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Study on Anti-Inflammatory and Moisturizing Effect of Extracts from Abelmoschus esculentus

오크라(Abelmoschus esculentus) 추출물의 항염증 및 보습 효과 연구

  • DanHee Yoo (College of Fusion and Convergence, Seowon University) ;
  • InChul Lee (Department of Bio-Cosmetic Science, Seowon University)
  • 유단희 (서원대학교 융복합대학) ;
  • 이인철 (서원대학교 바이오코스메틱학과)
  • Received : 2023.11.21
  • Accepted : 2024.01.30
  • Published : 2024.03.28

Abstract

In this study, we studied the anti-inflammatory and physiological activities Abelmoschus esculentus extracts by hot water (AEW) and 70% ethanol (AEE) and confirm the possibility to use it as a natural ingredient. For this study measure the antioxidative activity, total polyphenol content was measured, and DPPH and ABTS scavenging activity assays were conducted. Total polyphenol content of AEW and AEE was measured, and the results showed that they were 126.76 mg TAE/100 g and 144.21 mg TAE/100 g, respectively. DPPH and ABTS radical scavenging activities were measured to determine the antioxidative activity, and the results indicated that DPPH and ABTS radical scavenging activities increased in both extracts concentration-dependently. The moisturizing effect was measured by measuring the amount of hyaluronic acid (HA) produced within HaCaT cell using the ELISA kit. AEW and AEE increased the amount of HA production in a concentration-dependent manner. In order to determine the anti-inflammatory activity of AEW and AEE, the NO assay was conducted, and the inhibitory effects were found to be 11.46% and 25.28%, respectively in 100 ㎍/ml. In order to measure the anti-inflammatory activity, nitric oxide (NO) inhibitory activity was measured, and the inhibition of expression of iNOS, COX-2 proteins was measured and shown. Furthermore, inhibition of expression was found in inflammatory inducing factors iNOS and COX-2 proteins showing concentration-dependent inhibition. This study found the excellent effects of antioxidative, moisturizing effect, anti-inflammatory activity in Abelmoschus esculentus extracts, which indicates that can be used as functional materials for aesthetics, food and functional cosmetics.

Keywords

Acknowledgement

This research was supported by "Regional Innovation Strategy (RIS)" through the National Research Foundation of Korea(NRF) funded by the Ministry of Education(MOE)(2021RIS-001).

References

  1. Kim HJ, Shin JU, Lee KH. 2013. Atopic dermatitis and skin barrier dysfunction. Allergy Asthma Respir. Dis. 1: 20-28.
  2. Lee DG, Kim MJ, Kang SH, Kim YJ. 2017. Novel Sporichthyaceae Bacterium strain K-07 skin barrier, moisturizing and anti-inflammatory activity. J. Soc. Cosmet. Sci. Korea 43: 137-147.
  3. Oh JS, Jang HH. 2015. Epidermal differentiation and skin barrier. Asian J. Beauty Cosmetol. 13: 713-720.
  4. Kim Ch, Moon WS, Jang YA. 2023. Skin barrier and anti-inflammatory effect of petasites japonicus. J. Korean Appl. Sci. Technol. 40: 258-267.
  5. Medzhitov R. 2008. Origin and physiological roles of inflammation. Nature 454: 428-435.
  6. Noh KH, Jang JH, Min KH, Chinzorig R, Lee MO, Song YS. 2011. Suppressive effect of green tea seed coat ethyl acetate fraction on inflammation and its mechanism in RAW 264.7 macrophage cell. J. Korean Soc. Food Sci. Nut. 40: 625-634.
  7. Yun HY, Dawson VL, Dawson TM. 1996. Neurobiology of nitric oxide. Crit. Rev. Neurobiol. 10: 291-316.
  8. Jeong JB, Hong SC, Jeong HJ, Koo JS. 2012. Anti-inflammatory effects of ethyl acetate fraction from Cnidium officinale Makino on LPS-stimulated RAW 264.7 and THP-1 cells. Korean J. Plant Res. 25: 299-307.
  9. Hong HH, Lee KM, Park TJ, Chi WJ, Kim SY. 2021. Anti-inflammatory effect of Distylium racemosum leaf biorenovate extract in LPS-stimulated RAW 264.7 macrophages cells. J. Appl. Biol. Chem. 64: 375-382.
  10. Jang JH, Cho HW, Lee BY, Yu KY, Yoon JY. 2016. Anti-inflammatory effects of Oenanthe javanica ethanol extract and its fraction on LPS-induced inflammation response. J. Korean Soc. Food Sci. Nutr. 45: 1595-1603.
  11. Tindall HD. 1983. Vegetables in the Tropics. pp. 325-327. McMillan AVI. London.
  12. Lamont W. 1999. Okra a versatile vegetable crop. HortTechnology 9: 179-184.
  13. Majd NE, Tabandeh MR, Shahriari A, Soleimani Z. 2018. Okra (Abelmoschus esculentus) improved islets structure, and downregulated PPARs gene expression in pancreas of high-fat diet and streptozotocin-induced diabetic rats. Cell J. 20: 31-40.
  14. Olasantan FO, Bello NJ. 2004. Optimum sowing dates for okra (Abelmoschus esculentus) in monoculture and mixture with cassava (Manihot esculenta) during the rainy season in the south-west of Nigeria. J. Agric. Sci. 142: 49-58.
  15. Uhiara NS, Onwuka G. 2014. Suitability of protein-rich extract from okra seed for formulation of ready to use therapeutic foods (RUTF). Niger. Food J. 32: 105-109.
  16. Adelakun OE, Oyelade OJ, Ade-Omowaye BIO, Adeyemi IA, Van de Venter M. 2009. Chemical composition and the antioxidative properties of Nigerian okra seed (Abelmoschus esculentus Moench) flour. Food Chem. Toxicol. 47:1123-1126.
  17. Kim HS. 2018. Effect of Abelmoschus esculentus extract on antimelanogenesis and skin barrier function. Korean J. Food Sci. Technol. 50: 344-348.
  18. Yoo DH, Lee IC. 2021. Whitening effect of Abelmoschus esculentus on melanoma cells (B16F10). Microbiol. Biotechnol. Lett. 49: 485-492.
  19. Singleton VL, Orthofer R, Lamuela-Raventos RM. 1999. Analysis of total phenols and other oxidation substrates and antioxidants by means of folin-ciocalteu reagent. Methods Enzymol. 299: 152-178.
  20. Blois MS. 1958. Antioxidant determinations by the use or a stable free radical. Nature 181: 1199-1200.
  21. Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C. 1999. Antioxidant acitivity applying an improved ABTS radical cation decolorization assay. Free Radic. Biol. Med. 26: 1231-1237.
  22. Carmichael J, DeGraff WG, Gazdar AF, Minna JD, Mitchell JB. 1987. Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing. Cancer Res. 47: 936-942.
  23. Green LC, Wagner DA, Glogowski J, Skipper PL, Wishnok JS, Tannenbaum SR. 1982. Analysis of nitrate, nitrite, and [15N] nitrate in biological fluids. Anal. Biochem. 126: 131-138.
  24. Choi SY, Lin SH, Ha TY, Kim SR, Kang KS, Hwang IK. 2005. Evaluation of the estrogenic and antioxidant activity of some edible and medical plant. Korean J. Food Sci. Technol. 37: 549-556.
  25. Lee JH, Lee SR. 1994. Analysis of phenolic substances content in Korean plant food. Korean J. Food Sci. Technol. 26: 310-316.
  26. Que F, Mao L, Zhu C, Xie G. 2006. Antioxidant properties of Chineses yellow wine, its concentrate, and volatiles. LWT Food Sci. Technol. 39: 111-117.
  27. Cha JY, Ahn HY, Eom KE, Park BK, Jun BS, Cho YS. 2009. Antioxidative activity of aralia elata shoot and leaf extracts. J. Life Sci. 19: 652-658.
  28. Fellegrini N, Ke R, Yang M, Rice-Evans C. 1999. Screening of dietary carotenoids and carotenoid-rich fruit extracts for antioxidant activities applying 2,2'-azinobis (3-ethylenebenzothiazoline6-sulfonic acid) radical cation decolorization assay. Methods Enzymol. 299: 379-389.
  29. Kim MK. 2018. Antioxidant, antimicrobial and anti-inflammatory activities of broccoli leaf extracts. J. Invest. Cosmetol. 14: 153-159.
  30. Ukeda H, Maeda S, Ishii T, Sawamura M. 1997. Spectrophotometric assay for superoxide dismutase based on tetrazolium salt 3'-1-(phenylamino)-carbonyl-3,4-tetrazolium]-bis(4-methoxy-6-nitro) benzenesulfonic acid hydrate reduction by xanthine-xanthine oxidase. Anal. Biochem. 251: 206-209.
  31. Song HJ, Jin MH, Lee SH. 2013. Effect of ferulic acid isolated from Cnidium Officinale on the synthesis of hyaluronic acid. J. Soc. Cosmet. Sci. Korea 39: 281-288.
  32. Dahiya P, Kamal R. 2013. Hyaluronic acid: a boon in periodontal therapy. N. Am. J. Med. Sci. 5: 309-315.
  33. Madhu BP, Singh KP, Saminathan M, Singh R, Shivasharanappa N, Sharma A, et al. 2016. Role of nitric oxide in the regulation of immune responses during rabies virus infection in mice. Virusdisease 27: 387-399.
  34. Kim JY, Jung KS, Jeong HG. 2004. Suppressive effects of the kahweol and cafestol on cyclooxygenase-2 expression in macrophages. FEBS Lett. 569: 321-326.
  35. Lee DS, Kim KS, Ko W, Li B, Keo S, Jeong GS, et al. 2014. The neoflavonoid latifolin isolated from MeOH extract of Dalbergia odorifera attenuates inflammatory responses by inhibiting NF-κB activation via Nrf2-mediated heme oxygenase-1 expression. Phytother. Res. 28: 1216-1223.