ArticleBulletin of experimental biology and medicine2025
Studying the Influence of Ischemic Liver Damage on the Pharmacokinetics of a Phenolic Antioxidant.
Article in Bulletin of experimental biology and medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- The Mechanism of G Protein-Coupled Receptor Regulation of Ferroptosis in Hepatic Ischemia-Reperfusion Injury.International journal of molecular sciences · 2026Review
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A new approach has been developed to study the pharmacokinetics of 2,6-diisobornyl-4-methylphenol, a phenolic antioxidant, after intragastric administration at a dose of 10 mg/kg to male Wistar rats with ischemia/reperfusion liver injury. The control group consisted of rats without pathology. A catheter previously implanted into the jugular vein of the animals, allowed repeated blood sampling and monitoring of the pharmacokinetic profile of the substance in each animal. Pharmacokinetic studies usually involve healthy animals, but the ischemia/reperfusion injury of the liver disrupted its functions, potentially altering drug metabolism and pharmacokinetics. Analysis of actual blood plasma samples confirmed the effectiveness of the proposed approach: changes in the pharmacokinetics of the phenolic antioxidant were revealed during liver ischemia/reperfusion injury in rats.
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Registered trials
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