Renal - Pt 5 Hormonal Effects Flashcards

1
Q

Aldosterone is a [] saving hormonal pathway.

A

sodium

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2
Q

Aldosterone release pathway:

  1. Liver continuously produces [], which travels thorugout the circulation.
  2. If the kidney detects low sodium levels, through [] [] cells, the [] cells produce renin.
  3. Renin converts inactive angiotensinogen into [].
  4. Angiotensin I is converted to [] from the enzyme [] [] []. This process is usually done in the []
  5. Angiotensin II travels to the [] gland via the bloodstream where it stimulates the release of []
  6. Aldosterone travels to the late [] and [] where it effects reabsorption.
A
  1. Liver continuously produces angiotensinogen, which travels thorugout the circulation.
  2. If the kidney detects low sodium levels, through macula densa cells, the juxtaglomerular cells produce renin.
  3. Renin converts inactive angiotensinogen into angiotensin I.
  4. Angiotensin I is converted to Angiotensin II from the enzyme Angiotensin converting enzyme. This process is usually done in the lungs
  5. Angiotensin II travels to the adrenal gland via the bloodstream where it stimulates the release of Aldosterone
  6. Aldosterone travels to the late DCT and CD where it effects reabsorption.
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3
Q

Within the late DCT and CD, Aldosterone has 3 main effects:

  1. increases the synthesis and activity of the []/[] pump which is inserted into the [] membrane
  2. Increasesthe synthesis and insertion of [] leak channels in the [] membrane
  3. Increases the synthesis and insertion of [] channels in the [] membrane.
A
  1. increases the synthesis and activity of the sodium/potassium pump which is inserted into the basolateral membrane
  2. Increases the synthesis and insertion of potassium leak channels in the apical membrane
  3. Increases the synthesis and insertion of sodium channels in the apical membrane.
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4
Q

The net effect of aldosterones actions in the late DCT and CD is to increase [] ion secretion and [] ion reabsorption.

A

The net effect of aldosterones actions in the late DCT and CD is to increase potassium ion secretion and sodium ion reabsorption.

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5
Q

T/F

The PCT is always permeable to water?

A

TRUE!

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6
Q

The main sites of reabsorption are the [] and []

A

PCT and TAL

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7
Q

Main sites of net secretion are the late [] and []

A

DCT and CD

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8
Q

The main sites of tubuloglomerular feedback are the [] and []

A

TAL and Early DCT

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9
Q

[] is referred to as the diluting segment of the nephron

A

TAL

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10
Q

The [] is the site of action of furosemide

A

TAL

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11
Q

The [] and [] are the site of ADH action

A

TAL and late DCT

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12
Q

The [] and [] are the sites of aldosterone action

A

late DCT and CD

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13
Q

The [] is the site of NKCC transporters

A

TAL

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14
Q

The [] is the site of iso-osmotic reabsorption of sodium, chloride, and water.

A

PCT

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15
Q
  • ANP causes the kidney to [] water and sodium loss, after detecting and [] in blood volume.
  • ANP causes vaso-[] and a [] in TPR.
A
  • ANP causes the kidney to increase water and sodium loss, after detecting an increase in blood volume.
  • ANP causes vaso-dilation and a decrease in TPR.
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16
Q

Within the nephron, ANP has 3 main actions:

  • Relaxes​ the [] arteriole and constrict the [] arteriole –> [] in GFR –> [] in exretion of Na+ in urine
  • [] the sodium/potassium pump in the [] and [] –> [] Na+ reabsorption
A
  • Relaxes​ the afferent arteriole and constrict the efferent arteriole –> increase in GFR –> Increase in exretion of Na+ in urine
  • Inhibits the sodium/potassium pump in the late DCT and CD –> decreased Na+ reabsorption
17
Q

ANP can also act to systemically [] the vasculature, leading to a [] in blood pressure

A

vasodilate; drop

18
Q

In the kidney, ANP acts as an antagonist to []

A

Aldosterone

19
Q

[] is any substance that increases urine output

A

Diuretics

20
Q

Diuretics can be classified into 3 main types:

  1. Substances that [] GFR (mild increase in urine output)
  2. Substances that [] ADH release (potent increase in urine output)
  3. Osmotic or []-[]-[] substances (potent increase in urine output.)
A
  1. Substances that increase GFR (mild increase in urine output)
  2. Substances that inhibit ADH release (potent increase in urine output)
  3. Osmotic or renal-transport-inhibiting substances (potent increase in urine output.)
21
Q

Diuretics that affect GFR:

  1. Caffeine - [] afferent arteriole
  2. ANP - [] afferent arteriole, and [] the effeerent arteriole
  • Both of these create a urine product that is [] to plasma ~300 mOsm
A
  1. Caffeine - dilates afferent arteriole
  2. ANP - dilates afferent arteriole, and constricts the effeerent arteriole
  • Both of these create a urine product that is isomotic to plasma ~300 mOsm
22
Q
  • Examples of diretics that inhibit ADH: []and [].
  • In diabetes [], ADH is not produced and/or detected within the body
  • In these instances, the urine excreted by the body is []-osmotic compared to the plasma.
A
  • Examples of diretics that inhibit ADH: Ethanol and Narcotics.
  • In diabetes Insipidus, ADH is not produced and/or detected within the body
  • In these instances, the urine excreted by the body is hypo-osmotic compared to the plasma.
23
Q
A
24
Q
  • Example of diuresis due to osmotically active solutes: []
    • Glucoss [] the transport maximum for reabsorption
    • Water [] follows glucose
    • Usually due to diabetes []
  • The urine formed in these instances is relatively []-osmotic versus plasma.
A
  • Example of diuresis due to osmotically active solutes: Glucose
    • Glucoss exceeds the transport maximum for reabsorption
    • Water osmotically follows glucose
    • Usually due to diabetes mellitus
  • The urine formed in these instances is relatively iso-osmotic versus plasma.
25
Q

Carbonic Anhydrate Inhibitors:

  1. [] reabsorption of bicarbonate in []
  2. Some [] will follow the bicarbonate
  3. Can be limited by resultant []
A
  1. Inhibits reabsorption of bicarbonate in PCT
  2. Some sodium will follow the bicarbonate
  3. Can be limited by resultant acidosis
26
Q

Loop Diuretics (Potent)

  1. Example: []
  2. Interrupts counter-current [] system
  3. []-wasting diuretic..so patients oculd suffer form []
A
  1. Example: Furosemide
  2. Interrupts counter-current multiplier system
  3. Potassium-wasting diuretic..so patients oculd suffer form hypochalimia
27
Q

Thiazide-type Diuretic

  1. [] sodium chloride transporter in the []
A

Inhibits; Late DCT

28
Q

Aldosterone antagonists

  • []-saving diuretic
  • Affects are seen in the [] and []
  • Usually given when a patient isn’t tolerating [] [] and have a lot of sid effects
A
  • Potassium-saving diuretic
  • Affects are seen in the Late DCT and CD
  • Usually given when a patient isn’t tolerating loop diuretics and have a lot of sid effects