• 제목/요약/키워드: [$^3$H]thymidine incorporation

검색결과 143건 처리시간 0.028초

소양호 수중 생태계에서의 세균 생체물질량의 분포 (Distribution of bacterial biomass in the water column of Soyang lake)

  • 김명운;강찬수;김상종
    • 미생물학회지
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    • 제27권2호
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    • pp.130-138
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    • 1989
  • 소양호에서 측정된 세균 체적, 세균 생물량 및 세균 생산량 등의 미생물학적인 요인의 변화에 미치는 물리화학적 환경요인의 영향을 통계학적 방법으로 분석을 하였다. 상관관계 분석과 중회귀 분석 결과 수온은 대부분의 미생물학적 요인에 폭넓은 영향을 미침을 알 수 있었다. 총 세균수, 세균 체적, 세균 생물 량 및 saprophyte 수외 변화는 엽록소 a와 pheophytin a의 존재와 높은 상관관계를, $^{3}H$-thymidine incorporation rate에 의해 측정된 세균 생산량은 seston의 농도에 큰 영향을 받는 것으로 분석되었다. 소양호 수중생태계에서의 세균 체적 및 세균 생물량의 미생물학적 요인은 미생물 군집에게 탄소와 에너지원으로 작용하는 유기물질의 제공원인 식물성 플랑크톤의 분포와 seston의 농도에 의해 조절되고 있음을 시사하여 준다.

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T-2 Toxin이 병아리 비장세포의 유전질 발생에 미치는 영향 (Effect of T-2 Toxin on the Mitogen-Induced Blastogenesis in Chick Splenic Cell)

  • 전향숙;정덕화;이서래
    • 한국식품과학회지
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    • 제26권5호
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    • pp.585-589
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    • 1994
  • 시험관 내에서 T-2 toxin이 병아리 비장세포의 blastogenesis에 미치는 영향을 살펴본 결과, B-cell mitogen인 lipopolysaccharide 및 T-cell mitogen인 concanavalin A 자극에 대해 T-2 toxin의 농도가 증가함에 따라 억제정도가 증가하는 경향을 나타내었다. 노출시기를 달리하여 T-2 toxin을 투여한 병아리의 비장세포에서 mitogen 자극에 내한 반응을 안아 본 결과, 부화하기 전과 후에 계속 T-2 toxin에 노출시킨 실험군은 가장 영향을 많이 받은 것으로 나타났고 부화전 혹은 부화후 어느 한 시기에만 T-2 toxin에 노출된 실험군은 비교적 영향을 적게 받는 것으로 나타났다.

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항 방사선 인삼단백분획의 DNA수복능력 증진효과 (DNA Repair Enhancement by Radioprotective Ginseng Protein Fraction)

  • 김춘미;최미경
    • 약학회지
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    • 제36권5호
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    • pp.449-454
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    • 1992
  • The effect of radioprotective ginseng protein fraction on DNA repair capacity was determined by measuring the amount of $^{3}H-thymidine$ incorporated into DNA in the process of repair synthesis for UV damaged DNA. CHO-Kl cells were prepared whose semiconservative replication was inhibited by trimethylpsoralen plus near-UV(PUVA) treatment. When the cells were exposed to UV light alone, the DNA repair capacity was increased at first and then decreased as UV dose increased. However, when the ginseng fraction was treated to the cells, the DNA repair capacity was kept increasing regardless of UV dose increment. When the concentration of protein contained in the added fraction was increased gradually, the repair capacity was also increased almost linearly showing dose-response relationship of the effect. These results suggest that the enhancement of DNA repair capacity of the cell can be one of the mechanisms of radioprotection by the ginseng fraction.

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고려인삼이 마우스의 악하선 DNA 합성능에 미치는 영향( I ) (Influence of Panax Ginseng on DNA Synthesis of Submandibular Gland in Mice)

  • 권영진;채유병;장원상
    • The Korean Journal of Physiology
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    • 제8권1호
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    • pp.23-26
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    • 1974
  • 인삼주정추출액 투여에 의하여 마우스 악하선 조직의 DNA 합성능이 어떤 영향을 받는지를 알기 위하여 30마리의 마우스 (몸 무게 $18{\sim}20$ gm) 수컷을 15마리씩 두 무리로 나누어 한 무리에는 생리적 식염수를 다른 무리에는 인삼주정추출액(인삼주정추출물 4mg 을 생리적 식염수 1ml 속에 용해시켜 만든 용액)을 마우스의 몸 무게 10gm에 대하여 0.05ml씩 5일 동안 주사한 후 $[^3H]-thymidine$을 복강 속에 주사하고 1, 10 및 24시간 만에 도살하여 자기방사법을 이용하여 악하선의 합성능을 비교 관찰한 바 인삼주정추출액을 투여받은 마우스의 악하선 조직의 표지 세포수는 식염수만을 투여받은 마우스의 그것에 비하여 적었다. 그러므로 인삼주정추출액은 마우스의 악하선 조직 DNA 합성능을 어느 정도 억압한다고 믿어진다.

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Inhibitory effect of bisphenol A on the mixed lymphocyte reaction and TNF-$\alpha$ production of antigen presenting cells in mice

  • Hwang, Yoo-Kyung;Byun, Jung-A;Pyo, Myoung-Yun
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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    • pp.166.1-166.1
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    • 2003
  • We investigated the effects of bisphenol A (BPA), endocrine disruptor, on the mixed lymphocyte reaction and TNF-$\alpha$ production of antigen presenting cells in mice. Cells from mouse (C57BL/6) bone marrow were cultured with GM-CSF for 8 days and mature dendritic cells (DCs) were prepared. These DCs proliferation in response to Balb/c splenocytes was measured at 72 h of culture with BPA by tritiated thymidine incorporation ([3H]TdR) and [3H]TdR incorporation was determined by scintilation counting. (omitted)

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고려인삼이 ACTH를 받은 마우스의 간 조직 DNA 합성능에 미치는 영향(II) (Influence of Panax Ginseng on Hepatic DNA Synthesis in Mice Receiving ACTH ( II ))

  • 장원상;홍용하;김기연
    • The Korean Journal of Physiology
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    • 제8권2호
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    • pp.75-78
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    • 1974
  • 인삼주정추출액이 ACTH를 받은 마우스의 간 조직 DNA 합성능에 미치는 영향을 알기 위하여 30마리의 마우스 $(18{\sim}20\;gm)$ 수컷을 인삼-ACTH 군과 식염수-ACTH 군으로 나누어 다음과 같은 실험을 하였다. 인삼주정추출액 혹은 식염수 투여가 시작된지 5일째 되는 날에 해당 약물을 주사한 후 1시간만에 ACTH를 투여하고 다시 1시간만에 $[^3H]$ thymidine을 단 1회에 복강속에 주사하고 이어서 이를 마우스를 1, 10, 및 24시간 후에 각각 도살하여 간 조직을 적출하고 자기방사법을 이용하여 방사능 지수를 계수한 바 다음과 같은 결과를 얻었다 1. $[^3H]$ thymidine 주사 후 1, 10 및 24시간만에 관찰된 식염수-ACTH군의 간 조직 방사능 지수는 각각 $1.50{\pm}0.32,\;2.16{\pm}0.33$$2.79{\pm}0.31$이었다. 2. 인삼-ACTH군의 간 조직 방사능 지수는 1, 10 및 24시간만의 값이 각각 $2.71{\pm}0.22,\;3.85{\pm}0.29$$5.06{\pm}0.31$로 나타났다. 그러므로 인삼-ACTH군 간조직 방사능 지수는 식염수-ACTH군의 해당 값보다 현저하게 증가하였다. 이상의 결과로 미루어 보아 인삼-ACTH주사로 인하여 야기되는 마우스의 간 조직 DNA 합성능의 저하를 어느 정도 막는 것으로 추측된다.

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불화나트륨이 조골세포의 생리적 활성에 미치는 영향 (THE EFFECT OF SODIUM FLUORIDE ON THE PHYSIOLOGICAL ROLE OF OSTEOBLASTIC CELL)

  • 김대업
    • 대한소아치과학회지
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    • 제25권3호
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    • pp.635-648
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    • 1998
  • The clinical use of fluoride with a well known osteogenic action in osteoporotic patients is rational, because this condition is characterized by impaired bone formation. However, its anabolic effect has not been demonstrated well in vitro. The purpose of this study was to investigate the effects of sodium fluoride on the physiological role of osteoblastic cell. Osteoblastic cells were isolated from fetal rat calvaria. The results were as follows : 1. Mineralized nodules were shown in osteoblastic cell cultures, which had been maintained in the presence of ascorbic acid and ${\beta}-glycerophosphate$ up to 21 days. When cultures were treated with pulses of 48 hr duration before apparent mineralization was occurring, 2-fold increased in their number was detected. 2. Alkaline phosphatase activity of osteoblastic cells was inhibited by sodium fluoride in dose dependent manner. 3. The effect of sodium fluoride on the osteoblastic cell proliferation was measured by the incorporation of $[^3H]$-thymidine into DNA. As a result, sodium fluoride at $1{\sim}100{\mu}M$ increased the $[^3H]$-thymidine incorporation into DNA in a dose dependent manner. 4. The signaling mechanism activated by sodium fluoride dose-dependently enhanced the tyrosine phosphorylation of the adaptor molecule $Shc^{p66}$ and their association with Grb2, one of earlier events in a MAP kinase activation pathway cascade used by a significant subset of G protein-coupled receptors. 5. The phosphorylation of CREB(cAMP response element binding protein)was inhibited by the sodium fluoride in MC3T3E1 cells. In conclusion, the results of this study suggested that the mitogenic effect of the sodium fluoride in MC3T3E1 cell was stimulated in a dose-dependent manner and suggested "an important role for the interaction between She and Grb2" in controlling the proliferation of osteoblasts.

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Inhibitory Effects of Kimchi Extracts on the Growth and DNA Synthesis of Human Cancer Cells

  • Hur, young-Mi;Kim, So-Hee;Park, Kun-Young
    • Preventive Nutrition and Food Science
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    • 제4권2호
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    • pp.107-112
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    • 1999
  • Effect of solvent extracts and juice supernatants from kimchis on the growth of various human cancer cells was studied, comparing with the actions on the normal cells. Inhibitory effect of kimchi extracts on[3H] thymidine incorporation n cancer cells was also investigated. The methanol extract, hexane extract and methanol soluble fraction (MSF) of 3-week fermented kimchi did not have growth inhibitory effect on Ac2F rat normal liver cells at the concentrations of 0.5~2%. However, marked decrease in the growth of AGS human gastric cancer cells was shown by the treatment of those extacts. The juice from the kimchi samples also suppressed the growth of K-562 human leukemia cells and MG-63 human osteosarcoma cells. Especially, the juice of 3-week fermented kimchi exhibited the strong growth inhibitory effect in MG-63 human osteosarcoma cells. At the photomicrographs, growth inhibition and morphological change of the cells treated with kimchi juice were observed. And the solvent extracts of 3-week fermented kimchi suppressed the growth of cancer morethan the extracts or juices from fresh and 6-week fermented kimchi. When AGS human gastric cancer cels were treated with the extracts of 3-week fermented kimchi, [3H] thymidine incorporation in the cells also decreased. These results showed that kimchi extracts and juices had growth inhibitory effects on human osteosarcoma, leukemia and gastric cancer cells, but had no toxicity to the normal cells. We suggest that kimchi might have anticancer effect in part due to inhibition of the growth and DNA synthesis of cancer cells.

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인진청간탕(茵蔯淸肝湯)의 항암효과(抗癌效果)에 관(關)한 연구(硏究) (Study on the Anti-Cancer Effect of Injinchunggan-tang(Yinchenqinggan-tang))

  • 우홍정;이장훈;김영철
    • 대한한의학회지
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    • 제20권3호
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    • pp.94-104
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    • 1999
  • Objectives: Hepatoma is a very serious disease in Korea and worldwide. Hepatitis B virus (HBV) has proved the most significant cause of hepatoma. We carried out this study to investigate the effect of Injinchunggan-tang (Yinchenqinggan -tang) on inhibiting cell proliferation and DNA synthesis in HepG2.2.15 cell lines and on inhibiting phosphorilation of oncogene (MAP kinase) in NIT /3T3-HEx cells. Methods: First we confinned the Hepatitis B virus producing ability of HepG2.2.15 cells. To investigate the anti-cancer effect of Injinchunggan-tang (Yinchenqinggan-tang), we did the NTS/PMS assay, [3H]-thymidine incorporation assay and transfection of pcDNA-X. We also measured the gene expression through western blotting. Results: Injinchunggan-tang (Yinchenqing gan tang) showed the suppressing effect of HepG2.2.l5 increase in the MTS/PMS assay and the inhibiting effect of DNA synthesis of HepG2.2.15 in the [3H] thymidine incorporation assay. Injinchunggan-tang (Yinchenqinggan-tang) also showed the inhibiting phosphorilation effect of MAP kinase in HBV -X genes. Conclusions: From the above Injinchunggan-tang (Yinchenqinggan-tang) is thought to have an anti-cancer effect on the hepatoma from HBV. It is suggested that further studies on this prescription would give us a better medicine with an anti-cancer effect.

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고려인삼이 ACTH를 받은 마우스의 악하선 조직 DNA 합성능에 미치는 영향( II ) (Influence of Panax Ginseng on DNA Synthesis of Submandibular Gland in Mice Receiving ACTH(II))

  • 홍용하;김기연
    • The Korean Journal of Physiology
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    • 제8권2호
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    • pp.45-48
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    • 1974
  • It was planned to investigate, in mice that received ACTH, the influence of Panax Ginseng upon DNA synthesis of submandibular gland by observing incorporation of $[^3H]$ thymidine into the tissue cells. Thirty male mice $(body\;weight:\;18{\sim}20\;g)$ were divided equally into the ginseng-ACTIH and the saline-ACTH groups. Each animal of the ginseng-ACTH and the saline-ACTH groups received every day (subcutaneously) 0.05 m1/10 g body weight of ginseng extract(4 mg of ginseng alcohol extract in 1 ml of saline) and the same amount of saline, respectively, for 5 days. On the 5th experimental day, all animals received 0.01 unit of ACTH intraperitoneally one hour after the last medication, and $1\;{\mu}Ci/g$ body weight of $[^3H]$ thymidine after one more hour. Five animals, at a time, of each group were sacrificed 1, 10, and 24 hr after $[^3H]$ thymidine administration, and the radioactivity of cells in their mandibular gland was measured autoradiographically in terms of the % number of radioactive cells in 1,000 cell counts (Radioactive Index, R.1.). Results obtained were as follows: 1. The radioactive indices obtained from submandibular gland of the saline-ACTH group 1, 10 and 24 hr after $[^3H]$ thymidine administration were $15.2{\pm}0.32,\;20.1{\pm}0.30,\;and\;24.5{\pm}0.52(mean{\pm}S.D.)$ in the mucous cells, $13.0{\pm}0.22,\;10.2{\pm}0.05,\;and\;7.5{\pm}0.42$ in the serous cells. and $10.5{\pm}0.40,\;13.6{\pm}0.32,\;and\;15.9{\pm}0.42$ in the duct cells, while the $mean{\pm}S.D.$ of the values obtained from the 3 cell types 1, 10 and 24 hr after $[^3H]$ thymidine were $10.9{\pm}0.28,\;12.4{\pm}0.31,\;and\;10.0{\pm}0.39.$ Thus the radioactive indices obtained from the ginseng-ACTH group were generally lower than those obtained from the saline-ACTH group. It is inferred from the above results that the ginseng tends to promote the suppressive action of ACTH upon DNA synthesis of cells in the mandibular gland.

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