Furuhashi Masato, Ura Nobuyuki, Takizawa Hideki, Yoshida Daisuke, Moniwa Norihito, Murakami Hideyuki, Higashiura Katsuhiro, Shimamoto Kazuaki
Second Department of Internal Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan.
J Hypertens. 2004 Oct;22(10):1977-82. doi: 10.1097/00004872-200410000-00021.
Based on results of in vitro studies, it has been hypothesized that blockade of the renin-angiotensin system (RAS) promotes the recruitment and differentiation of pre-adipocytes and that increased formation of small insulin-sensitive adipocytes counteracts ectopic deposition of lipids, thereby improving insulin sensitivity. We investigated the effect of RAS blockade on insulin sensitivity, adipocyte size, and intramuscular lipid content in fructose-fed rats (FFR) as a model of insulin-resistant hypertension.
Six-week-old male Sprague-Dawley rats were divided into two groups: those fed a standard chow (control) and those fed a fructose-rich chow for 6 weeks. FFR were treated with a vehicle or with 1 mg/kg per day of temocapril, an angiotensin-converting enzyme inhibitor, or 0.1 mg/kg per day of olmesartan, an angiotensin II type 1 receptor blocker, for the last 2 weeks. Insulin sensitivity (M value: mg/kg per min) was estimated by the euglycemic hyperinsulinemic glucose clamp method. Sizes of adipocytes derived from epididymal fat and triglyceride content in the soleus muscle were determined.
FFR had lower M value, higher blood pressure, larger adipocyte size, higher ratio of epididymal fat pads over body weight (%fat pads), and higher intramuscular triglyceride than did the control rats. Both temocapril and olmesartan significantly improved the M value and decreased blood pressure and adipocyte size without change in %fat pads in FFR. Adipocyte size was negatively correlated with the M value. Treatment for 2 weeks decreased, but not significantly, intramuscular triglyceride.
RAS blockade decreases adipocyte size without change in epididymal %fat pads accompanied by improvement in insulin sensitivity.
基于体外研究结果,有人提出假说,即肾素 - 血管紧张素系统(RAS)的阻断可促进前脂肪细胞的募集和分化,并且增加小的胰岛素敏感脂肪细胞的形成可抵消脂质的异位沉积,从而改善胰岛素敏感性。我们研究了RAS阻断对果糖喂养大鼠(FFR)胰岛素敏感性、脂肪细胞大小和肌肉内脂质含量的影响,FFR作为胰岛素抵抗性高血压的模型。
将六周龄雄性Sprague-Dawley大鼠分为两组:一组喂食标准饲料(对照组),另一组喂食富含果糖的饲料六周。在最后两周,FFR分别接受载体、每天1mg/kg的替莫卡普利(一种血管紧张素转换酶抑制剂)或每天0.1mg/kg的奥美沙坦(一种1型血管紧张素II受体阻滞剂)治疗。通过正常血糖高胰岛素葡萄糖钳夹法评估胰岛素敏感性(M值:mg/kg每分钟)。测定附睾脂肪来源的脂肪细胞大小和比目鱼肌中的甘油三酯含量。
与对照大鼠相比,FFR的M值较低、血压较高、脂肪细胞较大、附睾脂肪垫与体重的比率(%脂肪垫)较高,且肌肉内甘油三酯含量较高。替莫卡普利和奥美沙坦均显著改善了FFR的M值,降低了血压和脂肪细胞大小,而%脂肪垫没有变化。脂肪细胞大小与M值呈负相关。治疗两周可降低但未显著降低肌肉内甘油三酯含量。
RAS阻断可减小脂肪细胞大小,附睾%脂肪垫无变化,同时改善胰岛素敏感性。