Institute for Experimental and Clinical Pharmacology and Toxicology, Doerenkamp-Chair for Innovations in Animal and Consumer Protection, Friedrich-Alexander University, Fahrstrasse 17, 91054 Erlangen, Germany.
Inflamm Res. 2013 Mar;62(3):251-8. doi: 10.1007/s00011-013-0592-5. Epub 2013 Jan 16.
Flupirtine was developed long before K(V)7 (KCNQ) channels were known. However, it was clear from the beginning that flupirtine is neither an opioid nor a nonsteroidal anti-inflammatory analgesic. Its unique muscle relaxing activity was discovered by serendipity. In the meantime, broad and intensive research has resulted in a partial clarification of its mode of action. Flupirtine is the first therapeutically used K(V)7 channel activator with additional GABA(A)ergic mechanisms and thus the first representative of a novel class of analgesics. The presently accepted main mode of its action, potassium K(V)7 (KCNQ) channel activation, opens a series of further therapeutic possibilities. One of them has now been realized: its back-up compound, the bioisostere retigabine, has been approved for the treatment of epilepsy.
氟吡汀的研发历史远早于 K(V)7 (KCNQ) 通道被发现。然而,从一开始就很清楚,氟吡汀既不是阿片类药物也不是非甾体抗炎镇痛药。它独特的肌肉松弛活性是偶然发现的。与此同时,广泛而深入的研究使得其作用模式部分得到阐明。氟吡汀是第一个被用于治疗的 K(V)7 通道激活剂,具有 GABA(A)能机制,因此是新型类镇痛药的第一个代表。目前公认的主要作用模式是钾 K(V)7 (KCNQ) 通道激活,这为一系列进一步的治疗可能性开辟了道路。其中一种可能性已经实现:其备用化合物,生物等排体瑞替加滨,已被批准用于治疗癫痫。