Planta Med 1997; 63(6): 561-563
DOI: 10.1055/s-2006-957767
Letters

© Georg Thieme Verlag Stuttgart · New York

4-Nerolidylcatechol from Pothomorphe Spp. Scavanges Peroxyl Radicals and Inhibits Fe(II)-Dependent DNA Damage

Cristian Desmarchelier1 , Silvia Barros2 , Marisa Repetto3 , Leandro Ribeiro Latorre4 , Masuo Kato4 , Jorge Coussio5 , Graciela Ciccia1
  • 1Cátedra de Microbiología Industrial y Biotecnología, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, 1113 Buenos Aires, Argentina
  • 2Departamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacéuticas, Universidade de São Paulo, Av. Lineu Prestes 580, 05508-900 São Paulo, Brazil
  • 3Cátedra de Química General e Inorgánica, Faucltad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, 1113 Buenos Aires, Argentina
  • 4Instituto de Química, Universidade de São Paulo, Av. Lineu Prestes 580, 05599-970 São Paulo, Brazil
  • 5Cátedra de Farmacognosia, (IQUIMEFA-CONICET), Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín 956, 1113 Buenos Aires, Argentina
Further Information

Publication History

1997

1997

Publication Date:
04 January 2007 (online)

Abstract

The total reactive antioxidant potential (TRAP) and total antioxidant reactivity (TAR) of 4-nerolidylcatechol (4-NC) and methanolic extracts of Pothomorphe umbellata and P.peltata were determined by monitoring the intensity of luminol enhanced chemiluminescence by peroxyl radicals derived from thermolysis of 2,2′-azobis(2-amidinopropane). The highest antioxidant potential was measured in the extract of P. umbellata (TRAP = 97.2 µM) while the highest reactivity was observed in the extract of P.peltata (TAR = 5.0 µM), measured as equivalents of Trolox concentration. These results were higher than those obtained for 4-NC (TRAP = 33.6 µM, TAR = 4.9 µM). DNA sugar damage induced by Fe(II) salts was also used to determine the capacity of 4-NC to suppress hydroxyl radical-mediated degradation of DNA. Calculated IC50 values for 4-NC and catechin, used as a standard, were 25 and 17 µM, respectively.

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