Avocado Seeds-Mediated Alleviation of Cyclosporine A-Induced Hepatotoxicity Involves the Inhibition of Oxidative Stress and Proapoptotic Endoplasmic Reticulum Stress

被引:11
作者
El-Magd, Mohammed A. [1 ]
Zedan, Amina M. G. [2 ]
Zidan, Nahla S. [3 ,4 ]
Sakran, Mohamed, I [5 ,6 ]
Bahattab, Omar [7 ]
Oyouni, Atif Abdulwahab A. [7 ,8 ]
Al-Amer, Osama M. [8 ,9 ]
Alalawy, Adel, I [5 ]
Elmoslemany, Amira M. [10 ]
机构
[1] Kafrelsheikh Univ, Fac Vet Med, Dept Anat, Kafrelsheikh 33516, Egypt
[2] Al Azhar Univ, Fac Home Econ, Biol & Environm Sci Dept, Tanta 31732, Egypt
[3] Tabuk Univ, Fac Home Econ, Dept Nutr & Food Sci, Tabuk 47512, Saudi Arabia
[4] Kafrelsheikh Univ, Fac Specif Educ, Dept Home Econ, Kafrelsheikh 33516, Egypt
[5] Univ Tabuk, Fac Sci, Dept Biochem, Tabuk 47512, Saudi Arabia
[6] Tanta Univ, Fac Sci, Chem Dept, Biochem Div, Tanta 31512, Egypt
[7] Univ Tabuk, Fac Sci, Biol Dept, Tabuk 47512, Saudi Arabia
[8] Univ Tabuk, Fac Sci, Genome & Biotechnol Unit, Tabuk 47512, Saudi Arabia
[9] Univ Tabuk, Fac Appl Med Sci, Dept Med Lab Technol, Tabuk 47512, Saudi Arabia
[10] Al Azhar Univ, Fac Home Econ, Nutr & Food Sci Dept, Tanta 31732, Egypt
来源
MOLECULES | 2022年 / 27卷 / 22期
关键词
avocado seeds; cyclosporine A; hepatotoxicity; oxidative stress; ER stress; UNFOLDED PROTEIN RESPONSE; PERSEA-AMERICANA MILL; ANTIOXIDANT ACTIVITY; LIVER; ERDOSTEINE; AUTOPHAGY; TOXICITY; EXTRACT; INJURY; DAMAGE;
D O I
10.3390/molecules27227859
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous studies reported disrupted hepatic function and structure following the administration of cyclosporine A (CsA) in humans and animals. Recently, we found that avocado seeds (AvS) ameliorated CsA-induced nephrotoxicity in rats. As a continuation, herein we checked whether AvS could also attenuate CsA-induced hepatotoxicity in rats. Subcutaneous injection of CsA (5 mg/kg) for 7 days triggered hepatotoxicity in rats, as indicated by liver dysfunction, redox imbalance, and histopathological changes. Oral administration of 5% AvS powder for 4 weeks ameliorated CsA-induced hepatotoxicity, as evidenced by (1) decreased levels of liver damage parameters (alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), and bilirubin), (2) resumed redox balance in the liver (reduced malondialdehyde (MDA) and increased superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx)), (3) downregulated hepatic expression of endoplasmic reticulum (ER) stress-related genes (X-box binding protein 1 (XBP1), binding immunoglobulin protein (BIP), C/EBP homologous protein (CHOP)), and apoptosis-related genes (Bax and Casp3), (4) upregulated expression of the anti-apoptotic gene Bcl2, (5) reduced DNA damage, and (6) improved liver histology. These results highlight the ability of AvS to ameliorate CsA-induced hepatotoxicity via the inhibition of oxidative stress and proapoptotic ER stress.
引用
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页数:14
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