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V. BOTTE and G. GRANATA

Instituto di Zoologia, Università di Napoli, Via Mezzocannone 8, Napoli, Italy

(Received 31 December 1976)

In the lizard Lacerta s. sicula sex steroids induce the synthesis of avidin in the oviduct in vivo (Botte, Segal & Koide, 1974). We report here evidence that these effects could be mediated, in vivo and in vitro, by RNA.

Adult female Lacerta s. sicula were maintained in terraria at 28 °C, and under a natural photoperiod. The lizards were ovariectomized and used 15 days after the operation. For the RNA preparation, three groups of ovariectomized females, each comprising 40 animals, were treated as follows: Group 1, four doses of 50 μg oestradiol dipropionate in 0·05 ml almond oil (every 3 days), administered intramuscularly; Group 2, treated with oestradiol as in Group 1, but only three times; on the fourth treatment given 0·5 mg progesterone in 0·05 ml almond oil; Group 3, injected with almond

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V. BOTTE, G. MATERAZZI, and G. CHIEFFI

SUMMARY

The placenta and the foetal membranes of rats (pregnant 5–21 days) have been assayed by histochemical methods for 3β-hydroxysteroid dehydrogenase (3β-HSDH), NAD-dependent, and 17α- and 17β-hydroxysteroid dehydrogenases (17α- and 17β-HSDH), both NAD and NADP-dependent.

3β-HSDH was limited to the trophoblastic giant cells of the first generation, whereas 17α- and 17β-HSDH were present in both the first- and second-generation giant cells and also in the endodermal cells of the inverted yolk sac placenta.

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V. BOTTE, S. TRAMONTANA, and G. CHIEFFI

SUMMARY

The placenta, foetal membranes and uterine mucosa of mice (pregnant for 8–17 days) have been investigated by histochemical methods for NAD-dependent 3β-hydroxysteroid dehydrogenase (3β-HSDH), and for NAD-and NADP-dependent 17α- and 17β-hydroxysteroid dehydrogenases (17α- and 17β-HSDH), 11α- and 11β-hydroxysteroid dehydrogenases (11α- and 11β-HSDH), and 20β-hydroxysteroid dehydrogenase (20β-HSDH).

3β-HSDH was found to be distributed in the trophoblastic giant cells of the first generation with both pregnenolone and DHA as substrates, and in the giant cells of the second generation and of the labyrinth and the endodermal cells of the inverted yolk sac placenta, but only with DHA as substrate.

17α-HSDH and 17β-HSDH, NAD-dependent, were present in both the first and second generation giant cells and in the giant cells of the labyrinth as well as in the endodermal cells of the inverted yolk sac placenta. With NADP as cofactor, 17α-HSDH and 17β-HSDH were weakly positive with all the substrates used in the giant cells of the second generation and of the labyrinth, while NADP-dependent 17β-HSDH was present in the first generation giant cells and in the endodermal cells of the inverted yolk sac placenta but only with oestradiol-17β as substrate.

The histochemical reaction for 11α-HSDH, both NAD- and NADP-dependent, was limited to trophoblastic giant cells of the second generation and of the labyrinth; 11β-HSDH, both NAD- and NADP- dependent, was distributed in the giant cells of the second generation and of the labyrinth, the epithelial cells of the uterine mucosa and the decidua basalis.

The histochemical reaction for 20β-HSDH, NAD- and NADP-dependent, was weakly positive in the giant cells of the first generation only.

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MM Di Fiore, L Assisi, V Botte, and A D'Aniello

In the present study we report the occurrence of D-aspartic acid (D-Asp) in the ovary of the green frog Rana esculenta and its putative involvement in testosterone production by the gonad. In the ovary, D-Asp concentrations undergo significant variations during the main phases of the sexual cycle. In spawning females (March), its concentration was low (2.5 +/- 1.1 nmol/g ovary) and during the post-reproductive period (June) it increased and reached its peak level (58.0 +/- 10.1 nmol/g) in October. In that month, vitellogenesis occurs in a new set of ovarian follicles and continues until the next spring. The concentrations of D-Asp in the ovary and of testosterone in the ovary and in the plasma were inversely correlated during the reproductive cycle: when endogenous D-Asp was low (March), testosterone was high (36.9 +/- 4.8 ng/g ovary; 23.1 +/- 2.76 ng/ml plasma) and, in contrast, when the D-Asp concentration was high (October), the testosterone concentration was low (0.86 +/- 0.21 ng/g ovary and 5.0 +/- 1.3 ng/ml plasma). In vivo experiments, consisting of injection of D-Asp (2.0 mumol/g body weight) into the dorsal lymphatic sac of adult female frogs, demonstrated that this amino acid accumulates significantly in the ovary. After 3 h, moreover, it caused a decrease in testosterone level in the plasma of about 80%. This inhibition was reversible: within 18 h after the amino acid injection, as the D-Asp concentration in the ovary decreased, the testosterone titre was restored in both ovary and plasma. In vitro experiments, conducted in isolated ovarian follicles, confirmed this phenomenon and identified these gonadal components as the putative D-Asp targets. Other amino acids (L-Asp, D-Glu, L-Glu, D-Ala and L-Ala) used instead of D-Asp were ineffective. These findings indicate that D-Asp is involved in the control of androgen secretion by the ovary in this amphibian species, revealing a more complex system for control of this androgen synthesis than was previously believed to exist.

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F Raucci, L Assisi, S D'Aniello, P Spinelli, V Botte, and MM Di Fiore

This study investigated the involvement of D-aspartic acid (D-Asp) in testicular steroidogenesis of the green frog Rana esculenta and its effect on stimulation of thumb pad morphology and glandular activity, a typical testosterone-dependent secondary sexual characteristic in this amphibian species. In the testis, D-Asp concentrations vary significantly during the reproductive cycle: they are low in pre- and post-reproductive periods, but reach peak levels in the reproductive period (140-236 nmol/g wet tissue). Moreover, the concentrations of D-Asp in the testis through the sexual cycle positively match the testosterone levels in the gonad and the plasma. The racemase activity evaluated during the cycle expresses its peak when D-Asp and testosterone levels are highest, that is, during the reproductive period, confirming the synthesis of D-Asp from L-Asp by an aspartate racemase. Short-term in vivo experiments consisting of a single injection of D-Asp (2.0 micro mol/g body weight) demonstrated that this amino acid accumulates significantly in the testis, and after 3 h its uptake is coupled with a testosterone increase in both testis and plasma. Moreover, within 18 h of amino acid administration, the D-Asp concentration in the testis decreased along with the testosterone titer to prestimulation levels. Other amino acids (L-Asp, D-Glu and L-Glu) used instead of D-Asp were ineffective, confirming that the significant increase in testicular testosterone was a specific feature of this amino acid. In long-term experiments, D-Asp had been administered chronically to frogs caught during the three phases of the reproductive cycle, inducing testosterone increase and 17beta-estradiol decrease in the gonad during the pre- and post-reproductive period, and vice versa during the reproductive period. The stimulatory effect of D-Asp on testosterone production by the testis is consistent with the stimulation of spermatogenesis and the maturation of thumb pads occurring in D-Asp-treated frogs. In these last animals, there was an increase of seminiferous ampoule area and a higher number of spermatids and sperm. Moreover, in spermatogonia I and II and in spermatocytes, a proliferating cell nuclear antigen (PCNA) intense immunopositivity was observed. In addition, the thumb pads of D-Asp-treated frogs compared with controls showed a significantly thicker epithelial lining, a wider area of their glands with taller secretion cells, and more numerous, PAS-positive-rich secretions. Finally, these results provide functional evidence for a biologic role of D-Asp in amphibian male steroidogenesis; therefore, this unusual amino acid could be considered a modulatory agent for reproductive processes.