Urinary Flashcards

(35 cards)

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?

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
Flow of blood in the kidney
interlobar artery - arcuate artery - interlobular artery - affarent glomerular arterioles - efferent arterioles - IN SUBCAPSULAR REGION: peritubular capillary network. IN JUXTAMEDULLARY REGION: vasa recta
26
What is the function of podocytes?
Foot processes assist in filtration barrier function by repelling negatively-charged molecules.
27
What is the function of mesangial cells?
Provides structure support and regulate diameter of capillaries.
28
What is the function of macula densa?
Senses blood pressure, regulates blood flow in afferent arteriole to maintain the glomerular filtration rate and stimulates release of renin.
29
What is the function of juxtaglomerular complex?
synthesize, store and release renin.
30
What happens where there are problems with polycystin 1 and 2?
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
What do intercalated cells do?
Dark cells. Secrete either H or HCO3 and reabsorb K in collecting duct. Have apical microvilli.
32
What do principal cells do?
Light cells. Reabsorb Na and water and secrete K. Primary cillium with polycystin 1 and 2.
33
What does aldosterone do?
Stimulates reabsorption of Na at the collecting tubule by the principal cells.
34
What does angiotensin II stimulate?
1. aldosterone secretion by adrenal cortex 2. arteriolar vasoconstriction 3. ADH secretion and thirst 4. reabsorption of NaCl by PCT
35
Describe the changes in the epithelium as urine moves from the ureter through the urethra.
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.