In vivo growth inhibition of sarcoma 180 by piperlonguminine, an alkaloid amide from the Piper species

被引:55
作者
Bezerra, Daniel P. [1 ]
Pessoa, Claudia [1 ]
de Moraes, Manoel Odorico [1 ]
de Alencar, Nylane M. N. [1 ]
Mesquita, Rodney O. [1 ]
Lima, Michael W. [1 ]
Alves, Ana Paula N. N. [2 ]
Pessoa, Otilia Deusdenia L. [3 ]
Chaves, Joao Henrique [3 ]
Silveira, Edilberto R. [3 ]
Costa-Lotufo, Leticia V. [1 ]
机构
[1] Univ Fed Ceara, Dept Physiol & Pharmacol, Fac Med, BR-60430270 Fortaleza, Ceara, Brazil
[2] Univ Fed Ceara, Dept Clin Odontol, BR-60430270 Fortaleza, Ceara, Brazil
[3] Univ Fed Ceara, Dept Quim Organ & Inorgan, BR-60021970 Fortaleza, Ceara, Brazil
关键词
Piper divaricatum; piperlonguminine; antitumor activity; toxicity; sarcoma; 180;
D O I
10.1002/jat.1311
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
Many authors have already emphasized that phytochemicals from spices have biological applications. Piperlonguminine is a known alkaloid amide from peppers, including Piper divaricatum. The aim of this study was to investigate the in vitro and in vivo antitumor effects of piperlonguminine in experimental models. In order to evaluate the toxicological aspects related to piperlonguminine treatment, hematological, biochemical, histopathological and morphological analyses of treated animals were performed. Piperionguminine did not show any significant in vitro cytotoxic effect at experimental exposure levels, but showed an in vivo antitumor effect. After 7 days of treatment, the inhibition rates were 38.71% and 40.68% at doses of 25 mg kg(-1) and 50 mg kg(-1), respectively. The histopathological analysis suggests that the liver and kidney were only weakly affected by piperlonguminine treatment. Neither the enzymatic activity of transaminases (AST and ALT) nor the urea levels were significantly altered. In the hematological analysis, all parameters analysed remained constant after piperlonguminine treatment. In conclusion, these data reinforce the anticancer potential of spice components. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:599 / 607
页数:9
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