Clinical Laboratories Sciences Department, College of Applied Medical Sciences at Al-Qurayyat, Jouf University, Al-Qurayyat, 77454, Saudi Arabia.
Biochemistry Department, Faculty of Science, Alexandria University, Alexandria 21511, Egypt.
Oxid Med Cell Longev. 2022 Oct 18;2022:4812993. doi: 10.1155/2022/4812993. eCollection 2022.
Neuroinflammation is documented to alter brain function as a consequence of metabolic changes linked with a high-fat diet (HFD). The primary target of this study is to see how geraniol is effective in manipulating age- and diet-associated multiple toxicity and neuroinflammation in HFD-fed rats. Sixty-four adult male Wistar rats were partitioned into two groups: Group 1 (untreated normal young and aged rats) and Group 2 (HFD-fed young and aged rats) that received HFD for 16 weeks before being orally treated with geraniol or chromax for eight weeks. The results revealed a dropping in proinflammatory cytokines (TNF- and IL-6) and leptin while boosting adiponectin in geraniol-supplemented rats. The liver, kidney, and lipid profiles were improved in geraniol-HFD-treated groups. HFD-induced brain insulin resistance decreased insulin clearance and insulin-degrading enzyme (IDE) levels significantly after geraniol supplementation. Geraniol suppressed acetylcholinesterase (AChE) activity and alleviated oxidative stress by boosting neuronal reduced glutathione (GSH), catalase (CAT), glutathione-S-transferase (GST), and superoxide dismutase (SOD) activities. It lowered malondialdehyde concentration (TBARS), nitric oxide (NO), and xanthine oxidase (XO) and restored the structural damage to the brain tissue caused by HFD. Compared with model rats, geraniol boosted learning and memory function and ameliorated the inflammation status in the brain by lowering the protein levels of IL-1, iNOS, NF-Bp65, and COX-2. In addition, the expression levels of inflammation-related genes (MCP-1, TNF-, IL-6, IL-1, and IDO-1) were lessened significantly. Remarkably, the supplementation of geraniol reversed the oxidative and inflammation changes associated with aging. It affected the redox status of young rats. In conclusion, our results exhibit the effectiveness of dietary geraniol supplementation in modifying age-related neuroinflammation and oxidative stress in rats and triggering off the use of geraniol as a noninvasive natural compound for controlling age- and diet-associated neuronal impairments and toxicity.
神经炎症被记录为代谢变化的结果,这种代谢变化与高脂肪饮食(HFD)有关。本研究的主要目的是观察香叶醇如何有效地操纵 HFD 喂养大鼠的年龄和饮食相关的多种毒性和神经炎症。64 只成年雄性 Wistar 大鼠被分为两组:第 1 组(未经处理的正常年轻和年老大鼠)和第 2 组(HFD 喂养的年轻和年老大鼠),它们在接受 HFD 喂养 16 周后,用香叶醇或 chromax 进行 8 周的口服治疗。结果显示,补充香叶醇的大鼠促炎细胞因子(TNF-α 和 IL-6)和瘦素水平下降,脂联素水平升高。肝、肾和血脂谱在 geraniol-HFD 治疗组得到改善。HFD 诱导的大脑胰岛素抵抗在补充香叶醇后,显著降低了胰岛素清除率和胰岛素降解酶(IDE)水平。香叶醇通过抑制乙酰胆碱酯酶(AChE)活性和增加神经元还原型谷胱甘肽(GSH)、过氧化氢酶(CAT)、谷胱甘肽-S-转移酶(GST)和超氧化物歧化酶(SOD)的活性来减轻氧化应激。它降低了丙二醛浓度(TBARS)、一氧化氮(NO)和黄嘌呤氧化酶(XO)的浓度,并恢复了 HFD 对脑组织造成的结构损伤。与模型大鼠相比,香叶醇通过降低 IL-1、iNOS、NF-Bp65 和 COX-2 的蛋白水平,提高了学习和记忆功能,改善了大脑的炎症状态。此外,炎症相关基因(MCP-1、TNF-α、IL-6、IL-1 和 IDO-1)的表达水平显著降低。值得注意的是,香叶醇的补充逆转了与衰老相关的氧化和炎症变化。它影响了年轻大鼠的氧化还原状态。总之,我们的结果表明,膳食香叶醇补充剂在调节大鼠与年龄相关的神经炎症和氧化应激方面具有有效性,并引发了使用香叶醇作为一种非侵入性天然化合物来控制与年龄和饮食相关的神经元损伤和毒性的可能性。