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Acta Scientiarum. Biological Sciences, 2013
Evaluation of semen characteristics after hormonal induction of the bullfrog could provide valuable information on the gametes of this species, which may be useful for projects related to artificial fertilization, animal improvement, and cryopreservation. Bullfrog males were induced to spermiate with buserelin acetate (GnRHa), and their semen was subsequently analyzed. GnRHa (0.4 μg) was administered to the bullfrog males with secondary sexual characteristics such as weight > 200 g, yellow chin, nuptial callus, and amplexus reflex, being the semen collected after 60 min. The semen volume was 5.76 mL, lightcolored. The other characteristics of the semen were: vigor of 4.80, motility of 93%, concentration of 14.24 × 10 6 mL -1 , and content of normal spermatozoa of 70%. The volume, color, vigor, motility, sperm concentration, and content of normal spermatozoa were adequate in these bullfrog semen samples. Evaluation of the bullfrog semen samples based on this set of parameters is essential for decision-making about the quality and destination of the semen.
Molecular and Cellular Endocrinology, 2003
Testicular androgens induce formation of the male urogenital tract in all mammals. In marsupials male development occurs after birth and over a prolonged period. For example, in the tammar wallaby virilization of the Wolffian ducts begins by day 20, prostate formation begins about day 25, and phallic development starts after day 80 of pouch life. Between days 20 and 40 5␣-androstane-3␣,17-diol (5␣-adiol) is formed in tammar testes and secreted into plasma. Administration of 5␣-adiol to pouch young females induces urogenital sinus virilization by day 40 and formation of a mature male prostate and phallus by day 150. 5␣-Adiol is synthesized in pouch young testes by two pathways, one involving testosterone and dihydrotestosterone and the other 5␣-pregnane-3␣,17␣-diol-20-one and androsterone as intermediates, both utilizing steroid 5␣-reductase. In target tissues 5␣-adiol acts via the androgen receptor after conversion to dihydrotestosterone but may have other actions as well. Whether 5␣-adiol plays a role in male development in placental mammals is uncertain.
Biology of Reproduction, 1978
Biology of Reproduction
Reproduction, 1990
Changes in the number and distribution of spermatozoa in the epididymis of the adult brown marsupial mouse were examined during July/August in mated and unmated males. The effects of mating on epididymal sperm populations were studied in 2 groups of males each mated 3 times and compared with the number and distribution of spermatozoa in the epididymides of 4 unmated control groups. One testis and epididymis were removed from each animal (hemicastration) either before or early in the mating season to provide information on initial sperm content and distribution. The contralateral side was removed later in the mating season to examine the effects of mating or sexual abstinence on epididymal sperm distribution. Epididymal sperm number peaked in both the distal caput and distal corpus/proximal cauda epididymidis in late July. The total number of spermatozoa, including those remaining in the testis, available to each male at the beginning of the mating season in early August was \m=~\4\m=.\4\m=x\ 106/side. Although recruitment of spermatozoa into the epididymis from the testis continued until mid-August, sperm content of the epididymis reached a peak ofabout 3\m=.\5\ m=x \ 106/epididymis in early August. At this time approximately 0\m=.\9\m=x\ 106 spermatozoa remained in the testis which had ceased spermatogenic activity. Throughout the mating season, epididymal spermatozoa were concentrated in the distal corpus/proximal cauda regions of the epididymis and were replenished by spermatozoa from upper regions of the duct. Relatively few spermatozoa were found in the distal cauda epididymidis, confirming a low sperm storage capacity in this region. A constant loss of spermatozoa from the epididymis, probably via spermatorrhoea, occurred throughout the mating season and very few spermatozoa remained in unmated males in late August before the annual male die-off. Mating studies showed that an average of 0\m=.\23\m=x\106 spermatozoa/epididymis were delivered per mating in this species, but the number of spermatozoa released at each ejaculation may be as few as 0\m=.\04\m=x\ 106/epididymis when sperm loss via spermatorrhoea is taken into account. We suggest that the unusual structure of the cauda epididymidis, which has a very restricted sperm storage capacity, may function to limit the numbers of spermatozoa available at each ejaculation and thus conserve the dwindling epididymal sperm reserves in order to maximize the number of successful matings which are possible during the mating season.
Andrologia, 2009
Consequently, a new terminology has arisen. It is used by different authors, in different languages, so that in context it has a different and sometimes opposite meaning to the old more classical nomenclature. Even if problems still remain to be clarified before a definitive understanding of the spermatogenic process is reached, the terminology should be standardized at least for the purpose of teaching students in the medical and allied areas. At the same time this would allow incorporation of the new advances that research in this field provides.
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