Front | Back |
Describe the anatomy of the kidney.
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- surrounded by insulating fat
- in connective tissue behind abdominal cavity (retroperitoneum) - concave aspect (hilum) where blood vessels, nerves and urinary tract enter - renal cortex is outer 1/3, inner 2/3 is medulla - medulla consists of pyramids whose bases face the cortex and tips have small openings of collecting duct that empty into renal pelvis |
Describe the anatomy of the urinary tract after the kidneys.
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- urine propelled by contractions along ureter
- ureter goes to bladder that holds 500 cc - bladder empties at base via urethra |
Differentiate between male and female urethras.
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- 20 cm in males
- 4 cm in females - higher incidence of urinary tract infection and incontinence in women - urethra passes through prostate in male - plays role in sexual function and when it enlarges, obstructs urinary tract in older men |
What filters the blood?
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- glomerulis (tuft of capillaries) with long epithelial tubes that collect and concentrate urine
- glomerulus surrounded by double walled epithelial capsule (bowman's) - space inside capsule collects fluid that is pressed through capillaries - fenestrations allow passage of fluid - glomerular basement memrane is mesh where small molecules pass through and proteins can't leave - GBM repel negatively charged proteins in blood - both physical and charge barrier - glomerular kidney disease - damage to GBM - final barrier from capillary space to urinary space - podocytes (finger like processes) with slits |
What happens to fluid after it leaves the glomerulus?
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- enter proximal convoluted tubule which reabsorbs 2/3 of filtered water and sodium, glucose, amino acids
- travels to loop of Henle that goes towards middle of kidney and then back to cortex - through active pumping, epithelial cells in loop are responsible for creation of concentration gradient that allows for further reabsorption of water and ions - enters distal convuluted tubule and leaves through collecting duct - this tubing forms the pyramids, and all cllecting ducts converge at tips of pyramids - urine empties into renal pelvis and is propelled to bladder |
Describe the anatomy of the pelvis, ureters, and bladder.
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- all lined by multilayered epithelium of transitional cells
- surrounded by smooth muscle |
What are the functions of the kidney?
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- elimination of drugs, toxins, poisons, metabolic waste
- maintenance of electrolyte concentrations - maintenance of water balance - regulation of pH - regulation of BP - regulation of vitamin D by converting it to active form - releasing hormone, erthropoietin |
What are the causes of renal failure?
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- pre-renal (septic shock, dehydration, hemorrhage, heart failure)
- renal (acute tubular necrosis, acute glomerulonephritis) - post-renal (urinary tract obstruction) |
What problems arise due to renal failure?
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- edema
- increased levels of sodium, potassium, phosphate - metabolic acidosis - build up of nitrogenous wastes in blood - decreased erythropoietin synthesis (anemia) - hypertension (sodium and water retention, increased renin - renin regulates BP) - bone disease (renal osteodystrophy) - increased blood phosphate and impaired reabsorption of calcium = low blood calcium... body reabsorbs more from bone; decreased activation of vit D - accumulation of waste products (itching, nausea, vomiting, decreased appetite, ulcers, inflammation of tissue, blood clotting problems, WBC dysfunction, nerve and muscle dysfunction, drowsiness, coma, death) |
What is the difference between acute and chronic renal failure?
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- acute is reversible , rapid onset of symptoms
- chronic is irreversible and loss of function, can result from loss of glomeruli, hypertension, chrnic urinary tract obstruction, diabetes, lupus... clinically silent at first |
Why are cystic diseases clinically important?
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- major causes of chronic renal failure
- can be confused with malignant tumours - some are hereditary and have implications for family members |
Describe adult polycystic kidney disease.
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- autosomal dominant inheritance
- mutations in three separate genes - PKD1 gene on chromosome 16 codes for polycystin which is involved in cell-cell and cell-matrix interactions in kidney, liver, pancreas - mechanisms are unclear, but los of protein results in altered growth regulation and differentiation of tubular epithelial cells... cysts form - one of most common causes of renal failure - affects BOTH kidneys... become enlarged and functional tissue replaced by thin-walled cysts which contain fluid - cysts destroy nephrons, chrnic renal failure occurs... affects liver, pancreas, spleen - predisposed to aneurysms in blood vessels of brain |
Describe infantile polycystic kidney disease.
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- different genes affected
- autsomal recessive inheritance - develop in childhilld... earlier symptoms - predisposed to liver fibrosis - dilated cortical and medullary collecting ducts arranged radially... external surface smooth |
What is the difference between primary and secondary glomerulopathies?
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- primary - affect glomerulus primarily or exclusively
- secondary - affect multiple organs, including kidney... diabetes, lupus, vasculitis |
What are glomerular disease usually a result of?
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- abnormal immune reaction resulting in deposition of antibodies or antigen-antibody immune complexes in GBM
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