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某些酯酶抑制剂对有机磷酸酯诱导的迟发性多神经病的促进作用。

Promotion of organophosphate induced delayed polyneuropathy by certain esterase inhibitors.

作者信息

Lotti Marcello

机构信息

Università degli Studi di Padova, Dipartimento di Medicina Ambientale e Sanità Pubblica, via Giustiniani 2, 35128 Padua, Italy.

出版信息

Toxicology. 2002 Dec 27;181-182:245-8. doi: 10.1016/s0300-483x(02)00291-3.

Abstract

Organophosphate induced delayed polyneuropathy (OPIDP) is an axonopathy caused by single doses of some organophosphates (OPs). Other OPs, sulphonyl halides, carbamates, thiocarbamates and phosphinates do not cause axonopathy but elicit or intensify the clinical expression of OPIDP when given after a neuropathic OP (promotion of OPIDP). One enzymatic activity (M200) was identified by means of selective inhibitors in hen peripheral nerve crude homogenates. Promotion of OPIDP initiated with several OPs was found to correlate with inhibition of M200 when various promoters were given to hens. Most M200 is in the soluble fraction of peripheral nerves and was separated from other esterases by means of molecular exclusion chromatography. In a second series of experiments, inhibition of this fraction also correlated with promotion when induced by the same chemicals. Further ion exchange chromatography identified a protein (60 kDa MW): the inhibition of its enzymatic activity correlated with promotion in another series of in vivo experiments. Biochemical and structural analyses of this protein are underway. Several experiments indirectly suggest that promotion may be related to mechanisms of repair and/or compensation of peripheral nerves. These include the observation that promotion results in clinical expression of biochemical lesions that otherwise would be well compensated, that promotion is not specific because axonopathies of other etiology are also exaggerated, and that promoters are effective when given several days before the neuropathic insult. Moreover, developing animals are more resistant to promotion.

摘要

有机磷酸酯诱导的迟发性多发性神经病(OPIDP)是一种由单次剂量的某些有机磷酸酯(OPs)引起的轴索性神经病。其他OPs、磺酰卤、氨基甲酸酯、硫代氨基甲酸酯和次膦酸酯不会引起轴索性神经病,但在给予神经病性OP后给予时会引发或加剧OPIDP的临床症状(OPIDP的促进作用)。通过选择性抑制剂在鸡外周神经粗匀浆中鉴定出一种酶活性(M200)。当给母鸡使用各种促进剂时,发现几种OPs引发的OPIDP促进作用与M200的抑制相关。大多数M200存在于外周神经的可溶部分,并通过分子排阻色谱法与其他酯酶分离。在第二系列实验中,当由相同化学物质诱导时,该部分的抑制也与促进作用相关。进一步的离子交换色谱法鉴定出一种蛋白质(分子量60 kDa):在另一系列体内实验中,其酶活性的抑制与促进作用相关。目前正在对该蛋白质进行生化和结构分析。几项实验间接表明,促进作用可能与外周神经的修复和/或补偿机制有关。这些包括以下观察结果:促进作用导致生化损伤的临床症状,否则这些损伤会得到很好的补偿;促进作用不具有特异性,因为其他病因的轴索性神经病也会被夸大;促进剂在神经病性损伤前几天给予时有效。此外,发育中的动物对促进作用更具抵抗力。

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