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1 Institute of Biomedicine,
Department of Anatomy, University of
Turku, Turku, Finland, and the
Department of Clinical Chemistry,
University of Oulu, Oulu, Finland
A microdissection procedure is described that allows
the isolation of segments of rat seminiferous tubules in
different stages of the epithelial cycle. This procedure
is based on spermatogenic stage-dependent differences
in the transillumination pattern along the freshly isolated, unstained seminiferous tubules. It allows collection of segments representing defined stages in
amounts sufficient for biochemical studies (5-10 mg
wet weight). Tubular segments at stages I, II-III, IV-V, VI,
VIIa-b, VIIc-d, VIII, IX-XI, XII, and XIII-XIV have
been used for measurement of endogenous concentrations of testosterone, 5 A number of morphologic and biochemical observations suggest unique changes in the metabolic activity
of both germ cells and Sertoli cells at stages VII and
VIII of the cycle. The possible androgen control of
these changes is discussed.
-dihydrotestosterone, progesterone, and 17
-hydroxyprogesterone by radioimmunoassays after Lipidex-5000 chromatography. Testosterone was the most abundant steroid at all stages of
the cycle, and its concentration at stage VIII was significantly higher than at any other stage. The concentration of 5
-dihydrotestosterone was markedly lower
and did not exhibit similar differences in distribution.
The levels of progesterone and 17
-hydroxyprogesterone were the same at all stages of the cycle of the
seminiferous epithelium.
Key words: androgens, seminiferous tubules, rats, stages of spermatogenesis, transillumination
Submitted on June 10, 1981
Revised on August 13, 1981
Accepted on September 29, 1981
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