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Effect of Inflammatory Responses to PLGA Films Incorporated Hesperidin: In vitro and In vivo Results

PLGA/헤스페리딘 함량별 필름에서 염증 완화 효과: In vitro, In vivo 결과

  • Song, Jeong Eun (Dept. of BIN Fusion Tech, and Dept. of PolymerNano Sci. & Tech., Chonbuk National University) ;
  • Shim, Cho Rok (Dept. of BIN Fusion Tech, and Dept. of PolymerNano Sci. & Tech., Chonbuk National University) ;
  • Lee, Yujung (Dept. of BIN Fusion Tech, and Dept. of PolymerNano Sci. & Tech., Chonbuk National University) ;
  • Ko, Hyun Ah (Dept. of BIN Fusion Tech, and Dept. of PolymerNano Sci. & Tech., Chonbuk National University) ;
  • Yoon, Hyeon (Dept. of BIN Fusion Tech, and Dept. of PolymerNano Sci. & Tech., Chonbuk National University) ;
  • Lee, Dongwon (Dept. of BIN Fusion Tech, and Dept. of PolymerNano Sci. & Tech., Chonbuk National University) ;
  • Khang, Gilson (Dept. of BIN Fusion Tech, and Dept. of PolymerNano Sci. & Tech., Chonbuk National University)
  • 송정은 (전북대학교 BIN 융합공학과, 고분자나노공학과) ;
  • 심초록 (전북대학교 BIN 융합공학과, 고분자나노공학과) ;
  • 이유정 (전북대학교 BIN 융합공학과, 고분자나노공학과) ;
  • 고현아 (전북대학교 BIN 융합공학과, 고분자나노공학과) ;
  • 윤현 (전북대학교 BIN 융합공학과, 고분자나노공학과) ;
  • 이동원 (전북대학교 BIN 융합공학과, 고분자나노공학과) ;
  • 강길선 (전북대학교 BIN 융합공학과, 고분자나노공학과)
  • Received : 2012.10.22
  • Accepted : 2013.01.06
  • Published : 2013.05.25

Abstract

Hesperidin (Hes) has known to having some functions like protection of blood circulatory system, anti-tumor effect, antioxidant effect and anti-inflammatory effect. The goal of this study is to demonstrate the relationship between Hes and inflammatory through in vitro and in vivo studies using poly(lactic-co-glycolic acid) (PLGA) film including Hes as a tissue engineered scaffold. To confirm the proliferation of cells on fabricated scaffold, cells (RAW 264.7 and NIH/3T3) were seeded on PLGA/Hes film then analyzed with MTT and SEM at 1 and 3 days after seeding. The results from ELISA, RT-PCR, and FACS for anti-oxident and anti-inflammatory effect showed that inflammatory response of PLGA/Hes film decreased more than that of PLGA film. Also, in vivo result confirmed that inflammatory response by implanted PLGA/Hes film decreased more comparing with PLGA film. This is because of anti-inflammatory effect of Hes reducing induced inflammatory cell and accumulation of fibrous capsule. The results showed that PLGA/Hes film's capacity on reducing inflammatory is better than PLGA film because of Hes.

헤스페리딘은 혈관 순환계 보호 효과, 항암 효과, 항산화 효과, 항염증 효과 등의 작용이 있다고 알려져 있다. 본 연구에서는 헤스페리딘을 함유한 poly(lactic-co-glycolic acid)(PLGA) 필름을 조직공학적 세포담체로 이용하고 생체 내/외의 실험을 통하여 헤스페리딘과 염증 반응의 상관관계를 알아보고자 하였다. 세포담체에서의 세포의 증식과 부착을 확인하고자 PLGA/헤스페리딘 필름에 세포(RAW 264.7, NIH/3T3)를 파종하여 1, 3일 후에 MTT와 SEM을 통하여 분석하였다. 또한 항산화 효과와 염증 완화 효과를 알아보고자 ELISA, RT-PCR, FACS 등을 평가한 결과 PLGA 필름보다는 헤스페리딘이 첨가된 PLGA 필름에서 염증 반응이 감소하는 것을 확인하였다. In vivo 실험에서도 헤스페리딘이 PLGA에 의해 유도된 염증세포와 섬유피막 축적을 감소시켜 헤스페리딘의 항염증 효과를 볼 수 있었다. 이 실험 결과 PLGA 필름보다는 PLGA/헤스페리딘 필름에서 염증 반응이 감소함을 확인하였다.

Keywords

References

  1. Y. K. Ko, S. H. Kim, H. J. Ha, M. S. Kim, C. W. Han, J. M. Rhee, Y. Son, H. B. Lee, and G. Khang, Tissue Eng. Regen. Med., 4, 67 (2007).
  2. G. Khang, M. S. Kim, and B. Y. Min, Tissue Eng. Regen. Med., 3, 376 (2004).
  3. G. Khang, M. S. Kim, and S. H. Cho, Tissue Eng. Regen. Med., 1, 9 (2004).
  4. S. J. Yoon, S. H. Kim, H. J. Ha, Y. K. Ko, J. W. So, M. S. Kim, Y. I. Yang, G. Khang, J. M. Rhee, and H. B. Lee, Tissue Eng. Part A, 14, 539 (2008). https://doi.org/10.1089/tea.2007.0129
  5. S. Munirah, S. H. Kim, J. S. Jeong, H. J. Ha, S. J. Yoon, J. M Rhee, M. S. Kim, H. B. Lee, and G. Khang, Polymer(Korea), 31, 14 (2007).
  6. Y. Song, J. Kwon, B. Kim, Y. Jeon, G. Khang, and D. Lee, J. Biomed. Mater. Res., 98A, 517 (2011). https://doi.org/10.1002/jbm.a.33135
  7. S. H. Oh, S. G. Kang, and J. H. Lee, J. Mater. Sci. Mater. Med., 17, 131, (2006). https://doi.org/10.1007/s10856-006-6816-2
  8. J. M. Chan, L. Zhang, K. P. Yuet, G. Liao, J. W. Rhee, R. Langer, and O. C. Farokhzad, Biomaterials, 30, 1627 (2009). https://doi.org/10.1016/j.biomaterials.2008.12.013
  9. O. Bostman, J. Bone Joint Surg. Am., 73, 148 (1991).
  10. M. S. Taylor, J. Appl. Biomater., 5, 151 (1994). https://doi.org/10.1002/jab.770050208
  11. M. S. Kim, H. H. Ahn, Y. N. Shin, M. H. Cho, G. Khang, and H. B. Lee, Biomaterials, 28, 5137 (2007). https://doi.org/10.1016/j.biomaterials.2007.08.014
  12. Y. P. Jeon, L. M. Mohammad, C. H. Park, J. H. Hong, G. D. Lee, J. C. Song, and G. S. Kim, J. Life Science, 19, 479 (2009). https://doi.org/10.5352/JLS.2009.19.4.479
  13. D. A. Willoughby, Ann. Rheum. Dis., 34, 471 (1975). https://doi.org/10.1136/ard.34.6.471
  14. E. J. Cho, L. Li, N. Yamabe, and H. Y. Kim, CNU J. Agricultural Science, 38, 717 (2011).
  15. E. Middleton, Annal Aller., 61, 523 (1988).
  16. Y. Lee, L. R. Howard, and B. Villalon, J. Food Sci., 60, 473 (1995). https://doi.org/10.1111/j.1365-2621.1995.tb09806.x
  17. H. S. Marie, L. Joel, and C. Marin, Toxicol. Appl. Pharmacol., 130, 73 (1995). https://doi.org/10.1006/taap.1995.1010
  18. H. H. Hong, S. J. Kim, S. H. Kim, H. L. Kim, J. H. Park, D. Lee, and G. Khang, Tissue Eng. Regen. Med., 6, 711 (2009).
  19. O. A. R. Sulaiman, and T. Gordon, Glia, 32, 234 (2000). https://doi.org/10.1002/1098-1136(200012)32:3<234::AID-GLIA40>3.0.CO;2-3
  20. C. R. Shim, Y. J. Lee, H. A. Ko, M. J. Kim, J. W. Bae, L. H. Lee, J. E. Song, and G. Khang, Int. J. Tissue Regen., 3, 50 (2012).
  21. G. E. Muschler, C. Nakamoto, and L. G. Griffith, J. Bone Joint Surg. Am., 86A, 1541 (2004).
  22. B. N. Amens, M. K. Shigenoga, and T. M. Hagen, Proc. Natl. Acad. Sci., 90, 7915 (1993). https://doi.org/10.1073/pnas.90.17.7915
  23. D. Harman, J. Gerontol., 2, 298 (1956).
  24. Y. Lee, J. Kwon, G. Khang, and D. Lee, Tissue Eng. Part A, 18, 1967 (2012). https://doi.org/10.1089/ten.tea.2012.0001
  25. A. V. Delgado, A. T. McManus, and J. P. Chambers, Neuropeptides, 37, 355 (2003). https://doi.org/10.1016/j.npep.2003.09.005
  26. B. B Aggarwal, Nat. Rev. Immunol., 3, 745 (2003). https://doi.org/10.1038/nri1184
  27. S. J. Kim, H. H. Hong, S. H. Kim, H. L. Kim, S. H. Kim, and G. Khang, Polymer(Korea), 1, 63 (2010).
  28. L. Meinel, S Hofmann, V Karageorgiou, C. Kirker-Head, J. McCool, G. Gronowicz, L. Zichner, R. Langer, G. Vunjak- Novakovica, and D. L. Kaplan, Biomaterials, 26, 147 (2005). https://doi.org/10.1016/j.biomaterials.2004.02.047
  29. J. C. Sy, G. Seshadri, S. C. Yang, M. Brown, T. Oh, S. Dikalov, N. Murthy, and M. E. Davis, Nat. Mater., 7, 863 (2008). https://doi.org/10.1038/nmat2299
  30. M. Chen, H. Gu, Y. Ye, B. Lin, L. Sun, W. Deng, J. Zhang, and J. Liu, Food Chem. Toxicol., 48, 2980 (2010). https://doi.org/10.1016/j.fct.2010.07.037
  31. N. Nandakumar, T. Rengarajan, L. Haribabu, S. Perumal, and M. P. Balasubramanian, Biomedicine & Preventive Nutrition, 1, 207 (2011). https://doi.org/10.1016/j.bionut.2011.07.001