Literature DB >> 30426249

Probiotics ameliorate renal ischemia-reperfusion injury by modulating the phenotype of macrophages through the IL-10/GSK-3β/PTEN signaling pathway.

Chenguang Ding1,2, Feng Han1,2, Heli Xiang1,2, Yuxiang Wang1,2, Yang Li1,2, Jin Zheng1,2, Wujun Xue1,2, Xiaoming Ding3,4, Puxun Tian5,6.   

Abstract

After renal ischemic reperfusion injury, a series of pathological changes, such as impaired intestinal barrier function, intestinal flora, and endotoxin translocation, are caused by intestinal ischemia and hypoxia, which then trigger systemic inflammatory responses and affect the condition and prognosis of the patients. In this study, a rat model of ischemia-reperfusion injury was established by examining changes in renal function, intestinal barrier function, inflammatory index, oxidative stress, and macrophage phenotypes to evaluate the effect of probiotic VSL#3 on renal ischemia-reperfusion injury. The results showed that, after VSL#3 intervention, the levels of BUN, Scr, Cys C, PRO, and NGAL were all significantly decreased compared with the I/R group, while the value of Ccr showed a significant increase. In addition, the concentrations of MPO, IL-1β, TNF-α, IL-6, ED-1, and PCNA were all significantly lower than those in the I/R group, while the levels of endotoxin, DOA, and D-lactic acid were significantly decreased. Furthermore, the proteins associated with intestinal barrier functions, such as ZO-1, Occludin, and Claudin-1, were significantly upregulated compared with the I/R group. Overall, the VSL#3 intervention group was able to maintain the required number of beneficial intestinal flora and to inhibit the proliferation of harmful bacteria. At the same time, the VSL#3 intervention could also prevent the decrease in the levels of CAT, GSH-PX, H2O2, and T-SOD, while downregulating the expression of Keap1 and Nrf2. After the intervention with the VSL#3, the expression levels of CD68 and CD86 proteins were significantly decreased, while the expression levels of CD163 and CD206 proteins were significantly higher. Further experiments confirmed that the expression of iNOS protein was significantly decreased after the VSL#3 intervention, and the expression of Arg-1 and Ym1 proteins was significantly increased. The VSL#3 was able to induce high expressions of p-GSK-3β and p-PTEN proteins, while the use of IL-10 antibody impaired the effect of the VSL#3. In summary, this research confirms that probiotics can alleviate renal dysfunction caused by ischemia and reperfusion by protecting the intestinal barrier function and maintaining the functions of intestinal flora. The pathway screening test of this study suggests that IL-10/GSK3β/PTEN may play an important role in the process of the prototypic VSL#3 inducing M2 transformation of macrophages.

Entities:  

Keywords:  IL-10/GSK-3β/PTEN signaling pathway; Macrophage phenotype; Probiotics; Renal ischemia-reperfusion injury

Year:  2018        PMID: 30426249     DOI: 10.1007/s00424-018-2213-1

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  18 in total

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3.  Atherosclerosis following renal injury is ameliorated by pioglitazone and losartan via macrophage phenotype.

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Journal:  Atherosclerosis       Date:  2015-07-04       Impact factor: 5.162

4.  PTEN regulation by the Akt/GSK-3β axis during RANKL signaling.

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5.  HMGB1 exacerbates renal tubulointerstitial fibrosis through facilitating M1 macrophage phenotype at the early stage of obstructive injury.

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6.  Impaired intestinal mucosal barrier upon ischemia-reperfusion: "patching holes in the shield with a simple surgical method".

Authors:  Olivér Rosero; Péter Ónody; Tibor Kovács; Dávid Molnár; Gábor Lotz; Szilárd Tóth; Zsolt Turóczi; András Fülöp; Dávid Garbaisz; László Harsányi; Attila Szijártó
Journal:  Biomed Res Int       Date:  2014-05-14       Impact factor: 3.411

7.  Intestinal mucosal barrier is injured by BMP2/4 via activation of NF-κB signals after ischemic reperfusion.

Authors:  Kang Chen; Wei Xie; Binyu Luo; Weidong Xiao; Daniel H Teitelbaum; Hua Yang; Kebin Zhang; Chaojun Zhang
Journal:  Mediators Inflamm       Date:  2014-07-16       Impact factor: 4.711

8.  Ginsenoside Rd alleviates mouse acute renal ischemia/reperfusion injury by modulating macrophage phenotype.

Authors:  Kaixi Ren; Chao Jin; Pengfei Ma; Qinyou Ren; Zhansheng Jia; Daocheng Zhu
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9.  Glutamine decreases intestinal mucosal injury in a rat model of intestinal ischemia-reperfusion by downregulating HMGB1 and inflammatory cytokine expression.

Authors:  Xiaoliang Shu; Jian Zhang; Qingxiu Wang; Zengguang Xu; Tingting Yu
Journal:  Exp Ther Med       Date:  2016-06-17       Impact factor: 2.447

10.  The interplay of BMP4 and IL‑7 regulates the apoptosis of intestinal intraepithelial lymphocytes under conditions of ischemia̸reperfusion.

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1.  Maternally expressed 3 protects the intestinal barrier from cardiac arrest-induced ischemia/reperfusion injury via miR-34a-3p/sirtuin 1/nuclear factor kappa B signaling.

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2.  Hirudin Regulates Vascular Function in Chronic Renal Failure through Modulating Macrophage Polarization.

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Review 3.  Crosstalk between gut microbiota and renal ischemia/reperfusion injury.

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Journal:  Front Cell Infect Microbiol       Date:  2022-09-05       Impact factor: 6.073

4.  Long Non-coding RNA MEG3 Promotes Pyroptosis in Testicular Ischemia-Reperfusion Injury by Targeting MiR-29a to Modulate PTEN Expression.

Authors:  Jin-Zhuo Ning; Kai-Xiang He; Fan Cheng; Wei Li; Wei-Min Yu; Hao-Yong Li; Ting Rao; Yuan Ruan
Journal:  Front Cell Dev Biol       Date:  2021-06-18

Review 5.  Large animal models for translational research in acute kidney injury.

Authors:  Balamurugan Packialakshmi; Ian J Stewart; David M Burmeister; Kevin K Chung; Xiaoming Zhou
Journal:  Ren Fail       Date:  2020-11       Impact factor: 2.606

  5 in total

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