• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

脾缺血预处理减轻肾缺血再灌注损伤。

Renal ischemia-reperfusion injury attenuated by splenic ischemic preconditioning.

机构信息

Department of Urology, Northern Jiangsu People's Hospital, Yangzhou, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Apr;22(7):2134-2142. doi: 10.26355/eurrev_201804_14747.

DOI:10.26355/eurrev_201804_14747
PMID:29687873
Abstract

OBJECTIVE

To investigate the therapeutic effect of splenic ischemic preconditioning (sIPC) on renal ischemia-reperfusion (IR) injury.

MATERIALS AND METHODS

A total of 18 adult male Sprague Dawley (SD) rats were treated by 45 min renal ischemia and followed by 24 h reperfusion. In the sIPC group, three cycles of splenic ischemic preconditioning including 5 min ischemia and 5 min reperfusion were carried out before renal ischemia. The blood samples and kidney tissues were collected after 24 h. The levels of Cr and BUN in serum were measured to evaluate the kidney function. The morphological changes in ischemia-reperfusion kidneys were determined by hematoxylin-eosin (HE) staining. The levels of pro-inflammatory cytokines including TNF-α and IL-6 in serum, and renal tissues, were measured by ELISA and Western Blotting. Furthermore, the levels of IKK-β, intra-nuclear NF-κB, p65, and IL-10 in renal tissues were also measured.

RESULTS

The results demonstrated that the level of Cr and BUN in the IR group were increased while decreased in the sIPC group. HE staining showed that the damage caused by renal ischemia-reperfusion was attenuated by sIPC with a low renal injury score in the sIPC group. ELISA and Western Blotting results showed that the production and secretion of TNF-α and IL-6 induced by IR were inhibited by sIPC. The expression level of IKK-β and intranuclear p65 in renal tissues were increased in the IR group while sIPC had exhibited the function of depressing the increased expression levels of IKK-β and intranuclear p65. Compared with the IR group, the expression level of IL-10 of serum and renal tissues in the sIPC group were increased.

CONCLUSIONS

sIPC exhibited a potent anti-inflammatory capacity to attenuated renal IR injury.

摘要

目的

探讨脾缺血预处理(sIPC)对肾缺血再灌注(IR)损伤的治疗作用。

材料与方法

18 只成年雄性 Sprague Dawley(SD)大鼠行 45 分钟肾缺血,随后再灌注 24 小时。在 sIPC 组,在肾缺血前进行了 3 个周期的脾缺血预处理,包括 5 分钟缺血和 5 分钟再灌注。24 小时后采集血样和肾组织。检测血清 Cr 和 BUN 水平以评估肾功能。通过苏木精-伊红(HE)染色观察缺血再灌注肾脏的形态变化。通过 ELISA 和 Western Blotting 检测血清和肾组织中促炎细胞因子 TNF-α和 IL-6 的水平。此外,还测量了肾组织中 IKK-β、核内 NF-κB、p65 和 IL-10 的水平。

结果

结果表明,IR 组 Cr 和 BUN 水平升高,sIPC 组降低。HE 染色显示 sIPC 减轻了肾缺血再灌注引起的损伤,sIPC 组的肾损伤评分较低。ELISA 和 Western Blotting 结果表明,sIPC 抑制了 IR 引起的 TNF-α和 IL-6 的产生和分泌。IR 组肾组织中 IKK-β 和核内 p65 的表达水平升高,而 sIPC 具有抑制 IKK-β 和核内 p65 表达水平升高的作用。与 IR 组相比,sIPC 组血清和肾组织中 IL-10 的表达水平升高。

结论

sIPC 具有抗炎作用,可减轻肾 IR 损伤。

相似文献

1
Renal ischemia-reperfusion injury attenuated by splenic ischemic preconditioning.脾缺血预处理减轻肾缺血再灌注损伤。
Eur Rev Med Pharmacol Sci. 2018 Apr;22(7):2134-2142. doi: 10.26355/eurrev_201804_14747.
2
Osthole Preconditioning Protects Rats Against Renal Ischemia-Reperfusion Injury.蛇床子素预处理可保护大鼠免受肾缺血再灌注损伤。
Transplant Proc. 2015 Jul-Aug;47(6):1620-6. doi: 10.1016/j.transproceed.2015.06.011.
3
Renal Ischemia-reperfusion Injury Attenuated by Exosomes Extracted From Splenic Ischemic Preconditioning Models.脾缺血预处理模型提取的外泌体减轻肾缺血再灌注损伤。
Transplantation. 2023 Apr 1;107(4):e90-e97. doi: 10.1097/TP.0000000000004514. Epub 2023 Feb 1.
4
Ischemic preconditioning improves rat kidney allograft function after ischemia/reperfusion injury: the role of tumor necrosis factor-alpha.缺血预处理改善大鼠肾脏移植术后缺血/再灌注损伤的功能:肿瘤坏死因子-α的作用
Transplant Proc. 2008 Dec;40(10):3316-20. doi: 10.1016/j.transproceed.2008.06.113.
5
Ischemic preconditioning ameliorates intestinal injury induced by ischemia-reperfusion in rats.缺血预处理可改善大鼠缺血再灌注所致的肠道损伤。
World J Gastroenterol. 2015 Jul 14;21(26):8081-8. doi: 10.3748/wjg.v21.i26.8081.
6
Splenic ischemic preconditioning attenuates oxidative stress induced by hepatic ischemia-reperfusion in rats.脾缺血预处理减轻大鼠肝脏缺血再灌注诱导的氧化应激。
Acta Cir Bras. 2019 Sep 16;34(7):e201900707. doi: 10.1590/s0102-865020190070000007.
7
Ischemic preconditioning attenuates renal ischemia-reperfusion injury by inhibiting activation of IKKbeta and inflammatory response.缺血预处理通过抑制 IKKβ 的激活和炎症反应来减轻肾缺血再灌注损伤。
Am J Nephrol. 2009;30(3):287-94. doi: 10.1159/000225928. Epub 2009 Jun 16.
8
Renal ischaemia-reperfusion injury is promoted by transcription factor NF-kB p65, which inhibits TRPC6 expression by activating miR-150.肾缺血再灌注损伤是由转录因子 NF-κB p65 促进的,它通过激活 miR-150 抑制 TRPC6 的表达。
Clin Hemorheol Microcirc. 2024;86(3):369-382. doi: 10.3233/CH-231979.
9
Dexmedetomidine Preconditioning Protects Rats from Renal Ischemia-Reperfusion Injury Accompanied with Biphasic Changes of Nuclear Factor-Kappa B Signaling.右美托咪定预处理可保护大鼠免受肾缺血再灌注损伤,并伴有核因子-κB 信号的双相变化。
J Immunol Res. 2020 Apr 17;2020:3230490. doi: 10.1155/2020/3230490. eCollection 2020.
10
Ischaemic preconditioning prevents the liver inflammatory response to lung ischaemia/reperfusion in a swine lung autotransplant model.缺血预处理可预防猪肺自体移植模型中肺缺血/再灌注引起的肝脏炎症反应。
Eur J Cardiothorac Surg. 2013 Jun;43(6):1194-201. doi: 10.1093/ejcts/ezs599. Epub 2012 Nov 23.

引用本文的文献

1
Nephroprotective role of resveratrol in renal ischemia-reperfusion injury: a preclinical study in Sprague-Dawley rats.白藜芦醇在肾缺血再灌注损伤中的肾保护作用:Sprague-Dawley 大鼠的临床前研究。
BMC Pharmacol Toxicol. 2024 Oct 28;25(1):82. doi: 10.1186/s40360-024-00809-8.
2
The Effect of Interleukin-10 Immunotherapy on Renal Ischemia-Reperfusion Injury: A Systematic Review and Meta-Analysis of Preclinical Studies.白细胞介素-10 免疫疗法对肾缺血再灌注损伤的影响:临床前研究的系统评价和荟萃分析。
Int J Mol Sci. 2024 Jun 5;25(11):6231. doi: 10.3390/ijms25116231.
3
-based feed supplement protects against renal ischaemia/reperfusion injury via downregulation of Bax/caspase 3 signaling.
基于[具体物质]的饲料补充剂通过下调Bax/半胱天冬酶3信号通路来预防肾缺血/再灌注损伤。
Front Nutr. 2024 Apr 23;11:1396864. doi: 10.3389/fnut.2024.1396864. eCollection 2024.
4
Comprehensive Overview of Innovative Strategies in Preventing Renal Ischemia-reperfusion Injury: Insights from Bibliometric and Analyses.预防肾缺血再灌注损伤创新策略的综合概述:文献计量学及分析见解
Curr Pharm Des. 2024;30(20):1578-1598. doi: 10.2174/0113816128283420240409050754.
5
Salidroside inhibits renal ischemia/reperfusion injury‑induced ferroptosis by the PI3K/AKT signaling pathway.红景天苷通过PI3K/AKT信号通路抑制肾缺血/再灌注损伤诱导的铁死亡。
Exp Ther Med. 2023 Sep 14;26(5):507. doi: 10.3892/etm.2023.12206. eCollection 2023 Nov.
6
Is Renal Ischemic Preconditioning an Alternative to Ameliorate the Short- and Long-Term Consequences of Acute Kidney Injury?肾缺血预处理是改善急性肾损伤短期和长期后果的替代方法吗?
Int J Mol Sci. 2023 May 6;24(9):8345. doi: 10.3390/ijms24098345.
7
TRPC6 ameliorates renal ischemic reperfusion injury by inducing Zn influx and activating autophagy to resist necrosis.瞬时受体电位阳离子通道蛋白6通过诱导锌内流和激活自噬来抵抗坏死,从而改善肾脏缺血再灌注损伤。
Ann Transl Med. 2022 Mar;10(5):249. doi: 10.21037/atm-21-5837.
8
Formononetin protects against cisplatin‑induced acute kidney injury through activation of the PPARα/Nrf2/HO‑1/NQO1 pathway.芒柄花素通过激活 PPARα/Nrf2/HO-1/NQO1 通路来防治顺铂诱导的急性肾损伤。
Int J Mol Med. 2021 Feb;47(2):511-522. doi: 10.3892/ijmm.2020.4805. Epub 2020 Dec 1.
9
Effect of sodium ()-2-hydroxyglutarate in male, and succinic acid in female Wistar rats against renal ischemia-reperfusion injury, suggesting a role of the HIF-1 pathway.(-)-2-羟基戊二酸对雄性Wistar大鼠的影响以及琥珀酸对雌性Wistar大鼠抗肾缺血再灌注损伤的影响,提示缺氧诱导因子-1(HIF-1)通路的作用。
PeerJ. 2020 Jul 10;8:e9438. doi: 10.7717/peerj.9438. eCollection 2020.
10
Splenic ischemic preconditioning attenuates oxidative stress induced by hepatic ischemia-reperfusion in rats.脾缺血预处理减轻大鼠肝脏缺血再灌注诱导的氧化应激。
Acta Cir Bras. 2019 Sep 16;34(7):e201900707. doi: 10.1590/s0102-865020190070000007.