PHASE DEPENDENT DISCREPANCY IN MURINE VAGINAL MICRO-ENVIRONMENT: A CORRELATIVE ANALYSIS OF pH, GLYCOGEN AND SERUM ESTROGEN UPON EXPOSURE TO LAPATINIB DITOSYLATE

Authors

  • Mahadevan Ganesan
  • Balamuthu Kadalmani Department of Animal Science, Bharathidasan University, Tiruchirappalli, Tamilnadu, India.

Keywords:

estrous cycle, vaginal pH, phenol red, glycogen, estrogen, correlation analysis

Abstract

Objective: This present investigation was designed to correlate the Hydrogen-ion concentration of vaginal fluid with glycogen content and serum estrogen level during different phases of mice reproductive cycle. These parameters were compared with the control and treated animals to set off this factor in the field of reproductive toxicological studies.

Methods: Female Swiss Albino mice [6-8 w] with regular estrous cyclicity were separated out into two groups as control [only HPMC] and treated [lapatinib in HPMC] animals. The treatment was carried out consecutively for 21 d via oral gavage at a dose of 20 mg/kg/d. Estrous cycle, pH and glycogen content of vaginal fluid was monitored on daily basis. At the end of the experiment period, serum estrogen level was quantified by ELISA method.

Results: Significant changes were observed in diestrus index, estrogen, and glycogen content with respect to their reproductive phases. In particular, the higher variations, seen within and between groups in estrous phase, suggest the maximum inhibitory potential exhibited by the drug used, was due to the elevated expression of its receptors [EGFR] at the time of oocyte maturation and ovulation.

Conclusion: Even, a change by one pH unit may illustrate the difference between healthy and heavily infected vaginal flora. Although, the pH value of vaginal secretions is not routinely used and compared with other parameters in the toxicological studies. This present study has become the trend set for considering pH as a valuable tool in in vivo studies.

Keywords: Estrous cycle, Vaginal pH, Phenol red, Glycogen, Estrogen, Correlation analysis

Downloads

Download data is not yet available.

References

Westwood FR. The female rat reproductive cycle: a practical histological guide to staging. Toxicol Pathol 2008;36:375-84.

McLean AC, Valenzuela N, Fai S, Bennett SAL. Performing vaginal lavage, crystal violet staining, and vaginal cytological evaluation for mouse estrous cycle staging identification. J Vis Exp 2012;67:e4389. Doi:10.3791/4389. [Article in Press].

Tsujikawa H, Yu AS, Xie J, Yue Z, Yang W, He Y, et al. Identification of key amino acid residues responsible for internal and external pH sensitivity of Orai1/STIM1 channels. Sci Rep 2015;5:16747.

Gorodeski GI, Hopfer U, Liu CC, E Margles. Estrogen acidifies vaginal pH by up-regulation of proton secretion via the apical membrane of vaginal-ectocervical epithelial cells. Endocrinology 2005;146:816–24.

Willyard C. pH paper trumps expensive kits in measuring acidity. Nat Med 2007;13:1128-9.

Hunt KK, Robb GL, Strom EA, Ueno NT. [Eds.] Breast cancer. 2nd ed. New York: Springer Science and Business Media; 2013. p. 384.

Baligar PN, Kaliwal BB. Reproductive toxicity of carbofuran to the female mice: effects on estrous cycle and follicles. Industrial Health 2002;40:345–52.

Balaci IM, PÃ ll E, Groza S. The influence of vaginal pH in mice over the sex of the offspring. Cluj Vet J 2009;162:41-5.

Krisma CR. A method for the calorimetric estimation of glycogen with iodine. Anal Biochem 1962;4:17-23.

Redondo-Lopez V, Cook RL, Sobel JD. The emerging role of lactobacilli in the control and maintenance of the vaginal bacterial microflora. Rev Infect Dis 1990;12:856–72.

Ito T, Bai T, Tanaka T, Yoshida K, Ueyama T, Miyajima M, et al. Semaphorin 4D induces vaginal epithelial cell apoptosis to control mouse postnatal vaginal tissue remodeling. Mol Med Rep 2015;11:829-36.

Whitten WK. Occurrence of anoestrus in mice caged in groups. J Endocrinol 1959;18:102–7.

Hiremath MB, Kaliwal BB. Effect of endosulfan on ovarian compensatory hypertrophy in hemicastrated albino mice. Reprod Toxicol 2002;16:783–90.

Schulz A. Evaluation of minimally-invasive methods to observe the cycle of the bitch in heat. Dissertation, Berlin; 2002.

Brabin L, Roberts SA, Fairbrother E, Mandal D, Higgins SP, Chandiok S, et al. Factors affecting vaginal pH levels among female adolescents attending genitourinary medicine clinics. Sex Transm Infect 2005;81:483–7.

Ehlers J. Standardisierung und reproduzierbarkeit der vaginalzytologie bei der hundin und ihr einsatz bei der bestimmung des optimalen belegungszeitraumers. Dissertation, Munchen; 2000.

Beilly JS, Kosch FC. Hydrogen ion concentration changes in the vaginal fluid of the rat during an estrous cycle. Endocrinology 2013;25:275-7.

Neill J. Knobil and Neill´s physiology of reproduction. 3rd ed. Cambridge: Academic Press; 2005. p. 117.

Berthois Y, Katzenellenbogen JA, Katzenellenbogen BS. Phenol red in tissue culture media is a weak estrogen: Implications concerning the study of estrogen-responsive cells in culture. Proc Natl Acad Sci USA 1986;83:2496-500.

Gault MH, Koch B, Dossetor JB. Phenolsulfonphthalein [PSP] in assessment of renal function. JAMA 1967;200:871-3.

Renn TR, Bitman J, Wood JR. Influence of local estrogen administration on vaginal glycogen. Endocrinology 1968;82:62-8.

Gregoire AT, Kandil 0, Ledger WJ. The glycogen content of human vaginal epithelial tissue. Fertil Steril 1971;22:64-8.

Mack HC, Ale T. Appraisal of estrogenic activity by the vaginal glycogen index; a comparison of oral and parenteral estrone. Clin Endocrinol 1942;2:361-4.

Mack HC. The glycogen index in the menopause. Am J Obstet Gynecol 1943;45:402-18.

Published

01-05-2016

How to Cite

Ganesan, M., and B. Kadalmani. “PHASE DEPENDENT DISCREPANCY IN MURINE VAGINAL MICRO-ENVIRONMENT: A CORRELATIVE ANALYSIS OF PH, GLYCOGEN AND SERUM ESTROGEN UPON EXPOSURE TO LAPATINIB DITOSYLATE”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 5, May 2016, pp. 404-7, https://innovareacademics.in/journals/index.php/ijpps/article/view/11171.

Issue

Section

Short Communication(s)