Samochocki Marek, Höffle Anja, Fehrenbacher Andreas, Jostock Ruth, Ludwig Jürgen, Christner Claudia, Radina Martin, Zerlin Marion, Ullmer Christoph, Pereira Edna F R, Lübbert Hermann, Albuquerque Edson X, Maelicke Alfred
Laboratory of Molecular Neurobiology, Institute of Physiological Chemistry and Pathobiochemistry, Johannes-Gutenberg University Medical School, Duesbergweg 6, D-55099 Mainz, Germany.
J Pharmacol Exp Ther. 2003 Jun;305(3):1024-36. doi: 10.1124/jpet.102.045773. Epub 2003 Mar 20.
Galantamine (Reminyl), an approved treatment for Alzheimer's disease (AD), is a potent allosteric potentiating ligand (APL) of human alpha 3 beta 4, alpha 4 beta 2, and alpha 6 beta 4 nicotinic receptors (nAChRs), and of the chicken/mouse chimeric alpha 7/5-hydroxytryptamine3 receptor, as was shown by whole-cell patch-clamp studies of human embryonic kidney-293 cells stably expressing a single nAChR subtype. Galantamine potentiates agonist responses of the four nAChR subtypes studied in the same window of concentrations (i.e., 0.1-1 microM), which correlates with the cerebrospinal fluid concentration of the drug at the recommended daily dosage of 16 to 24 mg. At concentrations >10 microM, galantamine acts as an nAChR inhibitor. The other presently approved AD drugs, donepezil and rivastigmine, are devoid of the nicotinic APL action; at micromolar concentrations they also block nAChR activity. Using five CHO-SRE-Luci cell lines, each of them expressing a different human muscarinic receptor, and a reporter gene assay, we show that galantamine does not alter the activity of M1-M5 receptors, thereby confirming that galantamine modulates selectively the activity of nAChRs. These studies support our previous proposal that the therapeutic action of galantamine is mainly produced by its sensitizing action on nAChRs rather than by general cholinergic enhancement due to cholinesterase inhibition. Galantamine's APL action directly addresses the nicotinic deficit in AD.
加兰他敏(雷米诺林)是一种已获批准用于治疗阿尔茨海默病(AD)的药物,它是人类α3β4、α4β2和α6β4烟碱型受体(nAChRs)以及鸡/小鼠嵌合α7/5-羟色胺3受体的强效变构增强配体(APL),对稳定表达单一nAChR亚型的人胚肾-293细胞进行的全细胞膜片钳研究表明了这一点。加兰他敏在相同的浓度范围内(即0.1 - 1微摩尔)增强了所研究的四种nAChR亚型的激动剂反应,这与该药物在推荐日剂量16至24毫克时的脑脊液浓度相关。在浓度>10微摩尔时,加兰他敏作为nAChR抑制剂起作用。目前其他已获批准的AD药物多奈哌齐和卡巴拉汀没有烟碱型APL作用;在微摩尔浓度下,它们也会阻断nAChR活性。使用五种CHO-SRE-Luci细胞系,每个细胞系表达不同的人类毒蕈碱受体,并通过报告基因检测,我们发现加兰他敏不会改变M1 - M5受体的活性,从而证实加兰他敏选择性地调节nAChRs的活性。这些研究支持了我们之前的提议,即加兰他敏的治疗作用主要是由其对nAChRs的敏化作用产生的,而不是由于胆碱酯酶抑制导致的一般胆碱能增强。加兰他敏的APL作用直接解决了AD中的烟碱缺乏问题。