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Regulation of cardiac ferroptosis in diabetic human heart failure: uncovering molecular pathways and key targets

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In the iron metabolism pathways, transferrin receptor 1 (TfR1) transport extracellular Fe 3+ to the nucleus and convert it into Fe 2+ , which is released from the nucleus through divalent metal transporter 1 (DMT1), triggering the Fenton reaction, activating lipoxygenases, and promoting the generation of lipid peroxides, resulting in ferroptosis ( (consisting of two subunits SLC3A2 and SLC7A11) ( decrease the uptake of cystine and reduce cysteine and suppress glutathione (GSH) production, further inactivating GPX4 ( Figure 1 Over the years, researches on the link between ferroptosis and clinical diseases have been gradually improved, with cancer and neurodegenerative diseases being the focus ( Ferroptosis and Cardiovascular Diseases Ferroptosis and Cardiomyopathy Cardiomyopathy is a group of myocardial diseases caused by heterogeneous factors, leading to myocardial and/or cardiac electrical dysfunction, with high mortality ( Doxorubicin (DOX), also known as adriamycin, is the second-generation anthracycline chemotherapy drug, a commonly used antitumor agent with fatal cardiotoxicity

Sleep 33 , 647656 (2010)

All of this financial security for women dramatically affects how they relate to a man, to a husband, to a partner

Environmental Toxins : Exposure to heavy metals, pollutants, and pesticides increases the demand for glutathione as the body works to detoxify these substances