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首页> 外文期刊>Archives of Toxicology >On the interactions between antimuscarinic atropine and NMDA receptor antagonists in anticholinesterase-treated mice.
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On the interactions between antimuscarinic atropine and NMDA receptor antagonists in anticholinesterase-treated mice.

机译:关于抗毒蕈碱型阿托品与NMDA受体拮抗剂在抗胆碱酯酶治疗小鼠中的相互作用。

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Both organophosphate (OP) and carbamate pesticides may produce seizures and death commonly attributed to the inhibition of acetylcholinesterase (AChE) and subsequent excess of acetylcholine (ACh). The anticonvulsant and neuroprotective properties of N-methyl-D-aspartate (NMDA) receptor antagonists in animals encouraged us to investigate their effects on the toxic and convulsant properties of OP and carbamate pesticides. Adult Swiss mice were systemically injected with the OP pesticide, chlorfenvinphos (CVP), or the carbamate pesticide, methomyl (MET). Both CVP and MET induced dose-dependent seizure activity and death in mice. Pretreatment with the muscarinic antagonist, atropine (ATR), at a dose of 1.8 mg/kg did not prevent seizures but decreased the lethal effects of CVP and MET. Pretreatment with the NMDA antagonists, dizocilpine (MK-801) at a dose of 1 mg/kg or 3-((R,S)-2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP) at a dose of 10 mg/kg, influenced neither MET-induced seizures nor CVP- or MET-induced death. However, both MK-801 and CPP blocked CVP-induced seizures. Concurrent administration of ATR and the NMDA antagonists prevented seizures produced by CVP, but not those produced by MET. Nevertheless, both MK801 and CPP coadministered with ATR markedly enhanced its antilethal effects in CVP- and MET-intoxicated mice. The antidotes had no influence upon brain AChE activities in mice treated with saline or CVP or MET. It seems that combined treatment with ATR and NMDA receptor antagonists might be of clinical relevance.
机译:有机磷酸酯(OP)和氨基甲酸酯类农药均可能引起癫痫发作和死亡,通常归因于对乙酰胆碱酯酶(AChE)的抑制和随后对乙酰胆碱(ACh)的过量抑制。 N-甲基-D-天门冬氨酸(NMDA)受体拮抗剂在动物中的抗惊厥和神经保护特性促使我们研究它们对OP和氨基甲酸酯农药的毒性和惊厥特性的影响。给成年瑞士小鼠全身性地注射OP农药氯芬灭磷(CVP)或氨基甲酸酯农药灭多威(MET)。 CVP和MET均可诱导剂量依赖性癫痫发作和小鼠死亡。用毒蕈碱拮抗剂阿托品(ATR)进行的1.8 mg / kg的预处理不能预防癫痫发作,但可以降低CVP和MET的致死作用。用NMDA拮抗剂,剂量为1 mg / kg的双唑西平(MK-801)或以(1)的3-((R,S)-2-羧基哌嗪-4-基)-丙基-1-膦酸(CPP)进行预处理剂量为10 mg / kg,既不影响MET引起的癫痫发作,也不影响CVP或MET引起的死亡。但是,MK-801和CPP均可阻止CVP诱发的癫痫发作。同时使用ATR和NMDA拮抗剂可预防CVP引起的癫痫发作,但不能预防MET引起的癫痫发作。尽管如此,MK801和CPP都与ATR共同使用显着增强了CVP和MET中毒小鼠的抗致死作用。解毒剂对用盐水或CVP或MET处理的小鼠的大脑AChE活性没有影响。似乎与ATR和NMDA受体拮抗剂联合治疗可能具有临床意义。

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