The effect of variation of dose, time toward cauli flower (Brassica oleracea var BotrytisL.) On hepatic cytochrome P-450 level rats given theophylline
Abstract
Cytochrome P-450 as a major component enzyme system in drug metabolism. Activity enzyme of cytochrome P-450 was influenced by internal and external factors. Vegetables of Brassicaceae such as cauli flower were often consumed in the long term, its has inductor activity of oxidation enzyme systems and conjugation reactions. Theophylline as a bronchodilator drugs have the unknown effects on hepatic microsomal enzyme, such as cytochrome P-450 and have not been many studies that tried to prove it. The purpose of this study was to prove the effects of Cauliflower and indol on level cytochrome P-450 enzyme. 90 rats were divided into 3 groups. Group I, were given Theophylline 20 mg/kg BW. In group II 30 rats were treated with indole 1,2; 2,4; 3,6 mg/kg BW, and group III 30 rats were treated with cauliflower extract respectively doses 100, 200, 300 g/kg BW. Each dose was given on 10 rats, each group were divided 2 sub-groups were treated for 5, 10 days. On the last day of treatment were given Theophylline 20 mg/kg BW. Cytochrome P-450 enzyme levels were determined by the method of Omura and Sato(Snell, and Mullock,1987). An induction cauliflower and indole did not increased levels of hepatic cytochrome P-450. The long treatment and the increased of administered dose did not enhanced the levels of hepatic cytochrome P-450 enzyme. cauliflower and indole contained in vegetables when consumed together with theophylline drug, would not affect the metabolism of theophylline
Key words: Cauli flower, cytochrome P-450, theophylline, indole, spectrofotometric.
Full Text:
UntitledReferences
Snell, K and Mullock, B, (editors) 1987, Biochemical toxicology, A Practical Approach IRL Press, Oxford Washington DC.
ndulski, JA and Lutz, W. 2000. Metabolic genotype in relation toindividual susceptibility to environmental carcinogenesis.Int Arch Occup Environ Health 73:71–85.
Akagah B, Lormier A.T, Fournet A, Figadere B, 2008., Oxidation of antiparasic 2- substituted quinolones using metalloporphyin catalysts : scale-up of a biomimetic reaction for metabolite production of drug candidates. Organic & Biomolecular Chemistry. 6. (24) : 4494-7.
Dalimartha, S. 2000. Atlas Tumbuhan Obat Indonesia.Jilid II. Jakarta : Trubus Agriwidya Lee S-A., Fowke J H., Lu W., Ye C., Zheng Y., Cai Q., Gu K., Gao y-T., Shu X-O., Zheng W; 2008; American Journal of Clinical Nutrition, March, vol. 87, No 3, 753-760.
Anonim, 1986, Sediaan Galenik, Departemen Kesehatan Republik Indonesia, Dirjen Pengawasan Obat Dan Makanan, Jakarta.
Anonim, (www.asiamaya.com, 2009).
Guengerich, F.P. 2005 Human cytochrome P450 enzymes. In Cytochrome P450: Structure Mechanism, and Biochemistry, 3rd ed.(Ortiz de Montellano, P. R., Ed.) pp 377–530, Kluwer Academic/Plenum Press, New York.
Oscarson M, Ingelman-Sundberg M, Daly AK, Nebert DW,2003.Human cytochrome P450 (CYP) alleles(web site) http://www.imm.ki.se/CYPalleles/
Nebert DW, & Russell DW. Clinical importance of the cytochromes P450. Lancet; 2002, 360:1155–1162.
Hallstrom H, Melhus, H, Glynn, A, Lind, L, Sylvanen, AC and Michaelsson, K, Coffee consumption and CYP1A2 genotype in relation to bone mineral density of the
proximal femur in elderly men and women : a cohort study, Nutrition & Metabolism, 2010, 7,(1) : 12.
Perera, V, CYP1A2*F is not a “rapid metabolizer” phenotype.Faculty of Pharmacy, The University of Sydney. (2011-06-21 17:55)
Murray,S. A.O.A,.Odupitan, B. P.,Murray, A.R.,Boobis and Edwards,R.J, 2001; Inhibition of human CYP1A2 activity in vitro by methylxanthines : potent competitive inhibition by 8-phenyltheophyllineVol. 31, No. 3, 135-151
Guengerich, F. P. 2001 Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity. Chem. Res. Toxicol. 14, 611–650.
Louisa, M., Suyatna, F.D., Setiawati, A., Jusman, S.W.A., 2009., The Effect of Lycopene on total cytochrome P-450, CYP1A2 and CYP2E1, Med.J.Indones., Flockhart, (2007) : 233-8., vol.Flockhart, (2007), No.4, Oktober-Desember 2009.
Donatus, I.A., 1994. Antaraksi kurkumin dengan parasetamol. Kajian terhadap aspekfarmakologi dan toksikologi perubahan hayati parasetamol.Desertasi S3Universitas Gadjah Mada, Yogyakarta, Indonesia.
Gorski JC, Huang S-M, Pinto A, Hamman MA, Hilligoss JK, Zaheer NA, Desai M, Miller M and Hall SD. 2004. The effect of echinacea on cytochrome P-450 activity in vivo. Clin Pharmacol Ther, 75:89-100,
Flockhart DA. 2007. Drug Interactions: Cytochrome P450 Drug Interaction Table. Indiana University School of Medicine. http://medicine.iupui.edu/ clinpharm/ddis/ table. Asp. Accessed [date].
DOI: http://dx.doi.org/10.14499/indonesianjpharm0iss0pp323-329
Refbacks
- There are currently no refbacks.
Copyright (c) 2017 INDONESIAN JOURNAL OF PHARMACY

This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
Indonesian J Pharm indexed by: