Proximal Tubular Dysfunctions and Disorders of Water Balance - Gosmanova Flashcards

1
Q

Which segments of the PT secrete organic compounds?

A

S2 and S3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the types of transport mechanisms present in the PT?

A

Primary active
Secondary active
Passive
Pinoctyosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What substances are reabsorbed via Na cotransport in the PT?

A

Sugars
Amino acids
Phosphate
Citrate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What substances are reabsorbed via Na antiport in the PT?

A

H

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What does angiotensin II promote in the PT?

A

Na / H antiporter (luminal)

HCO3 / Na cotransport (basolateral)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What can cause a defect in glucose reabsorption?

A

Mutation of SGLT2 glucose transporter (Hereditary Renal Glucosuria)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What can cause a defect in amino acid reabsorption?

A

Mutation of brush border transporter for cystine, ornithine, lysine, and arginine
Cystinuria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What can cause a defect in phosphate reabsorption?

A

Mutation in PHEX gene (X-linked hypophosphatemia - most common)
Mutation in FGF-23 (Hypophosphatemic rickets)
Increased FGF-23 production (Oncogenic hypophosphatemic osteomalacia)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is Fanconi syndrome?

A
Collection of symptoms (different underlying causes)
Aminoaciduria
Glucosuria
Hypophosphatemia
Hyperchloremic metabolic acidosis
Hypokalemia
Uricosuria
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is an inherited cause of Fanconi syndrome?

A

Cystinosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are acquired causes of Fanconi syndrome?

A
Drugs (Tenofovir)
Heavy Metals
Toxins
Dysproteinemias (Multiple myeloma)
Acute tubular necrosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the normal osmotic threshold for ADH and thirst?

A

ADH 280-290

Thirst 290-295

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is osmolar clearance?

A

Amount of water needed to excrete solutes at the concentration of solutes in plasma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the most common electrolyte disorder?

A

Hyponatremia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is hyperosmolar hyponatremia?

A

Dilutional hyponatremia due to presense of osmotically active substances (glucose, mannitol, glycine)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is psudohyponatremia?

A

This occurs with increased solid phase of plasma and is an artifact of Na assays

17
Q

What is true hyponatremia and what is the underlying mechanism?

A

Hypoosmolar hyponatremia

Impaired urinary dilution mechanisms

18
Q

What are causes of hypovolemic hyponatremia?

A

Renal losses
GI losses
Skin losses
Third spacing (Pancreatitis, bowel obstruction, burns)

19
Q

What causes euvolemic hyponatremia?

A

SIADH
Glucocorticoid deficiency
Hypothyroidism

20
Q

What causes hypervolemic hyponatremia?

A

CHF
Acute / Chronic kidney failure
Cirrhosis
Nephrotic syndrome

21
Q

How can you differentiate psychogenic polydipsia and SIADH?

A

Urine osmolality
Polydipsia - Low
SIADH - high

22
Q

What is the main defense against hypernatremia?

A

Thirst

23
Q

What is polyuria?

A

> 3 L urine / day

24
Q

What are two differences between DI and polydipsia?

A

DI - high Posm and 500 Uosm in response to water deprivation