Document Type

Article

Publication Date

5-23-2026

Abstract

Purpose

Cytochrome P450 (P450) metabolites of arachidonic acid (AA) are potential therapeutic targets in ischemia–reperfusion (IR) injury, yet their disposition and actions in hepatic IR are unknown. Cellular AA and its P450 metabolites are primarily bound to lipid membranes, resulting in negligible free concentrations. This study investigates how hepatic IR injury impacts the disposition of free AA and its major P450 metabolites in rats.

Methods

Rats underwent 60 min of partial (70%) ischemia or sham surgery, followed by 5 min, 3 h, or 24 h of reperfusion. The effects of IR injury on free concentrations of AA and its major P450-generated metabolites in the liver were studied using LC–MS/MS. The activities of phospholipase A2 (PLA2) enzymes, which release AA and its preformed metabolites from lipid membranes, were also measured in the liver and plasma. Additionally, in vitro rates of metabolite formation and the levels of major AA-metabolizing enzymes were assessed in microsomes.

Results

Hepatic IR injury significantly increased free liver concentrations of AA (sevenfold) and its metabolites (1.8–9.1-fold) only in the 5-min group. Similarly, PLA2 enzyme activity in the liver and plasma was higher only in this group. Conversely, liver IR injury caused a significant reduction or no change in the in vitro rate of AA metabolism to P450-mediated metabolites in the 5-min group.

Conclusions

Liver IR injury rapidly increases liver concentrations of free P450-mediated metabolites of AA, likely due to IR-induced release of preformed metabolites and AA from lipid membranes, rather than an increase in P450 enzymatic activity.

Comments

This article was originally published in Pharmaceutical Research in 2026. https://doi.org/10.1007/s11095-026-04108-1

11095_2026_4108_MOESM1_ESM.docx (1141 kB)
Electronic Supplementary Material: (The in vitro rates of metabolism of AA to its P450-mediated metabolites at an AA concentration of 62.5 µM are presented in the supplementary file. DOCX 1.11 MB)

Copyright

The authors

Creative Commons License

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.

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