Plasma catecholamines in patients with Addison's disease

SummaryBACKGROUND AND OBJECTIVE TWO endocrine tissues are present within the adrenal gland: the steroid producing cortical cells and the catecholamine producing chromaffin cells. Glucocorticolds occur in high concentrations in the adrenal medulla. In vitro, glucocorticolds have been shown to induce the enzyme phenyl‐N‐methyl‐transferase which is necessary for the production of adrenaline in adrenal medullary cells. The purpose of this study was to evaluate the possible significance of a local glucocorticold effect on adrenomedullary function. DESIGN Plasma catecholamine levels were measured in patients with autoimmune Addison's disease where local production of corticosterolds is deficient In the presence of intact chromaffin tissue.MEASUREMENTS Catecholamines were measured by high pressure liquid chromatography and ACTH, renin and adrenal steroids by radioimmunoassay.PATIENTS Nineteen Addisonian patients (9 females, 10 males) were treated according to a standard reglie with oral cortisone acetate (37·5 mg/day) and fludrocortisone (0·1 mg/day). All patients were clinically well.RESULTS Mean plasma adrenallne in patients with Addison's disease was significantly reduced compared to a sex and age matched control group (males (n= 10) 143 ± 36 pmol/1, controls (n= 27) 303 ± 30 pmol/1, P < 0·01; females (n= 9) 77 ± 25pmol/1, controls (n= 27) 293 ± 21 pmol, P < 0·001). The noradrenallne: adrenallne ratio was clearly higher in patients with Addison's disease (males 24 ± 4, controls 9 ± 1, P < 0·01; females 45 ± 6, controls 9 ± 1, P < 0·01CONCLUSION We conclude that the physiologically high local glucocorticold concentration may be responsible for normal adrenaline production under basal conditions.