Abstract

Rat pituitary, hypothalamic and cerebral cortical minces are demonstrated to effect the conversion of testosterone (T) to 5α-androstan-17β-o1-3-one (DHT) and Δ 4-androstene-3,17-dione (Δ 4A). The pituitary effected the greatest conversion of T to both DHT and Δ 4A. The hypothalamus converted more T to DHT than did the cerebral cortex; but the conversion of T to Δ 4A in these two tissues occured to approximately the same extent. Analysis of the time course of the conversion of T to DHT in these tissues demonstrated the conversion to increase in a linear fashion over 180 min., while the maximum conversions in the hypothalamus and cerebral cortex were reached by 120 min. The conversion of T to DHT and Δ 4A was also demonstrated in the human fetal hypothalamus and pituitary, and in the distal femoral epiphysis of the growing rat. In the femoral epiphysis, 5α-androstane-3α,17β-diol was also identified.

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