Kaempferol sophoroside glucoside mitigates acetaminophen-induced hepatotoxicity: Role of Nrf2/NF-κB and JNK/ASK-1 signaling pathways

被引:2
作者
Mohamed, Gamal A. [1 ]
El-Agamy, Dina S. [2 ]
Abdallah, Hossam M. [1 ]
Sindi, Ikhlas A. [3 ]
Almogaddam, Mohammed A. [4 ]
Alzain, Abdulrahim A. [4 ]
Andijani, Yusra Saleh [5 ]
Ibrahim, Sabrin R. M. [6 ,7 ]
机构
[1] King Abdulaziz Univ, Fac Pharm, Dept Nat Prod & Alternat Med, Jeddah 21589, Saudi Arabia
[2] Mansoura Univ, Fac Pharm, Dept Pharmacol & Toxicol, Mansoura 35516, Egypt
[3] King Abdulaziz Univ, Fac Sci, Dept Biol, Jeddah 21589, Saudi Arabia
[4] Univ Gezira, Fac Pharm, Dept Pharmaceut Chem, Wad Madani 21111, Sudan
[5] Taibah Univ, Coll Pharm, Dept Pharmacol & Toxicol, Al Madinah Al Munawwarah 30078, Saudi Arabia
[6] Batterjee Med Coll, Dept Chem, Preparatory Year Program, Jeddah 21442, Saudi Arabia
[7] Assiut Univ, Fac Pharm, Dept Pharmacognosy, Assiut 71526, Egypt
关键词
Kaempferol-3-sophoroside-7-glucoside; Acetaminophen; Hepatotoxicity; Acute liver injury; Health and wellbeing; Life on land; Drug discovery; Industrial development; INDUCED LIVER-INJURY; INHIBITOR; DOCKING; MICE; GLYCOSIDES; GLIDE; MECHANISMS; PROTECTS; DELETION; PROGRAM;
D O I
10.1016/j.heliyon.2024.e31448
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
APAP (Acetaminophen)-induced hepatic injury is a major public health threat that requires continuous searching for new effective therapeutics. KSG (Kaempferol-3-sophoroside-7-glucoside) is a kaempferol derivative that was separated from plant species belonging to different genera. This study explored the protective effects of KSG on ALI (acute liver injury) caused by APAP overdose in mice and elucidated its possible mechanisms. The results showed that KSG pretreatment alleviated APAP-induced hepatic damage as it reduced hepatic pathological lesions as well as the serum parameters of liver injury. Moreover, KSG opposed APAP-associated oxidative stress and augmented hepatic antioxidants. KSG suppressed the inflammatory response as it decreased the genetic and protein expression as well as the levels of inflammatory cytokines. Meanwhile, KSG enhanced the mRNA expression and level of anti-inflammatory cytokine, IL-10 (interleukin-10). KSG repressed the activation of NF-kappa B (nuclear-factor kappa-B), besides it promoted the activation of Nrf2 signaling. Additionally, KSG markedly hindered the elevation of ASK-1 (apoptosis-signal regulating-kinase-1) and JNK (c-Jun-N-terminal kinase). Furthermore, KSG suppressed APAP-induced apoptosis as it decreased the level and expression of Bax (BCL2associated X-protein), and caspase-3 concurrent with an enhancement of anti-apoptotic protein, Bcl2 in the liver. More thoroughly, Computational studies reveal indispensable binding affinities between KSG and Keap1 (Kelch-like ECH-associated protein-1), ASK1 (apoptosis signal-regulating kinase-1), and JNK1 (c-Jun N-terminal protein kinase-1) with distinctive tendencies for selective inhibition. Taken together, our data showed the hepatoprotective capacity of KSG against APAP produced ALI via modulation of Nrf2/NF- kappa B and JNK/ASK-1/caspase-3 signaling. Henceforth, KSG could be a promising hepatoprotective candidate for ALI.
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页数:18
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