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[新生期给予作用于自主神经系统药物的大鼠神经行为发育研究]

[Study on the neuro-behavioral development in rats treated neonatally with drugs acting on the autonomic nervous system].

作者信息

Watanabe T, Matsuhashi K, Takayama S

出版信息

Nihon Yakurigaku Zasshi. 1984 Sep;84(3):267-82.

PMID:6500402
Abstract

The drugs used were pargyrine, methamphetamine, reserpine, norepinephrine, epinephrine, propranolol, chlorpromazine, 6-hydroxydopamine, haloperidol, pilocarpine, neostigmine and atropine. The body The weight gain of pups receiving reserpine, chlorpromazine, 6-hydroxydopamine and pilocarpine was significantly inhibited. The mortality of pups given reserpine was significantly increased. The behavioral development of righting reflex, cliff drop avoidance and negative geotaxis of rats given reserpine, propranolol, 6-hydroxydopamine and haloperidol was significantly retarded in comparison with that of control pups. Spontaneous motor activity measured by Animex was increased in pups receiving norepinephrine, epinephrine, chlorpromazine, reserpine, propranolol and atropine. Furthermore, pharmacological challenge by the injection of methamphetamine exhibited an accentuated response to an increase in spontaneous motor activity in pups exposed to chlorpromazine, reserpine, propranolol, 6-hydroxydopamine and atropine. These findings suggest that an increase in spontaneous motor activity may be induced by the developmental impairment of central catecholamine mechanisms, especially the noradrenaline nervous system. Delayed latency, decreased rearing and preening of pups receiving propranolol were observed on the open field test. The conditioned avoidance responses using the shuttle box revealed deficits in acquisition of avoidance learning of rats given haloperidol, 6-hydroxydopamine and propranolol, suggesting that the learning deficits may be due to the developmental impairment of catecholamine mechanisms, especially the dopamine nervous system.

摘要

所使用的药物有帕吉林、甲基苯丙胺、利血平、去甲肾上腺素、肾上腺素、普萘洛尔、氯丙嗪、6-羟基多巴胺、氟哌啶醇、毛果芸香碱、新斯的明和阿托品。接受利血平、氯丙嗪、6-羟基多巴胺和毛果芸香碱的幼崽体重增加受到显著抑制。给予利血平的幼崽死亡率显著增加。与对照幼崽相比,给予利血平、普萘洛尔、6-羟基多巴胺和氟哌啶醇的大鼠的翻正反射、悬崖回避和负趋地性等行为发育明显迟缓。通过Animex测量,接受去甲肾上腺素、肾上腺素、氯丙嗪、利血平、普萘洛尔和阿托品的幼崽自发运动活动增加。此外,注射甲基苯丙胺进行药理学激发试验显示,暴露于氯丙嗪、利血平、普萘洛尔、6-羟基多巴胺和阿托品的幼崽对自发运动活动增加的反应增强。这些发现表明,自发运动活动的增加可能是由中枢儿茶酚胺机制,尤其是去甲肾上腺素神经系统的发育受损引起的。在旷场试验中观察到,接受普萘洛尔的幼崽潜伏期延长、竖毛和理毛行为减少。使用穿梭箱进行的条件回避反应显示,给予氟哌啶醇、6-羟基多巴胺和普萘洛尔的大鼠在回避学习的获得方面存在缺陷,这表明学习缺陷可能是由于儿茶酚胺机制,尤其是多巴胺神经系统的发育受损所致。

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