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Hepatoprotective Effects of Tamarix dioica Leaf Extracts on Paracetamol-Induced Hepatotoxicity in Mice

Hepatoprotective Effects of Tamarix dioica Leaf Extracts on Paracetamol-Induced Hepatotoxicity in Mice

Tahani Ahmad Al-Matrafi1, Zuhair M. Mohammedsaleh2, Mamdoh S. Moawadh2, Waheeb S. Aggad3, Rawabi Mohamed almuhimed4, Zamzam Alhuwaymil5, Aishah E Albalawi6, Ifat Alsharif7, Hailah M. Almohaimeed8, Fatima S. Alaryani9 and Mona H. Soliman10,11*

1Anatomy Department, College of Medicine, King Saudi University, Saudi Arabia
2Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences,University of Tabuk, Tabuk 71491, Saudi Arabia
3Department of Anatomy, College of Medicine, University of Jeddah, P.O. Box 8304, Jeddah23234, Saudi Arabia
4Saudi Authority for Intellectual Property (SAIP), Saudi Arabia
5Organic Department, College of Science and Humanities at Al-Quway’iyahl, Shaqra University, Saudi Arabia
6Faculty of Science, Department of Biology, University of Tabuk, Tabuk 47913, Saudi Arabia
7Department of Biology, Jamoum University College, Umm Al-Qura University, 21955, Makkah, Saudi Arabia
8Department of Basic Science, College of Medicine, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia
9University of Jeddah, College of Science, Department of Biological Sciences, Jeddah 21589, Saudi Arabia
10Botany and Microbiology Department, Faculty of Science, Cairo University, Giza 12613,Egypt
11Biology Department, Faculty of Science, Taibah University, Al-Sharm, Yanbu El-Bahr,Yanbu 46429, Kingdom of Saudi Arabia
 
*      Corresponding author: hmona@sci.cu.edu.eg

ABSTRACT

This study aimed to evaluate the hepatoprotective effects of aqueous, methanolic, and ethanolic extracts of Tamarix dioica leaves against paracetamol-induced toxicity. In this study, 36 albino mice were randomly grouped into six groups, each consisting of six mice: Group I (normal control), Group II (paracetamol-toxified), Group III (positive control with Silymarin @ 200 mg/Kg), Group IV (aqueous T. dioica extract @ 400 mg/Kg), Group V (methanolic T. dioica extract @ 400 mg/Kg), and Group VI (ethanolic T. dioica extract @ 400 mg/Kg). Hepatoprotective potential was assessed through liver function indicators (ALT, AST, ALP, total bilirubin, and total protein in blood serums), hepatic antioxidants (SOD, CAT, GSH, and GPx in liver homogenate), and inflammatory markers (IL-6, TNF-α, COX2), along with other liver biomarkers. Histopathological alterations in the liver were evaluated using Hematoxylin and Eosin staining. The leaf extracts effectively restored liver function indicators and hepatic antioxidants to normal levels, demonstrating a significant improvement compared to the elevated levels observed in the paracetamol control group (P < 0.001). Furthermore, a reversal of hepatoarchitecture was recorded. The study highlights the pronounced hepatoprotective effects of T. dioica leaf extracts against paracetamol-induced toxicity in albino mice. The extracts not only successfully normalized liver function indicators and hepatic antioxidants but also exhibited a significant reversal of hepatoarchitecture. These findings suggest the potential therapeutic value of T. dioica in mitigating liver disorders, emphasizing its promising role as a natural hepatoprotective agent.

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Pakistan Journal of Zoology

August

Pakistan J. Zool., Vol. 56, Iss. 4, pp. 1501-2000

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