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1.
Indian J Exp Biol ; 2007 May; 45(5): 480-5
Article in English | IMSEAR | ID: sea-63071

ABSTRACT

Antioxidant potential of leaves of three different species of Annona was studied by using different in vitro models eg., 1,1-diphenyl-2-picryl hydrazyl (DPPH), 2,2-azinobis-(3-ethylbenzothizoline-6-sulphonate) (ABTS), nitric oxide, superoxide, hydroxy radical and lipid peroxidation. The ethanolic extract of A. muricata at 500 microg/ml showed maximum scavenging activity (90.05%) of ABTS radical cation followed by the scavenging of hydroxyl radical (85.88%) and nitric oxide (72.60%) at the same concentration. However, the extract showed only moderate lipid peroxidation inhibition activity. In contrast, the extract of A. reticulata showed better activity in quenching DPPH (89.37%) and superoxide radical (80.88%) respectively. A.squamosa extract exhibited least inhibition in all in vitro antioxidant models excepting hydroxyl radical (79.79%). These findings suggest that the extracts of A. muricata possess potent in vitro antioxidant activity as compared to leaves of A. squamosa and A. reticulata suggesting its role as an effective free radical scavenger, augmenting its therapeutic


Subject(s)
Animals , Annona/chemistry , Antioxidants/analysis , Biphenyl Compounds/metabolism , Free Radical Scavengers/pharmacology , Free Radicals/metabolism , Goats , Hydrazines/metabolism , Lipid Peroxidation/drug effects , Liver/chemistry , Osmolar Concentration , Plant Extracts/chemistry , Plant Leaves/chemistry
2.
Ciênc. cult. (Säo Paulo) ; 48(1/2): 96-102, Jan.-Apr. 1996. ilus
Article in English | LILACS | ID: lil-191248

ABSTRACT

There are several hydrazine derivatives with pharmacological activity, all of which have carcinogenic properties in experimental animals. Several mono- and disubstituted derivatives have been shown to produce carbon-centered radicals upon oxidation by enzymatic systems such as HbO2' Cytochrome P-450, monoamine oxidases, horseradish peroxidase and myeloperoxidase. Proposed mechanisms of hydrazine metabolism leading to alkylating species are discussed. The in vitro induction of DNA alterations by carbon-centered radicals generated in hydrazine metabolism ascertains the possibility of its occurrence in vivo. Our results, discussed herein, established the induction of cytotoxicity, proliferation and transformation of cultured mouse fibroblasts by systems in which hydrazine-derived alkyl radicals are formed. These studies represent another step towards distinguishing the possible involvement of metabolism-generated carbon-centered radicals in the onset of carcinogenic processes, which reinforces the importance of additional experimental approaches in order to consolidate this hypothesis.


Subject(s)
Carbon/chemistry , Carcinogens/pharmacology , Hydrazines/pharmacology , Carcinogens/metabolism , Carcinogens/toxicity , Cell Division , DNA Damage/drug effects , Fibroblasts/cytology , Fibroblasts/metabolism , Free Radicals , Hydrazines/metabolism , Hydrazines/toxicity
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