The role of arginine vasotocin and prostaglandin F2 alpha on oviposition and luteolysis in the common snapping turtle Chelydra serpentina.

The administration of arginine vasotocin (AVT) to gravid snapping turtles with steroidogenically active corpora lutea and high plasma progesterone concentration (1480 +/- 155 pg/ml) did not trigger oviposition, whereas 12 days after ovulation when luteolysis occurred and plasma progesterone concentration was low (570 +/- 78 pg/ml), treatment with AVT caused oviposition. Controls with high plasma progesterone concentration (1605 +/- 185 pg/ml) oviposited 15-23 days after ovulation when plasma progesterone concentration dropped to 201 +/- 35 pg/ml. Deluteinization-induced oviposition was initiated 15 hr after surgery and was completed by 30 hr. Oviposition of complete clutches occurred and was correlated with a significant drop in plasma progesterone. Sham-operated turtles did not exhibit oviposition and no significant change in progesterone concentration was observed. A single injection of prostaglandin F2 alpha (PGF) in recently ovulated turtles induced early luteolysis and a significant decrease in plasma progesterone concentration after 24-30 hr. A single administration of PGF caused the disappearance of steroidogenic features such as the smooth endoplasmic reticulum and mitochondria with tubular cristae 48 hr later. Also PGF triggered the invasion of a hyaline-like material from the luteal theca into the luteal cell mass which eventually induced luteolysis. The role of AVT, PGF, and progesterone in relation to egg retention and oviposition is discussed.

Cytoplasmic progesterone receptors in uterine tissue of the snapping turtle (Chelydra serpentina).

A high affinity progesterone-binding component was detected in the cytosol of the uterus of the snapping turtle, Chelydra serpentina. Density gradient centrifugation indicated that binding of [3H]progesterone and [3H]promegestone (R5020) was to a fraction with a heavier sedimentation coefficient than bovine serum albumin (BSA) appearing as a broader peak in the 6-7 S region; it was not affected by excess cortisol. Another binding peak, lighter than BSA and appearing with [3H]R5020 and [3H]progesterone near the 4 S region, was affected by excess cortisol. Excess progesterone decreased both the heavier and lighter peaks. Analysis of steroid specificity revealed that, of the natural steroids, progesterone had the highest affinity for the uterine cytosol. This was followed by deoxycorticosterone, 5 alpha-pregnanedione, testosterone, oestradiol-17 beta, corticosterone, 5 alpha-dihydrotestosterone and cortisol. Non-linear regression analysis of saturation data indicated the presence of two classes of high affinity binding sites: progesterone-binding sites (R-sites) with equilibrium association constants (Ka) of 2.9 +/- 0.28 litres/nmol (mean +/- 95% confidence limit) for [3H]R5020 and 0.34 +/- 0.20 litres/nmol for [3H]progesterone, and corticosteroid-binding globulin-like sites (G-sites) with Ka of 4.5 +/- 1.6 litres/nmol for progesterone. The concentration of R-sites was between 0.66 +/- 0.10 and 2.6 +/- 0.55 pmol/mg protein while that of G-sites was between 0.73 +/- 0.05 and 5.0 +/- 0.27 pmol/mg protein. DEAE-cellulose filtration assay also confirmed the presence of R-sites and G-sites in the cytosol. R-sites were detectable without oestrogen priming during the preovulatory and vitellogenic phases (low progesterone, high oestrogen concentrations) when the ovarian follicles are mature (18-22 mm diameter).(ABSTRACT TRUNCATED AT 250 WORDS)

Ultrastructural changes in testes of the snapping turtle, Chelydra serpentina in relation to plasma testosterone, delta 5-3 beta-hydroxysteroid dehydrogenase, and cholesterol.

Ultrastructural changes in the testes of the common snapping turtle, Chelydra serpentina, were observed throughout the year. Plasma testosterone levels were measured and compared with the occurrence of delta 5-3 beta-hydroxysteroid dehydrogenase (3 beta-HSD), cholesterol, and steroidogenic ultrastructural features (smooth endoplasmic reticulum (SER), mitochondria with tubular cristae) in Sertoli and Leydig cells. The testosterone level is highest in May and October (mating) and relatively low during the rest of the year. Fluctuations in 3 beta-HSD and cholesterol are consistent with the interpretation that the Leydig cells are potentially active throughout the year. They undergo very little ultrastructural change, (tubular SER to vesiculate and loss of golgi during spermatogenesis and in the winter). Sertoli cells are active only during spermatogenesis from May through October and become inactive until the next cycle; 3 beta-HSD, cholesterol and ultrastructural features change more drastically in the Sertoli cells than in the Leydig cells. These results are discussed with reference to the hypothesis that testosterone of Leydig origin is concerned mainly with mating behavior and that of Sertoli origin with spermatogenesis and maturation of sperm.

Development of the ovarian follicles in relation to changes in plasma parameters and 5 delta 3 beta HSD in snapping turtle, Chelydra serpentina.

Follicular development in snapping turtle, Chelydra serpentina, was studied in relation to changes in plasma levels of estradiol-17 beta, total protein, calcium, inorganic phosphate and cholesterol. Histochemical reaction for 3 beta-HSD in granulosa and theca cells of the follicles is strong during the preovulatory and vitellogenic phases when the follicles attain their maximum size (18-22 mm) and estradiol is at a high level. The reaction for 3 beta-HSD is weal during the postovulatory phase when the developing follicles are at their minimum size (5-7 mm) and estradiol is low. Administration of estradiol-17 beta causes a rise in plasma calcium, total protein, inorganic phosphate and cholesterol.