Husted S E, Pedersen C, Nielsen H K, Apoil E, Nielsen O H, Lindvig K, Krusell L R, Høegholm A
Medical Department I, Aarhus County Hospital, Denmark.
Eur J Clin Pharmacol. 1988;34(3):221-6. doi: 10.1007/BF00540947.
In a double-blind cross-over study bepridil 900 mg followed by 300 mg daily for 11 days was given to 37 insulin (Type I) or non-insulin (Type II)-dependent diabetic patients. It did not modify the metabolic control of the patients as levels of glucose in blood and urine, doses of insulin and oral hypoglycaemic drugs, energy intake, and the number of hypoglycaemic attacks during therapy were unchanged. The serum concentration of C-peptide was not modified in either type of diabetic patient, and serum insulin in the Type I but not in the Type II patients was slightly higher during active drug treatment. No adverse organotoxic or arrhythmogenic effects or changes in possible atherogenic lipid fractions in serum could be demonstrated during bepridil therapy.
在一项双盲交叉研究中,37名胰岛素依赖型(I型)或非胰岛素依赖型(II型)糖尿病患者服用了每日900毫克随后每日300毫克共11天的苄普地尔。由于血液和尿液中的葡萄糖水平、胰岛素和口服降糖药的剂量、能量摄入以及治疗期间低血糖发作的次数均未改变,所以它并未改善患者的代谢控制。两种类型糖尿病患者的C肽血清浓度均未改变,在活性药物治疗期间,I型患者的血清胰岛素略有升高,而II型患者则未升高。在苄普地尔治疗期间,未发现有不良的器官毒性或致心律失常作用,也未发现血清中可能致动脉粥样硬化的脂质成分有变化。