Cadmium-Induced Hepatotoxicity in Mice - Prophylactic Supplementation of Quercetin Exerts Hepatoprotective Effect by Modulating PI3K/Akt/NF-kappaB Signaling Pathway.

IF 1.9 4区 医学 Q3 PHYSIOLOGY Physiological research Pub Date : 2024-11-12 DOI:10.33549/physiolres.935252
L Liu, Q Zhao, J Huang, S Lei
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Abstract

This current study seeks to examine the pre-protective function of Quercetin in Cadmium (Cd)-induced liver damage, along with its modulation of the PI3K/Akt/NF-kappaB signaling pathway. A total of 60 male C57BL/6J mice were randomly assigned to four groups: control (C), quercetin (Q, 100 mg/kg/day), Cd (Cd, 2.5 mg/kg/day), and quercetin and Cd (Q+Cd). Before receiving Cd treatment, quercetin was administered intragastrically for 4 weeks. In the present study, liver markers, oxidative stress parameters, pro-inflammatory cytokines, liver histopathology, apoptotic markers and PI3K/Akt/NF-kappaB signaling molecules were examined. We observed that the body weight of the Cd-treated mice dramatically rise after 4 weeks of quercetin pre-administration, and the Cd concentration was significantly decreased. Liver function markers like alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP), and lactate dehydrogenase (LDH) were significantly reduced in quercetin treatment in Cd-induced mice. Additionally, we observed that quercetin reduced Cd-mediated liver injury in mice by assessing the level of malondialdehyde (MDA), and the activities of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione (GSH) concentrations and the histological alterations. By monitoring tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), and interleukin-1beta (IL-1beta), quercetin successfully reduced the inflammatory cytokines that the Cd metal caused in the liver. Additionally, in the liver tissues of Cd-mediated, quercetin could enhance the expression of Bcl-2 and decrease the expression of p-Akt, p-PI3K, Bax, Caspase-9, Caspase-3, NF-kappaB. In conclusion, quercetin protects against Cd induced liver injury via several pathways, including oxidative stress, inflammation and apoptosis, and its protective effect correlates with antioxidant activity.

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镉诱导的小鼠肝毒性--预防性补充槲皮素可通过调节 PI3K/Akt/NF-kappaB 信号通路发挥保肝作用
本研究旨在探讨槲皮素对镉(Cd)诱导的肝损伤的预保护功能及其对PI3K/Akt/NF-kappaB信号通路的调节作用。60只雄性C57BL/6J小鼠被随机分为四组:对照组(C)、槲皮素组(Q,100毫克/千克/天)、镉组(Cd,2.5毫克/千克/天)和槲皮素与镉组(Q+Cd)。在接受镉治疗之前,先在胃内注射槲皮素 4 周。本研究检测了肝脏指标、氧化应激参数、促炎细胞因子、肝组织病理学、细胞凋亡指标和PI3K/Akt/NF-kappaB信号分子。我们观察到,预服槲皮素 4 周后,镉处理小鼠的体重显著增加,镉浓度明显降低。丙氨酸转氨酶(ALT)、天门冬氨酸转氨酶(AST)、碱性磷酸酶(ALP)和乳酸脱氢酶(LDH)等肝功能指标在槲皮素治疗镉诱导小鼠后明显降低。此外,我们还通过评估丙二醛(MDA)水平、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)和谷胱甘肽(GSH)浓度及组织学改变,观察到槲皮素能减轻镉介导的小鼠肝损伤。通过监测肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-1β(IL-1β),槲皮素成功地降低了镉金属在肝脏中引起的炎症细胞因子。此外,在镉介导的肝组织中,槲皮素能增强 Bcl-2 的表达,降低 p-Akt、p-PI3K、Bax、Caspase-9、Caspase-3、NF-kappaB 的表达。总之,槲皮素可通过多种途径(包括氧化应激、炎症和细胞凋亡)保护镉诱导的肝损伤,其保护作用与抗氧化活性相关。
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来源期刊
Physiological research
Physiological research 医学-生理学
CiteScore
4.00
自引率
4.80%
发文量
108
审稿时长
3 months
期刊介绍: Physiological Research is a peer reviewed Open Access journal that publishes articles on normal and pathological physiology, biochemistry, biophysics, and pharmacology. Authors can submit original, previously unpublished research articles, review articles, rapid or short communications. Instructions for Authors - Respect the instructions carefully when submitting your manuscript. Submitted manuscripts or revised manuscripts that do not follow these Instructions will not be included into the peer-review process. The articles are available in full versions as pdf files beginning with volume 40, 1991. The journal publishes the online Ahead of Print /Pre-Press version of the articles that are searchable in Medline and can be cited.
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