中华医学美学美容杂志
中華醫學美學美容雜誌
중화의학미학미용잡지
CHINESE JOURNAL OF MEDICAL AESTHETICS AND COSMETOLOGY
2009年
6期
405-409
,共5页
刘全忠%籍晓明%张秉新%侯淑萍%亓玉青%金洪喜
劉全忠%籍曉明%張秉新%侯淑萍%亓玉青%金洪喜
류전충%적효명%장병신%후숙평%기옥청%금홍희
维A酸%黑素瘤细胞%黑素细胞
維A痠%黑素瘤細胞%黑素細胞
유A산%흑소류세포%흑소세포
Retinoic acid%Mechanism%Melanocytes
目的 探讨维A酸治疗皮肤色斑的作用机制.方法 应用不同浓度的维A酸作用于B16F10黑素瘤细胞及正常人黑素细胞,观察肘酪氨酸酶mRNA的表达、酪氨酸酶活性、黑素含量及黑素细胞增殖率的影响.结果 维A酸的作用浓度为100μmol/L时,黑素细胞酪氨酸酶mRNA表达下调均值为30.13%;当浓度为500μmol/L以上时,可使酪氨酸酶活性降低82.79%,并随着浓度的增加作用越明显;而对黑素含量的降低则需要更高的浓度(1 000μmol/L);同时,还有促进黑素细胞增殖的作用.对照组氧醌对酪氰酸酶mRNA的表达无明显影响,对色素细胞有抑制和毒性作用.结论 维A酸能够抑制黑素产生,是通过下调酪氨酸酶的表达和活性来完成.
目的 探討維A痠治療皮膚色斑的作用機製.方法 應用不同濃度的維A痠作用于B16F10黑素瘤細胞及正常人黑素細胞,觀察肘酪氨痠酶mRNA的錶達、酪氨痠酶活性、黑素含量及黑素細胞增殖率的影響.結果 維A痠的作用濃度為100μmol/L時,黑素細胞酪氨痠酶mRNA錶達下調均值為30.13%;噹濃度為500μmol/L以上時,可使酪氨痠酶活性降低82.79%,併隨著濃度的增加作用越明顯;而對黑素含量的降低則需要更高的濃度(1 000μmol/L);同時,還有促進黑素細胞增殖的作用.對照組氧醌對酪氰痠酶mRNA的錶達無明顯影響,對色素細胞有抑製和毒性作用.結論 維A痠能夠抑製黑素產生,是通過下調酪氨痠酶的錶達和活性來完成.
목적 탐토유A산치료피부색반적작용궤제.방법 응용불동농도적유A산작용우B16F10흑소류세포급정상인흑소세포,관찰주락안산매mRNA적표체、락안산매활성、흑소함량급흑소세포증식솔적영향.결과 유A산적작용농도위100μmol/L시,흑소세포락안산매mRNA표체하조균치위30.13%;당농도위500μmol/L이상시,가사락안산매활성강저82.79%,병수착농도적증가작용월명현;이대흑소함량적강저칙수요경고적농도(1 000μmol/L);동시,환유촉진흑소세포증식적작용.대조조양곤대락청산매mRNA적표체무명현영향,대색소세포유억제화독성작용.결론 유A산능구억제흑소산생,시통과하조락안산매적표체화활성래완성.
Objective To investigate the effects and mechanism of retinoie acid on B16 marina mel-anoma cells and human melanocytes in vitro. Methods B16F10 murine melanoma cells and human mela-noeytes were cultured in culture medium which contains different concentration of components, including retinoic acid. Using reverse transcription-polymerase chain reaction (RT-PCR) mRNA expression of the tyrosinase was detected. Tyrosinase activity, melanin content and cell proliferation rate were also deter-mined. Results Retinoieacid exhibited an inhibitory effect on the expression of tyrosinase mRNA. As the concentration of retinoic acid was 100 μmol/L, treating for 72 h, the expression of tyrosinase mRNA de-creased 30.13 %, retinoic acid exhibited an inhibitory effect on tyrosinase activity and melanin production at high concentration (>500 μmol/L), and it could promote the cell proliferation. Retinoic acid and hy-droqninone could be cooperative at high concentration (1 000 μmol/L), and enhanced the down regulation of tyrosinase activity and melanin content. Retinoic acid could also mitigate the inhibitory effect of hydro-quinone on cell proliferation, so as to protect the cells from injury. Hydroquinone had no effect on tyrosi-nase gene expression at mRNA level. Conclusion Retinoic acid inhibits the synthesis of melanin by the genetic regulation at mRNA level.