5-hydroxy-4-oxo-L-norvaline depletes intracellular glutathione: A new modulator of drug resistance
1999
Tagashira, M. (Asahi Breweries Co. Ltd., Moriya, Ibaraki (Japan)) | Nozato, N. | Isonishi, S. | Okamoto, A. | Ochiai, K. | Ohtake, Y.
To search for compounds that reverse the drug resistanc induced by glutathione (GSH), an original screening system to detect intracellular GSH depleters was established. Among 8843 microbes derived from the soil samples tested, the extracts of two Streptomyces species, named KS6701 and KS8846, lowered the intracellular GSH level of Saccharomyces cerevisiae 5 x 47. From both the microbes, 5-hydroxy-4-oxo-L-norvaline (HON) was isolated as the active compound. At a concentration of 50-100/mu-g/ml, HON also decreased the GSH/protein level of the human ovarian tumor cell line, 2008/C13*5.25 and reversed its resistance to cisplatin. We also investigated the mechanism of the depletion. HON had little effect on gamma-glutamylcysteine synthetase (gamma-GCS) or glutathione synthetase, but HON decreased the quantity of thiol substances when it was spontaneously reacted with them. This suggested that the GSH depletion by HON occurred through a mechanism different from that of buthionine sulfo
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