Biol. Pharm. Bull. 30(4) 719—723 (2007)

نویسندگان

  • Yun - Hee CHANG
  • CheongTaek KIM
  • Minhwan JUNG
  • Young - Hee LIM
  • Sanghwa LEE
  • Sangjin KANG
چکیده

due to the destruction of the ozone layer. Our skin is more exposed to UV radiation and often suffers from various harmful effects of UV. Melanin prodcution in human skin is an important defense mechanism against UV and a major determinant of skin color. Melanocytes residing within the basal layer of the epidermis synthesize melanin in specialized organelles, designated as melanosomes, by coordinated action of various melanogenic enzymes such as tyrosinase, tyrosinase-related protein 1 (TRP-1), and tyrosinase-related protein 2 (TRP-2). Then, melanin-containing melanosomes are transferred to keratinocytes, providing protection against UV radiation and eventually disappear with desquamation of the skin. Despite the protective role of melanins, abnormal hyperpigmentation such as freckles, chloasma, and other forms of melanin hyperpigmentation sometimes can be serious aesthetic problems. Therefore potent active agents for the improvement of hyperpigmentation have been sought for cosmetic use. Many chemicals such as hydroquinone, arbutin, kojic acid, and ascorbic acid are well known for their melanogenicinhibitory functions. Even though these chemicals are often used in many skin-lightening, cosmetic formulations, they have some disadvantages such as poor safety and limited effectiveness. In this study, we screened more than 200 medicinal herbal extracts that have been known for their skin-lightening effects to develop a skin-lightening agent from traditional medicinal plants and found that Atractylodis Rhizoma Alba, which has been used in the treatment and prevention of diabetes and ulceration, has strong melanogenic-inhibitory activity. Its active compound was purified using bioactivityguided fractionation and identified as selina-4(14),7(11)dien-8-one (compound 1) by spectroscopic methods. The effects of compound 1 were evaluated on melan-a cells. Compound 1 markedly inhibited melanogenesis of melan-a cells by regulating the expression of melanogenic enzymes. MATERIALS AND METHODS

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Biol. Pharm. Bull. 30(9) 1599—1604 (2007)

In eukaryotic cells, combinatorial phosphorylation of the hydroxyl residues on the inositol ring of phosphatidylinositol (PtdIns) gives rise to seven phosphoinositides (eight if PtdIns itself is included) (Fig. 1). In the ‘canonical’ phosphoinositide (PI) cycles, phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2] serves as a precursor of the intracellular second The Physiology of Phosphoinos...

متن کامل

Antiinflammatory Constituents of Teramnus labialis

1. Alagarsamy, V., Raja Salomon, V., Vanikavitha, G., Paluchamy, V., Ravichandran, M., Arnold Sujin, A., Thangathirupathy, A., Amuthalakshmi, S. and Revathi R., Biol. Pharm. Bull., 2002, 25, 1432. 2. Alagarsamy, V., Muthukumar, V., Pavalarani, N., Vasanthanathan, P. and Revathi R., Biol. Pharm. Bull., 2003, 26(4), 557. 3. Chaurasia, M.R. and Sharma, S.K., Arch. Pharm., 1982, 315, 377. 4. Manabu...

متن کامل

Biol. Pharm. Bull. 30(3) 585—587 (2007)

major nosocomial pathogen, and biocides including antiseptics and disinfectants have been used in order to prevent its infections and spreading. Biocides have a wide variety of uses, and their concentrations and exposure times vary according to usage. Recently, MRSA isolates with decreased biocide susceptibilities have been isolated from clinical samples, and MRSA isolates carrying antiseptic-r...

متن کامل

Biol. Pharm. Bull. 28(3) 563—564 (2005)

Tomomi NOGUCHI, Chihiro SHINJI, Hisayoshi KOBAYASHI, Makoto MAKISHIMA, Hiroyuki MIYACHI, and Yuichi HASHIMOTO* Institute of Molecular & Cellular Biosciences, The University of Tokyo; 1–1–1 Yayoi, Bunkyo-ku, Tokyo 113–0032, Japan: and Department of Biochemistry, Nihon University, School of Medicine; 30–1 Oyaguchi-kamicho, Itabashi-ku, Tokyo 173–8610, Japan. Received January 13, 2005; accepted Ja...

متن کامل

Biol. Pharm. Bull. 30(8) 1580—1585 (2007)

that was selected from a series of sulphonamide-substituted phenylethylamines. It blocks both postsynaptic a1and b1adrenoceptors to almost the same extent. When administered to conscious, spontaneously hypertensive rats, it reduces blood pressure via its a1-blocking activity without causing reflex tachycardia because of its b1-blocking action. This drug exhibited dose-dependent hypotensive effe...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2007