Trygstad O, Foss I
Acta Endocrinol (Copenh). 1977 Jun;85(2):436-48. doi: 10.1530/acta.0.0850436.
Lipoatrophic diabetes has been produced in rabbits by injection of a fraction prepared from the urine from patients with congenital generalized lipodystrophy. Both these conditions are considered to be hypothalamic syndromes. The animals, and a patient with congenital generalized lipodystrophy and latent diabetes were treated with the dopamine receptor blocker, pimozide, for 4 and 17 months, respectively. The results were discouraging even though the patient got a daily dose of 16 mg pimozide. Fenfluramine has a lowering effect on brain serotonin, and peripheral effects on glucose and triglyceride metabolism. This drug improved the general condition of the rabbits with lipoatrophic diabetes, as well as that of the patient with congenital generalized lipodystrophy. The rabbits became normoglycaemic and insulin sensitive. In the patient a normalization of the urinary excretion of the serotonin metabolite 5-OH-indole acetic acid was observed. His voracious hunger and profuse perspiration were reduced, the hyperkeratotic layer of the skin peeled off, and the pigmentations of the skin decreased. There was observed an improvement of ALAT and ASAT, normalization of the fasting blood glucose, and increased sensitivity to exogenous insulin. After 11 months of 200 mg fenfluramine daily addtitional administration of 2 g clofibrate per day produced normalization of the serum triglyceride concentration and a marked reduction of the resistance to insulin. Three more patients with congenital generalized lipodystriphy, two of whom have manifest diabetes, have now started treatment with fenfluramine and are improving. The rabbits got relapse of their lipoatrophic diabetes when the fenfluramine treatment was stopped. It is suggested that a disturbance in the serotonin metabolism of the central nervous system may be of pathogenetic importance in congenital generalized lipodystrophy.
通过注射从先天性全身脂肪营养不良患者尿液中提取的一种成分,已在兔子身上诱发了脂肪萎缩性糖尿病。这两种病症都被认为是下丘脑综合征。分别用多巴胺受体阻滞剂匹莫齐特对这些动物以及一名患有先天性全身脂肪营养不良和潜伏性糖尿病的患者进行了4个月和17个月的治疗。尽管该患者每日服用16毫克匹莫齐特,但结果并不理想。芬氟拉明对大脑血清素具有降低作用,对葡萄糖和甘油三酯代谢具有外周作用。这种药物改善了患有脂肪萎缩性糖尿病的兔子以及患有先天性全身脂肪营养不良患者的总体状况。兔子血糖恢复正常且对胰岛素敏感。在该患者中,观察到血清素代谢物5-羟吲哚乙酸的尿排泄恢复正常。他的贪食和多汗症状减轻,皮肤的角化过度层脱落,皮肤色素沉着减少。观察到谷丙转氨酶和谷草转氨酶有所改善,空腹血糖恢复正常,对外源胰岛素的敏感性增加。在每日服用200毫克芬氟拉明11个月后,每天额外服用2克氯贝丁酯使血清甘油三酯浓度恢复正常,并显著降低了胰岛素抵抗。另外三名患有先天性全身脂肪营养不良的患者,其中两名患有明显的糖尿病,现已开始用芬氟拉明治疗且病情正在改善。当停止芬氟拉明治疗时,兔子的脂肪萎缩性糖尿病复发。提示中枢神经系统血清素代谢紊乱在先天性全身脂肪营养不良的发病机制中可能具有重要意义。