The Inhibitive Effects of Yukgunja-tang on the Cerebral Ischemia

대군자탕이 뇌허혈에 미치는 억제 효과

  • Kim Hee Seong (Department of Pathology, College of Oriental Medicine, Dongshin University) ;
  • Lee Sang Lock (Department of Pathology, College of Oriental Medicine, Dongshin University) ;
  • Jeong Hyun Woo (Department of Pathology, College of Oriental Medicine, Dongshin University)
  • 김희성 (동신대학교 한의과대학 병리학교실) ;
  • 이상록 (동신대학교 한의과대학 병리학교실) ;
  • 정현우 (동신대학교 한의과대학 병리학교실)
  • Published : 2004.04.01

Abstract

This experimental study was designed to investigate the effects of Yukgunja-tang(YGJT) on the inhibition of cerebral ischemia in rats. And We measured regional cerebral blood f1ow(rCBF) and pial arterial diameter(PAD) in cerebral ischemic rats, and cytokines production in serum Of cerebral ischemic rats. The results were as follows; Both rCBF and PAD were significantly and stably increased by YGJT(10 mg/kg, i.p.) during the period of cerebral reperfusion, which contrasted with the findings of rapid and marked increase in control group. In cytokine production of serum by drawing from femoral arterial blood after middle cerebral arterial occlusion(MCAO) 1 hr, IL-1β and TGF-β production of sample group were similar to that of control group, but sample group was decreased TNF-α production compared with control group, and was significantly increased IL-10 production in compared with control group. In cytokine production of serum by drawing from femoral arterial blood after reperfusion 1 hr, sample group was significantly decreased IL-1β and TNF-α production compared with control group, but TGF-β production of sample group was similar to that of control group, and sample group was significantly increased IL-10 production compared with control group. In cytokine production of serum by drawing from femoral arterial blood after reperfusion 4 hrs, sample group was significantly decreased IL-1β production compared with control group, and sample group was decreased TNF-α production in compared with control group, but TGF-β production of sample group was similar to that of control group, and sample group was increased IL-10 production compared with control group. This results were suggested that YGJT has inhibitive effect on the brain damage by inhibited IL-1β production and TNF-α production, but accelerated IL-10 production. We thought that YGJT should have an anti-ischemic effect through the improvement of cerebral hemodynamics and inhibitive effect on the brain damage.

Keywords

References

  1. 醫學正傳 虞 搏
  2. 東醫寶鑑 許 浚
  3. 景岳全書(上) 張介賓
  4. 뇌 김기석
  5. 병리학 대한병리학회
  6. J. Clin Invest v.27 The nitrous oxide method for the man ; theory, procedure and normal values Kety, S.S.; Schmidt, C.F. https://doi.org/10.1172/JCI101994
  7. J. Cereb Blood Flow Metab v.1 Changes in extracellular calcium activity in cerebral ischemia Harris, R.J.;Symon, L.;Branston, N.M.;Bayhan, M https://doi.org/10.1038/jcbfm.1981.21
  8. Pathol Biol v.30 Ischemic brain injury ; the importance of calcium, lipolytic activities and free fatty acids Wieloch, T.; Siesjo, B.K.
  9. 大韓神經科學會誌 v.8 no.1 허혈, 재관류 손상에서 뇌조직 아민 변동과 Free Radical과의 관련성 이경은;김경환
  10. 물리요법 의학교육연구원
  11. 신경외과학
  12. 대한한의학회지 v.22 no.1 牛黃淸心元이 중대뇌동맥 결찰로 유발된 뇌허혈에 미치는 영향 조규선;정승현;신길조;이원철
  13. 大韓韓醫學會誌 v.22 no.4 흰쥐의 중대뇌동맥 결찰로 유발된 腦虛血에서 星香正氣散과 藿香正氣散이 神經細胞에 미치는 효과 김선영;이원철
  14. 동의생리병리학회지 v.17 no.1 滋陰健脾湯加枳殼·天麻가 腦細胞 및 腦血流力學 變動에 미치는 영향 임광모;정현우
  15. 동의생리병리학회지 v.15 no.6 청피활성분획이 일과성 뇌허혈 병태모델의 뇌혈류역학에 미치는 실험적 효과 이원석;정현우
  16. 생약학회지 v.12 no.3 육군자탕이 위액분비 및 적출 위운동에 미치는 영향에 관한 연구 장인규;박성일
  17. 동국한의학연구소 논문집 v.2 no.1 육군자탕이 Cyclophosphamide로 손상된 비장조직의 회복에 미치는 영향 강윤호;권오성
  18. 東醫病理學會誌 v.18 no.1 四君子湯, 二陳湯, 六君子湯이 腦血流力學 變動에 미치는 實驗的 硏究 鄭鉉雨;金羲成
  19. New Eng J. Med. v.312 Mechanisms of disease : oxygen-derived free radicals in postischemic tissue injury McCord, J.M. https://doi.org/10.1056/NEJM198501173120305
  20. Stroke v.17 Polymorphonuclear leukocyteaccumulation in brain region with low blood flow during the early postischemic period Hallenbeck, J.M.;Dutka, A.J.;Tanishima, T.;Kochanek, P.M.; Kumaroo, K.K.; Thompson, C.B.; Obrenovich, T.P.; Contreras, T.J.
  21. Am J. Pathol. v.144 Influx of leukocytes and platelets in an evolving brain infarct(Wistar rat) Garcia, J.H.; Liu, K.F.; Yoshida, Y.; Lian, J.; Chen, S.; del Zoppo, G.J.
  22. 證脈·方藥合編 黃度淵
  23. 本草學 全國韓醫科大學 本草學敎授 (共編)
  24. Stroke v.20 no.1 Reversible middle cerebral artery occlusion without craniectomy in rats Longa, E.Z.;Weinstein, P.R.;Carlson, S.;Cummins, R.
  25. Stroke v.17 A model of focal ischemic stoke in the rat ; reproducible extension cortical infarction Chen, S.T.;Hsu, C.Y.;Hogan, E.L.;Maricque, H.; Balentine, J.D.
  26. J. Cereb Blood Flow Metab. v.6 no.1 Reactivity of rat pial arterioles and venules to adenosine and carbon dioxide ; with detailed description of the closed cranial window technique in rats Morii, S.;Ngai, A.C.;Winn, H.R. https://doi.org/10.1038/jcbfm.1986.5
  27. Stroke v.6 Detailed description of a cranial window technique for acute and chronic experimentals Joseph, E.;Lebasseur, M.S.;Wei, E.P.;Raper, A.J.; Kontos, H.A. and Patterson, J.L.
  28. J. Clin. Invest v.99 no.5 Injurious ventilatory strategiea increase cytokines and c-fos mRNA expression in an isolated rat lung model Trembaly, L.F.; Valenza, S.P. and Ribelro, J.Li. https://doi.org/10.1172/JCI119259
  29. Brain Res v.759 no.2 Increase of interleukin-1beta mRNA and protein in the spinal cord following experimental traumatic injury in the rat Wang, C.X.; Olschowka, J.A. and Wrathall, J.R. https://doi.org/10.1016/S0006-8993(97)00254-0
  30. J. Immunol. v.155 A comparative study of experimental autoimmune encephalomyelitis in Lewis and DA rats Stepaniak, J.A.; Gould, K.E.; Sun, D.; Swanborg, R.H.
  31. FASEB J. v.12 no.2 Interleukin-10 attenuates experimental fetal growth restriction and demise Rivera, D.L.; Olister, S.M.; Liu, X.; Thompson, J.H.; Zhang, X.J.; Pennline, K.; Azuero, R.; Clark, D.A.; Miller, M.J. https://doi.org/10.1096/fasebj.12.2.189
  32. Circ Res v.82 no.10 Recombinant murine interleukin-12 facilitates induction of cardiac myosin-specific type 1 helper T cells in rats Okura, Y.; Takeda, K.; Honda, S.; Hanawa, H.; Watanabe, H.; Kodama, M.; Izumi, T.; Aizawa, Y.; Seki, S.; Abo, T. https://doi.org/10.1161/01.RES.82.10.1035
  33. J. Exp. Med. v.187 no.9 Vaccination with DNA encoding an immunodominant myelin basic protein peptide targeted to Fc of immunoglobulin G suppresses experimental autoimmune encephalomyelitis Lobell, A.; Weissert, R.; Storch, M.K.; Svanholm, C.; de Graaf, K.L.; Lassmann, H.; Andersson, R.; Olsson, T.; Wigzell, H. https://doi.org/10.1084/jem.187.9.1543
  34. Horm. Res. v.42 no.1;2 Transforming growth factor-beta ; expression in normal and pathological conditions Kim, S.J.; Romeo, D.; Yoo, Y.D.; Park, K. https://doi.org/10.1159/000184136
  35. Cancer v.80 no.12 Expression of transforming growth factor-beta(TGF-beta) isoforms in osteosarcomas ; TGF-beta3 is related to disease progression Kloen, P.; Gebhardt, M.C.; Perez-Atayde, A.; Rosenberg, A.E.; Springfield, D.S.; Gold, L.I.; Mankin, H.J.
  36. Statistical Methods Snedecor, G.H. and Cocharn, W.G.
  37. 醫學入門 李 挻
  38. 丹溪心法 朱丹溪
  39. 醫方集解 汪 昻
  40. Stroke v.4 Correlation of continnous electroencephalograms with cerebral blood flow measurments during carotid endarterectomy Sharbrough, F.W.; Messick, M.K. Jr.; Sundt, T.M. Jr.
  41. Electroencephalogr Clin Neurophysiol v.34 Relation between EEG, regional cerebral blood flow and internal carotid artery pressure during carotid endarterectomy Trojaborg, W.; Boysen, G. https://doi.org/10.1016/0013-4694(73)90151-X
  42. Stroke v.34 no.3 Levels of anti-inflammatory cytokines and neurological worsening in acute ischemic stroke Vila, N.; Castillo, J.; Davalos, A.; Esteve, A.; Planas, A.M.; Chamorro, A.
  43. 면역학 하대유(외25인)
  44. Brain Res v.893 no.1;2 Immunohistochemical investigation of caspase-1 and effect of caspase-1 inhibitor in delayed neuronal death after transient cerebral ischemia Hayashi, Y.; Jikihara, I.; Yagi, T.; Fukumura, M.; Ohashi, Y.; Ohta, Y.; Takagi, H.; Maeda, M. https://doi.org/10.1016/S0006-8993(00)03307-2
  45. Crit Care Med v.27 no.7 Tumor necrosis factor-alpha and interleukin-1beta synergistically depress human myocardial function Cain, B.S.; Meldrum, D.R.; Dinarello, C.A.; Meng, X.; Joo, K.S.; Banerjee, A.; Harken, A.H. https://doi.org/10.1097/00003246-199907000-00018
  46. J. Thorac Cardiovasc Surg. v.124 no.2 Recipient intramuscular cotransfection of naked plasmid transforming growth factor beta1 and interleukin 10 ameliorates lung graft ischemia-reperfusion injury Daddi, N.; Suda, T.; D'Ovidio, F.; Kanaan, S.A.; Tagawa, T.; Grapperhaus, K.; Kozower, B.D.; Ritter, J.H.; Yew, N.S.; Mohanakumar, T.; Patterson, G.A. https://doi.org/10.1067/mtc.2002.122295
  47. Asian J. Surg. v.25 no.3 Induction of higher expression of IL-beta and TNF-alpha, lower expression of IL-10 and cyclic guanosine monophosphate by pulmonary arterial hypertension following cardiopulmonary bypass Lei, Y.; Zhen, J.; Ming, X.L.; Jian, H.K. https://doi.org/10.1016/S1015-9584(09)60176-7
  48. Ann. N. Y. Acad Sci. v.903 Cascading glia reactions ; a common pathomechanism and its differentiated control by cyclic nucleotide signaling Schubert, P.; Morino, T.; Miyazaki, H.; Ogata, T.; Nakamura, Y.; Marchini, C.; Ferroni, S. https://doi.org/10.1111/j.1749-6632.2000.tb06346.x