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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Gastrodin Reduces Blood Pressure by Intervening with RAAS and PPAR gamma in SHRs
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Gastrodin Reduces Blood Pressure by Intervening with RAAS and PPAR gamma in SHRs

机译:胃泌素通过在shrs中介入raas和pparγ来减少血压

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Gastrodin is a bioactive compound extracted from traditional Chinese medicine, Gastrodia elata Bl. It has a definite effect on reducing blood pressure in hypertensive patients. However, the mechanisms of gastrodin in lowering blood pressure still remain unclear. In this study, 4 weeks of administration of gastrodin (100mg/kg/d intraperitoneally injected) decreased the systolic blood pressure (SBP) in spontaneously hypertensive rats (SHRs) (190.2 +/- 8.9 versus 169.8 +/- 6.4, P 0.01). Among SHRs receiving gastrodin treatment, angiotensin II (Ang II) and aldosterone (ALD) in serum were significantly decreased (2022.1 +/- 53.0 versus 1528.7 +/- 93.9, 213.33 +/- 35.17 versus 179.65 +/- 20.31, and P 0.01, P 0.05, resp.) and dramatically downregulated expression of angiotensin type 1 receptor (AT1R) (4.9 +/- 0.9 versus 2.6 +/- 0.9, P 0.05) in myocardium in both mRNA and protein levels compared with their corresponding groups without gastrodin treatment. Additionally, gastrodin increased the mRNA expression (0.18 +/- 0.07 versus 0.82 +/- 0.10, P 0.01) and protein synthesis (0.40 +/- 0.10 versus 0.34 +/- 0.10, P 0.01) of peroxisome proliferator-activated receptor gamma (PPAR gamma) in myocardium tissues. Overall, our data demonstrated that gastrodin was able to decrease the SBP in SHR. Furthermore, this study showed that gastrodin intervened with the renin-angiotensin-aldosterone system (RAAS) and PPAR gamma effectively, which indicates its antihypertensive mechanism.
机译:Gastrodin是一种从中药胃肠榆树BL中提取的生物活性化合物。它对降低高血压患者血压有明确的影响。然而,在降低血压下胃生成的机制仍然尚不清楚。在这项研究中,4周的胃生成素(100mg / kg / d腹膜内注射)减少了自发性高血压大鼠的收缩压(SBP)(190.2 +/- 8.9与169.8 +/- 6.4,P& 0.01)。在接受胃素治疗的SHR中,血清中的血管素II(Ang II)和醛固酮(ALD)显着降低(2022.1 +/- 53.0与1528.7 +/- 93.9,213.33 +/- 35.17与179.65 +/- 20.31,以及P&P ; 0.01,P <0.05,REAC。)并显着下调血管紧张素1受体(AT1R)的表达(AT1R)(4.9 +/- 0.9对2.6 +/- 0.9,p <0.9,P <0.05),比较它们的相应群体没有胃脂素治疗。另外,胃生物素增加mRNA表达(0.18 +/- 0.07对0.82 +/- 0.10,p <0.01)和蛋白质合成(0.40 +/- 0.10与0.34 +/- 0.10,p <0.01)的过氧化物酶增殖物 - 心肌组织中的活化受体γ(PPARγ)。总体而言,我们的数据表明,胃生物素能够减少SHR中的SBP。此外,该研究表明,有效地利用了肾素 - 血管紧张素 - 醛固酮系统(RAAS)和PPARγ的胃毒素,这表明其抗高血压机制。

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