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Nociceptive Neurons Differentially Express Fast and Slow T-Type Ca2+ Currents in Different Types of Diabetic Neuropathy

机译:伤害性神经元在不同类型的糖尿病性神经病中差异性表达快和慢的T型Ca2 +电流

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摘要

T-type Ca2+ channels are known as important participants of nociception and their remodeling contributes to diabetes-induced alterations of pain sensation. In this work we have established that about 30% of rat nonpeptidergic thermal C-type nociceptive (NTCN) neurons of segments L4–L6 express a slow T-type Ca2+ current (T-current) while a fast T-current is expressed in the other 70% of these neurons. Streptozotocin-induced diabetes in young rats resulted in thermal hyperalgesia, hypoalgesia, or normalgesia 5-6 weeks after the induction. Our results show that NTCN neurons obtained from hyperalgesic animals do not express the slow T-current. Meanwhile, the fraction of neurons expressing the slow T-current did not significantly change in the hypo- and normalgesic diabetic groups. Moreover, the peak current density of fast T-current was significantly increased only in the neurons of hyperalgesic group. In contrast, the peak current density of slow T-current was significantly decreased in the hypo- and normalgesic groups. Experimental diabetes also resulted in a depolarizing shift of steady-state inactivation of fast T-current in the hyperalgesic group and slow T-current in the hypo- and normalgesic groups. We suggest that the observed changes may contribute to expression of different types of peripheral diabetic neuropathy occurring during the development of diabetes mellitus.
机译:T型Ca 2 + 通道被称为伤害感受的重要参与者,其重塑有助于糖尿病引起的疼痛感改变。在这项工作中,我们已经确定,大约30%的L4–L6段的大鼠非肽能热C型伤害性(NTCN)神经元表达缓慢的T型Ca 2 + 电流(T电流),而在这些神经元的其他70%中表达了快速的T电流。幼年大鼠中链脲佐菌素诱导的糖尿病导致热痛觉过敏,痛觉过敏或正常痛觉过敏。我们的结果表明,从痛觉过敏动物获得的NTCN神经元不表达慢T电流。同时,低速和正常镇痛糖尿病组中表达缓慢T电流的神经元比例没有明显变化。此外,仅在痛觉过敏组的神经元中快速T电流的峰值电流密度显着增加。相反,在低和正常组中,缓慢T电流的峰值电流密度显着降低。实验性糖尿病还导致痛觉过敏组中快速T电流的稳态失活发生去极化转变,而低痛觉和正常镇痛组的慢T电流的稳态失活发生去极化变化。我们建议观察到的变化可能有助于糖尿病发展过程中发生的不同类型的周围型糖尿病神经病变的表达。

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