Effects of Qian Lie Shuang Granule on the Expression of IL-10, TNF- in the Rat Model for Chronic Abacterial Prostatitis
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Effects of Qian Lie Shuang Granule on the Expression of IL-10, TNF- in the Rat Model for Chronic Abacterial Prostatitis
Chinese Journal of Experimental Traditional Medical FormulaeVol. 18, Issue 19, Pages: 267-270(2012)
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Published:2012
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FAN Yu-dong, HU Meng-ying, ZHANG Lan-lan, et al. Effects of Qian Lie Shuang Granule on the Expression of IL-10, TNF- in the Rat Model for Chronic Abacterial Prostatitis[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(19): 267-270.
DOI:
FAN Yu-dong, HU Meng-ying, ZHANG Lan-lan, et al. Effects of Qian Lie Shuang Granule on the Expression of IL-10, TNF- in the Rat Model for Chronic Abacterial Prostatitis[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(19): 267-270.DOI:
Effects of Qian Lie Shuang Granule on the Expression of IL-10, TNF- in the Rat Model for Chronic Abacterial Prostatitis
Objective:Investigate the influence of Qianlie Shuang granule on intereukin-10(IL-10)
tumor necrosis factor-α(TNF-α) in serum of chronic abacterial prostafitis(CAP)rats. Method:Sixty aged sprague dawley (SD) rats were randomly divided into six groups:control group
model group
Qianlie Huichun granule group
Qianlie Shuang low dose group
Qianlie Shuang medium dose group and Qianlie Shuang high dose group. The changes of prostate gland inflammation was investigated. The expression of IL-10 and TNF-α in rat prostatic tissue was detected by immunohistochemistry. Result:The inflammation of model group were similar to those in clinical CAP
the inflammation of treatment groups were obviously degraded. The IL-10 and TNF-α in model group were obviously higher than in control group(P<0.05).The TNF-α in Qianlie Huichun granule group
Qianlie Shuang medium dose group and high dose group were obviously lower than in model group. The IL-10 in those groups were obviously higher than in model group. Conclusions:Qianlie Shuang granule can regulate the secretion of inflammatory cytokines
which can be one of the mechanisms in the therapy of CAP.