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Mali-Nil 籼米糠水解物的降血压作用及其与 EDHF 介导的血管舒张和 L 型钙通道介导的血管收缩在 L-NAME 高血压大鼠中的机制。

Antihypertensive effect of Mali-Nil surin rice bran hydrolysate and its mechanisms related to the EDHF-mediated vasorelaxation and L-type Ca channel-mediated vasoconstriction in L-NAME hypertensive rats.

机构信息

Cardiovascular Research Group, Khon Kaen University, Khon Kaen 40002, Thailand; Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.

Surin Rice Research Center, Rice Department, Surin 32000, Thailand.

出版信息

Biomed Pharmacother. 2022 Jun;150:113003. doi: 10.1016/j.biopha.2022.113003. Epub 2022 Apr 21.

Abstract

Mali-Nil Surin rice bran hydrolysate (MRH) contains highly nutritional proteins and beneficial phenolic compounds. This study investigated an antihypertensive effect of MRH and evaluated the mechanisms mediating this action in N-nitro-L-arginine-methyl ester (L-NAME)-induced hypertensive rats. Antihypertensive activity was determined in male rats orally administered with MRH (100 or 300 mg/kg) or enalapril (15 mg/kg) daily together with L-NAME (50 mg/kg/day) in drinking water, for 21 days. Concurrent oral treatment with MRH lowered the high blood pressure in the L-NAME-induced hypertensive rats. MRH treatment improved endothelial function and increased the endothelium-derived hyperpolarizing factor-mediated vasorelaxation in L-NAME hypertensive rats. L-NAME rats treated with MRH had reduced adrenergic hypercontractility, which was associated with a decrease in L-type calcium channel-mediated vasoconstriction. In addition, MRH exhibited antioxidant activity in hypertensive rats, as indicated by suppression of vascular superoxide anion production and reduction of malondialdehyde levels, as well as magnification of superoxide dismutase and catalase activities in serum. This study demonstrated the nutraceutical potential of MRH to prevent oxidative stress-related vascular dysfunction in hypertension.

摘要

茉莉香米米糠水解物(MRH)含有高营养价值的蛋白质和有益的酚类化合物。本研究探讨了 MRH 的降压作用,并评估了其在 N-硝基-L-精氨酸甲酯(L-NAME)诱导的高血压大鼠中介导这种作用的机制。将雄性大鼠连续 21 天每天经口给予 MRH(100 或 300mg/kg)或依那普利(15mg/kg),同时给予 L-NAME(50mg/kg/天)于饮水中,测定其降压活性。MRH 治疗可降低 L-NAME 诱导的高血压大鼠的高血压。MRH 治疗可改善内皮功能,并增加 L-NAME 高血压大鼠中内皮衍生超极化因子介导的血管舒张作用。用 MRH 治疗的 L-NAME 大鼠的肾上腺素能过度收缩性降低,这与 L 型钙通道介导的血管收缩减少有关。此外,MRH 在高血压大鼠中表现出抗氧化活性,表现为抑制血管超氧阴离子的产生和降低丙二醛水平,以及增加血清中超氧化物歧化酶和过氧化氢酶的活性。本研究表明,MRH 具有预防高血压相关氧化应激性血管功能障碍的营养保健品潜力。

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