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Table 1 Summary of the mechanism of natural compounds

From: Research advances on molecular mechanism and natural product therapy of iron metabolism in heart failure

Natural compounds

Function

Reference

Berberine

Inhibits iron toxicity by reducing ROS production and lipid peroxidation in iron-treated cardiac cells

[168]

Resveratrol

Reduce oxidative stress and attenuating ferroptosis

[172]

Baicalin

Regulate ferroptosis by inhibiting ACSL4

[176]

Cyanidin-3-O-glucoside

Upregulate FTH1 and GPX4 expression

[181]

Naringenin

Activates the Nrf2/SLC7A11/GPX4 axis by upregulating Nrf2, SLC7A11, GPX4, FTH1, and ferroportin-1, and downregulating NOX1 NADPH oxidase to inhibit ferroptosis

[184]

Gossypol acetic acid

Decrease ACSL4 and Nrf2 protein levels, and upregulate GPX4 protein levels

[187]

Astragaloside IV

Activate the Nrf2/GPX4 pathway to alleviate myocardial ferroptosis induced by DOX

[192]

Ophiopogonin D

Regulate ferroptosis, thereby protect myocardial cells

[196]

Artesunate

Inhibit the PERK/ATF4/CHOP pathway activation

[200]

Luteolin

Enhance Nrf2 nuclear transcription and activate the Nrf2/Gpx4 pathway

[204]

Puerarin

Alleviate ferroptosis

[210]

Schizandrin B

Activate the Nrf2/HO-1/GPX4 signaling pathway

[216]

Salvianolic acid B

Upregulate the expression and phosphorylation of Cx43 protein

[221]

Apigenin

Activate the AMPK/Nrf2/HO-1 signaling pathway

[226]

Thymoquinone

Activate the Nrf2/HO-1 signaling pathway

[229]