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糖尿病猴模型中的肾缺血再灌注损伤及人骨髓间充质干细胞的治疗性试验。

Renal Ischemia-Reperfusion Injury in a Diabetic Monkey Model and Therapeutic Testing of Human Bone Marrow-Derived Mesenchymal Stem Cells.

机构信息

Department of Surgery, Division of Transplantation, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul 06351, Republic of Korea.

Graduate School of International Agricultural Technology and Institute of Green-Bio Science and Technology, Seoul National University, 1447 Pyeongchang-daero, Pyeongchang, Gangwon-do 25354, Republic of Korea.

出版信息

J Diabetes Res. 2018 Aug 1;2018:5182606. doi: 10.1155/2018/5182606. eCollection 2018.

Abstract

Clinically, acute kidney injury (AKI) episodes in diabetes mellitus (DM) patients are associated with a cumulative risk of developing end-stage renal disease. In this study, we asked whether the severity of AKI induced by renal ischemia-reperfusion injury (IRI) is more prominent in DM than in non-DM control using a cynomolgus monkey ( model. We also investigated whether human bone marrow-derived mesenchymal stem cells (hBM-MSCs) infused via the renal artery could ameliorate renal IRI in DM monkeys. The experimental data, including mortality rate, histologic findings, and urinary albumin secretion indicate that the severity of AKI was greater in DM monkeys than in control animals. Moreover, histological findings and qRT-PCR analysis of mRNA in renal biopsy tissue showed that hBM-MSC promoted the recovery of tubular damage caused by AKI. Serum analysis also revealed that the level of albumin and ALT was increased 24 and 48 hours after AKI, respectively, suggesting that AKI induced acute liver injury. We suggest that this nonhuman primate model could provide essential information about the renal and nonrenal impairment related to DM and help determine the clinical usefulness of MSCs in AKI.

摘要

临床上,糖尿病(DM)患者的急性肾损伤(AKI)发作与终末期肾病的发展累积风险相关。在这项研究中,我们使用食蟹猴(模型),询问了由肾缺血再灌注损伤(IRI)引起的 AKI 在 DM 患者中是否比在非 DM 对照中更为显著。我们还研究了经肾动脉输注的人骨髓间充质干细胞(hBM-MSCs)是否可以改善 DM 猴的肾 IRI。实验数据包括死亡率、组织学发现和尿白蛋白分泌表明,DM 猴的 AKI 严重程度大于对照动物。此外,肾脏活检组织的组织学发现和 qRT-PCR 分析表明,hBM-MSC 促进了 AKI 引起的肾小管损伤的恢复。血清分析还表明,AKI 后 24 小时和 48 小时,白蛋白和 ALT 水平分别升高,提示 AKI 引起急性肝损伤。我们建议该非人类灵长类动物模型可以提供与 DM 相关的肾脏和非肾脏损伤的重要信息,并有助于确定 MSC 在 AKI 中的临床应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0d0/6092988/573353a903b6/JDR2018-5182606.001.jpg

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