Targeting ferroptosis: a novel insight against myocardial infarction and ischemia–reperfusion injuries
Targeting ferroptosis: a novel insight against myocardial infarction and ischemia–reperfusion injuries
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靶向铁死亡:对抗心肌梗死和缺血再灌注损伤的新见解
DOI:
10.1007/s10495-022-01785-2
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发表时间:
2022-12
期刊:
影响因子:
7.2
通讯作者:
Caixia Guo
中科院分区:
文献类型:
--
作者:
Xuejie Han;Jie Zhang;Jian Liu;Hongxia Wang;Fenghe Du;Xiangjun Zeng;Caixia Guo
Ferroptosis, a newly discovered form of regulated cell death dependent on iron and reactive oxygen species, is mainly characterized by mitochondrial shrinkage, increased density of bilayer membranes and the accumulation of lipid peroxidation, causing membrane lipid peroxidation and eventually cell death. Similar with the most forms of regulated cell death, ferroptosis also participated in the pathological metabolism of myocardial infarction and myocardial ischemia/reperfusion injuries, which are still the leading causes of death worldwide. Given the crucial roles ferroptosis played in cardiovascular diseases, such as myocardial infarction and myocardial ischemia/reperfusion injuries, it is considerable to delve into the molecular mechanisms of ferroptosis contributing to the progress of cardiovascular diseases, which might offer the potential role of ferroptosis as a targeted treatment for a wide range of cardiovascular diseases. This review systematically summarizes the process and regulatory metabolisms of ferroptosis, discusses the relationship between ferroptosis and myocardial infarction as well as myocardial ischemia/reperfusion injuries, which might potentially provide novel insights for the pathological metabolism and original ideas for the prevention as well as treatment targeting ferroptosis of cardiovascular diseases such as myocardial infarction and myocardial ischemia/reperfusion injuries.
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影响因子:
14.8
作者:
Doll S;Proneth B;Tyurina YY;Panzilius E;Kobayashi S;Ingold I;Irmler M;Beckers J;Aichler M;Walch A;Prokisch H;Trümbach D;Mao G;Qu F;Bayir H;Füllekrug J;Scheel CH;Wurst W;Schick JA;Kagan VE;Angeli JP;Conrad M
通讯作者:
Conrad M
影响因子:
14.8
作者:
Kagan VE;Mao G;Qu F;Angeli JP;Doll S;Croix CS;Dar HH;Liu B;Tyurin VA;Ritov VB;Kapralov AA;Amoscato AA;Jiang J;Anthonymuthu T;Mohammadyani D;Yang Q;Proneth B;Klein-Seetharaman J;Watkins S;Bahar I;Greenberger J;Mallampalli RK;Stockwell BR;Tyurina YY;Conrad M;Bayır H
通讯作者:
Bayır H
影响因子:
64.5
作者:
Dixon SJ;Lemberg KM;Lamprecht MR;Skouta R;Zaitsev EM;Gleason CE;Patel DN;Bauer AJ;Cantley AM;Yang WS;Morrison B 3rd;Stockwell BR
通讯作者:
Stockwell BR
影响因子:
4
作者:
Dixon SJ;Winter GE;Musavi LS;Lee ED;Snijder B;Rebsamen M;Superti-Furga G;Stockwell BR
通讯作者:
Stockwell BR
影响因子:
8
作者:
Tadokoro, Tomonori;Ikeda, Masataka;Ide, Tomomi;Deguchi, Hiroko;Ikeda, Soichiro;Okabe, Kosuke;Ishikita, Akihito;Matsushima, Shouji;Koumura, Tomoko;Yamada, Ken-ichi;Imai, Hirotaka;Tsutsui, Hiroyuki
通讯作者:
Tsutsui, Hiroyuki