Azilsartan as a novel anti-ferriptotic agent via the upregulation of the Nrf2/HO-1/SLC7A11/GPX4 axis and downregulation of inflammatory pathways in folic acid-induced acute kidney injury in male mice

Azilsartan confers potent protection against FA-induced AKI by activating the Nrf2/HO-1/SLC7A11/GPX4 axis, reducing lipid peroxidation, normalizing iron metabolism, and attenuating inflammation. These findings support azilsartan's potential as a repurposed therapy for ferroptosis-driven renal injury.

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Publication Details

Journal
Toxicology Reports
Published
2026-01-08
DOI
https://doi.org/10.1016/j.toxrep.2026.102204
Citations
2
Primary Topic
Ferroptosis and cancer prognosis
Type
article
Field-Weighted Citation Impact
72.89
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article

Azilsartan as a novel anti-ferriptotic agent via the upregulation of the Nrf2/HO-1/SLC7A11/GPX4 axis and downregulation of inflammatory pathways in folic acid-induced acute kidney injury in male mice

Elaf Mahmood Shihab, Saja Majeed Shareef, Sohrab Abbas, Khulood Majid Alsaraf et al.
2 citations
Toxicology Reports
Ferroptosis and cancer prognosis
72.89
article

Azilsartan as a novel anti-ferriptotic agent via the upregulation of the Nrf2/HO-1/SLC7A11/GPX4 axis and downregulation of inflammatory pathways in folic acid-induced acute kidney injury in male mice

Elaf Mahmood Shihab, Saja Majeed Shareef, Sohrab Abbas, Khulood Majid Alsaraf, Hayder Adnan Fawzi, Rana Jawad Hasan
article en
2 citations

Abstract

Azilsartan confers potent protection against FA-induced AKI by activating the Nrf2/HO-1/SLC7A11/GPX4 axis, reducing lipid peroxidation, normalizing iron metabolism, and attenuating inflammation. These findings support azilsartan's potential as a repurposed therapy for ferroptosis-driven renal injury.

Toxicology ReportsVol. 16
University of Baghdad (IQ), Mustansiriyah University (IQ), Al Mansour University College (IQ)
Good health and well-being
Openalex Percentile: Top 0%
Ferroptosis and cancer prognosis
72.89
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