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Corticosteroids and other
hormone preparations
Glucocorticoids
Drugs used in thyroid disease
Oral contraceptives
Hormone replacement therapy
Glucocorticoids
The adrenal cortex releases two classes of steroidal hormones into the circulation:
Glucocorticoids (from the zona fasciculata and zona reticularis)
Mineralocorticoids (from the zona glomerulosa)
The main endogenous glucocorticoid in humans is hydrocortisone. Synthetic gluco-
corticoids include prednisolone, methylprednisolone, betamethasone, dexametha-
sone and triamcinolone. They havemetabolic, anti-inflammatoryandimmuno-
suppressiveeffects.
Metabolic effects
Glucocorticoids facilitate gluconeogenesis (i.e. synthesis of glucose from a non-
carbohydrate source, e.g. protein). Glycogen deposition and glucose release from
the liver are stimulated but the peripheral uptake of glucose is inhibited. Protein
catabolism is stimulated and synthesis inhibited.
When exogenous glucocorticoid is given in high doses or for prolonged periods, the
altered metabolism causes unwanted effects. Increased protein catabolism leads to
muscle weakness and wasting. The skin becomes thin leading to striae, and gastric
mucosa becomes susceptible to ulceration. Dietary protein will not reverse these
changes. Altered carbohydrate metabolism leads to hyperglycaemia and glycosuria.
Diabetes may be provoked. Fat is redistributed from the extremities to the trunk,
neck and face. Bone catabolism leads to osteoporosis.
Anti-inflammatory effects
Glucocorticoids reduce the production of tissue transudate and cell oedema in acute
inflammation. Circulating polymorphs and macrophages are prevented from reach-
ing inflamed tissue. The production of inflammatory mediators (prostaglandins,
leukotrienes and platelet-activating factor) is suppressed by the stimulation of
lipocortin, which inhibits phospholipase A 2 .Normally phospholipase A 2 would