WIDESPREAD TISSUE DISTRIBUTION OF STEROID SULFATASE, 3-BETA-HYDROXYSTEROID DEHYDROGENASE DELTA(5)-DELTA(4) ISOMERASE (3-BETA-HSD), 17-BETA-HSD 5-ALPHA-REDUCTASE AND AROMATASE ACTIVITIES IN THE RHESUS-MONKEY
C. Martel et al., WIDESPREAD TISSUE DISTRIBUTION OF STEROID SULFATASE, 3-BETA-HYDROXYSTEROID DEHYDROGENASE DELTA(5)-DELTA(4) ISOMERASE (3-BETA-HSD), 17-BETA-HSD 5-ALPHA-REDUCTASE AND AROMATASE ACTIVITIES IN THE RHESUS-MONKEY, Molecular and cellular endocrinology, 104(1), 1994, pp. 103-111
Dehydroepiandrosterone-sulfate (DHEA-S), the main secretory product of
the human adrenal, requires the presence of steroid sulfatase, 3 beta
-hydroxysteroid dehydrogenase/Delta(5)-Delta(4) isomerase (3 beta-HSD)
, 17 beta-hydroxysteroid dehydrogenase (17 beta-HSD), 5 alpha-reductas
e, and aromatase to form the active androgen dihydrotestosterone (DHT)
and the estrogens 17 beta-estradiol (E(2)) and 5-androst-ene-3 beta,1
7 beta-diol (Delta(5)-diol) in peripheral target tissues. Because huma
ns, along with non-human primates are unique in having adrenals that s
ecrete large amounts of DHEA-S, the present study investigated the tis
sue distribution of the enzymatic activity of the above-mentioned ster
oidogenic enzymes required for the formation of active sex steroids in
the male and female rhesus monkey. Estrone and DHEA sulfatase activit
ies were measured in all 25 tissues examined, and with the exception o
f the salivary glands, estrogenic and androgenic 17 beta-HSDs were pre
sent in all the tissues examined. The adrenal, small and large intesti
ne, kidney, liver, lung, fat, testis, prostate, seminal vesicle, ovary
, myometrium, and endometrium all possess the above-mentioned enzymati
c activities, thus suggesting that these tissues could possibly form t
he biologically active steroids E(2) and DHT from the adrenal precurso
r DHEA-S. On the other hand, the oviduct, cervix, mammary gland, heart
, and skeletal muscle possess all the enzymatic activities required to
synthesize E(2) from DHEA-S. The present study describes the widespre
ad tissue distribution of steroid sulfatase, 3 beta-HSD, 17 beta-HSD,
5 alpha-reductase, and aromatase activities in rhesus monkey periphera
l tissues. Such findings support the importance of developing therapeu
tic approaches to the treatment of sex steroid-sensitive diseases whic
h take into account the formation of androgens and estrogens in periph
eral target tissues.