Identification of potential pheromone source in sows.

Pheromones play a pivotal role in intra-species communication for reproduction and social behavior in a variety of mammals, such as boars. For boars, saliva is a rich source of pheromones, however, the identification of additional sources and relative abundance of pheromones in various body fluids of sows is also essential to understand the reproductive behaviors of pigs. The present study was designed to identify the source(s) of pheromones in sows. We collected urine, feces, saliva and cervical mucus/vaginal wash samples from sows at pre-estrus, estrus and post-estrus phases, and from gilts and exposed boars to each of these potential sources of pheromones. All the boars tested spent more time sniffing and hyper-salivating in response to urine from sows in estrus than that from sows not in estrus. The sniffing behavior of boars towards estrus samples differed from that towards the samples from non-estrus sows (P < 0.005) and gilts (P < 0.001). Further, hypersalivation behavior of boars differed between estrus samples and gilt samples (P < 0.05) and estrus samples compared to pre-estrus samples (P < 0.05). This is an indication that pheromones are abundant in the estrus samples. We conclude that urine of estrus sows can be a rich source of pheromones and the same can be used to identify, purify and characterize novel pheromone molecules.

Ultrastructural and physico-chemical characterization of saliva during menstrual cycle in perspective of ovulation in human.

Human saliva is a potential diagnostic fluid and any alteration in body might be reflected in saliva so that saliva is considered as "mirror of the body". Variations in salivary hormone level, ultra structure, pH, flow rate, buffering capacity and electrolytes level are found during menstrual cycle in regard to ovulation. Thirty healthy volunteers were used for the assessment of physico-chemical changes in saliva. Reproductive cycle was categorized as pre-ovulation phase (5 to 12 days), ovulation phase (13 or 14 days) and post-ovulation phase (15 to 25 days) according to salivary arborization test and hormonal analysis. Estradiol and luteinizing hormone was gradually increased and attained peak at the level of 2.28 ± 0.20 pg/mL and 1.35 ± 0.41 mIU/mL respectively during the ovulation phase. The electrolytes result clearly indicates that the influx of common electrolytes is important for crystallization and help to induce clear ferning pattern in ovulation phase. Sodium (Na) and chloride (Cl) were found to be high during ovulation phase only. Average salivary pH was 7.5, 7.1, and 7.3 during ovulation, pre- and post-ovulation phases respectively. Buffering capacity of saliva was normal during pre- and post- ovulation phases. In contrast, in ovulation phase the buffer capacity was slightly higher. At the first time, the scanning electron microscopy (SEM) studies revealed the ultra structure difference of saliva during menstrual cycle. During ovulation phase a compact network-shaped mesh was appeared; such structure was not appeared in pre- and post ovulation phases. Additionally, we observed the saliva is arrayed as a fine mosaic-like structure during ovulation. Based on physico-chemical properties and hormonal levels may lead to develop a detection kit/sensor for detecting the ovulation phase in human.