Li Min, Zhang Ya-Qiang, Wang Yan
Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing.
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2008 Nov;28(11):1018-21.
To explore the acting mechanism of Danpu Capsule (DPC) in treating chronic prostatitis by observing its effect on inflammatory factors in autoimmune prostatitis rat model.
The rat model was established by abdominal subcutaneous multiple points injection of rat's prostate tissue antigen. Thirty modeled rats were randamly divided into 3 groups, the DPC group, the Qianlietai Tablet (QLT) group and the model group. They were treated via gastrogavage respectively with DPC, Qianlietai Tablet and normal saline respectively. Besides, a control group was set up with 10 healthy rats. All animals were sacrificed 56 days after treatment. Pathologic change of prostatic tissue was observed by light microscopy, and the levels of interleukin 8 (IL-8), interleukin 10 (IL-10), tumor necrosis factor alpha (TNF-alpha) and prostaglandin E2 (PGE2) in blood serum and prostatic tissue were detected by enzyme linked immunosorbent assay (ELISA).
Compared with the normal group, the serum and prostatic levels of IL-8, IL-10 and TNF-alpha, as well as the prostatic level of PGE2 in the model group were higher (P <0.05 or P <0.01). In the DPC group, the serum and prostatic levels of IL-8 was 3.07 +/- 0.61 ng/L and 7.32 +/- 2.44 ng/L respectively, which was lower than those in the model group (4.73 +/- 1.95 ng/L and 10.14 +/- 3.64 ng/L, respectively); that of TNF-alpha in the DPC group (85.34 +/- 19.20 ng/L and 87.01 +/- 15.4 ng/L) was also lower in the model group (111.48 +/- 31.57 ng/L and 119.88 +/- 14.13 ng/L); similar difference between the two groups was also shown in prostatic level of IL-10 (34.05 +/- 7.56 ng/L vs 47.20 +/- 15.97 ng/L), and so was PGE2 (603.97 +/- 114.62 ng/L vs 712.58 +/- 117.10 ng/L), all with statistical significance (P <0.05 or P <0. 01).
DPC could reduce the prostatic inflammatory response of model rats, and regulate the local immune condition.
通过观察丹蒲胶囊(DPC)对自身免疫性前列腺炎大鼠模型炎症因子的影响,探讨其治疗慢性前列腺炎的作用机制。
采用大鼠前列腺组织抗原腹部皮下多点注射法建立大鼠模型。将30只造模大鼠随机分为3组,即DPC组、前列泰片(QLT)组和模型组,分别给予DPC、前列泰片及生理盐水灌胃。另设正常对照组,选取10只健康大鼠。治疗56天后处死所有动物,光镜下观察前列腺组织病理变化,采用酶联免疫吸附测定(ELISA)法检测血清及前列腺组织中白细胞介素8(IL-8)、白细胞介素10(IL-10)、肿瘤坏死因子α(TNF-α)和前列腺素E2(PGE2)水平。
与正常组比较,模型组血清及前列腺组织中IL-8、IL-10、TNF-α水平及前列腺组织中PGE2水平均升高(P<0.05或P<0.01)。DPC组血清及前列腺组织中IL-8水平分别为3.07±0.61 ng/L和7.32±2.44 ng/L,低于模型组(分别为4.73±1.95 ng/L和10.14±3.64 ng/L);DPC组TNF-α水平(85.34±19.20 ng/L和87.01±15.4 ng/L)也低于模型组(111.48±31.57 ng/L和119.88±14.13 ng/L);两组间前列腺组织IL-10水平(34.05±7.56 ng/L比47.20±15.97 ng/L)及PGE2水平(603.97±114.62 ng/L比712.58±117.10 ng/L)比较差异均有统计学意义(P<0.05或P<0.01)。
DPC可减轻模型大鼠前列腺炎症反应并调节局部免疫状态。