Acute intravenous antihypertensive and in vitro vasorelaxant effect of the hydroalcoholic stem bark extract of Hymenaea rubriflora Ducke in spontaneously hypertensive rats

阿托品 血管舒张 药理学 心动过缓 血压 四乙基铵 医学 抗氧化剂 化学 心率 内皮 麻醉 血流动力学 电阻抗肌描记术 平均动脉压 乙酰胆碱 毒蕈碱乙酰胆碱受体 血管平滑肌 内科学 生药学 抗胆碱能 内分泌学 树皮(声音) 一氧化氮
作者
Luciana Tavares Toscano,Milton Rocha Moraes,Robson Cavalcante Veras,Priscilla Maria Pereira Maciel,Kívia S. Assis,Franciely Oliveira Lima,Jayme César da Silva Júnior,Ângela Maria Tribuzy de Magalhães Cordeiro,Isac Almeida de Medeiros,Thiago dos Santos Rosa,Alexandre Sérgio Silva
出处
期刊:Journal of Pharmacy and Pharmacology [Oxford University Press]
卷期号:78 (7)
标识
DOI:10.1093/jpp/rgag082
摘要

OBJECTIVES: The cardioprotective potential of Hymenaea rubriflora Ducke's stem bark hydroalcoholic extract (HR-HAc) has not yet been investigated. This study aimed to quantify HR-HAc's antioxidant capacity and evaluate its effects on blood pressure (BP) and vascular reactivity in spontaneously hypertensive rats (SHR). METHODS: SHR and normotensive Wistar Kyoto (WKY) rats received intravenous HR-HAc (2.5-60 mg/kg). Mean arterial pressure (MAP) and heart rate (HR) were measured with or without atropine and propranolol. Isolated aortas from SHR and WKY rats were exposed to HR-HAc (0.1-729 μg/ml), with or without endothelium and K+ channel blockers. Phenolic content and antioxidant activity were quantified using standard colorimetric and chromatographic methods. KEY FINDINGS: In SHR rats, HR-HAc produced dose-dependent hypotension and bradycardia. MAP reduction in WKY rats was similar, while HR was unaffected. Atropine significantly attenuated HR-HAc-induced reductions in MAP and HR in SHR rats. HR-HAc induced potent endothelium-independent relaxation in SHR rat aortas, which was significantly reduced by tetraethylammonium or 4-aminopyridine. In WKY rats, vasorelaxant effects were endothelium-dependent. CONCLUSIONS: HR-HAc lowers MAP and induces bradycardia in SHR via muscarinic receptors, while also promoting vasodilation through activation of voltage- and calcium-activated K+ channels. These distinct mechanisms highlight HR-HAc as a promising preclinical antihypertensive candidate.

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