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Ro 16 - 6028和Ro 17 - 1812在小鼠体内的部分激动剂特性展示。

Demonstration of the partial agonist profiles of Ro 16-6028 and Ro 17-1812 in mice in vivo.

作者信息

Potier M C, Prado de Carvalho L, Venault P, Chapouthier G, Rossier J

机构信息

Laboratoire de Physiologie Nerveuse, C.N.R.S., Gif-sur-Yvette, France.

出版信息

Eur J Pharmacol. 1988 Oct 26;156(1):169-72. doi: 10.1016/0014-2999(88)90161-6.

Abstract

Benzodiazepine receptor occupancy by the full agonist, diazepam, and by the two putative partial agonists, Ro 16-6028 and Ro 17-1812, was measured by inhibition of in vivo [3H]Ro 15-1788 binding in mouse brain and was correlated with their pharmacological effects. The anticonvulsant effects of Ro 16-6028, Ro 17-1812 and diazepam (ED50 values) appeared at receptor occupancies of 40, 20 and less than 5%, respectively. Moreover, at the highest measurable receptor occupancy (90-100%), Ro 16-6028 and Ro 17-1812 did not induce any rotarod deficit whereas a complete deficit was observed with diazepam at 35% receptor occupancy.

摘要

通过抑制小鼠脑内的体内[3H]Ro 15 - 1788结合来测定全激动剂地西泮以及两种假定的部分激动剂Ro 16 - 6028和Ro 17 - 1812对苯二氮䓬受体的占有率,并将其与它们的药理作用相关联。Ro 16 - 6028、Ro 17 - 1812和地西泮的抗惊厥作用(ED50值)分别在受体占有率为40%、20%和小于5%时出现。此外,在可测量的最高受体占有率(90 - 100%)时,Ro 16 - 6028和Ro 17 - 1812未引起任何转棒试验缺陷,而地西泮在受体占有率为35%时观察到完全缺陷。

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