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Intracerebral ventricular injection of M receptor blocker,Atropine(10 μ L 1× 10- 7 mol/L), failed to block the gastric contraction effect of cerebral SP.

侧脑室注射 M 受体阻断剂阿托品 10 μ L(1× 10- 7 mol/L),不能阻断脑内 P物质对胃的收缩效应。

Objective:To investigate the effect of penehyclidine or atropine combined with midazolam on HR、mean arterial pressure,saturation of blood oxygen(SpO2),hypnosis,conscious-sedation and lapsus memoriae in patients during operation.

目的:观察盐酸戊乙奎醚或阿托品复合咪哒唑仑对病人术中心率,平均动脉压,血氧饱和度(SpO2)及催眠、镇静和遗忘作用的影响效果。

Group one use atropine 0.5mg, lumina 0.1 or diazepam 10mg, group two use nothing before the branchofiberoscope exam.

一组为检查前应用阿托品 0 。5mg、鲁米那 0 。1或安定 10mg ,一组为检查前不用任何药物。

Atropine is commonly administered to inhibit the effects of acetylcholine at muscarinic receptors, the authors note.

笔者提到,阿托品是最常用的抑制毒蕈碱受体中乙酰胆碱活性的药物。

Results: Compared with the baseline, REMS was significantly reduced in all groups treated with NBI in a dose-dependent manner, but not with vehicle.

考虑胆碱能系统对睡眠觉醒周期的作用,我们使用阿托品——M_1受体阻断剂,观察其对幼鼠睡眠的影响。

The relative standard derivations of migration time and peak area were 0.81 and 3.19%,respectively.

将该法用于注射液和人体尿液中硫酸阿托品的分离检测,回收率在90.9-99.6%之间。

A simple,rapid,sensitive and accurate RP HPLC for simultaneous determination of ketamine, phenobarbitone and atropine in plasma was established.

本文采用ZorbaxC8色谱柱,甲醇-磷酸盐缓冲液(69∶31)为流动相,220nm为检测波长,非那西丁为内标,建立了同时测定人血浆中氯胺酮、苯巴比妥和阿托品浓度的反相高效液相色谱法。

Ketamine ; phenobarbitone ; atropine ; plasma concentration ; RP HPLC

氯胺酮;苯巴比妥;阿托品;血药浓度;高效液相色谱法

RESULTS:Among the 116 eyes, 94 eyes presented identical optometric results or less than 0.50D difference while 22 eyes had more than 0.75D difference after the instillation of the two agents, with 81.0% in agreement with the degree of spherical lens, with 92.2% in agreement with the compound hyperopia cylinder lens, with 84.6% in agreement with the axis of astigmatism.

结果:远视球镜度数116眼两次验光结果相同或相差≤0.50D者94眼,相差0.75D以上22眼,远视球镜度数符合率为81.0%,52眼复性远视柱镜度数符合率为92.2%,散光轴向符合率为84.6%,28眼远视年龄在8~12岁者,两次验光结果验光度数相同和相差≤0.50D,散光轴向≤5°者7眼,符合率25.0%,88眼年龄在12~16岁,符合率97.7%,≥0.75D者两例均合并有内斜视,本组两种不同散瞳剂散瞳验光结果对比远视球镜或复性远视柱镜度数相差0.75D以上者均为美多丽散瞳年龄≤12岁者或有斜视者,低于阿托品散瞳验光度数。

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