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双丹明目胶囊通过调控微小RNA对大鼠糖尿病视网膜病变的影响

Effect of Shuangdan Mingmu Capsule on Diabetic Retinopathy in Rats via Regulation of miRNAs.

作者信息

Li Xiang, Yang Yijing, Song Yan, Nie Fujiao, Fu Chaojun, Qin Yuhui

机构信息

Ophthalmology Department, the First Affiliated Hospital, Hunan University of Chinese Medicine, Changsha, 410007, People's Republic of China.

Hunan Provincial Key Laboratory for the Prevention and Treatment of Ophthalmology and Otolaryngology Diseases with Chinese Medicine, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.

出版信息

Diabetes Metab Syndr Obes. 2022 Oct 19;15:3181-3194. doi: 10.2147/DMSO.S379611. eCollection 2022.

Abstract

PURPOSE

To evaluate the effects of Shuangdan Mingmu (SDMM) capsule on diabetic retinopathy in rats by regulating miRNAs.

MATERIALS AND METHODS

Streptozotocin (STZ) (50 mg/kg) was successfully used to induce diabetes in male Sprague-Dawley rats, which were randomly assigned to a group taking SDMM capsules ("diabetic+SDMM") or a control group ("diabetic"), and the normal group (n=10/group). The diabetic+SDMM capsule group received 1.89g/kg/d of SDMM capsule by gavage, whereas the other groups received the same amount of distilled water. After 12-weeks of gavage, the retina was removed from all rats for histopathological analysis, and miRNA sequencing experiments were carried out to identify the differential expression of miRNAs. These results were then confirmed by quantitative real-time polymerase chain reaction (qRT-PCR).

RESULTS

SDMM capsules improved retinal morphology, restored the number of cells in the ganglion cell layer (<0.0001) and reduced apoptosis in all retinal layers (p values in the outer nuclear layers, inner nuclear layers and ganglion cell layers 0.0001, 0.0147, 0.0034, respectively). In addition, miRNA expression was changed in rats taking SDMM capsules. Compared with the diabetic group, six miRNAs were up-regulated and four miRNAs were down-regulated in the diabetic+SDMM capsule group. The qRT-PCR validation results showed that the expression levels of miR-450b-5p, miR-1249 and miR-155-5p were consistent with the trend of miRNA sequencing results, and were all up-regulated after SDMM capsule treatment. Target gene prediction and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis of differentially expressed miRNAs showed that these pathways were mainly concentrated in the focal adhesions and PI3K/Akt, MAPK, and neural factor signaling pathways.

CONCLUSION

SDMM capsules may prevent and treat diabetic retinopathy by regulating the expression of miR-450b-5p, miR-1249 and miR-155-5p.

摘要

目的

通过调控微小RNA(miRNA)来评估双丹明目(SDMM)胶囊对大鼠糖尿病视网膜病变的影响。

材料与方法

采用链脲佐菌素(STZ)(50mg/kg)成功诱导雄性Sprague-Dawley大鼠患糖尿病,将其随机分为服用SDMM胶囊的组(“糖尿病+SDMM”)或对照组(“糖尿病”),以及正常组(每组n = 10)。糖尿病+SDMM胶囊组通过灌胃给予1.89g/kg/d的SDMM胶囊,而其他组给予等量的蒸馏水。灌胃12周后,从所有大鼠中取出视网膜进行组织病理学分析,并进行miRNA测序实验以鉴定miRNA的差异表达。然后通过定量实时聚合酶链反应(qRT-PCR)对这些结果进行验证。

结果

SDMM胶囊改善了视网膜形态,恢复了神经节细胞层中的细胞数量(<0.0001),并减少了所有视网膜层中的细胞凋亡(在外核层、内核层和神经节细胞层中的p值分别为0.0001、0.0147、0.0034)。此外,服用SDMM胶囊的大鼠中miRNA表达发生了变化。与糖尿病组相比,糖尿病+SDMM胶囊组中有6种miRNA上调,4种miRNA下调。qRT-PCR验证结果表明,miR-450b-5p、miR-1249和miR-15-5p的表达水平与miRNA测序结果的趋势一致,并且在SDMM胶囊治疗后均上调。对差异表达的miRNA进行靶基因预测和京都基因与基因组百科全书(KEGG)分析表明,这些途径主要集中在粘着斑以及PI3K/Akt、MAPK和神经因子信号通路中。

结论

SDMM胶囊可能通过调节miR-450b-5p、miR-1249和miR-155-5p的表达来预防和治疗糖尿病视网膜病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0308/9578787/17d4079d1cd9/DMSO-15-3181-g0001.jpg

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