Lecture 14: Water and salt balance Part 1 Flashcards

1
Q

Describe the negative feedback loop of ADH:

A

Water deficit -> Increased ECF osmolarity -> Osmoreceptors -> Increased ADH secretion -> Increased plasma ADH -> Increased water permeability DT and CD -> Increased water reabsorption and decreased water excretion (-ive feedback to water deficit)

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2
Q

Describe where ADH comes from:

A

ADH synthesised as part of precursor protein in hypothalamus, travels down axons to post. pituitary, wehere it is stored in granules in the nerve terminals. ADH is a nonapeptide

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3
Q

What determines ADH release?

A

Control of ADH release by osmolality and ‘volume’ of ECF

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4
Q

Where are osmoreceptors located?

A

Osmoreceptors in supraoptic and paraventricular nuclei sense high osmolality and result in stimulation of ADH release

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5
Q

What other regions of the brain contribute to ADH release? and how do they work?

A

Inputs to hypothalamus from the medullary vasomotor center increase ADH release in response to decreased circulating volume

Both initiate mechanisms that influence supraoptic and paraventricular ADH secreting neurons

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6
Q

What is the greater stimulus for ADH?

A

ADH is released in response to either increased osmolality (less than 1% chain) or decreased volume (greater than 10% change) of the ECF

Secretion of ADH in response to increased osmolality has a lower threshold and higher sensitivity (slope) than the response to decreased ECF.

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7
Q

What are the non-physiological stimuli for ADH secretion?

A
  • Pain and stress
  • Drugs: narcotics, nicotine
  • Carcinomas
  • Pulmonary disorders
  • CNS disorders
  • Alcohol (inhibits ADH secretion)
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8
Q

Describe the molecular mechanism of ADH:

A

ADH binds V2 receptor, increased cAMP -> PKA -> Phosphorylation and AQ2 insertion into apical membrane

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9
Q

What can develop if ADH is low?

A

Central and nephrogenic diabetes insipidus can develop if there is difficulty producing ADH or its action occuring.

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10
Q

What is central diabetes insipidus?

A
  • AKA neurogenic DI or pituitary DI
  • (Inadequate ADH secretion)
  • Problem with hypothalamus or post. pituitary
  • i.e due to brain injury, tumor or infection
  • Rarely hereditary
  • Treated with ADH analogues
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11
Q

What is nephrogenic DI?

A
  • CT unresponsive to ADH
  • Concentrated urine cannot be produced
  • Can be caused by certain drugs, commonly Li
  • Less commonly hereditary
    -> Congenital defect in V2 receptor
    -> Inherited defect in AQ2
  • Not currently treatable
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12
Q

Whats the difference b/w diabetes insipitus and diabetes mellitus?

A

DM = glucose in urine
DI = No glucose in urine

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13
Q

What is syndrome of inappropriate ADH secretion?

A

A defect in inappropriate ADH action
- High plasma ADH for osmolarity / volume
= Patients retain water inappropriately
= Patients have to be restrict water intake

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14
Q

What can cause SIADH?

A
  • Brain injury
  • Cancer
  • Anti-cancer drugs
  • Lung cancer
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15
Q

What does a decreased in BP stimulated?

A

Renin!

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16
Q

Describe the JGA and what stimulates renin?

A
  • Decreased afferent arteriolar pressure
  • Inc. sympathetic activity
  • Decreased macula densa NaCl delivery

= Renin secretion

17
Q

Describe the classical RAAS pathway:

A

Renin converts angiotensinogen into ANG 1, ACE converts ANG1 -> ANG2

18
Q

What does ANG2 do on its receptors?

A

AT2 receptor:
- Vasodilation

AT1 receptor:
- Increase aldosterone
- Vasoconstriction
- Increased proximal Na reabsorption
- Increased thirst
- Increased ADH release
- Decreased RBF, but maintains GFR

19
Q

Whats the non-classical RAAS pathway?

A

Alternative RAAS pathway with various effects, but just understand theres an alternative to the classical pathway

20
Q

Describe on a molecular level the action of ANG2:

A
  1. Increased aldosterone production
  2. Constriction of efferent arteriole.

3:
-> Increased basal Na/K ATPase
-> Increased Na/H (NH exchanger) (Apical)
-> Increased Na/HCO3 symporter (Basal)

Note: Drags water with it, thus increases BV w/o a change in osmolarity

21
Q

What are high levels of ANG2 implicated in?

A
  • Hypertension
  • HF
  • Kidney disease