Antitumor activity and antioxidant status of Streblus asper bark against Dalton's ascitic lymphoma in mice

Lour (Moraceae), commonly known as Siamee Rough Brush in English is widely distributed in subtropical Asia and traditionally used for several medicinal purposes. In the present study, the ethyl acetate fraction of the methanol extract from bark (EASA) was evaluated for antitumor effect against Dalto...

Full description

Saved in:
Bibliographic Details
Published inInterdisciplinary toxicology Vol. 8; no. 3; pp. 125 - 130
Main Authors Suresh Kumar, R.B., Kar, Biswakanth, Dolai, Narayan, Karmakar, Indrajit, Bhattacharya, Sanjib, Haldar, Pallab K.
Format Journal Article
LanguageEnglish
Published Slovakia De Gruyter Open 01.09.2015
De Gruyter Poland
Slovak Toxicology Society SETOX
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Lour (Moraceae), commonly known as Siamee Rough Brush in English is widely distributed in subtropical Asia and traditionally used for several medicinal purposes. In the present study, the ethyl acetate fraction of the methanol extract from bark (EASA) was evaluated for antitumor effect against Dalton’s ascitic lymphoma (DAL) in Swiss albino mice. Twenty-four hours after intraperitoneal inoculation of DAL cells in mice, EASA was administered intraperitoneally at 200 and 400 mg/kg body weight for 9 consecutive days. On the 10th day, half of the mice were sacrificed to determine the tumor growth parameters, and the rest were kept alive for survival assessment. Hematological, serum biochemical and tissue (liver, kidney) antioxidant profiles were also determined. EASA exhibited significant and dose dependent decrease in tumor growth parameters and increased survival of DAL bearing animals. EASA significantly and dose-dependently normalized the altered hematological, serum biochemical and tissue antioxidant parameters as compared with the DAL control mice. From the present study it may be concluded that bark possesses remarkable antitumor efficacy mediated by amelioration of oxidative stress by multiple mechanisms.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1337-6853
1337-9569
1337-9569
DOI:10.1515/intox-2015-0019