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International Journal of Analytical Chemistry
Volume 2011 (2011), Article ID 256106, 7 pages
Gas Chromatographic/Mass Spectrometric Analysis of Volatile Metabolites in Bovine Vaginal Fluid and Assessment of Their Bioactivity
1Department of Animal Science, Bharathidasan University, Tiruchirappalli 620 024, India
2Department of Animal Behaviour & Physiology, School of Biological Sciences, Madurai Kamaraj University, Madurai 625 021, India
Received 7 April 2011; Revised 6 July 2011; Accepted 7 July 2011
Academic Editor: P. Haglund
Copyright © 2011 R. Sankar and G. Archunan. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The chemical profiles of vaginal fluid collected from cows in oestrus and nonoestrus were analysed by gas chromatography-mass spectrometry (GC-MS) to establish any qualitative differences that might have potential value in bovine biocommunication. Eight different organic compounds were detected using the two chromatograms. The chemical profiles of oestrus vaginal fluid were distinguished significantly by the presence of three specific substances, namely, trimethylamine, acetic acid, and propionic acid that were not present in nonoestrus phase. The oestrus specific synthetic compounds were rubbed onto the genital region of nonoestrus animals (dummy cows), and the bulls were allowed to sniff the genital region and observed sexual behaviours. The statistical significance was higher () in bulls exhibiting repeated flehmen and mounting behaviours towards the mixture of acetic acid, propionic acid, and trimethylamine as compared to test these compounds separately. It was concluded that the volatile substances present in the bovine vaginal fluid during oestrus may act as chemical communicators.
The role of pheromones in reproduction has been well documented in several species of mammals [1–4]. The pheromonal cues excreted through faeces, urine, vaginal secretions, saliva, and specialised scent glands play a significant role in sexual and social behaviour . In cattle, it is known that bulls can detect pheromone odours and differentiate between oestrus and nonoestrus urine or vaginal fluid [6–8]. The physical and chemical properties of bovine vaginal mucus have been of long standing interest to reproductive biologists because the mucus enhances conception by facilitating viability and transport of sperm . The oestrus female attracts the male and informs its receptive state by means of chemical signals deriving from vaginal discharge  and urine . There is considerable evidence that olfactory components produced from vaginal fluid influence the male sexual behaviour in buffaloes , hamsters , sheep , and bovines [15, 16]. In addition, it has reported that vaginal secretions of heifers at oestrus stimulated sexual activity and mounting behaviour .
The individual animal may produce several volatile compounds from a single source but the influence of pheromone activity may be one compound or a mixture of compounds. Hence, it is necessary to analyse the bioactivity of individual volatile compounds identified in the bovine vaginal fluid. However, identification of the volatile compounds in bovine vaginal fluid and knowledge of how their biological activity may influence sexual behaviour remained to date. The present investigations were designed to analyse the chemistry of vaginal fluid and assess their bioactivity.
2. Materials and Methods
2.1. Sample Collection
Vaginal fluid was collected from twelve healthy cows, Bos taurus at the Exotic Cattle Breeding Centre, Tanjore, India. They were artificially bred, and the females were approximately 20 to 30 months old, and the males were 30 to 36 months old. The animals were fed a standard diet in which the presence of the chemicals has entirely differed from the identified compounds from the vaginal fluid. The same diet was provided throughout the study. Examination per rectum of each heifer was performed regularly at one- or two-week intervals to verify the normal morphological changes in the internal organ of uterus. Since the detection of vaginal fluid pheromones by bulls is more important for the success of oestrus detection under natural conditions, the samples were collected on the basis of bull behaviours such as licking, sniffing, flehmen, and mounting during oestrus and nonoestrus phases under natural conditions. The technique involved rectal massage of the reproductive tract or an infusion tube placed within the vagina prior to a.i. The samples were screened through cheese cloth or nylon mesh (60–120 μm) at the time of collection. Immediately after screening, the samples were stored frozen at −20°C and analyzed by gas chromatography mass spectrometry (GC-MS).
2.2. Sample Analysis
The samples collected from the particular stage as per the experimental protocol were pooled to minimise the effect of individual variation. In a preliminary study, nine organic solvents, namely, n-hexane, acetone, methanol, ethanol, petroleum ether, diethyl ether, chloroform, dichloromethane, and benzene were used to extract the compounds from the vaginal fluid samples. Among the different solvents used, the bull exhibited maximum response (i.e., Flehmen) when exposed to the sample dissolved in diethyl ether. Hence, this solvent was used throughout the study. Triplicate 15 mL of samples were taken from the pooled samples and separately mixed with 15 mL of diethyl ether. The supernatant was filtered through a silica-gel column (60–120 mesh) 30 min at room temperature. The filtered extract was reduced to 1/5 of its original volume by cooling with liquid nitrogen to condense it.
The sample was fractionated, and chemical compounds were identified by GC-MS (QP-5050, Shimadzu). Two microlitres of extract were injected into the GC-MS system on a 30 m glass capillary column with a film thickness of 0.25 μm (30 × 0.2 mm i.d. coated with UCON HB 2000) using the following temperature program: initial oven temperature of 40°C for 4 min, increasing to 250°C at 15°C/min, and then held at 250°C for 10 min. The GC-MS was run under computer control at 70 eV. The solvent (diethyl ether) peak was seen at 4.0 min. The vaginal fluids were analyzed repeatedly six times and subjected to cross-checking and confirmation. The identified compounds were then compared with the standard run under the same conditions. These data were already stored in a compact library of chemical substance (NIST 6221B).
2.3. Behavioural Assay
The synthetic compounds were procured and individually applied manually onto the genital region of nonoestrus animals (dummy cows). The bulls were allowed to sniff the genital region of experimental cows for a period of 30 min. The synthetic compounds were soaked with diethyl ether on cottonwool. The diethyl ether was used for GC-MS analysis as well as dissolving the synthetic compounds in various concentrations for example, 0.5%, 1.0%, 2.0%, 5.0%. Since 1% concentration of oestrus-specific compounds were found to be effective in eliciting the flehmen and other behaviours of penile erection and mounting, the same concentration was taken in the ratio of 1 : 1 : 1 and used throughout the experiment to assess the bioactivity. The duration of Flehmen behaviour exhibited by the bulls in response to dummy cows that received synthetic (oestrus and nonoestrus) compounds was recorded. Subsequently, other behaviour responses like penile erection, mounting, and act of copulation were also recorded.
2.4. Statistical Analyses
The data were compiled using SPSS statistical software 10th version and subjected to analysis of variance (ANOVA) with post hoc comparison (one-way) using Duncan’s Multiple Range Test (DMRT).
The GC-MS profiles shown in Figures 1 and 2 are the representative of vaginal fluid obtained in the oestrus and nonoestrus periods. The vaginal fluid of oestrus showed five peaks and of nonoestrus exhibited three peaks. Eight different peaks were noted in the vaginal fluid of two different phases (Figure 1). A single volatile, that is, 3-hexanol, was found in both the phases whereas other two volatiles, cyclohexane 3,3,5 trimethyl and phosphonic acid, were found only in nonoestrus vaginal fluid (Table 1). Of these, trimethylamine, acetic acid, and propionic acid were unique in the oestrus phase but were absent in the nonoestrus. The peaks between 5 and 6 and after the peak 7 in nonoestrus are referred as contaminants and not matching with any related compounds. The volatile compounds identified in the vaginal fluid have the molecular weight range between 59 and 174 dalton (Table 1).
The statistical analyses showed that the flehmen behaviour of bulls was greatly influenced by the mixture of three synthetic compounds () than that of individual compounds and control sample (Table 3). The number of mounting activity and flehmen (Table 3) was higher in response to mixture of the three compounds than that of individual and in combinations.
The results of Table 2 summarises the flehmen and mounting behaviour performed by the male responder on exposure to synthetic compounds. Among the individual synthetic compounds tested the combination of acetic and propionic acid showed higher sexual behaviour than that of individual and combination of acetic acid and trimethylamine; propionic acid and trimethylamine.
The present results revealed that the acetic acid, propionic acid, and trimethylamine appeared during oestrus phase but were not found in the nonoestrus phase. Among the compounds identified in oestrus vaginal fluid, the acetic and propionic acids belong to fatty acids, and the trimethylamine is in amine group. The identification of volatile fatty acids in the bovine vaginal fluid is consistent with the report of the predominant presence of short chain aliphatic acids, acetic acid, prop-, isotonic, in vaginal secretion of rhesus monkey . Such volatile aliphatics have also been demonstrated in the vaginal secretion of an inside range of primates, including human female . Furthermore,  reported that acetic, propionic, and isobutyric acid can act as pheromone in chimpanzee.
In the present study the bulls exhibited high frequency of flehmen response when exposed to oestrus sample as well as mixture of synthetic compounds tested. It clearly indicates that these three oestrus-specific compounds probably act as sex attractants (Table 1). It has been demonstrated that the olfactory chemical signals produced from oestrus females are mediated through the vomeronasal organ (VNO) facilitating the matting behaviour through expression of flehmen response in many species [20, 21]. The present findings further confirm that the identified compounds in oestrus and to activate the bull to mount are the sex attractants.
It is reported that in some mammals, pheromones are not single compounds but a mixture . Reference  reported that three oestrus-specific compounds, namely, acetic acid, propionic acid, and 1-iodo undecane of cattle (Bos taurus) were involved in the attraction of the opposite sex. Oestrus-specific bovine urinary signal, 1-iodo undecane, is identified successfully in our laboratory by gas chromatography linked with mass spectrometry . Similarly, in the present study the mixture of acetic, propionic, and trimethylamine revealed high incidence of precopulatory behaviour. The oestrus indication may have been initiated through urine followed by vaginal secretion, and accordingly the bull responded. It is, therefore, possible that the chemical signals produced from urine and vaginal fluid may act together for initiation of the precopulatory behaviours and successful coitus.
Chemical signals are less likely to be based on the presence of unique chemical compounds than on the relative ratios of concentrations in a complex mixture . This concept is commonly termed as “Bouquet effect” [25, 26], also proposed that volatile compounds in specific ratios and in the presence of unique components might confer pheromonal effects. Consistent with this suggestion, the present study also reveals that estrus vaginal fluid contains three specific compounds, which may be the basis of estrus odours. It is noteworthy that the present study on behaviour responses showed similar results using the mixture of synthetic compounds to that of oestrus vaginal fluid. We conclude that the specific volatile fatty acids present in bovine vaginal fluid during oestrus appear to be involved in sexual communication.
This paper was partially supported by UGC and DST- FIST, New Delhi. The authors thank the textiles committee, Bangalore, for GC-MS analysis.
- Z. T. Halpin, “Individual Odors among Mammals: Origins and Functions,” Advances in the Study of Behavior, vol. 16, no. C, pp. 39–70, 1986.
- C. J. Dominic, “Chemical communication in animals,” Journal of Science and Research, vol. 41, pp. 157–169, 1991.
- R. J. Beynon and J. L. Hurst, “Urinary proteins and the modulation of chemical scents in mice and rats,” Peptides, vol. 25, no. 9, pp. 1553–1563, 2004.
- G. Archunan, “Pheromones: chemical signals for reproductive behaviour,” in Proceedings of the 28th conference of the Ethological Society of India, pp. 38–42, 2003.
- E. B. Keverne, “Pheromonal influence on the endocrine regulation of reproduction,” Trends in Neurosciences, vol. 6, no. 9, pp. 381–384, 1983.
- H. H. Sambraus and Z. Waring, “Effect of urine from oestrous cows on libido in bulls,” Zoologie Saugetterkd, vol. 40, pp. 49–54, 1975.
- K. RameshKumar, G. Archunan, R. Jeyaraman, and S. Narasimhan, “Chemical characterization of Bovine urine with special reference to oestrous cycle,” Veterinary Research Communications, vol. 24, pp. 445–454, 2000.
- R. Sankar and G. Archunan, “Occurrence of flehmen reaction in bull towards bovine (Bos taurus) oestrus urine,” in Proceedings of the 20th National Symposium the Society for Reproduction Biology and Comparative Endocrinology, Tiruchirappalli, India, January 2002.
- R. H. Foote, “Estrus detection and estrus detection aids,” Journal of Dairy Science, vol. 58, no. 2, pp. 248–256, 1975.
- W. R. Klemm, G. N. Hawkins, and E. de Los Santos, “Identification of compounds in bovine cervico-vaginal mucus extracts that evoke male sexual behavior,” Chemical Senses, vol. 12, no. 1, pp. 77–87, 1987.
- K. Rameshkumar and G. Archunan, “1- iodoundecane. An effective sex attractant from bovine estrus urine,” in Proceedings of the 20th national symposium the society for reproduction biology and comparative endocrinology, Truchirappalli, India, January 2002.
- S. Rajanarayanan and G. Archunan, “Occurrence of flehmen in male buffaloes (Bubalus bubalis) with special reference to estrus,” Theriogenology, vol. 61, no. 5, pp. 861–866, 2004.
- A. G. Singer, A. N. Clancy, F. Macrides, and W. C. Agosta, “Chemical studies of hamster vaginal discharge: male behavioral responses to a high molecular weight fraction require physical contact,” Physiology and Behavior, vol. 33, no. 4, pp. 645–651, 1984.
- J. P. Signoret, “Sexual pheromones in the domestic sheep: Importance and limits in the regulation of reproductive physiology,” Journal of Steroid Biochemistry and Molecular Biology, vol. 39, no. 4, pp. 639–645, 1991.
- W. Ma, B. A. Clement, and W. R. Klemm, “Cyclic changes in volatile constituents of bovine vaginal secretions,” Journal of Chemical Ecology, vol. 21, no. 12, pp. 1895–1906, 1995.
- R. Sankar and G. Archunan, “Flehmen response in bull: Role of vaginal mucus and other body fluids of bovine with special reference to estrus,” Behavioural Processes, vol. 67, no. 1, pp. 81–86, 2004.
- K. Nishimura, K. Utsumi, T. Okano, and A. Iritani, “Separation of mounting-inducing pheromones of vaginal mucus from estrual heifers,” Journal of Animal Science, vol. 69, no. 8, pp. 3343–3347, 1991.
- A. M. Paleologou, “Detecting oestrus in cows by a method based on bovine sex pheromones,” Veterinary Record, vol. 100, no. 15, pp. 319–320, 1977.
- P. A. Brennan, “The vomeronasal system,” Cellular and Molecular Life Sciences, vol. 58, no. 4, pp. 546–555, 2001.
- D. F. Walker, “Causes of copulatory failure in beef bulls,” Modern Veterinary Practice, vol. 65, no. 4, pp. 252–256, 1984.
- S. Kannan and G. Archunan, “Chemistry of clitoral gland secretions of the laboratory rat: assessment of behavioural response to identified compounds,” Journal of Biosciences, vol. 26, no. 2, pp. 247–252, 2001.
- T. Hoverstad, A. Bjorneklett, O. Fausa, and T. Midtvedt, “Short-chain fatty acids in the small-bowel bacterial overgrowth syndrome,” Scandinavian Journal of Gastroenterology, vol. 20, no. 4, pp. 492–499, 1985.
- R. Sankar and G. Archunan, “Identification of putative pheromones in bovine (Bos taurus) faeces in relation to estrus detection,” Animal Reproduction Science, vol. 103, no. 1-2, pp. 149–153, 2008.
- M. L. Gorman, “A mechanism for individual recognition by odour in Herpestes auropunctatus (Carnivora: Viverridae),” Animal Behaviour, vol. 24, no. 1, pp. 141–145, 1976.
- C. J. Welsh, R. E. Moore, R. J. Bartelt, and L. L. Jackson, “Novel, species-typical esters from preputial glands of sympatric voles, Microtus montanus and M. pennsylvanicus,” Journal of Chemical Ecology, vol. 14, no. 1, pp. 143–158, 1988.
- P. F. Flood, S. R. Abrams, G. D. Muir, and J. E. Rowell, “Odor of the muskox—a preliminary investigation,” Journal of Chemical Ecology, vol. 15, no. 8, pp. 2207–2217, 1989.