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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Effect of SB-750364, a specific TRPV1 receptor antagonist, on injury-induced ectopic discharge in the lingual nerve.
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Effect of SB-750364, a specific TRPV1 receptor antagonist, on injury-induced ectopic discharge in the lingual nerve.

机译:SB-750364,一种特殊的TRPV1受体拮抗剂,对损伤引起的舌神经异位放电的影响。

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摘要

Abnormal neural activity generated at a site of nerve injury is thought to contribute to the development of dysaesthesia. Vanilloid receptor 1 (TRPV1), a transducer of noxious stimuli, may be involved in the initiation of this abnormal activity and could provide a useful therapeutic target. We investigated the effect of a specific TRPV1 antagonist (SB-750364) on injury-induced discharge in the lingual nerve. In 12 anaesthetised adult ferrets the left lingual nerve was sectioned and animals were allowed to recover for 3-7 days. In terminal experiments under general anaesthesia, the nerve was re-exposed and electrophysiological recordings made from spontaneously active axons in fine filaments dissected from the nerve central to both the injury site and the junction with the chorda tympani. SB-750364 was infused via the cephalic vein in order to achieve three increasing but stable systemic blood levels of the compound (0.3, 1.0 and 3.0 microM). Twenty-eight spontaneously active units were studied, with discharge frequencies ranging from 0.02 to 4.9 Hz. There was a significant reduction in spontaneous activity in 17 units (61%) at 1.0 microM or less of SB-750364 (p<0.01; Friedman test with Dunn's multiple comparisons). A further 4 units (14%) showed a significant reduction in activity at 3.0 microM (p<0.01). In the remaining 7 units (25%) the discharge was unaffected (p>0.05). These data show that the TRPV1 antagonist SB-750364 can reduce the level of spontaneous activity initiated in some axons following lingual nerve injury.
机译:在神经损伤部位产生的异常神经活动被认为导致感觉异常的发展。 Vanilloid受体1(TRPV1)是一种有害刺激物,可能参与了这种异常活动,并可能提供有用的治疗靶标。我们研究了特定的TRPV1拮抗剂(SB-750364)对舌神经损伤诱导放电的作用。在12只麻醉的成年雪貂中,将左舌神经切成薄片,让动物恢复3-7天。在全身麻醉下进行的终末实验中,将神经重新暴露,并用自发活动的轴突在神经中枢至损伤部位和与鼓膜的交界处切开的细丝中的自发活动轴突进行电生理记录。通过头静脉注入SB-750364,以实现该化合物的三种增加但稳定的全身血液水平(0.3、1.0和3.0 microM)。研究了28个自发活动单位,其放电频率范围为0.02至4.9 Hz。在SB-750364等于或小于1.0 microM时,自发活性显着降低了17个单位(61%)(p <0.01;采用Dunn多重比较的Friedman检验)。另外4个单位(14%)显示在3.0 microM时活性显着降低(p <0.01)。在剩余的7个单位(25%)中,放电不受影响(p> 0.05)。这些数据表明,TRPV1拮抗剂SB-750364可以降低舌神经损伤后某些轴突中起始的自发活动水平。

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