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首页> 外文期刊>Biochemical and Biophysical Research Communications >Spontaneous L-glutamate release enhancement in rat substantia gelatinosa neurons by (-)-carvone and (+)-carvone which activate different types of TRP channel
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Spontaneous L-glutamate release enhancement in rat substantia gelatinosa neurons by (-)-carvone and (+)-carvone which activate different types of TRP channel

机译:(-)-香芹酮和(+)-香芹酮激活不同类型的TRP通道可增强大鼠明胶质神经元自发的L-谷氨酸释放

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Transient receptor potential (TRP) channels in the spinal dorsal horn lamina II (substantia gelatinosa; SG), which are involved in the modulation of nociceptive transmission, have not yet been fully examined in property. Activation of the TRP channels by various plant-derived chemicals results in an increase in the spontaneous release of L-glutamate onto the SG neurons. We examined the effects of a monoterpene ketone (-)-carvone (contained in spearmint) and its stereoisomer (+)-carvone (in caraway) on glutamatergic spontaneous excitatory transmission in SG neurons of adult rat spinal cord slices by using the whole-cell patch-clamp technique. (-)-Carvone and (+)-carvone increased the frequency of spontaneous excitatory postsynaptic current (sEPSC) in a reversible and concentration-dependent manner with a small increase in its amplitude. Half-maximal effective concentrations of ()-carvone and ()-carvone in increasing sEPSC frequency were 0.70 mM and 0.72 mM, respectively. The ()-carvone but not (+)-carvone activity was inhibited by a TRPV1 antagonist capsazepine. On the other hand, the (+)-carvone but not ()-carvone activity was inhibited by a TRPA1 antagonist HC-030031. These results indicate that ()-carvone and (+)-carvone activate TRPV1 and TRPA1 channels, respectively, resulting in an increase in spontaneous L-glutamate release onto SG neurons, with almost the same efficacy. Such a difference in TRP activation between the stereoisomers may serve to know the properties of TRP channels in the SG. (C) 2015 Elsevier Inc. All rights reserved.
机译:脊髓背角椎板II(明胶质; SG)中的瞬态受体电位(TRP)通道参与了伤害性传递的调节,但尚未对其性质进行全面检查。各种植物来源的化学物质激活TRP通道会导致L-谷氨酸自发释放到SG神经元上。我们通过使用全细胞研究了单萜酮(-)-香芹酮(留在薄荷中)及其立体异构体(+)-香芹酮(在香芹籽中)对成年大鼠脊髓切片SG神经元中谷氨酸能自发性兴奋性传递的影响膜片钳技术。 (-)-香芹酮和(+)-香芹酮以可逆的和浓度依赖性的方式增加了自发性兴奋性突触后突触电流(sEPSC)的频率,其幅度略有增加。 (s-香芹酮)和()-香芹酮在sEPSC频率增加中的半数最大有效浓度分别为0.70 mM和0.72 mM。 TRPV1拮抗剂Capsazepine抑制()-香芹酮的活性,但不抑制(+)-香芹酮的活性。另一方面,TRPA1拮抗剂HC-030031抑制(+)-香芹酮但不抑制()-香芹酮的活性。这些结果表明(-)香芹酮和(+)-香芹酮分别激活TRPV1和TRPA1通道,导致自发性L-谷氨酸释放到SG神经元上的增加,具有几乎相同的功效。立体异构体之间的TRP活化的这种差异可以用来了解SG中的TRP通道的性质。 (C)2015 Elsevier Inc.保留所有权利。

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