Planta Med 1995; 61(4): 337-340
DOI: 10.1055/s-2006-958095
Papers

© Georg Thieme Verlag Stuttgart · New York

Effect of Peroxisomicine and Related Anthracenones on Catalase Activity

Myrthala Moreno-Sepúlveda, Rigoberto Vargas-Zapata, Dolores Esquivel-Escobedo, Noemí Waksman de Torres, Alfred Piñeyro-López
  • Departamento de Farmacologia y Toxicologia, Facultad de Medicina, Universidad Autónoma de Nuevo León, Apartado Postal 146, Col del Valle Garza García, N.L. 66220 México
Further Information

Publication History

1994

1994

Publication Date:
04 January 2007 (online)

Abstract

Dimeric anthracenones were isolated from toxic plants of the genus Karwinskia (Rhamnaceae). T 514 or peroxisomicine A1 is one of these toxic compounds which produces an irreversible and selective damage on the peroxisomes of yeast cells in vivo. In this paper we now report the inhibitory effect in vitro of peroxisomicine A1 and other structurally related anthracenones on liver catalase activity. The peroxisomicine A1 produces a non-competitive inhibition with respect to H2O2 on bovine, dog, and mouse liver catalases. In the three cases Vmax was decreased whereas Km was unaffected. Other dimeric anthracenones of natural origin were also found to be inhibitors of bovine liver catalase. There is a relationship between structure and degree of inhibition of all anthracenonic compounds tested. Peroxisomicine A1 and peroxisomicine A2 caused the highest degree of inhibition (IC50 = 3.34 and 3.64 µM, respectively).

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