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Positive Effect of Musa paradisiaca Peel Ethanolic Extract on Antioxidant Activity and Melanin Synthesis

바나나 껍질 에탄올 추출물이 멜라닌 합성에 미치는 영향

  • Received : 2018.02.23
  • Accepted : 2018.04.24
  • Published : 2018.07.30

Abstract

Aging is accompanied by changes in the body, such as graying hair, wrinkles, and black spots composed of lipid peroxides and proteins. Melanin is a polymer substance produced by an oxidation polymerization reaction from tyrosine, and it determines the color of hair and skin. It has been reported that melanin is synthesized by melanocyte, and its excessive production by reactive oxygen species is associated with aging. The purpose of this study was to determine the direct effects of Musa paradisiaca peel ethanolic extract (MPEE) on antioxidative activity and melanin synthesis. It was observed that the antioxidant activity of MPEE was similar to that of vitamin C, a positive control, in both DPPH radical scavenging assay and reducing power assay. In order to examine cytotoxicity prior to cell experimentation, 3-(4,5-dimethythiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was performed for B16F1 cells. MPEE was not cytotoxic at $32{\mu}g/ml$ or less. In addition, MPEE increased melanin synthesis in live cells in addition to tyrosinase activity and melanin synthesis in dihydroxyphenylalanine (DOPA)-oxidation assay in vitro. Moreover, MPEE increased melanin synthesis in cells aged by pretreatment with $H_2O_2$. The expression levels of tyrosinase-related protein (TRP)-1, TRP-2, and superoxide dismutase (SOD)-2 by western blot analysis were increased in the presence of MPEE. These results suggest that MPEE could promote the melanin synthesis as an antioxidative substance.

노화란 나이가 들면서 생기는 몸의 변화로 검은 머리가 흰 머리로 변하는 백발화, 과산화 지질과 단백질로 구성되어 생성되는 검버섯, 주름 등으로 나타난다. 멜라닌은 tyrosine에서 DOPA를 거쳐 산화 중합반응에 의해 생성되는 고분자 물질로 인체 내에 존재하는 머리카락 및 피부 색을 결정한다. 이러한 멜라닌은 melanocyte에서 합성되며, 활성산소에 의해 과도하게 생성되면 노화를 일으킨다는 연구가 보고되고 있다. 본 연구의 목적은 항산화 효과 및 멜라닌 합성에 대한 바나나 껍질 추출물(MPEE)의 직접적인 효과를 밝히는 것이다. MPEE는 DPPH radical scavenging assay와 reducing power assay를 수행한 결과, 두 실험 모두 양성대조군인 vitamin C와 비슷한 항산화 활성을 나타내었다. 세포 실험에 앞서 세포 독성을 알아보기 위해 B16F1 세포에서 MTT assay를 수행하였다. MPEE는 $32{\mu}g/ml$ 이하의 농도에서 세포독성이 없는 것으로 나타났다. 또한, MPEE는 invitro에서 tyrosinase 활성과 DOPA-oxidation 뿐만 아니라 살아있는 세포에서 멜라닌 합성을 증가시켰다. 더욱이, $H_2O_2$로 세포를 노화시켜 L-DOPA 실험을 수행한 결과, MPEE는 멜라닌 합성을 증가시켰다. 단백질 수준의 발현을 위한 Western blot 분석을 수행한 결과, TRP-1, TPR-2와 SOD-2의 발현 수준은 MPEE의 존재 하에서 증가되었다. 이상의 결과는 MPEE가 항산화 소재로 멜라닌 합성을 촉진시킨다는 것을 암시하고 있다.

Keywords

References

  1. An, Y. A., Hwang, J. Y., Lee, J. S. and Kim, Y. C. 2015. Cornus officinalis methanol extract upregulates melanogenesis in melan-a cells. Toxicol. Res. 31, 165. https://doi.org/10.5487/TR.2015.31.2.165
  2. Baek, S. H. and Lee, S. H. 2015. Sesamol decreases melanin biosynthesis in melanocyte cells and zebrafish: Possible involvement of MITF via the intracellular cAMP and p38/JNK signalling pathways. Exp. Dermatol. 24, 761-766. https://doi.org/10.1111/exd.12765
  3. Beckmann, S., Long, T., Scheld, C., Geyer, R., Caffrey, C. R. and Grevelding, C. G. 2014. Serum albumin and ${\alpha}$-1 acid glycoprotein impede the killing of Schistosoma mansoni by the tyrosine kinase inhibitor Imatinib. Int. J. Parasitol. Drugs Drug Resist. 4, 287-295. https://doi.org/10.1016/j.ijpddr.2014.07.005
  4. Beltran-Garcia, M. J., Prado, F. M., Oliveira, M. S., OrtizMendoza, D., Scalfo, A. C., Pessoa Jr, A., Medeiros, M. H., White, J. F. and Di Mascio, P. 2014. Singlet molecular oxygen generation by light-activated DHN-melanin of the fungal pathogen Mycosphaerella fijiensis in black Sigatoka disease of bananas. PloS. One 9, e91616. https://doi.org/10.1371/journal.pone.0091616
  5. Cabiscol, E., Tamarit, J. and Ros, J. 2000. Oxidative stress in bacteria and protein damage by reactive oxygen species. Int. Microbiol. 3, 3-8.
  6. Cheng, L. B., Cheng, L., Bi, H. E., Zhang, Z. Q., Yao, J., Zhou, X. Z. and Jiang, Q. 2014. Alpha-melanocyte stimulating hormone protects retinal pigment epithelium cells from oxidative stress through activation of melanocortin 1 receptor-Akt-mTOR signaling. Biochem. Biophys. Res. Commun. 443, 447-452. https://doi.org/10.1016/j.bbrc.2013.11.113
  7. Fajuyigbe, D. and Young, A. R. 2016. The impact of skin colour on human photobiological responses. Pigment. Cell. Melanoma. Res. 29, 607-618. https://doi.org/10.1111/pcmr.12511
  8. Feller, L., Masilana, A., Khammissa, R. A., Altini, M., Jadwat, Y. and Lemmer, J. 2014. Melanin: the biophysiology of oral melanocytes and physiological oral pigmentation. Head Face Med. 10, 8. https://doi.org/10.1186/1746-160X-10-8
  9. Gan, E., Haberman, H. and Menon, I. 1974. Oxidation of NADH by melanin and melanoproteins. Biochim. Biophys. Acta. 370, 62-69. https://doi.org/10.1016/0005-2744(74)90031-X
  10. Han, K. H., Oh, J. C. and Ryu, C. H. 2004. A study on the optimization for preparation conditions of germinated brown rice gruel. Prev. Nutr. Food. Sci. 33, 1735-1741.
  11. Jarrett, S. G., Horrell, E. M. W., Boulanger, M. C. and D'orazio, J. A. 2015. Defining the contribution of MC1R physiological ligands to ATR phosphorylation at Ser435, a predictor of DNA repair in melanocytes. J. Invest. Dermatol. 135, 3086-3095. https://doi.org/10.1038/jid.2015.280
  12. Jeon, S., Hwang, W., Hong, Y., Kim, M., Ahn, E. and Park, S. 2016. Inhibitory effects of hericium erinaceus extracts on melanin synthesis and oxidative stress. Asian J. Beauty Cosmetol. 14, 427-435. https://doi.org/10.20402/ajbc.2016.0075
  13. Jin, M. L., Park, S. Y., Kim, Y. H., Park, G., Son, H. J. and Lee, S. J. 2012. Suppression of ${\alpha}$-MSH and IBMX-induced melanogenesis by cordycepin via inhibition of CREB and MITF, and activation of PI3K/Akt and ERK-dependent mechanisms. Int. J. Mol. Med. 29, 119-124.
  14. Kim, S. R., Ahn, J. Y., Lee, H. Y. and Ha, T. Y. 2004. Various properties and phenolic acid contents of rices and rice brans with different milling fractions. Kor. J. Food Sci. Technol. 36, 930-936.
  15. Konieczkowski, D. J., Johannessen, C. M., Abudayyeh, O., Kim, J. W., Cooper, Z. A., Piris, A., Frederick, D. T., BarzilyRokni, M., Straussman, R. and Haq, R. 2014. A melanoma cell state distinction influences sensitivity to MAPK pathway inhibitors. Cancer Discov. 4, 816-827. https://doi.org/10.1158/2159-8290.CD-13-0424
  16. Lee, H. J., Lee, W. J., Chang, S. E. and Lee, G. Y. 2015. Hesperidin, a popular antioxidant inhibits melanogenesis via Erk1/2 mediated MITF degradation. Int. J. Mol. Sci. 16, 18384-18395. https://doi.org/10.3390/ijms160818384
  17. Lee, T. H., Seo, J. O., Baek, S. H. and Kim, S. Y. 2014. Inhibitory effects of resveratrol on melanin synthesis in ultraviolet B-induced pigmentation in Guinea pig skin. Biomol. Ther. (Seoul) 22, 35. https://doi.org/10.4062/biomolther.2013.081
  18. Malathi, M. and Thappa, D. M. 2013. Systemic skin whiten-ing/lightening agents: What is the evidence? Indian. J. Dermatol. Venereol. Leprol. 79, 842. https://doi.org/10.4103/0378-6323.120752
  19. McElnea, E. M., Hughes, E., McGoldrick, A., McCann, A., Quill, B., Docherty, N., Irnaten, M., Farrell, M., Clark, A. F. and O'Brien, C. J. 2014. Lipofuscin accumulation and autophagy in glaucomatous human lamina cribrosa cells. BMC Ophthalmol. 14, 153. https://doi.org/10.1186/1471-2415-14-153
  20. Murase, D., Hachiya, A., Takano, K., Hicks, R., Visscher, M. O., Kitahara, T., Hase, T., Takema, Y. and Yoshimori, T. 2013. Autophagy has a significant role in determining skin color by regulating melanosome degradation in keratinocytes. J. Invest. Dermatol. 133, 2416-2424. https://doi.org/10.1038/jid.2013.165
  21. Muthukumaran, P. and Rajalakshmi, N. 2014. Modulation of Banana Polyphenol Oxidase (PPO) activity by naturally occurring compounds. Int. J. Pharmaceut. Res. Allied. Sci. 3, 41-44.
  22. Oboh, G., Akinsanmi, O. A., Adefegha, S. A. and Akinyemi, A. J. 2015. Interaction of plantain (musa paradisiaca) peel extracts (unripe, ripe and over ripe) with key enzymes linked to hypertension (angiotensin-i converting enzyme) and their antioxidant activities (in vitro): a nutraceutical approach. AFS 37, 1-9.
  23. Park, S. Y., Jin, M. L., Kim, Y. H., Kim, Y. and Lee, S. J. 2011. Aromatic-turmerone inhibits ${\alpha}$-MSH and IBMX-induced melanogenesis by inactivating CREB and MITF signaling pathways. Arch. Dermatol. Res. 303, 737-744. https://doi.org/10.1007/s00403-011-1155-7
  24. Sabharwal, S. S. and Schumacker, P. T. 2014. Mitochondrial ROS in cancer: initiators, amplifiers or an Achilles' heel? Nat. Rev. Cancer 14, 709. https://doi.org/10.1038/nrc3803
  25. Shawa, I. T., Mponda, J., Msefula, C., Manda, H., Gondwe, M. and Maliwichi-Nyirenda, C. 2015. Brine shrimp lethality and phytochemical determination of aqueous extracts of Senna singueana, Musa paradisiaca, and Ziziphus mucronata in Malawi. J. Basic Appl. Res. 1, 82-88.
  26. Silva, A. A., Morais, S. M., Falcão, M. J., Vieira, I. G., Ribeiro, L. M., Viana, S. M., Teixeira, M. J., Barreto, F. S., Carvalho, C. A., Cardoso, R. P. and Andrade-Junior, H. F. 2014. Activity of cycloartane-type triterpenes and sterols isolated from Musa paradisiaca fruit peel against Leishmania infantum chagasi. Phytomedicine 21, 1419-1423. https://doi.org/10.1016/j.phymed.2014.05.005
  27. Skoczynska, A., Budzisz, E., Trznadel-Grodzka, E. and Rotsztejn, H. 2017. Melanin and lipofuscin as hallmarks of skin aging. Postepy. Dermatol. Alergol. 34, 97.
  28. Swope, V., Alexander, C., Starner, R., Schwemberger, S., Babcock, G. and Abdel Malek, Z. A. 2014. Significance of the melanocortin 1 receptor in the DNA damage response of human melanocytes to ultraviolet radiation. Pigment Cell Melanoma Res. 27, 601-610. https://doi.org/10.1111/pcmr.12252
  29. Tarafder, A. K., Bolasco, G., Correia, M. S., Pereira, F. J., Iannone, L., Hume, A. N., Kirkpatrick, N., Picardo, M., Torrisi, M. R. and Rodrigues, I. P. 2014. Rab11b mediates melanin transfer between donor melanocytes and acceptor keratinocytes via coupled exo/endocytosis. J. Invest. Dermatol. 134, 1056-1066. https://doi.org/10.1038/jid.2013.432
  30. Tuerxuntayi, A., Liu, Y. Q., Tulake, A., Kabas, M., Eblimit, A. and Aisa, H. A. 2014. Kaliziri extract upregulates tyrosinase, TRP-1, TRP-2 and MITF expression in murine B16 melanoma cells. BMC. Complement. Altern. Med. 14,166. https://doi.org/10.1186/1472-6882-14-166
  31. Vijayakumar, S., Vaseeharan, B., Malaikozhundan, B., Gopi, N., Ekambaram, P., Pachaiappan, R., Velusamy, P., Murugan, K., Benelli, G. and Kumar, R. S. 2017. Therapeutic effects of gold nanoparticles synthesized using Musa paradisiaca peel extract against multiple antibiotic resistant Enterococcus faecalis biofilms and human lung cancer cells (A549). Microb. Pathog. 102, 173-183. https://doi.org/10.1016/j.micpath.2016.11.029
  32. Vogt, G. 2015. Cell Biology Research on Stem Cells, Aging, Cancer Resistance, and Epigenetics in Marbled Crayfish and Relatives. Freshw. Crayfish. : A Global Overview, 115.
  33. Wang, Y., Zhao, Y., Liu, L., Zhang, L., Xiao, H., Wu, K., Xu, Y., Hu, Y., Fu, H. and Cao, W. 2014. Inhibitory effects of imatinib mesylate on human epidermal melanocytes. Clin. Exp. Dermatol. 39, 202-208. https://doi.org/10.1111/ced.12261
  34. Waterman, P. G. and Mole, S. 1994 Analysis. of. phenolic. plant. metabolites. : Blackwell Scientific.
  35. Yamaguchi, Y. and Hearing, V. J. 2009. Physiological factors that regulate skin pigmentation. Biofactors 35, 193-199. https://doi.org/10.1002/biof.29
  36. Ye, Y., Li, J. and Yuan, Z. 2013. Effect of antioxidant vitamin supplementation on cardiovascular outcomes: a meta-analysis of randomized controlled trials. PLoS One 8, e56803. https://doi.org/10.1371/journal.pone.0056803
  37. Zorov, D. B., Juhaszova, M. and Sollott, S. J. 2014. Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release. Physiol. Rev. 94, 909-950. https://doi.org/10.1152/physrev.00026.2013