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Pyrogens enhance beta-endorphin release in hypothalamus and trigger fever that can be attenuated by buprenorphine.

Abstract
At first, we investigated whether both beta-endorphin release level in the hypothalamus and body temperature can be altered after intracerebroventricular (i.c.v.) injection of either lipopolysaccharide (LPS), interleukin-1beta (IL-1beta), or prostaglandin E(2) (PGE(2)) in rats. It was found that in the rat, i.c.v. administration of either LPS (0.5 microg in 10 microl), IL-1beta (10 ng in 10 microl), or PGE(2) (200 ng in 10 microl), in addition to producing fever, upregulated the immunoreactivity of beta-endorphin in the preoptic anterior hypothalamus of rat brain. Secondarily, we assessed whether the fever induced by either LPS, IL-1beta, or PGE(2) can be altered by pretreatment with buprenorphine (an opioid receptor antagonist). The results revealed that i.c.v. administration of buprenorphine (1 - 10 microg in 10 microl) alone had an insignificant effect on the body temperature. However, the fever induced by i.c.v. injection of either LPS, IL-1beta, or PGE(2) was significantly attenuated by pretreatment with i.c.v. injection of buprenorphine 1 h before the pyrogen injection in rats. The results suggest that pyrogens enhance beta-endorphin release in the hypothalamus and trigger fever which can be attenuated by buprenorphine, an opioid receptor antagonist.
AuthorsShu-Ming Tsai, Mao-Tsun Lin, Jhi-Joung Wang, Wu-Tein Huang
JournalJournal of pharmacological sciences (J Pharmacol Sci) Vol. 93 Issue 2 Pg. 155-62 (Oct 2003) ISSN: 1347-8613 [Print] Japan
PMID14578583 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Interleukin-1
  • Lipopolysaccharides
  • Narcotic Antagonists
  • Pyrogens
  • Buprenorphine
  • beta-Endorphin
  • Dinoprostone
Topics
  • Animals
  • Buprenorphine (administration & dosage, pharmacology)
  • Dinoprostone (administration & dosage, pharmacology)
  • Fever (chemically induced, prevention & control)
  • Hypothalamus (drug effects, metabolism)
  • Immunohistochemistry
  • Injections, Intraventricular
  • Interleukin-1 (administration & dosage, pharmacology)
  • Lipopolysaccharides (administration & dosage, pharmacology)
  • Male
  • Narcotic Antagonists (administration & dosage, pharmacology)
  • Pyrogens (administration & dosage, antagonists & inhibitors, pharmacology)
  • Rats
  • Rats, Sprague-Dawley
  • beta-Endorphin (metabolism)

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