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Beta-adrenergic receptor blockade during exercise decreases intestinal lymphocyte apoptosis but not cell loss in mice.

Abstract
Catecholamines induce apoptosis in various lymphoid populations. This process can occur with both alpha- and beta-adrenoreceptors. Heavy exercise increases plasma catecholamine concentrations, and is also a cause of lymphocyte apoptosis, a possible explanation for postexercise lymphocytopenia. The purpose of this study was to examine the effects of adrenoreceptor antagonism on exercise-induced decreases and apoptosis of intestinal lymphocytes. Mice received an intraperitoneal injection of phentolamine (a nonselective alpha-blocker), nadolol (a nonselective beta-blocker), or saline (vehicle) prior to an exhaustive bout of exercise. Total intestinal lymphocyte numbers, percent and number of CD3+ lymphocytes, and cell viability were assessed. Neither alpha- nor beta-antagonism prevented exercise-induced cell loss in the intestine; however, pretreatment with nadolol significantly reduced the number of apoptotic and necrotic cells. Phentolamine administration appeared to increase the incidence of cell death among intestinal lymphocytes. Both drugs decreased the percentage of CD3+ intestinal lymphocytes. Our study suggests that catecholamines are not responsible for postexercise lymphocytopenia, but beta-adrenoceptor blockade may confer protection against exercise-induced apoptosis of intestinal lymphocytes.
AuthorsS Marra, L Hoffman-Goetz
JournalCanadian journal of physiology and pharmacology (Can J Physiol Pharmacol) Vol. 82 Issue 7 Pg. 465-73 (Jul 2004) ISSN: 0008-4212 [Print] Canada
PMID15389293 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adrenergic Antagonists
  • Adrenergic alpha-Antagonists
  • Adrenergic beta-Antagonists
  • Annexin A5
  • CD3 Complex
  • Receptors, Adrenergic, beta
  • Nadolol
  • Phentolamine
Topics
  • Adrenergic Antagonists (pharmacology)
  • Adrenergic alpha-Antagonists (pharmacology)
  • Adrenergic beta-Antagonists (pharmacology)
  • Animals
  • Annexin A5 (metabolism)
  • Apoptosis (drug effects)
  • CD3 Complex (metabolism)
  • Cell Survival (drug effects)
  • Female
  • Intestines (cytology, drug effects)
  • Lymphocyte Count
  • Lymphocytes (cytology, drug effects)
  • Mice
  • Mice, Inbred C57BL
  • Nadolol (pharmacology)
  • Phentolamine (pharmacology)
  • Physical Conditioning, Animal
  • Receptors, Adrenergic, beta (metabolism)

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