This mini-review discusses the probable mechanisms involved in pH regulation in sperm cells and how pH is involved in regulation of various sperm functions

Some insights into the action of TRP channels in regulating sperm fertility competence through both calcium-dependent and calcium-independent mechanisms

This study aimed to determine the thermoneutral zone (TNZ) in Sahiwal zebu calves under controlled environmental conditions. The experiment was conducted in the psychrometric chamber in two phases on six calves aged 8 to 11 months and weighing 120 to 150 Kg at the beginning of the experiment. In the first phase, to determine the upper critical temperature (UCT), calves were kept for six hours per day over 10 consecutive days at six different increasing temperature ranges from 24 to 39 °C with corresponding temperature humidity indexes (THIs) between 67 and 93. In the second phase, the same calves were exposed to decreasing temperatures (24 °C to 9 °C) to determine the lower critical temperature (LCT). On the 10th day of each temperature exposure, physiological parameters were recorded, and blood sampling was done. Using segmented regression analysis (SegReg standard version software), the breakpoints in linear regressions for different parameters with respect to exposure temperatures and THI in both phases were separately determined and considered to be the critical temperatures and threshold THIs, respectively. The LCT and UCT were arranged on a temperature scale. The temperature range between the highest LCT and the lowest UCT with respect to different studied parameters was considered as the thermoneutral zone (TNZ). The highest LCT was observed for granulocyte % at 18.15 °C, whereas the lowest UCT was observed at 30.10 °C (THI: 82.35). It was found that the LCT and UCT varied with respect to different physiological parameters. A subset of parameters displayed identifiable LCT and UCT values, while some did not exhibit clear breakpoints. The respiration rate (RR), rectal temperature (RT), total leukocyte count (TLC), granulocyte%, aspartate amino-transferase (AST), Alanine amino-transferase (ALT), cortisol, IL6, and HSP90 were the sensitive parameters for both cold stress and heat stress, whereas pulse rate (PR), triglyceride, and urea were only sensitive to cold stress, and erythrocytic parameters and lymphocyte % were sensitive only to heat stress. Based on heat stress responses, the UCT for zebu calves was identified at approximately 30.10 °C (THI: 82.35), whereas based on cold stress responses, the LCT for zebu calves was identified at approximately 18.15 °C. Thus, the TNZ for zebu calves can be proposed to be between 18.15 and 30.10 °C. These findings can inform climate-adaptive housing and management strategies for improving calf welfare and productivity in subtropical environments.

The present study was designed to evaluate the effect of supplementation of glutamine and replacement of Tris-egg yolk (TE) based buffer with defatted cow milk on the spermatozoa quality after equilibration and thawing. Semen was collected from five Bhadawari bulls biweekly, and a total of 30 ejaculates were taken. The semen ejaculates were pooled and divided into three equal parts. The pooled semen was diluted by TE based extender (control), TE + glutamine (8 mM) (T1) and 50% TE + 50% deffated cow milk + glutamine (8 mM) (T2). At two stages viz. after equilibration and after 12 h of cryopreservation (thawed samples), progressive motility, percent live, and percent acrosomal damage of the spermatozoa was assessed. Supplementation of glutamine improved (p<0.05) the spermatozoa quality with respect to the progressive motility, percent live and acrosomal damage both post-equilibration and post-thaw. T2 improved (p<0.05) the spermatozoa quality as compared to control, however; it was less (p<0.05) effective as compared T1 both post-equilibration and post-thaw. From the results of present study it can be concluded that glutamine supplementation was effective in maintaining post-equilibration and post-thaw spermatozoa quality whereas defatted cow milk was not as effective as TE based buffer in the extender in improving the spermatozoa quality.