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Anticancer activity of cissampelos pareira against dalton's lymphoma ascites bearing mice

BACKGROUND: Cissampelos pareira (Menispermaceae) is used in folk Indian system of alternative medicine, for its analgesic, antipyretic, diuretic, antilithic, and emmenagogue properties. OBJECTIVE: To evaluate Cissampelos pareira (C. pareira) for in vitro cytotoxicity and in vivo antitumor activity a...

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Autores principales: Thavamani, B. Samuel, Mathew, Molly, Dhanabal, S. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159910/
https://www.ncbi.nlm.nih.gov/pubmed/25210304
http://dx.doi.org/10.4103/0973-1296.137356
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author Thavamani, B. Samuel
Mathew, Molly
Dhanabal, S. P.
author_facet Thavamani, B. Samuel
Mathew, Molly
Dhanabal, S. P.
author_sort Thavamani, B. Samuel
collection PubMed
description BACKGROUND: Cissampelos pareira (Menispermaceae) is used in folk Indian system of alternative medicine, for its analgesic, antipyretic, diuretic, antilithic, and emmenagogue properties. OBJECTIVE: To evaluate Cissampelos pareira (C. pareira) for in vitro cytotoxicity and in vivo antitumor activity against Dalton's Lymphoma Ascites (DLA) cells in Swiss mice. MATERIALS AND METHODS: Cissampelos pareira was successively extracted using different solvents. In vitro cytotoxicity was assessed by the MTT assay. An in vivo study was carried out in methanol extract. Twenty-four hours after intraperitoneal inoculation of the DLA cells in mice, the methanol extract of C. pariera (MECP) was administered at 200 and 400 mg/kg body weight for 14 consecutive days. On day 14, six mice were sacrificed and the rest were kept alive for assessment of increase in life-span. The antitumor effect was assessed by evaluating the packed cell volume, viable tumor cell count, increase in body weight, and increase in life-span. The hematological and serum biochemical parameters and anti-oxidant properties were assessed by estimating the superoxide dismutase (SOD), catalase (CAT), and lipid peroxidation. RESULTS: Methanol Extract of Cissampelos pariera (MECP) showed a potent cytotoxic activity, with an IC(50) value of 95.5 μg/ml and a significant (P < 0.001) decrease in packed cell volume, viable cell count, and an increased lifespan (54 and 72%). The hematological and serum biochemical profiles were restored to normal levels in MECP-treated mice. The MECP-treated group significantly (P < 0.001) decreased SOD, lipid peroxidation, and CAT to normal. CONCLUSION: This study demonstrated that C. pariera exhibited significant in vitro and in vivo anti-tumor activities and that it was reasonably imputable to its increasing endogenous mechanism of antioxidant property.
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spelling pubmed-41599102014-09-10 Anticancer activity of cissampelos pareira against dalton's lymphoma ascites bearing mice Thavamani, B. Samuel Mathew, Molly Dhanabal, S. P. Pharmacogn Mag Original Article BACKGROUND: Cissampelos pareira (Menispermaceae) is used in folk Indian system of alternative medicine, for its analgesic, antipyretic, diuretic, antilithic, and emmenagogue properties. OBJECTIVE: To evaluate Cissampelos pareira (C. pareira) for in vitro cytotoxicity and in vivo antitumor activity against Dalton's Lymphoma Ascites (DLA) cells in Swiss mice. MATERIALS AND METHODS: Cissampelos pareira was successively extracted using different solvents. In vitro cytotoxicity was assessed by the MTT assay. An in vivo study was carried out in methanol extract. Twenty-four hours after intraperitoneal inoculation of the DLA cells in mice, the methanol extract of C. pariera (MECP) was administered at 200 and 400 mg/kg body weight for 14 consecutive days. On day 14, six mice were sacrificed and the rest were kept alive for assessment of increase in life-span. The antitumor effect was assessed by evaluating the packed cell volume, viable tumor cell count, increase in body weight, and increase in life-span. The hematological and serum biochemical parameters and anti-oxidant properties were assessed by estimating the superoxide dismutase (SOD), catalase (CAT), and lipid peroxidation. RESULTS: Methanol Extract of Cissampelos pariera (MECP) showed a potent cytotoxic activity, with an IC(50) value of 95.5 μg/ml and a significant (P < 0.001) decrease in packed cell volume, viable cell count, and an increased lifespan (54 and 72%). The hematological and serum biochemical profiles were restored to normal levels in MECP-treated mice. The MECP-treated group significantly (P < 0.001) decreased SOD, lipid peroxidation, and CAT to normal. CONCLUSION: This study demonstrated that C. pariera exhibited significant in vitro and in vivo anti-tumor activities and that it was reasonably imputable to its increasing endogenous mechanism of antioxidant property. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4159910/ /pubmed/25210304 http://dx.doi.org/10.4103/0973-1296.137356 Text en Copyright: © 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Thavamani, B. Samuel
Mathew, Molly
Dhanabal, S. P.
Anticancer activity of cissampelos pareira against dalton's lymphoma ascites bearing mice
title Anticancer activity of cissampelos pareira against dalton's lymphoma ascites bearing mice
title_full Anticancer activity of cissampelos pareira against dalton's lymphoma ascites bearing mice
title_fullStr Anticancer activity of cissampelos pareira against dalton's lymphoma ascites bearing mice
title_full_unstemmed Anticancer activity of cissampelos pareira against dalton's lymphoma ascites bearing mice
title_short Anticancer activity of cissampelos pareira against dalton's lymphoma ascites bearing mice
title_sort anticancer activity of cissampelos pareira against dalton's lymphoma ascites bearing mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159910/
https://www.ncbi.nlm.nih.gov/pubmed/25210304
http://dx.doi.org/10.4103/0973-1296.137356
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