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用链脲佐菌素诱导的糖尿病肾病小鼠模型的实验室和临床发现。

Laboratory and clinical findings in mouse models of diabetic nephropathy induced with streptozotocin.

机构信息

Medical Student, HangTuah University, Surabaya, Indonesia.

Department of Hyperbaric, Faculty of Medicine, Hang Tuah University, Surabaya, Indonesia.

出版信息

BMC Endocr Disord. 2023 Nov 22;23(1):254. doi: 10.1186/s12902-023-01504-1.

DOI:10.1186/s12902-023-01504-1
PMID:37990213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10664383/
Abstract

BACKGROUND

Diabetic nephropathy (DN) represents a microvascular complication of diabetes mellitus (DM). Despite the increasing incidence and prevalence of DN, conservative therapy only reduces risk factors and hemodialysis. This research aimed at finding DN animal model that can be tried to be given an alternative treatment. DN was assessed by evaluating body weight, blood glucose, proteinuria, and kidney histopathology.

METHODS

Wistar novergicus male rats were induced with 75 mg of streptozotocin per kg BW to obtain a diabetic nephropathy model. The 18 rats were divided into 2 groups consisting of 9 rats in the negative group (G0) and 9 rats in the positive group (G1). Indicators of body weight, blood glucose levels, urine protein and kidney histopathology determine the incidents of DN animal models.

RESULT

Rats induced using 75 mg of streptozotocin per kg body weight (BW) indicated weight loss, increased blood glucose, urine protein levels and histopathological features of DN.

CONCLUSION

Seventy-five mg of streptozotocin per kg BW can induce a diabetic nephropathy animal model in Wistar norvegicus rats.

摘要

背景

糖尿病肾病(DN)是糖尿病(DM)的一种微血管并发症。尽管 DN 的发病率和患病率不断上升,但保守治疗仅能降低风险因素和进行血液透析。本研究旨在寻找可尝试替代治疗的 DN 动物模型。通过评估体重、血糖、蛋白尿和肾脏组织病理学来评估 DN。

方法

使用 75mg/kg BW 的链脲佐菌素诱导雄性 Wistar norvegicus 大鼠建立糖尿病肾病模型。将 18 只大鼠分为两组,每组 9 只,分别为阴性组(G0)和阳性组(G1)。体重、血糖水平、尿蛋白和肾脏组织病理学等指标确定 DN 动物模型的发生率。

结果

使用 75mg/kg BW 的链脲佐菌素诱导的大鼠体重减轻、血糖升高、尿蛋白水平升高,并出现 DN 的组织病理学特征。

结论

75mg/kg BW 的链脲佐菌素可诱导 Wistar norvegicus 大鼠发生糖尿病肾病动物模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/06e5b789e04d/12902_2023_1504_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/6e54a3dfecdb/12902_2023_1504_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/53e5453a6099/12902_2023_1504_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/7417b67e9603/12902_2023_1504_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/24aee07951ef/12902_2023_1504_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/56e275ec6fba/12902_2023_1504_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/f357c4c366bd/12902_2023_1504_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/bfa2a5d70f20/12902_2023_1504_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/06e5b789e04d/12902_2023_1504_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/6e54a3dfecdb/12902_2023_1504_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/4231e157e416/12902_2023_1504_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/53e5453a6099/12902_2023_1504_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/7417b67e9603/12902_2023_1504_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/24aee07951ef/12902_2023_1504_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/56e275ec6fba/12902_2023_1504_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/f357c4c366bd/12902_2023_1504_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/bfa2a5d70f20/12902_2023_1504_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef39/10664383/06e5b789e04d/12902_2023_1504_Fig9_HTML.jpg

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本文引用的文献

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Up-Date on Diabetic Nephropathy.糖尿病肾病的最新进展
Life (Basel). 2022 Aug 8;12(8):1202. doi: 10.3390/life12081202.
2
Microtubule associated protein 4 phosphorylation-induced epithelial-to-mesenchymal transition of podocyte leads to proteinuria in diabetic nephropathy.微管相关蛋白 4 磷酸化诱导足细胞上皮-间质转化导致糖尿病肾病蛋白尿。
Cell Commun Signal. 2022 Jul 28;20(1):115. doi: 10.1186/s12964-022-00883-7.
3
could alleviate streptozotocin-induced diabetic nephropathy in rats by activating Nrf2 signaling.可以通过激活 Nrf2 信号通路来减轻链脲佐菌素诱导的大鼠糖尿病肾病。
Sci Prog. 2022 Apr-Jun;105(2):368504221102751. doi: 10.1177/00368504221102751.
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Recent therapeutic targets in diabetic nephropathy.糖尿病肾病的近期治疗靶点。
Int J Clin Pract. 2021 Nov;75(11):e14650. doi: 10.1111/ijcp.14650. Epub 2021 Aug 10.
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Diabetic Nephropathy: Challenges in Pathogenesis, Diagnosis, and Treatment.糖尿病肾病:发病机制、诊断和治疗的挑战。
Biomed Res Int. 2021 Jul 8;2021:1497449. doi: 10.1155/2021/1497449. eCollection 2021.
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Might hyperbaric oxygen therapy (HBOT) reduce renal injury in diabetic people with diabetes mellitus? From preclinical models to human metabolomics.高压氧疗法(HBOT)能否降低糖尿病患者的肾损伤?从临床前模型到人类代谢组学。
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Diabetic Kidney Disease: Challenges, Progress, and Possibilities.糖尿病肾病:挑战、进展与可能。
Clin J Am Soc Nephrol. 2017 Dec 7;12(12):2032-2045. doi: 10.2215/CJN.11491116. Epub 2017 May 18.
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Diabetic nephropathy - complications and treatment.糖尿病肾病——并发症与治疗
Int J Nephrol Renovasc Dis. 2014 Oct 15;7:361-81. doi: 10.2147/IJNRD.S40172. eCollection 2014.
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Trends in prevalence of diabetes in Asian countries.亚洲国家糖尿病患病率的变化趋势。
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Pathologic classification of diabetic nephropathy.糖尿病肾病的病理分类。
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