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1.
M. A. Ball T. Utsunomiya K. Ikemoto M. Kobayashi R. B. Pollard F. Suzuki 《Cellular and molecular life sciences : CMLS》1994,50(8):774-779
The antiviral effect of Keishi-ni-eppi-ichi-to (TJS-064), a traditional Chinese herbal medicine, was investigation in mice infected with influenza A2(H2N2) virus. When mice exposed to 5 LD50 dose of the virus were treated orally with a 70 mg/kg dose of TJS-064 1 day before and 1 day and 4 days after the infection, 100% survived over a 25-day experimental period. At the end of this period all the control mice, treated with saline alone, had died; their mean survival time in days (MSD) was 11.2 days. When mice infected with a 10 LD50 dose of the virus were treated with TJS-064, the MSD was >17.4 days and there was a 50% survival rate, while the control group had a MSD of 8.7 days and 0% survival rate. No significant antiviral effect TJS-064 was observed when the agent was administered orally to mice infected with a 100 LD50 or large dose of influenza virus. Pulmonary consolidation, virus titers in lung tissues and HAI titers in sera of infected mice treated with TJS-064 were all significantly lower than those of infected mice treated with saline. Interferon activities were detected in sera of mice treated with the agent at a dose of 100 mg/kg orally. Since viricidal and viristatic activities of the agent against influenza virus were not demonstrated, the antiviral effects of TJS-064 may be expressed through the host's antiviral functions including interferon production. 相似文献
2.
The role of hsp70 in protection and repair of luciferase activity in vivo; experimental data and mathematical modelling 总被引:1,自引:0,他引:1
J. E. M. Souren F. A. C. Wiegant R. Van Wijk 《Cellular and molecular life sciences : CMLS》1999,55(5):799-811
The stably transfected rat cell line HR24 expressing high levels of the inducible human hsp70 and its parental cell line
Rat-1 were used for in vivo studies to analyse the role of hsp70 during thermal protein denaturation and the subsequent renaturation.
In order to monitor denaturation and renaturation of a cellular protein in vivo, both cell lines were transiently transfected
with firefly luciferase (Luc). The continuous monitoring of Luc activity during and after heat stress allowed a detailed analysis
of the inactivation and reactivation kinetics in cells grown in monolayers. The aim of these studies was to distinguish a
protective effect of increased hsp70 levels during heat shock-induced protein inactivation from a stimulation of reactivation.
In this paper we show that in cells that are stably transfected with hsp70, thermal Luc inactivation decreased, and subsequent
reactivation yielded higher activity levels, compared with the parental cells. The difference in early inactivation kinetics
observed in the two cell lines suggests an immediate effect of the presence of an extra amount of hsp70 on enzyme inactivation.
Using different mathematical models, the heat-induced inactivation and reactivation kinetics was compared with simulations
of denaturation and renaturation. It is concluded that the model in which it is assumed that hsp70 is able to interact with
partially denatured proteins, which did not yet lose their enzymatic activity, most optimally explains the experimental observations.
Received 2 December 1998; received after revision 19 February 1999; accepted 18 March 1999 相似文献