A Possible Intracluster Origin for the Excess Soft X-ray Component in Some Clusters

The soft x-ray spectra of the Virgo and Coma clusters cannot be modeled by emission from the well-known hot intracluster medium attenuated by photoelectric absorption along the line of sight in our galaxy. If the excess soft emission is due to thermal emission in the clusters from gas at about 1 million kelvin, then the gas should be rapidly cooling. The high rate of cooling poses problems for the origin of the gas and its sink. A model in which the component is due to turbulent mixing layers around clouds scattered throughout the intracluster medium may explain the excess emission. The gas in the mixing layer is reheated after cooling, so that the total mass remains relatively small.     

Evaluation of the Karras Spermdensimeter in Relation to the Neubauer Counting Chamber for Sperm Concentration Measurement in Boar Semen

The correct measurement of spermatic concentration in boar semen is one of the basic tasks routinely performed at the Swine Artificial Insemination Center (CIAS). This article explains two experiments whose objectives were: Experiment 1: This trial had two objectives: (1) to evaluate the precision of the spermdensimeter (SPM) with relation to the Neubauer count chamber (CN) which is considered the standard technique in the field and (2) to correct the scale on the SPM table. Experiment 2: This trial also had two objectives: (1) to evaluate the time and repetitions required in the SPM and (2) to compare the SPM adjusted table produced in Expt 1 with the SPM standard table. The methods in Expt 1 were used to measure total spermatic concentration in 141 boar ejaculates. The average spermatic concentrations (10(6) spermatozoids/ml) and average dose number were 229.1 and 22.6 for CN, and 283.6 and 28.0 for SPM. These results indicate that the SPM has a tendency to overestimate spermatic concentration with relation to the CN. The SPM produced a smaller coefficient of variation and needed lesser examination time than the CN (p < 0.05). The SPM adjusted table created in Expt 1 produced similar results as the SPM and CN standard tables (2.96 billion live spermatozoids/dose vs 2.36 billion live spermatozoids/dose). Incorporation and evaluation of supplemental data from other CIAS regarding the use of the SPM adjusted table in the field entitled 'Adjusted Table for Karras Spermdensimeter LPS-FMVZ-USP' would be valuable to prove its efficiency.     

Early Development and Putative Primordial Germ Cells Characterization in Dogs

Previously, three distinct populations of putative primordial germ cells (PGCs), namely gonocytes, intermediate cells and pre‐spermatogonia, have been described in the human foetal testis. According to our knowledge, these PGCs have not been studied in any other species. The aim of our study was to identify similar PGC populations in canine embryos. First, we develop a protocol for canine embryo isolation. Following our protocol, 15 canine embryos at 21–25 days of pregnancy were isolated by ovaryhysterectomy surgery. Our data indicate that dramatic changes occur in canine embryo development and PGCs specification between 21 to 25 days of gestation. At that moment, only two PGC populations with distinct morphology can be identified by histological analyses. Cell population 1 presented round nuclei with prominent nucleolus and a high nuclear to cytoplasm ratio, showing gonocyte morphology. Cell population 2 was often localized at the periphery of the testicular cords and presented typical features of PGC. Both germ cell populations were positively immunostained with anti‐human OCT‐4 antibody. However, at day 25, all cells of population 1 reacted positively with OCT‐4, whereas in population 2, fewer cells were positive for this marker. These two PGCs populations present morphological features similar to gonocytes and intermediate cells from human foetal testis. It is expected that a population of pre‐spermatogonia would be observed at later stages of canine foetus development. We also showed that anti‐human OCT‐4 antibody can be useful to identify canine PGC in vivo.     

Anoestrus in the Dog: a Fascinating Story

In the bitch, progression from early to late anoestrus is characterized by a higher amplitude and a larger number of gonadotrophin-releasing hormone (GnRH) pulses generated by the hypothalamus, an increase in the sensitivity of the pituitary to GnRH, and an increase in ovarian responsiveness to gonadotrophins. An increase in basal plasma follicle-stimulating hormone (FSH) concentration is a critical event required for initiation of folliculogenesis. A period of increased luteinizing hormone pulsatility has been reported shortly before the onset of pro-oestrus. Apart from these changes in the hypothalamic-pituitary-ovarian axis, there is also involvement of dopaminergic influences in the initiation of a new follicular phase in the bitch. Administration of the dopamine-agonists bromocriptine and cabergoline shortens the anoestrus and is associated with a decrease in the plasma prolactin concentration, suggesting that the shortened anoestrus is the result of suppression of prolactin secretion. Yet, the anoestrus is not shortened in bitches treated with metergoline, a drug, which in a low dosage lowers the plasma prolactin concentration via a serotonin-antagonistic pathway. In addition, under physiological conditions low plasma prolactin concentrations are found during the entire anoestrus. Furthermore, a low dosage of bromocriptine, insufficient to cause a decrease in the plasma prolactin concentration, prematurely induces folliculogenesis. These observations indicate that not the decrease in the plasma prolactin concentration, but another dopamine-agonistic influence plays a critical role in the transition to a new follicular phase. The dopamine-agonist induced shortening of the anoestrus is associated with a rapid rise in the basal plasma FSH concentration, similar to what is observed during the physiological late anoestrus. This observation underlines the importance of an increase in the circulating plasma FSH concentration in the initiation of folliculogenesis in the bitch.