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DOI 10.1038/s41598-021-84734-4

Медицинская библиотека · Scientific reports · 2021

Smaller bladder capacity and stronger bladder contractility in patients with ketamine cystitis are associated with elevated TRPV1 and TRPV4.

Yang Hsueh-Hui, Jhang Jia-Fong, Hsu Yung-Hsiang, Jiang Yuan-Hong, Zhai Wei-Jun, Kuo Hann-Chorng

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Stronger contractility and smaller bladder capacity are common symptoms in ketamine cystitis (KC). This study investigates the association between expression levels of transient receptor potential cation channel subfamily V (TRPV) proteins and the clinical characteristics of KC. Bladder tissues were obtained from 24 patients with KC and four asymptomatic control subjects. Video urodynamic parameters were obtained before surgical procedures. The TRPV proteins were investigated by immunoblotting, immunofluorescence staining, and immunohistochemistry. The Pearson test was used to associate the expression levels of TRPV proteins with clinical characteristics of KC. The expression level of TRPV1 and TRPV4 was significantly higher in the severe KC bladders than in mild KC or control bladders. The TRPV1 proteins were localized in all urothelial cell layers, and TRPV4 was located in the basal cells and lamina propria. The expression of TRPV1 was negatively associated with maximal bladder capacity (r = - 0.66, P = 0.01). The expression of TRPV4 was positively associated with the velocity of detrusor pressure rise to the maximum flow rate (r = 0.53, P = 0.01). These observations suggest smaller bladder capacity and stronger contractility in KC are associated with an elevated expression of TRPV1 and TRPV4, respectively.

Для цитирования: Yang Hsueh-Hui, Jhang Jia-Fong, Hsu Yung-Hsiang, Jiang Yuan-Hong, Zhai Wei-Jun, Kuo Hann-Chorng. Smaller bladder capacity and stronger bladder contractility in patients with ketamine cystitis are associated with elevated TRPV1 and TRPV4.. Scientific reports. 2021. DOI: 10.1038/s41598-021-84734-4.

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