Influence of Clyster No.1 on the Express of Immunologic Targets of Mice with Ulcerative Colitis
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Influence of Clyster No.1 on the Express of Immunologic Targets of Mice with Ulcerative Colitis
Chinese Journal of Experimental Traditional Medical FormulaeVol. 14, Issue 7, Pages: 63-66(2008)
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Published:2008
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LIU Ping1, AN Xiao-xia2, LI Yan2, et al. Influence of Clyster No.1 on the Express of Immunologic Targets of Mice with Ulcerative Colitis[J]. Chinese journal of experimental traditional medical formulae, 2008, 14(7): 63-66.
DOI:
LIU Ping1, AN Xiao-xia2, LI Yan2, et al. Influence of Clyster No.1 on the Express of Immunologic Targets of Mice with Ulcerative Colitis[J]. Chinese journal of experimental traditional medical formulae, 2008, 14(7): 63-66.DOI:
Influence of Clyster No.1 on the Express of Immunologic Targets of Mice with Ulcerative Colitis
Objective:To compare the therapeutic effects of Clyster No.1(CN1
the Pulsatillae decoction) with salazosulfapyridine(SASP) to the ulcerative colitis(UC) model induced by dinitrochlorobenzene (DNCB)-acetic acid(AA) in mice
to research the pathogenesis.Methods:KM mice were randomly divided into four groups: normal control group
experimental colitis model group
SASP group and CN1 therapeutic group.Proportions of CD3+、CD4+ T cell、 in mesenteric lymph node and peripheral blood of each group were estimated by flow cytometry;and histological changes were evaluated by HE staining and histological score of intestine.Results: Compared with normal control group
the histological score was markedly higher and the length of colon became shorter in model group of experimental colitis.The proportion of CD3+、CD4+ T cells were markedly decreased(P<0.01) in model group compared with the control group.After two weeks' treatment with SASP and CN1
the histological score was reduced
the length of colon recovered almost to normal level
accompanied with increasing in the proportion of CD3+、CD4+ T cells compared with the model group.Conclusions: The effect was satisfactory for the UC mice treated with CN1 and it may serve as a tool for investigation of the pathogenesis and therapeutical effect for UC.