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首页> 外文期刊>Cell Reports >Report Loss of bhlha9 Impairs Thermotaxis and Formalin-Evoked Pain in a Sexually Dimorphic Manner
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Report Loss of bhlha9 Impairs Thermotaxis and Formalin-Evoked Pain in a Sexually Dimorphic Manner

机译:报告损失Bhlha9损害了热潮和福尔马林诱发的疼痛,性别二态

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C-LTMRs are known to convey affective aspects of touch and to modulate injury-induced pain in humans and mice. However, a role for these neurons in temperature sensation has been suggested, but not?fully demonstrated. Here, we report that deletion?of C-low-threshold mechanoreceptor (C-LTMR)-expressed bhlha9 causes impaired thermotaxis behavior and exacerbated formalin-evoked pain in male, but not female, mice. Positive modulators of GABAsubA/sub receptors failed to relieve inflammatory formalin pain and failed to decrease the frequency of spontaneous excitatory post-synaptic currents (sEPSCs) selectively in bhlha9 knockout (KO) males. This could be explained by a drastic change in the GABA content of lamina II inner inhibitory interneurons contacting C-LTMR central terminals. Finally, C-LTMR-specific deep RNA sequencing revealed more genes differentially expressed in male than in female bhlha9 KO C-LTMRs. Our data consolidate the role of C-LTMRs in modulation of formalin pain and provide in?vivo evidence of their role in the discriminative aspects of temperature sensation.
机译:已知C-LTMRS传达触感的情感方面,并调节人和小鼠的损伤疼痛。然而,已经提出了这些神经元在温度轰动中的作用,但没有?完全证明。在这里,我们报告删除?C-Low-Thresholly Mechenereptor(C-LTMR) - 表达的BHLHA9导致患有受损的热诱变行为,并且在雄性中加剧了福尔辛诱发的疼痛,但不是女性的小鼠。 GABA A 受体的阳性调节剂未能缓解炎症性福尔马林疼痛,并且未能在BHLHA9敲除(KO)雄性中选择性地减少自发兴奋性后电流(SEPSCs)的频率。这可以通过接触C-LTMR中央终端的椎板II内抑制性嵌入式中间核心的GABA含量的激烈变化来解释。最后,C-LTMR特异性的深RNA测序显示更多在男性中差异表达的基因,而不是雌性BHLHA9 KO C-LTMRS。我们的数据巩固C-LTMRS在调制福尔马林疼痛时的作用,并提供其在温度感应的辨别方面的作用的体内证据。

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