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Anti-diabetic activity of aerial parts of Sarcopoterium spinosum
BACKGROUND: Sarcopoterium spinosum (S. spinosum) is used by Bedouin medicinal practitioners for the treatment of diabetes. While the anti-diabetic activity of S. spinosum root extract was validated in previous studies, the activity of aerial parts of the same plants has not been elucidated yet. The...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501114/ https://www.ncbi.nlm.nih.gov/pubmed/28683738 http://dx.doi.org/10.1186/s12906-017-1860-7 |
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author | Elyasiyan, Uriel Nudel, Adi Skalka, Nir Rozenberg, Konstantin Drori, Elyashiv Oppenheimer, Rachela Kerem, Zohar Rosenzweig, Tovit |
author_facet | Elyasiyan, Uriel Nudel, Adi Skalka, Nir Rozenberg, Konstantin Drori, Elyashiv Oppenheimer, Rachela Kerem, Zohar Rosenzweig, Tovit |
author_sort | Elyasiyan, Uriel |
collection | PubMed |
description | BACKGROUND: Sarcopoterium spinosum (S. spinosum) is used by Bedouin medicinal practitioners for the treatment of diabetes. While the anti-diabetic activity of S. spinosum root extract was validated in previous studies, the activity of aerial parts of the same plants has not been elucidated yet. The aim of this study was to clarify the glucose lowering properties of the aerial parts of the shrub. METHODS: Anti-diabetic properties were evaluated by measuring the activity of carbohydrate digesting enzymes, glucose uptake into 3 T3-L1 adipocytes, and insulin secretion. Insulin signaling cascade was followed in L6 myotubes using Western blot and PathScan analysis. RESULTS: Activity of α-amylase and α-glucosidase was inhibited by extracts of all S. spinosum organs. Basal and glucose-induced insulin secretion was measured in Min6 cells and found to be enhanced as well. Glucose uptake was induced by all S. spinosum extracts, with roots found to be the most effective and fruits the least. The effect of S. spinosum on Akt phosphorylation was minor compared to insulin effect. However, GSK3β and PRAS40, which are downstream elements of the insulin cascade, were found to be highly phosphorylated by S. spinosum extracts. Inhibition of PI3K and Akt, but not AMPK and ERK, abrogated the induction of glucose uptake by the aerial parts of the shrub. CONCLUSION: The aerial organs of S. spinosum have anti-diabetic properties and may be used as a basis for the development of dietary supplements or to identify new agents for the treatment of type 2 diabetes. |
format | Online Article Text |
id | pubmed-5501114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55011142017-07-10 Anti-diabetic activity of aerial parts of Sarcopoterium spinosum Elyasiyan, Uriel Nudel, Adi Skalka, Nir Rozenberg, Konstantin Drori, Elyashiv Oppenheimer, Rachela Kerem, Zohar Rosenzweig, Tovit BMC Complement Altern Med Research Article BACKGROUND: Sarcopoterium spinosum (S. spinosum) is used by Bedouin medicinal practitioners for the treatment of diabetes. While the anti-diabetic activity of S. spinosum root extract was validated in previous studies, the activity of aerial parts of the same plants has not been elucidated yet. The aim of this study was to clarify the glucose lowering properties of the aerial parts of the shrub. METHODS: Anti-diabetic properties were evaluated by measuring the activity of carbohydrate digesting enzymes, glucose uptake into 3 T3-L1 adipocytes, and insulin secretion. Insulin signaling cascade was followed in L6 myotubes using Western blot and PathScan analysis. RESULTS: Activity of α-amylase and α-glucosidase was inhibited by extracts of all S. spinosum organs. Basal and glucose-induced insulin secretion was measured in Min6 cells and found to be enhanced as well. Glucose uptake was induced by all S. spinosum extracts, with roots found to be the most effective and fruits the least. The effect of S. spinosum on Akt phosphorylation was minor compared to insulin effect. However, GSK3β and PRAS40, which are downstream elements of the insulin cascade, were found to be highly phosphorylated by S. spinosum extracts. Inhibition of PI3K and Akt, but not AMPK and ERK, abrogated the induction of glucose uptake by the aerial parts of the shrub. CONCLUSION: The aerial organs of S. spinosum have anti-diabetic properties and may be used as a basis for the development of dietary supplements or to identify new agents for the treatment of type 2 diabetes. BioMed Central 2017-07-06 /pmc/articles/PMC5501114/ /pubmed/28683738 http://dx.doi.org/10.1186/s12906-017-1860-7 Text en © The Author(s). 2017 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 Elyasiyan, Uriel Nudel, Adi Skalka, Nir Rozenberg, Konstantin Drori, Elyashiv Oppenheimer, Rachela Kerem, Zohar Rosenzweig, Tovit Anti-diabetic activity of aerial parts of Sarcopoterium spinosum |
title | Anti-diabetic activity of aerial parts of Sarcopoterium spinosum |
title_full | Anti-diabetic activity of aerial parts of Sarcopoterium spinosum |
title_fullStr | Anti-diabetic activity of aerial parts of Sarcopoterium spinosum |
title_full_unstemmed | Anti-diabetic activity of aerial parts of Sarcopoterium spinosum |
title_short | Anti-diabetic activity of aerial parts of Sarcopoterium spinosum |
title_sort | anti-diabetic activity of aerial parts of sarcopoterium spinosum |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501114/ https://www.ncbi.nlm.nih.gov/pubmed/28683738 http://dx.doi.org/10.1186/s12906-017-1860-7 |
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