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Hepatoprotective effect of bone marrow-derived mesenchymal stromal cells in CCl(4)-induced liver cirrhosis

Bone marrow mesenchymal stromal cells (BM-MSCs) are multipotent stem cells which are ideal candidates for use in regenerative medicine. The objectives of this study were to evaluate the hepatoprotective effect of BM-MSC and its combination treatment with silymarin in carbon tetrachloride (CCl(4))-in...

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Autores principales: Aithal, Ashwini P., Bairy, Laxminarayana K., Seetharam, Raviraja N., Kumar, Naveen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847925/
https://www.ncbi.nlm.nih.gov/pubmed/33564610
http://dx.doi.org/10.1007/s13205-021-02640-y
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author Aithal, Ashwini P.
Bairy, Laxminarayana K.
Seetharam, Raviraja N.
Kumar, Naveen
author_facet Aithal, Ashwini P.
Bairy, Laxminarayana K.
Seetharam, Raviraja N.
Kumar, Naveen
author_sort Aithal, Ashwini P.
collection PubMed
description Bone marrow mesenchymal stromal cells (BM-MSCs) are multipotent stem cells which are ideal candidates for use in regenerative medicine. The objectives of this study were to evaluate the hepatoprotective effect of BM-MSC and its combination treatment with silymarin in carbon tetrachloride (CCl(4))-induced liver cirrhosis animal model and to investigate whether tail vein or portal vein infusion was the ideal route for BM-MSC transplantation. 36 female Wistar rats were randomly divided into six groups (n = 6): Group 1 (normal control), Group 2 (received only CCl(4), disease model), Group 3 (CCl(4) + BM-MSCs through tail vein), Group 4 (CCl(4) + BM-MSCs through portal vein), Group 5 (CCl(4) + silymarin), Group 6 (CCl(4) + BM-MSCs + silymarin). On the 21st day after treatment, blood samples were collected for biochemical estimations. After the experiment, the rats were sacrificed. Liver was dissected out and processed for histopathology and scanning electron microscopy studies. Liver enzyme and marker analysis, histopathological studies indicated that the combination of BM-MSCs and silymarin was effective in treating liver cirrhosis. Transplanted BM-MSCs in combination with silymarin ameliorated the liver tissue damage through their immunoregulatory activities. Among the two routes, the intravenous administration of cells through the tail vein was found to be more effective and safe.
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spelling pubmed-78479252021-02-08 Hepatoprotective effect of bone marrow-derived mesenchymal stromal cells in CCl(4)-induced liver cirrhosis Aithal, Ashwini P. Bairy, Laxminarayana K. Seetharam, Raviraja N. Kumar, Naveen 3 Biotech Original Article Bone marrow mesenchymal stromal cells (BM-MSCs) are multipotent stem cells which are ideal candidates for use in regenerative medicine. The objectives of this study were to evaluate the hepatoprotective effect of BM-MSC and its combination treatment with silymarin in carbon tetrachloride (CCl(4))-induced liver cirrhosis animal model and to investigate whether tail vein or portal vein infusion was the ideal route for BM-MSC transplantation. 36 female Wistar rats were randomly divided into six groups (n = 6): Group 1 (normal control), Group 2 (received only CCl(4), disease model), Group 3 (CCl(4) + BM-MSCs through tail vein), Group 4 (CCl(4) + BM-MSCs through portal vein), Group 5 (CCl(4) + silymarin), Group 6 (CCl(4) + BM-MSCs + silymarin). On the 21st day after treatment, blood samples were collected for biochemical estimations. After the experiment, the rats were sacrificed. Liver was dissected out and processed for histopathology and scanning electron microscopy studies. Liver enzyme and marker analysis, histopathological studies indicated that the combination of BM-MSCs and silymarin was effective in treating liver cirrhosis. Transplanted BM-MSCs in combination with silymarin ameliorated the liver tissue damage through their immunoregulatory activities. Among the two routes, the intravenous administration of cells through the tail vein was found to be more effective and safe. Springer International Publishing 2021-01-31 2021-02 /pmc/articles/PMC7847925/ /pubmed/33564610 http://dx.doi.org/10.1007/s13205-021-02640-y Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Aithal, Ashwini P.
Bairy, Laxminarayana K.
Seetharam, Raviraja N.
Kumar, Naveen
Hepatoprotective effect of bone marrow-derived mesenchymal stromal cells in CCl(4)-induced liver cirrhosis
title Hepatoprotective effect of bone marrow-derived mesenchymal stromal cells in CCl(4)-induced liver cirrhosis
title_full Hepatoprotective effect of bone marrow-derived mesenchymal stromal cells in CCl(4)-induced liver cirrhosis
title_fullStr Hepatoprotective effect of bone marrow-derived mesenchymal stromal cells in CCl(4)-induced liver cirrhosis
title_full_unstemmed Hepatoprotective effect of bone marrow-derived mesenchymal stromal cells in CCl(4)-induced liver cirrhosis
title_short Hepatoprotective effect of bone marrow-derived mesenchymal stromal cells in CCl(4)-induced liver cirrhosis
title_sort hepatoprotective effect of bone marrow-derived mesenchymal stromal cells in ccl(4)-induced liver cirrhosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847925/
https://www.ncbi.nlm.nih.gov/pubmed/33564610
http://dx.doi.org/10.1007/s13205-021-02640-y
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