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1.A trademark used for the sedative pentobarbital sodium.
宁眠泰尔戊巴比妥钠镇静药的商标收藏指正
2.All the subjects were sedated by pentobarbital sodium during ASSR testing.
测试状态为戊巴比妥钠镇静睡眠。收藏指正
3.The Biphasic Effect of DDT and 666 on the Biotransformation of Pentobarbital in vivo
滴滴涕和六六六对戊巴比妥体内转化的双相影响收藏指正
4.INFLUENCW OF ANTABUSE ON THE BIOTRANSFORMATION OF PENTOBARBITAL, CHLORPROMAZINE AND ρ-NITROBENZOIC ACID
安他布斯对戊巴比妥、氯丙嗪及对硝基苯甲酸生物转化的影响收藏指正
5.Dams were anesthetized with one of the following drugs or drug combinations: (1) sodium pentobarbital; (2) ketamine hydrochloride and xylazine; or (3) sodium pentobarbital and ketamine hydrochloride.
通过下列一种或多种药物对孕鼠进行麻醉:(1)戊巴比妥钠;(2)盐酸氯胺酮和甲苯噻嗪;(3)戊巴比妥钠和盐酸氯胺酮。收藏指正
6.Effect of DL-DOPA,L-5-HTP and Pentobarbital Sodium on Brain Encephalofluctuographs in rats
多巴、5-羟色胺酸和戊巴比妥钠对大白鼠脑涨落图的影响收藏指正
7.(1) sedation and anticonvulsant action: we observed the autonomic activity and improving sleep in combination with Pentobarbital-sodium in mice.
(1)镇静抗惊厥方面:观察了药物对小鼠自发活动、协同戊巴比妥钠睡眠实验及电惊厥、注射中枢兴奋药等小鼠惊厥模型的作用;收藏指正
8.Conclusion: PRN can obviously shorten hypnotic duration of pentobarbital sodium, which suggests that PRN could induce liver microsomal cytochrome P450 in mice.
结论 PRN能显著缩短戊巴比妥钠对小鼠的催眠时间 ,提示PRN能诱导小鼠肝微粒体细胞色素P4 5 0活性收藏指正
9.Methods 180Newzeland rabbits with the same age and weighed1.8-2.8kg were selected and un-derwent venous anesthesia by 30mg /L sodium pentobarbital.
方法同龄成年健康的新西兰兔180只,雌雄不限,体质量1.8~2.8kg。收藏指正
10.Thenifedipine-resistant [Ca2+]i increase was completely eliminated by JSTX-3. Theapplication of pentobarbital which blocked Ca2+-impermeable AMPA receptorscould also partly inhibit the AMPA-induced increase of [Ca2+]i andglutamate-induced current.
电压门控钙离子通道的阻断剂nifedipine灌流后残留的[Ca~(2+)]_i升高可以完全被JSTX-3所阻断。 单独应用JSTX-3或钙离子不通透AMPA受体(CIP-AMPAR)的阻断剂pentobarbital都只能部分的削弱AMPA引起的[Ca~(2+)]_i升高。收藏指正
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