Department of Urology, Zhongnan Hospital, Wuhan University, Wuhan 430071, China.
Department of Urology Research Lab/LIFE-Zentrum, University of Munich (LMU), München 81377, Germany.
Asian J Androl. 2019 Jul-Aug;21(4):360-364. doi: 10.4103/aja.aja_90_18.
We aimed to establish a novel rat model of seminal vesiculitis that would provide an effective approach to investigate the pathogenesis of this disease in the future. Eight male rats received the same operation, during which the root of one of the two seminal vesicles was partly ligatured with sutures and the other vesicle was left intact. The samples of seminal vesicles were harvested on the 8 day following the operation. Hematoxylin and eosin and Masson's trichrome stains were used to observe the histopathology and the presence of fibrous tissue in seminal vesicles, respectively. Immunoblotting and immunohistochemistry were applied to determine the tumor necrosis factor-alpha and cyclooxygenase-2 levels in seminal vesicle tissues. Real-time fluorescence quantitative polymerase chain reaction was performed to measure the gene expression levels of proinflammatory cytokines. HOlevelsin the seminal plasma from the seminal vesicle were also measured. Hematoxylin and eosin staining suggested that there was inflammatory cell infiltration into the seminal vesicles treated by partial root ligation. The tumor necrosis factor-alpha and cyclooxygenase-2 proteins were significantly upregulated in the treated seminal vesicles. The tumor necrosis factor-alpha, cyclooxygenase, interleukin 6, and inducible nitric oxide synthase mRNA expression levels were also upregulated in the treated seminal vesicles. The HO levels in the seminal plasma from seminal vesicles with partial root ligation were significantly elevated compared with those from vesicle left intact. In conclusion, partially ligating the root of the seminal vesicle via sutures in rats is an effective method to establish a seminal vesiculitis rat model.
我们旨在建立一种新的大鼠前列腺炎模型,为今后研究该病的发病机制提供有效的方法。8 只雄性大鼠接受相同的手术,其中一侧的两个精囊的根部用缝线部分结扎,另一侧的精囊保持完整。术后第 8 天采集精囊样本。苏木精和伊红染色和 Masson 三色染色分别用于观察精囊的组织病理学和纤维组织的存在。免疫印迹和免疫组织化学用于确定精囊组织中肿瘤坏死因子-α和环氧化酶-2 的水平。实时荧光定量聚合酶链反应用于测量促炎细胞因子的基因表达水平。还测量了来自精囊的精液中的 HO 水平。苏木精和伊红染色表明,部分结扎处理的精囊中存在炎症细胞浸润。处理过的精囊中肿瘤坏死因子-α和环氧化酶-2 蛋白明显上调。处理过的精囊中肿瘤坏死因子-α、环氧化酶、白细胞介素 6 和诱导型一氧化氮合酶的 mRNA 表达水平也上调。与保留的精囊相比,部分结扎精囊根部的精液中的 HO 水平显著升高。总之,通过缝线部分结扎大鼠的精囊根部是建立大鼠前列腺炎模型的有效方法。