Cargando…

Mechanistic In vitro Evaluation of Prosopis farcta Roots Potential as an Antidiabetic Folk Medicinal Plant

OBJECTIVE: Prosopis farcta has been used as a traditional herbal medicine for treating Diabetes mellitus. The aim of this study is to investigate the antidiabetic mechanisms of infusion (INF) extract of P. farcta and discovering the active extract for the first time. MATERIALS AND METHODS: Six diffe...

Descripción completa

Detalles Bibliográficos
Autores principales: Feyzmand, Saba, Shahbazi, Behzad, Marami, Marzieh, Bahrami, Gholamreza, Fattahi, Ali, Shokoohinia, Yalda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822511/
https://www.ncbi.nlm.nih.gov/pubmed/29491644
http://dx.doi.org/10.4103/pm.pm_162_17
_version_ 1783301700161896448
author Feyzmand, Saba
Shahbazi, Behzad
Marami, Marzieh
Bahrami, Gholamreza
Fattahi, Ali
Shokoohinia, Yalda
author_facet Feyzmand, Saba
Shahbazi, Behzad
Marami, Marzieh
Bahrami, Gholamreza
Fattahi, Ali
Shokoohinia, Yalda
author_sort Feyzmand, Saba
collection PubMed
description OBJECTIVE: Prosopis farcta has been used as a traditional herbal medicine for treating Diabetes mellitus. The aim of this study is to investigate the antidiabetic mechanisms of infusion (INF) extract of P. farcta and discovering the active extract for the first time. MATERIALS AND METHODS: Six different extracts of P. farcta were prepared using five different solvents (ethanol, n-hexane, acetone, ethanol:water (1:1 v/v), and water). Cytotoxicity and cell proliferation assays were performed on mouse pancreatic β-cells (β-TC(3)) using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium method. The effects of P. farcta on glucose metabolism (in a hepatocellular carcinoma cell line [HepG2]) and glucose diffusion across a dialysis membrane (as a model of cellular glucose absorption) were evaluated. The protective effect of various P. farcta extracts on cytotoxicity, mitochondrial membrane potential (MMP), and streptozotocin (STZ)-induced apoptosis in β-TC(3) cells was investigated. RESULTS: Cytotoxicity study indicated that extracts were safe on β-TC(3) and HepG2 (≤0.5 mg/ml). INF protected β-TC(3) cells from apoptosis induced by STZ and improved cell viability for 20% and significantly decrease depolarization of MMP (P < 0.005). The results showed that INF inhabited breaking/streaking the DNA. Proliferation study showed no significant increase in the number of cells either at single or multiple doses. In moderate hyperglycemia (11.1 mmol/l), a significant glucose-lowering effect was observed but glucose diffusion was not the probable mechanism of extracts antidiabetic effect. In conclusion, only INF, the traditionally used extract, has an antidiabetic potential by attenuating the death and apoptosis induced by STZ in β-TC(3) cells and increase glucose consumption. CONCLUSION: The present study demonstrates that only INF extract have an antidiabetic potential by attenuating the death and apoptosis induced by STZ in β-TC(3) cells and increase glucose consumption. SUMMARY: Six different extracts from P. farcta were prepared using five different solvents [ethanol, n-hexane, acetone, ethanol: water (1:1 v/v), and water]. The protective effect of various P. farcta extracts on cytotoxicity, mitochondrial membrane potential (MMP), and Streptozotocin-induced apoptosis in β-TC(3) cells were investigated. Infusion has an antidiabetic potential by attenuating the death and apoptosis induced by STZ in β-TC(3) cells and increase glucose consumption. The effect of infusion extract on glucose consumption in hepatocellular carcinoma cell line cells (a) and effect of infusion extract on glucose consumption in hepatocellular carcinoma cell line cells adjusted by optical density MTT (b). Significance was calculated by analysis of variance (*P ≤ 0.05). MTT: 3 (4,5 dimethylthiazol 2 yl) 2,5 diphenyltetrazolium. Abbreviations used: AC: Acetone extract; ANOVA: Analysis of variance; BSA: Bovine serum albumin; β-TC(3): Mouse pancreatic β-cells; DMEM: Dulbecco modified Eagle medium; DMSO: Dimethyl sulfoxide; ETH: Ethyl acetate extract; FBS: Fetal bovine serum; HDETH: Hydroethanolic extract; HepG2: Hepatocellular carcinoma cell line; HEX: Hexane extract; INF: Infusion; KUMS: Kermanshah University of Medical Sciences; MMP: Mitochondrial membrane potential; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium; NaCl: Natrium chloride; OD: Optical density; spp: Species; STZ: Streptozotocin; Tag: T-antigen; USA: United States of America.
format Online
Article
Text
id pubmed-5822511
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-58225112018-02-28 Mechanistic In vitro Evaluation of Prosopis farcta Roots Potential as an Antidiabetic Folk Medicinal Plant Feyzmand, Saba Shahbazi, Behzad Marami, Marzieh Bahrami, Gholamreza Fattahi, Ali Shokoohinia, Yalda Pharmacogn Mag Original Article OBJECTIVE: Prosopis farcta has been used as a traditional herbal medicine for treating Diabetes mellitus. The aim of this study is to investigate the antidiabetic mechanisms of infusion (INF) extract of P. farcta and discovering the active extract for the first time. MATERIALS AND METHODS: Six different extracts of P. farcta were prepared using five different solvents (ethanol, n-hexane, acetone, ethanol:water (1:1 v/v), and water). Cytotoxicity and cell proliferation assays were performed on mouse pancreatic β-cells (β-TC(3)) using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium method. The effects of P. farcta on glucose metabolism (in a hepatocellular carcinoma cell line [HepG2]) and glucose diffusion across a dialysis membrane (as a model of cellular glucose absorption) were evaluated. The protective effect of various P. farcta extracts on cytotoxicity, mitochondrial membrane potential (MMP), and streptozotocin (STZ)-induced apoptosis in β-TC(3) cells was investigated. RESULTS: Cytotoxicity study indicated that extracts were safe on β-TC(3) and HepG2 (≤0.5 mg/ml). INF protected β-TC(3) cells from apoptosis induced by STZ and improved cell viability for 20% and significantly decrease depolarization of MMP (P < 0.005). The results showed that INF inhabited breaking/streaking the DNA. Proliferation study showed no significant increase in the number of cells either at single or multiple doses. In moderate hyperglycemia (11.1 mmol/l), a significant glucose-lowering effect was observed but glucose diffusion was not the probable mechanism of extracts antidiabetic effect. In conclusion, only INF, the traditionally used extract, has an antidiabetic potential by attenuating the death and apoptosis induced by STZ in β-TC(3) cells and increase glucose consumption. CONCLUSION: The present study demonstrates that only INF extract have an antidiabetic potential by attenuating the death and apoptosis induced by STZ in β-TC(3) cells and increase glucose consumption. SUMMARY: Six different extracts from P. farcta were prepared using five different solvents [ethanol, n-hexane, acetone, ethanol: water (1:1 v/v), and water]. The protective effect of various P. farcta extracts on cytotoxicity, mitochondrial membrane potential (MMP), and Streptozotocin-induced apoptosis in β-TC(3) cells were investigated. Infusion has an antidiabetic potential by attenuating the death and apoptosis induced by STZ in β-TC(3) cells and increase glucose consumption. The effect of infusion extract on glucose consumption in hepatocellular carcinoma cell line cells (a) and effect of infusion extract on glucose consumption in hepatocellular carcinoma cell line cells adjusted by optical density MTT (b). Significance was calculated by analysis of variance (*P ≤ 0.05). MTT: 3 (4,5 dimethylthiazol 2 yl) 2,5 diphenyltetrazolium. Abbreviations used: AC: Acetone extract; ANOVA: Analysis of variance; BSA: Bovine serum albumin; β-TC(3): Mouse pancreatic β-cells; DMEM: Dulbecco modified Eagle medium; DMSO: Dimethyl sulfoxide; ETH: Ethyl acetate extract; FBS: Fetal bovine serum; HDETH: Hydroethanolic extract; HepG2: Hepatocellular carcinoma cell line; HEX: Hexane extract; INF: Infusion; KUMS: Kermanshah University of Medical Sciences; MMP: Mitochondrial membrane potential; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium; NaCl: Natrium chloride; OD: Optical density; spp: Species; STZ: Streptozotocin; Tag: T-antigen; USA: United States of America. Medknow Publications & Media Pvt Ltd 2017 2018-01-31 /pmc/articles/PMC5822511/ /pubmed/29491644 http://dx.doi.org/10.4103/pm.pm_162_17 Text en Copyright: © 2018 Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Feyzmand, Saba
Shahbazi, Behzad
Marami, Marzieh
Bahrami, Gholamreza
Fattahi, Ali
Shokoohinia, Yalda
Mechanistic In vitro Evaluation of Prosopis farcta Roots Potential as an Antidiabetic Folk Medicinal Plant
title Mechanistic In vitro Evaluation of Prosopis farcta Roots Potential as an Antidiabetic Folk Medicinal Plant
title_full Mechanistic In vitro Evaluation of Prosopis farcta Roots Potential as an Antidiabetic Folk Medicinal Plant
title_fullStr Mechanistic In vitro Evaluation of Prosopis farcta Roots Potential as an Antidiabetic Folk Medicinal Plant
title_full_unstemmed Mechanistic In vitro Evaluation of Prosopis farcta Roots Potential as an Antidiabetic Folk Medicinal Plant
title_short Mechanistic In vitro Evaluation of Prosopis farcta Roots Potential as an Antidiabetic Folk Medicinal Plant
title_sort mechanistic in vitro evaluation of prosopis farcta roots potential as an antidiabetic folk medicinal plant
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822511/
https://www.ncbi.nlm.nih.gov/pubmed/29491644
http://dx.doi.org/10.4103/pm.pm_162_17
work_keys_str_mv AT feyzmandsaba mechanisticinvitroevaluationofprosopisfarctarootspotentialasanantidiabeticfolkmedicinalplant
AT shahbazibehzad mechanisticinvitroevaluationofprosopisfarctarootspotentialasanantidiabeticfolkmedicinalplant
AT maramimarzieh mechanisticinvitroevaluationofprosopisfarctarootspotentialasanantidiabeticfolkmedicinalplant
AT bahramigholamreza mechanisticinvitroevaluationofprosopisfarctarootspotentialasanantidiabeticfolkmedicinalplant
AT fattahiali mechanisticinvitroevaluationofprosopisfarctarootspotentialasanantidiabeticfolkmedicinalplant
AT shokoohiniayalda mechanisticinvitroevaluationofprosopisfarctarootspotentialasanantidiabeticfolkmedicinalplant