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首页> 外文期刊>Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association >Beneficial and adverse renal and vascular effects of the vasopeptidase inhibitor omapatrilat in renovascular hypertensive rats.
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Beneficial and adverse renal and vascular effects of the vasopeptidase inhibitor omapatrilat in renovascular hypertensive rats.

机译:血管肽酶抑制剂omapatrilat对肾血管性高血压大鼠的有益和不利的肾脏和血管作用。

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BACKGROUND: Vasopeptidase inhibitors are a new class of compounds that inhibit both angiotensin-converting enzyme (ACE) and neutral endopeptidase. This study determined whether treatment with the vasopeptidase inhibitor omapatrilat (OMA) produced different effects on renal and cardiovascular structure compared with inhibition of ACE by enalapril (ENP) in rats with two-kidney, one clip hypertension (2K1C). METHODS: Hypertensive 2K1C rats were randomized into four groups and studied for another 8 weeks: no treatment, OMA, ENP or ENP combined with the diuretic hydrochlorothiazide (ENP + HCTZ). Albuminuria, vascular and renal histology as well as glomerular expression of transforming growth factor-beta (TGF-beta) were determined at the end of the experiment. RESULTS: OMA decreased blood pressure slightly better than ENP. However, combination of ENP with a diuretic lowered blood pressure equally effective as OMA. OMA was numerically more efficient in reducing cardiovascular and renal hypertensive changes compared with ENP. In contrast, the combination of ENP + HCTZ was as efficient as OMA. However, OMA lowered overexpression of TGF-beta in the non-clipped kidney better than ENP or ENP +HCTZ. Antihypertensive therapy surprisingly decreased renal function as shown by increased plasma creatinine and urea and decreased creatinine clearance. CONCLUSION: OMA is marginally more potent compared with ENP alone in lowering blood pressure and preventing cardiovascular and renal injury. This effect may be due to slightly better blood pressure reduction because addition of HCTZ enhances the cardio- and nephroprotective capacity of ENP. In contrast, OMA reduces TGF-beta overexpression in the non-clipped kidney better than ENP or ENP + HCTZ. Therefore, vasopeptidase inhibition is not superior to ACE inhibition in the prevention of cardiovascular and renal damage Goldblatt hypertension.
机译:背景:血管肽酶抑制剂是一类同时抑制血管紧张素转换酶(ACE)和中性内肽酶的新型化合物。这项研究确定了血管肽酶抑制剂omapatrilat(OMA)与二肾一夹高血压(2K1C)大鼠相比,依那普利(ENP)对ACE的抑制作用是否对肾脏和心血管结构产生了不同的影响。方法:将高血压2K1C大鼠随机分为四组,并进行另外8周的研究:不治疗,OMA,ENP或ENP联合利尿剂氢氯噻嗪(ENP + HCTZ)。在实验结束时确定蛋白尿,血管和肾脏的组织学以及转化生长因子-β(TGF-β)的肾小球表达。结果:OMA降低的血压略好于ENP。但是,ENP与利尿剂的组合降低血压与OMA一样有效。与ENP相比,OMA在减少心血管和肾脏高血压变化方面更有效。相反,ENP + HCTZ的组合与OMA一样有效。但是,OMA可以比ENP或ENP + HCTZ更好地降低非唇肾中TGF-β的过表达。降压治疗令人惊讶地降低了肾功能,如血浆肌酐和尿素增加以及肌酐清除率降低所表明的。结论:与单独使用ENP相比,OMA在降低血压和预防心血管和肾脏损伤方面的效力略强。这种效果可能是由于降压效果更好,因为添加HCTZ可以增强ENP的心脏和肾脏保护能力。相比之下,OMA可以比ENP或ENP + HCTZ更好地减少非唇肾中TGF-β的过度表达。因此,在预防心血管和肾脏损害Goldblatt高血压方面,血管肽酶抑制作用不优于ACE抑制作用。

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