Yong-hao, Y., Nai-qiang, C., Qiang, F. et al. Change of Th1/Th2 cytokine equilibrium in rats with severe sepsis and therapeutic effect of recombinant interleukin-12 and Shenmai injection., Chin. J. Integr. Med. 11, 136–141 (2005). https://doi.org/10.1007/BF02836471
Yu Yong-hao, Cui Nai-qiang, Fu Qiang, et al. Change of Th1/Th2 cytokine equilibrium in rats with severe sepsis and therapeutic effect of recombinant interleukin-12 and Shenmai injection[J]. Chinese Journal of Integrative Medicine, 2005,11(2):136-141.
Yong-hao, Y., Nai-qiang, C., Qiang, F. et al. Change of Th1/Th2 cytokine equilibrium in rats with severe sepsis and therapeutic effect of recombinant interleukin-12 and Shenmai injection., Chin. J. Integr. Med. 11, 136–141 (2005). https://doi.org/10.1007/BF02836471DOI:
Yu Yong-hao, Cui Nai-qiang, Fu Qiang, et al. Change of Th1/Th2 cytokine equilibrium in rats with severe sepsis and therapeutic effect of recombinant interleukin-12 and Shenmai injection[J]. Chinese Journal of Integrative Medicine, 2005,11(2):136-141. DOI: 10.1007/BF02836471.
Change of Th1/Th2 cytokine equilibrium in rats with severe sepsis and therapeutic effect of recombinant interleukin-12 and Shenmai injection
摘要
Objective: To evaluate the dynamic change of Thl/Th2 cytokines in serum
peritoneal lavage fluid (PLF) and splenic macrophages (SM) in rats with severe peritonitis
and to observe the therapeutic effects of recombinant interleukin-12 (rlL-2) and Shenmai injection (SMI)
a Chinese medicinal preparation.Methods: Severe peritonitis (SP) model was induced by intraperitoneal injection of E. coli and B. frag
and mild peritonitis (MP) model was induced by cecal ligation and punching. Then the following experiments were done: (1) Survival rates of animals after every 6 hrs in the 72 hrs after modeling were recorded
serum and PLF levels of cytokines
including tumor necrosis factor-α (TNF-α)
interferon-γ (IFN-γ)
and interleukin-10 (IL-10)
6 hrs
12 hrs
24 hrs and 48 hrs after modeling were measured. (2) Model rats were treated with rIL-12 or SMI
the survival rate was recorded and serum levels of TNF-α
INF-γ
and IL-10 before and after treatment were measured
and (3) amount of these cytokines produced by SM were determined 6 hrs
12 hrs and 24 hrs after treatment. The survival rates and levels of cytokines were then compared between the groups (model group treated with rIL-12 or SMI
untreated model group
and blank group).Results: Serum and PLF levels of IFN-γ
TNF-α at all the time points in SP rats were significantly lower than those in MP rats while those of IL-10 6 hrs and 12 hrs after modeling were significantly higher in the former than that in the latter (P<0.05). IFN-γ secretion of SM in SP rats was significantly higher than that in MP rats 6 hrs after modeling (P<0. 05). Administration of rlL-12 or SMI given before modeling could improve the survival rate of the model rats (P<0.05) and cause significant increase of the serum level and SM secretion of IFN-γ.Conclusion: Imbalance in promoting/antagonizing inflammatory cytokines and Th2 response dominance appear in SP rats early at the initiating stage
and SM secretion of inflammation promoting factor also reduces. Administration in time of rIL-12 and SMI
may increase the survival rate
and its mechanism may be related with their immuno-stimulating action.
Abstract
Objective: To evaluate the dynamic change of Thl/Th2 cytokines in serum
peritoneal lavage fluid (PLF) and splenic macrophages (SM) in rats with severe peritonitis
and to observe the therapeutic effects of recombinant interleukin-12 (rlL-2) and Shenmai injection (SMI)
a Chinese medicinal preparation.Methods: Severe peritonitis (SP) model was induced by intraperitoneal injection of E. coli and B. frag
and mild peritonitis (MP) model was induced by cecal ligation and punching. Then the following experiments were done: (1) Survival rates of animals after every 6 hrs in the 72 hrs after modeling were recorded
serum and PLF levels of cytokines
including tumor necrosis factor-α (TNF-α)
interferon-γ (IFN-γ)
and interleukin-10 (IL-10)
6 hrs
12 hrs
24 hrs and 48 hrs after modeling were measured. (2) Model rats were treated with rIL-12 or SMI
the survival rate was recorded and serum levels of TNF-α
INF-γ
and IL-10 before and after treatment were measured
and (3) amount of these cytokines produced by SM were determined 6 hrs
12 hrs and 24 hrs after treatment. The survival rates and levels of cytokines were then compared between the groups (model group treated with rIL-12 or SMI
untreated model group
and blank group).Results: Serum and PLF levels of IFN-γ
TNF-α at all the time points in SP rats were significantly lower than those in MP rats while those of IL-10 6 hrs and 12 hrs after modeling were significantly higher in the former than that in the latter (P<0.05). IFN-γ secretion of SM in SP rats was significantly higher than that in MP rats 6 hrs after modeling (P<0. 05). Administration of rlL-12 or SMI given before modeling could improve the survival rate of the model rats (P<0.05) and cause significant increase of the serum level and SM secretion of IFN-γ.Conclusion: Imbalance in promoting/antagonizing inflammatory cytokines and Th2 response dominance appear in SP rats early at the initiating stage
and SM secretion of inflammation promoting factor also reduces. Administration in time of rIL-12 and SMI
may increase the survival rate
and its mechanism may be related with their immuno-stimulating action.
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