DOI QR코드

DOI QR Code

실크 단백질의 식이 공급이 아토피 피부염 동물 모델 NC/Nga Mice 표피의 스핑고이드 베이스 및 인산화물 함량 변화에 미치는 영향

Dietary effect of silk protein on epidermal levels of free sphingoid bases and phosphate metabolites in NC/Nga mice

  • 김영애 (경희대학교 동서의학대학원 의학영양학과) ;
  • 송은화 (경희대학교 동서의학대학원 의학영양학과) ;
  • 신경오 (충북대학교 약학대학) ;
  • 이용문 (충북대학교 약학대학) ;
  • 조윤희 (경희대학교 동서의학대학원 의학영양학과)
  • Kim, Young-Ae (Department of Medical Nutrition, Graduate School of East-West Medical Science, Kyung Hee University) ;
  • Song, Eun-Hwa (Department of Medical Nutrition, Graduate School of East-West Medical Science, Kyung Hee University) ;
  • Shin, Kyoung-Oh (College of Pharmacy, Chungbuk National University) ;
  • Lee, Yong-Moon (College of Pharmacy, Chungbuk National University) ;
  • Cho, Yun-Hi (Department of Medical Nutrition, Graduate School of East-West Medical Science, Kyung Hee University)
  • 투고 : 2011.12.14
  • 심사 : 2012.02.09
  • 발행 : 2012.04.30

초록

In our previous studies, dietary supplements of silk protein, sericin, and fibroin, were beneficial for improving epidermal levels of ceramides, which are the major lipids for maintaining the epidermal barrier. In this study, we investigated the dietary effects of silk protein on epidermal levels of free sphingoid bases and their phosphates such as $C_{18}$ sphingosine (So), $C_{18}$ sphinganine (Sa), $C_{18}$ sphingosine-1-phosphate (S1P), and $C_{18}$ sphinganine-1-phosphate (Sa1P), which are either synthetic substrate or degradative metabolites of ceramides. Forty-five male NC/Nga mice, an animal model of atopic dermatitis (AD), were divided into three groups: group CA was an atopic control and fed a control diet, group S was fed a 1% sericin diet, and group F was fed a 1% fibroin diet. Fifteen male BALB/c mice served as group C (control group) and were fed the control diet. All mice were fed with diets and water $ad$ $libitum$ for 10 weeks. Sa in group CA was lower than that in group C, but So in group CA was similar to that in group C. So and Sa were higher in groups S and F than those in group CA; So level was even higher than that in group C, and Sa level was similar to that of group C. The So/Sa ratio in group CA, which is reported to increase in AD, was significantly higher than that of group C. The So/Sa ratio was lower in groups S and F than that in group CA, and decreased further in group F. However, S1P and Sa1P in groups S and F were similar to those in group CA. Taken together, we demonstrated that silk protein, sericin and fibroin dietary supplements, increased So and Sa levels, and decreased the So/Sa ratio.

키워드

참고문헌

  1. Coderch L, López O, de la Maza A, Parra JL. Ceramides and skin function. Am J Clin Dermatol 2003; 4(2): 107-129 https://doi.org/10.2165/00128071-200304020-00004
  2. Bartke N, Hannun YA. Bioactive sphingolipids: metabolism and function. J Lipid Res 2009; 50 Suppl: S91-S96 https://doi.org/10.1194/jlr.R800080-JLR200
  3. Bibel DJ, Aly R, Shinefield HR. Antimicrobial activity of sphingosines. J Invest Dermatol 1992; 98(3): 269-273 https://doi.org/10.1111/1523-1747.ep12497842
  4. Vogler R, Sauer B, Kim DS, Schafer-Korting M, Kleuser B. Sphingosine-1-phosphate and its potentially paradoxical effects on critical parameters of cutaneous wound healing. J Invest Dermatol 2003; 120(4): 693-700 https://doi.org/10.1046/j.1523-1747.2003.12096.x
  5. Elias PM, Wood LC, Feingold KR. Epidermal pathogenesis of inflammatory dermatoses. Am J Contact Dermat 1999; 10(3): 119-126 https://doi.org/10.1016/S1046-199X(99)90054-4
  6. Horn EJ, Domm S, Katz HI, Lebwohl M, Mrowietz U, Kragballe K; International Psoriasis Council. Topical corticosteroids in psoriasis: strategies for improving safety. J Eur Acad Dermatol Venereol 2010; 24(2): 119-124 https://doi.org/10.1111/j.1468-3083.2009.03358.x
  7. Majoie IM, Oldhoff JM, van Weelden H, Laaper-Ertmann M, Bousema MT, Sigurdsson V, Knol EF, Bruijnzeel-Koomen CA, de Bruin-Weller MS. Narrowband ultraviolet B and mediumdose ultraviolet A1 are equally effective in the treatment of moderate to severe atopic dermatitis. J Am Acad Dermatol 2009; 60(1): 77-84 https://doi.org/10.1016/j.jaad.2008.08.048
  8. Warren RB, Griffiths CE. Systemic therapies for psoriasis: methotrexate, retinoids, and cyclosporine. Clin Dermatol 2008; 26(5): 438-447 https://doi.org/10.1016/j.clindermatol.2007.11.006
  9. Kim J, Kim H, Jeong do H, Kim SH, Park SK, Cho Y. Comparative effect of gromwell (Lithospermum erythrorhizon) extract and borage oil on reversing epidermal hyperproliferation in guinea pigs. Biosci Biotechnol Biochem 2006; 70(9): 2086-2095 https://doi.org/10.1271/bbb.60038
  10. Lee KG, Yeo JH, Lee YW, Kweon HY, Kim JH. Bioactive and skin-compatible properties of silk sericin. Korean J Sericult Sci 2001; 43(2): 109-115
  11. Padamwar MN, Pawar AP, Daithankar AV, Mahadik KR. Silk sericin as a moisturizer: an in vivo study. J Cosmet Dermatol 2005; 4(4): 250-257 https://doi.org/10.1111/j.1473-2165.2005.00200.x
  12. Kato N, Sato S, Yamanaka A, Yamada H, Fuwa N, Nomura M. Silk protein, sericin, inhibits lipid peroxidation and tyrosinase activity. Biosci Biotechnol Biochem 1998; 62(1): 145-147 https://doi.org/10.1271/bbb.62.145
  13. Zhaorigetu S, Yanaka N, Sasaki M, Watanabe H, Kato N. Silk protein, sericin, suppresses DMBA-TPA-induced mouse skin tumorigenesis by reducing oxidative stress, inflammatory responses and endogenous tumor promoter TNF-alpha. Oncol Rep 2003; 10(3): 537-543
  14. Nagai N, Murao T, Ito Y, Okamoto N, Sasaki M. Enhancing effects of sericin on corneal wound healing in rat debrided corneal epithelium. Biol Pharm Bull 2009; 32(5): 933-936 https://doi.org/10.1248/bpb.32.933
  15. Choi MJ, Maibach HI. Role of ceramides in barrier function of healthy and diseased skin. Am J Clin Dermatol 2005; 6(4): 215-223 https://doi.org/10.2165/00128071-200506040-00002
  16. Farwanah H, Raith K, Neubert RH, Wohlrab J. Ceramide profiles of the uninvolved skin in atopic dermatitis and psoriasis are comparable to those of healthy skin. Arch Dermatol Res 2005; 296(11): 514-521 https://doi.org/10.1007/s00403-005-0551-2
  17. Imokawa G, Abe A, Jin K, Higaki Y, Kawashima M, Hidano A. Decreased level of ceramides in stratum corneum of atopic dermatitis: an etiologic factor in atopic dry skin? J Invest Dermatol 1991; 96(4): 523-526 https://doi.org/10.1111/1523-1747.ep12470233
  18. Meguro S, Arai Y, Masukawa Y, Uie K, Tokimitsu I. Relationship between covalently bound ceramides and transepidermal water loss (TEWL). Arch Dermatol Res 2000; 292(9): 463-468 https://doi.org/10.1007/s004030000160
  19. Motta S, Monti M, Sesana S, Caputo R, Carelli S, Ghidoni R. Ceramide composition of the psoriatic scale. Biochim Biophys Acta 1993; 1182(2): 147-151 https://doi.org/10.1016/0925-4439(93)90135-N
  20. Reiter LV, Torres SM, Wertz PW. Characterization and quantification of ceramides in the nonlesional skin of canine patients with atopic dermatitis compared with controls. Vet Dermatol 2009; 20(4): 260-266 https://doi.org/10.1111/j.1365-3164.2009.00759.x
  21. Madyarov S, Lee KG, Yeo JH, Nam J, Lee YW. Improved method for the preparation of silk fibroin hydrolysates. Korean J Sericult Sci 1999; 41(2): 108-115
  22. Suto H, Matsuda H, Mitsuishi K, Hira K, Uchida T, Unno T, Ogawa H, Ra C. NC/Nga mice: a mouse model for atopic dermatitis. Int Arch Allergy Immunol 1999; 120 Suppl 1: 70-75 https://doi.org/10.1159/000053599
  23. Takagi Y, Nakagawa H, Yaginuma T, Takema Y, Imokawa G. An accumulation of glucosylceramide in the stratum corneum due to attenuated activity of beta-glucocerebrosidase is associated with the early phase of UVB-induced alteration in cutaneous barrier function. Arch Dermatol Res 2005; 297(1): 18-25 https://doi.org/10.1007/s00403-005-0567-7
  24. Doering T, Holleran WM, Potratz A, Vielhaber G, Elias PM, Suzuki K, Sandhoff K. Sphingolipid activator proteins are required for epidermal permeability barrier formation. J Biol Chem 1999; 274(16): 11038-11045 https://doi.org/10.1074/jbc.274.16.11038
  25. Min JK, Yoo HS, Lee EY, Lee WJ, Lee YM. Simultaneous quantitative analysis of sphingoid base 1-phosphates in biological samples by o-phthalaldehyde precolumn derivatization after dephosphorylation with alkaline phosphatase. Anal Biochem 2002; 303 (2): 167-175 https://doi.org/10.1006/abio.2002.5579
  26. Flamand N, Justine P, Bernaud F, Rougier A, Gaetani Q. In vivo distribution of free long-chain sphingoid bases in the human stratum corneum by high-performance liquid chromatographic analysis of strippings. J Chromatogr B Biomed Appl 1994; 656(1): 65-71 https://doi.org/10.1016/0378-4347(94)80021-9
  27. Caligan TB, Peters K, Ou J, Wang E, Saba J, Merrill AH Jr. A high-performance liquid chromatographic method to measure sphingosine 1-phosphate and related compounds from sphingosine kinase assays and other biological samples. Anal Biochem 2000; 281(1): 36-44 https://doi.org/10.1006/abio.2000.4555
  28. Park KH, Choi YS, Kim HA, Lee KG, Yeo JH, Jung DH, Kim SH, Cho YH. Dietary effect of silk protein on ceramide synthesis and the expression of ceramide metabolic enzymes in the epidermis of NC/Nga mice. J Korean Soc Food Sci Nutr 2007; 36(5): 554-562 https://doi.org/10.3746/jkfn.2007.36.5.554
  29. Macheleidt O, Kaiser HW, Sandhoff K. Deficiency of epidermal protein-bound omega-hydroxyceramides in atopic dermatitis. J Invest Dermatol 2002; 119(1): 166-173 https://doi.org/10.1046/j.1523-1747.2002.01833.x
  30. Arikawa J, Ishibashi M, Kawashima M, Takagi Y, Ichikawa Y, Imokawa G. Decreased levels of sphingosine, a natural antimicrobial agent, may be associated with vulnerability of the stratum corneum from patients with atopic dermatitis to colonization by Staphylococcus aureus. J Invest Dermatol 2002; 119(2): 433-439 https://doi.org/10.1046/j.1523-1747.2002.01846.x
  31. Elias PM, Menon GK. Structural and lipid biochemical correlates of the epidermal permeability barrier. Adv Lipid Res 1991; 24: 1- 26
  32. Melnik B. Disturbances of antimicrobial lipids in atopic dermatitis. J Dtsch Dermatol Ges 2006; 4(2): 114-123 https://doi.org/10.1111/j.1610-0387.2006.05902.x
  33. Bibel DJ, Aly R, Shinefield HR. Inhibition of microbial adherence by sphinganine. Can J Microbiol 1992; 38(9): 983-985 https://doi.org/10.1139/m92-158
  34. Loiseau N, Moradian S, Elias PM, Holleran WM, Uchida Y. Ceramide metabolites in epidermal permeability barrier function and atopic dermatitis [abstract]. J Invest Dermatol 2009; 129 Suppl 1: S68. Abstract no. 405
  35. Stewart ME, Downing DT. Free sphingosines of human skin include 6-hydroxysphingosine and unusually long-chain dihydrosphingosines. J Invest Dermatol 1995; 105(4): 613-618 https://doi.org/10.1111/1523-1747.ep12323736
  36. Hait NC, Oskeritzian CA, Paugh SW, Milstien S, Spiegel S. Sphingosine kinases, sphingosine 1-phosphate, apoptosis and diseases. Biochim Biophys Acta 2006; 1758(12): 2016-2026 https://doi.org/10.1016/j.bbamem.2006.08.007
  37. Gómez-Muñoz A. Ceramide 1-phosphate/ceramide, a switch between life and death. Biochim Biophys Acta 2006; 1758(12): 2049- 2056 https://doi.org/10.1016/j.bbamem.2006.05.011
  38. Prieschl EE, Csonga R, Novotny V, Kikuchi GE, Baumruker T. The balance between sphingosine and sphingosine-1-phosphate is decisive for mast cell activation after Fc epsilon receptor I triggering. J Exp Med 1999; 190(1): 1-8 https://doi.org/10.1084/jem.190.1.1
  39. Mondal M, Trivedy K, Nirmal Kumar S. The silk proteins, sericin and fibroin in silkworm, Bombyx mori Linn., -a review. Casp J Environ Sci 2007; 5(2): 63-76
  40. Voegeli R, Meier J, Blust R. Sericin silk protein: unique structure and properties. Cosmet Toilet 1993; 108: 101-108
  41. Aramwit P, Sangcakul A. The effects of sericin cream on wound healing in rats. Biosci Biotechnol Biochem 2007; 71(10): 2473- 2477 https://doi.org/10.1271/bbb.70243

피인용 문헌

  1. Manufacture and Characterization of Silkworm Gland Hydrolysate vol.50, pp.2, 2012, https://doi.org/10.7852/jses.2012.50.2.76
  2. Comparative effect of dietary borage oil and safflower oil on anti-proliferation and ceramide metabolism in the epidermis of essential fatty acid deficient guinea pigs vol.48, pp.4, 2015, https://doi.org/10.4163/jnh.2015.48.4.319