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Possible mechanisms of action of the hypotensive effect of Annona muricata (soursop) in normotensive Sprague-Dawley rats
被引:36
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+.
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页码:1436 / 1441
页数:6
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