DOI QR코드

DOI QR Code

Neuroprotective Effect of Insamyangyung-tang

인삼양영탕(人蔘養營湯)의 산화적 stress에 대한 뇌세포 보호효과

  • Kim, Seung-Hyun (Dept. of Oriental Medicine, Graduate School, Kyung Hee University) ;
  • Lee, Chang-Hoon (Dept. of Oriental Medicine, Graduate School, Kyung Hee University) ;
  • Lee, Jin-Moo (Dept. of Oriental Medicine, Graduate School, Kyung Hee University) ;
  • Cho, Jung-Hoon (Dept. of Oriental Medicine, Graduate School, Kyung Hee University) ;
  • Jang, Jun-Bock (Dept. of Oriental Medicine, Graduate School, Kyung Hee University) ;
  • Lee, Kyung-Sub (Dept. of Oriental Medicine, Graduate School, Kyung Hee University)
  • 김승현 (경희대학교 한의과대학 한방부인과학 교실) ;
  • 이창훈 (경희대학교 한의과대학 한방부인과학 교실) ;
  • 이진무 (경희대학교 한의과대학 한방부인과학 교실) ;
  • 조정훈 (경희대학교 한의과대학 한방부인과학 교실) ;
  • 장준복 (경희대학교 한의과대학 한방부인과학 교실) ;
  • 이경섭 (경희대학교 한의과대학 한방부인과학 교실)
  • Published : 2009.02.27

Abstract

Purpose: Oxidative stress was thought to play a critical role in neurodegenerative disease. Many in vivo and in vitro reports explained the possible pathway of human aging. But in therapeutic aspects, there was no clear answers to prevent aging associated with neural diseases. In this study, we investigated the antioxidant and neuroprotective effects of the Insamyangyung-tang (IYT). Methods: To estimate the antioxidant effects, we carried out 1.1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging assay, 2,2'-azinobis-(3- ethylbenzothiazoline-6- sulfonic acid (ABTS) radical cation decolorization assay, and measurement of total polyphenolic content. To evaluate neuroprotective effect of IYT in vitro. We performed thiazolyl blue tetrazolium bromide (MTT) assay, reactive oxygen species (ROS) creation in SH-SY5Y. Tyrosine hydroxylase (TH) immunocytochemistry, nitric oxide (NO) assay, and TNF-${\alpha}$ assay in primary rat mesencephalic dopaminergic neurons. Results: The $IC_{50}$ values were $571.6{\mu}g/m{\ell}$ and $202.3{\mu}g/m{\ell}$ in DPPH and ABTS assay respectively. Total polyphenolic content was 1.05%. In SH-SY5Y culture, IYT significantly increased the decreased cell viability by 6-OHDA at the concentrations of $10{\mu}g/m{\ell}$ in pre-treatment group, $10-100{\mu}g/m{\ell}$ in post-treatment group, and $100{\mu}g/m{\ell}$ in co-treatment group. The production of ROS induced by 6-OHDA was significantly inhibited in IYT treated group. In mesencephalic dopaminergic cell culture, the IYT group reduced the dopaminergic cell loss against 6-OHDA toxicity and the production of No and TNF-${\alpha}$ at the concentration of $0.2{\mu}g/m{\ell}$. Conclusion: These results showed that IYT has antioxidant and neuroprotectctive effects in the dopaminergic cells through decreasing the production of ROS, NO and TNF-${\alpha}$ which can cause many neurodegenerative changes in brain cell.

Keywords

References

  1. Workshop report. Aging-from molecules to populations. Mechanisms of ageing and development. 2008;199:614-623.
  2. 노인복지총람편찬위원회. 노인복지총람. 서울: 대한노인신문사. 2006:3-7, 677-686.
  3. 통계청. 연령,성별,인구 읍면동 조사. 2005.
  4. 김동일 등. 갱년기클리닉의 운영방안과 활용 약물에 관한 고찰. 대한한방부인과학회지. 2000;13(2):418-436.
  5. 대한노인병학회. 노인병학. 서울: 의학출판사. 2000:3-49, 808-830.
  6. Sayre LS, Perry G, Smith MA. Oxidative stress and neurotoxicity. Chem Res Toxicol. 2008;21:172-188. https://doi.org/10.1021/tx700210j
  7. Facchinetti F, Dawson VL, Dawson TM. Free radicals as mediators of neuronal injury. Cellular and molecular neurobiology. 1998;18(6):667-682. https://doi.org/10.1023/A:1020221919154
  8. Papa S, Skulachev VP. Reactive oxygen species, mitochondria, apoptosis and aging. Molecularand cellular biochemistry. 1997;174:305-319. https://doi.org/10.1023/A:1006873518427
  9. Halliwell B. Oxidative stress and neurodegeneration: where are we now? Journal of neurochemistry. 2006;97: 1634-1658. https://doi.org/10.1111/j.1471-4159.2006.03907.x
  10. Kurz T, Terman A, Brunk UT. Autophagy, ageing and apoptosis: the role of oxidative stress and lysosomal iron. Arc of biochemistry and biophysics. 2007;42:222-230.
  11. 대한폐경학회 편찬위원회. 폐경기 여성의 관리. 서울: 군자출판사. 2001 :62-65.
  12. Jung JW et al. Estrogen replacement effect of Korean ginseng saponin on learning and memory of ovariectomized mice. J Ginseng Res. 2000;24(1):8-17.
  13. Zhao L, Mao Z, Brinton RD. A select combination of clinically relevant phytoestrogens enhances estrogen receptor $\beta$-binding selectivity and neuroprotective activities in vitro and in vivo. Endocrinoloty. 2008.
  14. Currie LJ et al. Postmenopausal estrogen use affects risk for parkinson disease. Arc Neurol. 2004;61:886-888. https://doi.org/10.1001/archneur.61.6.886
  15. Wise PM. Estrogens and neuroprotection. Trends in endocrinology & metabolism. 2002;13(6):229-230. https://doi.org/10.1016/S1043-2760(02)00611-2
  16. 張介賓. 부인규. 서울: 법인문화사. 1999:13-33.
  17. 한의부인과학교재편찬위원회. 한의부인과학. 서울: 정담출판사. 2002:221-233.
  18. 반혜란 등. 人蔘養榮湯 투여로 호전된 갱년기장애 15례에 대한 임상 고찰. 대한한방부인과학회지. 2006;19(3) :257-266.
  19. 하지용, 조성연. 人蔘養榮湯이 항암 및 면역조절작용에 미치는 영향. 대한동의병리학회지. 1998;12(1):60-71.
  20. Huang S, Lin CM, Chian BH. Protective effects of Angelica sinensis extract on amyloid $\beta$-peptide-induced neurotoxicity. Phytomedicine. 2008;15:710-721. https://doi.org/10.1016/j.phymed.2008.02.022
  21. 박홍주 등. 한국약식동원 식물자원의 항산화 활성 비교. 한국지역사회생활과학회지. 2004;15(4):11-1622.
  22. 뢰영성 등. 인삼고본환과 그 구성약물군의 항산화 효과. 대한본초학회지. 2003;18(3):41-50.
  23. Sohn EH et al. Effects of nonsaponin red ginseng components on the function of brain cells. J Ginseng Res. 2008;32(1):62-66. https://doi.org/10.5142/JGR.2008.32.1.062
  24. 권후자, 박찬성. 오미자 추출물의 생리활성. 한국식품저장유통학회. 2008;15(4):587-592.
  25. 서운교, 정효원, 박용지. 생강 클로로로포름 분획의 활성화된 뇌신경교세 포에서 염증반응 억제효과. 대한본초학회지. 2008;23(3):73-83.
  26. 박찬성, 김동한. 황금, 산조인, 백출 추출물의 생리활성. 대한본초학회지. 2008;23(3):41-51.
  27. 이수배, 성낙설, 이영종. 원지가 NMDA로 유발된 신경세포 손상에 미치는 효과. 대한본초학회지. 2005;20(2):115-125.
  28. 박찬성, 김동한, 김미림. 산수유, 황기, 감초 추출물의 생리활성. 대한본초학회지. 2008;28(1):98-101.
  29. 허준. 동의보감. 서울: 법인문화사. 2002:1176-1177.
  30. Yoo KM, Kim DO, Lee CY. Evaluation of different methode of antioxidant measurement. Food Sci Biotechnol. 2007;16(2):177-182.
  31. Halliwell B. Are polyphenols antioxidants or pro-oxidants? what do we learn from cell cultre and in vivo studies?. Arc Biochem and Biophysics. 2008;476:107-112. https://doi.org/10.1016/j.abb.2008.01.028
  32. Doris LL, Stanley SL. Microglia and myeloperoxidase: a deadly partnership in neurodegenerative disease. Free radical biology & medicine. 2008;45:726-731. https://doi.org/10.1016/j.freeradbiomed.2008.05.021
  33. Pieper HC et al. Different methylation of the TNF-alpha promoter in cortex and substantia nigra: implications for selective neuronal vulnerability. Neurobiology of disease. 2008;4:1-741. https://doi.org/10.1006/nbdi.1997.0137
  34. 강재성 등. 세포분자면역학. 서울: 범문사. 2005:287-288.
  35. McCOy MK, Tansey MG. TNF signaling inhibition in the CNS: implication for normal brain function and neurodegenerative disease. Journal of neuroinflammation. 2008;45:1-13.
  36. Rapp SR et al. Effect of estrogen plus progestin on global cognitive function in postmenopausal women: the women;s health initiative menory test: a randomized controlled trial. JAMA. 2003;289(20):2663-2672. https://doi.org/10.1001/jama.289.20.2663
  37. Drechsel DA, Patel M. Role of reactive oygen speces in the neurotoxicity of environmental agents implicated in Parkinson's disease. Free radical biology & medicine. 2008;44:1873-1886. https://doi.org/10.1016/j.freeradbiomed.2008.02.008