Sanke T, Nanjo K, Kondo M, Nishi M, Moriyama Y, Miyamura K
Metabolism. 1986 Oct;35(10):924-7. doi: 10.1016/0026-0495(86)90055-7.
The clinical usefulness of calcium antagonists was studied in four patients with reactive hypoglycemia including two with alimentary and two with idiopathic. All patients had hyperresponses of plasma insulin (IRI) and C-peptide (CPR) during an oral glucose tolerance test (OGTT). A calcium antagonist (diltiazem 90 mg/d, or nifedipine 30 mg/d, or nicardipine 60 mg/d) was administered orally for about two months. After two months of treatment, plasma IRI and CPR responses during the OGTT were clearly suppressed in all patients and symptomatic reactive hypoglycemia disappeared. One month after the discontinuation of the treatment in two patients, plasma IRI and CPR responses during the OGTT became higher again and symptomatic reactive hypoglycemia recurred. In addition, an intravenous glucose tolerance test was performed before and after two months of the treatment with calcium antagonists in the two patients with reactive hypoglycemia and seven patients with hypertension, who were free from glucose intolerance and were also treated with a calcium antagonist. In these patients, plasma IRI and CPR responses were also reduced after the treatment compared with those before the treatment. These results suggest that calcium antagonists are useful as therapeutic agents for the treatment of reactive hypoglycemia associated with hyperinsulinemia, and that one of the main mechanisms of action of calcium antagonists is a direct action on the pancreatic B-cell to inhibit glucose-induced insulin release.
对4例反应性低血糖患者(其中2例为饮食性,2例为特发性)研究了钙拮抗剂的临床效用。所有患者在口服葡萄糖耐量试验(OGTT)期间血浆胰岛素(IRI)和C肽(CPR)均有高反应。口服一种钙拮抗剂(地尔硫䓬90毫克/天,或硝苯地平30毫克/天,或尼卡地平60毫克/天)约两个月。治疗两个月后,所有患者OGTT期间的血浆IRI和CPR反应均明显受到抑制,有症状的反应性低血糖消失。在两名患者停药一个月后,OGTT期间的血浆IRI和CPR反应再次升高,有症状的反应性低血糖复发。此外,对两名反应性低血糖患者和七名高血压患者在使用钙拮抗剂治疗两个月前后进行了静脉葡萄糖耐量试验,这些患者无糖耐量异常,也接受了钙拮抗剂治疗。在这些患者中,与治疗前相比,治疗后血浆IRI和CPR反应也降低了。这些结果表明,钙拮抗剂可作为治疗与高胰岛素血症相关的反应性低血糖的治疗药物,并且钙拮抗剂的主要作用机制之一是对胰腺B细胞的直接作用,以抑制葡萄糖诱导的胰岛素释放。