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Effects of nerve growth factor neutralization on TRP channel expression in laser-captured bladder afferent neurons in mice with spinal cord injury

机译:神经生长因子中和对脊髓损伤小鼠激光捕获的膀胱传入神经元TRP通道表达的影响

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摘要

Nerve growth factor (NGF) is reportedly involved in the changes in C-fiber bladder afferent pathways that induce detrusor overactivity (DO) following spinal cord injury (SCI). This study examined the roles of NGF in TRP channel expression in bladder afferent neurons in mice with SCI using laser-capture microdissection (LCM) methods. Spinal intact (SI) and SCI mice were divided into 3 groups: (1) SI with vehicle treatment; (2) SCI with vehicle treatment; and (3) SCI with anti-NGF antibody. Two weeks after SCI, an osmotic pump was placed subcutaneously into the back of the mice and vehicle or anti-NGF antibody was administered at a rate of 10 μg/kg per hour for two weeks. Four weeks after SCI, the L6 dorsal root ganglia (DRG) were removed. Expression of the TRPV1, TRPC1, TRPC3, and TRPC6 genes was analyzed using real-time polymerase chain reaction (PCR) following LCM of the bladder afferent neurons, which were labeled by Fast Blue injected into the bladder wall 1 week prior to tissue removal. The mRNA expression of TRPV1 was found to be higher in vehicle-treated SCI mice than in SI mice. The expression level of TRPC3 and TRPC6 in vehicle-treated SCI mice was lower than in SI mice. However, in SCI mice treated with anti-NGF antibody, the mRNA expression of TRPV1 was lower, and the mRNA levels of TRPC3 and TRPC6 were higher than in vehicle-SCI mice. These results suggest that the NGF-dependent changes in specific TRP channel genes, such as TRPV1, TRPC3, and TRPC6, could be involved in SCI-induced afferent hyperexcitability and DO.
机译:据报道,神经生长因子(NGF)参与了C纤维膀胱传入途径的变化,这些变化导致脊髓损伤(SCI)后逼尿肌过度活动(DO)。这项研究使用激光捕获显微切割(LCM)方法检查了NGF在SCI小鼠膀胱传入神经元TRP通道表达中的作用。完整脊髓(SI)和SCI小鼠分为3组:(1)接受媒介物治疗的SI; (2)SCI进行车辆处理; (3)具有抗NGF抗体的SCI。 SCI后两周,将渗透泵皮下置于小鼠背部,并以每小时10μg/ kg的速度施用媒介物或抗NGF抗体,持续两周。 SCI后四周,移除L6背根神经节(DRG)。膀胱传入神经元的LCM之后,使用实时聚合酶链反应(PCR)分析TRPV1,TRPC1,TRPC3和TRPC6基因的表达,并通过在组织切除前1周将快速蓝注射到膀胱壁中进行标记。发现在媒介物处理的SCI小鼠中TRPV1的mRNA表达高于SI小鼠。载体治疗的SCI小鼠中TRPC3和TRPC6的表达水平低于SI小鼠。然而,在抗NGF抗体治疗的SCI小鼠中,TRPV1的mRNA表达较低,而TRPC3和TRPC6的mRNA水平高于载体-SCI小鼠。这些结果表明特定TRP通道基因,如TRPV1,TRPC3和TRPC6,依赖NGF的变化可能与SCI引起的传入性过度兴奋和DO有关。

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