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OST 529 Systems Biology: Endocrinology Keith Lookingland Associate Professor Dept. Pharmacology & Toxicology Adrenocorticosteroids Goodman & Gilman’s “The Pharmacological Basis of Therapeutics” 10th Edition Chapter 60: 1649-1677 Hormone Negative Feedback Hypothalamic-Pituitary Systems • • • • Thyroid Axis (Thyroid Hormones) Adrenocortical Axis (Glucocorticoids) Ovarian Axis (Estrogen/Progesterone) Testicular Axis (Testosterone) Peripheral Substrate Systems • Glucose - Insulin/Glucagon • Sodium/Potassium - Aldosterone • Calcium - PTH/Calcitonin/Vitamin D Adrenocorticosteroids • Glucocorticoids + Mineralocorticoids – Synthesis and metabolism – Secretion – Actions • Adrenocortical Insufficiency – Addison’s disease (primary & secondary) • Adrenocortical Hyperactivity – Congenital adrenal hyperplasia – Cushing’s disease – Conn’s syndrome (primary aldosteronism) Adrenal Gland Adrenocorticosteroids Glucocorticoids Transport of Cortisol • 95% bound to corticosteroid binding globulin (CBG) • 5% free, bioactive • cortisol half-life (90-110 min) Metabolism of Cortisol Hypothalamic-Pituitary-Adrenal (HPA) Axis Circadian Rhythm of Cortisol Secretion Mechanism of Glucocorticoid Action Physiological Actions of Glucocorticoids • Metabolic Glucose Availability for the Brain • Anti-inflammatory • Immunosuppression Metabolic Actions of Cortisol Anti-inflammatory Actions of Cortisol • phagocytic cell function pyrogens,elastase,collagenase • reduces edema capillary permeability arteriole vasoconstriction • blocks basophil histamine Immunosuppressive Actions of Cortisol Mineralocorticoids Transport and Metabolism of Aldosterone • • • • weakly bound to plasma proteins 95% free, bioactive aldosterone half-life (20-30 min) degraded in liver, secreted in urine as a water soluble conjugate Control of Aldosterone Secretion Mechanisms of Aldosterone Action Adrenocortical Insufficiency • Primary (Addison’s Disease) – hyposecretion of both cortisol & aldosterone – hypersecretion of ACTH (loss of negative feedback) – glucocorticoid insufficiency • weakness, fatigue • inability to maintain fasting plasma glucose – mineralocorticoid insufficiency • sodium loss, potassium retention • dehydration • Secondary – defect in hypothalamic-pituitary axis – hyposecretion of ACTH and cortisol Synthetic Glucocorticoids • Cortisol – short-acting – orally active – glucocorticoid replacement adrenal insufficiency • Triamcinolone – intermediate-acting – topical – localized allergic and arthritic disorders • Dexamethasone – long-acting – diagnostic • Dexamethasone Suppression Test Side Effects of Glucocorticoid Therapy Synthetic Mineralocorticoids Synthetic Mineralocorticoids Fludrocortisone – oral, injectable, topical compilations – mimics aldosterone action • sodium retention • potassium excretion – mineralocorticoid replacement adrenal insufficiency Adrenocortical Hyperactivity • Congenital Adrenal Hyperplasia – primary defect in cortisol biosynthetic enzymes • 21-B hydroxylase • shunts precursors into androgen pathway – – – – compensatory increase in ACTH (loss of negative feedback) adrenal hypertrophy virilization of physical features im cortisone/dexamethasome to suppress ACTH – oral cortisol Adrenocortical Hyperactivity • Cushing’s Syndrome – adrenal hyperplasia – secondary to ACTH-secreting pituitary or ectopic tumor – loss of negative feedback unresponsive to low dose dexamethasone Adrenocortical Hyperactivity • Cushing’s Syndrome – excessive glucocorticoid activity • muscle atrophy, thinning of skin (protein catabolism) • facial & truncal obesity (lipid deposition insulin-dependent adipocytes) • poor wound healing (immunosuppression) – surgical removal of tumor (oral cortisol) – adrenalectomy (oral cortisol & fludrocortisone) Adrenocortical Hyperactivity • Primary Aldosteronism (Conn’s Syndrome) – aldosterone-secreting adrenal adenoma – excessive mineralocorticoid activity (electrolyte imbalance) • hypertension (sodium retention) • muscle weakness, tetany (potassium excretion) – adrenalectomy (oral cortisol & fludrocortisone) – spironolactone • aldosterone receptor antagonist • genomic actions (slow onset of action)