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Sex Glands (sex + gland)

Distribution by Scientific Domains
Life Sciences57%
Medical Sciences42%

Kinds of Sex Glands

  • accessory sex gland
    		•

    Selected Abstracts

    The Gross and Micro Anatomy of the Accessory Sex Glands of the Male Agouti (Dasyprocta leporina)

    ANATOMIA, HISTOLOGIA, EMBRYOLOGIA, Issue 3 2009
    W. M. Mollineau
    Summary This study was a follow up to the study on the gross anatomy of the male agouti (Dasyprocta leporina) reproductive system. The seminal vesicles of the agouti are lobulated structures. The mean diameter of the large lumen is 883.6 ± 76.83 ,m. The mucosa (24.1 ± 0.92 ,m), which is lined by pseudo-stratified columnar epithelium is thrown into folds, which often branch. The lamina muscularis mucosa is thin and is made of loose connective tissue containing blood vessels. The mucosa of the leaf-like coagulating glands of the agouti is folded. The mean diameter of the lumen is 488.3 ± 41.96 ,m. The mucosa contains tubuloalveolar glands, which have a mean length of 199.5 ± 28.83 ,m. The thin epithelium, 15.0 ± 1.25-,m wide, consists mostly of pseudo-stratified columnar cells. The epithelium also has surface modifications in the form of apical blebs and cilia. The epithelium of the agouti's lobulated prostate gland is also folded creating a large lumen with a mean diameter of 995.5 ± 55.70 ,m. The mucosa contains tubular and tubuloalveolar glands, each having a mean length of 134.4 ± 13.59 ,m. The epithelium (13.9 ± 1.16 ,m) consists of pseudo-stratified columnar cells. The pea-shaped bulbourethral gland (BG) of the agouti consists of convoluted tubular, mucous secretory units, which are irregularly shaped each with a mean length of 177.9 ± 7.10 ,m and a mean width of 63.5 ± 3.97 ,m. The BG of the agouti are ventro-lateral to the rectum and dorsally positioned to the pubic symphysis, and connected to the urethra by short ducts. [source]

    Photoperiod-induced apoptosis in the male genital tract epithelia of the golden hamster

    INTERNATIONAL JOURNAL OF ANDROLOGY, Issue 2 2007
    Rosa Carballada
    Summary The aim of this study was to identify some details of the changes induced by a short-day light regime (8:16 light:dark) on the male genital tract and accessory sex glands of the golden hamster Mesocricetus auratus. We principally examined the presence of apoptotic cells in the epithelium from different regions of the epididymis, seminal vesicles, prostate and coagulating gland. We detected an increase in the percentage of apoptotic cells in situ using the TUNEL technique in animals that were maintained for 6, 8 or 12 weeks in a short photoperiod. That those cells were indeed undergoing apoptosis was confirmed by the immunodetection of the active fragment of caspase-3. The apoptotic indices in the different tissues analysed were low, but were maintained for weeks, suggesting cell loss at a steady rate. We tried to correlate these changes with the testosterone levels in serum as well as with the oxidative stress in the tissue. On the other hand, the increase in size and number of lipofuscin granules indicated the possibility that a parallel increase in oxidative stress occurred in the tissues. The normalization in the number of apoptotic cells and lipofuscin granules in animals treated with testosterone suggests that both phenomena might be related to changes in the hormone levels. [source]

    Morphology and ultrastructure of the female accessory sex glands in various crickets (Orthoptera, Saltatoria, Gryllidae)

    MITTEILUNGEN AUS DEM MUSEUM FUER NATURKUNDE IN BERLIN-DEUTSCHE ENTOMOLOGISCHE ZEITSCHRIFT, Issue 2 2002
    Robert Sturm
    Abstract In the present study, the morphology and ultrastructure of the accessory sex glands in females of the three cricket species Teleogryllus commodus, Gryllus bimaculatus, and Gryllus assimilis were subject to a detailed comparison. Within the observed crickets, the pairy glands are uniformly located in the 6th and 7th abdominal segment, joining the genital chamber lateral to the terminal papilla. Each gland is composed of an apical region (R3), consisting of the end tubules which produce the main amount of secretion, a middle region (R2) storing and leading the secretion to the orifice, and a basal region (R1) defining the orifice and most basal part of the gland. Concerning the size, number of ramifications, and length/width ratio, the investigated organs are marked by great variations among the species, ranging from anisometric glands (length/width < or > 1) with low number of ramifications in Teleogryllus commodus and Gryllus assimilis to nearly isometric glands with very numerous (up to 30) ramifications in Gryllus bimaculatus. The morphology of the respective glands is uniformly expressed by an epithelium composed of a basal lamina, one layer of gland cells, and a luminal, duct-less cuticular intima forming specific spines and hair-like processes. The ultrastructure of single gland cells is marked by a basal region with a large elliptic nucleus and intracellular cisternae formed by deep invaginations of the basal cell membrane. The apical part contains numerous lipid- and protein-forming compartments, mitochondria of cristae type, vesicles, and lipid drops. The apical cell surface is enlarged by forming a dense layer of microvilli. The lipophilic secretion produced by the glands is thought to be used as a lubricant in the ovipositor during egg-laying. [source]

    Proteins of the accessory sex glands associated with the oocyte-penetrating capacity of cauda epididymal sperm from holstein bulls of documented fertility

    MOLECULAR REPRODUCTION & DEVELOPMENT, Issue 2 2007
    Arlindo A. Moura
    Abstract We previously reported that accessory sex gland fluid (AGF) from high fertility (HF) bulls influenced the oocyte-penetrating capacity of cauda epididymal sperm from low fertility (LF) bulls, based on in vitro fertilization (IVF) assays. The present study determined if AGF proteins were associated with these effects. Nineteen IVF assays with 12 bulls were grouped as follows. Group I (n,=,8): assays where sperm from LF bulls exposed to AGF from HF bulls had greater oocyte penetration than exposed to homologous AGF. Group II (n,=,7): sperm from LF bulls to AGF from HF bulls versus homologous AGF showed no significant differences. Group III (n,=,4): sperm from LF bulls treated with homologous AGF had greater fertility than sperm treated with AGF from HF bulls. Sire fertility was based on nonreturn rates (NNR) and AGF collected by artificial vagina from bulls with cannulated vasa deferentia. Two-dimensional SDS,PAGE maps of AGF were analyzed by PDQuest and proteins identified by tandem mass spectrometry and Western blots. Differences in spot intensity between AGF of HF and LF bulls were compared across groups of IVF assays (P,<,0.05). The expression of BSP A1/A2 and A3, BSP 30 kDa, clusterin, albumin, phospholipase A2 (PLA2), and osteopontin was greater in the AGF of HF bulls in Group I as compared to Groups II and III. Conversely, there was less nucleobindin in the AGF of HF bulls in Group I than in Groups II and III. This is the first report of nucleobindin (58 kDa/pI 5.6) in male reproductive fluids, using both immunoblots and mass spectrometry. Thus, the effect of AGF from HF bulls on epididymal sperm is likely the result of specific proteins expressed in the AGF. Mol. Reprod. Dev. © 2006 Wiley-Liss, Inc. [source]

    Reproductive Development of Santa Inęs Rams During the First Year of Life: Body and Testis Growth, Testosterone Concentrations, Sperm Parameters, Age at Puberty and Seminal Plasma Proteins

    REPRODUCTION IN DOMESTIC ANIMALS, Issue 4 2010
    CEA Souza
    Contents We have investigated the reproductive development of the tropically adapted Santa Inęs ram, the most common hair sheep in Brazil. From 8 to 48 weeks of age, 16 animals were evaluated for body and testis growth, semen parameters, testosterone concentrations and seminal plasma proteins, using two-dimensional SDS-PAGE. Animals were weaned at 30 days and kept in feedlots thereafter, receiving hay, concentrate (18% of crude protein) and mineral supplement. Body weight increased from 12.3 ± 0.7 to 54.3 ± 1.6 kg between 8 and 48 weeks (p < 0.05), but changes in thoracic perimeter and scrotal circumference were non-significant after 36 weeks (p > 0.05). The percentage of motile sperm increased slowly until 23 weeks and more rapidly after that age, but significant changes in progressive motility occurred after 25 weeks. Presence of abnormal sperm related inversely to age. Most significant changes in sperm concentration occurred between 38 and 44 weeks (0.38 ± 0.05 to 1.14 ± 0.24 × 109 cells/ml, p < 0.05) and testosterone reached its highest concentrations at 42 weeks, decreasing afterwards. Rams reached puberty at 28.2 ± 0.8 weeks. The number of protein spots on seminal plasma gels was similar from 15 to 18 weeks (45 and 47 spots; p > 0.05), increased until 24 weeks (141 spots) and 28 weeks (170 spots; p < 0.05) and remained without significant (p > 0.05) changes from 28 to 48 weeks (186 ± 10 spots). Furthermore, the intensity of selected spots on 2D maps increased (p < 0.05) between 15 and 28 weeks, which preceded or coincided with the main developmental changes in sperm motility and percentage of defective sperm in the ejaculates. These results will support future studies designed to characterize specific seminal plasma proteins whose expression relate to the development of testis, epididymis and accessory sex glands. [source]

    The Origin of Membrane Vesicles in Ram Seminal Plasma

    REPRODUCTION IN DOMESTIC ANIMALS, Issue 2 2006
    R El-Hajj Ghaoui
    Contents The hypothesis tested in this study was that the membrane vesicles present in ram seminal plasma are of testicular origin, rather than being secreted by the accessory sex glands as has been previously reported for a number of species. Membrane vesicles were present in cellular extracts from reproductive organs and accessory sex glands of six rams, and in the seminal plasma of a further eight rams. When four of the latter rams were subjected to vasectomy, to isolate ejaculate contents to only the secretions of the accessory sex glands, the vesicles were largely eliminated from their ejaculates, while vesicles were still present in the ejaculates of the four control rams. The constituents of the cytoplasmic droplets and membrane vesicles derived from the seminal plasma were compared by transmission electron microscopy (TEM). Vesicles present in the cytoplasmic droplets were similar in morphology but smaller on average than those in the seminal plasma. It was concluded that the membrane vesicles in ram seminal plasma originate from either the cytoplasmic droplets, or a combination of vesicles from the droplets and the epididymis. [source]