Adrenal Gland Anatomy & Zones - Gland Central
- Location: Suprarenal (on superior kidney poles), retroperitoneal.
- Parts: Outer Cortex (~90%), Inner Medulla (~10%).
- Cortex Zones (OuterāInner): š GFR (Salt, Sugar, Sex)
- Zona Glomerulosa (ZG): Aldosterone (Mineralocorticoids)
- Zona Fasciculata (ZF): Cortisol (Glucocorticoids)
- Zona Reticularis (ZR): Androgens (e.g., DHEA)
- Blood Supply: Rich; 3 suprarenal arteries. 1 central medullary vein.
- Innervation: Medulla: direct preganglionic sympathetic fibers (splanchnic nerves). Cortex: minimal.

ā R. adrenal vein ā IVC; L. adrenal vein ā L. renal vein.
Cortisol & Glucocorticoids - Stress Steroid Saga

- Synthesis: Zona fasciculata (adrenal cortex) from cholesterol.
- Key enzyme: 17α-hydroxylase.
- Regulation (HPA Axis): CRH (hypothalamus) ā ACTH (anterior pituitary) ā Cortisol.
- Negative feedback by cortisol on CRH & ACTH. Diurnal rhythm.
- Transport: ~90% bound to Corticosteroid-Binding Globulin (CBG), ~5-10% free (active).
- Key Actions (Stress Adaptation & Permissive Effects):
- Metabolic: āGluconeogenesis, āProteolysis, āLipolysis. Insulin resistance (diabetogenic).
- Anti-inflammatory & Immunosuppressive: Inhibits Phospholipase A2, ācytokines (e.g., IL-2).
- Cardiovascular: āBP (maintains vascular tone, permissive for catecholamines).
- Musculoskeletal: āBone formation, āmuscle catabolism.
- CNS: Influences mood, memory, sleep.
ā Cortisol exhibits a diurnal rhythm: peak in early morning, nadir at night.
Aldosterone & Mineralocorticoids - Salt Saver Star
- Source: Zona Glomerulosa (Adrenal Cortex). š GFR: Salt (Glomerulosa), Sugar (Fasciculata), Sex (Reticularis).
- Primary Mineralocorticoid: Aldosterone.
- Synthesis: From cholesterol; key enzyme Aldosterone Synthase (stimulated by Angiotensin II & āK+).
- Regulation: Renin-Angiotensin-Aldosterone System (RAAS) is primary.
- Actions: Acts on principal & intercalated cells (late Distal Convoluted Tubule & Collecting Ducts).
- ā Na+ reabsorption (via ENaC channels)
- ā K+ secretion (via ROMK channels)
- ā H+ secretion (via H+-ATPase)
- Water follows Na+ ā ā ECF volume, ā Blood Pressure.
ā Aldosterone escape: In primary hyperaldosteronism, chronic aldosterone excess leads to volume expansion, but edema is limited due to pressure natriuresis and ANP action.

Adrenal Androgens & Cortex Pathologies - Cortex Chaos
- Adrenal Androgens: DHEA, Androstenedione (Zona Reticularis). Peripheral conversion to sex steroids.
- Cushing's Syndrome: ā Cortisol. Features: central obesity, striae, HTN. Screen: Low-dose DST, 24hr UFC.
- Addison's Disease: ā Cortisol, ā Aldosterone. Features: weakness, pigmentation, hypotension, āK+, āNa+. ACTH stim test.
- Conn's Syndrome: ā Aldosterone. Features: HTN, āK+, alkalosis. Aldosterone:Renin ratio > 20.
- CAH: Enzyme defects (e.g., 21-hydroxylase def.). ā Cortisol, ā/normal Aldo, ā Androgens (virilization). š Salt wasting, virilization.

ā Nelson's syndrome: Rapid enlargement of pituitary ACTH-secreting adenoma after bilateral adrenalectomy for Cushing's disease. Presents with hyperpigmentation & visual field defects.
Adrenal Medulla & Pheochromocytoma - Catecholamine Rush
- Adrenal Medulla: Chromaffin cells (neural crest) secrete catecholamines: Epinephrine (E), Norepinephrine (NE).
- PNMT (cortisol-induced) converts $NE \rightarrow E$.
- Actions: "Fight-or-flight" (āHR, āBP, āglucose).
- Pheochromocytoma: Chromaffin cell tumor.
- š Rule of 10s (approximate values for malignant, bilateral, extra-adrenal, pediatric, familial).
- Symptoms (episodic): 5 P's - Pressure (HTN), Pain (headache), Perspiration, Palpitations, Pallor.
- Diagnosis: ā 24hr urinary/plasma metanephrines & VMA.
- Treatment: Pre-op α-blockade (e.g., phenoxybenzamine) THEN β-blockade, then surgery.
ā Plasma free metanephrines are the most sensitive screening test for pheochromocytoma.
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HighāYield Points - ā” Biggest Takeaways
- Adrenal cortex: Glomerulosa (Aldosterone), Fasciculata (Cortisol), Reticularis (Androgens).
- Aldosterone: Regulated by RAAS & K+; acts on DCT/CD for Na+ reabsorption.
- Cushing's syndrome: Excess cortisol; features central obesity, striae, hypertension.
- Addison's disease: āCortisol & āAldosterone; causes hypotension, hyperpigmentation, hyperkalemia.
- Pheochromocytoma: Medullary tumor of catecholamines; causes paroxysmal hypertension, palpitations, headache.
- 21-hydroxylase deficiency: Most common CAH; āCortisol, āAldosterone, āAndrogens, causing virilization.
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