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Drug Chem Toxicol. 2016;39(2):206-12. doi: 10.3109/01480545.2015.1079916. Epub 2015 Aug 31.

The fibrosis of ketamine, a noncompetitive N-methyl-d-aspartic acid receptor antagonist dose-dependent change in a ketamine-induced cystitis rat model.

Author information

1
a Department of Urology , Soonchunhyang University School of Medicine , Seoul , Korea .
2
b Department of Urology and.
3
c Department of Biomedical Sciences , Asan Medical Center, University of Ulsan College of Medicine , Seoul , Korea , and.
4
d Yonsei University Underwood International College Comparative Literature and Culture , Seoul , Korea.

Abstract

Ketamine abusers have greatly increased in number worldwide during recent years. The consumption of ketamine has increased, as have the number of published accounts of devastating urological sequelae. However, the mechanism of ketamine-associated urinary tract dysfunction remains unclear. This study was to evaluate the ketamine dose-dependency of ketamine-induced cystitis (KC) in a rat model. A total of 42 Sprague-Dawley rats (female, 10-week-old) were used. Each of the 7 KC rat models were induced by 1, 5, 10, 25 and 50 mg/kg ketamine intravenous injection for two weeks. For the sham group (n = 7), a phosphate-buffered saline (PBS) vehicle was used rather than ketamine hydrochloride. The cystometric parameters, histological examinations, staining for Masson's trichome, cytokeratin, toluidine blue and quantitative PCR were measured at two weeks following the intervention. The voiding interval gradually decreased depending upon the ketamine dose of 1, 5, 10, 25, or 50 mg/kg, respectively, and was decreased compared with Sham. Bladder capacity was decreased as ketamine dose increased. In particular, the increase of fibrosis and submucosal apoptosis were found according to the increase of the ketamine dose. The bladder apoptosis in the KC rat model makes the fibrotic bladder change, and led us to hypothesize that fibrosis could contribute to the lower urinary-tract symptoms. We suggest that according to the pathophysiology evidence, fibrosis induced by apoptosis plays a key role in KC.

KEYWORDS:

Apoptosis; cystitis; cystometry; fibrosis; ketamine

PMID:
26324997
DOI:
10.3109/01480545.2015.1079916
[Indexed for MEDLINE]

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