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[Intracellular calcium mobilization and effects of ATP on ampullate crista hair cells of the guinea pig].

OBJECTIVE: To further understand the intracellular calcium mobilization features of the isolated ampullate crista vestibular hair cells(VHCs) and ATP effects on intracellular free calcium concentration([Ca2+]i) in VHCs of the guinea pig. METHODS: Vestibular hair cells were isolated from the guinea pig crista ampullaris by enzymatic and mechanical methods. The influence of high K+ solution and ATP on [Ca2+]i was investigated. The [Ca2+]i of VHC was examined using laser scanning confocal microscopy(LSCM) and the Ca2+ sensitive dye Fluo-3. RESULTS: (1) 75 mmol/L K+ Hank's solution resulted in an increase of [Ca2+]i in both the cytoplasm and the cuticular plate of 5 type I VHCs. In the Ca(2+)-free medium, however, 75 mmol/L K+ solution could not induce [Ca2+]i an increase in observed 5 type I VHCs. (2) In the presence of 1.0 mmol/L or 0.1 mmol/L of ATP, there was a rapid reversible rise of the [Ca2+]i in 18/19 type I VHCs. A small response of ATP-induced [Ca2+]i was found only in 1/10 of type I VHC in Ca(2+)-free medium. There was no significant increase in [Ca2+]i when the same volume of Hank's solution was applied to the chamber containing VHCs. CONCLUSIONS: The result suggests that high K+ solution led to Ca2+ influx via voltage-dependent calcium channels. Extracellular Ca2+ influx is a major source of the ATP-induced [Ca2+]i increase.

Adenosine Triphosphate↗

Bilateral seminal vesiculitis and ampullitis in a stallion.

A Thoroughbred stallion suspected of having venereal disease was found to have an infection of the accessory sex glands. Purulent debris, blood, and Pseudomonas aeruginosa were recovered from all ejaculates. Treatment with gentamicin sulfate, tobramycin, and amikacin sulfate was unsuccessful in eliminating the infection. The stallion's seminal plasma, collected during treatment with gentamicin sulfate, did not contain any appreciable antibacterial activity. Apparently, negligible amounts of gentamicin diffused across the mucosal cell borders of the accessory sex glands into the seminal plasma. Bilateral seminal vesiculitis and ampullitis were evident on examination of the reproductive tract when the stallion was euthanatized.

Animals↗

Optimum thawing temperature and time for bovine semen processed by three methods and packaged in 1 ml ampules.

A central composite rotatable design was used to determine optimum temperature and time for thawing semen which was processed in egg yolk-tris-glycerol (ETG), egg yolk-citrate-glycerol (ECG) and skim milk-glycerol (SMG) diluents. Percentage of progressive motility (PPM) and percentage of intact acrosomes (PIA) immediately after thawing (0-hr) and after 3-hr incubation at 37 degrees C were measured. The optimum conditions for temperature and time (C/sec) to sustain maximal PIA response after 3-hr incubation (PIA) were: ETG 42 degrees 121 , ECG 33 degrees 175 , and SMG 38 degrees 128 . Average conditions predicted to be "shared" by all three processing methods were 35 degrees C for 150 sec. Final seminal temperature (FST) was measured at each of these points for ETG, ECG and SMG. Each of the above conditions has a FST above 30 degrees C. A strip plot design was used to compare the optimum and predicted "shared" (35 degrees C 150 sec ) conditions with recommended method (35 degrees C 65 sec ) presently in use, denoted as "present". The predicted "shared" thawing conditions resulted in greater (P<0.01) cell viability (PPM and PIA) than did the "present" thawing method both before and after 3-hr incubation. The viability of semen thawed by the predicted "shared" method did not differ (P<0.05) from that resulting from the optimum thawing condition for each processing method (ETG, ECG and SMG) at 0-hr or 3-hr incubation. Cell viability of skim milk-glycerol processed semen degraded faster over the 3-hr incubation period that did that of ETG or ECG processed semen.

Journal Article↗