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从L.根部分离出的苯醌通过抑制TLR4/NF-κB信号通路对链脲佐菌素诱导的糖尿病小鼠的保护作用。

Protective Effect of Benzoquinone Isolated from the Roots of L. on Streptozotocin-Induced Diabetic Mice by Inhibiting the TLR4/NF-κB Signaling Pathway.

作者信息

Qin Luhui, Zhang Xiaolin, Zhou Xing, Wu Xingchun, Huang Xiang, Chen Ming, Wu Yani, Lu Shunyu, Zhang Hongliang, Xu Xiaohui, Wei Xiaojie, Zhang Shijun, Huang Renbin

机构信息

Pharmaceutical College, Guangxi Medical University, Nanning, Guangxi, People's Republic of China.

Center for Translational Medicine, Key Laboratory of Longevity and Aging-Related Diseases, Ministry of Education, School of Preclinical Medicine, Guangxi Medical University, Nanning, Guangxi, People's Republic of China.

出版信息

Diabetes Metab Syndr Obes. 2020 Jun 22;13:2129-2138. doi: 10.2147/DMSO.S241998. eCollection 2020.

DOI:10.2147/DMSO.S241998
PMID:32606871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7319517/
Abstract

BACKGROUND

Studies have demonstrated that the roots of L. , a traditional Chinese medicine, can be used to treat diabetes and diabetes-related diseases. Nevertheless, the potential beneficial effects and mechanism of benzoquinone isolated from the roots of L. (BACR) on diabetes remain unclear.

METHODS

Diabetic Kunming mice were injected with STZ (120 mgkg) in the tail vein. Fasting blood glucose (FBG) and the change of body weight were measured after oral administration of BACR (120, 60, 30 mg/kg/d) every week. The levels of the total cholesterol (TC), triglyceride (TG), free fatty acids (FFA), glucosylated hemoglobin (GHb), fasting insulin (FINS), tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) were measured. The histological examination of pancreatic tissues and the TLR4/NF-κB pathway was analyzed by RT-PCR, immunohistochemistry and Western blot.

RESULTS

The study found that clearly the BACR obviously reduced the blood glucose, serum lipids, GHb and FINS. In addition, BACR treatment markedly reduced the release of inflammatory factors, including IL-6 and TNF-α, and down-regulated the expression of the TLR4/NF-κB pathway.

CONCLUSION

BACR has potential benefits for the treatment of diabetes by ameliorating metabolic functions and attenuating the inflammatory response via inhibition of the activation of theTLR4/NF-κB pathway.

摘要

背景

研究表明,中药[植物名称未给出]的根可用于治疗糖尿病及糖尿病相关疾病。然而,从[植物名称未给出]的根中分离出的苯醌(BACR)对糖尿病的潜在有益作用及其机制仍不清楚。

方法

将链脲佐菌素(STZ,120mg/kg)尾静脉注射到糖尿病昆明小鼠体内。每周口服BACR(120、60、30mg/kg/d)后测量空腹血糖(FBG)和体重变化。检测总胆固醇(TC)、甘油三酯(TG)、游离脂肪酸(FFA)、糖化血红蛋白(GHb)、空腹胰岛素(FINS)、肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)的水平。通过RT-PCR、免疫组织化学和蛋白质印迹法分析胰腺组织的组织学检查及TLR4/NF-κB信号通路。

结果

研究发现,BACR明显降低了血糖、血脂、GHb和FINS。此外,BACR治疗显著降低了包括IL-6和TNF-α在内的炎症因子的释放,并下调了TLR4/NF-κB信号通路的表达。

结论

BACR通过改善代谢功能和抑制TLR4/NF-κB信号通路的激活来减轻炎症反应,对糖尿病治疗具有潜在益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/15d06e37f8dc/DMSO-13-2129-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/b5ef96782ae1/DMSO-13-2129-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/7e38aac6ab73/DMSO-13-2129-g0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/a825b323b76a/DMSO-13-2129-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/0c51e98f5087/DMSO-13-2129-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/ed88911985ab/DMSO-13-2129-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/4d5ea26c85df/DMSO-13-2129-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/5c2216f7a7c3/DMSO-13-2129-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/15d06e37f8dc/DMSO-13-2129-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/b5ef96782ae1/DMSO-13-2129-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/7e38aac6ab73/DMSO-13-2129-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/63507f61a8dc/DMSO-13-2129-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/a825b323b76a/DMSO-13-2129-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/0c51e98f5087/DMSO-13-2129-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/ed88911985ab/DMSO-13-2129-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/4d5ea26c85df/DMSO-13-2129-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/5c2216f7a7c3/DMSO-13-2129-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcb5/7319517/15d06e37f8dc/DMSO-13-2129-g0009.jpg

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