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关于百草枯处理的成纤维细胞中胶原蛋白合成抑制作用的研究。

Studies on the inhibition of collagen synthesis in fibroblasts treated with paraquat.

作者信息

Darr D, Combs S, Murad S, Pinnell S

机构信息

Duke University Medical Center, Division of Dermatology, Durham, North Carolina 27710.

出版信息

Arch Biochem Biophys. 1993 Oct;306(1):267-71. doi: 10.1006/abbi.1993.1510.

Abstract

Paraquat (methyl viologen) is an industrial herbicide which upon entering many cell types can be enzymatically reduced and in the presence of oxygen, subsequently generate the superoxide radical anion (O2-). This is its mode of toxicity in many of these cells. In vivo, it has been shown to preferentially accumulate in lung tissue, leading to tissue destruction and marked fibrosis. Collagen accumulation has also been noted in paraquat-treated lung slices in vitro. In studies designed to investigate these effects, it has been found, unexpectedly, that paraquat inhibits collagen synthesis in isolated fibroblasts. This inhibition is not due to overt cellular toxicity nor to inhibition of prolyl hydroxylase (directly or by cofactor depletion). While this effect could be unique to paraquat, it may be relevant to a more generalized role for free radicals in regulating collagen synthesis at the level of the individual cell.

摘要

百草枯(甲基紫精)是一种工业除草剂,进入多种细胞类型后可被酶促还原,在有氧存在的情况下,随后产生超氧阴离子自由基(O2-)。这是它在许多这类细胞中的毒性作用方式。在体内,已证明它优先在肺组织中蓄积,导致组织破坏和明显的纤维化。在体外,经百草枯处理的肺切片中也观察到了胶原蛋白的蓄积。在旨在研究这些作用的实验中,意外地发现百草枯在分离的成纤维细胞中抑制胶原蛋白合成。这种抑制作用并非由于明显的细胞毒性,也不是由于脯氨酰羟化酶的抑制(直接抑制或因辅因子耗竭而抑制)。虽然这种作用可能是百草枯所特有的,但它可能与自由基在个体细胞水平调节胶原蛋白合成的更普遍作用有关。

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