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首页> 外文期刊>Journal of Functional Foods >Involvement of nitric oxide and prostacyclin in the antihypertensive effect of low-molecular-weight procyanidin rich grape seed extract in male spontaneously hypertensive rats.
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Involvement of nitric oxide and prostacyclin in the antihypertensive effect of low-molecular-weight procyanidin rich grape seed extract in male spontaneously hypertensive rats.

机译:一氧化氮和前列环素参与低分子富含原花青素的葡萄籽提取物对雄性自发性高血压大鼠的降压作用。

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摘要

The aim of this study was to evaluate the involvement of endothelial-relaxing factors as possible antihypertensive mechanism of low-molecular-weight procyanidin rich grape seed extract (LM-GSPE). Thirty 17-20-week-old male spontaneously hypertensive rats (SHR) were administered water or 375 mg/kg LM-GSPE by intragastric gavage. One millilitre of saline, 30 mg/kg NG-Nitro-L-arginine methyl ester (L-NAME) or 5 mg/kg indomethacin was administrated intraperitoneally. Systolic blood pressure (SBP) and diastolic blood pressure (DBP) were recorded before and 6 h after oral administration. Plasma concentration of 6-keto-prostaglandin F1 alpha (PGF1 alpha) was quantified. In addition, we evaluated the relaxation caused by LM-GSPE in different aorta preparations. The antihypertensive effect of LM-GSPE was completely and partially abolished by L-NAME and indomethacin, respectively. In addition, plasma PGF1 alpha was increased in LM-GSPE-administered rats. Finally, LM-GSPE relaxed the intact aorta preparations but did not relax the endothelium-denuded aorta rings. L-NAME inhibited the relaxation caused by LM-GSPE in the SHR aorta rings, but indomethacin did not. Therefore, the antihypertensive effect of LM-GSPE in SHR is endothelium dependent, and it could be mediated by changes in endothelium-derived nitric oxide bioavailability. Nevertheless, prostacyclin could also contribute additionally to this effect
机译:这项研究的目的是评估内皮松弛因子作为低分子量富含原花青素的葡萄籽提取物(LM-GSPE)可能的降压机制。通过胃管灌胃法对30只17-20周大的雄性自发性高血压大鼠(SHR)进行饮水或375 mg / kg LM-GSPE。腹膜内注射1毫升盐水,30 mg / kg NG-硝基-L-精氨酸甲酯(L-NAME)或5 mg / kg消炎痛。在口服之前和之后6小时记录收缩压(SBP)和舒张压(DBP)。定量6-酮-前列腺素F1α(PGF1 alpha)的血浆浓度。此外,我们评估了LM-GSPE在不同主动脉制剂中引起的松弛。 LM-GSPE的降压作用被L-NAME和消炎痛分别完全和部分消除。另外,在LM-GSPE给药的大鼠中血浆PGF1α增加。最后,LM-GSPE放松了完整的主动脉准备,但没有放松内皮剥除的主动脉环。 L-NAME抑制了SHR主动脉环中LM-GSPE引起的松弛,但吲哚美辛没有。因此,LM-GSPE在SHR中的降压作用是内皮依赖性的,并且可以由内皮衍生的一氧化氮生物利用度的变化介导。然而,前列环素也可能另外有助于这种作用

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