Luteinizing hormone-releasing hormone modulates nicotinic ACh-receptor sensitivity in amphibian cholinergic transmission

Brain Res. 1983 Nov 21;279(1-2):347-51. doi: 10.1016/0006-8993(83)90208-1.

Abstract

Luteinizing hormone-releasing hormone (LH-RH; 100 nM-50 microM) reduced the sensitivity of the nicotinic ACh-receptor in amphibian sympathetic ganglion cells and skeletal muscle end-plates. Analyses of LH-RH action, based on a Michaelis-Menten type kinetics, revealed that LH-RH depressed the maximum response (Vmax) of the dose-response curve of ACh currents without changing the affinity (Km) of ACh to the receptor. It was suggested that LH-RH reduced the sensitivity of nicotinic receptor by acting on a certain allosteric site of the receptor-ionic channel complex. Probably, LH-RH reduces the ACh current by decreasing the number of channels available.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dose-Response Relationship, Drug
  • Ganglia, Sympathetic / drug effects*
  • Gonadotropin-Releasing Hormone / pharmacology*
  • Membrane Potentials / drug effects
  • Motor Endplate / drug effects*
  • Neuromuscular Junction / drug effects*
  • Ranidae
  • Receptors, Cholinergic / drug effects*
  • Sciatic Nerve / drug effects
  • Synaptic Transmission / drug effects*

Substances

  • Receptors, Cholinergic
  • Gonadotropin-Releasing Hormone