Harris L W, Stitcher D L, Hey W C
Life Sci. 1982 May 31;30(22):1867-73. doi: 10.1016/0024-3205(82)90466-0.
The effects of hemicholinium-3 (HC-3) or 4-(l-naphthylvinyl)pyridine (4-NVP) alone and together with cholinolytics and/or cholinesterase inhibitors on brain acetylcholine (ACh) levels and survival were studied. Intracerebroventricular (ICVT) injection of 10 micrograms HC-3 280 min before euthanasia by microwave irradiation reduced rat cerebral ACh levels from 28.4 to 5.4 nmoles ACh/g wet tissue. In rats pretreated with HC-3 alone or with other pretreatment drugs prior to giving up to 2.7 LD50 of soman, iv, cerebral ACh levels increased very little, but in animals not receiving HC-3, brain ACh levels increased to 67.1 nmoles. Treatment of unpoisoned rats with 4-NVP resulted in a significant (26%) reduction in ACh. The inclusion of atropine with 4-NVP caused sign-free doses of physostigmine to produce toxic signs in rabbits and did not enhance the efficacy of carbamate pretreatment against soman. Pretreatment of rabbits with pyridostigmine and atropine methyl nitrate (AMN) failed to provide any protection against soman, but when HC-3, ICVT, was included with those drugs, the protective ratio (PR), against soman was increased excess ACh is a primary lesion in organophosphorus anticholinesterase intoxication and that the central nervous system is quite sensitive to excesses of ACh.
研究了单独使用半胱氨酸-3(HC-3)或4-(1-萘基乙烯基)吡啶(4-NVP)以及它们与胆碱能解药剂和/或胆碱酯酶抑制剂联合使用对脑乙酰胆碱(ACh)水平和存活率的影响。在通过微波辐射实施安乐死280分钟前,脑室内(ICVT)注射10微克HC-3可使大鼠脑内ACh水平从28.4纳摩尔ACh/克湿组织降至5.4纳摩尔。在用HC-3单独预处理或与其他预处理药物联合预处理的大鼠中,静脉注射高达2.7倍半数致死剂量的梭曼后,脑内ACh水平几乎没有增加,但在未接受HC-3的动物中,脑内ACh水平增至67.1纳摩尔。用4-NVP处理未中毒的大鼠导致ACh显著降低(26%)。4-NVP与阿托品联合使用使无明显中毒症状剂量的毒扁豆碱在兔身上产生中毒症状,且未增强氨基甲酸酯预处理对梭曼的效果。用吡啶斯的明和硝酸甲基阿托品(AMN)预处理兔未能提供对梭曼的任何保护,但当将HC-3经ICVT与这些药物联合使用时,对梭曼的保护率(PR)增加,过量的ACh是有机磷抗胆碱酯酶中毒的主要损伤,且中枢神经系统对过量的ACh相当敏感。