Histopathological assessment of inflammation and expression of inflammatory markers in patients with ketamine-induced cystitis

氯胺酮诱发膀胱炎患者炎症的组织病理学评估和炎症标志物的表达

阅读:5
作者:Hsin-Chung Lin, Herng-Sheng Lee, Tzong-Shi Chiueh, Yu-Chieh Lin, Hsin-An Lin, Yu-Chun Lin, Tai-Lung Cha, En Meng

Abstract

The aim of the current study was to evaluate the histopathological features of inflammation and the expression levels of inflammatory markers in tissue samples from patients with ketamine‑induced cystitis. Bladder biopsy samples for histological analysis were obtained from 23 patients (18 men and 5 women) with a self‑reported history of ketamine use and who were treated for cystitis at the Tri‑Service General Hospital of Taipei, Taiwan. Immunohistochemical staining for cyclooxygenase‑2 (COX‑2), inducible nitric oxide synthase (iNOS), matrix metallopeptidase‑9 (MMP‑9), mammalian target of rapamycin (mTOR), and phosphorylated 40S ribosomal protein S6 (Phos‑S6) was performed. The results revealed urothelial atypia in all patients, and intravascular eosinophil accumulation in 22 patients. Histopathological features included denuded urothelial mucosa, ulceration, collagen deposition, smooth muscle degeneration and vessel proliferation. Tissue samples were immunopositive for all of the inflammation markers, including the urothelium, vessel walls, and smooth muscle. COX‑2 staining revealed a significant difference between the inflammatory levels in the urothelium and smooth muscle, and iNOS staining differed significantly between inflammatory levels in smooth muscle (p=0.029). A positive correlation was observed between the percentage of Phos‑S6‑positive cells and the levels of inflammation in the urothelium. These results add to the descriptive literature on the histopathological aspects of ketamine‑induced cystitis, emphasizing the inflammatory nature and a possible role for proteins such as COX‑2, iNOS and Phos‑S6 in the degree of inflammation.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。