香叶醇在高脂肪饮食诱导的NAFLD中的保护作用:平衡脂质稳态、抗氧化防御和炎症反应。

IF 3.2 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Sakeena Noor, Fakhria A Al-Joufi, Ambreen Malik Uttra, Sumera Qasim, Aiman Afzal
{"title":"香叶醇在高脂肪饮食诱导的NAFLD中的保护作用:平衡脂质稳态、抗氧化防御和炎症反应。","authors":"Sakeena Noor, Fakhria A Al-Joufi, Ambreen Malik Uttra, Sumera Qasim, Aiman Afzal","doi":"10.1093/jpp/rgaf053","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to evaluate the preventive effects of geraniol on non-alcoholic fatty liver disease (NAFLD) induced by a high fat diet (HFD) in a rat model, focusing on its impact on lipid metabolism, oxidative stress, and inflammation.</p><p><strong>Methods: </strong>NAFLD was induced in male Sprague-Dawley rats by feeding them a HFD for 10 weeks. Geraniol was administered orally at doses of 50, 100, and 200 mg/kg. The following parameters were assessed: body weight, hepatic index, lipid profile (total cholesterol, triglycerides, HDL, LDL), serum hepatic enzymes (ALT, AST, ALP), oxidative stress markers (MDA, SOD, CAT, GSH), and inflammatory markers (TNF-α, IL-6, IL-10). Histopathological evaluation of liver tissues was performed to assess structural changes and inflammation.</p><p><strong>Key findings: </strong>Geraniol treatment, particularly at 100 and 200 mg/kg, significantly reduced body weight gain and hepatic index in HFD-fed rats. It improved lipid profiles by lowering total cholesterol, triglycerides, and LDL while increasing HDL levels. Hepatic enzyme levels were markedly decreased, indicating hepatoprotection. Geraniol also restored antioxidant enzyme activity and reduced markers of oxidative stress. Moreover, it lowered pro-inflammatory cytokines and elevated anti-inflammatory cytokines. Histopathological analysis confirmed reduced hepatic steatosis and inflammation.</p><p><strong>Conclusions: </strong>Geraniol demonstrated potent protective effects against HFD-induced NAFLD in rats by improving lipid metabolism, mitigating oxidative stress, and modulating inflammatory responses. These findings support its potential as a therapeutic agent for the prevention and management of NAFLD.</p>","PeriodicalId":16960,"journal":{"name":"Journal of Pharmacy and Pharmacology","volume":" ","pages":"1439-1449"},"PeriodicalIF":3.2000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Protective role of geraniol in high fat diet-induced NAFLD: balancing lipid homeostasis, antioxidant defence, and inflammatory responses.\",\"authors\":\"Sakeena Noor, Fakhria A Al-Joufi, Ambreen Malik Uttra, Sumera Qasim, Aiman Afzal\",\"doi\":\"10.1093/jpp/rgaf053\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>This study aimed to evaluate the preventive effects of geraniol on non-alcoholic fatty liver disease (NAFLD) induced by a high fat diet (HFD) in a rat model, focusing on its impact on lipid metabolism, oxidative stress, and inflammation.</p><p><strong>Methods: </strong>NAFLD was induced in male Sprague-Dawley rats by feeding them a HFD for 10 weeks. Geraniol was administered orally at doses of 50, 100, and 200 mg/kg. The following parameters were assessed: body weight, hepatic index, lipid profile (total cholesterol, triglycerides, HDL, LDL), serum hepatic enzymes (ALT, AST, ALP), oxidative stress markers (MDA, SOD, CAT, GSH), and inflammatory markers (TNF-α, IL-6, IL-10). Histopathological evaluation of liver tissues was performed to assess structural changes and inflammation.</p><p><strong>Key findings: </strong>Geraniol treatment, particularly at 100 and 200 mg/kg, significantly reduced body weight gain and hepatic index in HFD-fed rats. It improved lipid profiles by lowering total cholesterol, triglycerides, and LDL while increasing HDL levels. Hepatic enzyme levels were markedly decreased, indicating hepatoprotection. Geraniol also restored antioxidant enzyme activity and reduced markers of oxidative stress. Moreover, it lowered pro-inflammatory cytokines and elevated anti-inflammatory cytokines. Histopathological analysis confirmed reduced hepatic steatosis and inflammation.</p><p><strong>Conclusions: </strong>Geraniol demonstrated potent protective effects against HFD-induced NAFLD in rats by improving lipid metabolism, mitigating oxidative stress, and modulating inflammatory responses. These findings support its potential as a therapeutic agent for the prevention and management of NAFLD.</p>\",\"PeriodicalId\":16960,\"journal\":{\"name\":\"Journal of Pharmacy and Pharmacology\",\"volume\":\" \",\"pages\":\"1439-1449\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pharmacy and Pharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/jpp/rgaf053\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmacy and Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/jpp/rgaf053","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

目的:本研究旨在评估香叶醇对大鼠高脂饮食(HFD)诱导的非酒精性脂肪性肝病(NAFLD)的预防作用,重点关注其对脂质代谢、氧化应激和炎症的影响。方法:雄性sd大鼠饲喂HFD 10周诱导NAFLD。香叶醇口服剂量分别为50、100和200 mg/kg。评估以下参数:体重、肝脏指数、血脂(总胆固醇、甘油三酯、HDL、LDL)、血清肝酶(ALT、AST、ALP)、氧化应激标志物(MDA、SOD、CAT、GSH)和炎症标志物(TNF-α、IL-6、IL-10)。对肝组织进行组织病理学评估,以评估结构变化和炎症。主要发现:香叶醇治疗,特别是100和200 mg/kg的剂量,显著降低了饲喂hfd的大鼠的体重增加和肝脏指数。它通过降低总胆固醇、甘油三酯和低密度脂蛋白来改善脂质谱,同时增加高密度脂蛋白水平。肝酶水平明显降低,提示肝保护作用。香叶醇还能恢复抗氧化酶活性,降低氧化应激标志物。此外,它还能降低促炎细胞因子和升高抗炎细胞因子。组织病理学分析证实肝脂肪变性和炎症减轻。结论:香叶醇通过改善脂质代谢、减轻氧化应激和调节炎症反应,对hfd诱导的大鼠NAFLD具有有效的保护作用。这些发现支持其作为NAFLD预防和治疗药物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective role of geraniol in high fat diet-induced NAFLD: balancing lipid homeostasis, antioxidant defence, and inflammatory responses.

Objectives: This study aimed to evaluate the preventive effects of geraniol on non-alcoholic fatty liver disease (NAFLD) induced by a high fat diet (HFD) in a rat model, focusing on its impact on lipid metabolism, oxidative stress, and inflammation.

Methods: NAFLD was induced in male Sprague-Dawley rats by feeding them a HFD for 10 weeks. Geraniol was administered orally at doses of 50, 100, and 200 mg/kg. The following parameters were assessed: body weight, hepatic index, lipid profile (total cholesterol, triglycerides, HDL, LDL), serum hepatic enzymes (ALT, AST, ALP), oxidative stress markers (MDA, SOD, CAT, GSH), and inflammatory markers (TNF-α, IL-6, IL-10). Histopathological evaluation of liver tissues was performed to assess structural changes and inflammation.

Key findings: Geraniol treatment, particularly at 100 and 200 mg/kg, significantly reduced body weight gain and hepatic index in HFD-fed rats. It improved lipid profiles by lowering total cholesterol, triglycerides, and LDL while increasing HDL levels. Hepatic enzyme levels were markedly decreased, indicating hepatoprotection. Geraniol also restored antioxidant enzyme activity and reduced markers of oxidative stress. Moreover, it lowered pro-inflammatory cytokines and elevated anti-inflammatory cytokines. Histopathological analysis confirmed reduced hepatic steatosis and inflammation.

Conclusions: Geraniol demonstrated potent protective effects against HFD-induced NAFLD in rats by improving lipid metabolism, mitigating oxidative stress, and modulating inflammatory responses. These findings support its potential as a therapeutic agent for the prevention and management of NAFLD.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信