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强化血糖控制对糖尿病溃疡患者血清外泌体miR-126-3p和miR-125b-1-3p水平及伤口愈合的影响

Effects of Intensive Glycemic Control on Serum Exosome miR-126-3p and miR-125b-1-3p Levels and Wound Healing in Patients with Diabetic Ulcers.

作者信息

Wang Lin, Zheng Aitian, Zeng Na, Li Zheng, Tang Lizhu, Long Caidan, Wu Biaoliang

机构信息

Department of Endocrinology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China.

Department of Endocrinology, Pingshan District People's Hospital, Pingshan General Hospital of Southern Medical University, Shenzhen, Guangdong, China.

出版信息

Evid Based Complement Alternat Med. 2023 Jan 30;2023:2523245. doi: 10.1155/2023/2523245. eCollection 2023.

DOI:10.1155/2023/2523245
PMID:36756041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9902161/
Abstract

OBJECTIVE

Intensive glycemic control and exosomal miRNAs have both been reported to improve wound repair in diabetic ulcers. In this study, we aimed to investigate the effects of intensive glycemic control on serum exosome microRNA-126-3p (miR-126-3p), microRNA-125b-1-3p (miR-125b-1-3p), and wound healing in patients with diabetic ulcers.

METHODS

Herein, 45 diabetic patients with an ulcer, aged 35-75 years old, were randomly assigned to the intensive glycemic control group ( = 21) and the conventional glycemic control group ( = 24). Serum exosomes were extracted in the laboratory and assessed by Western blotting, transmission electron microscopy, and nanoparticle tracking analysis. The expression of miR-126-3p and miR-125b-1-3p was validated using quantitative real-time polymerase chain reaction. The wound healing of each diabetic ulcer patient was measured and imaged; additionally, clinical and follow-up data were collected. Finally, the clinical and laboratory data were combined for statistical analysis.

RESULTS

Intensive glycemic control was significantly more conducive to wound healing and infection control than conventional glycemic control ( < 0.05). Serum exosomal miR-126-3p was negatively correlated with fasting plasma glucose levels ( = 0.34, < 0.05) and positively associated with the wound healing rate ( = 0.45, < 0.01). The level of miR-126-3p in the intensive glycemic control group was significantly higher than that in the conventional glycemic control group ( < 0.01). Serum exosomal miR-125b-1-3p was not correlated with blood glucose levels ( = 0.03, > 0.05) and was positively associated with the wound healing rate ( = 0.33, < 0.05). No significant difference was observed in the level of miR-125b-1-3p between the intensive and conventional glycemic control groups. Regarding the prognosis of diabetic ulcers, the intensive glycemic control group was better than the conventional group ( = -2.02, < 0.05).

CONCLUSION

Serum exosome (miR-125b-1-3p and miR-126-3p) levels are correlated with wound healing in diabetic ulcers. Intensive glycemic control increases the serum exosomal miR-126-3p level, which might be one of the mechanisms that promotes wound healing in diabetic ulcers.

摘要

目的

强化血糖控制和外泌体微小RNA(miRNA)均已被报道可改善糖尿病溃疡的伤口愈合。在本研究中,我们旨在探讨强化血糖控制对糖尿病溃疡患者血清外泌体微小RNA-126-3p(miR-126-3p)、微小RNA-125b-1-3p(miR-125b-1-3p)及伤口愈合的影响。

方法

在此,45例年龄在35至75岁之间患有溃疡的糖尿病患者被随机分为强化血糖控制组(n = 21)和传统血糖控制组(n = 24)。在实验室中提取血清外泌体,并通过蛋白质免疫印迹法、透射电子显微镜和纳米颗粒跟踪分析进行评估。使用定量实时聚合酶链反应验证miR-126-3p和miR-125b-1-3p的表达。测量并拍摄每位糖尿病溃疡患者的伤口愈合情况;此外,收集临床和随访数据。最后,将临床和实验室数据合并进行统计分析。

结果

与传统血糖控制相比,强化血糖控制在促进伤口愈合和控制感染方面明显更具优势(P < 0.05)。血清外泌体miR-126-3p与空腹血糖水平呈负相关(r = 0.34,P < 0.05),与伤口愈合率呈正相关(r = 0.45,P < 0.01)。强化血糖控制组中miR-126-3p的水平显著高于传统血糖控制组(P < 0.01)。血清外泌体miR-125b-1-3p与血糖水平无相关性(r = 0.03,P > 0.05),与伤口愈合率呈正相关(r = 0.33,P < 0.05)。强化血糖控制组和传统血糖控制组之间miR-125b-1-3p的水平未观察到显著差异。关于糖尿病溃疡的预后,强化血糖控制组优于传统组(P = -2.02,P < 0.05)。

结论

血清外泌体(miR-125b-1-3p和miR-126-3p)水平与糖尿病溃疡的伤口愈合相关。强化血糖控制可提高血清外泌体miR-126-3p水平,这可能是促进糖尿病溃疡伤口愈合的机制之一。

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本文引用的文献

1
New Horizons of Macrophage Immunomodulation in the Healing of Diabetic Foot Ulcers.巨噬细胞免疫调节在糖尿病足溃疡愈合中的新视野
Pharmaceutics. 2022 Sep 27;14(10):2065. doi: 10.3390/pharmaceutics14102065.
2
Hydrogen Sulfide Improves Angiogenesis by Regulating the Transcription of pri-miR-126 in Diabetic Endothelial Cells.硫化氢通过调节糖尿病内皮细胞中 pri-miR-126 的转录促进血管生成。
Cells. 2022 Aug 25;11(17):2651. doi: 10.3390/cells11172651.
3
Exosomes from mmu_circ_0001052-modified adipose-derived stem cells promote angiogenesis of DFU via miR-106a-5p and FGF4/p38MAPK pathway.
脂肪间充质干细胞来源外泌体通过 miR-106a-5p 和 FGF4/p38MAPK 通路促进糖尿病足溃疡的血管生成。
Stem Cell Res Ther. 2022 Jul 23;13(1):336. doi: 10.1186/s13287-022-03015-7.
4
Exosome-cargoed microRNAs: Potential therapeutic molecules for diabetic wound healing.外泌体携带的 microRNAs:糖尿病创面愈合的潜在治疗分子。
Drug Discov Today. 2022 Oct;27(10):103323. doi: 10.1016/j.drudis.2022.07.008. Epub 2022 Jul 20.
5
miR-199a-5p Plays a Pivotal Role on Wound Healing via Suppressing and in Diabetic Ulcer Foot.miR-199a-5p 通过抑制和在糖尿病溃疡足中发挥关键作用促进伤口愈合。
Oxid Med Cell Longev. 2022 Apr 7;2022:4791059. doi: 10.1155/2022/4791059. eCollection 2022.
6
Regulation of endothelial progenitor cell functions during hyperglycemia: new therapeutic targets in diabetic wound healing.高血糖症对内皮祖细胞功能的调控:糖尿病创面愈合中新的治疗靶点。
J Mol Med (Berl). 2022 Apr;100(4):485-498. doi: 10.1007/s00109-021-02172-1. Epub 2022 Jan 8.
7
MiR-195-5p and miR-205-5p in extracellular vesicles isolated from diabetic foot ulcer wound fluid decrease angiogenesis by inhibiting VEGFA expression.来源于糖尿病足溃疡伤口液的细胞外囊泡中的 miR-195-5p 和 miR-205-5p 通过抑制 VEGFA 表达来减少血管生成。
Aging (Albany NY). 2021 Aug 9;13(15):19805-19821. doi: 10.18632/aging.203393.
8
Early and Intensive Glycemic Control for Diabetic Foot Ulcer Healing: A Prospective Observational Nested Cohort Study.早期强化血糖控制对糖尿病足溃疡愈合的影响:一项前瞻性观察性巢式队列研究。
Int J Low Extrem Wounds. 2023 Sep;22(3):578-587. doi: 10.1177/15347346211033458. Epub 2021 Jul 19.
9
Macrophage polarization and diabetic wound healing.巨噬细胞极化与糖尿病创面愈合。
Transl Res. 2021 Oct;236:109-116. doi: 10.1016/j.trsl.2021.05.006. Epub 2021 Jun 2.
10
Human Adipose-derived mesenchymal stem cells promote lymphocyte apoptosis and alleviate atherosclerosis via miR-125b-1-3p/BCL11B signal axis.人脂肪间充质干细胞通过miR-125b-1-3p/BCL11B信号轴促进淋巴细胞凋亡并减轻动脉粥样硬化。
Ann Palliat Med. 2021 Feb;10(2):2123-2133. doi: 10.21037/apm-21-49.