Abstract
It is now well established that the prostate and other androgen-sensitive peripheral structures (seminal vesicles, sebaceous gland, kidney, etc.) metabolise testosterone into 5α-androstan-17β-ol-3-one (dihydrotestosterone, DHT) and subsequently into 5α-androstan-3α,17β-diol (3α-diol) (Wilson and Gloyna, 1970; Robel et al., 1971; Schmidt et al., 1972; Massa and Martini, 1972, 1974). In the peripheral androgen-responding tissues small amounts of 5α-androstan-3α, 17β-diol (3β-diol) are also formed (Shimazaki et al., 1972; Levy et al., 1974; Taurog et al., 1975). These conversions occur under the influence of a 5α-reductase 3α- and 3β-hydroxysteroid dehydrogenase system (figure 1). According to the most widely accepted theory, these αa-reduced metabolites act as the intracellular mediators of the multiple actions testosterone exerts on its target structures (Bruchovsky and Wilson, 1968; Wilson and Gloyna, 1970; Robel et al., 1971; Schmidt et al., 1973).
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© 1981 Institute of Biology Endowment Trust Fund
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Martini, L., Avogadri, N., Ferraboschi, P., Celotti, F., Motta, M. (1981). Control of androgen metabolism in the peripheral and central structures: physiological implications. In: Lewis, G.P., Ginsburg, M. (eds) Mechanisms of Steroid Action. Biological Council The Co-ordinating Committee for Symposia on Drug Action. Palgrave, London. https://doi.org/10.1007/978-1-349-81345-2_10
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DOI: https://doi.org/10.1007/978-1-349-81345-2_10
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