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Microsphere analysis of beta 2-adrenergic control of resistance in different vascular areas after hemorrhage.

Abstract
In cats exposed to bleeding (exsanguination of 15 ml X kg bwt-1) the microsphere technique was used to determine regional vascular resistances in a large number of tissues before and after i.v. administration of the 'selective' beta 2-adrenoceptor antagonist ICI 118,551. beta 2-blockade significantly raised vascular resistance in the stomach (+ 26%), small (+ 25%) and large (+ 38%) intestine, pancreas (+ 29%), kidney (+ 39%), omental (+ 33%) and subcutaneous (+ 26%) fat, 'white' skeletal muscle (+ 19%), and skin (+ 24%). These findings indicate that, with intact beta-adrenoceptors, beta 2-adrenergic dilator interaction counteracted the hemorrhage evoked vasoconstrictor influences. beta 2-blockade also evoked quite a strong increase of total peripheral resistance (19%) and led to some redistribution of cardiac output. It is concluded that beta 2-adrenergic inhibition of vascular tone significantly seems to improve tissue perfusion during bleeding in several vascular areas. Such effects may be of special significance during severe hemorrhage. In the intestine, pancreas, and adipose tissue, for example, protection against excessive vasoconstriction may serve to minimize the severe metabolic disturbances with secondary release of toxic factors into the circulation reported during hemorrhagic shock.
AuthorsD Gustafsson, L Andersson, L Mårtensson, J Lundvall
JournalActa physiologica Scandinavica (Acta Physiol Scand) Vol. 121 Issue 2 Pg. 119-26 (Jun 1984) ISSN: 0001-6772 [Print] England
PMID6147953 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adrenergic beta-Antagonists
  • Propanolamines
  • ICI 118551
Topics
  • Adrenergic beta-Antagonists (pharmacology)
  • Animals
  • Blood Pressure (drug effects)
  • Cardiac Output (drug effects)
  • Cats
  • Female
  • Heart Rate (drug effects)
  • Hemorrhage (physiopathology)
  • Male
  • Microspheres
  • Muscles (blood supply)
  • Propanolamines (pharmacology)
  • Regional Blood Flow (drug effects)
  • Stroke Volume (drug effects)
  • Vascular Resistance (drug effects)

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