Journals / Turkish Journal of Biology / 2015 / Cilt: 39 - Sayı: 3

Eugenol biologic activity in immunosuppressed rat females with Candida albicans genital infection: histocytological changes

Pages
455–460
Publication Date
2015-08-13
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The efficiency in the in vivo experimental candidiasis exerted by eugenol upon the tissues' histoarchitecture allows us to seriously consider it as a promising antifungal active substance, useful therapeutically in genital candidiasis and, in our opinion, with comparable biologic activity to that of nystatin.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:From our prior studies concerning eugenol's biologic activity we observed the very good in vitro antifungal efficiency of this natural compound.
📊
Key Findings & Data:Those positive results generated the need to supplement the available information with a comparative in vivo animal model.
💡
Conclusion & Impact:The efficiency in the in vivo experimental candidiasis exerted by eugenol upon the tissues' histoarchitecture allows us to seriously consider it as a promising antifungal active substance, useful therapeutically in genital candidiasis and, in our opinion, with comparable biologic activity to that of nystatin.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Candida albicans · eugenol · genital infection

Abstract

From our prior studies concerning eugenol's biologic activity we observed the very good in vitro antifungal efficiency of this natural compound. Those positive results generated the need to supplement the available information with a comparative in vivo animal model. In this context, our current study was proposed to ascertain and compare the effects of eugenol with nystatin with a placebo control group (saline solution) by evaluating the cytohistological alterations in immunosuppressed Wistar female rats genitally infected with Candida albicans. The observed histological alterations were most apparent in the placebo group. Candidiasis affected the liver, ovaries, kidneys, and spleen of the infected female rats. When compared to the groups treated with eugenol and nystatin, these alterations were either less discernible or were not reported at all, except for the liver degenerations, which were attributed to the immunosuppressive activity of drugs used and not to the Candida infection. The efficiency in the in vivo experimental candidiasis exerted by eugenol upon the tissues' histoarchitecture allows us to seriously consider it as a promising antifungal active substance, useful therapeutically in genital candidiasis and, in our opinion, with comparable biologic activity to that of nystatin.

Özet

From our prior studies concerning eugenol's biologic activity we observed the very good in vitro antifungal efficiency of this natural compound. Those positive results generated the need to supplement the available information with a comparative in vivo animal model. In this context, our current study was proposed to ascertain and compare the effects of eugenol with nystatin with a placebo control group (saline solution) by evaluating the cytohistological alterations in immunosuppressed Wistar female rats genitally infected with Candida albicans. The observed histological alterations were most apparent in the placebo group. Candidiasis affected the liver, ovaries, kidneys, and spleen of the infected female rats. When compared to the groups treated with eugenol and nystatin, these alterations were either less discernible or were not reported at all, except for the liver degenerations, which were attributed to the immunosuppressive activity of drugs used and not to the Candida infection. The efficiency in the in vivo experimental candidiasis exerted by eugenol upon the tissues' histoarchitecture allows us to seriously consider it as a promising antifungal active substance, useful therapeutically in genital candidiasis and, in our opinion, with comparable biologic activity to that of nystatin.

🔖

Cite This Article

CRISTINA, R. T., OBISTIOIU, D., DUMITRESCU, E., NICHITA, İ., MUSELIN, F., BREZOVAN, D., CERNEA, M. S. (2015). Eugenol biologic activity in immunosuppressed rat females with Candida albicans genital infection: histocytological changes. Turkish Journal of Biology, Cilt: 39 - Sayı: 3, 455–460. https://ajindex.com/articles/181781

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (10)

  1. Baykan Erel Ş, Reznicek G, Şenol SG, Karabay YavaşoğuluNÜ, Konyalıoğlu S, Zeybek AU (2012). Antimicrobial and antioxidant properties of Artemisia L. species from western Anatolia. Turk J Biol 36: 75–84.
  2. Cavaleiro C, Pinto E, Gonçalves MJ, Salgueiro L (2006). Antifungal activity of Juniperus essential oils against dermatophyte, Aspergillus and Candida strains. J Appl Microbiol 100: 1333– 1338. Chami N, Chami F, Bennis S (2004). Antifungal treatment with carvacrol and eugenol of oral candidiasis in immunosuppressed rats. Braz J Inf Dis 8: 217–226.
  3. CLSI (2009). Clinical and Laboratory Standards Institute. Method for Antifungal Disk Diffusion Susceptibility Testing of Yeasts; Approved Guideline - Second Edition. CLSI Document M44-A2. Wayne, PA, USA: CLSI. Donaldson JR, Warner SL, Cates RG, Young DG (2005). Assessment of antimicrobial activity of fourteen essential oils when using dilution and diffusion methods. Pharm Biol 43: 687–695.
  4. Dupont BF, Dromer F, Improvisi L (1996). The problem of resistance to azoles in Candida. J Mycol Med 6: 12–29.
  5. ECPVAEOSP (1986). European Convention for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes. Strasbourg, France: Council of Europe. European Parliament (2010). Directive 2010/63/EU of the European Parliament and of the Council on the Protection of Animals Used for Scientific Purposes, 22 September 2010. Official Journal of the European Union 2010 L 276, 33–79.
  6. Brussels, Belgium: European Parliament. Fidel PL Jr, Sobel JD (1996). Immunopathogenesis of recurrent vulvovaginal candidiasis. Clin Microbiol Rev 9: 335–348.
  7. Fındık D, Tuncer İ (2002). Nosocomial fungal infections in a teaching hospital in turkey: identification of the pathogens and their antifungal susceptibility patterns. Turk J Med Sci 32: 35–38.
  8. Ghaly MF, Shalaby MA, Shash SMS, Shehata MN, Ayad AA (2009). Synergistic effect of antibiotics and plant extract to control clinical bacterial isolates implicated in urinary tract infections. J Appl Sci Res 5: 1298–1306.
  9. Giordani R, Regli P, Kaloustian J, Mikaïl C, Abou L, Portugal H (2004). Antifungal effect of various essential oils against Candida albicans. Potentiation of antifungal action of amphotericin B by essential oil from Thymus vulgaris. Phytother Res 18: 990–995.
  10. Hammer KA, Carson CF, Riley TV (1998). In vitro activity of essential oils, in particular Melaleuca alternifolia (Tea tree) oil and tea tree oil products against Candida spp. J Antimicrob Chemoth 42: 591–595.