열다한소탕(熱多寒少湯)이 저산소성(低酸素性) 대뇌신경세포(大腦神經細胞) 손상에 미치는 영향(影響)

Influence of Yeoldahanso-tang on the Hypoxic Damage of Cultured Cerebral Neurons from mouse and SK-N-MC cells

  • 김형순 (원광대학교 한의과대학 사상체질과) ;
  • 배영춘 (원광대학교 한의과대학 사상체질과) ;
  • 이상민 (원광대학교 한의과대학 사상체질과) ;
  • 김경요 (원광대학교 한의과대학 사상체질과) ;
  • 원경숙 (계명대학교 의과대학 핵의학과) ;
  • 심규헌 (상지대학교 사상체질의학과 대학원) ;
  • 박수정 (원광대학교 한의과대학 사상체질과)
  • Kim, Hyoung-Soon (Dept. of Sasang Constitutional Medicine, College of Oriental Medicine, Wonkwang Univ.) ;
  • Bae, Young-Chun (Dept. of Sasang Constitutional Medicine, College of Oriental Medicine, Wonkwang Univ.) ;
  • Lee, Sang-Min (Dept. of Sasang Constitutional Medicine, College of Oriental Medicine, Wonkwang Univ.) ;
  • Kim, Kyung-Yo (Dept. of Sasang Constitutional Medicine, College of Oriental Medicine, Wonkwang Univ.) ;
  • Won, Kyoung-Sook (Dept. of Nuclear Medicine, College of Medicine, Keimyung Univ.) ;
  • Sihm, Gyue-Hearn (Dept. of Sasang Constitutional Medicine, College of Oriental Medicine, Sang-ji Univ.) ;
  • Park, Su-Jeong (Dept. of Sasang Constitutional Medicine, College of Oriental Medicine, Wonkwang Univ.)
  • 발행 : 2003.06.30

초록

To elucidate the neuroprotective effect of Yeoldahanso-tang(YHT) on nerve cells damaged by hypoxia, the cytotoxic effects of exposure to hypoxia were determined by XTT(SODIUM3,3'-{I-[(PHENYLAMINO) CARBONYL]-3,4-TETRAZOLIUM}- BIS (4-METHOXY-6-NITRO) BENZENE SULFONIC ACID HYDRATE), NR(Neutral red), MTT(3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) and SRB(Sulforhodamin B) asssay. The activity of catalase and SOD(Superoxide dismutase) was measured by spectrophometry, and $TNF-{\alpha}$(Tumor cell necrosis $fector-{\alpha}$) and PKC(Protein kinase C) activity was measured after exposure to hypoxia and treatment of YHTWE. Also the neuroprotective effect of YHTWE was researched for the elucidatioion of neuroprotective mechanism. The results were as follows; 1. Hypoxia decreased cell viability measured by XTT, NR assay when cultured cerebral neurons were exposed to 95% N2/5% CO2 for $2{\sim}26$ minutes in these cultures and YHTWE inhibited the decrease of cell viability. 2. H2O2 treatment decreased cell viability measured by MTT, and SRB assay when cultured cerebral neurons were exposed to 1-80 ${\mu}M$ for 6 hours, but YHTWE inhibited the decrease of cell viability. 3. Hypoxia decreased catalase and SOD activity, and also $TNF-{\alpha}$ and PKC activity in these cultured cerebral neurons, but YHTWE inhibited the decrease of the catalase and SOD activity in these cultures. 4. Hypoxia triggered the apoptosis via caspase activation and internucleosomal DNA fragmentation. Also hypoxia stimulate the release of cytochrome c forom mitochondria. YHTWE inhibited the apoptosis via caspase activation induced by hypoxia. From these results, it can be suggested that brain ischemia model induced hypoxia showed neurotoxicity on cultured mouse cerebral neurons, and the YHTWE has the neuroprotective effect in blocking the neurotoxicity induced by hypoxia in cultured mouse cerebral neurons.

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