Transmitters and Pathways Mediating Inhibition of Spinal Itch-Signaling Neurons by Scratching and Other Counterstimuli

被引:85
作者
Akiyama, Tasuku [1 ]
Carstens, Mirela Iodi [1 ]
Carstens, Earl [1 ]
机构
[1] Univ Calif Davis, Dept Neurobiol Physiol & Behav, Davis, CA 95616 USA
来源
PLOS ONE | 2011年 / 6卷 / 07期
基金
美国国家卫生研究院;
关键词
DORSAL-HORN NEURONS; HISTAMINE-INDUCED ITCH; DRY SKIN; PAR-2; AGONIST; ACTIVATED RECEPTORS; SENSORY NEURONS; FOS EXPRESSION; POTENTIAL ROLE; PAIN; MOUSE;
D O I
10.1371/journal.pone.0022665
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Scratching relieves itch, but the underlying neural mechanisms are poorly understood. We presently investigated a role for the inhibitory neurotransmitters GABA and glycine in scratch-evoked inhibition of spinal itch-signaling neurons in a mouse model of chronic dry skin itch. Superficial dorsal horn neurons ipsilateral to hindpaw dry skin treatment exhibited a high level of spontaneous firing that was significantly attenuated by cutaneous scratching, pinch and noxious heat. Scratch-evoked inhibition was nearly abolished by spinal delivery of the glycine antagonist, strychnine, and was markedly attenuated by respective GABAA and GABAB antagonists bicuculline and saclofen. Scratch-evoked inhibition was also significantly attenuated (but not abolished) by interruption of the upper cervical spinal cord, indicating the involvement of both segmental and suprasegmental circuits that engage glycine- and GABA-mediated inhibition of spinal itch-signaling neurons by noxious counterstimuli.
引用
收藏
页数:10
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