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1.
Tissue Cell ; 41(3): 214-21, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19131082

ABSTRACT

Eggshells were randomly collected from turtle nests immediately after oviposition and at the end of incubation to examine the ultrastructural features using scanning JSM-5600LV microscopy. Three layers were recognized; an outer calcareous, a middle multistrata and an inner membrane. The calcareous layer had loose nodular units varying in shape and size without interlocking attachments. In freshly laid eggs, each nodular unit had spicules arranged in folded stacks. The spicules became unfolded during incubation, to form radiating configurations. Elemental composition and mapping of the layers were analyzed using energy dispersive spectroscopy (EDS). The elements were unevenly distributed throughout the eggshell and Ca(2+) decreased significantly after hatching. X-ray diffraction was used to identify the crystals of the eggshells. It revealed that nodular units of the calcareous were made up of CaCO(3), as aragonite (91%), calcite (6%) and vaterite (3%). The middle layer consisted of organic amorphous material with aragonite (89%) and calcite (11%). The shell membrane consisted of reticular fibers with crystals predominantly of NaCl halite. Thermogravimetry analysis of the calcareous layer indicated a complete evaporation of bonded H(2)O at 480 degrees C and CO(2) at 830 degrees C. Using the differential thermal analysis (DTA), aragonite was transformed to stable calcite at 425 degrees C.


Subject(s)
Elements , Turtles/anatomy & histology , Zygote/chemistry , Zygote/ultrastructure , Animals , Calcium/analysis , Calcium/chemistry , Calcium/metabolism , Calcium Carbonate/chemistry , Calcium Carbonate/metabolism , Chorioallantoic Membrane/chemistry , Chorioallantoic Membrane/metabolism , Chorioallantoic Membrane/ultrastructure , Crystallography, X-Ray , Female , Microscopy, Electron, Scanning , Sodium Chloride/chemistry , Sodium Chloride/metabolism , Spectrum Analysis , Temperature , Turtles/physiology , Water/chemistry , Water/metabolism , Zygote/metabolism
2.
Article in English | MEDLINE | ID: mdl-15596394

ABSTRACT

SDS-polyacrylamide gel electrophoresis was used to separate the secretory proteins produced by the epithelial and endometrial glands of the uterine tube and uterus in the snapping turtle Chelydra serpentina. The proteins were analyzed throughout the phases of the reproductive cycle from May to August, including preovulatory, ovulatory, postovulatory or luteal, and vitellogenic phases. The pattern of secretory proteins is quite uniform along the length of the uterine tube, and the same is true of the uterus, but the patterns for uterine tube and uterus are clearly different. We identify 13 major proteins in C. serpentina egg albumen. Bands co-migrating with 11 of these are found in the uterine tube, but at most 4 are found in the uterus, suggesting that the majority of the albumen proteins are most likely secreted in the uterine tube, not in the uterus. Although some of the egg albumen proteins are present in the uterine tube only at the time of ovulation, most of the bands corresponding to albumen proteins are present throughout the breeding season even though the snapping turtle is a monoclutch species. These results suggest that the glandular secretory phase in the uterine tube is active and quite homogeneous in function regardless of location or phase of the reproductive cycle.


Subject(s)
Oviducts/metabolism , Reptilian Proteins/metabolism , Turtles/metabolism , Albumins/metabolism , Animals , Female , Mucous Membrane/metabolism , Uterus/metabolism
3.
Tissue Cell ; 33(4): 361-7, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11521952

ABSTRACT

In this study we investigated the effects of treatment by luteinizing hormone-releasing hormone (LHRH) on the morphology and steroid release of ovarian tissues in the Western painted turtle, (Chrysemys picta). In Experiment I, four adult female turtles were injected with synthetic mammalian LHRH (i.p., 500 pg/g bodyweight) and four with saline 2-3 weeks prior to ovulation. Granulosa cells from LHRH-treated turtles vs controls contained both preovulatory follicles (16-20 mm in diameter) and small follicles (0.5-1.00mm in diameter) with increased RER, free ribosomes and mitochondria with swollen cristae. An increase in the amount of cytoskeletal material (microfilaments) was observed in granulosa cells of the experimental turtles compared to the controls. Cytoplasmic extensions of the oocyte and granulosa cells were longer in the small follicles of treated animals, accounting for the observed increase in the thickness of the zona pellucida (ZP) over the controls. In Experiment II, administration of LHRH (i.p.) to 10 turtles during the same period triggered a substantial increase in plasma progesterone and estradiol-17beta levels over the 10 saline-injected controls. This supports the idea that in this species, as in mammals, steroidogenic activity in the ovarian follicles are under the control of the hypothalamic-pituitary axis. The ultrastructure and hormonal levels of the experimental animals were typical of untreated turtles just prior to ovulation. In this species the development of follicles and steroidogenesis can be stimulated prematurely by a releasing hormone from a nonreptilian origin.


Subject(s)
Estradiol/blood , Gonadotropin-Releasing Hormone/pharmacology , Granulosa Cells/drug effects , Progesterone/blood , Animals , Female , Fertility Agents, Female/administration & dosage , Fertility Agents, Female/pharmacology , Gonadotropin-Releasing Hormone/administration & dosage , Granulosa Cells/ultrastructure , Microscopy, Electron , Sexual Maturation , Turtles , Zona Pellucida/drug effects , Zona Pellucida/ultrastructure
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