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叶提取物对高脂饮食诱导的肥胖小鼠模型中胰岛素抵抗和炎症的预防作用,该模型对罗格列酮有反应。

Preventive effects of leaf extract on insulin resistance and inflammation in a model of high fat diet-induced obesity in mice that responds to rosiglitazone.

作者信息

Ben Khedher Mohamed R, Hammami Mohamed, Arch Jonathan R S, Hislop David C, Eze Dominic, Wargent Edward T, Kępczyńska Małgorzata A, Zaibi Mohamed S

机构信息

Biochemistry Department, Research Laboratory 'Nutrition-Functional Food & Vascular Health', Faculty of Medicine, University of Monastir, Monastir, Tunisia.

Buckingham Institute for Translational Medicine (BITM), Clore Laboratory, University of Buckingham, Buckingham, United Kingdom.

出版信息

PeerJ. 2018 Jan 9;6:e4166. doi: 10.7717/peerj.4166. eCollection 2018.

Abstract

BACKGROUND

(sage) is a native plant to the Mediterranean region and has been used for a long time in traditional medicine for various diseases. We investigated possible anti-diabetic, anti-inflammatory and anti-obesity effects of sage methanol (MetOH) extract in a nutritional mouse model of obesity, inflammation and insulin resistance, as well as its effects on lipolysis and lipogenesis in 3T3-L1 cells.

METHODS

Diet-induced obese (DIO) mice were treated for five weeks with sage methanol extract (100 and 400 mg kg/day bid), or rosiglitazone (3 mg kg/day bid), as a positive control. Energy expenditure, food intake, body weight, fat mass, liver glycogen and lipid content were evaluated. Blood glucose, and plasma levels of insulin, lipids leptin and pro- and anti-inflammatory cytokines were measured throughout the experiment. The effects of sage MetOH extract on lipolysis and lipogenesis were tested in 3T3-L1 cells.

RESULTS

After two weeks of treatment, the lower dose of sage MetOH extract decreased blood glucose and plasma insulin levels during an oral glucose tolerance test (OGTT). An insulin tolerance test (ITT), performed at day 29 confirmed that sage improved insulin sensitivity. Groups treated with low dose sage and rosiglitazone showed very similar effects on OGTT and ITT. Sage also improved HOMA-IR, triglycerides and NEFA. Treatment with the low dose increased the plasma levels of the anti-inflammatory cytokines IL-2, IL-4 and IL-10 and reduced the plasma level of the pro-inflammatory cytokines IL-12, TNF-α, and KC/GRO. The GC analysis revealed the presence of two PPARs agonist in sage MetOH extract. , the extract reduced in a dose-related manner the accumulation of lipid droplets; however no effect on lipolysis was observed.

CONCLUSIONS

Sage MetOH extract at low dose exhibits similar effects to rosiglitazone. It improves insulin sensitivity, inhibits lipogenesis in adipocytes and reduces inflammation as judged by plasma cytokines. Sage presents an alternative to pharmaceuticals for the treatment of diabetes and associated inflammation.

摘要

背景

鼠尾草是地中海地区的本土植物,长期以来在传统医学中用于治疗各种疾病。我们在肥胖、炎症和胰岛素抵抗的营养小鼠模型中研究了鼠尾草甲醇提取物可能的抗糖尿病、抗炎和抗肥胖作用,以及其对3T3-L1细胞脂肪分解和脂肪生成的影响。

方法

饮食诱导肥胖(DIO)小鼠用鼠尾草甲醇提取物(100和400毫克/千克/天,每日两次)或罗格列酮(3毫克/千克/天,每日两次)作为阳性对照治疗五周。评估能量消耗、食物摄入量、体重、脂肪量、肝糖原和脂质含量。在整个实验过程中测量血糖以及胰岛素、脂质、瘦素和促炎及抗炎细胞因子的血浆水平。在3T3-L1细胞中测试鼠尾草甲醇提取物对脂肪分解和脂肪生成的影响。

结果

治疗两周后,较低剂量的鼠尾草甲醇提取物在口服葡萄糖耐量试验(OGTT)期间降低了血糖和血浆胰岛素水平。在第29天进行的胰岛素耐量试验(ITT)证实鼠尾草改善了胰岛素敏感性。用低剂量鼠尾草和罗格列酮治疗的组在OGTT和ITT上显示出非常相似的效果。鼠尾草还改善了HOMA-IR、甘油三酯和NEFA。低剂量治疗增加了抗炎细胞因子IL-2、IL-4和IL-10的血浆水平,并降低了促炎细胞因子IL-12、TNF-α和KC/GRO的血浆水平。气相色谱分析显示鼠尾草甲醇提取物中存在两种PPARs激动剂。该提取物以剂量相关的方式减少了脂滴的积累;然而,未观察到对脂肪分解的影响。

结论

低剂量的鼠尾草甲醇提取物表现出与罗格列酮相似的效果。它改善胰岛素敏感性,抑制脂肪细胞中的脂肪生成,并根据血浆细胞因子判断减少炎症。鼠尾草为糖尿病及相关炎症的治疗提供了一种药物替代品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9531/5765810/f5db988332c9/peerj-06-4166-g001.jpg

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