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Study on protective effect of bakuchiol on photoaging HSF cells |
LIU Guoliang1 YAO Yuan1 ZHANG Ning1 GUO Wei2 WANG Yao2 LIU Bin1 |
1.College of Jiamusi, Heilongjiang University of Chinese Medicine, Heilongjiang Province, Jiamusi 154007, China;
2.the First Clinical Medical College, Heilongjiang University of Chinese Medicine, Heilongjiang Province, Harbin 150040, China |
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Abstract Objective To study the protective effect of bakuchiol on photoaging human skin fibroblasts (HSF) induced by ultraviolet radiation B (UVB) irradiation. Methods HSF cells were cultured in vitro and divided into blank group (normal culture, no UVB radiation), UVB model group (UVB radiation), estradiol group and bakuchiol low (1 μmol/L), medium (10 μmol/L) and high dose (100 μmol/L) groups. Cell viability was detected by MTT assay. The protein expressions of type Ⅰ collagen (COL Ⅰ), matrix metalloproteinase-1 (MMP-1) and matrix metalloproteinase-3 (MMP-3) were detected by Western blot. The expression levels of COL Ⅰ and MMP-1 mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR). Results The optimal UVB radiation dose for photoaging HSF cell model was 25 mJ/cm2. Compared with the blank group, there was no significant difference in cell viability and secretion of MMP-1, MMP-3 and COL Ⅰ between the low, medium and high dose groups of bakuchiol (P > 0.05); the cell viability and COL Ⅰ expression level in the UVB model group decreased significantly (P < 0.05), the protein expression levels of MMP-1 and MMP-3 increased significantly (P < 0.05); the mRNA expression levels of MMP-1 and COL Ⅰ decreased significantly (P < 0.05). Compared with the UVB model group, the cell viability and COL Ⅰ expression in the low, middle and high dose groups of bakuchiol increased significantly (P < 0.05), the protein expression levels of MMP-1 and MMP-3 decreased significantly (P < 0.05), the mRNA expression levels of MMP-1 and COL Ⅰ increased significantly (P < 0.05). Conclusion Bakuchiol can promote the expression of COL Ⅰ in HSFs, inhibit the expression of MMP-1 and MMP-3, protect UVB from damage to HSFs and exert anti-photoaging effects on skin.
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[1] 吴斯敏,杨慧龄.紫外线引起皮肤光老化机制及防治的研究进展[J].医学综述,2018(2):341-346.
[2] 杨锐,陈丽娟.中西医防治皮肤光老化新进展[J].中医药信息,2017,34(3):117-120.
[3] 刘少英,孟祥璟,张祥奎,等.皮肤光老化机制及抗光老化药物[J].生理科学进展,2018,49(4):265-269.
[4] 张昕,李承新.皮肤光老化治疗进展[J].中国激光医学杂志,2018,27(1):47-51.
[5] 左俊,李勤,吴燕虹.雌激素调控皮肤衰老作用机制的研究进展[J].中国美容整形外科杂志,2013,24(2):122-124.
[6] 张欢,李青峰.雌激素对皮肤衰老的调控[J].组织工程与重建外科,2009,5(1):58-60.
[7] 雷秀东.雌激素抗皮肤老化的作用机制探讨[J].医学信息,2014(39):284-284.
[8] 倪晨宁.皮肤光老化的中医药治疗研究进展[J].名医,2018(2):96,98.
[9] Antoniou C,Kosmadaki MG,Stratigos AJ,et al. Photoaging [J].Am J Clin Dermatol,2010,11(2):95-102.
[10] Zegarska B,Jó■wicki W,Zegarski W,et al. Histopathological lesions in different types of skin aging [J]. Acta Dermatovenerol Alp Pannonica Adriat,2010,19(2):17-21.
[11] Chiu AE,Ab JLC,Ms DGK,et al. Double-Blinded,Placebo-Controlled Trial of Green Tea Extracts in the Clinical and Histologic Appearance of Photoaging Skin [J].Dermatol Surg,2005,31(Supplement s1):855-860.
[12] Jung HY,Shin JC,Park SM,et al. Pinus densiflora,extract protects human skin fibroblasts against UVB-induced photoaging by inhibiting the expression of MMPs and increasing type Ⅰ procollagen expression [J]. Toxicol Rep,2014(1):658-666.
[13] 刘俊岑,刘海洋,刘国良,等.异补骨脂素对紫外线诱导人真皮成纤维细胞损伤的保护作用及机制研究[J].国际中医中药杂志,2018,40(4):339-344.
[14] 刘俊岑,董蕊,朴成玉,等.松脂醇二葡萄糖苷对UVB诱导HDF细胞损伤的保护作用及机制研究[J].中药材,2017,40(6):1410-1414.
[15] 周勇,谢臻蔚,金杭美.雌激素在抗皮肤衰老中的生物学作用[J].中国美容医学,2017,26(1):27-30.
[16] Sjerobabskimasnec I,Situm M. Skin aging [J]. Acta Clinica Croatica,2010,49(4):515-518.
[17] 魏毅君,张荣军,罗文颖,等.补骨脂酚通过抑制凋亡、氧化应激和炎症反应缓解小鼠脓毒症脑病[J].现代生物医学进展,2018,18(20):3840-3844.
[18] Xin Z,Wu X,Ji T,et al. Bakuchiol:A newly discovered warrior against organ damage [J]. Pharmacol Res,2019, 141.
[19] 徐美娇.二苯乙烯苷对中波紫外线诱导人皮肤成纤维细胞光老化的保护作用研究[D].杭州:浙江中医药大学,2016.
[20] 王继慧.绞股蓝总皂苷对人皮肤成纤维细胞光老化模型凋亡信号通路的影响[D].沈阳:辽宁中医药大学,2014.
[21] 任捷.中草药对紫外线照射下真皮成纤维细胞保护作用的研究[D].上海:复旦大学,2010. |
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