The effect of yucca on proliferation, apoptosis, and steroidogenesis of porcine ovarian granulosa cells

Authors

  • Aneta Štochmaľová Constantine the Philosopher University, Tr. A. Hlinku 1, Department of Zoology and Anthropology, 949 74 Nitra
  • Attila Kadasi Slovak University of Agriculture in Nitra, Faculty of Biotechnology and and Food Science, Department of Animal Physiology, Tr. A. Hlinku 2, 949 76 Nitra
  • Richard Alexa Constantine the Philosopher University, Department of Zoology and Anthropology, Tr. A. Hlinku 1, 949 74 Nitra
  • Roland Grossman Department of Functional Genomics and Bioregulation, Institute of Animal Science, Mariensee, Neustadt
  • Alexander Sirotkin Alexander Sirotkin, Institute for Genetics and Reproduction of Farm Animals, Animal Production Research Centre Nitra, Hlohovecka 2, 951 41 Lužianky, Slovak Republic and Department of Zoology and Anthropology, Constantine the Philosopher University, Tr. A

DOI:

https://doi.org/10.5219/357

Keywords:

yucca, proliferation, apoptosis, steroidogenesis, porcine granulosa cell

Abstract

Yucca shidigera is a medicinal plant native to Mexico. Is a plant widely used in folk medicine to treat a variety of ailmentary disorders, but its action on reproductive processes and possible mechanisms of such action remains unknown. Yucca schidigera extract contains a number of steroidal saponins that, because of their biological activity, have attracted attention from the food industry for many years. Yucca extract is used as a natural feed additive with positive effect to microflora, digestion, metabolism and to improve animal muscle growth. Its extract has been used as a foodstuff and folk medicine to treat a wide variety of diseases for many years. Nevertheless, it remaines unknown, whether consumption of yucca can affect reproductive system. The aim of this study was to examine the effects of yucca on basic ovarian cell functions - proliferation, apoptosis and steroidogenesis. Porcine ovarian granulosa cells were cultured with and without yucca extract (added at doses 0; 1; 10 and 100 μg.mL-1 of medium). Markers of proliferation (% of PCNA-positive cells) and apoptosis (% cells containing bax) were analysed by immunocytochemistry. Release of steroid hormones (progesterone and testosterone) was measured by EIA. It was observed, that addition of yucca inhibited proliferation (expression of PCNA), increased apoptosis (expression of bax), stimulated progesterone and inhibited testosterone release. The ability of yucca to reduce ovarian cell proliferation, to promote ovarian cell apoptosis and affect steroidogenesis demonstrates the direct influence of yucca on female gonads. Furthermore, our observations suggest the multiple sites of action (proliferation, apoptosis, steroidogenesis) of yucca on porcine ovarian cell functions. It is not to be excluded, that consumption of yucca can suppress female reproductive functions.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

References

Abaza, I. M., El-Said, H. 2005. Effect of using Yucca Schidigera as feed additive on performance of growing rabbits. The 4th Inter. Con. on Rabbit Prod. in Hot Clim., Sharm El-Sheikh, Egypt, p. 259-266. Retrieved from the web: http://www.abazacenter.8m.net/rich_text.html

Al-Dabbas, F. M., Hamra, A. H., Awawdeh, F. T. 2008. The effect of arginine supplementation on some blood parameters, ovulation rate and concentrations of estrogen and progesterone in female Awassi sheep. Pakistan Journal of Biological Science, vol. 11, p. 2389-2394. https://doi.org/10.3923/pjbs.2008.2389.2394 PMid:19137847 DOI: https://doi.org/10.3923/pjbs.2008.2389.2394

Balazi, A., Foldesiova, M., Chrastinova, L., Sirotkin, A. V., Chrenek, P. 2013. Effect of the herbal additive "Yucca" on rabbit spermatozoa characteristics. 2013. Journal of Microbiology, Biotechnology and Food Sciences, vol. 2, p. 1829-1837.

Blaszczyk, B., Stankiewicz, T., Udala, J., Gaczarzewicz, D. 2009. Plasma progesterone analysis by time-resolved fluorescent antibody test to monitor estrous cycles in goats. Journal of Veterinary Diagnostic Investigations, vol. 21, p. 80-87. http://dx.doi.org./10.1177/104063870902100112 PMid:19139505 DOI: https://doi.org/10.1177/104063870902100112

Cheeke, P. R. 1998. Saponins: Surprising benefits of desert plants. The linus Pauling Institute Newsletter; Oregon state university, p. 4-5.

Cheeke, P., R., Piacente, S., Oleszek, W. 2006. Anti-inflammatory and anti-arthritic effects of Yucca shidigera: A review. Journal of Inflammation, vol. 3, p. 6. http://dx.doi.org./10.1186/1476-9255-3-6 PMid:16571135 DOI: https://doi.org/10.1186/1476-9255-3-6

Cox, R. M., John-Alder, H. B. 2005. Testosterone has opposite effects on male growth in lizards (Sceloporus spp.) with opposite patterns of sexual size dimorphism. Journal of Experimental Biology, vol. 208, no. 24, p. 4679-4687. http://dx.doi.org./10.1242/jeb.01948 PMid:16326949 DOI: https://doi.org/10.1242/jeb.01948

Duffy, C., Brooks, P. 2007. Using Yucca shidigera in Pig Diets: Effects on Nitrogen Metabolism. [cit.2014-02-24] Available at: http://en.engormix.com/MA-pig-industry/management/articles/using-yucca-schidigera-pig-t717/124-p0.htm

Hagan, C. R., Faivre, E. J., Lange, C. A. 2009. Scaffolding actions of membraneassociated progestrerone receptors. Steroids, vol. 74, no. 7, p. 568-572. https://doi.org/10.1016/j.steroids.2008.12.004 PMid:19135465 DOI: https://doi.org/10.1016/j.steroids.2008.12.004

Department of Animal science, Oregon State University, Corvallis, OR 97333, USA.

Jaques, K. A. 1989. Yucca sarsaponin mode of action: Effects independent of air quality problems. Animal feed, Biological additives: Proceeding, Veterinary science University of Sydney, no. 119, p. 39-46.

Kolesárová, A., Roychoudhury, S., Slivková, J., Sirotkin, A., Capcarová, M., Massanyi, P. 2010a. In vitro study on the effect of lead and mercury on porcine ovarian granulosa cells. Journal of Environmental Science and Health, Part A Toxic/ Hazard Substances Environmental Engeneering, vol. 45, p. 320-331. https://doi.org/10.1080/10934520903467907 PMid:20390873 DOI: https://doi.org/10.1080/10934520903467907

Kolesárová, A., Capcarová, M., Sirotkin, A., Medveďová, M., Kováčik, J. 2010b. Cobalt-induced changes in the IGF-I and progesteron release, expression of proliferation- and apoptosis-related peptides in porcine ovarian granulosa cells in vitro. Journal of Environmental Science and Health, Part A Toxic/ Hazard Substances Environmental Engeneering, vol. 45, no. 3, p. 810-817. http://dx.doi.org./10.1080/10934521003708968 PMid:20397087 DOI: https://doi.org/10.1080/10934521003708968

Münster, E., 1989. Entwicklung von enzymimmunologischen Messverfahren auf Mikrotitrationsplatten zur Bestimmung von Testosteron und Progesteron im Blutplasma. Doctoral Thesis. Institut for Animal Production and Breeding of the University of Hohemheim, p. 154.

Oakenfull, D., Sidhu, G.S., Cheeke, P., R. 1989. Saponins. Toxicants of Plant Origin, vol. 2, p. 97-141.

Olas, B., Wachowicz, B., Stochmal, A., Olezsek, W. 2003. Inhibition of oxidative stress in blood platelets by different phenolics from Yucca schidigera roezl. bark. Nutrition, vol. 19, p. 633-640. PMid:12831950 DOI: https://doi.org/10.1016/S0899-9007(03)00036-4

Oleszek, W., Sitek, M., Stochmal, A., Piacente, S., Pizza, C., Cheeke, P. 2001. Resveratrol and other phenolics from the bark of Yucca schidigera roezl. Journal if Agricultural and Food Chemistry, vol. 49, p. 747-752. PMid:11262023 DOI: https://doi.org/10.1021/jf001056f

Prakash, B. S., Meyer, H. H., Schallenberger, E., van de Wiel, D. F. 1987. Development of a sensitive enzyme immunoassay (EIA) for progesterone determination in unextracted bovine plasma using the second antibody technique. Journal of Steroid Biochemistry, vol. 28, no. 6, p. 623-627. https://doi.org/10.1016/0022-4731(87)90389-X PMid:3320573 DOI: https://doi.org/10.1016/0022-4731(87)90389-X

Reed, W. L., Clark, M. E., Parker, P. G., Raouf, S. A., Arguedas, N., Monk, D. S., Snajdr, E., Nolan, V., Ketterson, E. D. 2006. Physiological effects on demography: a long-term experimental study of testosterone's effects on fitness. The American Naturalist, vol. 167, no. 5, p. 667-83. https://doi.org/10.1086/503054 PMid:16671011 DOI: https://doi.org/10.1086/503054

Santoso, B., Mwenya, C., Sar, C., Takahashi, J. 2006. Ruminal fermentation and nitrogen metabolism in sheep fed a silage-based diet supplemented with Yucca Schidigera or Yucca schidigera and nisin. Animal Feed Science and Technology, vol. 129, no. 3-4, p. 187-195. https://doi.org/10.1016/j.anifeedsci.2006.01.001 DOI: https://doi.org/10.1016/j.anifeedsci.2006.01.001

Sirotkin, A. V., Chrenek, P., Darlak, K., Valenzuela, F., Kuklova, Z. 2008. Some endocrine traits of transgenic rabbits. II. Changes in hormone secretion and response of isolated ovarian tissue to FSH and ghrelin. Physiological Research, vol. 57, p. 745-751. PMid:17949242 DOI: https://doi.org/10.33549/physiolres.931150

Sirotkin, A. V., Rafay, J., Kotwica, J. 2009. Leptin controls rabbit ovarian function in vivo and in vitro: possible interrelationships with ghrelin. Theriogenology,

vol. 72, no. 6, p. 765-72. https://doi.org/10.1016/j.theriogenology.2009.05.011 PMid:19616295 DOI: https://doi.org/10.1016/j.theriogenology.2009.05.011

Sirotkin, A. V. 2010. Effect of two types of stress (heat shock/high temperature and malnutrition/serum deprivation) on porcine ovarian cell functions and their response to hormones. The Journal of Experimental Biology, vol. 213, p. 2125-2130. https://doi.org/10.1242/jeb.040626 PMid:20511527 DOI: https://doi.org/10.1242/jeb.040626

Sirotkin, A. V. 2014. Regulators of Ovarian Functions. Nova Publishers, New York, p. 193. ISBN 978-1-61324-468-5

Southon, S., Wright, A. J. A., Price, K. R., Fairweather-Tait, S. J., Fenwick, G. R. 1988. The effect of three types of saponin on iron and zinc absorption from a single meal in the rat. British Journal of Nutrition, vol. 59, p. 389-396. https://doi.org/10.1079/BJN19880048 PMid:3395602 DOI: https://doi.org/10.1079/BJN19880048

Swaab, D. F., Garcia-Falgueras, A. 2009. Sexual differentiation of the human brain in relation to gender identity and sexual orientation. Functional Neurology, vol. 24, no. 1, p. 17-28. PMid:19403051

Tanaka, O., Tamura, Y., Masuda, H., Mizutani, K. 1996. Application of saponins in foods and cosmetics: saponins of Mohave yucca and Sapindus mukurossi. Advances in Experimental Medicine and Biology, vol. 405, p. 1-11. https://doi.org/10.1007/978-1-4613-0413-5_1 PMid:8910691 DOI: https://doi.org/10.1007/978-1-4613-0413-5_1

Watanabe, C. M. H., Wolfram, S., Ader, P., Rimbach, G., Packer, L., Maguire, J. J. 2001. The in vivo neuromodulatory effects of the herbal medicine ginkgo biloba. Proceedings of the National Academy of Sciences, vol. 98, p. 6577-6580. https://doi.org/10.1073/pnas.111126298 PMid:11381109 DOI: https://doi.org/10.1073/pnas.111126298

Downloads

Published

2014-04-29

How to Cite

Štochmaľová, A. ., Kadasi, A. ., Alexa, R. ., Grossman, R. ., & Sirotkin, A. . (2014). The effect of yucca on proliferation, apoptosis, and steroidogenesis of porcine ovarian granulosa cells. Potravinarstvo Slovak Journal of Food Sciences, 8(1), 87–91. https://doi.org/10.5219/357

Most read articles by the same author(s)