Literature DB >> 26629116

Influence of mesenchymal stem cells on expression of AQP1 and AQP2 in rats with nephropathy induced by adriamycin.

Yi-Hua Bai1, Hong-Ying Jiang1, Xi-Yan Lian1, Jian-Song Wang2, Jia-Ping Wang3.   

Abstract

This study aims to explore the therapeutic effect of bone marrow mesenchymal stem cells on adriamycin nephrosis, and the potential mechanism. The rat experimental nephropathy model was established by unilateral nephrectomy combined repeated injecting adriamycin (ADR). Thirty adriamycin nephrosis rats were randomly divided into three groups, including ADR (n=10), MSCs transplantation through peripheral veins groups (M-V, n=10), and MSCs transplantation through right renal artery groups (M-A, n=10), and there was another normal control group (N, n=10). This study lasted 8 weeks, 24 hours urine was collected through simple metabolic cage to measure urinary volume and urine protein quantitation in 24 hours. The levels of plasma albumin (ALB), sodium were measured by biochemical analysis. The expressions of AQP1-2 were measured by immuno-histochemistry assay. Kidney medulla ultramicroscopic structure was observed by TEM. The results indicated that the ALB and 24 h urinary volume have significant increased in M-V and M-A group compared to the ADR group (P<0.05). Furthermore, the serum sodium and urine protein quantitation in 24 hours were decreased in M-V and M-A group compared to ADR group (P<0.05). Protein expression of AQP1-2 had been remarkably decreased (P<0.05). It showed degenerative changes of kidney ultra microscopic structures of the ADR rats, while MSCs transplantation could significantly improve the damage. In conclusion, in adriamycin nephropathy rats, MSCs transplantation exerts its therapeutic effects by decrease urinary albumin excretion, increase ALB, decrease sodium and the expression of AQP1-2 in renal tubules.

Entities:  

Keywords:  AQP1; AQP2; Mesenchymal stem cells; adriamycin nephropathy; urinary volume

Year:  2015        PMID: 26629116      PMCID: PMC4659005     

Source DB:  PubMed          Journal:  Int J Clin Exp Med        ISSN: 1940-5901


  11 in total

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3.  Novel autosomal recessive gene mutations in aquaporin-2 in two Chinese congenital nephrogenic diabetes insipidus pedigrees.

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5.  Association of nitric oxide production and apoptosis in a model of experimental nephropathy.

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6.  The effect of mesenchymal stromal cells on doxorubicin-induced nephropathy in rats.

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Journal:  Cytotherapy       Date:  2013-03-14       Impact factor: 5.414

7.  Transplantation of bone marrow-derived MSCs improves cisplatinum-induced renal injury through paracrine mechanisms.

Authors:  Kang Cheng; Partab Rai; Andrei Plagov; Xiqian Lan; Dileep Kumar; Divya Salhan; Shabina Rehman; Ashwani Malhotra; Kuldeep Bhargava; Christopher J Palestro; Sanjeev Gupta; Pravin C Singhal
Journal:  Exp Mol Pathol       Date:  2013-03-25       Impact factor: 3.362

8.  Ulinastatin attenuates cerebral ischemia-reperfusion injury in rats.

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Journal:  Int J Clin Exp Med       Date:  2014-05-15

Review 9.  Autologous and allogeneic mesenchymal stem cells in organ transplantation: what do we know about their safety and efficacy?

Authors:  Senthilkumar Alagesan; Matthew D Griffin
Journal:  Curr Opin Organ Transplant       Date:  2014-02       Impact factor: 2.640

10.  Neph1 is reduced in primary focal segmental glomerulosclerosis, minimal change nephrotic syndrome, and corresponding experimental animal models of adriamycin-induced nephropathy and puromycin aminonucleoside nephrosis.

Authors:  Jenny Hulkko; Jaakko Patrakka; Mark Lal; Karl Tryggvason; Kjell Hultenby; Annika Wernerson
Journal:  Nephron Extra       Date:  2014-09-19
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