Urinary Flashcards

1
Q

Functions of the urinary system

A

Filtration of blood/excretion of wast, regulation of water and electrolyte balance, regulation of arterial blood pressure, regulation of erythropoesis, production of vitamin D

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2
Q

Why are chronic renal diseases associate with anemia?

A

Because of a decrease in the production of erythropoietin

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3
Q

What is a renal lobe?

A

triangular-shaped structure consisting of a medullary pyramid covered by the corresponding cortex.

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4
Q

What is a renal lobule

A

portion of the cortex between two adjacent interlobular arteries

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5
Q

What is a medullary ray?

A

Single collecting duce collecting the fluid of the corresponding interlobular nephrons

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6
Q

Where are renal lobules and renal lobes?

A

Renal lobules are cortical. Renal lobes are combined cortical-medullary structures. Renal lobules are subcomponents of renal lobes

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7
Q

Where is the peritubular capillary network

A

surrounds the cortical segments of the uriniferous tubules

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8
Q

where is the vasa recta

A

an descending arteriolar-capillary and ascending capillary-venous component that are alongside the loop of Henle

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9
Q

What is the uriniferous tubule

A

nephron and collecting tubule/duct

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10
Q

What are the components of the nephron?

A

Renal corpuscle and the renal tubule

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11
Q

What are the components of the renal corpuscle?

A

capsule of bowman and glomerular capillaries (the glomerulus)

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12
Q

What are the components of the renal tubule?

A

PCT, loop of Henle, and DCT

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13
Q

What are the components of the glomerulus?

A

glomerular capillaries (fenestrated), mesangium (mesangial matrix), podocytes. NOTE does NOT include bowman’s capsule.

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14
Q

What do mesangial cells do?

A

have contractile and phagocytic properties. Provide mechanical support to capillaries, turn over basal lamina components, and secrete vasoactive substances (protaglandins and endothelians)

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15
Q

What are the layers of the glomerular filtration barrier

A

fenestrated endothelial cells, dual glomerular basal lamina, podocytes

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16
Q

Defects in the podocytes filtration slit diaphragm lead to…?

A

Hereditary proteinuria syndromes

17
Q

Congenital nephrotic syndrome is caused by?

A

Mutations in the nephrin gene

18
Q

What are the differences between acute proliferative glomerulonephritis and rapid progressive glomerulonephritis?

A

Acute: reversible in children. Caused by proliferation of endothelial and mesangial cells in the presence of neutrophiles. Rapid: proliferation of parietal cells in bowman’s capsule and infiltration of macrophages forming a crescent-like mass within the glomerulus. Observed in Goodpasture syndrome.

19
Q

What are the components of the juxtaglomerular apparatus

A

macula densa, extraglomerular mesangial cells, renin-producing juxtaglomerular cells.

20
Q

What is fanconi syndrome?

A

amino acids and glucose are not reabsorbed and are found in urine. Defect in the cellular energy metabolism decreasing levels of ATP and impairing the Na/K pump

21
Q

Difference in brush border btwn PCT and DCT?

A

DCT is less well defined. Both are simple cuboidal.

22
Q

What are the cell types of the collecting duct?

A

Principal cells (light) and intercalated cells (dark)

23
Q

What do principal cells respond to?

A

Aldosterone

24
Q

What does aldosterone do?

A

Reduces the excretion of NaCl in the thick ascending loop of Henle, the DCT, and the collection tubule.

25
Q

Flow of blood in the kidney

A

interlobar artery - arcuate artery - interlobular artery - affarent glomerular arterioles - efferent arterioles - IN SUBCAPSULAR REGION: peritubular capillary network. IN JUXTAMEDULLARY REGION: vasa recta

26
Q

What is the function of podocytes?

A

Foot processes assist in filtration barrier function by repelling negatively-charged molecules.

27
Q

What is the function of mesangial cells?

A

Provides structure support and regulate diameter of capillaries.

28
Q

What is the function of macula densa?

A

Senses blood pressure, regulates blood flow in afferent arteriole to maintain the glomerular filtration rate and stimulates release of renin.

29
Q

What is the function of juxtaglomerular complex?

A

synthesize, store and release renin.

30
Q

What happens where there are problems with polycystin 1 and 2?

A

They are primarily in the primary cilium of principle cells (in the collecting duct). Mutations in either gene leads to autosomal dominant polycystic kidney disease.

31
Q

What do intercalated cells do?

A

Dark cells. Secrete either H or HCO3 and reabsorb K in collecting duct. Have apical microvilli.

32
Q

What do principal cells do?

A

Light cells. Reabsorb Na and water and secrete K. Primary cillium with polycystin 1 and 2.

33
Q

What does aldosterone do?

A

Stimulates reabsorption of Na at the collecting tubule by the principal cells.

34
Q

What does angiotensin II stimulate?

A
  1. aldosterone secretion by adrenal cortex 2. arteriolar vasoconstriction 3. ADH secretion and thirst 4. reabsorption of NaCl by PCT
35
Q

Describe the changes in the epithelium as urine moves from the ureter through the urethra.

A

The ureter and bladder have a transitional epithelium. The initial segment of the urethra has a stratified epithelium, and the final segment has a stratified squamous epithelium.