Abstract | OBJECTIVES: BACKGROUND: The mechanisms underlying postischemic LV dysfunction are largely unknown. METHODS: Percutaneous transluminal coronary angioplasty (PTCA) provides a clinical model of ischemia and reperfusion. In 50 patients undergoing coronary stenting for 77+/-5% stenosis, LV function was monitored by transesophageal echocardiography during and 30-min after PTCA. Fifteen minutes after stenting, 15 patients received 12 microg/kg body weight of the alpha-blocker phentolamine intracoronarily, 15 patients received 600 microg/kg of the alpha1-blocker urapidil intravenously, 10 patients received the combination of phentolamine and 1.2 mg of propranolol intracoronarily, and 10 patients received saline. RESULTS: Fifteen minutes after successful coronary dilation, significant contractile dysfunction occurred in previously ischemic and nonischemic myocardium. LV dysfunction was accompanied by an increase in coronary resistance and diffuse vasoconstriction. Alpha-blockers counteracted LV dysfunction and coronary resistance and the increase in vasoconstriction. Phentolamine and urapidil increased global LV shortening from 34+/-9% to 45+/-8% and to 49+/-8%, respectively (p < 0.05). After the administration of propranolol combined with phentolamine, LV dysfunction remained unchanged (34+/-6%), as in control subjects. CONCLUSIONS:
LV dysfunction occurs after PTCA, as described in animal models after ischemia. Alpha-blockers abolished LV, macrocirculatory and microcirculatory dysfunction, whereas the alpha-blocker effect was prevented by combining alpha- and beta-blockers. The evidence of diffuse rather than regional dysfunction, together with the opposite effects of alpha- and beta-blockade, supports the hypothesis of neural mechanisms eliciting postischemic LV dysfunction.
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Authors | L Gregorini, J Marco, C Palombo, M Kozàkovà, G B Anguissola, B Cassagneau, M Bernies, A Distante, I Marco, J Fajadet, A Zanchetti |
Journal | Journal of the American College of Cardiology
(J Am Coll Cardiol)
Vol. 31
Issue 5
Pg. 992-1001
(Apr 1998)
ISSN: 0735-1097 [Print] United States |
PMID | 9561999
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Adrenergic alpha-Antagonists
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Topics |
- Adrenergic alpha-Antagonists
(pharmacology, therapeutic use)
- Aged
- Angioplasty, Balloon, Coronary
- Coronary Vessels
(diagnostic imaging)
- Echocardiography, Transesophageal
- Female
- Hemodynamics
(drug effects)
- Humans
- Male
- Middle Aged
- Myocardial Ischemia
(complications, physiopathology, therapy)
- Stents
- Vascular Resistance
(drug effects)
- Ventricular Dysfunction, Left
(diagnostic imaging, drug therapy, etiology)
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