Adrenal Gland Disorders Study Notes
Adrenal Gland Anatomy and Hormone Regulation
Adrenal gland location and organization
Located above each kidney
Outer cortex and inner medulla
Cortex consists of three zones with distinct steroidogenic outputs:
Zona glomerulosa → mineralocorticoids (Aldosterone)
Zona fasciculata → glucocorticoids (Cortisol)
Zona reticularis → gonadocorticoids (Androgen)
Inner medulla contains chromaffin cells that secrete catecholamines (Adrenaline and Noradrenaline)
Regulation of adrenal hormones (HPA axis and sympathetic inputs)
Hypothalamus releases CRH (corticotropin-releasing hormone)
Pituitary gland releases ACTH (adrenocorticotropic hormone)
Adrenal cortex produces cortisol (glucocorticoid) in response to ACTH
Adrenal medulla is innervated by sympathetic nerves and secretes catecholamines (Adrenaline and Noradrenaline) directly
The cascade links to systemic effects via cortisol and catecholamines
Hormones associated with adrenal gland function include}
Cortisol (stress response, metabolism, immune modulation)
Aldosterone (sodium and water retention, potassium excretion via kidney)
Androgens (gonadal effects; minor adrenal source)
Catecholamines (acute sympathetic responses: fight/flight)
Actions of Cortisol
Liver- Increases gluconeogenesis from amino acids and fatty acids
Decreases glycogen and protein synthesis
Adipose tissue and muscle- Decreases glucose uptake and utilization
Increases protein catabolism and lipolysis
Vascular system- Increases vascular reactivity
Immune and tissue effects- Long-term immunosuppressive effects reduce wound healing
Systemic/survival roles- Supports the long-term stress response
Suppresses non-essential organ functions (e.g., digestion, reproduction) to mobilize glucose stores and help maintain blood pressure
Actions of Aldosterone
Target: kidney
Regulatory role- Increases sodium (and water) reabsorption via the Renin–Angiotensin–Aldosterone system (RAAS)
Regulates blood levels of potassium by increasing potassium excretion (decreases potassium reabsorption)
Hyposecretion of Adrenocortical Hormones (Cortisol & Aldosterone) – Addison Disease
Causes- Autoimmune destruction of the adrenal cortex
Infections/disease (e.g., Tuberculosis)
Adrenal hemorrhage
Pathophysiology- Increased ACTH due to loss of cortisol feedback → hyperpigmentation of the skin (ACTH shares precursors with melanocyte-stimulating hormone)
Addison Disease as the clinical syndrome when cortisol and aldosterone are deficient
Clinical features due to specific deficiencies- Decreased Aldosterone
Hyponatremia (Na+), Hyperkalemia (K+)
Dehydration and hypotension
Weight loss
Muscle weakness and potential cardiac arrhythmias
Nausea, vomiting, and diarrhea (gastrointestinal symptoms)
Decreased Cortisol
Hypoglycemia
Irritability, depression, confusion, lethargy
Decreased Androgens
Loss of axillary and pubic hair
Loss of libido and amenorrhea
Hypersecretion of Adrenocortical Hormones – Cushing’s Syndrome
Causes- Endogenous sources: adrenal tumour or pituitary tumour (Cushing’s disease)
Exogenous: corticosteroid administration
Hypercortisolism cascade- Elevated cortisol leads to metabolic and systemic changes
Hyperglycemia → Hyperinsulinemia and increased fat deposition
Common phenotypic features- Weight gain with trunk obesity and fat distributions (Moon face, buffalo hump)
Muscle and bone wasting due to protein catabolism
Osteoporosis with fractures and potentially kyphosis; may contribute to kidney stones
Increased androgens causing hirsutism, oligomenorrhea, deepening of voice, acne
Decreased libido
Other Common Clinical Manifestations and Consequences
Cardiovascular and integumentary effects- Hypertension
Thin skin with purple striae
Easy bruising
Pigmentation and immune effects- Hyperpigmentation (often due to elevated ACTH)
Increased susceptibility to infection; poor wound healing
Neurological and mood effects- Mood swings, irritability, depression or euphoria
Summary and Learning Objectives (Recap)
You should be able to:- Describe the causes of hyposecretion and hypersecretion of adrenal hormones (cortisol, aldosterone, androgens)
Describe the symptoms associated with hyposecretion and hypersecretion
Explain the pathophysiology underlying the adrenal hormone disorders described (Addison’s and Cushing’s syndromes)
Foundational context and relevance- Relates to regulation of metabolism, fluid balance, stress response, immune function, and reproductive physiology
Demonstrates how endocrine feedback loops (hypothalamus-pituitary-adrenal axis) and adrenal outputs interact to maintain homeostasis
Clinical implications include potential for metabolic derangements, cardiovascular risk, immune compromise, and quality-of-life impacts
Conceptual Connections and Practical Implications
Clinical reasoning- Distinguish between cortisol-driven and aldosterone-driven symptoms when patient presents with fatigue, hypotension, hyponatremia/hyperkalemia, or features of Cushing’s
Therapeutic considerations (high-level)- Treatment strategies depend on whether the issue is hypo- or hypersecretion and whether etiologies are autoimmune, neoplastic, infectious, or iatrogenic (steroid-induced)
Ethical and societal context- Not explicitly discussed in the material; standard medical ethics apply to diagnosis, treatment, and patient autonomy in managing chronic endocrine disorders