毒扁豆碱

幼虫5.3sAChE对毒扁豆碱的敏感度抗性品系和敏感品系相差达123倍，而成虫则没有差异。

The sensitivity of 5.3s form of AChE to eserine sulfate shows 123 times of difference between R and S strains in larvae , however no difference in adults .

第Ⅲ脑室注射ACh或毒扁豆碱均可使猫产生升压反应。

Administration of ACh or physostigmine into the third ventricle caused pressor response in cats .

家兔侧脑室注射P物质和毒扁豆碱对心血管控制的影响及其相互关系

On the relation between substance P and physostigmine on cardio vascular control in rabbit brain

中枢抑制药对毒扁豆碱石杉碱甲LD（50）的影响

Effects of Central Nervous System Depressants on LD_ ( 50 ) of Physostigmine or Huperzine A in Mice

目的：探讨毒扁豆碱对血管性痴呆（VD）的治疗效果。

Objective : To investigate the curative effect of physostigmine on vascular dementia patients .

此外还讨论了对氧磷、敌敌畏、速灭威、毒扁豆碱、TPP和异稻瘟净对RM、RD和S品系α-NACarE的抑制作用。

The inhibition of the a-NA CarE from RM , RD and S strains by paraoxon , DDVP , MTMC , eserine , TPP and IMP is also discussed .

用定点记录胃运动法，观察脑室注射（icv）毒扁豆碱（PHY）对大鼠胃运动的影响。

Using the fix-points method for recording gastric motility , the effects of intracerebroventricular ( icv ) microinjection of physostigmine ( PHY ) were observed in Wistar rats .

方法：以双盲对照方法，检测应用毒扁豆碱治疗的50例由于缺血性脑血管病所致的轻、中度VD，观察其疗效及治疗前后的电生理学改变。

Methods : Fifty patients with mild to moderate vascular dementia caused by ischemic cerebral vascular disease were treated by physostigmine , and the curative effect and the changes of electrophysiology before and after treatment were evaluated using double-blind contrast method .

侧脑室内微量注射毒扁豆碱对大鼠胃运动的影响

Effect of Intracerebroventricular Microinjection of Physostigmine on Gastric Motility in Rats

毒扁豆碱催醒作用的实验研究

A study on the analeptic action of physostigmine in anesthetized animals

内源性精氨酸加压素在毒扁豆碱引起大鼠低温反应中作用

Role of Endogenous Arginine Vasopressin in Physostigmine Induced Hypothermic Response in Rats

毒扁豆碱鼻腔给药对小鼠学习记忆功能的影响

Effects of physostigmine intranasal administration on learning and memory function in mice

毒扁豆碱对豌豆幼苗的伤害机制

Toxicological mechanism of CALABARINE to affect pea seedling

目的比较新斯的明、毒扁豆碱和毛果芸香碱对兔眼的缩瞳作用。

Objective To compare the myotic effects of physostigmine , pilocarpine and neostigmine in rabbits .

第Ⅲ脑室注射乙酰胆碱和毒扁豆碱对猫肾上腺髓质释放儿茶酚胺的影响

Influence of Third Ventricle Injection of ACh and Physostigmine on Adrenal Medulla CA Release in Cats

发现毒扁豆碱不能明显缩短小鼠的翻正反射消失持续时间；

It was found that physostigmine could not shorten the recovery time in any of the mice groups ( p0.05 ) .

毒扁豆碱是胆碱酯酶抑制剂，能促进中枢乙酰胆碱含量，拮抗东莨菪碱所致健忘；

Physostigmine was cholinesterase inhibitor , it could improve the content of center Ach and antagonize the amnesia induced by Scopolamine .

目的：研究毒扁豆碱阻断交感节神经元烟碱受体的作用机理。

IM : To study the blocking mechanism of physostigmine ( Phy ) on nicotinic acetylcholine receptors ( NAChR ) in sympathetic neurons .

论新斯的明、毒扁豆碱和毛果芸香碱滴眼给药，均能缩小兔眼瞳孔，其时效关系相似。

Conclusion Physostigmine , neostigmine and pilocarpine , when applied locally to the eye in rabbits , could cause myosis and their time-effect relationships were comparable .

毒扁豆碱组21例中死亡1例，成功20例，成功率为95.24%，平均清醒时间为11.69小时。

As to the physostigmine group , 20 of 21 patients were brought to life and only 1 died , the average revival time was 11.69 hours .

胆碱酯类（乙酰胆碱、氨甲酰胆碱和乙酰甲胆碱）及毒扁豆碱对肝片形吸虫呈抑制作用而对鸡蛔虫则呈兴奋作用。

The rhythmical activity of the liver fluke was inhibited and those of chicken roundworm was stimulated by choline esters ( acetylcholine , carbacholine and acetyl - β - methylcholine ) and eserine .

用对氧磷、马拉氧磷、西维因及毒扁豆碱等4种抑制剂对这两个种群飞蝗的酯酶进行体外抑制实验，结果表明，这两个种群的大部分酯酶属于B-型。

Inhibition studies of the esterases using four inhibitors ( i. e. , paraoxon , malaoxon , eserine , and carbaryl ) indicated that most of general esterases in the two populations were B-type .

初步临床观察表明，化合物Ⅱ4（现命名为催醒安）比毒扁豆碱的催醒效果好，而毒性小。

Preliminary clinical observations showed that compound ⅱ _4 , introduced under the name of " CUI XING AN ", is less toxic and more effective than physostigmine as analeptic in traditional medicine anesthesia .

在兔，毒扁豆碱可缩短静注安定或氯丙嗪的翻正反射消失持续时间，但对戊巴比妥钠或氯丙嗪加东莨菪碱麻醉则否。

In rabbits , physostigmine hastened the recovery of righting reflex in the diazepam and the chlorpromazine groups ( p0.05 ), but did not in the pentobarbital group and the chlorpromazine plus scopolamine group ( p0.05 ) .