In vitro and in vivo antiproliferative activity of Calotropis procera stem extracts

被引:43
|
作者
Magalhaes, Hemerson I. F. [1 ]
Ferreira, Paulo M. P. [2 ]
Moura, Eraldo S. [3 ]
Torres, Marcia R. [1 ]
Alves, Ana P. N. N. [4 ]
Pessoa, Otilia D. L. [5 ]
Costa-Lotufo, Leticia V. [1 ]
Moraes, Manoel O. [1 ]
Pessoa, Claudia [1 ]
机构
[1] Univ Fed Ceara, Dept Fisiol & Farmacol, Fac Med, BR-60430270 Fortaleza, Ceara, Brazil
[2] Univ Fed Piaui, BR-64600000 Picos, PI, Brazil
[3] Univ Fed Ceara, Fac Med, Dept Cirurgia, BR-30416160 Fotaleza, Ceara, Brazil
[4] Univ Fed Ceara, Dept Clin Odontol, BR-60430270 Fortaleza, Ceara, Brazil
[5] Univ Fed Ceara, Dept Quim Organ & Inorgan, BR-60455970 Fortaleza, Ceara, Brazil
来源
关键词
antimitotic; antiproliferative; Calotropis procera; Sarcoma; 180; tumor; stem extracts; AEDES-AEGYPTI; LATEX; DERIVATIVES; ANTICANCER; TOXICITY; FLOWERS;
D O I
10.1590/S0001-37652010000200017
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The cytotoxic potential of stem organic extracts from Calotropis procera (Asclepiadaceae) was firstly evaluated against cancer cell lines by MTT assay. Subsequently, samples considered cytotoxic were tested for antimitotic activity on sea urchin egg development and for in vivo antiproliferative activity in mice bearing Sarcoma 180 tumor. Among the five extracts (hexane, dichloromethane, ethyl acetate, acetone and methanol), ethyl acetate and acetone extracts displayed higher cytotoxic potential against tumor cells, with IC50 ranging from 0.8 to 4.4 mu g/mL, while methanolic extract was weakly cytotoxic. Cytotoxic extracts also exhibited cell division inhibition capacity by antimitotic assay, revealing IC50 values lower than 5 mu g/mL. In the in vivo antitumor assessments, ethyl acetate-and acetone-treated animals showed tumor growth inhibition ratios of 64.3 and 53.1%, respectively, with reversible toxic effects on liver and kidneys. Further studies are in progress in order to identify C. procera cytotoxic compound(s) and to understand the mechanism of action responsible for this tumor-decreasing potential.
引用
收藏
页码:407 / 416
页数:10
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