Identification of immunoreactive somatostatin in the rat harderian gland: regulation of its content by growth hormone, beta-adrenergic agonists and calcium channel blockers

Peptides. 1988 May-Jun;9(3):571-4. doi: 10.1016/0196-9781(88)90166-0.

Abstract

Immunoreactive somatostatin (IRS) was identified in the male rat Harderian gland (HG) by radioimmunoassay. Tissue was extracted and a displacement curve performed; there were no significant differences between values obtained with serial dilutions of extracted tissue and those from purified somatostatin standard used in the radioimmunoassay. Basal values of HG-IRS were found to be in the nanomolar range (10.8 +/- 3.5 ng IRS/mg protein). Hypophysectomy did not change the HG-IRS but, in vivo growth hormone (GH) treatment led to a dramatic increase (6-7-fold) in the levels of IRS in the HG. Isoproterenol, a beta-adrenergic agonist, when administered in vivo significantly decreased the HG-IRS content. The effect of two different calcium channel blockers on the isoproterenol-induced decrease of HG-IRS was studied; no changes were observed with nifedipine but verapamil, injected one hour after isoproterenol administration, prevented the drop in HG-IRS levels. These data demonstrate the existence of IRS in a new location, the rat Harderian gland, and support a classical endocrine regulation for its tissue concentration.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Growth Hormone / pharmacology*
  • Harderian Gland / drug effects
  • Harderian Gland / metabolism*
  • Hypophysectomy
  • Isoproterenol / pharmacology*
  • Lacrimal Apparatus / metabolism*
  • Male
  • Nifedipine / pharmacology*
  • Radioimmunoassay / methods
  • Rats
  • Reference Values
  • Somatostatin / immunology
  • Somatostatin / metabolism*
  • Verapamil / pharmacology*

Substances

  • Somatostatin
  • Growth Hormone
  • Verapamil
  • Nifedipine
  • Isoproterenol