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缝隙连接有助于调节成年泥螈(黄斑蝾螈)的类似行走活动。

Gap Junctions Contribute to the Regulation of Walking-Like Activity in the Adult Mudpuppy (Necturus Maculatus).

作者信息

Lavrov Igor, Fox Lyle, Shen Jun, Han Yingchun, Cheng Jianguo

机构信息

Institute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.

Departments of Pain Management and Neurosciences, Anesthesiology Institute, Cleveland Clinic, Cleveland, Ohio, United States of America.

出版信息

PLoS One. 2016 Mar 29;11(3):e0152650. doi: 10.1371/journal.pone.0152650. eCollection 2016.

Abstract

Although gap junctions are widely expressed in the developing central nervous system, the role of electrical coupling of neurons and glial cells via gap junctions in the spinal cord in adults is largely unknown. We investigated whether gap junctions are expressed in the mature spinal cord of the mudpuppy and tested the effects of applying gap junction blocker on the walking-like activity induced by NMDA or glutamate in an in vitro mudpuppy preparation. We found that glial and neural cells in the mudpuppy spinal cord expressed different types of connexins that include connexin 32 (Cx32), connexin 36 (Cx36), connexin 37 (Cx37), and connexin 43 (Cx43). Application of a battery of gap junction blockers from three different structural classes (carbenexolone, flufenamic acid, and long chain alcohols) substantially and consistently altered the locomotor-like activity in a dose-dependent manner. In contrast, these blockers did not significantly change the amplitude of the dorsal root reflex, indicating that gap junction blockers did not inhibit neuronal excitability nonselectively in the spinal cord. Taken together, these results suggest that gap junctions play a significant modulatory role in the spinal neural networks responsible for the generation of walking-like activity in the adult mudpuppy.

摘要

尽管缝隙连接在发育中的中枢神经系统中广泛表达,但在成体脊髓中,神经元与神经胶质细胞通过缝隙连接进行电偶联的作用在很大程度上仍不清楚。我们研究了美西螈成熟脊髓中是否表达缝隙连接,并在体外美西螈标本中测试了应用缝隙连接阻滞剂对由N-甲基-D-天冬氨酸(NMDA)或谷氨酸诱导的类行走活动的影响。我们发现,美西螈脊髓中的神经胶质细胞和神经细胞表达不同类型的连接蛋白,包括连接蛋白32(Cx32)、连接蛋白36(Cx36)、连接蛋白37(Cx37)和连接蛋白43(Cx43)。应用来自三种不同结构类别的一系列缝隙连接阻滞剂(羧苄索龙、氟芬那酸和长链醇),以剂量依赖的方式显著且持续地改变了类运动活动。相比之下,这些阻滞剂并未显著改变背根反射的幅度,这表明缝隙连接阻滞剂不会在脊髓中非选择性地抑制神经元兴奋性。综上所述,这些结果表明,缝隙连接在负责成体美西螈类行走活动产生的脊髓神经网络中发挥着重要的调节作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63b3/4811563/8b4dfb9b5197/pone.0152650.g001.jpg

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