Ro 19-6327的中心效应急性和反复给予。

G Skuza, Z Rogóz
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摘要

低剂量(1或3 mg/kg)给予Ro 19-6327不影响小鼠的运动活性,但高剂量(10 mg/kg)增加了运动活性。在大鼠中,ro19 -6327对运动活动有抑制作用,但其作用不具有剂量依赖性,且并不总是显著的。Ro 19-6327不改变左旋多巴(外加苯塞拉肼——外周脱羧酶抑制剂)诱导小鼠的运动活性。该药对利血平所致小鼠体温过低和上睑下垂有抑制作用,对阿吗啡所致体温过低有部分抵消作用。10 mg/kg显著增强大鼠安非他明诱导的刻板印象。r19 -6327对l -5-羟色氨酸(L-5-HTP)诱导的头抽搐反应无明显影响。给药三次,在强制游泳试验中无效。重复使用Ro 19-6327(每天两次,连续14天)可增强(+)-安非他明和诺非芬辛诱导的大鼠多动症。与许多抗抑郁药不同,Ro 19-6327不会增强小鼠对可乐定的攻击性,相反,它会抑制这种攻击性。结果表明,反复给予Ro 19-6327对α -肾上腺素能系统的反应性没有影响(参考α - 1肾上腺素受体介导的作用)。多巴胺系统的适应性变化值得怀疑。
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Central effects of Ro 19-6327 given acutely and repeatedly.

Some central effects of Ro 19-6327--a new MAO-B inhibitor--were studied in mice and rats. Given in low doses (1 or 3 mg/kg) Ro 19-6327 did not affect the locomotor activity of mice but its high dose (10 mg/kg) increased the activity. In rats Ro 19-6327 inhibited the locomotor activity but the effect was not dose dependent and not always significant. Ro 19-6327 did not change the locomotor activity in mice induced by L-DOPA (plus benserazide--an inhibitor of peripheral decarboxylase). The drug suppressed the reserpine-induced hypothermia and ptosis in mice and partly counteracted the apomorphine-induced hypothermia. It markedly enhanced (10 mg/kg) the amphetamine-induced stereotypy in rats. L-5-Hydroxytryptophan (L-5-HTP)-induced head twitch response was unchanged by Ro 19-6327. The drug given three times was inactive in forced swimming test. Repeated treatment with Ro 19-6327 (twice daily for 14 days) produced the enhancement of (+)-amphetamine- and nomifensine-induced hyperactivity in rats. Unlike a number of antidepressants, Ro 19-6327 did not potentiate the clonidine aggressiveness in mice, but--in contrast--inhibited it. The results suggest that Ro 19-6327 given repeatedly produces no changes in the responsiveness of the alpha-adrenergic system (in references to effects mediated by alpha 1-adrenoceptors). Adaptive changes in dopamine system are doubtful.

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