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May 6, 2026International Journal of Pharmacology0 citationsOpen Access

Hepatoprotective Effects of Ajwa Seed Oil Against CCl4-Induced Acute Liver Injury in Mice

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AAAbdulrahman A. AljabriTATurki Hathal AlfehaidiAAAmer Fadhi Alarawi

Key Points

  • This study aims to investigate the hepatoprotective effects of Ajwa seed oil against CCl4-induced liver injury in mice.
  • Conducted an experimental study using 24 adult male mice divided into four groups.
  • Administered CCl4 to induce liver injury, followed by treatments with either Ajwa seed oil or silymarin.
  • Collected blood and liver samples for biochemical and histological analyses 24 hours after CCl4 administration.
  • Ajwa seed oil significantly reduced liver enzyme levels (alanine aminotransferase, aspartate aminotransferase, lactate dehydrogenase), indicating lower liver damage.
  • Treatment restored cholesterol and triglyceride levels, and increased albumin levels.
  • Histological analysis showed preserved liver architecture and reduced collagen deposition, confirming hepatoprotective effects.

Abstract

Background: As a major metabolic organ, the liver is constantly exposed to toxic substances. Although the flesh and seeds of Ajwa dates have been established to have antioxidant and anti-inflammatory properties, the hepatoprotective potential of Ajwa seed oil (ASO) against CCl4-induced damage has yet to be ascertained. Methods: Twenty-four adult male mice were randomly assigned to one of four groups (n = 6 per group): control (oral saline for 12 days), CCl4-treated saline for 12 days plus a single dose of CCl4 dissolved in corn oil 1:1 (1 mL/kg), CCl4 + ASO (100 mg/kg ASO administered daily for 12 days, followed by CCl4), and CCl4 + silymarin (100 mg/kg silymarin administered daily for 12 days, followed by CCl4). Blood and liver samples were collected 24 h after CCl4 administration for biochemical and histological analyses. Results: ASO treatment substantially reduced CCl4-induced liver damage by restoring normal serum liver enzyme levels (alanine aminotransferase, aspartate aminotransferase, and lactate dehydrogenase; p 0.05). Conclusion: Our findings in this study revealed that ASO has beneficial hepatoprotective effects against CCl4-induced injury, which can be attributed largely to its antioxidant properties, as evidenced by restored total antioxidant capacity and reduced lipid peroxidation. Anti-inflammatory mechanisms may also contribute, as suggested by the histological reduction in inflammatory cell infiltration; however, direct measurement of inflammatory biomarkers warrants investigation in future studies.

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Cite This Study

Aljabri et al. (2026) studied this question.

synapsesocial.com/papers/69faa2b504f884e66b533595https://doi.org/10.31083/ijp49020
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