TESTOSTERONE METABOLISM IN TARGET TISSUES - HYPOTHALAMIC AND PITUITARY TISSUES OF ADULT RAT AND HUMAN FETUS, AND IMMATURE RAT EPIPHYSIS

被引:152
作者
JAFFE, RB
机构
[1] Steroid Research Unit, Reproductive Endocrinology Program, Department of Obstetrics and Gynecology, Ann Arbor
关键词
D O I
10.1016/S0039-128X(69)80043-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 Δ4-androstene-3,17-dione (Δ4A). The pituitary effected the greatest conversion of T to both DHT and Δ4A. The hypothalamus converted more T to DHT than did the cerebral cortex; but the conversion of T to Δ4A 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 Δ4A 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. © 1968 Holden-Day, Inc.
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页码:483 / &
相关论文
共 29 条
[1]   STUDIES IN FETAL METABOLISM .2. METABOLISM OF PROGESTERONE-4-C14 AND PREGNENOLONE-7ALPHA-H3 IN HUMAN FETAL TESTES [J].
ACEVEDO, HF ;
ISHIKAWA, E ;
AXELROD, LR ;
TAKAKI, F .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1963, 23 (09) :885-+
[3]   SELECTIVE RETENTION OF DIHYDROTESTO-STERONE BY PROSTATIC NUCLEI [J].
ANDERSON, KM ;
LIAO, S .
NATURE, 1968, 219 (5151) :277-&
[4]   METABOLISM OF 4-14C-PROGESTERONE BY HUMAN FETAL TESTIS + OVARIES [J].
BLOCH, E .
ENDOCRINOLOGY, 1964, 74 (06) :833-&
[5]  
BRUCHOVSKY N, 1968, J BIOL CHEM, V243, P5953
[6]  
BRUCHOVSKY N, 1968, J BIOL CHEM, V243, P2012
[8]  
DORFMAN RI, 1956, ANDROGENS BIOCHEMIST, P118
[9]  
GAY VL, 1969, P SOC EXP BIOL MED, V130, P1344
[10]  
GROSSER BI, 1968, STEROIDS, V11, P829