Cargando…

Effects of Panax notoginseng saponins on severe acute pancreatitis through the regulation of mTOR/Akt and caspase-3 signaling pathway by upregulating miR-181b expression in rats

BACKGROUND: In China, Panax notoginseng has been used to treat oxidative stress-related diseases for a long time. Panax notoginseng saponins is an extract from Panax notoginseng Ledeb. Its therapeutic potential is related to antioxidant activity, but related mechanisms are still unclear. The study a...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Ming-wei, Wei, Rui, Su, Mei-xian, Li, Hui, Fang, Tian-wen, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800027/
https://www.ncbi.nlm.nih.gov/pubmed/29402262
http://dx.doi.org/10.1186/s12906-018-2118-8
_version_ 1783298122891395072
author Liu, Ming-wei
Wei, Rui
Su, Mei-xian
Li, Hui
Fang, Tian-wen
Zhang, Wei
author_facet Liu, Ming-wei
Wei, Rui
Su, Mei-xian
Li, Hui
Fang, Tian-wen
Zhang, Wei
author_sort Liu, Ming-wei
collection PubMed
description BACKGROUND: In China, Panax notoginseng has been used to treat oxidative stress-related diseases for a long time. Panax notoginseng saponins is an extract from Panax notoginseng Ledeb. Its therapeutic potential is related to antioxidant activity, but related mechanisms are still unclear. The study aims to assess the protection effects of Panax notoginseng saponins in the taurocholate-induced rat model of acute pancreatitis (AP) and explore underlying mechanisms. METHODS: A rat model of severe acute pancreatitis (SAP) was established in rats induced with taurocholate. Panax notoginseng saponins was firstly administered in the treatment group via intravenous injection. After 2 h, taurocholate administration was performed. After 24 h, the expression levels of miR-181b, Beclin1, LC3-II, Akt and mTOR from pancreas tissues were measured by Western Blotting and RT-PCR. Then the expression levels of Caspase-3 and Blc-2 were determined by immunohistochemistry. Apoptosis was assessed by the TUNEL assay. Amylase and lipase in serum were determined by ELISA and pancreatic water contents in pancreatic tissue were measured. After eosin and hematoxylin staining, the histologic analysis was performed. RESULTS: After SAP induction by taurocholate and the treatment with Panax notoginseng saponins for 24 h, we detected the up-regulated miR-181b, the reduced Bcl-2 expression, the increased activity of mTOR/Akt, the blocked Beclin1 and LC3-II expressions, and the enhanced Caspase-3 expression. Serum lipase and amylase levels were significantly decreased in the treatment group of Panax notoginseng saponins compared to the control group. Histological analysis results verified the attenuation effects of Panax notoginseng saponins on taurocholate-induced pancreas injury, apoptosis, and autophagy. CONCLUSION: By up-regulating the miR-181b expression level, Panax notoginseng saponins significantly reduced taurocholate-induced pancreas injury and autophagy and increased apoptosis. The significant protection effects of Panax notoginseng saponins suggested its potential in treating taurocholate induced-acute pancreatitis.
format Online
Article
Text
id pubmed-5800027
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-58000272018-02-13 Effects of Panax notoginseng saponins on severe acute pancreatitis through the regulation of mTOR/Akt and caspase-3 signaling pathway by upregulating miR-181b expression in rats Liu, Ming-wei Wei, Rui Su, Mei-xian Li, Hui Fang, Tian-wen Zhang, Wei BMC Complement Altern Med Research Article BACKGROUND: In China, Panax notoginseng has been used to treat oxidative stress-related diseases for a long time. Panax notoginseng saponins is an extract from Panax notoginseng Ledeb. Its therapeutic potential is related to antioxidant activity, but related mechanisms are still unclear. The study aims to assess the protection effects of Panax notoginseng saponins in the taurocholate-induced rat model of acute pancreatitis (AP) and explore underlying mechanisms. METHODS: A rat model of severe acute pancreatitis (SAP) was established in rats induced with taurocholate. Panax notoginseng saponins was firstly administered in the treatment group via intravenous injection. After 2 h, taurocholate administration was performed. After 24 h, the expression levels of miR-181b, Beclin1, LC3-II, Akt and mTOR from pancreas tissues were measured by Western Blotting and RT-PCR. Then the expression levels of Caspase-3 and Blc-2 were determined by immunohistochemistry. Apoptosis was assessed by the TUNEL assay. Amylase and lipase in serum were determined by ELISA and pancreatic water contents in pancreatic tissue were measured. After eosin and hematoxylin staining, the histologic analysis was performed. RESULTS: After SAP induction by taurocholate and the treatment with Panax notoginseng saponins for 24 h, we detected the up-regulated miR-181b, the reduced Bcl-2 expression, the increased activity of mTOR/Akt, the blocked Beclin1 and LC3-II expressions, and the enhanced Caspase-3 expression. Serum lipase and amylase levels were significantly decreased in the treatment group of Panax notoginseng saponins compared to the control group. Histological analysis results verified the attenuation effects of Panax notoginseng saponins on taurocholate-induced pancreas injury, apoptosis, and autophagy. CONCLUSION: By up-regulating the miR-181b expression level, Panax notoginseng saponins significantly reduced taurocholate-induced pancreas injury and autophagy and increased apoptosis. The significant protection effects of Panax notoginseng saponins suggested its potential in treating taurocholate induced-acute pancreatitis. BioMed Central 2018-02-05 /pmc/articles/PMC5800027/ /pubmed/29402262 http://dx.doi.org/10.1186/s12906-018-2118-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Liu, Ming-wei
Wei, Rui
Su, Mei-xian
Li, Hui
Fang, Tian-wen
Zhang, Wei
Effects of Panax notoginseng saponins on severe acute pancreatitis through the regulation of mTOR/Akt and caspase-3 signaling pathway by upregulating miR-181b expression in rats
title Effects of Panax notoginseng saponins on severe acute pancreatitis through the regulation of mTOR/Akt and caspase-3 signaling pathway by upregulating miR-181b expression in rats
title_full Effects of Panax notoginseng saponins on severe acute pancreatitis through the regulation of mTOR/Akt and caspase-3 signaling pathway by upregulating miR-181b expression in rats
title_fullStr Effects of Panax notoginseng saponins on severe acute pancreatitis through the regulation of mTOR/Akt and caspase-3 signaling pathway by upregulating miR-181b expression in rats
title_full_unstemmed Effects of Panax notoginseng saponins on severe acute pancreatitis through the regulation of mTOR/Akt and caspase-3 signaling pathway by upregulating miR-181b expression in rats
title_short Effects of Panax notoginseng saponins on severe acute pancreatitis through the regulation of mTOR/Akt and caspase-3 signaling pathway by upregulating miR-181b expression in rats
title_sort effects of panax notoginseng saponins on severe acute pancreatitis through the regulation of mtor/akt and caspase-3 signaling pathway by upregulating mir-181b expression in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800027/
https://www.ncbi.nlm.nih.gov/pubmed/29402262
http://dx.doi.org/10.1186/s12906-018-2118-8
work_keys_str_mv AT liumingwei effectsofpanaxnotoginsengsaponinsonsevereacutepancreatitisthroughtheregulationofmtoraktandcaspase3signalingpathwaybyupregulatingmir181bexpressioninrats
AT weirui effectsofpanaxnotoginsengsaponinsonsevereacutepancreatitisthroughtheregulationofmtoraktandcaspase3signalingpathwaybyupregulatingmir181bexpressioninrats
AT sumeixian effectsofpanaxnotoginsengsaponinsonsevereacutepancreatitisthroughtheregulationofmtoraktandcaspase3signalingpathwaybyupregulatingmir181bexpressioninrats
AT lihui effectsofpanaxnotoginsengsaponinsonsevereacutepancreatitisthroughtheregulationofmtoraktandcaspase3signalingpathwaybyupregulatingmir181bexpressioninrats
AT fangtianwen effectsofpanaxnotoginsengsaponinsonsevereacutepancreatitisthroughtheregulationofmtoraktandcaspase3signalingpathwaybyupregulatingmir181bexpressioninrats
AT zhangwei effectsofpanaxnotoginsengsaponinsonsevereacutepancreatitisthroughtheregulationofmtoraktandcaspase3signalingpathwaybyupregulatingmir181bexpressioninrats