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首页> 外文期刊>Hypertension research: Official journal of the Japanese Society of Hypertension >Effect of cilnidipine on insulin sensitivity in patients with essential hypertension.
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Effect of cilnidipine on insulin sensitivity in patients with essential hypertension.

机译:西尼地平对原发性高血压患者胰岛素敏感性的影响。

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摘要

To clarify the effect of cilnidipine, a long-acting dihydropyridine Ca-antagonist that blocks both L- and N-type Ca(2+)-channels, on insulin sensitivity, cilnidipine at 5 to 10 mg/day was administered to ten patients with essential hypertension for 12 weeks. Mean age and body mass index (BMI) were 57.7 +/- 5.0 (SEM) years old and 27.1 +/- 1.5, respectively. Blood pressure, serum levels of catecholamines, glucose and lipid were determined before and after the treatment. Insulin sensitivity was also measured by a euglycemic hyperinsulinemic clamp method using an artificial pancreas (STG-22; Nikiso, Tokyo, Japan) before and after the treatment. Cilnidipine administration significantly lowered blood pressure from 154/96 to 137/84 mmHg (p<0.05). The glucose infusion rate was significantly increased by 20.8%, from 3.27 +/- 0.36 to 3.95 +/- 0.55 mg/kg/min (p<0.05). HbA1C and serum lipid levels such as total cholesterol and triglyceride were not altered. In addition, cilnidipine treatment did not significantlyincrease serum norepinephrine levels (278 +/- 25.2 vs. 332 +/- 33.6 pg/ml). Our results suggest that cilnidipine improves insulin sensitivity, possibly due to its exerting a vasodilatory action without stimulating sympathetic nervous activity.
机译:为阐明西尼地平的长效二氢吡啶类钙拮抗剂对胰岛素敏感性的影响,该药可阻断L型和N型Ca(2+)通道对胰岛素敏感性的作用,对10例患有糖尿病的患者给予西尼地平5至10 mg / day原发性高血压持续12周。平均年龄和体重指数(BMI)分别为57.7 +/- 5.0(SEM)岁和27.1 +/- 1.5岁。在治疗前后测定血压,儿茶酚胺的血清水平,葡萄糖和脂质。在治疗之前和之后,还通过使用人工胰腺(STG-22; Nikiso,东京,日本)的正常血糖高胰岛素钳夹法测量胰岛素敏感性。西尼地平的给药将血压从154/96毫米汞柱显着降低到137/84 mmHg(p <0.05)。葡萄糖输注速率显着提高了20.8%,从3.27 +/- 0.36增至3.95 +/- 0.55 mg / kg / min(p <0.05)。 HbA1C和血清脂质水平(如总胆固醇和甘油三酸酯)未改变。此外,西尼地平治疗并未显着增加血清去甲肾上腺素水平(278 +/- 25.2 vs. 332 +/- 33.6 pg / ml)。我们的结果表明,西尼地平可改善胰岛素敏感性,这可能是由于其发挥了血管舒张作用而不刺激交感神经活动。

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