FK143, a novel nonsteroidal inhibitor of steroid 5α-reductase: (1) In vitro effects on human and animal prostatic enzymes
1995
Abstract Steroid 5α-reductase is an enzyme which converts testosterone into 5α-dihydrotestosterone (DHT) and is implicated in the pathogenesis of benign prostatic hyperplasia (BPH) in men. We studied in vitro effects of FK143, a nonsteroidal new compound, on 5α-reductase in human and animal prostates. Prostates were obtained from Wistar rats, Beagle dogs, and Cynomolgus monkeys as well as prostatic tissue from BPH patients obtained by the prostatectomy. Nuclear membrane fraction of prostates showed pH dependent 5α-reductase activities, and inhibitory effects of drugs were assayed at pH 6.5. FK143 inhibited human prostatic 5α-reductase in a dose-dependent manner with an IC 50 of 1.9nM and also inhibited animal 5α-reductases with similar IC 50 values. FK143 inhibited human and rat 5α-reductases in a noncompetitive fashion while finasteride, a steroidal 5α-reductase inhibitor, showed competitive inhibition. The affinities of FK143 for the human 5α-reductase is constant at pH 5 and 6.5. No inhibitory effects were shown to other oxidoreductases. These results indicate that FK143 is a new type of potent and selective 5α-reductase inhibitor.
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