Suppr超能文献

口服 T2 抗原对慢性前列腺炎/慢性盆腔疼痛综合征小鼠模型的影响。

Effect of Oral T2 Antigen on Chronic Prostatitis/Chronic Pelvic Pain Syndrome in Mice Model.

机构信息

Department of Clinical Pharmacy, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, 211198, Jiangsu Province, China.

Department of Surgery, Nanjing Shuiximen Hospital, Nanjing, 211198, Jiangsu Province, China.

出版信息

Inflammation. 2019 Dec;42(6):2086-2094. doi: 10.1007/s10753-019-01072-4.

Abstract

The exact etiology and pathogenesis of chronic prostatitis (CP/CPPS) remain unclear. However, autoimmunity is a widely known theory. Precise treatment of CP/CPPS is not available. Here, we developed a new effective treatment method to prevent the occurrence of CP/CPPS. A total of 40 male C57BL/6 mice were randomly divided into four groups (n = 10): i.e., naive, model, high-dose (500 μg/ml), and low-dose (50 μg/ml) groups. High-dose and low-dose groups were orally given 0.4 ml of T2-containing soybean trypsin inhibitor (STI) at once after every 2 days for a total of 10 days. On day 10 and day 24 all the groups except naïve group were subcutaneously injected with 0.2 ml of T2 peptide along with CFA to make valid CP/CPPS models. Hematoxylin and eosin staining were used to evaluate the variation in CP/CPPS manifestation. Voiding behavior was recorded for the evaluation of urine frequencies. ELISA was used to measure the serum level of TNF-α in each group. The high- and low-dose groups of T2-containing STI displayed a reduction in urine frequencies, and inflammation, and there was a slight inflammatory infiltration as compared to the model group. In contrast, there was no difference observed in the TNF-α concentration of model as well as high- and low-dose groups compared to the naïve group. Our study demonstrates that oral T2-containing STI prevents CP/CPPS and provides an effective approach for the treatment of CP/CPPS.

摘要

慢性前列腺炎/慢性骨盆疼痛综合征(CP/CPPS)的确切病因和发病机制尚不清楚。然而,自身免疫是一个广为人知的理论。目前还没有针对 CP/CPPS 的精确治疗方法。在这里,我们开发了一种新的有效治疗方法来预防 CP/CPPS 的发生。将 40 只雄性 C57BL/6 小鼠随机分为四组(n = 10):即对照组、模型组、高剂量(500μg/ml)组和低剂量(50μg/ml)组。高剂量和低剂量组在第 2 天开始,每隔 2 天给予 0.4ml 含 T2 的大豆胰蛋白酶抑制剂(STI)一次,共 10 天。第 10 天和第 24 天,除对照组外,所有组均皮下注射 0.2ml T2 肽和 CFA 以建立有效的 CP/CPPS 模型。用苏木精和伊红染色评估 CP/CPPS 表现的变化。记录排尿行为以评估尿频率。用 ELISA 法测定各组血清 TNF-α水平。与模型组相比,含 T2 的 STI 的高、低剂量组的尿频率和炎症均减少,炎症浸润轻微。然而,与对照组相比,模型组以及高、低剂量组的 TNF-α浓度没有差异。我们的研究表明,口服含 T2 的 STI 可预防 CP/CPPS,并为 CP/CPPS 的治疗提供了一种有效方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验