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阿利吉仑对链脲佐菌素诱导的雌性大鼠糖尿病肾病的抗糖尿病和肾脏保护作用。

Anti-diabetic and renoprotective effects of aliskiren in streptozotocin-induced diabetic nephropathy in female rats.

作者信息

Mahfoz Amal M, El-Latif Hekma A Abd, Ahmed Lamiaa A, Hassanein Nahed M, Shoka Afaf A

机构信息

Department of Pharmacology, National Organization for Drug Control and Research (NODCAR), Giza, 35521, Egypt.

Faculty of Pharmacy, Cairo University, Kasr El Aini St., Cairo, 11562, Egypt.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2016 Dec;389(12):1315-1324. doi: 10.1007/s00210-016-1299-2. Epub 2016 Sep 9.

Abstract

Since chronic kidney disease due to diabetic nephropathy (DN) is becoming an ever larger health burden worldwide, more effective therapies are desperately needed. In the present study, the anti-diabetic and renoprotective effects of aliskiren have been evaluated in streptozotocin (STZ)-induced DN in rats. DN was induced by a single intraperitoneal injection of STZ (65 mg/kg). Three weeks after STZ, rats were divided into four groups; normal, diabetic, diabetic treated with gliclazide (10 mg/kg/day) for 1 month, and diabetic treated with aliskiren (50 mg/kg/day) for 1 month. At the end of the experiment, mean arterial blood pressure and heart rate were recorded. Rats were then euthanized and serum was separated for determination of glucose, insulin, kidney function tests, superoxide dismutase activity (SOD), adiponectin, and tumor necrosis factor-alpha (TNF-α). One kidney was used for estimation of malondialdehyde (MDA), reduced glutathione (GSH), and nitric oxide (NO) contents. Other kidney was used for histopathological study and immunohistochemical measurement of caspase-3 and transforming growth factor beta (TGF-β). In addition, islets of Langerhans were isolated from normal rats by collagenase digestion technique for in vitro study. Aliskiren normalized STZ-induced hyperglycemia, increased insulin level both in vivo and in vitro, normalized kidney function tests and blood pressure, and alleviated STZ-induced kidney histopathological changes. This could be related to the ability of aliskiren toward preserving hemodynamic changes and alleviating oxidative stress and inflammatory and apoptotic markers induced by STZ in rats. However, aliskiren was more effective than gliclazide in relieving STZ-induced DN. These findings support the beneficial effect of aliskiren treatment in DN which could be attributed to its anti-diabetic, renoprotective, antioxidant, anti-inflammatory, and anti-apoptotic effects. Moreover, clinical studies are required to establish the effectiveness of aliskiren treatment in patients suffering from hypertension and diabetes.

摘要

由于糖尿病肾病(DN)所致的慢性肾脏病在全球范围内正成为日益沉重的健康负担,因此迫切需要更有效的治疗方法。在本研究中,已在链脲佐菌素(STZ)诱导的大鼠DN模型中评估了阿利吉仑的抗糖尿病和肾脏保护作用。通过单次腹腔注射STZ(65 mg/kg)诱导DN。STZ注射三周后,将大鼠分为四组;正常组、糖尿病组、用格列齐特(10 mg/kg/天)治疗1个月的糖尿病组和用阿利吉仑(50 mg/kg/天)治疗1个月的糖尿病组。实验结束时,记录平均动脉血压和心率。然后对大鼠实施安乐死并分离血清,用于测定血糖、胰岛素、肾功能指标、超氧化物歧化酶活性(SOD)、脂联素和肿瘤坏死因子-α(TNF-α)。取一侧肾脏用于评估丙二醛(MDA)、还原型谷胱甘肽(GSH)和一氧化氮(NO)含量。另一侧肾脏用于组织病理学研究以及caspase-3和转化生长因子β(TGF-β)的免疫组织化学测定。此外,通过胶原酶消化技术从正常大鼠中分离胰岛用于体外研究。阿利吉仑使STZ诱导的高血糖正常化,在体内和体外均提高胰岛素水平,使肾功能指标和血压正常化,并减轻STZ诱导的肾脏组织病理学变化。这可能与阿利吉仑维持血流动力学变化以及减轻STZ在大鼠中诱导的氧化应激、炎症和凋亡标志物的能力有关。然而,在缓解STZ诱导的DN方面,阿利吉仑比格列齐特更有效。这些发现支持了阿利吉仑治疗DN的有益作用,这可能归因于其抗糖尿病、肾脏保护、抗氧化、抗炎和抗凋亡作用。此外,需要进行临床研究以确定阿利吉仑治疗对高血压和糖尿病患者的有效性。

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