Journal of Traditional Chinese Medicine >
Pharmacological effect and possible mechanism of Mudan Huaban recipe (牡丹化斑方) on melasma in mice induced by ultraviolet B and progesterone
Received date: 2024-03-23
Accepted date: 2024-07-12
Online published: 2025-05-21
Supported by
Beijing University of Chinese Medicine Transversal Project: "Internal and External" Product and Technology Development for Herbal Acne and Blemish Removal(2019110031001241);Youth Project Under the National Natural Science Foundation of China: Revealing the Scientific Connotation of Tongfu Chinese Herb Rhubarb in Treating Ischemic Stroke from the Perspective of "Intestinal Tryptophan Metabolism and Central Microglia Polarisation"(82104440)
OBJECTIVE: To analyze the chemical components of Mudan Huaban recipe (牡丹化斑方, MHR) and evaluate its efficacy and possible mechanism in melasma mice.
METHODS: The chemical compositions of MHR were determined by the ultra-high performance liquid chromatography coupled with quadrupole-exactive mass spectrometry method. Female C57BL/6 mice were exposed to ultraviolet B and progesterone for 21 d to induce melasma, and Fontana-Masson staining was used to assess the effects of MHR on melasma. Luteinizing hormone (LH), estradiol, and follicle-stimulating hormone levels were detected by enzyme-linked immunosorbent assay. The superoxide dismutase (SOD) activity and malonic dialdehyde content were detected by chemiluminescence. Tyrosinase and related proteins expressions were detected by Western blots and immunohistochemistry.
RESULTS: A total of 43 chemical components were identified in MHR, MHR significantly decreased the melanin particles of melasma mice. MHR treatment significantly reversed the high contents of LH and low activity of SOD in models. MHR significantly reduced the higher levels of tyrosinase, tyrosinase-related proteins-1 (TRP-1), TRP-2, microphthalmia-associated transcription factor and phosphorylation of cyclic adenosine monophosphate response element-binding protein (p-CREB)/CREB in the skin of melasma mice.
CONCLUSIONS: MHR protects against melasma via regulation of sex hormones, oxidative stress, and melanogenesis-related proteins, suggesting its possible use as a supplement and alternative drug therapy for melasma.
Xiaoyao LIU , Jialin LI , Weiling WANG , Qiongyin FAN , Zeqi SU , Cheng HE , Chunguo WANG , Jian GAO , Ting WANG . Pharmacological effect and possible mechanism of Mudan Huaban recipe (牡丹化斑方) on melasma in mice induced by ultraviolet B and progesterone[J]. Journal of Traditional Chinese Medicine, 2025 , 45(3) : 518 -527 . DOI: 10.19852/j.cnki.jtcm.2025.03.001
| 1. | Passeron T, Picardo M. Melasma, a photoaging disorder. Pigm Cell Melanoma R 2018; 31: 461-5. |
| 2. | Rajanala S, Maymone MBC, Vashi NA. Melasma pathogenesis: a review of the latest research, pathological findings, and investigational therapies. Dermatol Online J 2019; 25: 13030/qt47b7r28c. |
| 3. | Ogbechie-Godec OA, Elbuluk N. Melasma: an up-to-date comprehensive review. Dermatol Ther (Heidelb) 2017; 7: 305-18. |
| 4. | Handel AC, Miot LD, Miot HA. Melasma: a clinical and epidemiological review. An Bras Dermatol 2014; 89: 771-82. |
| 5. | Babbush KM, Babbush RA, Khachemoune A. The therapeutic use of antioxidants for melasma. J Drugs Dermatol 2020; 19: 788-92. |
| 6. | Lee AY. Recent progress in melasma pathogenesis. Pigm Cell Melanoma R 2015; 28: 648-60. |
| 7. | Filoni A, Mariano M, Cameli N. Melasma: How hormones can modulate skin pigmentation. J Cosmet Dermatol-US 2019; 18: 458-63. |
| 8. | Choubey V, Sarkar R, Garg V, Kaushik S, Ghunawat S, Sonthalia S. Role of oxidative stress in melasma: a prospective study on serum and blood markers of oxidative stress in melasma patients. Int J Dermatol 2017; 56: 939-43. |
| 9. | Komirishetty P, Areti A, Yerra VG, et al. PARP inhibition attenuates neuroinflammation and oxidative stress in chronic constriction injury induced peripheral neuropathy. Life Sci 2016; 150: 50-60. |
| 10. | Kim HJ, Moon SH, Cho SH, Lee JD, Kim HS. Efficacy and safety of tranexamic acid in melasma: a Meta-analysis and systematic review. Acta Derm Venereol 2017; 97: 776-81. |
| 11. | Lee HC, Thng TGS, Goh CL. Oral tranexamic acid (TA) in the treatment of melasma: a retrospective analysis. J Am Acad Dermatol 2016; 75: 385-92. |
| 12. | Mishra SN, Dhurat RS, Deshpande DJ, Nayak CS. Diagnostic utility of dermatoscopy in hydroquinone-induced exogenous ochronosis. Int J Dermatol 2013; 52: 413-7. |
| 13. | Nomakhosi M, Heidi A. Natural options for management of melasma, a review. J Cosmet Laser Ther 2018; 20: 470-81. |
| 14. | Zhang Y, Zheng X, Chen Z, Lu L. Laser and laser compound therapy for melasma: a Meta-analysis. J Dermatolog Treat 2020; 31: 77-83. |
| 15. | Manuskiatti W, Yan C, Tantrapornpong P, Cembrano KAG, Techapichetvanich T, Wanitphakdeedecha R. A prospective, split-face, randomized study comparing a 755-nm picosecond laser with and without diffractive lens array in the treatment of melasma in Asians. Laser Surg Med 2021; 53: 95-103. |
| 16. | Nair AB, Jacob S. A simple practice guide for dose conversion between animals and human. J Basic Clin Pharm 2016; 7: 27-31. |
| 17. | Deshpande SS, Khatu SS, Pardeshi GS, Gokhale NR. Cross-sectional study of psychiatric morbidity in patients with melasma. Indian J Psychiat 2018; 60: 324-8. |
| 18. | Feng L, Shi N, Cai S, et al. De novo molecular design of a novel octapeptide that inhibits in vivo melanogenesis and has great transdermal ability. J Med Chem 2018; 61: 6846-57. |
| 19. | Norimoto H, Yomoda S, Fujita N, et al. Effects of keishibukuryoganryokayokuinin (Gui-Zhi-Fu-Ling-Wanliao-Jia-Yiyiren) on the epidermal pigment cells from DBA/2 mice exposed to ultraviolet B (UVB) and/or progesterone. Yakugaku zasshi 2011; 131: 1613-9. |
| 20. | You YJ, Wu PY, Liu YJ, et al. Sesamol inhibited ultraviolet radiation-induced hyperpigmentation and damage in C57BL/ 6 mouse skin. Antioxidants (Basel) 2019; 8: 207. |
| 21. | Kumar KJS, Vani MG, Wang SY, et al. In vitro and in vivo studies disclosed the depigmenting effects of gallic acid: a novel skin lightening agent for hyperpigmentary skin diseases. Biofactors 2013; 39: 259-70. |
| 22. | Liu-Smith F, Meyskens FL. Molecular mechanisms of flavonoids in melanin synthesis and the potential for the prevention and treatment of melanoma. Mol Nutr Food Res 2016; 60: 1264-74. |
| 23. | Kim YJ. Hyperin and quercetin modulate oxidative stress-induced melanogenesis. Biol Pharm Bull 2012; 35: 2023-7. |
| 24. | Ye Y, Chou GX, Wang H, Chu JH, Yu ZL. Flavonoids, apigenin and icariin exert potent melanogenic activities in murine B16 melanoma cells. Phytomedicine 2010; 18: 32-5. |
| 25. | Enogieru AB, Haylett W, Hiss DC, Bardien S, Ekpo OE. Rutin as a potent antioxidant: implications for neurodegenerative disorders. Oxid Med Cell Longev 2018; 2018: 6241017. |
| 26. | Khan BA, Mahmood T, Menaa F, et al. New perspectives on the efficacy of gallic acid in cosmetics & nanocosmeceuticals. Curr Pharm Design 2018; 24: 5181-7. |
| 27. | Su TR, Lin JJ, Tsai CC, et al. Inhibition of Melanogenesis by gallic acid: possible involvement of the PI3K/Akt, MEK/ERK and Wnt/beta-catenin signaling pathways in B16F10 cells. Int J Mol Sci 2013; 14: 20443-58. |
| 28. | Cho YH, Kim JH, Park SM, Lee BC, Pyo HB, Park HD. New cosmetic agents for skin whitening from Angelica dahurica. J Cosmet Sci 2006; 57: 11-21. |
| 29. | Baek SH, Lee SH. Sesamol decreases melanin biosynthesis in melanocyte cells and zebrafish: possible involvement of MITF via the intracellular cAMP and p38/JNK signalling pathways. Exp Dermatol 2015; 24: 761-6. |
| 30. | Lin KY, Chen CM, Lu CY, Cheng CY, Wu YH. Regulation of miR-21 expression in human melanoma via UV-ray-induced melanin pigmentation. Environ Toxicol 2017; 32: 2064-9. |
| 31. | Quillen EE, Bauchet M, Bigham AW, et al. OPRM1 and EGFR contribute to skin pigmentation differences between indigenous Americans and Europeans. Hum Genet 2012; 131: 1073-80. |
| 32. | Robinson N, Ganesan R, Hegedus C, Kovacs K, Kufer TA, Virag L. Programmed necrotic cell death of macrophages: focus on pyro-ptosis, necroptosis, and parthanatos. Redox Biol 2019; 26: 101239. |
| 33. | Zhao MX, Wen JL, Wang L, Wang XP, Chen TS. Intracellular catalase activity instead of glutathione level dominates the resistance of cells to reactive oxygen species. Cell Stress Chaperones 2019; 24: 609-19. |
| 34. | Wang W, Cheng YY, Chen DD, et al. The catalase gene family in cotton: genome-wide characterization and bioinformatics analysis. Cells-basel 2019; 8: 86. |
| 35. | Titz B, Boue S, Phillips B, et al. Effects of cigarette smoke, cessation, and switching to two heat-not-burn tobacco products on lung lipid metabolism in C57BL/6 and Apoe(-/-) mice-an integrative systems toxicology analysis. Toxicol Sci 2016; 149: 441-57. |
| 36. | Hseu YC, Vudhya Gowrisankar Y, Wang LW, et al. The in vitro and in vivo depigmenting activity of pterostilbene through induction of autophagy in melanocytes and inhibition of UVA-irradiated alpha-MSH in keratinocytes via Nrf2-mediated antioxidant pathways. Redox Biol 2021; 44: 102007. |
| 37. | Pillaiyar T, Manickam M, Jung SH. Downregulation of melanogenesis: drug discovery and therapeutic options. Drug Discov Today 2017; 22: 282-98. |
| 38. | Doolan BJ, Gupta M. Melasma. Aust J Gen Pract 2021; 50: 880-5. |
| 39. | Young Kang H, Ortonne JP. Melasma update. Actas Dermosifiliogr 2009; 100 Suppl 2: 110-3. |
| 40. | Muallem MM, Rubeiz NG. Physiological and biological skin changes in pregnancy. Clin Dermatol 2006; 24: 80-3. |
| 41. | Maeda K, Naganuma M, Fukuda M, Matsunaga J, Tomita Y. Effect of pituitary and ovarian hormones on human melanocytes in vitro. Pigment Cell Res 1996; 9: 204-12. |
| 42. | Lee BW, Schwartz RA, Janniger CK. Melasma. G Ital Dermatol Venereol 2017; 152: 36-45. |
| 43. | Liao S, Shang J, Tian X, et al. Up-regulation of melanin synthesis by the antidepressant fluoxetine. Exp Dermatol 2012; 21: 635-7. |
| 44. | D'Mello SA, Finlay GJ, Baguley BC, Askarian-Amiri ME. Signaling pathways in melanogenesis. Int J Mol Sci 2016; 17: 1144. |
| 45. | Pillaiyar T, Manickam M, Jung SH. Recent development of signaling pathways inhibitors of melanogenesis. Cell Signal 2017; 40: 99-115. |
| 46. | Otreba M, Rok J, Buszman E, Wrzesniok D. Regulation of melanogenesis: the role of cAMP and MITF. Postepy Hig Med Dosw 2012; 66: 33-40. |
| 47. | Lyu J, An X, Jiang S, Yang Y, Song G, Gao R. Protoporphyrin IX stimulates melanogenesis, melanocyte dendricity, and melanosome transport through the cGMP/PKG pathway. Front Pharmacol 2020; 11: 569368. |
| 48. | Zhang M, Chen X, Zhang J, Li J, Bai Z. Cloning of a HcCreb gene and analysis of its effects on nacre color and melanin synthesis in Hyriopsis cumingii. PLoS One 2021; 16: e0251452. |
| 49. | Rzepka Z, Buszman E, Beberok A, Wrzesniok D. From tyrosine to melanin: signaling pathways and factors regulating melanogenesis. Postepy Hig Med Dosw 2016; 70: 695-708. |
| 50. | Ito S, Wakamatsu K. Chemistry of mixed melanogenesis-pivotal roles of dopaquinone. Photochem Photobiol 2008; 84: 582-92. |
| 51. | Tanaka H, Yamashita Y, Umezawa K, Hirobe T, Ito S, Wakamatsu K. The pro-oxidant activity of pheomelanin is significantly enhanced by UVA irradiation: benzothiazole moieties are more reactive than benzothiazine moieties. Int J Mol Sci 2018; 19: 2889. |
| 52. | Morgan AM, Lo J, Fisher DE. How does pheomelanin synthesis contribute to melanomagenesis? Two distinct mechanisms could explain the carcinogenicity of pheomelanin synthesis. Bioessays 2013; 35: 672-6. |
/
| 〈 |
|
〉 |