Husain Kazim, Ansari Rais A, Ferder Leon
Department of Physiology, Pharmacology and Toxicology, Ponce School of Medicine, Ponce, PR 00732, USA.
Indian J Exp Biol. 2010 Jul;48(7):642-50.
Organophosphorus pesticide poisoning causes tens of thousands of deaths each year across the world. Poisoning includes acute cholinergic crisis as a result of AChE inhibition, intermediate syndrome (IMS) due to neuromuscular necrosis and organophosphate-induced delayed neuropathy (OPIDN) due to inhibition of neuropathy target esterase (NTE). Standard treatment for acute poisoning involves administration of intravenous atropine, oxime 2-PAM to counter AChE inhibition and diazepam for CNS protection. However clinical trials showed ineffectiveness of the standard therapy regimen. Although new oximes that can reactivate both peripheral and cerebral AChE and other prophylactic agents such as human serum butyrylcholinesterase (Hu BChE), sodium bicarbonate, huperzine A (a reversible ChE inhibitor) with imidazenil (a GABAA receptor modulator) have been proved effective in animal models, systematic clinical trials in patients are warranted. For IMS which is non-responsive to standard therapy, supportive therapy specifically artificial respiration followed by recovery is indicated. For OPIDN which has a different target (NTE) than AChE, standard therapy is ineffective. However neuroprotective drugs such as corticosteroids proved partially effective. Pretreatment with protease inhibitor PMSF has been shown to protect the aging of NTE and prevent the development of delayed symptoms in hens. Since the biology of NTE is being explored, new pharmacological agents should be developed in future. OP pesticide poisoning is a serious condition that needs rapid diagnosis and treatment. Since respiratory failure is the major reason for mortality, artificial respiration, careful monitoring, appropriate treatment and early recognition of OP pesticide poisoning may decrease the mortality rate among these patients.
每年,有机磷农药中毒在全球导致数万人死亡。中毒包括因乙酰胆碱酯酶(AChE)抑制引起的急性胆碱能危象、因神经肌肉坏死导致的中间综合征(IMS)以及因神经病变靶酯酶(NTE)抑制引起的有机磷诱导的迟发性神经病(OPIDN)。急性中毒的标准治疗包括静脉注射阿托品、肟类药物2 - PAM以对抗AChE抑制,以及使用地西泮进行中枢神经系统保护。然而,临床试验表明标准治疗方案无效。尽管新型肟类药物能够使外周和脑AChE重新激活,以及其他预防药物如人血清丁酰胆碱酯酶(Hu BChE)、碳酸氢钠、石杉碱甲(一种可逆性胆碱酯酶抑制剂)与咪达唑仑(一种GABAA受体调节剂)已在动物模型中被证明有效,但仍需在患者中进行系统的临床试验。对于对标准治疗无反应的IMS,建议进行支持性治疗,特别是人工呼吸,随后患者恢复。对于具有与AChE不同靶点(NTE)的OPIDN,标准治疗无效。然而,神经保护药物如皮质类固醇已被证明有部分疗效。蛋白酶抑制剂苯甲基磺酰氟(PMSF)预处理已显示可保护母鸡的NTE老化并预防迟发性症状的发展。由于正在探索NTE生物学,未来应开发新的药理药物。有机磷农药中毒是一种严重疾病,需要快速诊断和治疗。由于呼吸衰竭是主要死亡原因,人工呼吸、仔细监测、适当治疗以及早期识别有机磷农药中毒可能会降低这些患者的死亡率。