Yoshioka S, Nishino H, Shiraki T, Ikeda K, Koike H, Okuno A, Wada M, Fujiwara T, Horikoshi H
Biological Research Laboratories, Sankyo, Tokyo, Japan.
Metabolism. 1993 Jan;42(1):75-80. doi: 10.1016/0026-0495(93)90175-n.
The association of hypertension with obesity has been well recognized, but the etiology remains poorly understood. Obesity is characterized by hyperinsulinemia, which reflects peripheral insulin resistance. Insulin resistance may participate in the development of hypertension with obesity. CS-045 [(I)-5-[4-(5-hydroxy-2,5,7,8-tetramethylchroman-2-yl-methoxy)be nzy l]-2,4- thiazolidiendion] is a new orally effective antidiabetic agent that potentiates insulin action and reduces insulin resistance in obese Zucker rats and other obese diabetic animals. In this study, we examined the antihypertensive effect of CS-045 in obese male and female Zucker rats as a model of hypertension associated with obesity. CS-045 was administered as a food admixture (approximately 16 and approximately 70 mg/kg/d) for 4 weeks (female) and (approximately 15 and approximately 67 mg/kg/d) 8 weeks (male) in obese Zucker rats at 5 to 7 months of age. CS-045 slightly but significantly decreased plasma glucose levels. Plasma insulin levels were significantly decreased in obese male rats, but were not significantly decreased in obese female rats. Drug administration led to significant decreases in plasma triglyceride and cholesterol levels and systolic blood pressure (SBP) in a dose-dependent manner from 1 week after administration in obese Zucker rats. CS-045 increased urinary sodium excretion, sodium/potassium ratio, and creatine clearance in a dose-dependent manner, and also led to a remarkable decrease in urinary protein excretion. However, CS-045 did not reduce urinary catecholamine excretion. These data indicate that CS-045 may promote renal sodium excretion and improve decreased glomerular filtration rates, which may reflect the amelioration of insulin resistance.(ABSTRACT TRUNCATED AT 250 WORDS)
高血压与肥胖之间的关联已得到充分认识,但其病因仍知之甚少。肥胖的特征是高胰岛素血症,这反映了外周胰岛素抵抗。胰岛素抵抗可能参与了肥胖相关性高血压的发生发展。CS - 045 [(I)-5 - [4 - (5 - 羟基 - 2,5,7,8 - 四甲基色满 - 2 - 基 - 甲氧基)苄基] - 2,4 - 噻唑烷二酮]是一种新型口服有效的抗糖尿病药物,可增强胰岛素作用并降低肥胖的 Zucker 大鼠及其他肥胖糖尿病动物的胰岛素抵抗。在本研究中,我们以肥胖 Zucker 大鼠作为肥胖相关性高血压模型,研究了 CS - 045 的降压作用。对 5 至 7 月龄的肥胖 Zucker 大鼠,CS - 045 以食物添加剂形式给药(雌性约 16 和约 70 mg/kg/d,持续 4 周;雄性约 15 和约 67 mg/kg/d,持续 8 周)。CS - 045 轻微但显著降低了血糖水平。肥胖雄性大鼠的血浆胰岛素水平显著降低,但肥胖雌性大鼠的血浆胰岛素水平未显著降低。给药后 1 周起,药物给药以剂量依赖方式显著降低了肥胖 Zucker 大鼠的血浆甘油三酯和胆固醇水平以及收缩压(SBP)。CS - 045 以剂量依赖方式增加尿钠排泄、钠/钾比值和肌酐清除率,还导致尿蛋白排泄显著减少。然而,CS - 045 并未降低尿儿茶酚胺排泄。这些数据表明,CS - 045 可能促进肾钠排泄并改善肾小球滤过率降低,这可能反映了胰岛素抵抗的改善。(摘要截断于 250 字)