Osmoregulation Flashcards

1
Q

Evidence for countercurrent hypothesis by micropuncture

A

Gottschalk and Mylle (1959)

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2
Q

Net transtubular movement of water and urea; primarily from descending limb; compatible with passive movement of water/urea

A

Lassiter et al (1961)

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3
Q

Model for countercurrent multiplication where loop of Henle operates passively

A

Kokko and Rector (1972)

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4
Q

Model of secondary active Cl- transport; removal of K+ conductance reduced Isc; compatible with NCKK exchanger

A

Greger and Schlatter (1981)

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5
Q

Evidence for electroneutral NaCl cotransport (NCKK) in cortical thick ascending limb

A

Greger et al (1983)

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6
Q

UT-A knockouts have urinary concentrating defects caused by failure of urea transport

A

Fenton et al (2005)

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7
Q

Transgenic restoration of urea transporter A1 confers maximal urinary concentration in the absence of urea transporter A3

A

Klein et al (2015)

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8
Q

Active urea secretion into pars recta = urea-selective improvement in urine concentrating ability

A

Layton and Bankir (2013)

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9
Q

Urea actively secreted by straight segments of superficial and juxtamedullar PT

A

Karamura and Kokko (1976)

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10
Q

Compatible with passive urea secretion in PST but not a significant degree of active secretion

A

Knepper (1983)

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11
Q

Secondary active secretor urea transport in inner medullar collecting ducts upregulated in diuretic rats

A

Kato and Sands (1998)

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12
Q

Supaoptic neurones of rat hypothalamus are osmosensitive

A

Mason (1980)

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13
Q

• Changes in firing rate of magnocellular neurosecretory cells (MNCs) following OVLT stimulation selectively mediated by changes in synaptic excitation

A

Richard and Bourque (1995)

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14
Q

OVLT detects NaCl to elevate sympathetic nerve activity and blood pressure; intrinsic

A

Kinsman et al (2017)

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15
Q

NaCl and osmolarity produce different responses in organum vasculosum of the lamina terminalis neurons, sympathetic nerve activity and blood pr

A

Kinsman et al (2017)

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16
Q

Extracellular signal-regulated kinase phosphorylation in forebrain neurones contributes to osmoregulatory mechanisms

A

Dine et al (2014)

17
Q

Physial shrinking necessary and sufficient to medaite hypertonicity; mechanical process involved TRPV1 but not TRPV4

A

Ciura et al (2011)

18
Q

TRPV4 responds to volume changes, but is a lack of evidence for involvement in some studies

A

Toft-Bertelson et al (2018)

19
Q

TRPV4 knockout mice drink less water and become more hyperosmolar, with lower ADH levels

A

Liedke and Friedman (2003)

20
Q

No difference in cumulative water intake in TRPV1/TRPV4/double knockouts; smaller increase in Fos-positive subfornical organ in knockouts; TRPV1/4 not primary mechanism of dehydration response

A

Kinsman et al (2014)

21
Q

Dehydration doubled AQP3 mRNA with slight increase in protein expression

A

Ishibashi et al (1997)

22
Q

Vasopressin increases water permeability of kidney collecting duct by inducing translocation of aquaporin-CD water channels to plasma membrane

A

Nielsen et al (1995)

23
Q

AQP2 trafficking to vesicles is phosphorylation independent and to membrane is phosphorylation dependent

A

van Balkom et al (2002)

24
Q

AQP2 plasma membrane diffusion altered by degree of AQP2 phosphorylation

A

Arnspang et al (2016)

25
Q

Phosphorylation of AQP2 controls interaction with LIP5 lysosomal trafficking protein

A

Roche et al (2017)

26
Q

Vasopressin-induced phosphorylation reduces Sipa1|1-mediated AQP2 endocytosis

A

Wang et al (2017)

27
Q

Partial nephrogenic diabetes insipidus caused by novel AQP2 variation impairing trafficking of AQP2 water channel

A

Dollerup et al (2015)

28
Q

Decrease in AQP3 expression in rats with unilateral partial ureteral obstruction

A

Lee et al (2013)

29
Q

EDH4 is a novel regulator of urinary water homeostasis; knockouts have higher volume of more dilute urine with more dispersed AQP2

A

Rahman et al (2017)