Apoptotic role of natural isothiocyanate from broccoli (Brassica oleracea italica) in experimental chemical lung carcinogenesis

被引:25
作者
Priya, D. Kalpana Deepa [1 ]
Gayathri, R. [1 ]
Gunassekaran, G. R. [1 ]
Murugan, S. [1 ]
Sakthisekaran, D. [1 ]
机构
[1] Univ Madras, Dept Med Biochem, Dr ALM Post Grad Inst Basic Med Sci, Chennai 600113, Tamil Nadu, India
关键词
Apoptosis; DNA-protein crosslinks; chemical carcinogenesis; cytoprotection; genomic base modification; glycosylation; H2O2; production; isothiocyanate; membrane damage; potein carbonyls; SENSITIVE ASSAY; SULFORAPHANE; INDUCTION; TUMORIGENESIS; PURIFICATION; ANTIOXIDANT; INHIBITION; ENZYMES; BENZYL; DAMAGE;
D O I
10.3109/13880209.2012.761242
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context: Sulforaphane (SFN) [1-isothiocyanato-4-(methylsulfinyl)butane] is a naturally occurring isothiocyanate found in cruciferous vegetables such as broccoli [Brassica oleracea L. var. italica Plenck. (Brassicaceae)]. Since it is among the most potent bioactive components with antioxidant and antitumor properties, it has received intense attention in the recent years for its chemopreventive properties. Objective: The present work determined the rehabilitating role in alleviating the oxidative damage caused by benzo(a)pyrene [B(a)P] to biomolecules and the apoptotic cascade mediated by orally administered isothiocyanate-SFN (9 mu mol/mouse/day) against B(a)P (100 mg/kg body weight, i.p.) induced pulmonary carcinogenesis in Swiss albino mice. Materials and methods: Oxidative damage was assessed by measuring lipid peroxidation, 8-hydroxydeoxyguanosine, hydrogen peroxide (H2O2) production, glycoprotein components, protein carbonyl levels and DNA-protein crosslinks. DNA fragmentation by agarose gel electrophoresis and caspase-3 activity by ELISA proved apoptotic induction by SFN along with the protein expression of Bcl-2, Bax and Cyt c. Results: SFN treatment was found to decrease the H2O2 production (p < 0.001) in cancer induced animals, proving its antioxidant potential. Apoptosis was induced by increasing the release of Cyt c (p < 0.001) from mitochondria, decreasing and increasing the expression of Bcl-2 (p < 0.01) and Bax (p < 0.001), respectively. Caspase-3 activity was also enhanced (p < 0.001) which leads to DNA fragmentation in SFN treated groups. Conclusion: Our results reflect the rehabilitating role of SFN in B(a)P induced lung carcinogenesis.
引用
收藏
页码:621 / 628
页数:8
相关论文
共 31 条
[1]   THE EFFECT OF L-BUTHIONINE SULFOXIMINE ON THE AEROBIC RADIATION RESPONSE OF A549 HUMAN-LUNG CARCINOMA-CELLS [J].
BIAGLOW, JE ;
VARNES, ME ;
TUTTLE, SW ;
OLEINICK, NL ;
GLAZIER, K ;
CLARK, EP ;
EPP, ER ;
DETHLEFSEN, LA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1986, 12 (07) :1139-1142
[2]   Regulation of apoptosis by Bcl-2 family proteins [J].
Burlacu, A .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2003, 7 (03) :249-257
[3]   Increased levels of 8-hydroxydeoxyguanosine and its relationship with lipid peroxidation and antioxidant vitamins in lung cancer [J].
Caliskan-Can, Emel ;
Firat, Hikmet ;
Ardic, Sadik ;
Simsek, Bolkan ;
Torun, Meral ;
Yardim-Akaydin, Sevgi .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2008, 46 (01) :107-112
[4]  
DISCHE Z, 1948, J BIOL CHEM, V175, P595
[5]   Direct oxidative modifications of signalling proteins in mammalian cells and their effects on apoptosis [J].
England, K ;
Cotter, TG .
REDOX REPORT, 2005, 10 (05) :237-245
[6]   The chemical diversity and distribution of glucosinolates and isothiocyanates among plants [J].
Fahey, JW ;
Zalcmann, AT ;
Talalay, P .
PHYTOCHEMISTRY, 2001, 56 (01) :5-51
[7]   Sulforaphane inhibits extracellular, intracellular, and antibiotic-resistant strains of Helicobacter pylori and prevents benzo[a]pyrene-induced stomach tumors [J].
Fahey, JW ;
Haristoy, X ;
Dolan, PM ;
Kensler, TW ;
Scholtus, I ;
Stephenson, KK ;
Talalay, P ;
Lozniewski, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (11) :7610-7615
[8]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[9]  
Halliwell B, 1999, NUTR REV, V57, P104, DOI 10.1111/j.1753-4887.1999.tb06933.x
[10]   Inhibition of carcinogenesis by isothiocyanates [J].
Hecht, SS .
DRUG METABOLISM REVIEWS, 2000, 32 (3-4) :395-411