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细胞的氧化还原特征:性别视角

Redox features of the cell: a gender perspective.

作者信息

Malorni Walter, Campesi Ilaria, Straface Elisabetta, Vella Stefano, Franconi Flavia

机构信息

Department of Drug Research and Evaluation, Istituto Superiore di Sanita', Rome, Italy.

出版信息

Antioxid Redox Signal. 2007 Nov;9(11):1779-801. doi: 10.1089/ars.2007.1596.

Abstract

Reactive oxygen and nitrogen species have been implicated in diverse subcellular activities, including cell proliferation,differentiation and, in some instances, cell injury and death. The implications of reactive species inhuman pathology have also been studied in detail. However, although the role of free radicals in the pathogenesis of human diseases has been extensively analyzed in different systems (i.e., in vitro, ex vivo, and in vivo),it is still far from elucidated. In particular, the possible role of gender 4 differences in human pathophysiology associated with reactive species is a promising new field of investigation. Although the complex scenario this presents is still incomplete, important gender-associated "redox features" of cells have already been described in the literature. Here we summarize the different aspects of redox-associated molecules and enzymes in regard to gender differences in terms of the intracellular production and biochemical activity of reactive species. These are often associated with the pathogenetic mechanisms underlying several human morbidities(e.g., degenerative diseases) and can represent a specific target for new pharmacologic strategies. Gender differences may thus pose an important challenge for future studies aimed at the clinical management of diseases characterized by a redox imbalance.

摘要

活性氧和氮物种参与了多种亚细胞活动,包括细胞增殖、分化,在某些情况下还包括细胞损伤和死亡。活性物种在人类病理学中的影响也已得到详细研究。然而,尽管自由基在人类疾病发病机制中的作用已在不同系统(即体外、离体和体内)中得到广泛分析,但仍远未阐明。特别是,性别差异在与活性物种相关的人类病理生理学中的可能作用是一个有前途的新研究领域。尽管这所呈现的复杂情况仍不完整,但文献中已经描述了细胞重要的与性别相关的“氧化还原特征”。在这里,我们从活性物种的细胞内产生和生化活性方面,总结了氧化还原相关分子和酶在性别差异方面的不同方面。这些通常与几种人类疾病(如退行性疾病)的发病机制相关,并且可以代表新药物策略的特定靶点。因此,性别差异可能对未来旨在临床管理以氧化还原失衡为特征的疾病的研究构成重大挑战。

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