Urinary System
Urinary System Overview
Discussion on Glomerular Filtration Rate (GFR)
Filtration occurs at a high level in kidneys.
Massive amounts of fluid filtered daily; entire liquid portion of blood filters approximately every 20 minutes.
Tubular Reabsorption and Secretion
Essential for reclaiming large amounts of fluid post-filtration.
Proximal Convoluted Tubule (PCT)
Primary site for reabsorption due to high pressure and large surface area.
Microvilli on PCT cells increase surface area.
Reabsorption processes include:
Passive diffusion and osmosis.
Active transport mechanisms:
Sodium-potassium pump (Na+/K+ ATPase) critical for powering reabsorption.
Secondary active transport for glucose, amino acids, etc.
Pinocytosis for small proteins.
Reabsorption occurs throughout nephron but predominantly in PCT.
Tubular secretion also occurs along nephron length:
Major sites include Distal Convoluted Tubule (DCT) and Collecting Duct.
Key secretions:
Hydrogen ions for pH regulation.
Potassium ions.
Other substances: creatinine, ammonia, toxins, drug metabolites.
Regulation of Potassium: Rigid control necessary to maintain balance and prevent toxicity.
Mechanisms of Reabsorption
Routes of Reabsorption
Paracellular: passive movement between cells; ~50% reabsorption in PCT.
Transcellular: through cells; facilitated by various transport systems.
Nutrient Reabsorption: linked to sodium transport.
Sodium coupled transport: e.g., Na+-glucose symporter.
Reabsorption of water is osmotically driven (follows solutes).
Two types of water reabsorption:
Obligatory: through always-open aquaporin-1 channels, occurring automatically.
Facultative: through aquaporin-2 channels, regulated by Antidiuretic Hormone (ADH).
Glucosuria and Transport Maximum
Glucosuria: presence of glucose in urine (also known as glycosuria).
Transports glucose until plasma concentration exceeds transport maximum (Tmax) of 180 mg/dL, leading to glucose in urine.
Commonly associated with diabetes mellitus (lack of insulin or resistance).
Other causes: high-carb meals can temporarily exceed Tmax.
Genetic variations may lead to inefficient glucose transport.
Bicarbonate Reabsorption
Bicarbonate reclamation prevents acidosis.
Process involves:
Bicarbonate freely filtered at glomerulus; important to reclaim.
Deamination of glutamine in PCT helps produce ammonia, aiding pH regulation.
Bicarbonate enters blood, hydrogen ion enters tubule, contributing to acid-base balance without altering pH directly.
Distal Convoluted Tubule and Collecting Duct Functions
DCT and Collecting Duct: final adjustments of filtrate.
Further Na+ and Cl- reabsorption; reabsorbs Ca2+ regulated by Parathyroid Hormone.
Final urine concentration adjustments influenced by ADH presence:
Dilute urine formation when ADH is absent.
Concentrated urine formation when ADH is present (inserting more aquaporin-2 channels).
Principal Cells: sensitive to aldosterone; manage sodium reabsorption and potassium secretion.
Intercalated Cells: primarily pH regulation; manage bicarbonate and hydrogen ion levels.
Hormonal Regulation and Kidney Function
Renin-Angiotensin-Aldosterone System (RAAS):
Triggered by low blood flow, leading to renal reabsorption.
Aldosterone increases Na+ reabsorption, affecting blood pressure and volume.
Atrial Natriuretic Peptide (ANP): regulates blood pressure; can counteract effects of aldosterone when fluid volume increases.
Antidiuretic Hormone (ADH): maintains water balance by regulating water reabsorption in the kidneys.
Countercurrent Multiplication and Concentration of Urine
Two mechanisms: Countercurrent Multiplier and Countercurrent Exchange.
Countercurrent Multiplier
Establishes osmolarity gradient in the medulla through Na+ pumps in the ascending limb of Loop of Henle.
Descending limb permeable to water; ascension concentrates tubular fluid.
Resulting high osmolarity (up to 1200 mOsm/L) ensures maximal concentration of urine when necessary.
Countercurrent Exchange (via vasa recta):
Maintains osmotic gradient; prevents dilution by balancing movement of water and solutes.
Diuretics: Effects and Use
Diuretics promote urine formation; common for managing hypertension and congestive heart failure.
Types include osmotic (e.g., mannitol), loop diuretics (e.g., furosemide/Lasix), thiazides, and aldosterone antagonists.
Osmotic Diuretics: retain water in tubules by preventing reabsorption.
Loop Diuretics: impair the concentration gradient, leading to increased urine output.
Thiazides: calcium-sparing effects useful in particular patient populations.
Evaluating Kidney Function
Tests for BUN and creatinine levels to assess kidney function.
Urinalysis to detect abnormalities (e.g., glucose, proteins).
Oliguria (<400 mL/day) and anuria (<50 mL/day): assess for potential kidney dysfunction.
Kidney Injuries and Renal Failure
Acute Kidney Injury (AKI) recognized through decreased GFR.
Types of kidney injury:
Prerenal: due to insufficient blood distribution to kidneys (dehydration, hemorrhage).
Renal: direct damage to kidney tissue (inflammation, nephritis).
Postrenal: obstruction hindering urine flow from kidneys (stones, tumors).
Chronic Kidney Disease (CKD): persistent damage requiring assessment and management plans.
Diabetes mellitus as Cause for Urinary Symptoms
Diabetes leads to osmotic diuresis, common in type 1 and type 2 diabetes due to blood glucose levels exceeding Tmax.
Gestational diabetes parallels type 2 behavior. Renal diabetes linked to ineffective glucose transporter function.
Diabetes insipidus: absence of ADH, leading to excessive urination.
Dialysis: Life-sustaining Treatment
Patients undergoing dialysis experience extensive management due to end-stage renal disease.
Different forms of dialysis: hemodialysis and peritoneal dialysis with varying patient implications.
HD: typically requires vascular access via AV fistula for sustained treatments.
Structure and Function of the Ureters and Bladder
Ureters: Deliver urine from kidneys; retroperitoneal orientation.
Bladder: Elastic, muscular sac, sits below uterus in females; undergoes contraction during voiding (urination).
Micturition Reflex: Stretch receptors activate the detrusor muscle.
Sphincters: Internal (involuntary) and external (voluntary, skeletal muscle).
Urethra: Shorter in females, longer in males; differentiated structure with various regions as per anatomy.
Urinary Incontinence and Control
Types include stress incontinence (sudden pressure events) and urge incontinence (sudden detrusor muscle contractions).
Kegel exercises encouraged for women to strengthen pelvic floor to improve symptom management.