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

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), lowering elevated levels of cholesterol and triglycerides, and increasing albumin levels (p < 0.05). The treatment significantly reduced lipid peroxidation, as evidenced by decreased malondialdehyde levels (p < 0.0001), and concurrently restored the total antioxidant capacity. Histological analysis revealed the preservation of liver architecture, reduced collagen deposition, and maintenance of glycogen storage (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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Journal
International Journal of Pharmacology
Published
2026-04-24
DOI
https://doi.org/10.31083/ijp49020
Primary Topic
Date Palm Research Studies
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article
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article

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

Bandar D. Alrehaili, Faris S. Alnezary, Ammar Abdulraheem Bahauddin, Abdulrahman A. Aljabri et al.
International Journal of Pharmacology
Date Palm Research Studies
article

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

Bandar D. Alrehaili, Faris S. Alnezary, Ammar Abdulraheem Bahauddin, Abdulrahman A. Aljabri, Heba M. Zahid, Lujain A. Almohammadi, Amer Fadhi Alarawi, Turki Hathal Alfehaidi, Heba Eltahir, Mohammed H. Alsubhi, Suhayb W. Alamri, Abdulrahman G. Alharbi
article en

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), lowering elevated levels of cholesterol and triglycerides, and increasing albumin levels (p < 0.05). The treatment significantly reduced lipid peroxidation, as evidenced by decreased malondialdehyde levels (p < 0.0001), and concurrently restored the total antioxidant capacity. Histological analysis revealed the preservation of liver architecture, reduced collagen deposition, and maintenance of glycogen storage (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.

International Journal of PharmacologyVol. 22(2)
Taibah University (SA)
Good health and well-being
Openalex Percentile: Top 8%
Date Palm Research Studies
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