PMID- 25523514 OWN - NLM STAT- MEDLINE DCOM- 20150916 LR - 20181113 IS - 1791-3004 (Electronic) IS - 1791-2997 (Print) IS - 1791-2997 (Linking) VI - 11 IP - 4 DP - 2015 Apr TI - Histopathological assessment of inflammation and expression of inflammatory markers in patients with ketamine-induced cystitis. PG - 2421-8 LID - 10.3892/mmr.2014.3110 [doi] AB - 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. FAU - Lin, Hsin-Chung AU - Lin HC AD - Department of Pathology, Tri‑Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan, R.O.C. FAU - Lee, Herng-Sheng AU - Lee HS AD - Department of Pathology, Tri‑Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan, R.O.C. FAU - Chiueh, Tzong-Shi AU - Chiueh TS AD - Department of Pathology, Tri‑Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan, R.O.C. FAU - Lin, Yu-Chieh AU - Lin YC AD - Department of Pathology, Tri‑Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan, R.O.C. FAU - Lin, Hsin-An AU - Lin HA AD - Division of Infection, Department of Medicine, Tri‑Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan, R.O.C. FAU - Lin, Yu-Chun AU - Lin YC AD - Department of Pathology, Tri‑Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan, R.O.C. FAU - Cha, Tai-Lung AU - Cha TL AD - Division of Urology, Department of Surgery, Tri‑Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan, R.O.C. FAU - Meng, En AU - Meng E AD - Division of Urology, Department of Surgery, Tri‑Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan, R.O.C. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20141218 PL - Greece TA - Mol Med Rep JT - Molecular medicine reports JID - 101475259 RN - 0 (Analgesics) RN - 0 (Biomarkers) RN - 0 (Inflammation Mediators) RN - 690G0D6V8H (Ketamine) SB - IM MH - Adolescent MH - Adult MH - Analgesics/*adverse effects MH - Biomarkers MH - Cystitis/diagnosis/*etiology/metabolism/*pathology MH - Female MH - Humans MH - Immunohistochemistry MH - Inflammation Mediators/metabolism MH - Ketamine/*adverse effects MH - Male MH - Mucous Membrane/metabolism/pathology MH - Urinary Bladder/metabolism/pathology MH - Young Adult PMC - PMC4337510 EDAT- 2014/12/20 06:00 MHDA- 2015/09/17 06:00 PMCR- 2014/12/18 CRDT- 2014/12/20 06:00 PHST- 2014/01/09 00:00 [received] PHST- 2014/10/24 00:00 [accepted] PHST- 2014/12/20 06:00 [entrez] PHST- 2014/12/20 06:00 [pubmed] PHST- 2015/09/17 06:00 [medline] PHST- 2014/12/18 00:00 [pmc-release] AID - mmr-11-04-2421 [pii] AID - 10.3892/mmr.2014.3110 [doi] PST - ppublish SO - Mol Med Rep. 2015 Apr;11(4):2421-8. doi: 10.3892/mmr.2014.3110. Epub 2014 Dec 18.