Antiulcerogenic effect and cytotoxic activity of semi-synthetic crotonin obtained from Croton cajucara Benth.

被引:30
|
作者
de Almeida, ABA
Melo, PS
Hiruma-Lima, CA
Gracioso, JS
Carli, L
Nunes, DS
Haun, M
Brito, ARMS
机构
[1] Univ Estadual Campinas, Dept Fisiol & Biofis, Inst Biol, BR-13083970 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Dept Farmacol, Fac Ciencias Med, BR-13083970 Campinas, SP, Brazil
[3] Univ Estadual Campinas, Dept Bioquim, Inst Biol, BR-13083970 Campinas, SP, Brazil
[4] Univ Estadual Paulista, Dept Fisiol, Inst Biociencias, Botucatu, SP, Brazil
[5] Univ Estadual Ponta Grossa, Dept Quim, Ponta Grossa, PR, Brazil
关键词
crotonin; semi-synthetic; V79; cell; cytotoxicity; hepatocyte toxicity; gastric ulcer;
D O I
10.1016/S0014-2999(03)01909-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Trans-dehydrocrotonin, the major diterpene isolated from the bark of Croton cajucara, has good antiulcerogenic activity which, however, is accompanied by toxic effects. On the basis of these results, a semi-synthetic crotonin, named 4SRC, was prepared to determine whether this substance has similar antiulcerogenic activity with lower or no toxicity. The natural crotonin was also isolated from the bark of C. cajucara but was not used due to the small amount obtained. The cytotoxic effect of semi-synthetic crotonin, expressed as cell viability, was assessed in (a) lung fibroblast cell line (V79) derived from Chinese hamsters, a system commonly used for cytotoxicity studies, and (b) rat hepatocytes isolated from male Wistar rats. After treatment, cell viability was determined by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide reduction (MTT reduction), total acid content and neutral red uptake assays. To evaluate V79 cell viability, different concentrations of semi-synthetic crotonin were incubated with the cells. To evaluate the antiulcerogenic effects of semi-synthetic crotonin (50, 100 and 200 mg/kg), we used the models of gastric ulcer induced by ethanol/HCl, stress, indomethacin/bethanechol, and ethanol in male Swiss mice and male Wistar rats. The substance had an IC50 = 500 muM in the neutral red uptake and MTT reduction tests and an IC50 = 200 muM in the nucleic acid content test. With regard to hepatocyte viability after treatment with semi-synthetic crotonin at different concentrations, semi-synthetic crotonin had an IC50 = 10-500 muM in the nucleic acid content and MTT reduction tests and an IC50 = 120 muM in the neutral red uptake test. In another experiment, V79 cells were incubated with the metabolites produced by hepatocytes treated with different concentrations of semi-synthetic crotonin. After a 4-h incubation, semi-synthetic crotonin had an IC50 = 500 muM in the MTT reduction and neutral red uptake tests and an IC50 = 370 muM in nucleic acid content test. The substance had significant antiulcerogenic activity in all models studied, suggesting the presence of a possible antisecretory effect combined with a cytoprotective effect. For this reason, the effect of semi-synthetic crotonin was also evaluated on biochemical parameters of gastric juice and gastric wall mucus, both obtained from pylorus-ligated mice. No significant differences were observed in these parameters between semi-synthetic crotonin-treated and control animals. The results obtained with semi-synthetic crotonin are promising, with a significant preventive effect against gastric ulcer induced by different agents. Our data also show that semi-synthetic crotonin was less toxic than dehydrocrotonin and that the cytotoxic effects decreases with the time that isolated hepatocytes were in culture. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:205 / 212
页数:8
相关论文
共 50 条
  • [21] Isolation and cytotoxic activity of buchariol from Salvia leriifolia Benth.
    Loizzo, M. R.
    Tundis, R.
    Menichini, F.
    Bonesi, M.
    Conforti, F.
    Statti, G. A.
    Nadjafi, F.
    Nicoletti, M.
    Menichini, F.
    PLANTA MEDICA, 2009, 75 (09) : 967 - 967
  • [22] The lipid-lowering effect of trans-dehydrocrotonin, a clerodane diterpene from Croton cajucara Benth. in mice fed on high-fat diet
    Silva, RM
    Santos, FA
    Rao, VSN
    Maciel, MAM
    Pinto, AC
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (04) : 535 - 539
  • [23] Cytotoxic effect of the diterpene lactone dehydrocrotonin from Croton cajucara on human promyelocytic leukemia cells
    Freire, ACG
    Melo, PD
    Aoyama, H
    Haun, M
    Durán, N
    Ferreira, CV
    PLANTA MEDICA, 2003, 69 (01) : 67 - 69
  • [24] Comparison of the gastroprotective effect of a diterpene lactone isolated from Croton cajucara with its synthetic derivatives
    Melo, PS
    Durán, N
    Hiruma-Lima, CA
    Souza-Brito, ARM
    Haun, M
    JOURNAL OF ETHNOPHARMACOLOGY, 2003, 87 (2-3) : 169 - 174
  • [25] Cytotoxic potential of dihydrochalcones from Eriosema glomeratum and their semi-synthetic derivatives
    Tabakam, Gaetan Tchangou
    Kodama, Takeshi
    Tchuenmogne, Marthe Aimee Tchuente
    Hoang, Nhat Nam
    Nomin-Erdene, Battsengel
    Ngouela, Silvere Augustin
    Tene, Mathieu
    Morita, Hiroyuki
    Awouafack, Maurice Ducret
    NATURAL PRODUCT RESEARCH, 2024, 38 (02) : 186 - 197
  • [26] Anti-tumour activity of two 19-nor-clerodane diterpenes, trans-dehydrocrotonin and trans-crotonin, from Croton cajucara
    Grynberg, NF
    Echevarria, A
    Lima, JE
    Pamplona, SSR
    Pinto, AC
    Maciel, MAM
    PLANTA MEDICA, 1999, 65 (08) : 687 - 689
  • [27] Solid-state 13C NMR and molecular modeling studies of acetyl aleuritolic acid obtained from Croton cajucara Benth
    da Silva San Gil, Rosane Aguiar
    Albuquerque, Magaly Girao
    de Alencastro, Ricardo Bicca
    Pinto, Angelo da Cunha
    Santo Gomes, Fabiano do Espirito
    de Castro Dantas, Tereza Neuma
    Medeiros Maciel, Maria Aparecida
    JOURNAL OF MOLECULAR STRUCTURE, 2008, 885 (1-3) : 82 - 88
  • [28] Anti-biofilm activity of a semi-synthetic molecule obtained from resveratrol against Candida albicans biofilm
    Juin, Camille
    Perrin, Flavie
    Puy, Thomas
    Bernard, Clement
    Mollichella, Marie Laure
    Girardot, Marion
    Costa, Damien
    Guillard, Jerome
    Imbert, Christine
    MEDICAL MYCOLOGY, 2020, 58 (04) : 530 - 542
  • [29] In vitro shistosomicidal activity of (-)-6,6-dinitrohinokinin: a semi-synthetic lignan derivative obtained from (-)-hinokinin
    Silva, M. L. A.
    Rodrigues, V
    Albuquerque, S.
    Bastos, J. K.
    Silva, R.
    Pereira Junior, O. S.
    Bianco, T. N. C.
    Cunha, W. R.
    Santos, F. F.
    Donate, P. M.
    Magalhaes, L. G.
    Pereira, A. C.
    Da Silva Filho, A. A.
    PLANTA MEDICA, 2009, 75 (09) : 945 - 945
  • [30] Cytotoxic Effect of Euphol and Semi-Synthetic Ingenol Derived from Euphorbia Tirucalli on Human Melanomas Cell Lines
    Silva, V.
    Rosa, M.
    Vazquez, V.
    Pianowski, L. F.
    Reis, R.
    JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT, 2013, 11 : 70 - 70