Human testicular steroidogenesis was studied by determining the concentration of dehydroepiandrosterone (DHA), androstenediol (AD), testosterone (T), androstenedione (Δ
4A), DHA-sulfate, AD-sulfate, T-sulfate and gonadotropins in venous blood samples collected from spermatic veins during castration. Blood samples were drawn from spermatic and peripheral veins at 0, 15, 30, 60, 90 and 120 min after injection of 100μg LH-RH. The concentrations of gonadotropin and steroid were measured by radioimmunoassay. The results were as follows : 1) LH and FSH levels in spermatic venous blood were very close to those in peripheral venous blood after the LH-RH injection. 2) The concentrations of DHA, AD and T increased promptly at 5 min and was significantly greater than the 0 min level at 5-120 min after LH-RH injection. The post-injection levels of Δ
4A were higher than the 0 min level, but statistically significant (p<0.05) elevation of Δ
4A occurred only at 90 min after the LH-RH injection. Although there was significant correlation between T levels, DHA levels and AD levels at 30-120 min after LH-RH injection, Δ
4A levels did not correlate with T, DHA or AD levels. 3) The concentrations of T-sulfate and AD-sulfate did not increase significantly but the concentrations of DHA-sulfate increased significantly at 5-90 min after LH-RH injection compared with the 0 min level. The DHA-sulfate levels correlated with the AD-sulfate levels at 5-120 min. On the basis of the results from these stimulation studies, we concluded that human testicular steroidogenesis responds to intrinstic LH induced by LH-RH injection
in vivo. In this human testicular steroidogenesis, it is strongly suggested that the Δ
5-pathway is preferred to the Δ
4-pathway. It is suggested that the human testis secretes DHA-sulfate
in vivo.
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