Farnesol attenuates cadmium-induced kidney injury by mitigating oxidative stress, inflammation and necroptosis and upregulating cytoglobin and PPARγ in rats

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Reem S. Alruhaimi , Emad H.M. Hassanein , Ahmad F. Ahmeda , Ahmed M. Atwa , Sulaiman M. Alnasser , Ghadir A. Sayed , Meshal Alotaibi , Mohammed A. Alzoghaibi , Ayman M. Mahmoud
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Abstract

Heavy metals are environmental pollutants that can harm animals and humans even at low concentrations. Cadmium (Cd) is known for its serious health effects on different organs and its toxicity is associated with oxidative stress (OS) and inflammation. Farnesol (FAR), a sesquiterpene alcohol found in many vegetables and fruits, possesses promising anti-inflammatory and antioxidant activities. This study evaluated the effect of FAR on Cd-induced kidney injury, pinpointing its effect of the redox status, inflammation, fibrosis and necroptosis. Rats in this study received FAR for 14 days and Cd on day 7. Elevated serum creatinine, urea and uric acid, and several kidney histopathological alterations were observed in Cd-administered rats. Cd increased MDA, decreased antioxidants, downregulated PPARγ and upregulated NF-κB p65, IL-6, TNF-α, and IL-1β. Necroptosis mediators (RIP1, RIP3, MLKL, and caspase-8) and α-SMA were upregulated, and collagen deposition was increased in Cd-administered rats. FAR ameliorated kidney injury markers and tissue damage, attenuated OS, suppressed NF-κB and inflammatory mediators, and enhanced antioxidants. In addition, FAR suppressed RIP1, RIP3, MLKL, caspase-8, and α-SMA, and enhanced kidney cytoglobin and PPARγ. In conclusion, FAR protects against Cd nephrotoxicity by suppressing OS, inflammatory response and necroptosis, effects associated with enhanced antioxidants, cytoglobin, and PPARγ.

法呢醇通过减轻氧化应激、炎症和坏死,上调大鼠的细胞色素和 PPARγ 来减轻镉引起的肾损伤
重金属是一种环境污染物,即使浓度很低,也会对动物和人类造成伤害。众所周知,镉(Cd)对不同器官的健康有严重影响,其毒性与氧化应激(OS)和炎症有关。法尼醇(FAR)是一种倍半萜醇,存在于许多蔬菜和水果中,具有良好的抗炎和抗氧化活性。本研究评估了 FAR 对镉诱导的肾损伤的影响,明确了其对氧化还原状态、炎症、纤维化和坏死的影响。本研究中的大鼠接受了 14 天的 FAR 治疗,并在第 7 天接受了镉治疗。在服用镉的大鼠中观察到血清肌酐、尿素和尿酸升高,以及一些肾脏组织病理学改变。镉使 MDA 增加,抗氧化剂减少,PPARγ 下调,NF-κB p65、IL-6、TNF-α 和 IL-1β 上调。Cd 给药大鼠的坏死介质(RIP1、RIP3、MLKL 和 caspase-8)和 α-SMA 上调,胶原沉积增加。FAR 可改善肾损伤指标和组织损伤,减轻 OS,抑制 NF-κB 和炎症介质,并增强抗氧化能力。此外,FAR 还能抑制 RIP1、RIP3、MLKL、caspase-8 和 α-SMA,增强肾脏细胞色素和 PPARγ。总之,FAR可通过抑制OS、炎症反应和坏死来防止镉肾毒性,这些效应与抗氧化剂、细胞血红蛋白和PPARγ的增强有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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