Renal/Urinary system Flashcards

1
Q

What is the role of the urinary system?

A

→ Maintain water and chemical balance in the body
→ Endocrine roles
- RBC production
- Blood pressure

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2
Q

What are the main components of the urinary system?

A

1) The kidneys
2) 2 ureters (one for each kidney)
3) Bladder
4) Urethra
5) Regulatory nerves & muscles

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3
Q

What does the kidney structure allow?

A
  • Blood to be brought into close proximity w/ nephron for filtering
  • A pathway for urine to be removed from the kidney (to be stored then secreted)
  • Protection
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4
Q

Kidneys:

  • Location
  • Vessels passing through hilum
A
  • Behind the peritoneum, surrounded by fat pad, below adrenal gland; right kidney lower bc of liver
  • Located at the T12-L3 vertebral level
  • Arteries, veins, lymphatics and nerves pass through hilum
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5
Q

What are the structures of the kidneys?

A
  1. Cortex
  2. medulla
  3. pelvis
  4. fibrous capsule
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6
Q

Inner medulla structure

A
  • Divided into pyramids

- Each medullary pyramid ends in a papilla

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7
Q

Outer cortex structure

A
  • Continuous layer

- Renal columns

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8
Q

Direction of urine flow

A

papilla → minor calyx → major calyx → renal pelvis → ureter

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9
Q

Features of blood supply to the kidney

  • What region does filtration occur
  • Structure of the arteries leading up to the kidney
A
  • Filtration occurs in the cortex of the kidney
  • Renal arteries arise from the abdominal aorta
  • Branching arteries get smaller & smaller until they reach the cortex
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10
Q

Flow of blood to/through the kidneys

A

Renal arteries → series of arteries → afferent arterioles → glomerulus → efferent arteriole → peritubular capillaries → series of veins → renal vein → IVC

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11
Q

What are vasa recta?

A
  • Blood vessels alongside the loop of Henle of Juxtamedullary nephrons
  • extensions of the peritubular capillaries
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12
Q

What specialised cells do afferent arterioles have?
What do they form part of?
What is their function?

A
  • Juxtagomerular cells
  • Form part of JGA
  • Detect change in pressure (mechanoreceptors)
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13
Q

What is the nerve supply to kidneys?

A
  • Renal plexus (network of autonomic nerves and ganglia)

- Sympathetic nerves act to adjust diameter of renal arterioles and thus regulate blood flow

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14
Q

What are the two types of nephron?

A
  • Cortical nephron

- Juxtamedullary nephron

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15
Q

Cortical nephron features

A
  • 85% (most abundant type)

- Lies mainly in cortex

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16
Q

Juxtamedullary nephron features

A
  • Extends deep into medulla

- Important for the formation of concentrated urine

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17
Q

Nephron functions?

A

1) Selectively filter blood
2) Return anything to be kept to the blood
3) Carry waste away for storagee & expulsion

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18
Q

Nephron components

A
  1. Bowmans capsule
  2. Renal tubules
  3. Collecting duct
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19
Q

What is each nephron associated with?

A
  • A glomerulus
  • Peritubular capillaries
  • Vasa recta
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20
Q

Glomerulus features

A
  • Filtration
  • Thin-walled, single layer of fenestrated endothelial cells
  • Fed and drained by arterioles
  • High pressure and tightly regulated
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21
Q

Peritubular capillaries

  • Function
  • Location
  • Arise from?
  • High/low pressure?
A
  • Absorption
  • Adjacent to renal tubules
  • Arise from efferent arterioles draining glomerulus
  • Low pressure
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22
Q

Structure of renal corpuscle

A
  • Consists of the glomerulus surrounded by the Bowmans capsule
  • B/w these two structures is the blood-urine barrier
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23
Q

Structure of Bowmans capsule

A
→ Two layers
- Outer parietal layer - simple squamous
- Inner visceral layer - podocytes
→ b/w two layers - "bowmans space"
→ Pedicels wrap around podocytes to form filtration slits
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24
Q

Podocyte features

A
  • Surround the glomerular capillaries
  • V branched, v specialised epithelium
  • Branches form interwining foor processes - ‘pedicels’
  • Filtration slits form b/w pedicels
  • Filtered blood (filtrate) goes thr’ slits & passes into Bowmans space
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25
Q

What does/doesn’t the Blood-urine Barrier filter?

A
  • Allows free passage of water and small molecules
  • Restricts passage of most proteins
  • RBCs not filtered
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26
Q

What are the 3 layers of the Blood-urine barrier?

A

1) Fenestrated endothelium of glomular capillary
2) Fused basement membrane
3) Filtration slits b/w the pedicels of the podocytes

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27
Q

What are the 4 section of the nephron and what do they allow?

A
  • Proximal convoluted tubule (PCT)
  • Loop of Henle
  • Distal convoluted tube (DCT)
  • Collecting duct
    They allow reabsorption
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28
Q

Proximal convoluted tubule (PCT)

  • Function
  • Structure
  • Surrounded by?
A
→ Bulk reabsorption
→ Surrounded by peritubular capillaries
→ Structure 
- Cuboidal epithelial cells
- Dense microvilli (brush border)
- Rich in mitochondria for active transport
- Leaky epithelium
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29
Q

Loop of Henle

  • Surrounded by?
  • Function
  • Structure
A

→ Surrounded by vasa recta (Juxtamedullary nephrons only)
→ Length is important in production of highly concentrated urine
→ Structure
- Descending limb: reabsorption of water from filtrate
- Thick (superior) section: similar to PCT
- Thin (inferior) section: simple squamous epithelium
- Ascending limb: reabsorption of NaCl from filtrate
- Thin (inferior) section: simple squamous epi
- Thick (superior) section: similar to DCT

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30
Q

Distal convoluted tube (DCT)

  • Function
  • Structure
  • Specialised cells?
A

→ Fine tuning
→ Cuboidal epithelium (thinner than PCT)
→ Fewer mitochondria and microvilli (no brush border)
→ Macula dense cells located where DCT contacts afferent arteriole; chemoreceptors which detect Na+ conc.

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31
Q

Collecting duct

  • Function (incl. what controls it)
  • Structure (incl. cell types)
A

→ Fine tuning
→ Filtrate from several DCTs drains into one collecting duct, which empty at papilla
→ simple cuboidal epithelium
- Principal cells - reabsorption
- Intercalated cells - acid/base balance
→ Reabsorption influence by ADH, thr’ use of aquaporins

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32
Q

Juxtaglomerular apparatus (JGA): where is it and what does it do?

A

→ Located where DCT lies against afferent arteriole
→ Controls glomerular filtration rate ensuring system working at full capacity
→ Stabilises blood pressure

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33
Q

Specialised cells and main role of the

  • Afferent arteriole
  • DCT
A
→ Afferent arteriole
- JG cells 
- Mechanoreceptors
- Release renin in response to blood pressure, which stimulates angiotensin II formation
→ DCT
- Macula densa cells 
- Chemo receptors
- Detect sodium concentration in filtrate
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34
Q

Ureters:

  • Arise from?
  • Descend where relative to the peritoneum?
  • Motility pattern?
A
  • Arise from each renal pelvis at each hilum
  • Descend retroperitoneally through abdomen, vertically
  • Peristaltic waves move urine → bladder
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35
Q

Layers of the Ureters and what they’re made of

A

1) Mucosa - transitional epithelium, stratified
2) Muscularis - inner longitudinal, outer circular smooth muscle layer (opposite to GI tract, prevents backflow)
3) Adventitia - FCT

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36
Q

What motility pattern do the ureters use?

A

Peristalsis

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37
Q

What are the ureters lined with? What does it do?

A
  • Protein plaques

- For protection; stops urine from leaking

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38
Q

What is the significance of the way in which the ureters join connect to the bladder?

A
  • Run obliquely through the wall of bladder at its posterolateral (side, back) corners
    → Act as sphincter/valve;
  • compressed by increase bladder pressure to prevent back flow of urine
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39
Q

Urinary bladder

  • What it is and what it does
  • Structure when empty and when full
  • How many openings?
  • Contains what region?
A
  • Collapsible, muscular sac, stores and expels urine
  • When empty, collapses along rugae (folds)
  • When full, expands w/out great ↑ in pressure
  • 3 openings: 2 for entry of ureters, 1 for urethra
  • Trigone: triangular region b/w openings; infections persist here
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40
Q

Position of bladder: Males vs Females

A
→ Male bladder
- Anterior to rectum
- Superior to prostate gland
→ Female bladder
- Anterior to vagina and uterus
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41
Q

What are the 3 layers of the bladder wall?

What are they made up of?

A

1) Mucosa
- Transitional epithelium
2) Detrusor muscle
- Meshwork of longitudinal, circular & oblique smith muscle fibres (squeeze urine from bladder during urination - no motility pattern)
3) Adventitia
- Connective tissue

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42
Q

Urethra

  • structure
  • function
  • Epithelium (incl. changes)
A
  • Thin walled muscular tube
  • Drains urine from bladder → out of body
    → Epithelium changes:
    1) Transitional near bladder
    2) Columnar (provides goblet cells → produce mucous)
    3) Stratified squamous near external opening
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43
Q

Male vs Female urethra

A
→ Male
- Long
- Part of reproductive system
- Male urethra has 3 sections (due to length) 
1) Prostatic urethra
2) Membranous urethra
3) Spongy/penile urethra
→ Female
- Short
- Separate from RS
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44
Q

Internal urethral sphincter features

A
  • Junction of bladder and urethra
  • Detrusor muscle (smooth)
  • Involuntary control - parasympathetic innervation
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45
Q

External urethral sphincter features

A
  • Where urethra passes through the urogenital diaphragm
  • Skeletal muscle
  • Voluntary control
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46
Q

Process of urination

A

Bladder expands → APs to brain → urgency → inner sphincter relaxes → conscious relaxation of external sphincters → urination

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47
Q

Urine composition - Normal

A
  • 95-98% water (approx. 1.5L/day)
  • Creatinine
  • Urea
  • H+, NH3
  • Na+, K+
  • Drugs (anti-viral, diuretics)
  • Toxins
48
Q

Urine composition - Pathogenic

A
  • Glucose
  • Protein
  • Blood
  • Haemoglobin
  • Leucocytes
  • Bacteria
49
Q

What is normal Urine

  • Look
  • Taste
  • Smell
A
→ Look
- Clear, light or dark amber
→ Taste
- Acidic (pH 5-7) - not sweet
       ↳ depends on diet
→ Smell
- None
50
Q

What is pathogenic Urine

  • Look
  • Taste
  • Smell
A
→ Look
- Golden red, brown, blue
→ Taste
- Sweet (diabetes)
→ Smell
- Like fruits (diabetes, ketosis, chronic alcohol abuse)
- Rotten (infection, tumour)
51
Q

Functions of the kidneys (8)

A

1) Water and salt homeostasis
2) Filteration
3) Reabsorption
4) Hormone production (EPO)
5) Metabolism
6) Gluconeogenesis
8) Excretion drugs, endogenous metabolites & toxins (aspirin, anti-viral drugs, urea, uric acid, herbal toxins)
9) pH regulation
- Excrete excess HCO3-, H+

52
Q

What are the basic nephron functions?

A

1) Filtration
2) Secretion
3) Re-absorption

53
Q

How much of the cardiac output does the kidney receive?

A

20-25%

54
Q

What does reabsorption do?
Which of the following are partially/completely reabsorbed:
- Na+ and K+
- glucose

A
  • Removes useful solutes from the filtrate & returns them to blood
  • Na+ and K+ partially reabsorbed
  • glucose entirely reabsorbed
55
Q

Function of basic nephron secretion

A

gets rid of substances that can’t make it through the filtration barrier but need to be excreted in the urine

56
Q

What defines renal filtration?

A
  • Renal blood flow
  • Filtration barrier
  • Driving forces
57
Q

Kidney filtration:

  • Rate
  • Produces what amount?
A
  • Takes place at a rate of 125mL/min (180L/day)

- Produces only 1.5 of urine/day

58
Q

How is blood pressure monitored in the kidney?

A

DCT senses how much vol. is filtered and thus monitors BP

59
Q

What is the rate of blood supply to the kidney?

A

1-1.2L/min

60
Q

What substances are filtered by the glomerular?

And not filtered?

A
  • Small substances → freely filtered

- Large substances → NOT filtered

61
Q

What is Glomerular filtration influenced by?

A

1) Pressure gradient b/w glomerular capillary and Bowmans space
2) Permeability of glomerular capillary
3) SA of glomerular capillary

62
Q

How do you calculate effective filtration pressure?

A

Effective filtration pressure = (glomerular hydrostatic pressure + capsular osmotic pressure) - (glomerular osmotic pressure + capsular hydrostatic pressure)

63
Q

What are the glomerular driving forces?

A

→ Blood pressure (PGC) is the main driver for filtration
→ Forces opposing filtration are osmotic pressure in the glomerular capillary (πGC) and fluid pressure in Bowman capsule (PBS)

64
Q

Blood vs. primary urine composition in terms of:

  1. NaCl conc.
  2. albumin conc.
A
  • Both have NaCl conc. of 145mM (thus, isotonic primary filtrate)
  • Blood contains 50g/L albumin, whereas urine contains none
65
Q

What is renal clearance?

How do you calculate it?

A

The RATE at which substances (that can be detected in plasma and urine) is CLEARED by the kidneys per unit time. (unit mL/min)
Clearance = conc. of substrate in urine x (vol. of urine produced/conc. of substrate in plasma)

66
Q

Glomerular filtration rate (GFR):

  • What is it?
  • Normal value
  • How can it be estimated?
A
  • Amount of fluid filtered per unit time.// Vol. of plasma filtered per time.
  • Normally 125mL/min
  • Tightly regulated: variation b/w people; ↓ slowly from age 30
  • Can be estimated using renal clearance
67
Q

Which substances can be used as a measure of GFR?

A

Inulin and Creatinine

68
Q

Inulin and Creatinine can be used as a measure of GFR bc they? (3 reasons)

A

1) Aren’t reabsorbed from the tubule
2) Aren’t secreted into the tubule
3) Aren’t metabolised

69
Q

What is more commonly used out of Inulin and creatinine? Why ?

A

Creatinine bc its already in the body and is only filtered, not reabsorbed

70
Q

How does Creatinin conc. indicate kidney function?

A
  • Plasma creatinin is low if both kidneys are working

- Plasma creatinin fairly normal if only one is working

71
Q

What is the filtration fraction?

A

FF = GFR/Renal Plasma Flow

→ ratio b/w blood flow and filtration in the kidney

72
Q

What is the filtered load?

How to calculate?

A
  • Amount of a particular substance/solute filtered per minute.
  • FL = GFR x Solute plasma conc.
73
Q

Solutes which are only reabsorbed? (not secreted)

A
  • Glucose
  • Water
  • Na+
  • Cl-
  • PO4-
  • Ca2+
74
Q

Solutes which are only secreted? (not reabsorbed)

A
Organic cations
- Monoamines
- Drugs
Organic anions
- Endogenous compounds (eg bile salts)
- Drugs (eg penicillin; 'PAH')
75
Q

Where is PAH (organic anion) secreted?

Active or passive?

A

Proximal tubules

Active transport

76
Q

What substances are both reabsorbed and filtered, depending on homeostatic requirements?

A
  • K+
  • NH3
  • H+
  • HCO3-
  • Urea
77
Q

What are the routes of transport?

A

1) Between cells - Paracellular

2) Through cells - Transcellular

78
Q

Paracellular (between cells) features

A
  • “leaky” = bulk reabsorption (PCT)
  • Single barrier; permeability depends on ‘tightness’ of tight junction
  • No transport proteins
79
Q

Transcellular (through cells) features

A
  • “tight” channels/energy
  • More selective: hormonal control
  • 2 barriers; apical (mucosal) and basolateral membrane
  • usually involves membrane transport proteins
80
Q
Proximal tubule:
- Function
- Reabsorbs what proportion of:
sodium, water, chloride, glucose, AAs, K+, PO43-, Ca2+, HCO3-, urea
- Secretes?
A
→ BULK reabsorption/secretion
- 66% sodium, water, chloride
- All filtered glucose & AAs
- Most of K+, PO43-, Ca2+
- 80% of filtered HCO3-
- 1/2 of urea
→ Secretes organic acids, drugs, H+
81
Q

How does sodium reabsorption happen?

A

Transport of many solutes is coupled to Na+ reabsorption (glucose, AAs); Na+/K+ pump keeps [Na+] in cell low so this can keep occurring.
- 3 Na+ into interstitial, 2K+ into cell

82
Q

Where does sodium reabsorption happen?

A

→ Occurs

  • PCT (66%)
  • TAL (25%)
  • DCT (5%)
  • CCT (3%)
83
Q

PCT:

  • what type of epithelium
  • Permeability to water
  • Which pathway(s)?
A
  • Leaky epithelium
  • High water permeability
  • Transcellular (AQP1) and paracellular
84
Q

CCT:

  • what type of epithelium
  • Permeability to water
  • Which pathway(s)?
A
  • Tight epithelium
  • Low water permeability
  • ONLY trancellular (AQP2)
85
Q

Loop of Henle:

  • Function of each section
  • Effect on filtrate
A

→ Descending limb (tDLH): removes water from filtrate (leaky), impermeable to salt
→ Thick ascending limb (TAL): removes NaCl from filtrate (tight), impermeable to water; makes surrounding interstitial in medulla hyperosmotic - ‘Hyperosmotic medullary gradient’ (HOMG)
- Leaves filtrate inside tubules v. dilute

86
Q

Distal tubule &collecting duct

  • Function
  • Hormonal control
A

→ Fine tuning of electrolytes, pH & water
- Reabsorb remaining NaCl & water
- Secrete K+ & H+
→ Hormonal control
- Na+ reabsorption/K+ secretion: aldosterone
- Water reabsorption: ADH

87
Q

Body water volume?

A
TBW = 55-60% of body weight
→ 2/3 ICF
→ 1/3 ECF
      - 1/5 plasma
      - 4/5 interstitial fluid
88
Q

What is osmolarity?

A

No. of ions or solutes per volume of water

- e.g. 145mM NaCl = 145mM Na+ + 145mM Cl- = 290mosmol/L

89
Q

What is

  • ISO osmolarity
  • HYPO osmolarity
  • HYPER osmolarity
A
ISO = same
HYPO = lower
HYPER = higher
90
Q

What is tonicity

A

Effect of a solution on cells

91
Q

What proportion of water is reabsorbed in different parts of the nephron?

A
  • PCT: 66%
  • tDLH: 25%
  • CCT: 2-8%
92
Q

What is PCT driven by?

A

Na+ reabsorption (isotonic)

93
Q

Urine tonicity through the nephron

A
  • isotonic in PCT (300mosmol/L)
  • hypertonic in tDLH
  • hypotonic in TAL
  • hypertonic in CCT (anti-diuresis)
94
Q

Body osmolarity:

  • Relative osmolarity of ECF and ICF (incl. value/s)
  • How does dehydration and rehydration affect vol?
A
  • Fluid shifts b/w ECF & ICF to equalise
    → Have the same osmolarity: 275-295mosmol/L
  • Dehydration: water is lost only from ECF
  • Hyperhydration: water is gained only by ECF
95
Q

How does ADH regulate body osmolarity?

A

TBW alters plasma (ECF) osmolarity

1) detected by osmoreceptors in hypothalamus
2) Stimulates pituitary gland
3) ADH alters permeability of renal collecting duct (CD), so water is retained/excreted to balance initial TBW
4) Plasma osmolarity stable
5) Cell vol. stable

96
Q

ADH synthesis; location and direction of travel

A

→ In cell body of central neurons (hypothalamus)

→ Axonal transport to posterior pituitary

97
Q

ADH release; location and stimulus

A
  • From posterior pituitary into bloodstream
    → Stimulated by:
  • increase ECF osmolarity
  • decrease blood volume
98
Q

ADH actions/role:

A

1) Inserts water channels (aquaporins - AQP2) into luminal membrane of CD
2) Increase H2O reabsorption in the collecting duct

99
Q

How is filtrate altered when ADH is present?

A

→ ANTI-DIURESIS

  • Collecting duct more permeable to water; reabsorbed from CD
  • Small vol. of concentrated (high osmolarity) urine
100
Q

How is filtrate altered when ADH is absent?

A

→ DIURESIS

  • Collecting duct impermeable to water; majority remains in CD
  • Large vol. of dilute (low osmolarity) urine
101
Q

Water homeostasis: Fast system

  • Reacts to?
  • Corrected by?
A
  • Reacts to changes in osmolarity

- ADH system

102
Q

Water homeostasis: Slow system

  • Reacts to?
  • Corrected by?
  • Affect of loss/gain of isosmotic solutions?
A
→ Reacts to changes in volume
→ corrected via sodium retention/excretion
→ Losses from ECF don't change osmolarity (bc isosmotic)
- no gradient change
- no movement of water in/out cells
- Thus, volume loss restricted to ECF
- circulating vol. ↓, BP ↓
→ gains of isosmotic solutions
- vol. gain restricted to ECF
- Circulating vol. ↑ & BP ↑
103
Q

What 3 sensor mechanisms defect ΔECF vol. (in response to haemorrhage)

A

1) High pressure baroreceptors (aorta, carotid)
- pressure sensors
2) Low pressure baroreceptors (vena cava, right atrium)
- volume sensors
3) Intra-renal baroreceptors (kidney: JG cells in afferent arteriole and macula densa cells in distal tubule)

104
Q

How do high pressure baroreceptors regulate pressure?

A

→ Signal to brainstem; CVS centres
→ Regulates via:
- Renal nerve activity (sympathetic)
- ADH

105
Q

How do low pressure baroreceptors regulate pressure?

A

→ Signals to brainstem; CVS centres
→ If stimulated by high vol, atrial release of ANP (ANH)
- ANP promotes loss of sodium in the urine → promotes water excretion

106
Q

How do Intra-renal sensors regulate pressure?

A
→ Afferent arteriole (mechanoreceptors)
- Senses changes in BP
- Alters renin secretion (JGA): renin stimulates angiotensin ll formation
→ Macula densa (chemoreceptors)
- Senses flow rate via Na+ conc in DT
- Alters renin secretion (JGA)
107
Q

ECF vol. regulation Renin-Angiotensin System (RAs)

A

1) Renin (enzyme) secreted by JGA
2) Renin cleaves angiotensinogen into angiotensin l
3) Angiotensin l → angiotensin ll by angiotensin converting enzyme (ACE)
4) Angiotensin ll: vasoconstrictor (incr. TPR) and stimulates aldosterone release (incr. Na+ reabsorption)

108
Q

Renal blood flow regulation?

A

1) Intrinsic (auto regulation)
- Myogenic vascular smooth muscle (afferent arteriole)
- Tubuloglomerular feedback (TGF): via JGA
2) Extrinsic
- Sympathetic vasoconstrictor nerves
- Angiotensin ll

109
Q

Integration of systems @ HIGH circulating vol. & renal flow

A
  • Mechanisms adjust to ↑ Na+ exretion
  • Causes osmotic gradient → water loss
  • ↓ vol. (BP)
110
Q

Integration of systems @ LOW circulating vol. & renal flow

A
  • Mechanisms activated to retain Na+
  • Retain water
  • Restore vol. (BP
111
Q

ANP:

  • Secreted by?
  • In response to?
  • Effects?
A
→ ANP secreted by atria in response to ↑ vol.; which:
- ↑ Filtered load of Na+
- ↓ Tubular reabsorption of Na+
- ↓ Renin secretion
therefore
- ↑ Na+ excretion
- ↑ water excretion
- ↓ vol. & BP
112
Q

RAS: Stimuli for renin release from JGA when ECF vol. low

A

1) ↓ renal flow pressure in afferent arteriole
2) ↓ delivery of NaCl to macula densa (low vol. = low filtration = less in tubules)
3) Renal sympathetic nerves (activated by baroreceptors) each of these stimuli are activated when the body needs to conserve or restore vol.)

113
Q

RAS: Effects to ↑ vol

A
  • Stimulates reabsorption of Na+
  • ↑ aldosterone secretion which also stimulates Na+ reabsorption
  • Powerful vasoconstrictor (ATll): ↑ total peripheral resistance
  • Hypothalamus: thirst, ADH release
114
Q

Aldosterone:

  • What is it
  • Secreted from?
  • Stimulated by?
  • Acts on?
  • Effect?
A
  • Steroid hormone secreted from adrenal gland
  • Stimulated by Angiotensin ll (& ↑ extracellular k+ levels)
  • Acts on distal tubule & collecting duct; ↑ reabsorption of Na+ (& secretion of k+)
115
Q

Isosmotic losses

A
  • Diarrhea
  • Vomiting
  • Burns (bleeding)
116
Q

Isosmotic gains

A
  • Renal failure

- Excess IV fluids