본문 바로가기
KERD
논문KCI 등재

Inhibitory Effects on Oral Microbial Activity and Production of Lipopolysaccharides-Induced Pro-Inflammatory Mediators in Raw264.7 Macrophages of Ethanol Extract of Perilla flutescens (L.) Britton

1

조회

0

다운로드

2

인용

0

참고문헌

키워드

주제분류치의학

초록

Background: The leaves of Perilla frutescens, commonly called perilla and used for food in Korea, contain components with a variety of biological effects and potential therapeutic applications. The purpose of this study was to identify the components of 70% ethanol extracted Perilla frutescens (EEPF) and determine its inhibitory effects on oral microbial activity and production of nitric oxide (NO) and prostaglandin E2 (PGE2) in lipopolysaccharides (LPS)-stimulated Raw264.7 macrophages, consequently, to confirm the possibility of using EEPF as a functional component for improving the oral environment and preventing inflammation. Methods: One kg of P. frutescens leaves was extracted with 70% ethanol and dried at −70oC. EEPF was analyzed using high-performance liquid chromatography analysis, and antimicrobial activity against oral microorganisms was revealed using the disk diffusion test. Cell viability was elucidated using a methylthiazolydiphenyl-tetrazolium bromide assay, and the effect of EEPF on LPS-induced morphological variation was confirmed through microscopic observation. The effect of EEPF on LPS-induced production of pro-inflammatory mediators, NO and PGE2 was confirmed by the NO assay and PGE2 enzyme-linked immunosorbent assay. Results: The main component of EEPF was rosemarinic acid, and EEPF showed weak anti-bacterial and anti-fungal effects against microorganisms living in the oral cavity. EEPF did not show toxicity to Raw264.7 macrophages and had inhibitory effects on the morphological variations and production of pro-inflammatory mediators, NO and PGE2 in LPS-stimulated Raw264.7 macrophages. Conclusion: EEPF can be used as a functional material for improving the oral environment through the control of oral microorganisms and for modulating inflammation by inhibiting the production of inflammatory mediators.

Abstract

Background: The leaves of Perilla frutescens, commonly called perilla and used for food in Korea, contain components with a variety of biological effects and potential therapeutic applications. The purpose of this study was to identify the components of 70% ethanol extracted Perilla frutescens (EEPF) and determine its inhibitory effects on oral microbial activity and production of nitric oxide (NO) and prostaglandin E2 (PGE2) in lipopolysaccharides (LPS)-stimulated Raw264.7 macrophages, consequently, to confirm the possibility of using EEPF as a functional component for improving the oral environment and preventing inflammation. Methods: One kg of P. frutescens leaves was extracted with 70% ethanol and dried at −70oC. EEPF was analyzed using high-performance liquid chromatography analysis, and antimicrobial activity against oral microorganisms was revealed using the disk diffusion test. Cell viability was elucidated using a methylthiazolydiphenyl-tetrazolium bromide assay, and the effect of EEPF on LPS-induced morphological variation was confirmed through microscopic observation. The effect of EEPF on LPS-induced production of pro-inflammatory mediators, NO and PGE2 was confirmed by the NO assay and PGE2 enzyme-linked immunosorbent assay. Results: The main component of EEPF was rosemarinic acid, and EEPF showed weak anti-bacterial and anti-fungal effects against microorganisms living in the oral cavity. EEPF did not show toxicity to Raw264.7 macrophages and had inhibitory effects on the morphological variations and production of pro-inflammatory mediators, NO and PGE2 in LPS-stimulated Raw264.7 macrophages. Conclusion: EEPF can be used as a functional material for improving the oral environment through the control of oral microorganisms and for modulating inflammation by inhibiting the production of inflammatory mediators.

참고문헌 (22)

  1. Liu J, "Determination of the content of rosmarinic acid by HPLC and analytical comparison of volatile constituents by GC-MS in different parts of Perilla frutescens (L.) Britt", Chem Cent J, 7, pp.61~ (2013)[DOI]
  2. Hyun-Ah Lee, "Anti-inflammatory Effect of Perilla frutescens (L.) Britton var. frutescens Extract in LPS-stimulated RAW 264.7 Macrophages", Preventive Nutrition and Food Science, 17(2), pp.109~115 (2012), 한국식품영양과학회[DOI]
  3. Meng L, "Antioxidant activities of polyphenols extracted from Perilla frutescens varieties", Molecules, 14, pp.133~140 (2008)[DOI]
  4. Makino T, "Anti-allergic effect of Perilla frutescens and its active constituents", Phytother Res, 17, pp.240~243 (2003)[DOI]
  5. Ueda H, "Inhibitory effect of Perilla leaf extract and luteolin on mouse skin tumor promotion", Biol Pharm Bull, 26, pp.560~563 (2003)[DOI]
  6. Kangwan N, "Rosmarinic acid enriched fraction from Perilla frutescens leaves strongly protects indomethacin-induced gastric ulcer in rats", Biomed Res Int, 2019, pp.9514703~ (2019)[DOI]
  7. Moon DO, "Rosmarinic acid sensitizes cell death through suppression of TNFalpha-induced NF-kappaB activation and ROS generation in human leukemia U937 cells", Cancer Lett, 288, pp.183~191 (2010)[DOI]
  8. Parnham MJ, "Rosmarinic acid", Drugs Future, 10, pp.756~757 (1985)
  9. Yamamoto H, "Antimicrobial activity of perilla seed polyphenols against oral pathogenic bacteria", Biosci Biotechnol Biochem, 66, pp.921~924 (2002)[DOI]
  10. Petit MD, "Prevalence of periodontitis and suspected periodontal pathogens in families of adult periodontitis patients", J Clin Periodontol, 21, pp.76~85 (1994)[DOI]
  11. Bernardes WA, "Antimicrobial activity of Rosmarinus officinalis against oral pathogens:relevance of carnosic acid and carnosol", Chem Biodivers, 7, pp.1835~1840 (2010)[DOI]
  12. Pokrowiecki R, "Oral microbiome and peri-implant diseases: where are we now?", Ther Clin Risk Manag, 13, pp.1529~1542 (2017)[DOI]
  13. 양수현, "오미자추출액의 구강미생물에 대한 항균과 구취억제 효과", 한국구강보건과학회지, 4(2), pp.93~98 (2016), 한국구강보건과학회
  14. Eswar P, "Anti-microbial activity of Tulsi {Ocimum sanctum (Linn.)} extract on a periodontal pathogen in human dental plaque: an invitro study", J Clin Diagn Res, 10, pp.ZC53~ZC56 (2016)[DOI]
  15. Kim MY, "Induction of apoptosis by Citrus unshiu peel in human breast cancer MCF-7 cells:involvement of ROS-dependent activation of AMPK", Biol Pharm Bull, 41, pp.713~721 (2018)[DOI]
  16. Bauer AW, "Antibiotic susceptibility testing by a standardized single disk method", Am J Clin Pathol, 45, pp.493~496 (1966)[DOI]
  17. 이승연, "Secretory leukocyte protease inhibitor reduces inflammation and alveolar bone resorption in LPS-induced periodontitis in rats and in MC3T3-E1 preosteoblasts", Animal Cells and Systems, 20(6), pp.344~352 (2016), 한국통합생물학회[DOI]
  18. Jeong JW, "Ethanol extract of Poria cocos reduces the production of inflammatory mediators by suppressing the NF-kappaB signaling pathway in lipopolysaccharide-stimulated RAW 264.7 macrophages", BMC Complement Altern Med, 14, pp.101~ (2014)[DOI]
  19. Kwon DH, "Schisandrin A suppresses lipopolysaccharide-induced inflammation and oxidative stress in RAW 264.7 macrophages by suppressing the NF-κB, MAPKs and PI3K", Akt pathways and activating Nrf2, Int J Mol Med, pp.2018, 41[DOI]
  20. Huang N, "Rosmarinic acid in Prunella vulgaris ethanol extract inhibits lipopolysaccharideinduced prostaglandin E2 and nitric oxide in RAW 264.7mouse macrophages", J Agric Food Chem, 57, pp.10579~10589 (2009)[DOI]
  21. 나희삼, "Nuclear Factor-κB Dependent Induction of TNF-α and IL-1β by the Aggregatibacter actinomycetemcomitans Lipopolysaccharide in RAW 264.7 Cells", International Journal of Oral Biology, 39(1), pp.15~22 (2014), 대한구강생물학회[DOI]
  22. Kang HJ, "An ethanol extract of Aster yomena(Kitam. )Honda inhibits lipopolysaccharideinduced inflammatory responses in murine RAW 264. 7macrophages", Biosci Trends, 11, pp.85~94 (2017)[DOI]

관련 논문AI추천

이 간행물의 다른 논문 (8건)