Urological Research Institute of PLA, Southwest Hospital, Third Military Medical University, Chongqing, People's Republic of China.
J Urol. 2010 Jul;184(1):364-9. doi: 10.1016/j.juro.2010.03.003. Epub 2010 May 20.
Nanobacteria are thought to be a pathopoiesis bacterium in urological disease. We observed pathological changes in nanobacteria infected prostates in Sprague-Dawley(R) rats and investigated the possible etiological relationships of nanobacteria and type III prostatitis.
We randomized 40 adult male Sprague-Dawley rats each to the control and model groups. Rat prostate infection models were reproduced by infusing nanobacteria suspension transurethrally. Rats were sacrificed 1, 2, 4 and 8 weeks later, respectively. Prostatic pathology, and the cytokines interleukin-1beta and tumor necrosis factor-alpha were assessed. Nanobacteria isolation, culture and characterization were also analyzed.
In model rats we observed prostatic acute inflammatory changes 1 to 2 weeks after nanobacteria infusion and chronic inflammatory changes after 4 weeks. At 8 weeks we noted microcalculous formation in the prostatic glandular cavity in 7 of the 10 model rats, which was not seen in controls. Interleukin-1beta and tumor necrosis factor-alpha in prostatic tissues were higher in model rats than in controls at different time points (p <0.01). In model rats interleukin-1beta and tumor necrosis factor-alpha were higher 2 weeks after infusion than at 1, 4 and 8 weeks (p <0.05). Prostatic tissue was nanobacteria positive in 35 model rats and in 0 controls.
Nanobacteria may be an important etiological factor for type III prostatitis.
纳米细菌被认为是泌尿系统疾病的病理细菌。我们观察到感染纳米细菌的前列腺组织在斯普拉格-道利(Sprague-Dawley)大鼠中的病理变化,并研究了纳米细菌与 III 型前列腺炎的可能病因关系。
我们将 40 只成年雄性斯普拉格-道利大鼠随机分为对照组和模型组。通过经尿道注入纳米细菌悬浮液来复制大鼠前列腺感染模型。分别在 1、2、4 和 8 周后处死大鼠。评估前列腺病理学和细胞因子白细胞介素-1β和肿瘤坏死因子-α。还分析了纳米细菌的分离、培养和鉴定。
在模型大鼠中,我们在纳米细菌输注后 1 至 2 周观察到前列腺急性炎症变化,4 周后观察到慢性炎症变化。在 8 周时,我们在 10 只模型大鼠中的 7 只中观察到前列腺腺腔中的微结石形成,而在对照组中未观察到。在不同时间点,模型大鼠前列腺组织中的白细胞介素-1β和肿瘤坏死因子-α均高于对照组(p<0.01)。在模型大鼠中,输注后 2 周白细胞介素-1β和肿瘤坏死因子-α高于 1、4 和 8 周(p<0.05)。35 只模型大鼠的前列腺组织呈纳米细菌阳性,而对照组为 0 只。
纳米细菌可能是 III 型前列腺炎的重要病因。