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손윤희,임종국,최혜경,남경수,배만종 경산대학교 생명자원개발연구소 1999 생명자원과 산업 Vol.3 No.-
한방에서 염증, 종양 억제 등에 사용되는 금은화로 약침액을 조제하여 쥐와 사람의 암세포 성장억제효과를 살펴 보았을 때 금은화 약침액 10×, 5×농도는 mouse EATC에 대해 90% 및 86% 세포 성장 억제율이 있었으며, 열수추출액 10×, 5× 농도는 89% 및 87% 세포 성장억제효과가 있었다. 같은 농도의 약침액을 Hepalclc7에 처리했을 때는 89.5%, 69.7%의 억제효과가 있었고 열수추출액은 85.7%, 67.3%의 hepalclc7 세포 성장억제율을 보였다. 사람의 암세포주 A549, HeLa 세포에 대한 금은화 약침액 및 열수추출액의 세포독성 실험에서도 A549 세포에 약침액 10×, 5×를 처리했을 때 82.0%, 46.1% 세포 성장억제효과가 나타났으며 금은화 역수추출액은 75%, 50%의 세포 성장 억제율이 나타났다. HeLa 세포에서는 약침액이 열수추출액보다 세포 성장 억제효과가 더 높았다. 금은화 약침액을 처리한 세포(EATC,Hepalclc7과 human A549, HeLa)의 현미경 관찰에서는 세포수의 감소와 형태의 변화를 관찰할 수 있었다. Lonicerae flos Aqua-acupuncture Solution(LFAS) and Lonicerae flos Water-extracted Solution(LFWS) were prepared and tested for their potential antitumor activities. It was shown to possess considerable toxicity toward various tumor cell lines. Concentration of LFAS at 10× and 5× resulted in more than 50% inhibition of growth in Ehrich ascites tumor cells(EATC), Hepalclc7, and HeLa cells after 72 hours. Toxicity of LFWS to A549 revealed that more than 50% inhibition of growth at LFAS conentration of 10× after 72 hours. Concentration of LFWS at 10× and 5× showed more than 50% inhibition of growth with EATC, Hepalclc7, HeLa and A549. In morphological study, the number of cells were decreased, and the shape of cells was round form in EATC, Hepalclc7, HeLa, and A549.
Chlorpromazine의 유전적 안전성에 관한 연구
김한규,손윤희,이광현,윤태호,남경수 大韓神經精神醫學會 2000 신경정신의학 Vol.39 No.3
연구목적 ; 항 정신성약물로 사용빈도가 높은 chlorpromazine을 사용하여 이 약물의 돌연변이원성과 유전독성을 알아보았다. 방 법 : Bacillus subtilis을 사용한 DNA손상성검토(rec assay), Salmonella typhimurium을 이용한 돌연변이원성실험(Ames test 및 SOS umu test) 그리고 생쥐에 chlorpromazine를 직접 주입하여 대사 후에 돌연변이원성을 확인하는 host-mediated assay법을 각각 사용하였다. 결 과 ; Rec assay에서 chlorpromazine은 Bacillus subtilis의 DNA에는 별다른 영향을 미치지 않았으며, salmonella typhomurium TA 98 및 TA100을 이용한 돌연별이원성 실험에서도 chlorpromazine은 어느 균에도 돌연변이원성을 나타내지 않았으며, S-9 mixture의 첨가에 의해 대사가 된 후에도 돌연변이원성을 나타내지 않았다. 또한 SOS umu test의 경우에도 β-galactosidase활성에는 별다른 영향을 미치지 않는 것으로 보아 chlorpromazine은 돌연별이원성을 일으키지 않는 것으로 판정되었으며 S-9 mixture 처리 후에도 이와 유사한 결과를 얻었다. 한편 생쥐를 이용한 host mediated assay에서도 Ames test에서 S-9 mixture를 첨가 한 경우와 같이 돌연변이원성이 없는 것으로 판정되었다. 결 론 : 이상을 종합해 볼 때 chlorpromazine은 본 실험에 사용한 4가지 방법에서는 돌연병이원성과 유전독성을 일으키지 않는 것으로 나타났다. Object : The aim of this study is to determine whether exposure to chlorpromazine causes mutagenicity and genetic disorders. Method : Ames(Salmonella typhimurium) test and Rec assay(Bacillus subtilis) were used as indicators for DNA damage. Furthermore, the levels of umu operon expression by measuring the β-galactosidase activity were monitered with the SOS umu test using S. typhimurium 1535 containing plasmid pSK1002. And the host-mediated assay was used to investigate the mutagenicity of chlorpromazine after the activation with in vivo metabolic systems. Results : From the results, chlorpromazine did not affect DNA of S. typhimurium and B.subtilis strains and showed no mutagenicity at the all concentrations tested. These phenomena was also similar to that after metabolic activation of chlorpromazine in in vivo system. Conclusion : These results suggested that chlorpromazine did not show the mutagenicity and genotoxicity by four different methods used in this study.
Yun-Hee Shon,Kyung-Soo Nam 대한약학회 2006 Archives of Pharmacal Research Vol.29 No.3
We investigated the effect of protein extract of Asterina pectinifera on the activity of 4 enzymes that may play a role in adenocarcinoma of the colon: quinone reductase (QR), glutathione Stransferase (GST), ornithine decarboxylase (ODC), and cyclooxygenase (COX)-2. QR and GST activity increased in HT-29 human colon adenocarcinoma cells increased that had been exposed to 4 concentrations of the protein extract (80, 160, 200, and 240 µg/mL). Additionally, 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced ODC activity decreased significantly in cells exposed to the extract in concentrations of 160 µg/mL (p<0.05), 200 µg/mL (p<0.005), and 240 µg/mL (p<0.005). TPA-induced COX-2 activity also decreased in cells exposed to extract concentrations of 10, 20, 40, and 60 µg/mL. COX-2 expression was also inhibited in cells exposed to this extract. These results suggest that this protein extract of A pectinifera has chemopreventive activity in HT-29 human colon adenocarcinoma cells, and therefore, may have the potential to function as a chemopreventive agent in human colorectal cancer.
Antimutagenic Activity of Chitosan Oligosaccharides
Shon, Yun-Hee,Ha, Young-Min,Nam, Kyung-Soo 동국대학교 자연과학연구원 2000 자연과학연구 논문집 Vol.5 No.-
The antimutagenic effects of chitosan oligosaccharide I and chitosan oligosaccharide Ⅱ were examined using the Ames/Salmonella test. No antimutagenic activity was found against the directly-acting mutagens, 4-nitro-o-phenylenediamine(NPD) using the tester strain TA 98 and sodium azide (NaN3) using the tester strain TA 100 in the absence of S9 mix. In contrast, chitosan oligosaccharide showed inhibitory effect on the mutagenicities of the indirectly-acting mutagens, 2-aminofluorene (2-AF) and 2-amino-3,8-dimethylimidazo[4,5-f] quinoxaline(MeIQx) using the tester strain TA 98 and benzo[a]pyrene (B[a]P) using the tester strain TA 100 in the presence of S9. These results suggested that chitosan oligosaccharide had antimutagenic properties and may play a role in the prevention of cancer.