Possible mechanisms of action of the hypotensive effect of Annona muricata (soursop) in normotensive Sprague-Dawley rats

被引:33
|
作者
Nwokocha, Chukwuemeka R. [1 ]
Owu, Daniel U. [2 ]
Gordon, Angeline [1 ]
Thaxter, Karen [1 ]
McCalla, Garsha [1 ]
Ozolua, Raymond I. [3 ]
Young, Lauriann [1 ]
机构
[1] Univ W Indies, Dept Basic Med Sci, Physiol Sect, Kingston 7, Jamaica
[2] Univ Calabar, Dept Physiol, Calabar, Nigeria
[3] Univ Benin, Dept Pharmacol, Benin, Nigeria
关键词
Aorta; calcium antagonism; hypertension; rats; in vitro; in vivo; HEAVY-METAL ACCUMULATION; CHEMICAL-COMPOSITION; VASCULAR REACTIVITY; MEDICINAL-PLANT; ESSENTIAL OILS; WISTAR RATS; L; LEAVES; IN-VITRO; ACETOGENINS; EXTRACT;
D O I
10.3109/13880209.2012.684690
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context: Annona muricata Linn (Annonaceae) (soursop) is a food plant reported to have antihypertensive properties. Objective: We investigated the blood pressure reducing effect of its aqueous leaf extract and the possible mechanisms that may be responsible. Methods: Intravenous administration of an aqueous leaf extract (9.17-48.5 mg/kg) of A. muricata on the mean arterial pressure and heart rate were recorded invasively on anaesthetized, normotensive Sprague-Dawley rats. Contractile responses of rat aortic rings to the extract (0.5-4.0 mg/mL) were studied using standard organ bath techniques. Results: A. muricata (9.17-48.5 mg/kg) caused significant (p < 0.05) dose-dependent reduction in blood pressure without affecting the heart rates. The hypotensive effects were unaffected by atropine (2 mg/kg), mepyramine (5 mg/kg), propranolol (1 mg/kg) and l-NAME (5 mg/kg). A. muricata leaf aqueous extract significantly (p < 0.05) relaxed phenylephrine (10(-9)-10(-4) M) and 80 mM KCl induced contractions in endothelium intact and denuded aortic rings; and caused a significant (p < 0.05) rightward shift of the Ca2+ dose response curves in Ca2+-free Kreb's solution containing 0.1 mM EGTA. Conclusions: The hypotensive effects of A. muricata are not mediated through muscarinic, histaminergic, adrenergic and nitric oxide pathways, but through peripheral mechanisms involving antagonism of Ca2+.
引用
收藏
页码:1436 / 1441
页数:6
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