Froestl Wolfgang, Gallagher Michela, Jenkins Helen, Madrid Annette, Melcher Thorsten, Teichman Sam, Mondadori Cesare G, Pearlman Rodney
Neuroscience Research, Novartis Pharma AG, WKL-136.5.25, CH-4002 Basel, Switzerland.
Biochem Pharmacol. 2004 Oct 15;68(8):1479-87. doi: 10.1016/j.bcp.2004.07.030.
The GABA(B) receptor antagonist SGS742 (CGP36742) displays pronounced cognition enhancing effects in mice, young and old rats and in Rhesus monkeys in active and passive avoidance paradigms, in an eight-arm radial maze and a Morris water maze and in a social learning task. SGS742 blocks the late inhibitory postsynaptic potential and the paired-pulse inhibition of population spikes recorded from CA1 pyramidal neurons of the hippocampus of rats in vitro and in vivo. SGS742 significantly enhances the release of glutamate, aspartate, glycine and somatostatin in vivo. Chronic administration of SGS742 causes an up-regulation of GABA(B) receptors in the frontal cortex of rats. Single doses cause a significant enhancement of the mRNA and protein levels of NGF and BDNF in the cortex and hippocampus of rats. The observed antidepressant effects of SGS742 in rats may be explained by these findings. SGS742 was well tolerated in experimental animals as well as in young and elderly human volunteers with an absolute bioavailability in humans of 44%. In a Phase II double-blind, placebo-controlled study in 110 patients with mild cognitive impairment (MCI), oral administration of SGS742 at a dose of 600 mg t.i.d. for 8 weeks significantly improved attention, in particular choice reaction time and visual information processing as well as working memory measured as pattern recognition speed. A second Phase II clinical trial in 280 Alzheimer's disease patients is underway.
GABA(B)受体拮抗剂SGS742(CGP36742)在主动和被动回避范式、八臂辐射迷宫、莫里斯水迷宫以及社会学习任务中,对小鼠、幼年和成年大鼠以及恒河猴均显示出显著的认知增强作用。SGS742在体外和体内均可阻断大鼠海马CA1锥体神经元记录到的晚期抑制性突触后电位和群体峰电位的双脉冲抑制。SGS742在体内可显著增强谷氨酸、天冬氨酸、甘氨酸和生长抑素的释放。长期给予SGS742可导致大鼠额叶皮质中GABA(B)受体上调。单次给药可显著提高大鼠皮质和海马中NGF和BDNF的mRNA和蛋白水平。SGS742在大鼠中观察到的抗抑郁作用可能可以用这些发现来解释。SGS742在实验动物以及年轻和老年人类志愿者中耐受性良好,在人类中的绝对生物利用度为44%。在一项针对110例轻度认知障碍(MCI)患者的II期双盲、安慰剂对照研究中,口服SGS742,剂量为600 mg,每日三次,持续8周,显著改善了注意力,特别是选择反应时间和视觉信息处理能力以及以模式识别速度衡量的工作记忆。一项针对280例阿尔茨海默病患者的II期临床试验正在进行中。