B Pharmacy Sem 2: Human Anatomy and Physiology II
Subject: Human Anatomy and Physiology II
- Cardiovascular & Lymphatic Systems
- Respiratory System
- Digestive System & Metabolism
- Urinary System & Fluid & Electrolyte Balance
- Endocrine Glands & Hormonal Regulation
- Reproductive System & Developmental Physiology
Unit 1: Cardiovascular & Lymphatic Systems
This unit covers the heart, blood vessels, blood, and lymphatic system. You’ll learn the structure and function of the heart, the cardiac cycle, blood circulation types, blood components, hemostasis, and lymphatic organs—essential for understanding drug distribution, pathology, and immune responses.
1.1 Heart Anatomy
The heart is a muscular, four-chambered pump that maintains blood circulation.
Chambers: Right atrium, right ventricle, left atrium, left ventricle
Valves: Tricuspid (RA–RV), pulmonary (RV–pulmonary artery), mitral/bicuspid (LA–LV), aortic (LV–aorta)
Layers of Heart Wall:
Endocardium: inner lining
Myocardium: thick muscle layer
Epicardium: outer protective layer
Pericardium: double-walled sac enclosing heart; pericardial fluid reduces friction.
1.2 Conducting System of the Heart
The heart has an intrinsic electrical system that coordinates contraction:
SA Node (Sinoatrial Node): natural pacemaker; initiates impulse
AV Node (Atrioventricular Node): delays impulse for ventricular filling
Bundle of His: conducts impulse to ventricles
Purkinje Fibers: spread impulse through ventricular myocardium
This system creates the cardiac cycle, a repeating sequence of systole (contraction) and diastole (relaxation).
1.3 Cardiac Cycle
Atrial Systole: atria contract → ventricles fill
Ventricular Systole: ventricles contract → blood ejected into aorta and pulmonary artery
Diastole: both atria and ventricles relax → chambers refill
Heart sounds:
S1 (“lub”): closure of AV valves
S2 (“dub”): closure of semilunar valves
1.4 Blood Vessels & Circulation
Arteries: carry blood away from heart (high pressure)
Veins: return blood to heart (low pressure, valves prevent backflow)
Capillaries: microscopic vessels for exchange of gases, nutrients, wastes
Circulatory pathways:
Systemic circulation: LV → body → RA
Pulmonary circulation: RV → lungs → LA
Coronary circulation: supplies heart muscle
1.5 Blood
Blood is a fluid connective tissue (5–6 L in adults).
Components:
Plasma (55%): water, proteins (albumin, globulin, fibrinogen), nutrients, hormones, waste products
Formed elements (45%):
Erythrocytes (RBCs): carry oxygen via hemoglobin
Leukocytes (WBCs): immune defense
Thrombocytes (platelets): blood clotting
1.6 Hemostasis & Blood Coagulation
Hemostasis stops bleeding after vessel injury:
Vascular spasm: immediate vasoconstriction
Platelet plug formation: platelets adhere and aggregate
Coagulation cascade: fibrin mesh forms clot
Intrinsic & Extrinsic pathways converge at factor X → thrombin → fibrin.
1.7 Blood Groups
ABO System: A, B, AB, O blood types based on antigen presence
Rh factor: positive (+) or negative (–); important in transfusion and pregnancy
Cross-matching: prevents transfusion reactions.
1.8 Lymphatic System
The lymphatic system drains tissue fluid (lymph) back to circulation, filters pathogens, and helps immunity.
Lymph vessels: parallel veins, return lymph via thoracic duct & right lymphatic duct
Lymph nodes: filter lymph, house lymphocytes
Organs: spleen (filters blood), thymus (T-cell maturation), tonsils (first defense in oral/nasal cavities)
Functions:
Maintain fluid balance
Absorb fats from intestine (lacteals)
Provide immune surveillance
1.9 Clinical Correlations
Hypertension: sustained high blood pressure; risks heart attack, stroke
Atherosclerosis: plaque buildup in arteries; leads to coronary artery disease
Anemia: reduced RBCs/hemoglobin; causes fatigue, pallor
Leukemia: cancer of WBCs; abnormal proliferation
Lymphedema: lymphatic blockage; swelling of tissues
1.10 Key Points for Exams
✔ Be able to label heart chambers and valves
✔ Explain cardiac cycle phases and heart sounds
✔ List blood components and their functions
✔ Describe hemostasis steps
✔ Understand ABO/Rh blood grouping
✔ Recall major lymphatic organs and their roles
Unit 2: Respiratory System
This unit explores the structures and functions of the respiratory tract, the mechanics of breathing, pulmonary volumes and capacities, gas exchange and transport, and neural and chemical regulation of respiration.
2.1 Anatomy of the Respiratory Tract
Upper Respiratory Tract:
Nasal cavity & sinuses: filter, warm and humidify inspired air
Pharynx & larynx: conduct air; larynx houses vocal cords
Lower Respiratory Tract:
Trachea: C‑shaped cartilaginous rings maintain patency
Bronchi & bronchioles: branching network; terminal bronchioles lead to respiratory zone
Alveoli: thin‑walled sacs for gas exchange; Type I (structure) and Type II (surfactant secretion) pneumocytes
2.2 Mechanics of Breathing (Pulmonary Ventilation)
Breathing depends on pressure differences between alveoli and atmosphere:
Inspiration (active):
Diaphragm contracts (flattens)
External intercostals elevate ribs
Intrapulmonary pressure ↓ → air flows in
Expiration (passive at rest):
Diaphragm and intercostals relax
Elastic recoil ↑ intrapulmonary pressure → air expelled
Forced breathing uses accessory muscles (sternocleidomastoids, abdominals).
2.3 Lung Volumes & Capacities
Measured by spirometry to assess pulmonary function:
Volume/Capacity | Definition |
---|---|
Tidal Volume (TV) | Air moved in/out in a normal breath (~500 mL) |
Inspiratory Reserve Volume (IRV) | Extra air inhaled after normal inspiration (~3 000 mL) |
Expiratory Reserve Volume (ERV) | Extra air exhaled after normal expiration (~1 100 mL) |
Residual Volume (RV) | Air remaining after maximal expiration (~1 200 mL) |
Capacities | |
Vital Capacity (VC) = TV+IRV+ERV | Max air exhaled after maximal inhalation (~4 600 mL) |
Total Lung Capacity (TLC) = VC+RV | Total volume lungs can hold (~5 800 mL) |
Functional Residual Capacity (FRC) = ERV+RV | Air in lungs after normal expiration (~2 300 mL) |
Inspiratory Capacity (IC) = TV+IRV | Max air inhaled after normal expiration (~3 500 mL) |
2.4 Gas Exchange & Transport
External Respiration:
Alveolar gas exchange across respiratory membrane (thin barrier)
Fick’s law: rate ∝ surface area × pressure gradient ÷ thickness
Internal Respiration:
Exchange of O₂ and CO₂ between blood and tissues
O₂ Transport:
~98 % bound to hemoglobin (forms oxyhemoglobin)
~2 % dissolved in plasma
CO₂ Transport:
~70 % as bicarbonate (HCO₃⁻)
~23 % bound to hemoglobin (carbaminohemoglobin)
~7 % dissolved
Oxyhemoglobin Dissociation Curve: factors shifting curve:
Right shift (↓ pH, ↑ CO₂, ↑ temperature) promotes O₂ release
Left shift (↑ pH, ↓ CO₂, ↓ temperature) promotes O₂ binding
2.5 Regulation of Respiration
Neural Control:
Medullary respiratory centers: dorsal (inspiration), ventral (expiration)
Pontine centers: fine‑tune rhythm
Chemical Control:
Central chemoreceptors (medulla): respond to ↑ PCO₂ (via H⁺)
Peripheral chemoreceptors (carotid & aortic bodies): respond to ↓ PO₂, ↑ PCO₂, ↓ pH
Other Influences:
Stretch reflexes (Hering–Breuer) prevent over‑inflation
Higher brain centers (voluntary control, emotions)
2.6 Clinical Correlations
Asthma: chronic bronchoconstriction, inflammation; measured by ↓ FEV₁/ FVC ratio
Chronic Obstructive Pulmonary Disease (COPD): emphysema + chronic bronchitis; ↑ RV, ↓ VC
Acute Respiratory Distress Syndrome (ARDS): increased alveolar membrane permeability → hypoxemia
Pneumonia: alveolar fluid/inflammation impairs gas exchange
Hypoxia Types: hypoxemic, anemic, circulatory, histotoxic
2.7 Key Points for Exams
Be able to draw and label respiratory volumes and capacities
Explain mechanics of inspiration and expiration
Describe gas exchange mechanisms and O₂/CO₂ transport
Know factors that shift the oxyhemoglobin dissociation curve
Recall neural vs. chemical controls of breathing
Recognize basic spirometric patterns in obstructive vs. restrictive diseases
Unit 3: Digestive System & Metabolism
This unit examines the structure and function of the gastrointestinal (GI) tract, accessory organs, digestive secretions, mechanisms of nutrient digestion and absorption, and key metabolic pathways that transform food into usable energy and biomolecules.
3.1 Anatomy of the Gastrointestinal Tract
Alimentary Canal (mouth → anus):
Mouth & Pharynx: ingestion, mastication, bolus formation
Esophagus: muscular tube; peristalsis transports bolus
Stomach: storage; mechanical churning and acid–pepsin digestion
Small Intestine (duodenum, jejunum, ileum): primary site of digestion and absorption
Large Intestine (cecum, colon, rectum): water absorption, feces formation
Accessory Organs:
Salivary Glands: secrete amylase‑rich saliva
Liver: produces bile for fat emulsification
Gallbladder: concentrates and stores bile
Pancreas: exocrine (digestive enzymes, bicarbonate) and endocrine (insulin, glucagon) functions
3.2 Digestive Secretions & Enzymes
Secretion | Source | Major Components & Actions |
---|---|---|
Saliva | Parotid, submandibular, sublingual glands | Amylase (starch → maltose), mucin |
Gastric Juice | Gastric glands | HCl (protein denaturation), pepsinogen → pepsin (protein → peptides), intrinsic factor (B₁₂ absorption) |
Pancreatic Juice | Pancreas (acinar cells) | Trypsin, chymotrypsin (proteins), amylase, lipase, bicarbonate (neutralizes duodenal pH) |
Bile | Liver hepatocytes | Bile salts (emulsify fats), bilirubin, cholesterol |
Intestinal Juice | Crypts of Lieberkühn | Brush‑border enzymes: lactase, sucrase, peptidases |
3.3 Mechanisms of Digestion & Absorption
Carbohydrates: starch → maltose (amylases) → monosaccharides (glucose, galactose, fructose) via brush‑border enzymes; absorbed by secondary active transport (SGLT) and facilitated diffusion (GLUT).
Proteins: pepsin in stomach; trypsin/chymotrypsin → small peptides; brush‑border peptidases → amino acids; absorbed via active transport.
Lipids: emulsified by bile salts → micelles; lipases → monoglycerides + free fatty acids; re‑esterified to triglycerides in enterocytes; packaged into chylomicrons for lymphatic transport.
Vitamins & Minerals:
Fat‑soluble (A, D, E, K) with fats via micelles
Water‑soluble (B‑complex, C) by diffusion or transporters
Minerals (e.g., Ca²⁺ by vitamin D–dependent active transport; Fe²⁺ via DMT1)
3.4 Blood Supply & Portal Circulation
Arterial Supply: celiac trunk, superior and inferior mesenteric arteries
Portal System: nutrient‑rich blood from GI tract → hepatic portal vein → liver sinusoids for detoxification and metabolism → hepatic veins → systemic circulation
3.5 Overview of Metabolism
Anabolic vs. Catabolic Pathways:
Catabolism: breakdown of macronutrients to generate ATP
Anabolism: synthesis of complex molecules (glycogen, fatty acids, proteins) using ATP
Key Pathways:
Glycolysis (cytosol): glucose → 2 pyruvate + 2 ATP + 2 NADH
Pyruvate Dehydrogenase Complex (mitochondria): pyruvate → acetyl‑CoA + NADH + CO₂
Citric Acid Cycle (mitochondria): acetyl‑CoA → CO₂ + 3 NADH + FADH₂ + GTP
Electron Transport Chain & Oxidative Phosphorylation (inner mitochondrial membrane): NADH/FADH₂ → ATP (≈ 34 ATP per glucose)
Gluconeogenesis: non‑carbohydrate → glucose (liver, kidney)
Glycogenesis & Glycogenolysis: glucose ↔ glycogen (storage and mobilization)
3.6 Regulation of Metabolism
Hormonal Control:
Insulin: secreted by β‑cells in response to ↑ blood glucose; promotes uptake and storage (glycogenesis, lipogenesis, protein synthesis)
Glucagon: secreted by α‑cells when glucose low; stimulates glycogenolysis and gluconeogenesis
Epinephrine & Cortisol: stress hormones; mobilize energy stores (glycogenolysis, lipolysis)
Allosteric & Covalent Regulation:
Phosphofructokinase‑1 (PFK‑1): key glycolysis control (activated by AMP, fructose‑2,6‑bisphosphate; inhibited by ATP, citrate)
Glycogen Phosphorylase: regulated by phosphorylation (activated by glucagon/epinephrine via PKA)
3.7 Clinical Correlations
Peptic Ulcer Disease: erosion of mucosa by excess HCl or H. pylori infection
Malabsorption Syndromes: celiac disease, pancreatic insufficiency → nutrient deficiencies
Jaundice: hyperbilirubinemia due to impaired bile flow or liver disease
Diabetes Mellitus: Type 1 (insulin deficiency) and Type 2 (insulin resistance) disrupt glucose homeostasis
Inborn Errors of Metabolism: e.g., phenylketonuria (phenylalanine hydroxylase deficiency)
3.8 Key Points for Exams
Identify regions of the GI tract and major accessory organs
List digestive enzymes and their sources/actions
Describe absorption mechanisms for carbs, proteins, and fats
Outline major metabolic pathways (glycolysis, TCA cycle, etc.) and their net ATP yields
Understand hormonal regulation of fuel metabolism
Recognize clinical manifestations of digestive and metabolic disorders
Unit 4: Urinary System & Fluid & Electrolyte Balance
This unit covers the anatomy and function of the kidneys and urinary tract, mechanisms of urine formation, compartments of body fluid, and the homeostatic regulation of water and key electrolytes.
4.1 Anatomy of the Urinary System
Kidneys
Location: retroperitoneal, T12–L3 level
External Regions: cortex (outer), medulla (inner pyramids), pelvis (collecting funnel)
Blood Supply: renal artery → segmental → interlobar → arcuate → cortical radiate arteries; venous return via matching veins
Ureters: muscular tubes conveying urine from renal pelvis to bladder via peristalsis
Urinary Bladder: distensible storage; detrusor muscle; trigone region sensitive to stretch
Urethra: conveys urine out; sphincters (internal involuntary, external voluntary)
4.2 The Nephron: Functional Unit
Components
Renal Corpuscle: glomerulus (capillary tuft) + Bowman’s capsule
Renal Tubule:
Proximal Convoluted Tubule (PCT)
Loop of Henle (descending & ascending limbs)
Distal Convoluted Tubule (DCT)
Collecting Duct (cortical → medullary)
Nephron Types
Cortical Nephrons (85 %): short loops, primarily for solute reabsorption
Juxtamedullary Nephrons (15 %): long loops, create medullary osmotic gradient for urine concentration
4.3 Mechanisms of Urine Formation
4.3.1 Glomerular Filtration
Filtration Barrier: fenestrated endothelium + basement membrane + podocyte slits
Forces (Starling’s):
Glomerular hydrostatic pressure (~55 mm Hg) ↑ filtration
Capsular hydrostatic pressure (~15 mm Hg) ↓
Oncotic pressure (~30 mm Hg) ↓
Glomerular Filtration Rate (GFR): ~125 mL/min; regulated by afferent/efferent arteriole tone
4.3.2 Tubular Reabsorption
Segment | Major Reabsorbed Substances | Mechanism |
---|---|---|
PCT | 65 % Na⁺, H₂O, glucose, amino acids | Secondary active transport, osmosis |
Descending Loop | H₂O | Aquaporins, osmotic gradient |
Ascending Loop | 25 % Na⁺, K⁺, Cl⁻ | Na⁺–K⁺–2Cl⁻ co‑transporter |
DCT | Na⁺, Cl⁻, Ca²⁺ (PTH‑regulated) | Cotransporters, channels |
Collecting Duct | H₂O (ADH‑regulated), urea | Aquaporins, urea recycling |
4.3.3 Tubular Secretion
Active transport of H⁺, K⁺, organic acids/bases into tubule for excretion
4.3.4 Excretion
Urine Output = Filtration – Reabsorption + Secretion
Typical volume: 1–2 L/day; osmolarity: 50–1,200 mOsm/kg
4.4 Body Fluid Compartments & Water Balance
Total Body Water ~60 % of body weight (42 L in 70 kg adult)
Intracellular Fluid (ICF) ~40 % (28 L)
Extracellular Fluid (ECF) ~20 % (14 L):
Plasma (~3 L)
Interstitial Fluid (~11 L)
Water Movement via osmotic gradients across cell membranes
Regulation
Thirst mechanism (hypothalamic osmoreceptors)
Antidiuretic Hormone (ADH): increases water reabsorption in collecting ducts
Atrial Natriuretic Peptide (ANP): promotes water and Na⁺ excretion
4.5 Electrolyte Balance
Electrolyte | Location & Function | Regulation |
---|---|---|
Sodium (Na⁺) | Major ECF cation; key in fluid balance & membrane potential | RAAS (aldosterone ↑ reabsorption), ADH |
Potassium (K⁺) | Major ICF cation; nerve/muscle excitability | Aldosterone ↑ secretion in DCT/collecting duct |
Calcium (Ca²⁺) | Bone structure, muscle contraction, neurotransmission | Parathyroid hormone (↑ reabsorption), calcitonin (↓), vitamin D (↑ intestinal absorption) |
Phosphate (HPO₄²⁻) | Bone buffer, ATP, DNA/RNA | PTH (↑ excretion), vitamin D (↑ absorption) |
Acid–Base | Normal pH 7.35–7.45 | Buffers (bicarbonate, phosphate, proteins), respiratory (CO₂ removal), renal (H⁺ secretion, HCO₃⁻ reabsorption) |
4.6 Hormonal Control of Renal Function
Renin–Angiotensin–Aldosterone System (RAAS)
Decreased renal perfusion → juxtaglomerular cells release renin
Renin converts angiotensinogen → angiotensin I → ACE → angiotensin II
Angiotensin II: vasoconstriction, stimulates aldosterone release → ↑ Na⁺/H₂O retention
Antidiuretic Hormone (ADH)
Released by posterior pituitary in response to ↑ plasma osmolarity
Inserts aquaporin‑2 channels in collecting duct → ↑ water reabsorption
Atrial Natriuretic Peptide (ANP)
Secreted by atrial myocytes in response to ↑ atrial stretch
Inhibits renin, aldosterone, ADH → ↑ Na⁺ and water excretion
4.7 Clinical Correlations
Acute Kidney Injury (AKI): abrupt GFR decline; prerenal, intrinsic, or postrenal causes
Chronic Kidney Disease (CKD): progressive nephron loss; stages based on GFR
Edema: excess interstitial fluid—cardiac, renal, or hepatic origin
Electrolyte Disorders:
Hyponatremia: confusion, seizures (excess water or Na⁺ loss)
Hyperkalemia/Hypokalemia: arrhythmias, muscle weakness
Metabolic Acidosis/Alkalosis: pH disturbances due to renal or respiratory dysfunction
4.8 Key Points for Exams
Label kidney regions and nephron segments
Explain Starling forces in glomerular filtration
Trace tubular reabsorption and secretion steps with major solutes
Differentiate ICF vs. ECF compartments and regulatory mechanisms
Describe RAAS, ADH, and ANP actions on fluid/electrolyte balance
Recognize lab findings and presentations of renal and electrolyte disorders
Unit 5: Endocrine Glands & Hormonal Regulation
This unit explores the structure and function of major endocrine glands, the hormones they secrete, mechanisms of hormone action, feedback control loops, and clinical disorders arising from hormonal imbalances.
5.1 Overview of the Endocrine System
Endocrine vs. Exocrine: endocrine glands secrete hormones into bloodstream; exocrine glands use ducts.
Hormone Types:
Peptide/Protein (e.g., insulin, growth hormone)
Steroid (e.g., cortisol, aldosterone, sex steroids)
Amine (e.g., thyroid hormones, catecholamines)
Mechanisms of Action:
Cell-surface receptors for peptide/amine hormones → second messengers (cAMP, IP₃/DAG)
Intracellular receptors for steroid/thyroid hormones → direct gene transcription
5.2 Hypothalamic–Pituitary Axis
Structure | Hormones Secreted | Major Actions |
---|---|---|
Hypothalamus | Releasing/inhibiting factors (TRH, CRH, GHRH, GHIH, GnRH, PIH) | Regulate anterior pituitary secretion |
Anterior Pituitary | GH, TSH, ACTH, FSH, LH, PRL | Growth/metabolism, thyroid function, adrenal cortisol, gonads, lactation |
Posterior Pituitary | ADH (vasopressin), oxytocin | Water retention; uterine contraction, milk ejection |
Feedback Loops:
Negative feedback: rising hormone levels inhibit upstream release (e.g., cortisol ↓ CRH/ACTH).
Positive feedback: less common (e.g., oxytocin surge during labor).
5.3 Thyroid Gland
Anatomy: two lobes connected by isthmus; follicles lined with follicular cells.
Hormones:
Thyroxine (T₄) & Triiodothyronine (T₃): regulate basal metabolic rate, growth, and development
Calcitonin: from parafollicular C‑cells; lowers blood Ca²⁺
Synthesis Pathway: iodide uptake → oxidation & iodination of thyroglobulin → coupling to form T₃/T₄ → release.
Regulation: TRH → TSH → ↑ thyroid hormone.
5.4 Adrenal Glands
Cortex Zone | Hormones | Functions |
---|---|---|
Zona Glomerulosa | Aldosterone (mineralocorticoid) | ↑ Na⁺ reabsorption, K⁺ excretion, water retention |
Zona Fasciculata | Cortisol (glucocorticoid) | Gluconeogenesis, stress response, anti‑inflammatory |
Zona Reticularis | Androgens (DHEA, androstenedione) | Secondary sex characteristics (weak) |
| Medulla | Epinephrine & Norepinephrine | Fight-or-flight: ↑ HR, BP, blood glucose |
Control: ACTH stimulates cortisol & androgens; renin–angiotensin controls aldosterone; sympathetic preganglionic fibers control medulla.
5.5 Pancreatic Islets
Cell Types & Hormones:
α‑cells: glucagon → ↑ blood glucose (glycogenolysis, gluconeogenesis)
β‑cells: insulin → ↓ blood glucose (glycogenesis, uptake by muscle/adipose)
δ‑cells: somatostatin → inhibits insulin, glucagon, GH release
PP‑cells: pancreatic polypeptide → regulates exocrine secretions
Regulation: blood glucose is primary stimulus; incretins (GLP‑1) enhance insulin release.
5.6 Other Endocrine Glands
Parathyroid Glands:
Parathyroid Hormone (PTH): ↑ blood Ca²⁺ by bone resorption, ↑ renal Ca²⁺ reabsorption, activates vitamin D.
Pineal Gland:
Melatonin: regulates circadian rhythms; secreted in darkness.
Gonads:
Ovaries: estrogen & progesterone regulate menstrual cycle, secondary sexual traits
Testes: testosterone controls spermatogenesis, male characteristics
Thymus (functional in childhood):
Thymosins: T‑cell maturation
5.7 Hormone Action & Signal Transduction
Second Messenger Systems:
cAMP pathway (e.g., ACTH, glucagon)
IP₃/DAG pathway (e.g., GnRH, ADH via V1 receptors)
Receptor Types: G‑protein–coupled, tyrosine kinase (insulin), intracellular nuclear receptors (steroid/thyroid)
Amplification & Termination: enzyme cascades amplify signal; phosphodiesterases and receptor internalization terminate signals.
5.8 Clinical Correlations
Hypo/Hyperpituitarism: pituitary adenomas can cause dwarfism, acromegaly, Cushing’s disease
Thyroid Disorders:
Hypothyroidism (e.g., Hashimoto’s): fatigue, weight gain, cold intolerance
Hyperthyroidism (e.g., Graves’): weight loss, heat intolerance, exophthalmos
Adrenal Disorders:
Addison’s Disease: cortisol/aldosterone deficiency → hypotension, hyperpigmentation
Cushing’s Syndrome: cortisol excess → central obesity, hypertension, hyperglycemia
Diabetes Mellitus: Type 1 (β‑cell destruction) vs. Type 2 (insulin resistance); complications include neuropathy, nephropathy
Hyperparathyroidism/Hypoparathyroidism: Ca²⁺ imbalance → bone fragility or tetany
5.9 Key Points for Exams
Match each gland with its hormones and functions
Describe feedback loops in the hypothalamic–pituitary axes
Outline thyroid hormone synthesis and regulation
Differentiate adrenal cortex vs. medulla hormones and controls
Explain insulin vs. glucagon actions on blood glucose
Know clinical features of major endocrine disorders
Unit 6: Reproductive System & Developmental Physiology
This unit examines the anatomy and physiology of the male and female reproductive systems, gamete formation, hormonal regulation of reproduction, pregnancy and parturition, and early developmental processes.
6.1 Anatomy of the Male Reproductive System
Testes: paired oval glands housed in the scrotum; produce sperm and testosterone
Seminiferous Tubules: site of spermatogenesis; supported by Sertoli cells (nourish germ cells, form blood‑testis barrier)
Interstitial (Leydig) Cells: secrete testosterone under LH stimulation
Duct System:
Epididymis: sperm maturation and storage
Vas Deferens: transports sperm during ejaculation
Ejaculatory Duct & Urethra: passage through prostate and penis
Accessory Glands:
Seminal Vesicles: fructose, prostaglandins, coagulating proteins
Prostate Gland: alkaline fluid, citrate, enzymes
Bulbourethral (Cowper’s) Glands: mucus for lubrication
6.2 Anatomy of the Female Reproductive System
Ovaries: paired glands in pelvic cavity; produce ova and secrete estrogen & progesterone
Ovarian Follicles: contain oocytes; mature through primordial → primary → secondary → Graafian stages
Fallopian (Uterine) Tubes: capture ovulated oocyte; site of fertilization
Uterus:
Layers: endometrium (stratum functionalis & basalis), myometrium (smooth muscle), perimetrium
Phases: proliferative, secretory, menstrual
Cervix: mucus secretion; barrier to pathogens
Vagina: acidic environment; conduit for sperm and birth canal
External Genitalia: labia majora/minora, clitoris, vestibular glands
6.3 Gametogenesis
Spermatogenesis (in seminiferous tubules):
Spermatogonia (2n) → mitotic divisions →
Primary Spermatocytes (2n) → Meiosis I →
Secondary Spermatocytes (1n) → Meiosis II →
Spermatids (1n) → spermiogenesis → mature spermatozoa
Oogenesis:
Begins prenatally: oogonia → primary oocytes (arrested in Prophase I)
At puberty: each menstrual cycle, one primary oocyte completes Meiosis I → secondary oocyte (arrested in Metaphase II) + first polar body
After fertilization: secondary oocyte completes Meiosis II → ovum + second polar body
6.4 Hormonal Regulation of Reproduction
Hypothalamic–Pituitary–Gonadal Axis:
GnRH (hypothalamus) → FSH & LH (anterior pituitary)
In Males:
FSH → Sertoli cells → support spermatogenesis, produce inhibin (– feedback on FSH)
LH → Leydig cells → testosterone production (– feedback on LH & GnRH)
In Females:
Follicular Phase: FSH stimulates follicle growth & estrogen secretion
Mid‑cycle LH Surge: triggers ovulation
Luteal Phase: ruptured follicle forms corpus luteum → secretes progesterone (and estrogen) to prepare endometrium; inhibin reduces FSH
6.5 Menstrual Cycle
Phase | Days (approx.) | Hormone Profile | Endometrial Changes |
---|---|---|---|
Menstrual | 1–5 | ↓ estrogen & progesterone | Shedding of stratum functionalis |
Proliferative | 6–14 | ↑ estrogen (follicle) | Regeneration & thickening of endometrium |
Ovulation | ~14 | Peak LH & FSH; estrogen peak | Release of oocyte |
Secretory (Luteal) | 15–28 | ↑ progesterone & estrogen (corpus luteum) | Endometrial gland secretion; vascularization |
If no fertilization | 26–28 | ↓ progesterone & estrogen → menstruation | Breakdown of stratum functionalis |
6.6 Pregnancy, Parturition & Lactation
Fertilization & Implantation:
Occurs in ampulla of fallopian tube within 24 h of ovulation
Blastocyst implants in endometrium ~6–7 days post‑fertilization
Hormonal Changes in Pregnancy:
hCG (from syncytiotrophoblast) maintains corpus luteum first 8–10 weeks
Estrogen & Progesterone (placenta) support uterine growth and inhibit myometrial contractions
Relaxin: softens cervix and pelvic ligaments
Parturition (Childbirth):
↑ estrogen:progesterone ratio → ↑ oxytocin receptors on uterus
Ferguson reflex: stretch of cervix → oxytocin release → uterine contractions
Positive feedback: contractions → more oxytocin
Lactation:
Prolactin (anterior pituitary) stimulates milk synthesis
Oxytocin triggers milk ejection (let‑down reflex) via myoepithelial cell contraction
6.7 Early Developmental Physiology
Gastrulation: formation of three germ layers (ectoderm, mesoderm, endoderm) around week 3
Neurulation: neural tube formation from ectoderm (future CNS)
Organogenesis: weeks 4–8; major organs begin to form
Fetal Circulation: special shunts bypass lungs (foramen ovale, ductus arteriosus, ductus venosus)
Birth Adaptations: clamping of umbilical cord, first breath → closure of shunts
6.8 Clinical Correlations
Infertility: anovulation, tubal blockages, low sperm count/motility
Polycystic Ovary Syndrome (PCOS): hyperandrogenism, irregular cycles, insulin resistance
Ectopic Pregnancy: implantation outside uterus (often in fallopian tube)
Pre‑eclampsia: hypertension & proteinuria after 20 weeks gestation
Testicular Disorders: cryptorchidism, varicocele, testicular torsion
6.9 Key Points for Exams
Label male/female reproductive organs and stages of follicle development
Outline spermatogenesis vs. oogenesis, including arrest points
Describe hormonal control of menstrual cycle and feedback mechanisms
Explain pregnancy hormones, implantation timing, and parturition reflexes
Recall germ layer formation and major embryonic milestones
Recognize features of common reproductive disorders