692 research outputs found

    A Mathematical Model for Estimating Biological Damage Caused by Radiation

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    We propose a mathematical model for estimating biological damage caused by low-dose irradiation. We understand that the Linear Non Threshold (LNT) hypothesis is realized only in the case of no recovery effects. In order to treat the realistic living objects, our model takes into account various types of recovery as well as proliferation mechanism, which may change the resultant damage, especially for the case of lower dose rate irradiation. It turns out that the lower the radiation dose rate, the safer the irradiated system of living object (which is called symbolically "tissue" hereafter) can have chances to survive, which can reproduce the so-called dose and dose-rate effectiveness factor (DDREF).Comment: 22 pages, 6 Figs, accepted in Journal of the Physical Society of Japa

    Virtual hand illusion: The alien finger motion experiment

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    In VIVO anti-tumor activities of gelatin

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    Aim: As reported previously, porcine skin gelatin exerted direct anti-tumor effect in vitro and induced anti-tumor peritoneal macrophages in vitro. The present study investigated whether or not the gelatin exerted anti-tumor effect in vivo. Methods: In vitro anti-tumor activities of peritoneal macrophages and the gelatin were evaluated with tritium thymidine uptake by target tumor cells. In vivo anti-tumor activity was evaluated with the survival of tumor-bearing animals and the size of the tumor. Results: Intraperitoneal daily administration of 12.5 mg of the gelatin prolonged the survival of mice which had been intraperitoneally inoculated with MH134 (hepatic cell carcinoma cell line) or Colon 26 (colon carcinoma cell line) tumor cells, and there were no tumors in case of MH134 cells inoculation. Intraperitoneal daily administration of 12.5 mg of the gelatin did not affect growth of subcutaneous MH134 tumor. The gelatin administered subcutaneously did not affect the survival of mice with intraperitoneal MH134 tumor. On the other hand, bovine skin gelatin administered subcutaneously achieved statistically significant prolongation of the survival. The contact of MH134 cells with porcine skin gelatin for 5 min was required for the gelatin to exert its anti-tumor activity in vitro. Porcine skin gelatin of 12.5 mg injected intraperitoneally was detected as protein in the peritoneal cavity 5 min after the injection. Peritoneal macrophages elicited by intraperitoneal injection with porcine skin gelatin suppressed tritium thymidine uptake by MH134 cells more strongly than those elicited by thioglycollate injection. Conclusion: Porcine skin gelatin administered intraperitoneally prolonged the survival of tumor-bearing mice via activation of peritoneal macrophages and involvement of direct anti-tumor activity of porcine skin gelatin. Key Words: porcine skin, gelatin, dissemination

    Serum factors that suppress cytotoxic effect of methotrexate

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    To study the phenomenon that human erythroid leukemia K-562 cells are more sensitive to cytotoxic effect of antimetabolites when cultured in a serum-free medium than in a conventional medium containing fetal calf serum (FCS). Methods: Cytotoxic effects of methotrexate, azaserine and 5-fluorouracil were estimated by accessing the lactate dehydrogenase (LDH) activity of viable tumor cells. Proteins of FCS were separated using two-dimensional electrophoresis followed by mass spectrometry analysis. Results: Addition of 10% FCS attenuated anti-tumor activity of methotrexate and azaserine against K-562 cells compared with serum-free medium. Such an activity of FCS was different for each serum lot. Comparison of the proteins in active serum lot with those in not active one using two-dimensional electrophoresis showed that in the active serum there were proteins 150 kDa, which were absent in the not active serum lot. Mass spectrometry indicated that all those proteins had the amino acid sequence of albumin. Sera of one healthy volunteer and two patients with thyroid cancer also attenuated the activity of the agent. Conclusion: Several lots of FCS and human serum demonstrated the ability to attenuate the cytotoxic effect of methotrexate in vitro, possibly due to the formation of albumin dimers/MTX complexes

    Anti-tumor activity of murine peritoneal macrophages induced by porcine skin gelatin

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    Aim: To study the induction of anti-tumor activity of murine peritoneal macrophages in vitro by porcine skin gelatin. Methods: Anti-tumor activity of the macrophages was evaluated with tritium thymidine uptake by target tumor cells. ELISA was used to measure amounts of cytokines secreted in culture medium. Results: The ability of the gelatin to induce anti-tumor activity of the macrophages was stronger than that of lipopolysaccharide of E. coli. Combination of the lipopolysaccharide and interferon-g synergistically stimulated the macrophages but that of the gelatin and interferon-g additionally did. The culture supernatant of the macrophages incubated with the gelatin also showed higher anti-tumor activity than that with the lipopolysaccharide though the lipopolysaccharide was more excellent than the gelatin in stimulating secretion of anti-tumor cytokines (IL-1, IL-6, TNF-a, IFN-g) by the macrophages. Anti-TNF-a antibody partially suppressed the anti-tumor activity of the culture supernatant of the macrophages incubated with the lipopolysaccharide but not with the gelatin. The gelatin induced anti-tumor activity of the macrophages of C3H/HeJ as well as C3H/HeN mice whereas the lipopolysaccharide did only in C3H/HeN mice. The macrophages stimulated in vitro by the gelatin exerted anti-tumor activity in vivo. Moreover, the gelatin stimulated peritoneal exudates cells in vivo when subcutaneously administered with them. Conclusions: Porcine skin gelatin induces anti-tumor activity of macrophages in mice and its magnitude is greater than that of lipopolysaccharide of E. coli. Its mechanism is different from that of the lipopolysaccharide but not fully clarified.ЦСль: ΠΈΠ·ΡƒΡ‡ΠΈΡ‚ΡŒ in vitro ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΡƒΡŽ Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ ΠΌΡ‹ΡˆΠΈΠ½Ρ‹Ρ… ΠΏΠ΅Ρ€ΠΈΡ‚ΠΎΠ½Π΅Π°Π»ΡŒΠ½Ρ‹Ρ… ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΎΠ², ΠΈΠ½Π΄ΡƒΡ†ΠΈΡ€ΠΎΠ²Π°Π½Π½ΡƒΡŽ ΠΆΠ΅Π»Π°Ρ‚ΠΈΠ½ΠΎΠΌ ΠΊΠΎΠΆΠΈ свиньи. ΠœΠ΅Ρ‚ΠΎΠ΄Ρ‹: ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΡƒΡŽ Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΎΠ² ΠΎΡ†Π΅Π½ΠΈΠ²Π°Π»ΠΈ ΠΏΠΎ Π²ΠΊΠ»ΡŽΡ‡Π΅Π½ΠΈΡŽ ΠΌΠ΅Ρ‡Π΅Π½Π½ΠΎΠ³ΠΎ Ρ‚ΠΈΠΌΠΈΠ΄ΠΈΠ½Π° ΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²Ρ‹ΠΌΠΈ ΠΊΠ»Π΅Ρ‚ΠΊΠ°ΠΌΠΈ-мишСнями. Π£Ρ€ΠΎΠ²Π΅Π½ΡŒ Ρ†ΠΈΡ‚ΠΎΠΊΠΈΠ½ΠΎΠ², сСкрСтируСмых Π² ΠΊΡƒΠ»ΡŒΡ‚ΡƒΡ€Π°Π»ΡŒΠ½ΡƒΡŽ срСду, опрСдСляли с ΠΏΠΎΠΌΠΎΡ‰ΡŒΡŽ ELISA. Π Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Ρ‹: cΠΏΠΎΡΠΎΠ±Π½ΠΎΡΡ‚ΡŒ ΠΆΠ΅Π»Π°Ρ‚ΠΈΠ½Π° ΠΈΠ½Π΄ΡƒΡ†ΠΈΡ€ΠΎΠ²Π°Ρ‚ΡŒ ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΡƒΡŽ Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΎΠ² Π±Ρ‹Π»Π° сильнСС, Ρ‡Π΅ΠΌ Ρƒ липополисахарида E. coli. ΠšΠΎΠΌΠ±ΠΈΠ½Π°Ρ†ΠΈΡ липополисахарида ΠΈ ΠΈΠ½Ρ‚Π΅Ρ€Ρ„Π΅Ρ€ΠΎΠ½Π°-Ξ³ (IFN-Ξ³) синСргично стимулировала ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΈ, Ρ‡Ρ‚ΠΎ ΠΏΠΎΠΊΠ°Π·Π°Π½ΠΎ ΠΈ для ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Ρ†ΠΈΠΈ ΠΆΠ΅Π»Π°Ρ‚ΠΈΠ½Π° с IFN-Ξ³. ΠŸΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²Π°Ρ Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ ΠΊΡƒΠ»ΡŒΡ‚ΡƒΡ€Π°Π»ΡŒΠ½ΠΎΠ³ΠΎ супСрнатанта ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΎΠ², ΠΈΠ½ΠΊΡƒΠ±ΠΈΡ€ΠΎΠ²Π°Π½Π½Ρ‹Ρ… с ΠΆΠ΅Π»Π°Ρ‚ΠΈΠ½ΠΎΠΌ, Π±Ρ‹Π»Π° Π²Ρ‹ΡˆΠ΅, Ρ‡Π΅ΠΌ Π² случаС примСнСния липополисахарида, хотя липополисахарид ΠΈΠ½Π΄ΡƒΡ†ΠΈΡ€ΠΎΠ²Π°Π» Π±ΠΎΠ»Π΅Π΅ ΡΠΈΠ»ΡŒΠ½ΡƒΡŽ ΡΠ΅ΠΊΡ€Π΅Ρ†ΠΈΡŽ ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²Ρ‹Ρ… Ρ†ΠΈΡ‚ΠΎΠΊΠΈΠ½ΠΎΠ² (IL-1, IL-6, TNF-Ξ±, IFN-Ξ³) ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³Π°ΠΌΠΈ. АнтитСла ΠΏΡ€ΠΎΡ‚ΠΈΠ² TNF-Ξ± частично ΡƒΠ³Π½Π΅Ρ‚Π°Π»ΠΈ ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΡƒΡŽ Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ ΠΊΡƒΠ»ΡŒΡ‚ΡƒΡ€Π°Π»ΡŒΠ½ΠΎΠ³ΠΎ супСрнатанта ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΎΠ², ΠΈΠ½ΠΊΡƒΠ±ΠΈΡ€ΠΎΠ²Π°Π½Π½Ρ‹Ρ… с липополисахаридом, Π½ΠΎ Π½Π΅ с ΠΆΠ΅Π»Π°Ρ‚ΠΈΠ½ΠΎΠΌ. Π–Π΅Π»Π°Ρ‚ΠΈΠ½ ΠΈΠ½Π΄ΡƒΡ†ΠΈΡ€ΠΎΠ²Π°Π» ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΡƒΡŽ Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΎΠ² ΠΊΠ°ΠΊ C3H/HeJ ΠΌΡ‹ΡˆΠ΅ΠΉ, Ρ‚Π°ΠΊ ΠΈ ΠΌΡ‹ΡˆΠ΅ΠΉ C3H/ HeN, Π² Ρ‚ΠΎ врСмя ΠΊΠ°ΠΊ липополисахарид влиял Ρ‚ΠΎΠ»ΡŒΠΊΠΎ Π½Π° ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΈ C3H/HeN ΠΌΡ‹ΡˆΠ΅ΠΉ. ΠœΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΈ, стимулированныС in vitro, ΠΏΠΎΠΊΠ°Π·Ρ‹Π²Π°Π»ΠΈ ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΡƒΡŽ Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ in vivo. Π‘ΠΎΠ»Π΅Π΅ Ρ‚ΠΎΠ³ΠΎ, ΠΆΠ΅Π»Π°Ρ‚ΠΈΠ½ стимулировал ΠΊΠ»Π΅Ρ‚ΠΊΠΈ ΠΏΠ΅Ρ€ΠΈΡ‚ΠΎΠ½Π΅Π°Π»ΡŒΠ½ΠΎΠ³ΠΎ экссудата in vivo ΠΏΡ€ΠΈ ΠΎΠ΄Π½ΠΎΠ²Ρ€Π΅ΠΌΠ΅Π½Π½ΠΎΠΌ ΠΏΠΎΠ΄ΠΊΠΎΠΆΠ½ΠΎΠΌ Π²Π²Π΅Π΄Π΅Π½ΠΈΠΈ. Π’Ρ‹Π²ΠΎΠ΄Ρ‹: ΠΆΠ΅Π»Π°Ρ‚ΠΈΠ½ свиной ΠΊΠΎΠΆΠΈ ΠΈΠ½Π΄ΡƒΡ†ΠΈΡ€ΡƒΠ΅Ρ‚ ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΡƒΡŽ Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ ΠΌΠ°ΠΊΡ€ΠΎΡ„Π°Π³ΠΎΠ² Ρƒ ΠΌΡ‹ΡˆΠ΅ΠΉ, ΠΏΡ€ΠΈΡ‡Π΅ΠΌ Π±ΠΎΠ»Π΅Π΅ эффСктивно, Ρ‡Π΅ΠΌ липополисахарид E. coli. ΠœΠ΅Ρ…Π°Π½ΠΈΠ·ΠΌ дСйствия ΠΆΠ΅Π»Π°Ρ‚ΠΈΠ½Π° отличаСтся ΠΎΡ‚ ΠΌΠ΅Ρ…Π°Π½ΠΈΠ·ΠΌΠ° дСйствия липополисахарида ΠΈ остаСтся ΠΏΠΎΠΊΠ° нСвыяснСнным Π΄ΠΎ ΠΊΠΎΠ½Ρ†

    A New Possibility of Dynamical Study on Solid State Ionic Materials by Inelastic Neutron Scattering

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    A new technique of inelastic neutron scattering measurement utilizing the multiple incident energies is applied to the dynamical study of vitreous silica. A wide variety of extracted information from a series of two-dimensional maps of dynamical structure factor with multiple different incident energies are greatly valuable. The applicability and its expected contribution of new experimental technique into the further progress of scientific activities in solid state ionic materials are discussed.Received: 30 September 2010; Revised: 25 October 2010; Accepted: 26 October 201
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