Excretory System MCQ for RRB & SSC and other Competitive exams
91
What is the process of micturition (urination) controlled by?
✓ Answer:
B
A combination of involuntary (autonomic) and voluntary (somatic) control - micturition reflex via sacral spinal cord plus voluntary control of external sphincter
Micturition (urination) is controlled by: Involuntary (Autonomic) component = Parasympathetic (S2-S4) contracts detrusor muscle, relaxes internal urethral sphincter (promotes urination) and Sympathetic (L1-L2) relaxes detrusor, contracts internal sphincter (promotes urine storage). Voluntary (Somatic) component = Pudendal nerve (S2-S4) controls external urethral sphincter (skeletal muscle) - voluntary hold or release. Higher cortical centres (frontal lobe) override the reflex - social continence. Micturition reflex: Bladder stretch > sacral cord > detrusor contraction + internal sphincter relaxation. Spinal cord injury above sacral level causes neurogenic bladder (reflex but no voluntary control).
92
What is the significance of protein in urine during pregnancy?
✓ Answer:
B
Significant proteinuria (>300 mg/24h) after 20 weeks gestation, especially with hypertension, suggests pre-eclampsia
Pre-eclampsia is a serious pregnancy complication defined as: Hypertension (BP >=140/90 mmHg) after 20 weeks gestation + Significant proteinuria (>=300 mg/24h or urine protein:creatinine ratio >=30 mg/mmol). Symptoms: headache, visual disturbances, epigastric pain, oedema (especially facial/hand). Complications: Eclampsia (seizures in a pre-eclamptic patient - life-threatening), HELLP syndrome (Haemolysis + Elevated Liver enzymes + Low Platelets), Placental abruption, IUGR, preterm birth. Pathophysiology: Poor placentation > inadequate trophoblast invasion > placental ischaemia > release of vasoconstrictive factors > systemic endothelial dysfunction. Treatment: antihypertensives, magnesium sulphate (prevent seizures), delivery (definitive treatment).
93
What is the role of atrial natriuretic peptide (ANP) in kidney function?
✓ Answer:
B
ANP is released by the heart when blood volume is high - it causes natriuresis (sodium excretion) and diuresis, lowering blood pressure
Atrial Natriuretic Peptide (ANP) is a hormone released by atrial cardiomyocytes when atrial walls are stretched (indicating high blood volume/pressure). Its effects on the kidney: Increases GFR (dilates afferent arteriole, constricts efferent arteriole), Inhibits Na+ reabsorption in collecting duct (natriuresis - Na+ excretion), Increases water excretion (diuresis), Inhibits renin and aldosterone release, and Inhibits ADH release. Net effect: Reduces blood volume and blood pressure. ANP acts as a counter-regulatory hormone to the RAAS - when volume is too high, ANP brings it back down. BNP (Brain/B-type Natriuretic Peptide) is released by ventricles - used as a marker of heart failure.
94
What are renal casts and what do they indicate?
✓ Answer:
B
Cylindrical protein structures formed in the tubules - different types indicate specific kidney diseases
Renal Casts are cylindrical structures formed when proteins (mainly Tamm-Horsfall protein/uromodulin) precipitate in the tubular lumen, trapping cells or debris. Types and significance: Hyaline casts (normal finding in small numbers; concentrated urine, exercise), RBC casts (Red cell casts) = pathognomonic of glomerulonephritis - most important, WBC casts = pyelonephritis/interstitial nephritis, Granular casts (muddy brown) = Acute Tubular Necrosis (ATN) - ischaemia/nephrotoxins, Fatty casts = nephrotic syndrome (lipiduria), Waxy casts = advanced CKD (slow tubular flow), and Epithelial cell casts = ATN/heavy metal toxicity. Casts are seen on urine microscopy - a key part of urinalysis in kidney disease workup.
95
What is renal osteodystrophy?
✓ Answer:
B
Bone disease occurring in CKD due to disturbances in calcium, phosphate, PTH, and vitamin D metabolism
Renal Osteodystrophy (CKD-Mineral Bone Disorder / CKD-MBD) is the bone disease of Chronic Kidney Disease due to complex metabolic disturbances: 1) Reduced GFR > phosphate retention (hyperphosphataemia). 2) Damaged kidney > reduced 1-alpha hydroxylase > reduced calcitriol (active Vit D). 3) Reduced calcitriol > reduced intestinal calcium absorption > hypocalcaemia. 4) Hyperphosphataemia + Hypocalcaemia > stimulate parathyroid glands > secondary hyperparathyroidism (excess PTH). 5) Excess PTH > bone resorption > osteitis fibrosa cystica (bone pain, fractures, brown tumours). Treatment: Phosphate binders (calcium carbonate, sevelamer), Active Vitamin D (alfacalcidol), Cinacalcet (reduces PTH), dialysis.
96
What is incontinence?
✓ Answer:
B
Involuntary leakage of urine due to loss of bladder control
Urinary Incontinence is the involuntary leakage of urine. Types: Stress incontinence (leakage on coughing, sneezing, laughing, exercise - increased intra-abdominal pressure overcomes urethral sphincter - common in women after childbirth/pelvic floor weakness. Treatment: pelvic floor exercises/Kegel exercises), Urge incontinence (sudden strong urge followed by involuntary leakage - overactive bladder. Treatment: anticholinergics/oxybutynin), Overflow incontinence (bladder unable to empty fully - overflow leakage - common in men with prostate enlargement), and Total incontinence (complete loss of sphincter control - spinal cord injury). Risk factors: age, childbirth, menopause, obesity, prostate problems, neurological conditions.
97
What is the concept of clearance in kidney physiology?
✓ Answer:
B
The volume of plasma completely cleared of a given substance by the kidneys per unit time
Renal Clearance (C) is the volume of plasma from which a given substance is completely removed (cleared) by the kidneys per unit time (mL/min). Formula: C = (U x V) / P where U = urine concentration, V = urine flow rate (mL/min), P = plasma concentration. Clinical applications: Inulin clearance = GFR (freely filtered, not secreted or reabsorbed - gold standard but impractical), Creatinine clearance is approximately equal to GFR (slight overestimation due to tubular secretion), PAH (Para-aminohippuric acid) clearance = Renal Plasma Flow (RPF) - completely filtered + secreted. If clearance of substance > GFR = substance is secreted by tubules. If clearance < GFR = substance is reabsorbed by tubules.
98
What is the clinical importance of urine osmolality?
✓ Answer:
B
It measures the concentration of solutes in urine and reflects the kidney's concentrating/diluting ability
Urine Osmolality measures the concentration of all solutes dissolved in urine (mOsm/kg). Normal range: 50-1200 mOsm/kg (reflects extreme diluting to concentrating ability). Clinical significance: Maximum concentration = ~1200-1400 mOsm/kg (severe dehydration, ADH maximum). Minimum dilution = ~50-100 mOsm/kg (maximum water intake, ADH suppressed). Isosthenuria (fixed ~300 mOsm/kg = plasma osmolality) = Severe CKD - loss of concentrating ability. Water deprivation test: If urine osmolality fails to rise = Diabetes insipidus. SIADH = Urine osmolality inappropriately high (>100 mOsm/kg) despite hyponatraemia. Prerenal AKI: High urine osmolality (>500) = kidney conserving water (appropriate response to dehydration).
99
What is the significance of measuring serum electrolytes in kidney disease?
✓ Answer:
B
The kidney regulates electrolyte balance - kidney disease causes dangerous imbalances in Na+, K+, HCO3-, Ca2+, and phosphate
The kidney is the primary regulator of electrolyte balance. In kidney disease, dangerous abnormalities occur: Hyperkalaemia (K+ >5.5 mmol/L) - most life-threatening complication of CKD/AKI - cardiac arrhythmias, cardiac arrest. ECG changes: peaked T waves - widened QRS - sine wave - VF. Hyponatraemia (Na+ <135 mmol/L) - confusion, seizures, cerebral oedema. Metabolic acidosis (low HCO3-) - due to failure to excrete H+. Hypocalcaemia - due to reduced Vit D activation (CKD). Hyperphosphataemia - due to reduced excretion (CKD). Hypomagnesaemia - can occur with diuretics. Regular monitoring of renal panel (U&E - urea, electrolytes, creatinine) is essential in all kidney disease patients.
100
What is the overall importance of the excretory system in maintaining homeostasis?
✓ Answer:
B
The excretory system maintains homeostasis by regulating fluid balance, electrolyte levels, blood pressure, acid-base balance, and removing metabolic wastes
The excretory system - primarily through the kidneys - maintains homeostasis through multiple functions: 1) Waste elimination (urea, creatinine, uric acid, drugs, toxins), 2) Fluid balance (regulates body water content - produces concentrated or dilute urine), 3) Electrolyte regulation (Na+, K+, Ca2+, Mg2+, phosphate, HCO3- balance), 4) Blood pressure regulation (RAAS, pressure natriuresis, prostaglandins), 5) Acid-base balance (H+ excretion, HCO3- reabsorption), 6) Hormone production (EPO - erythropoiesis, Renin - RAAS, Calcitriol - Vitamin D activation), and 7) Gluconeogenesis (contributes to blood glucose during fasting). Without the excretory system, toxic waste would accumulate leading to uraemia, acidosis, fluid overload, electrolyte imbalances, and hypertension - all life-threatening. The kidneys are truly the body's master chemists.