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甘氨酸转运体 2 型(GlyT2)抑制剂改善大鼠膀胱过度活动和痛觉行为。

Glycine transporter type 2 (GlyT2) inhibitor ameliorates bladder overactivity and nociceptive behavior in rats.

机构信息

Department of Urology, University of Pittsburgh, Pittsburgh, PA 15213, USA.

出版信息

Eur Urol. 2012 Oct;62(4):704-12. doi: 10.1016/j.eururo.2012.01.044. Epub 2012 Feb 1.

Abstract

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 (3μM). 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 α1 and β 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.

摘要

背景

甘氨酸是脊髓中的一种主要抑制性神经递质,其浓度受两种甘氨酸转运体(GlyTs):GlyT1 和 GlyT2 调节。我们假设抑制 GlyTs 可以改善下尿路的膀胱过度活动和/或疼痛感觉。

目的

研究 GlyT 抑制剂对大鼠膀胱过度活动和疼痛行为的影响。

设计、设置和参与者:在环磷酰胺(CYP)处理的大鼠中,在乌拉坦麻醉下进行膀胱测压。在使用清醒大鼠的行为研究中,通过膀胱内给予树脂毒素(3μM)诱导疼痛反应。鞘内给予选择性 GlyT1 或 GlyT2 抑制剂,评估其作用。

测量

测量膀胱测压参数、疼痛行为(舔舐和冻结)以及背根脊髓(L6-S1)中 GlyTs 和甘氨酸受体(GlyR)亚基的信使 RNA(mRNA)水平。

结果和局限性

在 CYP 处理的大鼠中进行膀胱测压时,选择性 GlyT2 抑制剂 ALX-1393 引起的收缩间期和排尿压力阈值显著增加,但 GlyT1 抑制剂肌氨酸没有。这些作用被甘氨酸受体拮抗剂士的宁完全逆转。ALX-1393 还以剂量依赖性方式显著抑制疼痛行为。在假手术大鼠中,背根脊髓中 GlyT2 mRNA 的表达水平(23 倍)明显高于 GlyT1 mRNA。在 CYP 处理的大鼠中,GlyT2 和 GlyR α1 和 β 亚基的 mRNA 水平显著降低。

结论

这些结果表明 GlyT2 在脊髓中清除细胞外甘氨酸方面起着主要作用,抑制 GlyT2 可改善 CYP 诱导的膀胱过度活动和疼痛行为。GlyT2 可能是治疗膀胱过度活动和/或膀胱高敏感疾病(如膀胱疼痛综合征/间质性膀胱炎)的新的治疗靶点。

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