Compound K induces expression of hyaluronan synthase 2 gene in transformed human keratinocytes and increases hyaluronan in hairless mouse skin

被引:86
作者
Kim, S
Kang, BY
Cho, SY
Sung, DS
Chang, HK
Yeom, MH
Kim, DH
Sim, YC
Lee, YS
机构
[1] Amore Pacific Corp, R&D Ctr, Kyounggi 449729, South Korea
[2] Hanyang Univ, Coll Med, Dept Biochem, Seoul 133791, South Korea
关键词
cDNA microarray; ginsenosides; compound K; hyaluronan synthase 2; HaCaT cell; skin;
D O I
10.1016/j.bbrc.2004.02.046
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ginsenosides, the major active ingredients of ginseng, have a variety of biomedical efficacies such as anti-aging, anti-oxidation, and anti-inflammatory activities. To understand the effects of compound K (20-0-beta-D-glucopyranosyl-20(S)-protopanaxadiol), one of the major metabolites of ginsenosides, on the skin, we assessed the expression levels of about 100 transcripts in compound K-treated HaCaT cells using cDNA microarray analysis. One gene up-regulated by compound K was hyaluronan synthase2 (HAS2). Semi-quantitative RT-PCR showed that compound K increased HAS2 mRNA in time- and dose-dependent manners. ELISA and immunocytochemistry using hyaluronan (HA)-binding protein showed that compound K effectively increased HA production in HaCaT cells. Finally, treatment of compound K on hairless mouse skin increased the amount of HA in the epidermis and papillary dermis. Our study suggests that topical application of compound K might prevent or improve the deteriorations, such as xerosis and wrinkles, partly ascribed to the age-dependent decrease of the HA content in human skin. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:348 / 355
页数:8
相关论文
共 32 条
[1]   Intestinal bacterial hydrolysis is required for the appearance of compound K in rat plasma after oral administration of ginsenoside Rb1 from Panax ginseng [J].
Akao, T ;
Kida, H ;
Kanaoka, M ;
Hattori, M ;
Kobashi, K .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1998, 50 (10) :1155-1160
[2]   Metabolism of ginsenoside Rc by human intestinal bacteria and its related antiallergic activity [J].
Bae, EA ;
Choo, MK ;
Park, EK ;
Park, SY ;
Shin, HY ;
Kim, DH .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2002, 25 (06) :743-747
[3]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[4]   The impact of herbal medicines on dermatologic surgery [J].
Chang, LK ;
Whitaker, DC .
DERMATOLOGIC SURGERY, 2001, 27 (08) :759-763
[5]   Epidermis proliferative effect of the Panax ginseng ginsenoside Rb2 [J].
Choi, S .
ARCHIVES OF PHARMACAL RESEARCH, 2002, 25 (01) :71-76
[6]   Does estrogen prevent skin aging? Results from the first national health and nutrition examination survey (NHANES I) [J].
Dunn, LB ;
Damesyn, M ;
Moore, AA ;
Reuben, DB ;
Greendale, GA .
ARCHIVES OF DERMATOLOGY, 1997, 133 (03) :339-342
[7]   HUMAN DERMAL GLYCOSAMINOGLYCANS AND AGING [J].
FLEISCHMAJER, R ;
BASHEY, RI ;
PERLISH, JS .
BIOCHIMICA ET BIOPHYSICA ACTA, 1972, 279 (02) :265-+
[8]   HYALURONIC-ACID IN CUTANEOUS INTRINSIC AGING [J].
GHERSETICH, I ;
LOTTI, T ;
CAMPANILE, G ;
GRAPPONE, C ;
DINI, G .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1994, 33 (02) :119-122
[9]   Panax ginseng pharmacology: A nitric oxide link? [J].
Gillis, CN .
BIOCHEMICAL PHARMACOLOGY, 1997, 54 (01) :1-8
[10]   Ginseng intestinal bacterial metabolite IH901 as a new anti-metastatic agent [J].
Hasegawa, H ;
Sung, JH ;
Huh, JD .
ARCHIVES OF PHARMACAL RESEARCH, 1997, 20 (06) :539-544