Opioid modulation of normal and pathological human chromaffin tissue

J Clin Endocrinol Metab. 1986 Mar;62(3):577-82. doi: 10.1210/jcem-62-3-577.

Abstract

To evaluate whether opioid receptor blockade might modulate sympathetic-adrenal activity, we studied the effects of placebo or naloxone administration on plasma catecholamine (CA) levels in a group of 13 normal subjects and 15 hypertensive patients suspected to have a pheochromocytoma. Diagnostic evaluation confirmed the presence of pheochromocytoma in 9 patients. Among these, 4 had a unilateral epinephrine (E)-secreting tumor, 3 had bilateral E-secreting tumors due to multiple endocrine adenomatosis type IIa, and 2 had a unilateral norepinephrine (NE)-secreting tumor. In each subject studied, CA secretion was evaluated by calculating the area (0-30 min) under the plasma hormone curves after placebo or naloxone administration. In normal subjects naloxone caused a significant increase (P less than 0.005) of E secretion, whereas NE did not change. Similarly, in the group of hypertensive patients, E secretion increased after naloxone (P less than 0.01). In pheochromocytoma patients naloxone caused a significant increase in E (P less than 0.05) and NE (P less than 0.01) secretion from E-producing tumors but no increase in the patients with NE-secreting pheochromocytomas. The study suggests that CA secretion from normal and pathological chromaffin tissue is modulated by endogenous opioids; this modulation seems particularly evident in patients with E-secreting pheochromocytoma.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adrenal Gland Neoplasms / blood
  • Adult
  • Aged
  • Catecholamines / blood*
  • Chromaffin System / metabolism*
  • Female
  • Humans
  • Hypertension / blood
  • Male
  • Middle Aged
  • Naloxone / pharmacology
  • Pheochromocytoma / blood
  • Receptors, Opioid / drug effects
  • Receptors, Opioid / physiology*

Substances

  • Catecholamines
  • Receptors, Opioid
  • Naloxone