates —— ——— thereby causing an elevation of ——– which in turn opens the —- channel in the apical membrane of the crypt epithelial cells. This causes a prolonged secretion of —–, —- and —– which can be fatal.

Enterotoxins produced by the bacterial microorganism raise intracellular —–, —– or —– leading to the stimulation of — secretion.

A

Secretory diarrhoea results from disturbances in secretion.

Elevation of secretory activity of cells in unidirectional secretory flux may exceed unidirectional absorptive flux and net secretion prevails.

Cholera toxin permanently activates adenylate cyclase thereby causing an elevation of cAMP which in turn opens the Cl channel in the apical membrane of the crypt epithelial cells. This causes a prolonged secretion of Cl, Na and water which can be fatal.

Enterotoxins produced by the bacterial microorganism raise intracellular cAMP, cGMP or calcium ions, leading to the stimulation of Cl secretion

65
Q

How can we treat diarrhoea?

A

Oral rehydration solution

When you have diarrhoea the glucose transporters are not affected so if a solution with sodium and glucose is given, when sodium moves into the cell it takes glucose with it. Chloride follows and bicarbonate (to combat acidosis)

66
Q

Molecules containing hydrogen atoms that can release hydrogen ions in solutions are referred to as —-.

A

Acids

67
Q

A —- is an ion or a molecule that can accept an H+

A

Base

68
Q

Proteins in the body also function as ——- because some of the amino acids that make up proteins have a net —— charge that readily accepts H+.

A

Proteins in the body also function as base because some of the amino acids that make up proteins have a net negative charge that readily accepts H+.

69
Q

What is the normal pH of atrial blood?

A

7.4

70
Q

Is the pH of venous blood and interstitial fluid above the normal atrial blood pH or below?

A

Below because of the extra amounts of carbon dioxide released from the tissues to form H2CO3 in these fluids.

71
Q

Is the pH of venous blood and interstitial fluid above the normal atrial blood pH or below?

A

Below because of the extra amounts of carbon dioxide released from the tissues to form H2CO3 in these fluids.

72
Q

A person is considered to have acidosis when the pH falls below ——- (addition of H+) and to have alkalosis when the pH rises above —– (removal of H+)

A

A person is considered to have acidosis when the pH falls below 7.4 (addition of H+) and to have alkalosis when the pH rises above 7.4 (removal of H+)

73
Q

Name the mechanisms of pH control from immediate reaction to slow reaction.

A

Acid-Base buffer system

Respiratory center

Kidneys

74
Q

Acid base buffer system

The chemical acid-base buffer system of the body fluids, immediately combine with —- or —- to prevent excessive changes in —- concentration.

This is the —- line of defense.

When there is a change in — concentration, the buffer systems of the body fluids react within seconds to —— these changes.

Buffer systems do not eliminate —- from or add them to the body but only keep them tied up until balance can be re-established.

A

The chemical acid-base buffer system of the body fluids, immediately combine with acid or base to prevent excessive changes in H+ concentration.

This is the first line of defence.

When there is a change in H+ concentration, the buffer systems of the body fluids react within seconds to minimise these changes.

Buffer systems do not eliminate H+ from or add them to the body but only keep them tied up until balance can be re-established.

75
Q

Acid base buffer system

The chemical acid-base buffer system of the body fluids, immediately combine with —- or —- to prevent excessive changes in —- concentration.

This is the —- line of defense.

When there is a change in — concentration, the buffer systems of the body fluids react within seconds to —— these changes.

Buffer systems do not eliminate —- from or add them to the body but only keep them tied up until balance can be re-established.

A

The chemical acid-base buffer system of the body fluids, immediately combine with acid or base to prevent excessive changes in H+ concentration.

This is the first line of defence.

When there is a change in H+ concentration, the buffer systems of the body fluids react within seconds to minimise these changes.

Buffer systems do not eliminate H+ from or add them to the body but only keep them tied up until balance can be re-established.

76
Q

The respiratory center

Regulates the removal of —— and therefore ——–, from the ——— fluid.

This is the ——- line of defence.

A

Regulates the removal of CO2 and therefore H2CO3, from the extracellular fluid.

This is the second line of defence.

77
Q

The kidneys

Can excrete either —– or —– urine, thereby readjusting the ———- fluid — concentration toward normal during acidosis or alkalosis.
This is the last line of defense

Although the kidneys are relatively slow to respond compared with the other defenses, over a period of hours to several days, they are by far the most powerful of the acid—base regulatory systems.

A

Can excrete either acidic or basic urine, thereby readjusting the extracellular fluid H+ concentration toward normal during acidosis or alkalosis.

This is the last line of defense

78
Q

The more ——– ions the greater the pH.

A

The more bicarbonate ions (HCO3-) the greater the pH (pH is directly proportional to HCO3-)

79
Q

Higher ——- the lower the pH

A

Higher Pco2 the lower the pH (pH is inversely proportional to Pco2)

80
Q

Name the buffer systems.

A

Bicarbonate buffers
phosphate buffers
Proteins

81
Q

———- buffers are ubiquitous, act fast to sort out pH but are not strong.

A

Bicarbonate buffers

82
Q

——– buffers are limited to the kidney tubules but are strong buffers

A

Phosphate buffers

83
Q

Bicarbonate buffer

H2CO3 is an unstable compound so it breaks down into __ and ____

If there is an increase in _, they will combine with ______ to produce ____ which will then dissociate into ____ and ____, catalysed by —– —–. (breathe faster to remove CO2)

For alkalines (NaOH) combines with H2CO3 to form an inert compound (NaHCO3) and water.

Bicarbonate buffer system to be powerful, for two reasons:

First, the pH of the extracellular fluid is about 7.4, whereas the pK of the bicarbonate buffer system is 6.1 (the best pH at which the buffer exists as both a base and acid). This means that there is about 20 times as much of the bicarbonate buffer system in the form of HCO3 (acidic)— as in the form of dissolved CO2 (basic). For this reason, this system operates on the portion of the buffering curve where the slope is low and the buffering power is poor.

Second, the concentrations of the two elements of the bicarbonate system, CO2 and HCO3, are not great.

A

H2CO3 is an unstable compound so it breaks down into H+ and HCO3-

If there is an increase in H+, they will combine with bicarbonate to produce H2CO3 which will then dissociate into CO2 and H20, catalysed by carbonic anhydrase. (breathe faster to remove CO2)

For alkalines (NaOH) combines with H2CO3 to form an inert compound (NaHCO3) and water.

Bicarbonate buffer system to be powerful, for two reasons:

First, the pH of the extracellular fluid is about 7.4, whereas the pK of the bicarbonate buffer system is 6.1 (the best pH at which the buffer exists as both a base and acid). This means that there is about 20 times as much of the bicarbonate buffer system in the form of HCO3— as in the form of dissolved CO2. For this reason, this system operates on the portion of the buffering curve where the slope is low and the buffering power is poor.

Second, the concentrations of the two elements of the bicarbonate system, CO2 and HCO3, are not great.

84
Q

In our body we are basic at a pH of — so the buffer is operating at that pH, so it exists more as a —– rather than as an —— so it’s not that powerful because it doesn’t exist in equal amounts of acid and base

This is a limiting factor

A

In our body we are basic at a pH of 7.4 so the buffer is operating at that pH, so it exists more as a base rather than as an acid so it’s not that powerful because it doesn’t exist in equal amounts of acid and base

85
Q

Phosphate buffers

The main elements of the phosphate buffer system are —- and —–.

The buffer system has a pk of —-.

The phosphate buffer is especially important in the —- fluids of the —-.

The phosphate buffer is especially important in the —— fluids of the ——-, for two reasons:

(1) phosphate usually becomes greatly ———- in the tubules, thereby ——- the buffering power of the phosphate system
(2) the tubular fluid usually has a —— pH than the extracellular fluid does, bringing the operating range of the buffer —— to the pK (6.8) of the system.

A

The main elements of the phosphate buffer system are H2PO4- and HPO4-.

The buffer system has a pk of 6.8.

The phosphate buffer is especially important in the tubular fluids of the kidney.

The phosphate buffer is especially important in the tubular fluids of the kidney, for two reasons:

(1) Phosphate usually becomes greatly concentrated in the tubules, thereby increasing the buffering power of the phosphate system
(2) The tubular fluid usually has a lower pH than the extracellular fluid does, bringing the operating range of the buffer closer to the pK (6.8) of the system.

86
Q

Respiratory regulation of acid-base balance

Acts rapidly and keeps the — concentration from changing too much until the slowly responding —— can eliminate the imbalance

It is one to 2 times greater as the buffering power of all other chemical buffers. So 1 to 2 times as much acid and base can normally be buffered by this mechanism.

A

Acts rapidly and keeps the H+ concentration from changing too much until the slowly responding kidneys can eliminate the imbalance

87
Q

Respiratory regulation of acid-base balance

increased alveolar ventilation,

——- removal of CO2 so
——– partial pressure of CO2, so ———- CO2 combining with water, ———- carbonic acid, ——— H+ concentration in the extracellular fluid and — back to normal
This is the —– line of defense, which controls extracellular fluid —– concentration by the lungs.

Changes in either ——– ventilation or the rate of —– formation by the tissues can change the extracellular fluid —–.

A

Respiratory regulation of acid-base balance

increased alveolar ventilation,
increased removal of CO2 so decreased partial pressure of CO2, so decreased CO2 combining with water, decreased carbonic acid, decreased H+ concentration in the extracellular fluid and pH back to normal

This is the second line of defense, which controls extracellular fluid CO2 concentration by the lungs.

Changes in either pulmonary ventilation or the rate of CO2 formation by the tissues can change the extracellular fluid PCO2.

88
Q

Respiratory regulation of acid-base balance

increased alveolar ventilation,

——- removal of CO2 so
——– partial pressure of CO2, so ———- CO2 combining with water, ———- carbonic acid, ——— H+ concentration in the extracellular fluid and — back to normal
This is the —– line of defense, which controls extracellular fluid —– concentration by the lungs.

Changes in either ——– ventilation or the rate of —– formation by the tissues can change the extracellular fluid —–.

A

Respiratory regulation of acid-base balance

increased alveolar ventilation,
increased removal of CO2 so decreased partial pressure of CO2, so decreased CO2 combining with water, decreased carbonic acid, decreased H+ concentration in the extracellular fluid and pH back to normal

This is the second line of defense, which controls extracellular fluid CO2 concentration by the lungs.

Changes in either pulmonary ventilation or the rate of CO2 formation by the tissues can change the extracellular fluid PCO2.

89
Q

Increase in ventilation ——- pH

Decrease in ventilation ——– pH

The normal rate of alveolar ventilation is —-. At this rate the change in pH of body fluids is —.

The alveolar ventilation rate doesn’t change much during changes in atrial blood pH from 7.4 to 7.2 because of the acting ——-.

A

Increase in ventilation increases pH

Decrease in ventilation decreases pH

The normal rate of alveolar ventilation is 1. At this rate the change in pH of body fluids is 0.

The alveolar ventilation rate doesn’t change much during changes in atrial blood pH from 7.4 to 7.2 because of the acting buffers.

90
Q

How does the kidney regulate pH?

A

Secretion of H+

Reabsorption of filtered HCO3-

Production of new HCO3-

91
Q

kidney regulation of pH

Secretion of H+

There are ——- ——- (3 Na out, 2K in), there is always a drive for sodium to move —- the cell

There is a filtrate in the tubular lumen, there is sodium and bicarbonates (phosphate buffers) filtering in.

The sodium is taken — the cell and a — ion is exchanged into the lumen via Na/H+ exchangers, which then goes onto combine with the ————- to form H2CO3, which then dissociates into —— and ——-.

The —— then goes into the cell and combines with —— to produce H2CO3 which dissociates into ——- and —-, with the ——- moving out of the cell and into the blood

It’s complicated because the kidney doesn’t have a system that can actively reabsorb bicarbonates

A

There are Na/K ATPases (3 Na out, 2K in), there is always a drive for sodium to move into the cell

There is a filtrate in the tubular lumen, there is sodium and bicarbonates (phosphate buffers) filtering in.

The sodium is taken into the cell and a H+ ion is exchanged into the lumen via Na/H+ exchangers, which then goes onto combine with the bicarbonate to form H2CO3, which then dissociates into CO2 and H20.

The CO2 then goes into the cell and combines with H20 to produce H2CO3 which dissociates into HCO3- and H+, with the HCO3- moving out of the cell and into the blood

92
Q

kidney regulation of pH

Active secretion of H+

When there is a lot of acid in the body it actively secretes __ ions

This is done via —-exchangers, which are secondary active transporters turning ATP to ADP when removing the —— into the lumen

The bicarbonate goes back into the cell

A

When there is a lot of acid in the body it actively secretes H+ ions

This is done via H/Cl exchangers, which are secondary active transporters turning ATP to ADP when removing the H+ into the lumen

The bicarbonate goes back into the cell

93
Q

kidney regulation of pH

Addition of new HCO3-

There are ——— ——-(3 Na out, 2K in), there is always a drive for sodium to move —- the cell

There is a filtrate in the tubular lumen, there is phosphate buffers filtering in, the —- is taken into the cell and a — ion is exchanged into the lumen (sodium hydrogen exchangers), which then goes onto combine with ——- to form NaH2PO4, which is excreted out of the body.

The —- in the blood goes into the cell and combines with —— to produce H2CO3 which dissociates into —- and —-, with the HCO3- moving out of the cell and into the blood.

A

There are Na/K ATPases (3 Na out, 2K in), there is always a drive for sodium to move into the cell

There is a filtrate in the tubular lumen, there is phosphate buffers filtering in, the sodium is taken into the cell and a H+ ion is exchanged into the lumen (sodium hydrogen exchangers), which then goes onto combine with NaHPO4- to form NaH2PO4, which is excreted out of the body.

The CO2 in the blood goes into the cell and combines with water to produce H2CO3 which dissociates into HCO3- and H+, with the HCO3- moving out of the cell and into the blood.

94
Q

kidney regulation of pH

Addition of new HCO3-

Glutamine dissociates into —- and —– ions which get exchanged into the lumen with sodium ions.

The —- and — gets lost in the urine

The body gains – bicarbonate ions

A

Glutamine dissociates into HCO3- and NH4+ ions which get exchanged into the lumen with sodium ions.

The NH4+ and Cl gets lost in the urine

The body gains 2 bicarbonate ions

95
Q

Respiratory acidosis (pCO2)

The pH is ——– 7.4

There is ——- H+

There is ——– PCO2

A

The pH is below 7.4

There is increased H+

There is increased PCO2

96
Q

Respiratory alkalosis (PCO2)

The pH is ——- 7.4.

There is ——- H+.

There is ——- PO2.

A

The pH is above 7.4

There is decreased H+

There is decreased PCO2

97
Q

Metabolic acidosis (HCO3-)

The pH is ——- 7.4

There is —– H+.

There is ——– HCO3-

A

The pH is below 7.4

There is increased H+.

There is decreased HCO3-

98
Q

Metabolic alkalosis (HCO3-)

The pH is ——- 7.4

There is —– H+.

There is ——– HCO3-

A

The pH is above 7.4

There is decreased H+.

There is increased HCO3-

99
Q

What is the function of the kidney?

A

Maintains homeostasis of hydration. blood volume and pressure

100
Q

If you drink more water than you need the excess volume is excreted as ——.

If you drink less water than you need, you try and —– the fluid ingested to maintain ——.

A

If you drink more water than you need the excess volume is excreted as urine.

If you drink less water than you need, you try and reabsorb the fluid ingested to maintain homeostasis.

101
Q

What is the normal intake and output of the kidney?

A

2300ml/day and 900 output respectively

102
Q

What is the outer part of the kidney called?

A

Cortex

103
Q

What is the inside of the kidney called?

A

Medulla

104
Q

What is the functional unit of the kidney?

A

Nephrons

105
Q

The afferent arteriole goes —– the bowman’s capsule.

The efferent arteriole goes —- the bowman’s capsule.

A

The afferent arteriole goes into the bowman’s capsule.

The efferent arteriole goes out the bowman’s capsule.

106
Q

What are the two types of nephrons?

Whats the difference between them?

A

Cortical - have small loop of henle’s

Juxtamedullary - long loop of henle’s

107
Q

What is glomerular filtration rate (GFR)?

A

The rate at which fluid which is virtually free of protein is filtered from the glomerular capillaries into Bowman’s capsule.

108
Q

What is the normal average GFR?

A

125 ml/min or 144-180L/day

109
Q

Most substances in the plasma are freely filtered so the concentration of the glomerular filtrate in the bowman’s capsule is almost the ——- as the plasma.

As the filtrate passes through the ———, it is modified by both the ———– of water and certain solutes back into the blood as well as by the ——— of substances from the peritubular capillaries into the tubules thereby forming urine

A

Most substances in the plasma are freely filtered so the concentration of the glomerular filtrate in the bowman’s capsule is almost the same as the plasma.

As the filtrate passes through the nephron, it is modified by both the reabsorption of water and certain solutes back into the blood as well as by the secretion of substances from the peritubular capillaries into the tubules thereby forming urine.

110
Q

Subtle changes in —– can lead to relatively —– changes in renal excretion if the tubular ——- remained constant.

A

Subtle changes in GFR can lead to relatively large changes in renal excretion if the tubular reabsorption remained constant.

111
Q

If the pressure in the ——- is greater than the pressure in the —— you get filtration

A

If the pressure in the capillaries is greater than the pressure in the capsule you get filtration

112
Q

What pressures make up the GFR?

A

Hydrostatic pressure

Osmotic pressure

glomerular capillary filtration coefficient

113
Q

When the efferent arteriole constricts there is an increase ——- in the glomerulus resulting in the GFR ——-.

When the afferent arteriole constricts —– fluid will be filtered

A

When the efferent arteriole constricts there is an increased pressure in the glomerulus resulting in the GFR increasing.

When the afferent arteriole constricts less fluid will be filtered

114
Q

What mechanism of GFR control is described below?

The concentration of —— and —— in the ——- tubule is sensed by the —– —— cells.

If the GFR is high the concentration of — and —- would be —– causing the —- ——- cells to ——. This is sensed by the ——– arteriole and as a result it ———- to ——- the GFR.

If the GFR is low the concentration of — and —-would be —– causing the — —– cells to ——-. This is sensed by the —— arteriole and as a result it ———- to ——- the GFR.

This is a —— feedback system

This is an ——- mechanism and is called ————- Feedback

A

The concentration of Na and Cl in the distal tubule is sensed by the macula densa cells.

If the GFR is high the concentration of Na and Cl would be high causing the macula densa cells to swell. This is sensed by the afferent arteriole and as a result it vasoconstricts to decrease the GFR.

If the GFR is low the concentration of Na and Cl would be low causing the Macula densa cells to shrink. This is sensed by the afferent arteriole and as a result it vasodilates to increase the GFR.

This is a negative feedback system

This is an intrinsic mechanism and is called tubuloglomerular Feedback

115
Q

Is the afferent or efferent arteriole more innervated by the sympathetic nerves?

A

Afferent arteriole

116
Q

Sympathetic nerve innervation and GFR.

There are —- types of sympathetic fibres that innervate the kidney.

Type 1 fibres innervate just the —— arteriole, while type 2 innervates —– and ——– arterioles. As a result the —— arteriole is more innervated than the ——- and therefore will ———– more than the ——–, so more blood passes through and doesn’t get ——.

When you want to retain fluid the sympathetic nerve activity ——— and GFR —–.

If you want to get rid of fluid sympathetic nerve activity —— and GFR ——-.

If you lose blood volume there is an ——– in sympathetic nerve activity causing ————, of the ——- arteriole, ——— GFR, increasing —– —-, therefore not allowing a lot of fluid to be ——–.

Increase in fluid consumption causes a ——— in renal sympathetic nerve activity, causing ———- of the ——– arteriole (efferent doesn’t open up much), ——– GFR and all the fluid is filtered into bowman’s capsule

A

Sympathetic nerve innervation and GFR.

There are 2 types of sympathetic fibres that innervate the kidney.

Type 1 fibres innervate just the afferent arteriole, while type 2 innervates afferent and efferent arterioles. As a result the afferent arteriole is more innervated than the efferent and therefore will vasoconstrict more than the efferent, so more blood passes through and doesn’t get filtered.

When you want to retain fluid the sympathetic nerve activity increases and GFR decreases.

If you want to get rid of fluid sympathetic nerve activity decreases and GFR increases.

If you lose blood volume there is an increase in sympathetic nerve activity causing vasocontriction, of the afferent arteriole, decreaseing GFR, increasing blood pressure, therefore not allowing a lot of fluid to be filtered.

Increase in fluid consumption causes a decrease in renal sympathetic nerve activity, causing vasodilation of the afferent arteriole (efferent doesn’t open up much), increase GFR and all the fluid is filtered into bowman’s capsule

117
Q

Tubular reabsorption

The —- passes along a tube that has ——– that are impermeable to urea.

——- moves into the cell or intercellular space and gets reabsorbed by the ——– capillary.

——- passes through via osmosis because of the higher —- pressure in the —– than in the —— fluid.

The cell has —- Na and —-K due to the ——– ——- in the basolateral membrane.

The cell has a ——— potential of ——.

A

The filtrate passes along a tube that has aquaporens that are impermeable to urea.

Na+ moves into the cell or intercellular space and gets reabsorbed by the peritubular capillary.

water passes through via osmosis because of the higher osmotic pressure in the lumen than in the interstitual fluid.

The cell has low Na and high K due to the Na/K ATPase in the basolateral membrane.

The cell has a negative potential of -70mV.

118
Q

Secondary active reabsorption

The —— gradient is maintained by the —- ——–.

The ——- ———– cotransporter, ——–, brings ——- and —– into the cell. The ——- then leaves the cell via ——- and gets absorbed into the capillaries.

A

The sodium gradient is maintained by the Na/K ATPase.

The sodium glucose cotransporter, SGLT, brings sodium and glucose into the cell. The glucose then leaves the cell via GLUT and gets absorbed into the capillaries.

119
Q

In the first 1/4 of the proximal convoluted tubule most of the —– and ——- acids are reabsorbed.

A lot of —— is reabsorbed but the concentration remains the same because —— is being dragged along with it.

A

In the first 1/4 of the proximal convoluted tubule most of the glucose and amino acids are reabsorbed.

A lot of sodium is reabsorbed but the concentration remains the same because water is being dragged along with it.

120
Q

Glucose filtration

All the glucose gets ——-.

You are trying to ——– the glucose using the —– —— co transporter, but it can only go so fast.

At some point it cannot ——- at a faster rate so it starts ——– down

Once it starts slowing down glucose starts to show in the ——–, dragging ——with it, ——– urine output

At some point your glucose transporter becomes ———, your plasma glucose levels still ———, so you start —— glucose.

A

All the glucose gets filtered.

You are trying to reabsorb the glucose using the sodium glucose co transporter, but it can only go so fast.

At some point it cannot reabsorb at a faster rate so it starts slowing down

Once it starts slowing down glucose starts to show in the urine, dragging water with it, increasing urine output

At some point your glucose transporter becomes saturated, your plasma glucose levels still increase, so you start excreting glucose.

121
Q

At the end of the proximal tubule

Around –% of the tubular fluid from the glomerulus has been ———-.

This means a decrease from —L/hr to around — L/hr.

There has been no change in ——- concentration because —– passively follows the —–.

All of the ——– and —— acids have been reabsorbed

The tubular fluid is also ——- with the initial filtrate - missing osmoles (sodium) is replaced by ——

Urea concentration is ~ 2-4x higher than it was in the original glomerular filtrate (and ECF of course) because the proximal convoluted tubule is impermeable to urea

A

Around 80% of the tubular fluid from the glomerulus has been reabsorbed.

This means a decrease from 6L/hr to around 1.2 L/hr.

There has been no change in sodium concentration because water passively follows the sodium.

All of the glucose and amino acids have been reabsorbed

The tubular fluid is also isoosmoitic with the initial filtrate - missing osmoles (sodium) is replaced by urea.

Iso-osmotic; the missing osmoles are made up by urea (the number of osmoles per unit solution is the same at the end of the proximal convoluted tubule as at the beginning even though the total volume is less by about 80%

Urea concentration is ~ 2-4x higher than it was in the original glomerular filtrate (and ECF of course) because the proximal convoluted tubule is impermeable to urea

122
Q

The thin descending part of the loop of henle is permeable to —— but the thick ascending part is not

A

The thin descending part of the loop of henle is permeable to water but the thick ascending part is not

123
Q

The thick ascending limb of the loop of Henle

The remaining —– is reabsorbed and the excess —— is reabsorbed via the ——-

A

The remaining potassium is reabsorbed and the excess Cl is reabsorbed via the sodium, potassium, chloride co transporter.

124
Q

Counter current mechanism

There is no initial ——— gradient in the kidney’s interstitial fluid, the osmolarity is —– mOsm/L throughout the interstitium. This is the —– as the osmolarity of normal body fluids, including the fluid moving inside the —- of ——.
——- is transported out of the ———- limb of the loop of Henle and accumulates in the ——— interstitium. —— exits the —— ascending limb by ——- ——–, and is pumped out of the ——– ascending limb by the ———- cotransporter. The ——— ascending limb is ———- to water, so water stays ——- the loop of henle and the osmolarity of the —— ascending fluid ——-. The —– is added to the interstitial fluid, ———— its osmolarity. This creates a —– mOsm/L difference in the osmolarities of the ——— fluid and the fluid in the —— ascending limb.
——- then diffuses out of the — ——— limb until the fluid there has equilibrated with the ——– fluid at ——- mOsm/L.
Once the ————- limb has equilibrated, —— mOsm/L fluid from the proximal tubule enters the top of the ———– limb. This pushes the ——- osmolarity fluid below it down towards the hairpin curve in the loop of Henle.
The osmolarities of the fluids in the ———– limb and the interstitium are once again mismatched due to —– leaving the —— limb and the movement of fluid in the tube. This causes ——- to leave the ——- limb until the two fluids have re-equilibrated.
You can see a corticopapillary gradient starting to appear. Interstitial fluid in the cortex has an osmolarity of —— mOsm/L, while the papillary interstitial fluid is —— mOsm/L
Steps __-__ are repeated, with each cycle enhancing the ———. At its maximum, the gradient reaches —— mOsm/L between the —— and the inner ——-.

A
  1. There is no initial osmotic gradient in the kidney’s interstitial fluid, the osmolarity is uniform mOsm/L throughout the interstitium. This is the same as the osmolarity of normal body fluids, including the fluid moving inside the tubules of nephrons.
  2. Sodium is transported out of the thin descending limb of the loop of Henle and accumulates in the medullary interstitium. Sodium exits the thick ascending limb by active transport, and is pumped out of the thick ascending limb by the sodium-potassium cotransporter. The thick ascending limb is impermeable to water, so water stays in the loop of Henle and the osmolarity of the ascending fluid increases. The sodium is added to the interstitial fluid, increasing its osmolarity. This creates a 200 mOsm/L difference in the osmolarities of the tubular fluid and the fluid in the thick ascending limb.
  3. Sodium then diffuses out of the thin descending limb until the fluid there has equilibrated with the interstitial fluid at 300 mOsm/L.
  4. Once the thin descending limb has equilibrated, 300 mOsm/L fluid from the proximal tubule enters the top of the thin ascending limb. This pushes the lower osmolarity fluid below it down towards the hairpin curve in the loop of Henle.
  5. The osmolarities of the fluids in the thin ascending limb and the interstitium are once again mismatched due to sodium leaving the thin limb and the movement of fluid in the tube. This causes sodium to leave the thin limb until the two fluids have re-equilibrated.
  6. You can see a corticopapillary gradient starting to appear. Interstitial fluid in the cortex has an osmolarity of 300 mOsm/L, while the papillary interstitial fluid is 1200 mOsm/L
    Steps 2-5 are repeated, with each cycle enhancing the gradient. At its maximum, the gradient reaches 1200 mOsm/L between the cortex and the inner medulla.
125
Q

The longer the loop of henle you have the greater the —– gradient you will achieve, so the ——- the concentration of the —–.

A

The longer the loop of henle you have the greater the osmotic gradient you will achieve, so the higher the concentration of the urine.

126
Q

What can you change to allow more fluid to be retained/ less urine?

A

The longer the loop of henle, the higher the concentration

Change how well or how much the sodium potassium chloride cotransporter there is in the thick ascending limb

127
Q

What are some signs of dehydration?

A

Thirst
Fatigue
Dry mouth
Concentrated urine

128
Q

Osmoreceptors

Monitor —– deficit

These are specialised cells that sit in the —— —– of the ———, in close contact with ——– that run through the ———. In response to changes in ——– they can —— or ——–, which changes the ——- activity of these cells which signal the supraoptic neurons to release —–.

A

Monitor water deficit

These are specialised cells that sit in the posterior pituitary of the hypothalamus, in close contact with capillaries that run through the hypothalamus. In response to changes in osmolarity they can expand or shrink, which changes the electrical activity of these cells which signal the supraoptic neurons to release ADH.

129
Q

Antidiuretic hormone (ADH)/Vassopression (AVP)

ADH is manufactured and secreted from the ——- —– of the ——–.

ADH travels down to the —— and binds to — receptors which cause insertions of ——- on the —— —— side, allowing —— to move along its concentration gradient and into the —— interstitial fluid to be absorbed into the ———.

If actions of ADH are impaired (low ADH) it can result in either —— or ——– diabetes insipidus.

——– diabetes insipidus - the pituitary is unable to ——- ADH

———- diabetes insipidus - have the ——– amounts of ADH but the ——— in the kidney do not work.

A

ADH is manufactured and secreted from the posterior pituitary of the hypothalamus.

ADH travels down to the kidney and binds to V2 receptors which cause insertions of aquaporens on the tubular lumen side, allowing water to move along its concentration gradient and into the interstitial fluid to be absorbed into the capillaries.

If actions of ADH are impaired (low ADH) it can result in either central or nephrogenic diabetes insipidus.

Central diabetes insipidus - the pituitary is unable to secrete ADH

Nephrogenic diabetes insipidus - have the right amounts of ADH but the receptors in the kidney do not work.

130
Q

Why are there high levels of ADH in heart failure?

A

The heart isn’t beating well, so isn’t perfusing blood to all of its organs, forcing the body to vasoconstrict and keep pressure up and retain as much water as it can.
The high levels of ADH are in response to trying to retain water

131
Q

Does an increase in osmolarity increase ADH levels?

A

Yes

132
Q

Does a decrease in blood volume increase ADH levels?

A

Yes

133
Q

Does an increase in ADH levels result in dilute urine?

A

No

134
Q

ngiotensin and aldosterone

Angiotensinogen gets formed to ———— by the actions of —– which is secreted by the —– cells in the kidneys.

——– is the rate limiting factor - the more —– you have the more ——– you have.

———- gets converted into ——– by the ——– —– enzymes (ACE) in the ——–.

———- can bind to a ——(causes vasoconstriction) or ——- (reabsorption of sodium and water) receptor

Angiotensin 2 activates the —- —— exchanger on the ——- membrane as well as the —– ——— on the —— membrane. Both of these cause ——- to be ———- from the ——- lumen to the ———- space and then into the ——— and the ——– follows

There are about 95% —- receptors and 5% —— receptors, so if ———- binds to both receptors the action of the —– receptor will be expressed almost all the time

So when you inject —– or ——- you get ——— blood pressure

——– can bind to certain cells in the ———- medulla and produce ———-

———- binds to the ——— (MR) receptor and causes insertion of —— channels, which cause reabsorption of ——- into the interstitial fluid

A

Angiotensinogen gets formed to angiotensin 1 by the actions of renin which is secreted by the granular cells in the kidneys.

renin is the rate limiting factor - the more renin you have the more angiotensin 1 you have.

Angiotensin 1 gets converted into angiotensin 2 by the enzymes (ACE) in the lungs.

Angiotensin 2 can bind to a AT1 (causes vasoconstriction) or AT2 (reabsorption of sodium and water) receptors.

Angiotensin 2 activates the sodium hydrogen exchanger on the apical membrane as well as the sodium potassium ATPase on the basolateral membrane. Both of these cause sodium to be reabsorbed from the tubular lumen to the interstitial space and then into the capillaries and the water follows

There are about 95% AT1 receptors and 5% AT2 receptors, so if angiotensin 2 binds to both receptors the action of the AT1 receptor will be expressed almost all the time

So when you inject renin or angiotensin 2 you get increased blood pressure

Angiotensin 2 can bind to certain cells in the adrenal medulla and produce aldosterone

Aldosterone binds to the mineralocorticoid (MR) receptor and causes insertion of ENac channels, which cause reabsorption of sodium into the interstitial fluid

135
Q

What factors determine renin release from the granular cells in the kidney?

A

Afferent arteriolar pressure

Macula densa NaCl delivery

Sympathetic nerve activity

136
Q

Renin release

Renin promotes increased ——- —– via ———.

If blood pressure is high, there will be ——– renin release.

If blood pressure is low, there will be ——- renin release.

If there is decreased Na concentration in the —– —- cells, there will be ——- renin release.

If there is increased Na concentration in the —– —- cells, there will be ——- renin release.

If sympathetic nerve activity to the kidney increases, there will be —– renin release along with ——- of the ——- arteriole.

A

Renin promotes increased blood pressure via angiotensin 2.

If blood pressure is high, there will be decreased renin release.

If blood pressure is low, there will be increased renin release.

If there is decreased Na concentration in the macula densa cells, there will be increased renin release.

If there is increased Na concentration in the macula densa cells, there will be decreased renin release.

If sympathetic nerve activity to the kidney increases, there will be increased renin release along with vasoconstriction of the afferent arteriole.

137
Q

If there is an elevated extracellular ——— concentration you can directly regulate the release of ——– from the adrenal medulla

A

If there is an elevated extracellular potassium concentration you can directly regulate the release of aldosterone from the adrenal medulla

138
Q

What can block the actions of aldosterone?

A

Spironolactone which binds to the receptor for aldosterone

139
Q

What can block the actions of aldosterone?

A

Spironolactone which binds to the receptor for aldosterone

140
Q

What regulates Osmolality?

A

Renal water handling - ADH

141
Q

What regulates ECF volume?

A

Renal sodium handling - renin-angiotensin and sympathetic systems.

142
Q

Changes in ECF volume are compensated by changes in —- reabsorption by the kidney.

Decreased EFC volume is compensated by ——- renal reabsorption of ——– via the — —- —- system and the — — system.

Increased ECF volume is compensated by ——- renal reabsorption of ——— via decreased activity of the —— —– —- system and —- ——-

A

Changes in ECF volume are compensated by changes in sodium reabsorption by the kidney.

Decreased EFC volume is compensated by increased renal reabsorption of sodium via the renin angiotensin aldosterone system and the sympathetic nervous system.

Increased ECF volume is compensated by decreased renal reabsorption of sodium via decreased activity of the renin angiotensin aldosterone system and sympathetic nervous

Also increased secretion of Atrial natriuretic peptide (ANP) by the cardiac muscle cells in the atrial wall in response to increased stretch in the atrial wall due to increased volume, reduces extracellular matrix volume by increasing sodium excretion.

143
Q

What are some Anti-hypertensive medication (high BP)?

A

irbesartan, candesartan - block AT1 receptors

Prils (ramipril, captoprils) which are the ACE (in the lungs converts angiotensin 1 to 2) inhibitors

Once this medication is consumed the blood pressure is going to be low irrespectively

144
Q

Does an increase in macula densa NaCl concentration lead to a decrease in renin secretion?

A

yes

145
Q

Does increased production of angiotensin 2 inhibit the sodium hydrogen exchanger?

A

No

146
Q

Does an increase in angiotensin 2 result in excretion of salt and water in the urine?

A

No

147
Q

What happens when you eat a lot of salt chips?

There is no change in volume.

As soon as the ——– is reabsorbed the osmolarity will ———-

This increase is sensed by the ———– in the ——— which then secrete ——–.

Increased ——- levels, increases the amount of —– retained through the signalling of ———.

This balances the osmolality

There is now an increased blood ——– which is sensed by the ———- receptors (sense how much the heart stretches). Increased blood volume, increases ——- return to the heart, these receptors fire signals which ——– sympathetic drive to the kidney which allows the excretion of —– and ——-, bringing volume back to its normal (reflex pathway - slow response).

If the increase in blood volume is substantial the ——– is going to increase. If the ——– increased then the carotid and aortic baroreceptors will sense that

A

As soon as the sodium is reabsorbed the osmolarity will increase

This increase is sensed by the osmoreceptors in the hypothalamus which then secrete ADH.

Increased ADH levels, increases the amount of water retained through the signalling of aquaporins.

This balances the osmolality

There is now an increased blood volume which is sensed by the cardiopulmonary receptors (sense how much the heart stretches). Increased blood volume, increases venous return to the heart, these receptors fire signals which decreases sympathetic drive to the kidney which allows the excretion of sodium and water, bringing volume back to its normal (reflex pathway - slow response).

If the increase in blood volume is substantial the pressure is going to increase. If the pressure increased then the carotid and aortic baroreceptors will sense that

148
Q

Does a high salt pasta meal lead to a decrease in angiotensin 2 levels?

A

Yes

149
Q

Does dehydration lead to a decrease in ADH levels?

A

No

150
Q

Is the angiotensin response to haemorrhage decreases if the renal nerves to the kidney are denervated?

A

yes

Denervated - cut,

Angiotensin 2 response to haemorrhage - decrease in blood volume, so increased renin = increase.

Response is decreased because the renin response also depends on an increase in sympathetic nerve activity to the kidney

151
Q

Does an increase in angiotensin 2 levels result in excretion of salt and water in the urine?

A

No

152
Q

Is angiotensin released by the juxtaglomerular cells when renal perfusion pressure increases?

A

No

Angiotensin is not released by the juxtaglomerular cells, renin is.

153
Q

Does stenosis of the renal artery lead to increased sodium and water reabsorption?

A

A
Yes

Stenosis = narrowing, when you have stenosis there is plaque build up in the artery which decreases the amount of flow to the kidney, there is decreased pressure, which increases renin, angiotensin 2 and therefore sodium and water reabsorption

154
Q

Change in blood volume

Decreased blood volume leads to ——— blood pressure.

The ——– receptors in the —- and —– and —– baroreceptors sense this change.

The cardiovascular system responds by —— cardiac output and ————.

——— intake results in increase ——- and —– fluid volume.

Both these factors ——– blood pressure.

Kidneys act to conserve —– by increased ———– —– activity, ———- of the ——- arteriole and via the —— —– —— system.

A

Decreased blood volume leads to decreased blood pressure.

The volume receptors in the atria and aortic and carotid baroreceptors sense this change.

The cardiovascular system responds by increasing cardiac output and vasoconstriction.

Water intake results in increase extracellular and intracellular fluid volume.

Both these factors increase blood pressure.

Kidneys act to conserve water by increased sympathetic nerve activity, vasoconstriction of the afferent arteriole and via the renin angiotensin aldosterone system (sodium and water retention).

155
Q

Osmolarity, Blood volume, Blood pressure

Increased osmolarity is sensed by the ———— in the ——- ——- of the ——–.

Decreased blood volume is sensed by the —– —– receptors.

Decreased blood pressure is sensed by the —- and —– baroreceptors.

—— is released which binds to —– receptors causing insertion of ——- on the tubular lumen side. This allows —— to be reabsorbed along its concentration gradient and into the capillaries.

There is increased —— reabsorption, which decreases ——–, increases blood —– and ———.

A

Increased osmolarity is sensed by the osmoreceptors in the posterior pituitary of the hypothalamus.

Decreased blood volume is sensed by the atrial stretch receptors.

Decreased blood pressure is sensed by the carotid and aortic baroreceptors.

ADH is released which binds to V2 receptors causing insertion of aquaporins on the tubular lumen side. This allows water to be reabsorbed along its concentration gradient and into the capillaries.

There is increased water reabsorption, which decreases osmolarity, increases blood volume and pressure.