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首页> 外文期刊>Physiological Research >TRPV1 receptors contribute to mediate paclitaxel-induced c-Fos expression in spinal cord dorsal horn neurons.
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TRPV1 receptors contribute to mediate paclitaxel-induced c-Fos expression in spinal cord dorsal horn neurons.

机译:TRPV1受体有助于介导紫杉醇诱导的脊髓背角神经元中c-Fos表达。

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Transient receptor potential vanilloid type 1 (TRPV1) receptorsare important in the development of different pathologicalchronic pain states. Here we examined the role of spinal cordTRPV1 receptors in the mechanisms leading to activation ofdorsal horn neurons after paclitaxel (PAC) treatment. PAC isa widely used chemotherapeutic drug that often leads todevelopment of painful neuropathy. Immunohistochemicalanalysis of c-Fos protein expression in dorsal horn neurons wasused as a marker of neuronal activation. Rat spinal cord sliceswere processed for in vitro incubation with PAC (100 nM) andTRPV1 receptor antagonists (SB366791 and AMG9810; 10 μM).PAC treatment induced significant upregulation of c-Fos nuclearexpression in superficial dorsal horn neurons that was diminishedby TRPV1 receptor antagonists pre-incubation. These resultsfurther substantiated the role of spinal TRPV1 receptors in thedevelopment of paclitaxel-induced neuropathic pain andcontribute to better understanding of the pathologicalmechanisms involved.
机译:瞬态受体潜在的香草类1型(TRPV1)受体在不同病理性慢性疼痛状态的发展中很重要。在这里,我们检查了紫杉醇(PAC)治疗后脊髓TRPV1受体在导致背角神经元活化的机制中的作用。 PAC是一种广泛使用的化学治疗药物,通常会导致疼痛性神经病的发展。背角神经元中c-Fos蛋白表达的免疫组织化学分析被用作神经元激活的标志物。将大鼠脊髓切片与PAC(100 nM)和TRPV1受体拮抗剂(SB366791和AMG9810; 10μM)一起进行体外培养。孵化。这些结果进一步证实了脊柱TRPV1受体在紫杉醇诱导的神经性疼痛发生中的作用,并且有助于更好地理解所涉及的病理机制。

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