Al-Salami H, Mamo J C, Mooranian A, Negrulj R, Lam V, Elahy M, Takechi R
Curtin Health Innovation Research Institute-Biosciences, Curtin University, WA, Australia.
Exp Clin Endocrinol Diabetes. 2017 Jan;125(1):28-32. doi: 10.1055/s-0042-106084. Epub 2016 May 24.
Hypertension is a significant comorbidity associated with insulin resistance and type-2 diabetes. Limited evidence show that ursodeoxycholic acid (UDCA) has some anti-hypertensive effects. However, the potential effect of UDCA on hypertension induced by type-2 diabetic insulin resistance has not been reported. In C57Bl6 wild-type mice, insulin resistance was induced by the chronic ingestion of diet enriched in fat and fructose (HFF). HFF mice were randomized to treatment with UDCA or candersartan incorporated into the diet to achieve an ingested dose of approximately 70 mg/kg/day of UDCA or 3 mg/kg/day respectively. Systolic and diastolic blood pressure were measured with tail-cuff method. At 4 weeks of dietary treatment systolic and diastolic blood pressure were comparable in HFF and low-fat (LF) control mice. Co-administration of candesartan at 4 weeks significantly decreased systolic and diastolic blood pressure, UDCA showed no anti-hypertensive effect at 4 weeks. At 24 weeks of dietary intervention, HFF fed mice had substantially elevated systolic blood pressure compared to LF controls. The provision of UDCA substantially attenuated the dietary HFF induced increase in systolic blood pressure concomitant with significantly lower plasma angiotensin II. The anti-hypertensive effect of UDCA in HFF mice was comparable to candesartan. The data suggests that long term supplementation of UDCA effectively lowers hypertension in a dietary induced model of type-2 diabetic insulin resistance.
高血压是一种与胰岛素抵抗和2型糖尿病相关的重要合并症。有限的证据表明,熊去氧胆酸(UDCA)具有一定的抗高血压作用。然而,UDCA对2型糖尿病胰岛素抵抗所致高血压的潜在作用尚未见报道。在C57Bl6野生型小鼠中,通过长期摄入富含脂肪和果糖的饮食(HFF)诱导胰岛素抵抗。将HFF小鼠随机分为两组,分别给予掺入饮食中的UDCA或坎地沙坦进行治疗,以使摄入剂量分别达到约70mg/kg/天的UDCA或3mg/kg/天。采用尾套法测量收缩压和舒张压。在饮食治疗4周时,HFF小鼠和低脂(LF)对照小鼠的收缩压和舒张压相当。在4周时联合使用坎地沙坦可显著降低收缩压和舒张压,UDCA在4周时未显示出抗高血压作用。在饮食干预24周时,与LF对照组相比,喂食HFF的小鼠收缩压大幅升高。给予UDCA可显著减轻饮食HFF诱导的收缩压升高,同时血浆血管紧张素II显著降低。UDCA对HFF小鼠的抗高血压作用与坎地沙坦相当。数据表明,在饮食诱导的2型糖尿病胰岛素抵抗模型中,长期补充UDCA可有效降低高血压。