结合网络药理分析与动物实验探讨张炎明片治疗糖尿病视网膜病变的药理机制。

IF 2.8 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Mengmeng Yang, Hualin Liu, Jiewen Zhou, Kewei Wang, Yujing Sun, Na Ning, Qiuling Huang, Jiajia Hu, Jidong Liu, Fei Yan, Xinguo Hou, Li Chen, Lingshu Wang, Fuqiang Liu
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引用次数: 0

摘要

背景:张炎明片(ZYMT)是一种含多种中药的中成药,可用于治疗多种眼病,但其对糖尿病视网膜病变(DR)的确切疗效和具体机制尚不清楚。方法:采用网络药理学分析方法,对ZYMT治疗DR的关键调控基因和潜在治疗靶点进行评价。分别给予糖尿病db/db小鼠低剂量(330 mg/kg)和高剂量(660 mg/kg) ZYMT,检测相关代谢指标。采用组织化学染色和光学相干断层扫描血管造影(OCTA)评价小鼠视网膜的组织病理结构,采用RT-qPCR、TUNEL染色和免疫荧光染色评价ZYMT对dr的抗凋亡和抗血管生成作用。网络拓扑分析结果显示,ZYMT中排名前10位的中药成分分别为槲皮素、木犀草素、山奈酚、木犀草素、柚皮素、β-谷甾醇、黄芩素、异鼠李素、阿卡辛、豆甾醇。ZYMT通过AKT1、TNF、MAPK8、RELA、VEGFA、HIF1A、IL6、CASP3、BCL2、STAT3、ICAM1等关键节点治疗DR。ZYMT对DR有直接影响,而不是对代谢指标的二次改善。组织染色表明,ZYMT改善了db/db小鼠视网膜血管形态,延缓了视网膜变薄。OCTA成像也显示ZYMT增加了db/db小鼠的血流密度。TUNEL染色和RT-qPCR结果显示,ZYMT可减少db/db小鼠视网膜细胞凋亡,RT-qPCR和免疫荧光染色显示,ZYMT可抑制视网膜新生血管形成。结论:本研究通过网络药理分析发现了ZYMT改善DR的潜在靶点,并验证了ZYMT通过发挥抗凋亡和抗新生血管的作用改善DR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combining Network Pharmacological Analysis and Animal Experiments to Explore the Pharmacological Mechanism of Zhangyanming Tablets in Diabetic Retinopathy.

Background: Zhangyanming Tablets (ZYMT) is a proprietary Chinese medicine containing a variety of traditional Chinese medicines, which can be used to treat a wide range of eye diseases, but its exact effect on diabetic retinopathy (DR) and the specific mechanism are still unclear. This study aims to investigate the ameliorative effects and specific mechanisms of ZYMT on DR.

Methods: Key regulatory genes and potential therapeutic targets of ZYMT for DR were evaluated using network pharmacological analysis. Diabetic db/db mice were given low-dose ZYMT (330 mg/kg) and high-dose ZYMT (660 mg/kg), and relevant metabolic indices were tested. Histochemical staining and optical coherence tomography angiography (OCTA) were used to evaluate the histopathological structure of mice retina, RT-qPCR, TUNEL staining and immunofluorescence staining were used to evaluate the anti-apoptosis and anti-angiogenesis effect of ZYMT on DR.

Results: The results of network topology analysis showed that the top 10 Traditional Chinese Medicine (TCM) ingredients of ZYMT were quercetin, luteolin, kaempferol, wogonin, naringenin, β-sitosterol, baicalein, isorhamnetin, acacetin, and stigmasterol. ZYMT treats DR through key nodes such as AKT1, TNF, MAPK8, RELA, VEGFA, HIF1A, IL6, CASP3, BCL2, STAT3, and ICAM1. ZYMT has a direct effect on DR rather than secondary improvement of metabolic indices. Tissue staining demonstrated that ZYMT improved retinal vascular morphology and delayed retinal thinning in db/db mice. The OCTA imaging also showed that ZYMT increased blood flow density in db/db mice. TUNEL staining and RT-qPCR results showed that ZYMT could reduce the apoptosis of retinal cells in db/db mice, and RT-qPCR and immunofluorescence staining showed that ZYMT could inhibit retinal neovascularization.

Conclusion: This study found the potential target of ZYMT to ameliorate DR through network pharmacological analysis, and verified that ZYMT can improve DR by exerting anti-apoptosis and anti-neovascularization.

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来源期刊
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.90
自引率
6.10%
发文量
431
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal. The journal is committed to the rapid publication of the latest laboratory and clinical findings in the fields of diabetes, metabolic syndrome and obesity research. Original research, review, case reports, hypothesis formation, expert opinion and commentaries are all considered for publication.
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