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Effects of coronary occlusion on arterial baroreflex control of heart rate and vascular resistance.

Abstract
This study was planned to assess whether circumflex coronary occlusion (CO) impairs the arterial baroreflex control of heart rate (HR) and hindlimb vascular resistance (HVR), and to determine the mechanisms involved in the mediation of these phenomena. Increasing doses of phenylephrine and nitroglycerin were given intravenously to anesthetized dogs with a constant flow-perfused hindlimb before and during 30-s CO. The reflex responses were assessed by the changes in HR and hindlimb perfusion pressure evoked by changes in arterial pressure following phenylephrine and nitroglycerin administration. During CO, there was an attenuation of the reflex control of HR and HVR as compared with control conditions. The application of lidocaine on the left ventricular epicardial surface was able to prevent the effect of CO on both the baroreflex responses. The intravenous administration of atropine prevented only the impairment in arterial baroreflex control of HR induced by CO. After the injection of phentolamine into the perfused hindlimb, the baroreflex had no effect on HVR either before or during CO. Finally, intravenous administration of propranolol failed to modify the effect of CO on both the baroreflex responses. These data indicate that CO attenuates the arterial baroreflex control of both HR and HVR through the stimulation of left ventricular receptors. The effect on HR is mediated by the parasympathetic system, whereas the effect on HVR is due to sympathetic efferents.
AuthorsB Trimarco, B Ricciardelli, A Cuocolo, M Volpe, N De Luca, A F Mele, M Condorelli
JournalThe American journal of physiology (Am J Physiol) Vol. 252 Issue 4 Pt 2 Pg. H749-59 (Apr 1987) ISSN: 0002-9513 [Print] United States
PMID3105333 (Publication Type: Journal Article)
Chemical References
  • Phenylephrine
  • Atropine
  • Lidocaine
  • Propranolol
  • Nitroglycerin
  • Phentolamine
Topics
  • Animals
  • Atropine (pharmacology)
  • Coronary Circulation
  • Coronary Disease (physiopathology)
  • Dogs
  • Female
  • Heart Rate (drug effects)
  • Lidocaine (pharmacology)
  • Male
  • Nitroglycerin (pharmacology)
  • Phentolamine (pharmacology)
  • Phenylephrine (pharmacology)
  • Pressoreceptors (physiology)
  • Propranolol (pharmacology)
  • Reflex (drug effects, physiology)
  • Vascular Resistance (drug effects)

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