Effect of thyrotropin-releasing hormone on pentobarbitone-induced sleep in rats: continuous treatment with a sustained release injectable formulation

J Pharm Pharmacol. 1993 Feb;45(2):94-7. doi: 10.1111/j.2042-7158.1993.tb03690.x.

Abstract

The mode of action and the time course of the effects of continuous thyrotropin-releasing hormone (TRH) treatment using a two-week sustained release injectable formulation of TRH-containing copoly((+/-)-lactic/glycolic acid) microspheres (TRH-SR) on pentobarbitone-induced sleeping time were studied in rats. Subcutaneous treatment with TRH-SR at doses corresponding to 0.05 and 0.2 mg of TRH kg-1 day-1 caused a dose-related shortening of pentobarbitone-induced sleeping time with a minimum effective dose (MED) of 0.05 mg kg-1 day-1, without affecting the body weight gain. On the other hand, the MED of TRH when given as a bolus subcutaneous injection was 40 mg kg-1. The effect of TRH-SR treatment was blocked by intraperitoneal scopolamine (0.1 mg kg-1) and mecamylamine (2 mg kg-1) but not by scopolamine methyl bromide (0.1 mg kg-1). The results indicate that continuous TRH treatment using TRH-SR causes shortening of pentobarbitone-induced sleeping time at doses lower than those required using bolus injection and probably by a mechanism involving the central cholinergic system.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Body Weight / drug effects
  • Delayed-Action Preparations
  • Male
  • Microspheres
  • Molecular Sequence Data
  • Parasympatholytics / pharmacology
  • Pentobarbital / antagonists & inhibitors*
  • Pentobarbital / pharmacology
  • Rats
  • Rats, Wistar
  • Sleep / drug effects*
  • Thyrotropin-Releasing Hormone / administration & dosage
  • Thyrotropin-Releasing Hormone / pharmacology*

Substances

  • Delayed-Action Preparations
  • Parasympatholytics
  • Thyrotropin-Releasing Hormone
  • Pentobarbital