4.3 Article

Cardiovascular Autophagy: Crossroads of Pathology, Pharmacology and Toxicology

期刊

CARDIOVASCULAR TOXICOLOGY
卷 13, 期 3, 页码 220-229

出版社

HUMANA PRESS INC
DOI: 10.1007/s12012-013-9200-8

关键词

Autophagy; Cardiovascular disease; Drug-eluting stents; LC3; Rapamycin; Verapamil

资金

  1. NIH [NIGMS RR024489, HL89380]

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Cardiovascular disease (CVD) remains the leading cause of death worldwide, despite the significant advances in medicine. Autophagy, a process of self-cannibalization employed by mammalian cells for the recycling of cellular contents, is altered not only in a number of CVDs, but in other diseases, as well. Many FDA-approved drugs are known to induce autophagy-mediated side effects in the cardiovascular system. In some cases, such drug-induced autophagy could be harnessed and used for treating CVD, greatly reducing the duration and cost of CVD treatments. However, because the induction of autophagy in cardiovascular targets can be both adaptive and maladaptive under specific settings, the challenge is to determine whether the changes stimulated by drug-induced autophagy are, in fact, beneficial. In this review, we surveyed a number of CVDs in which autophagy is known to occur, and we also address the role of FDA-approved drugs for which autophagy-mediated side effects occur within the cardiovascular system. The therapeutic potential of using small molecule modulators of autophagy in the management of CVD progression is discussed.

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