Glycine Transporter Type 2 (GlyT2) Inhibitor Ameliorates Bladder Overactivity and Nociceptive Behavior in Rats

被引:29
作者
Yoshikawa, Satoru
Oguchi, Tomohiko
Funahashi, Yasuhito
de Groat, William C. [2 ]
Yoshimura, Naoki [1 ,2 ]
机构
[1] Univ Pittsburgh, Dept Urol, Sch Med, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Pharmacol & Chem Biol, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
Glycine; Glycine transporter; Overactive bladder; Rat; Spinal cord; Bladder pain syndrome; SPINAL-CORD-INJURY; NEUROPATHIC PAIN; SCHIZOPHRENIA; RECEPTOR; MODEL; NEUROTRANSMISSION; SARCOSINE; CNS;
D O I
10.1016/j.eururo.2012.01.044
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Background: Glycine is a major inhibitory neurotransmitter in the spinal cord, the concentration of which is regulated by two types of glycine transporters (GlyTs): GlyT1 and GlyT2. We hypothesized that the inhibition of GlyTs could ameliorate bladder overactivity and/or pain sensation in the lower urinary tract. Objective: Investigate the effects of GlyT inhibitors on bladder overactivity and pain behavior in rats. Design, setting, and participants: Cystometry was performed under urethane anesthesia in cyclophosphamide (CYP)-treated rats. In behavioral studies using conscious rats, nociceptive responses were induced by intravesical administration of resiniferatoxin (3 mu M). Selective GlyT1 or GlyT2 inhibitors were administered intrathecally to evaluate their effects. Measurements: Cystometric parameters, nociceptive behaviors (licking and freezing), and messenger RNA (mRNA) levels of GlyTs and glycine receptor (GlyR) subunits in the dorsal spinal cord (L6-S1) were measured. Results and limitations: During cystometry in CYP-treated rats, significant increases in intercontraction interval and micturition pressure threshold were elicited by ALX-1393, a selective GlyT2 inhibitor, but not by sarcosine, a GlyT1 inhibitor. These effects were completely reversed by strychnine, a GlyR antagonist. ALX-1393 also significantly suppressed nociceptive behaviors in a dose-dependent manner. In sham rats, GlyT2 mRNA was expressed at a much higher level (23-fold) in the dorsal spinal cord than GlyT1 mRNA. In CYP-treated rats, mRNA levels of GlyT2 and the GlyR alpha 1 and beta subunits were significantly reduced. Conclusions: These results indicate that GlyT2 plays a major role in the clearance of extracellular glycine in the spinal cord and that GlyT2 inhibition leads to amelioration of CYP-induced bladder overactivity and pain behavior. GlyT2 may be a novel therapeutic target for the treatment of overactive bladder and/or bladder hypersensitive disorders such as bladder pain syndrome/interstitial cystitis. (C) 2012 European Association of Urology. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:704 / 712
页数:9
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