Homeostasis Flashcards

1
Q

Define homeostasis

A

Homeostasis=maintenance of constant internal environment
Keep set point stable within narrow limits in body
Irrespective of changes in external environment
*Factors such as temperature, water potential, glucose concentration must be maintained in the tissues fluid because it affects cell function
*So that internal environment can:
➡️Be stable
➡️Function optimally

*Control systems often work by using a negative feedback mechanism

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2
Q

What is negative feedback and what are the components needed for negative feedback?

A

Components needed:
*Stimulus
*Receptor
*Control center
*Effector
*Response

➡️Restoration of norm or set point

*Continuous monitoring of the factor affecting the internal environment
*Resulting in many “corrective actions”
*Factors thus fluctuates around the norm/set point stable

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3
Q

What is a stimulus?

A

Stimulus refers to internal or external change in factor away from norm/set-point

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4
Q

What is a receptor?

A

Cells/tissue/organ which detect the stimulus

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5
Q

What is a coordinating centre?

A

Consists of tissue which receives and processes messages, in the form of hormones or nerve impulses from the receptors and determines the appropriate response.

Only if the stimulus reaches a certain threshold/is strong enough, it sends messages to an effector.

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6
Q

What is an effector?

A

Tissues/organs which receive messages from coordinating centre and carry out a corrective reaction.

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7
Q

What is a response?

A

The reaction carried out by the effectors.
In negative feedback response counteract the stimulus. Return to set point/ norm

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8
Q

Compare positive vs negative feedback response

A

Positive feedback:
*Response reinforce the original stimulus
*Very uncommon
*Response worsen/intensifies the initial change

E.g. Labour pains, ripening of fruit, inhalation of CO2

Negative feedback:
*Response counteracts the original stimulus
*Common in the body
*To maintain homeostasis/stable internal environment

E.g. maintaining blood glucose levels, temperature,oxygen levels, water content in blood etc

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9
Q

What is excretion

A

Removal of unwanted products of metabolism
→Toxic,poisonous, will cause damage to tissues
Main excretory products:
a)Carbon dioxide
→From aerobic respiration
→Excreted via bloodstream and lungs
b)Urea (nitrogenous waste)
→Produced in liver
→From excess amino acids
→Excreted via kidneys
c)Creatinine (Nitrogenous waste)
→Small amounts produced in liver
→From certain amino acids
→Most used as energy storage in muscles
→Excreted via kidneys
d)Uric acid (Nitrogenous waste)
→Produced in liver
→From excess purines of nucleotides
→Excreted via kidneys

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10
Q

Describe Urea

A

*Main nitrogenous excretory product
*Formed from excess amino acids
*In liver cells

  1. Deamination
    →Remove amine group and a H atom from amino acid
    →Produce ammonia,NH3
    →Toxic if allowed to accumulate
  2. Urea cycle(aka ornithine cycle)
    NH3 + CO2 →Urea→Excreted (kidneys)
    *Keto acid remains→Respired or converted to glucose/glycogen/fat
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11
Q

What are the blood vessels anmd excretory tubes related to the kidney?

A

Blood vessels:
Renal artery(in)
Renal vein (out)
Excretory tubes:
*Ureter -Urine from kidney into urinary bladder
*Urethra-Urine out from urinary bladder

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12
Q

Describe te structure of the kidney

A

*Capsule
→Tough, protective layer

*3 main regions:
a)Cortex
b)Medulla
c)Pelvis

*Nephrons-tiny tubes in the kidney in coretx and medulla

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13
Q

Describe the structure of a nephron

A

1) Bowman’s capsule @ cortex aka renal capsule
2) Proximal convulated tubule @ cortex
3) Loop of Henle @ Medulla
subdivided to:
a)Descending limb
b)Ascending limb
4)Distal convulated tubule @ cortex
5)Collecting duct @ medulla
→Ureter @ pelvis

*Branch of renal artery
→Afferent arteriole
→Glomerulus (tangle of capillaries in the “cup” of the bowman’s capsule)
→Efferent arteriole
→Network of blood capillaries
Surrounding the rest of the nephron
→Branch of renal vein

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14
Q

What are the two stages involved in the mechanism of extraction in the kidneys?

A

2 stages:
1) Ultrafiltration
*Filtering of small molecules, incl. urea out of the blood @ bowman’s capsule
2)Selective reabsorption
*Absorbing any useful molecules from fluid in nephron
@proximal convulated tubules,loop of Henle, distal convulated tubule and collecting duct

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15
Q

What is ultrafiltration?

A

*Filtering of small molecules, incl. urea
*Out of the blood in glomerulus
→Into filtrate in bowman’s capsule space/lumen
*Glomerular filtrate is produced
*Flows along the entire nephron
→Into ureter

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16
Q

Describe the structure of glomerular wall and bowman’s capsule wall

A

Blood in glomerulus is seperated from lumen of bowmans capsule by 3 layers:
1) Endothelium of blood capillaries of the glomerulus
*With many more gaps/fenestrations
2)Basement membrane
*Mesh of collagen and glycoprotein fibres
*Acts as main selective barrier/filter
3)Epithelial cells of bowman’s capsule
*Inner lining of bowman’s capsule (podocytes)
*Wrap around capillaries of the glomerulus
*Podocytes have many finger-like projections that forms gaps/filtration slits

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17
Q

How is the structure of the kidney adapted for ultrafiltration?

A

1) Many large gaps in capillary endothelium + filtration slits between foot processes of podocytes
*Allow movement of substances from blood plasma easily into bowman’s capsule lumen
2) Diameter of the lumen of afferent arteriole is wider than efferent arterioles
*leads to high blood pressure/hydrostatic pressure in the glomerulus than the bowman’s capsule
*Fluid forced out of glomerulus into bowman’s capsule
3)Basement membrane acts as a filter
→Prevents RBCs,WBCs and large plasma proteins (RMM>68000Da) from passing through

Resulting glomerular filtrate contains:
*No cells and large proteins
*Soluble molecules: water,amino acids, glucose, urea, inorganic ions (Na+,K+,Cl-),uric acid,creatinine,vitamins

→Glomerular filtrate passes through gaps betweens podocytes and into renal capsule

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18
Q

What is selective reabsorption?

A

*Necessary
*To reabsorb essential substances from filtrate
*Back into blood
*Selective reabsorption so only certain substances are reabsorbed
*E.g. Glucose,amino acids,vitamins,Cl-,Na+,H2O

@proximal convulated tubule, loop of henle. distal convulated tubule and collecting duct

19
Q

Describe selective reabsorption @ proximal convulated tubule (PCT)

A

*Main site for glucose/amino acid/vitamin/Cl- reabsorbtion
*Walls made of single layer of cuboidal epithelial cells
1)Active transport of Na+ ions
*From PCT cells into blood in capillary
*VIA Na+/K+ pumps
*Concentration of Na+ ions in the PCT cell decreases
2)Na+ ions in PCT lumen diffuse down its gradient into cells lining the PCT
*By faciliated diffusion
*Via co-transported carrier proteins
*Na+ co-transported with glucose/amino acids/vitamins/Cl- ions into cell
3)Glucose/amino acid/vitamins/Cl- ions diffuse into blood via transport protein
*By faciliatated diffusion

20
Q

What is the result of selective reabsorption @ proximal convulated tubule (PCT)?

A

*Glucose is
→ALL actively reabsorbed into blood
→No glucose in urine

*Amino acids,vitamins and Cl- ions
→Actively reabsorbed

*Water, urea
→Some passively reabsorbed

*Uric acid and creatinine → NOT reabsorbed
→Creatinine→Actively secreted/transported into lumen of PCT

21
Q

What are the adaptations of Proximal convulated tubules cells for selective reabsorption?

A

a)Numerous microvilli (facing lumen)
-Large surface arwa for absorption
b)Presense of different transport proteins in membranes (facing lumen)
i.e cotransporters,pumps, aquaporins
c)High density of mitochondria
-Provides energy in the form of ATP for active transport
d) High infolding of basal membranes (facing blood capillaries)
e)Tight junctions holding adjacent cells together
-Seperate proteins of front and basal membrane
-So fluid cannot pass between cells,substance must pass through cells

22
Q

Describe the structure of the loop of Henle

A

Loop of Henle is located at the medulla
Mainly for water reabsorption
2 parts:
1)Descending limb
*Permeable to both water and Na+ and Cl- ions
2)Ascending limb
*Impermeable to water
*Permeable to Na+ and Cl- ions

23
Q

How does selective reabsorption occur at the loop of Henle?

A

@Ascending limb
1. Na+ and Cl- ions move out of the tube
→By active transport
→Into tissue fluid of medulla space
2. High concentrations of Na+ and Cl- ions in the medulla space
→Renal fluid becomes more dilute and enters distal convulated tubule
→Longer loop results in higher concentration of solute built up in the medulla space, more water reabsorption, more conc urine formed!

@Descending limb
*Permeable to both water and Na+ and Cl- ions

Due to high concentrations of solute in the medulla
3. Water moves out into medulla tissue fluid
→By osmosis
→Water is reabsorbed
4. Urea, Na+ and Cl- ions in medulla space diffuse into descending limb
→Fluid in the descending limb becomes very concentrated as it moves down the loop.

24
Q

Describe how selective reabsorption @ distal convulated tubule occurs.

A

Distal convulated tubule is located in the cortex
1st part of DCT=Similar to ascending limb of loop of Henle
*Na+ and Cl- ions again actively transported into blood
2nd part of DCT=Similar to collecting duct
*Water is reabsrobed into blood
*Plus secretion of K+,H+ ions and urea into lumen from blood

25
Q

Describe how selective reabsorption occurs @ collecting duct

A

*Located at medulla
*Tissue fluid of medullah has high concentrations of solutes
*So water moves out of collecting duct
*High reabsorption of water back into blood
→Formation of urine

*Rate of water reabsorption is controlled by ADH (antidiuretic hormone)

26
Q

Describe osmoregulation

A

Osmoregulation=control of the water potential of body fluids
Uses negative feedback mechanism
Stimuli:Water potential of blood is low
Receptor:Osmoreceptors at the hypothalamus detect water potential of blood
Effector:Neuroscretory cells of the hypothalamus send nerve impulse to posterior pituitary glands
*ADH (antidiuretic hormone) released from posterior pituitary
→Enter blood stream
→Target organ: Distal convulated tubule/collecting duct of kidneys

27
Q

Describe the response to ADH in osmoregulation

A
  1. ADH in blood bind to receptors on plasma membrane of disital convulated tubule/collecting duct
  2. Activate a series of enzyme-controlled reactions/enzyme cascade in cells
    →Production of active phosphorylase enzyme
    3.Vescicles containing aquaporins fuse with plasma membrane of lumen side
28
Q

Describe the result of ADH in osmoregulation

A

Result:
*ADH increases membrane permeablity of collecting duct
*Increases water reabsorption
*More water flows out of distal convulated tubule/collecting duct into blood down water potential convulated gradient
*so smaller volume of more conc urine produced
*Water potential of blood increases
*Returns to norm/set point

29
Q

What happens if there is an increase in the water potential of blood?

A

*Osmorecpetors are no longer stimulated
*Neurons stop secreting ADH
*Aquaporins move out of cell surface membrane of collecting duct, back into vesicles in the cytoplasm
*Collecting duct is less permeable to water
*Dilute urine and larger volume of urine produced
*Water potential of blood decreases
*Returns to set point

30
Q

What are endocrine glands?

A

Secretory cells
Releases secretions directly into blood capillaries in the glands
Secretions:Hormones
E.g. pituitary glands,thyroid,adrenal,ovary, testes, pancreas

31
Q

What are Exocrine glands?

A

Secretory cells
Releases secretion into ducts/tubes (not capillaries)
Secretions: not hormones
E.g. stomach,salivary glands,pancreas

32
Q

What are hormones

A

*Secreted by endocrine glands
*Hormones can be globular proteins OR steroids
E.g. Insulin-protein hormone
Testosterone/steroid hormone

Characteristics:
1.Small molecules, chemical messengers
2. Needed in small quantities
3.Secreted quickly upon receiving stimulus
4.Short life span,quickly broken down by enzymes/excreted via urine
5. Transported in the blood stream to target cells
6. Specific- bind to receptors on target cells
Receptors can be on cell surface membrane OR inside cell

33
Q

What are the types of hormone receptors?

A

1)Receptors for protein hormones-on plasma membrane
➡️Water soluble, cannot pass through plasma membrane
2)Receptors for steroid hormones-in cytoplasm
➡️Lipid soluble, can pass easily through plasma membrane

34
Q

Describe the pancreas

A

The pancreas:
*Acts as BOTH endocrine and exocrine gland
*Exocrine-secretes pancreatic juice
➡️VIA pancreatic duct to duodenum
*Endocrine-secretes insulin and glucagon hormones into blood
➡️Islets of langerhans (group of secretory cells) composed of:
*Alpha cells that secrete glucagon
*Beta cells that secrete insulin

35
Q

Describe Insulin vs Glucagon

A

Glucagon and insulin are antagonist hormones
*Glucogan secreted by alpha cells → used to increase blood sugar
*Insulin secreted by beta cells→used to decrease blood sugar

36
Q

What are the stimuli, receptors and effectors for insulin?

A

Stimuli: Blood glucose level increases
Receptors: Detected by α and β cells in islet of langerhans of the pancreas
Effectors:β cells secrete more insulin into blood and α cells stop secreting glucagon

Insulin acts on liver cells, muscle cells and adipose (fat) cells

37
Q

How does insulin work?

A

1.Insulin bind to receptors on cell surface membrane of liver cells/muscle cell/adipose cell
2.Increase permeability of membrane to glucose in liver and muscle cells.
*Trigger vesicles with glucose transported proteins (GLUT proteins) to move and fuse with plasma membrane
*More facilitated diffusion of glucose into cells
3. Increase glucose uptake/absorption from blood
*Stimulate activation of enzyme glucokinase→phosphorylates glucose
*Glucose trapped in cells
4. Increase rate of respiration of glucose
5. Increase conversion of glucose→glycogen (glycogenesis)
*By activating two enzymes (phosphofructokinase,glycogen synthetase)
→Store in liver and muscles
6. Increase protein and lipid synthesis
7. Inhibit secretion of glucagon from α cells
→Inhibit glycogen breakdown into glucose (glycogenolysis)
8.Inhibit production of glucose from proteins and fats (gluconeogenesis)

Result:
*Decrease in glucose concentration and return to norm/set point

38
Q

What is the stimuli, recpetors and effectors of glucagon?

A

Stimuli: Blood glucose level decreases
Receptors: Both α and β cells in islet of langerhans of the pancreas
Effectors:
α cells secrete glucagon into blood
β cells stop secreting insulin

Glucagon acts on liver cells ONLY

39
Q

How does glucagon work?

A
  1. Glucagon binds to receptor on cell surface membrane of liver cells
    *Receptor changes shape
  2. Activates G proteins,
    *Which activates adenyl cyclase
  3. Adenyl cyclase produces cyclic AMP (cAMP)
    *From ATP
    *cAMP acts as the second messenger
    *Activates protein kinase
    *Triggers an enzyme cascade/ a series of enzyme-controlled reactions
    *Signal is amplified

Response:
4. cAMP activates enzyme glycogen phosphorylase
*Increase breakdown of glucogen to glucose (glycogenolysis)
5. Use fatty acids and proteins as respiratory substrate instead of glucose
6. Increase production of glucose from proteins and fats (gluconeogenesis)

*Glucose diffuse through glucose transported proteins-GLUT proteins from liver
*Liver releases glucose into blood
*Increase in blood glucose conc. and return to norm/set point

40
Q

Describe adrenaline

A

*Fight or flight hormone
*Produced during excercise and stress
*Secreted by adrenal gland into blood
*To increase glucose levels in blood
→So muscles can undergo aerobic/anaerobic respiration and produce more ATP

41
Q

Describe diabetes melitus

A

*High glucose concentration in blood
There are two types
*Symptoms same in both forms
*High glucose concentration in blood and urine
→Due to glucose not taken up by cells
→Less glucose converted to glycogen/fat
→Not all glucose can be reabsorbed in kidneys

*Decrease in water potentiol of blood
→Water and salts move out of cells down concentration gradient
→Dehyrdration, production of dilute urine, loss of saltys and cramps
→Detected by osmoreceptors in the hypothalamus→feeling thirsty

*Fat and proteins used in respiration instead of glucose→weight loss
→Build up of keto acids/ketones in blood →blood pH lowers, can cause coma

42
Q

How does urine analysis work?

A

Urine can be collected from patient to test

Presense of glucose and keto acids/ketons in urine
*Not all glucose is reabsorbed at the PCT
*May have diabetes mellitus

Long term presense of proteins in urine:
*Most protein molecules do not pass through the basement membrane at the bowman’s capsule
*Other protein should be reabsorbed at the PCT
*May have kidney infection or disease affecting the glomeruli
*Also associated with high blood pressure
*Short-term presense common during during high fever, vigorous excercise, pregancy

43
Q

How do dipstick tests work?

A

*Used to measure glucose concentration in urine (not blood!)
*Specific test for glucose detection

1)Glucose oxidase and peroxidase immobolised onto pad on disptick
2)Dip stick lowered into urine
3)Glucose catalysed by glucose oxidase→gluconolactone + hydrogen peroxide
Hydrogen peroxide + chromogen(colourless chemical) catalysed by peroxidase→darker compound
4)Compare with colour chart
*Darkness of colour is porportional to concentration of glucose
*The more glucose present, the darker the colour!

44
Q

Describe how biosensors work

A

*Biosensors can directly measure glucose concentration in blood
*Reusable, more precise

1)Glucose oxidase immobolized on pad
2)Place small smaple of blood on pad and insert into machine
3)Glucose is catalysed by glucose oxidase→gluconolactone + hydrogen peroxide
*Small electric current is generated at the same time
4)Current detected by electrode
*Current amplified and reading is produced
*Gives numerical value of blood glucose concentration
*More glucose present, greater current, greater reading from bio sensor