Maeda N, Matsuoka N, Yamazaki M, Arakawa H, Ohkubo Y, Yamaguchi I
Tsukuba Research Laboratories, Fujisawa Pharmaceutical Co., Ltd, Ibaraki, Japan.
Jpn J Pharmacol. 1994 Mar;64(3):147-53. doi: 10.1254/jjp.64.147.
Starting from the hypothesis that drugs which specifically activate the hippocampal cholinergic nerve activity may ameliorate memory impairments, we carried out a series of evaluations for a novel cognitive enhancer using enhancement of penile erection as a sign of cholinergic activation, and found FR64822. The compound facilitated penile erection in naive rats, and it ameliorated scopolamine-induced amnesia of rats in passive avoidance tasks with bell-shaped dose-response curves, while it dose-dependently reduced body weight gain in Zucker fatty rats. Pretreatment with sulpiride (32 mg/kg, p.o.) hardly affected the former two activities, but significantly reduced the anorectic activity in Zucker rats. Further evaluation of FR64822 derivatives characterized a second compound, FR121196, which induces penile erection and memory enhancement, but not body weight reduction. Memory enhancing and erection stimulating activities of FR121196 were abolished in rats treated with either cysteamine (200 mg/kg, s.c.), a somatostatin depletor, or lesioning of the serotonergic raphe nuclei. Thus, classic whole animal studies based on a hypothesis proved to be efficient for reaching our objective, the discovery of a new drug. They also gave us insight into the common somatostatinergic and serotonergic mechanisms underlying penile erection and memory improvement.
基于特定激活海马胆碱能神经活动的药物可能改善记忆障碍这一假设,我们以阴茎勃起增强作为胆碱能激活的标志,对一种新型认知增强剂进行了一系列评估,发现了FR64822。该化合物可促进正常大鼠的阴茎勃起,并改善东莨菪碱诱导的大鼠在被动回避任务中的失忆,呈现钟形剂量反应曲线,而在 Zucker 肥胖大鼠中它可剂量依赖性地降低体重增加。舒必利(32 mg/kg,口服)预处理对前两种活性影响不大,但显著降低了 Zucker 大鼠的厌食活性。对FR64822衍生物的进一步评估鉴定出第二种化合物FR121196,它可诱导阴茎勃起和记忆增强,但不会导致体重减轻。在用生长抑素耗竭剂半胱胺(200 mg/kg,皮下注射)或损伤5-羟色胺中缝核的大鼠中,FR121196的记忆增强和勃起刺激活性被消除。因此,基于假设的经典整体动物研究被证明对实现我们发现新药的目标是有效的。它们还让我们深入了解了阴茎勃起和记忆改善背后共同的生长抑素能和5-羟色胺能机制。