Suzuki Katsunori, Nakagawa Osamu, Aizawa Yoshifusa
Division of Endocrinology and Metabolism, Saiseikai Niigata Second Hospital, Niigata, Japan.
Clin Exp Hypertens. 2008 Jul;30(5):309-14. doi: 10.1080/10641960802269927.
As the effect of renin-angiotensin system (RAS) blockade on beta-cells in clinical situations remains unclear, new evidence has been presented that angiotensin-converting enzyme (ACE) inhibitors and angiotensin vertical line vertical line receptor blockers (ARBs) may delay or prevent the development of insulin resistance and diabetes through novel mechanisms. This study aimed to determine the effects of ARBs on insulin excretion by beta-cells. Hypertensive patients with impaired glucose tolerance were randomly divided into two groups: group A (n = 6), which received 8 mg/day of oral candesartan for three months, and controls (n = 6). Before and after administration, a 75 g oral glucose tolerance test was conducted to compare various parameters. No significant differences in age, body mass index (BMI), systolic blood pressure (SBP), diastolic blood pressure (DBP), fasting glucose, or fasting immunoreactive insulin (IRI) were identified between the groups before administration. After three months, there were no significant changes in BMI, SBP, and DBP for the controls and in BMI and DBP for group A. However, SBP was significantly decreased from 144 +/- 2.6 mmHg to 125 +/- 4.6 mmHg in group A. Insulinogenic index tended to be slightly decreased for controls, but was significantly increased from 0.32 +/- 0.0 to 0.47 +/- 0.1 for group A. No significant changes in HOMA-R were identified in either group. To the best of our knowledge, no previous studies have documented a RAS inhibitor improving early-phase insulin response; thus, the present study may be the first of its kind.
由于肾素-血管紧张素系统(RAS)阻断在临床情况下对β细胞的影响仍不清楚,新的证据表明,血管紧张素转换酶(ACE)抑制剂和血管紧张素Ⅱ受体阻滞剂(ARBs)可能通过新机制延缓或预防胰岛素抵抗和糖尿病的发生。本研究旨在确定ARBs对β细胞胰岛素分泌的影响。糖耐量受损的高血压患者被随机分为两组:A组(n = 6),口服坎地沙坦8mg/天,持续三个月,以及对照组(n = 6)。给药前后,进行75g口服葡萄糖耐量试验以比较各项参数。给药前两组在年龄、体重指数(BMI)、收缩压(SBP)、舒张压(DBP)、空腹血糖或空腹免疫反应性胰岛素(IRI)方面无显著差异。三个月后,对照组的BMI、SBP和DBP以及A组的BMI和DBP均无显著变化。然而,A组的SBP从144±2.6mmHg显著降至125±4.6mmHg。对照组的胰岛素生成指数略有下降趋势,但A组从0.32±0.0显著增至0.47±0.1。两组的HOMA-R均无显著变化。据我们所知,以前没有研究记录过RAS抑制剂可改善早期胰岛素反应;因此,本研究可能是首例此类研究。