Sasson S, Kunievsky B, Nathan C, Cerasi E
Department of Pharmacology, Hebrew University Hadassah Medical Center, Jerusalem, Israel.
Biochem Pharmacol. 1989 Aug 15;38(16):2655-61. doi: 10.1016/0006-2952(89)90551-0.
Fenfluramine is an effective appetite suppressant that mediates its action via serotoninergic neurons. We studied the effect of pure d- and l-fenfluramine on in vitro hexose transport in isolated rat soleus muscles and skeletal muscle cells in culture. We found no evidence to suggest that the fenfluramine enantiomers affect the basal transport activity. Furthermore, the drugs did not interfere with the ability of glucose to regulate its own transport. Muscle responsiveness to insulin was not altered by the enantiomers, nor did insulin unmask any effect of fenfluramine on muscle hexose transport. These conclusions are based on experiments performed with a wide concentration range of drug and insulin, from the therapeutic to suprapharmacological levels. We discuss our results in view of published data on the effects of fenfluramine on peripheral glucose metabolism.
芬氟拉明是一种有效的食欲抑制剂,它通过血清素能神经元介导其作用。我们研究了纯d-和l-芬氟拉明对离体大鼠比目鱼肌和培养的骨骼肌细胞体外己糖转运的影响。我们没有发现证据表明芬氟拉明对映体影响基础转运活性。此外,这些药物不会干扰葡萄糖调节自身转运的能力。对映体不会改变肌肉对胰岛素的反应性,胰岛素也不会揭示芬氟拉明对肌肉己糖转运的任何影响。这些结论是基于在从治疗水平到超药理水平的广泛药物和胰岛素浓度范围内进行的实验得出的。我们根据已发表的关于芬氟拉明对外周葡萄糖代谢影响的数据来讨论我们的结果。