Urinary Flashcards
(35 cards)
Functions of the urinary system
Filtration of blood/excretion of wast, regulation of water and electrolyte balance, regulation of arterial blood pressure, regulation of erythropoesis, production of vitamin D
Why are chronic renal diseases associate with anemia?
Because of a decrease in the production of erythropoietin
What is a renal lobe?
triangular-shaped structure consisting of a medullary pyramid covered by the corresponding cortex.
What is a renal lobule
portion of the cortex between two adjacent interlobular arteries
What is a medullary ray?
Single collecting duce collecting the fluid of the corresponding interlobular nephrons
Where are renal lobules and renal lobes?
Renal lobules are cortical. Renal lobes are combined cortical-medullary structures. Renal lobules are subcomponents of renal lobes
Where is the peritubular capillary network
surrounds the cortical segments of the uriniferous tubules
where is the vasa recta
an descending arteriolar-capillary and ascending capillary-venous component that are alongside the loop of Henle
What is the uriniferous tubule
nephron and collecting tubule/duct
What are the components of the nephron?
Renal corpuscle and the renal tubule
What are the components of the renal corpuscle?
capsule of bowman and glomerular capillaries (the glomerulus)
What are the components of the renal tubule?
PCT, loop of Henle, and DCT
What are the components of the glomerulus?
glomerular capillaries (fenestrated), mesangium (mesangial matrix), podocytes. NOTE does NOT include bowman’s capsule.
What do mesangial cells do?
have contractile and phagocytic properties. Provide mechanical support to capillaries, turn over basal lamina components, and secrete vasoactive substances (protaglandins and endothelians)
What are the layers of the glomerular filtration barrier
fenestrated endothelial cells, dual glomerular basal lamina, podocytes
Defects in the podocytes filtration slit diaphragm lead to…?
Hereditary proteinuria syndromes
Congenital nephrotic syndrome is caused by?
Mutations in the nephrin gene
What are the differences between acute proliferative glomerulonephritis and rapid progressive glomerulonephritis?
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.
What are the components of the juxtaglomerular apparatus
macula densa, extraglomerular mesangial cells, renin-producing juxtaglomerular cells.
What is fanconi syndrome?
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
Difference in brush border btwn PCT and DCT?
DCT is less well defined. Both are simple cuboidal.
What are the cell types of the collecting duct?
Principal cells (light) and intercalated cells (dark)
What do principal cells respond to?
Aldosterone
What does aldosterone do?
Reduces the excretion of NaCl in the thick ascending loop of Henle, the DCT, and the collection tubule.