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有效简化的阿霉素诱导的慢性肾病小鼠模型:眶后静脉注射与尾静脉注射对比

Effectively simplified Adriamycin-induced chronic kidney disease mouse model: Retro-orbital vein injection versus tail-vein injection.

作者信息

Watanabe Masaki, Takimoto Hayato R, Hashimoto Kazuki, Ishii Yuki, Sasaki Nobuya

机构信息

Laboratory of Laboratory Animal Science and Medicine, School of Veterinary Medicine, Kitasato University, Towada, Japan.

出版信息

Animal Model Exp Med. 2025 Mar;8(3):568-572. doi: 10.1002/ame2.12553. Epub 2025 Jan 22.

DOI:10.1002/ame2.12553
PMID:39843403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11904100/
Abstract

This study aimed to investigate the impact of administration routes in establishing the Adriamycin (ADR)-induced chronic kidney disease (CKD) model. Using BALB/c mice, we compared the effects of conventional tail-vein injection (TV10, 10 mg/kg) to those of retro-orbital sinus (orbital vein) injection (OV10, 10 mg/kg; OV8, 8 mg/kg). The results indicated that the OV10 group exhibited CKD pathology similar to the TV10 group, with both groups demonstrating significantly higher urinary albumin/creatinine ratio (p < 0.05), tubular injury (p < 0.05), and degree of renal fibrosis (p < 0.05) than the OV8 group. No significant differences were observed between the OV10 and TV10 groups in urinary albumin/creatinine ratio, tubular injury, and degree of renal fibrosis. These findings demonstrated that retro-orbital administration of 10 mg/kg ADR induces comparable effects to conventional tail-vein administration. This technique's technical simplicity may improve experimental efficiency, reproducibility, and animal welfare in CKD research. In conclusion, this study validates the utility of retro-orbital injection in CKD model establishment, demonstrating its potential to standardize and improve the reliability of future CKD research protocols.

摘要

本研究旨在探讨给药途径对建立阿霉素(ADR)诱导的慢性肾脏病(CKD)模型的影响。我们使用BALB/c小鼠,比较了传统尾静脉注射(TV10,10mg/kg)与眶后窦(眶静脉)注射(OV10,10mg/kg;OV8,8mg/kg)的效果。结果表明,OV10组表现出与TV10组相似的CKD病理学特征,两组的尿白蛋白/肌酐比值(p<0.05)、肾小管损伤(p<0.05)和肾纤维化程度(p<0.05)均显著高于OV8组。OV10组和TV10组在尿白蛋白/肌酐比值、肾小管损伤和肾纤维化程度方面未观察到显著差异。这些发现表明,眶后注射10mg/kg ADR产生的效果与传统尾静脉注射相当。该技术操作简单,可能会提高CKD研究中的实验效率、可重复性和动物福利。总之,本研究验证了眶后注射在建立CKD模型中的实用性,表明其有潜力规范并提高未来CKD研究方案的可靠性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3998/11904100/1e90f01bcfc1/AME2-8-568-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3998/11904100/53df6c1ae534/AME2-8-568-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3998/11904100/e8cc00b39bf1/AME2-8-568-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3998/11904100/1e90f01bcfc1/AME2-8-568-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3998/11904100/53df6c1ae534/AME2-8-568-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3998/11904100/e8cc00b39bf1/AME2-8-568-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3998/11904100/1e90f01bcfc1/AME2-8-568-g002.jpg

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本文引用的文献

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Development and Characterization of a Novel FVB- Mouse Model for Adriamycin-Induced Nephropathy.一种用于阿霉素诱导的肾病的新型FVB-小鼠模型的建立与表征
Genes (Basel). 2024 Apr 4;15(4):456. doi: 10.3390/genes15040456.
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Kidney fibrosis: from mechanisms to therapeutic medicines.肾脏纤维化:从机制到治疗药物。
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Genetic background strongly influences the transition to chronic kidney disease of adriamycin nephropathy in mice.遗传背景强烈影响阿霉素肾病小鼠向慢性肾病的转变。
Exp Anim. 2023 Feb 21;72(1):47-54. doi: 10.1538/expanim.22-0057. Epub 2022 Sep 3.
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Different Patterns of Kidney Fibrosis Are Indicative of Injury to Distinct Renal Compartments.不同模式的肾纤维化提示肾脏不同节段的损伤。
Cells. 2021 Aug 6;10(8):2014. doi: 10.3390/cells10082014.
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A single amino acid substitution in PRKDC is a determinant of sensitivity to Adriamycin-induced renal injury in mouse.PRKDC 中的单个氨基酸取代是决定小鼠对阿霉素诱导的肾损伤敏感性的因素。
Biochem Biophys Res Commun. 2021 Jun 4;556:121-126. doi: 10.1016/j.bbrc.2021.03.150. Epub 2021 Apr 8.
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