Skip to main content
Log in

Extract of Oplopanax elatus Adventitious Roots Inhibits Melanogenesis in B16F10 Cells by Regulating cAMP/MAPK Pathways

  • Research Paper
  • Published:
Iranian Journal of Science and Technology, Transactions A: Science Aims and scope Submit manuscript

Abstract

Oplopanax elatus Nakai is an endangered perennial shrub of the Araliaceae family with various bioactive compounds, but its practical application is limited by the shortage of plant resource. Adventitious root (AR) culture is a novel approach for obtaining plant materials; thus, this study used the extract from bioreactor cultured O. elatus ARs (OAE) as experimental material and investigated the effect of OAE on inhibiting melanin synthesis of mouse melanoma cells (B16-F10) to utilize the ARs in production of related products in the future. The results showed that tyrosinase activity and melanin content of B16-F10 cells were inhibited by the treatments of 12.5, 25, and 50 μg/mL OAE, but those did not significantly decrease at 6.25 μg/mL OAE, indicating the anti-melanin effect of OAE (≥12.5 μg/mL). OAE down-regulated the expressions of microphthalmia-associated transcription factor, tyrosinase, and tyrosinase-related proteins-I or -II. Furthermore, phosphorylation of cyclic adenosine monophosphate (cAMP) response element-binding protein was inhibited by OAE. Meanwhile, phosphorylation of mitogen-activated protein kinases (MAPKs) of p38 and c-Jun N-terminal kinase was also inhibited by OAE, whereas that of extracellular regulated protein kinases was promoted. These findings demonstrated that the anti-melanin effect of OAE is probably caused by the regulation of the cAMP and MAPK signaling pathways. In conclusion, O. elatus ARs possess good anti-melanin effect and could be used in production of whitening products.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Alam M, Bajpai V, Lee JL, Zhao P, Byeon JH, Ra JS, Majumder R, Lee JS, Yoon JL, Rather LA (2017) Inhibition of melanogenesis by jineol from Scolopendra subspinipes mutilans via MAP-Kinase mediated MITF downregulation and the proteasomal degradation of tyrosinase. Sci Rep 7:45858

    Article  Google Scholar 

  • Alexander NS, Olga NP, Valery GM, Yang WZ, Guo DA (2014) Oplopanax elatus (Nakai) Nakai: chemistry, traditional use and pharmacology. Chin J Nat Med 12:721–729

    Google Scholar 

  • Aoki H, Moro O (2002) Involvement of microphthalmia-associated transcription factor (MITF) in expression of human melanocortin-1 receptor (MC1R). Life Sci 71:2171–2179

    Article  Google Scholar 

  • Azam MS, Joung EJ, Choi JK, Kim HR (2017) Ethanolic extract from Sargassum serratifolium attenuates hyperpigmentation through CREB/ERK signaling pathways in α-MSH-stimulated B16F10 melanoma cells. J Appl Phycol 29:2089–2096

    Article  Google Scholar 

  • Baek SH, Lee SH (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

    Article  Google Scholar 

  • Chen JZ, Ao ZH, Chen JM (2010) Determination of chlorogenci acid in Fructus chaenomelis and its wine processing products of different area by HPLC. J Med Res 39:86–88

    Google Scholar 

  • Chiang HM, Chien YC, Wu CH, Kuo YH, Wu CH, Pan YY, Su YH, Wen KC (2014) Hydroalcoholic extract of Rhodiola rosea L. (Crassulaceae) and its hydrolysate inhibit melanogenesis in B16F0 cells by regulating the CREB/MITF/tyrosinase pathway. Food Chem Toxicol 65:129–139

    Article  Google Scholar 

  • García-Borrón JC, Abdel-Malek Z, Jiménez-Cervantes C (2014) MC1R, the cAMP pathway, and the response to solar UV: extending the horizon beyond pigmentation. Pigm Cell Melanoma R 27:699–720

    Article  Google Scholar 

  • Han L, Piao XC, Jiang J, Jiang XL, Yin CR, Lian ML (2019) A high production of flavonoids and anthraquinones via adventitious root culture of Oplopanax elatus and evaluating antioxidant activity. Plant Cell Tiss Organ Cult 137:173–179

    Article  Google Scholar 

  • Jiang YJ, Piao XC, Liu JS, Jiang J, Lian ZX, Kim MJ, Lian ML (2015) Bioactive compound production by adventitious root culture of Oplopanax elatus in balloon-type airlift bioreactor systems and bioactivity property. Plant Cell Tiss Organ Cult 123:413–425

    Article  Google Scholar 

  • Jiang XL, Piao XC, GaoR JMY, Jiang J, Jin XH, Lian ML (2017a) Improvement of bioactive compound accumulation in adventitious root cultures of an endangered plant species. Oplopanax Elatus Acta Physiol Plant 39:226

    Article  Google Scholar 

  • Jiang XL, Dai Y, Jin XA, Piao XH, Lian ML, Yang LX (2017b) Effect of extraction technology on tyrosinase activity of extraxcts from adventitious roots of Oplopanax elatus. Agricult Sci J Yanbian Univ 39:23–28

    Google Scholar 

  • Jin MY, Piao XC, Wu XH, Fan MZ, Li XF, Yin CR, Lian ML (2020) Oplopanax elatus adventitious root production through fed-batch culture and their anti-bacterial effects. Plant Cell Tiss Organ Cult 140:447–457

    Article  Google Scholar 

  • Lee HD, Lee WH, Roh E, Seo CS, Son JK, Lee SH, Hwang BY, Jung SH, Han SB, Kim YS (2011) Manassantin A inhibits cAMP-induced melanin production by down-regulating the gene expressions of MITF and tyrosinase in melanocytes. Exp Dermatol 20:761–763

    Article  Google Scholar 

  • Li HR, Habasi M, Xie LZ, Aisa HA (2014) Effect of Chlorogenic acid on melanogenesis of B16 melanoma cells. Molecules 19:12940–12948

    Article  Google Scholar 

  • Li HX, Park JU, Su XD, Kim KT, Kang JS, Kim YR, Kim YH, Yang SY (2018) Identification of anti-melanogenesis constituents from Morus alba L. leaves. Molecules 23:1–11

    Google Scholar 

  • Liang Y, Liu Y, Hou BL, Zhang W, Liu M, Sun YE, Ma ZL, Gu XP (2016) CREB-regulated transcription coactivator 1 enhances CREB-dependent gene expression in spinal cord to maintain the bone cancer pain in mice. Mol Pain 12:1–11

    Google Scholar 

  • Mamat N, Dou J, Lu LUXY, Eblimit A, Akber AH (2017) Isochlorogenic acid A promotes melanin synthesis in B16 cell through the β-catenin signal pathway. Acta Bioch Bioph Sin 49:800–807

    Article  Google Scholar 

  • Martinon F, Burns K, Tschopp J (2002) The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of pro IL-beta. Mol Cell 10:417–426

    Article  Google Scholar 

  • Piao XC, Zhang WB, Jiang J, Jin YH, Park PJ, Kim SE, Lian ML (2017) Cell suspension culture of Orostachys cartilaginous in bioreactor systems for bioactive compound production and evaluation of their antioxidant properties. Acta Physiol Plant 39:70–80

    Article  Google Scholar 

  • Prasad KN, Yang B, Yang SY, Yl C, Zhao MM, Ashraf M, Jiang YM (2009) Identification of phenolic compounds and appraisal of antioxidant and antityrosinase activities from litchi (Litchi sinensis Sonn.) seeds. Food Chem 116:1–7

    Article  Google Scholar 

  • Serre C, Busuttil V, Botto JM (2018) Intrinsic and extrinsic regulation of human skin melanogenesis and pigmentation. Int J Cosmetic Sci 40:328–347

    Article  Google Scholar 

  • Song HS, Sim SS (2010) Acteoside inhibits alpha-MSH-induced melanin production in B16 melanoma cells by inactivation of adenyl cyclase. J Pharm Pharmacol 61:1347–1351

    Article  Google Scholar 

  • Tian W, Piao XC, Yin CR, Jiang XL, Sun HD, An XL, Jiang J, Lian ML (2019) Adventitious root cultures of Oplopanax elatus inhibit LPS-induced inflammation via suppressing MAPK and NF-κB signaling pathways. In Vitro Cell Dev Biol 55:766–775

    Article  Google Scholar 

  • Taira J, Tsuchida E, Uehara M, Ohhama N, Ohmine W, Ogi T (2015) The leaf extract of Mallotus japonicus and its major active constituent, rutin, suppressed on melanin production in murine B16F1 melanoma. Asian Pac J Trop Biomed 5:819–823

    Article  Google Scholar 

  • Tsang TF, Chan B, Tai WCS, Huang GX, Wang JR, Li XA, Jiang ZH, Hsiao WLW (2019) Gynostemma pentaphyllum saponins induce melanogenesis and activate cAMP/PKA and Wnt/β-catenin signaling pathways. Phytomedicine 60:1–8

    Article  Google Scholar 

  • Wei KC, Chen RF, Chen YF, Lin CH (2019) Hinokitiol suppresses growth of B16 melanoma by activating ERK/MKP3/proteosome pathway to downregulate survivin expression. Toxicol Appl Pharmacol 366:35–45

    Article  Google Scholar 

  • Wu LC, Lin YY, Yang SY, Weng YT, Tsai YT (2011) Antimelanogenic effect of c-phycocyanin through modulation of tyrosinase expression by upregulation of ERK and downregulation of p38 MAPK signaling pathways. J Biomed Sci 18:74–85

    Article  Google Scholar 

  • Wu CJ, Fang YH, Zhang LP (2021) Research progress of plant-based skin whitening ingredients. Deterg Cosmet 44:49–52

    Google Scholar 

  • Zhao N, Su XM, Wang YY, Chen JG, Zhuang WY (2020) Traditional chinese herbal medicine for whitening. Nat Prod Commun 15:1–12

    Google Scholar 

  • Ziaullah BKS, Warnakulasuriya SN, Rupasinghe HPV (2013) Biocatalytic synthesis, structural elucidation, antioxidant capacity and tyrosinase inhibition activity of long chain fatty acid acylated derivatives of phloridzin and isoquercitrin. Bioorg Med Chem 21:684–692

    Article  Google Scholar 

Download references

Funding

This work was supported by National Natural Science Foundation of China (81960685).

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Jun Jiang or Mei-Lan Lian.

Ethics declarations

Conflict of interest

No potential conflict of interest was reported by the authors.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 2084 KB)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jiang, XL., Wu, XH., Hao, YJ. et al. Extract of Oplopanax elatus Adventitious Roots Inhibits Melanogenesis in B16F10 Cells by Regulating cAMP/MAPK Pathways. Iran J Sci Technol Trans Sci 46, 771–779 (2022). https://doi.org/10.1007/s40995-022-01310-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40995-022-01310-9

Keywords

Navigation