Neuroprotective effect of interleukin-6 regulation of voltage-gated Na+ channels of cortical neurons is time- and dose-dependent

Interleukin-6 has been shown to be involved in nerve injury and nerve regeneration, but the effects of long-term administration of high concentrations of interleukin-6 on neurons in the central nervous system is poorly understood. This study investigated the effects of 24 hour expo-sure of interleuk...

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Published in:Neural regeneration research Vol. 10; no. 4; pp. 610 - 617
Main Authors: Xia, Wei, Peng, Guo-Yi, Sheng, Jiang-Tao, Zhu, Fang-Fang, Guo, Jing-Fang, Chen, Wei-Qiang
Format: Journal Article
Language:English
Published: India Medknow Publications and Media Pvt. Ltd 01-04-2015
Medknow Publications & Media Pvt. Ltd
Department of Interventional Radiology, First Afifliated Hospital, Shantou University Medical College, Shantou, Guangdong Province, China%Department of Neurosurgery, First Afifliated Hospital, Shantou University Medical College, Shantou, Guangdong Province, China%Department of Pathogenic Microbiology and Immunology, Shantou University Medical College, Shantou, Guangdong Province, China
Medknow Publications & Media Pvt Ltd
Wolters Kluwer Medknow Publications
Subjects:
EGF
EPO
FGF
Wnt
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Summary:Interleukin-6 has been shown to be involved in nerve injury and nerve regeneration, but the effects of long-term administration of high concentrations of interleukin-6 on neurons in the central nervous system is poorly understood. This study investigated the effects of 24 hour expo-sure of interleukin-6 on cortical neurons at various concentrations (0.1, 1, 5 and 10 ng/mL) and the effects of 10 ng/mL interleukin-6 exposure to cortical neurons for various durations (2, 4, 8, 24 and 48 hours) by studying voltage-gated Na+ channels using a patch-clamp technique. Volt-age-clamp recording results demonstrated that interleukin-6 suppressed Na+ currents through its receptor in a time- and dose-dependent manner, but did not alter voltage-dependent activation and inactivation. Current-clamp recording results were consistent with voltage-clamp recording results. Interleukin-6 reduced the action potential amplitude of cortical neurons, but did not change the action potential threshold. The regulation of voltage-gated Na+channels in rat corti-cal neurons by interleukin-6 is time- and dose-dependent.
Bibliography:Wei Xia,Guo-yi Peng,Jiang-tao Sheng,Fang-fang Zhu,Jing-fang Guo,Wei-qiang Chen
nerve regeneration; brain injury; inflammatory reaction; interleukin-6; voltage-gated Na+ channel; cortical neurons; cerebrospinal fluid; neuroimmunomodulation; neuroprotection; action potential; patch clamp; neurophysiology; NSFC grants; neural regeneration
Interleukin-6 has been shown to be involved in nerve injury and nerve regeneration, but the effects of long-term administration of high concentrations of interleukin-6 on neurons in the central nervous system is poorly understood. This study investigated the effects of 24 hour expo-sure of interleukin-6 on cortical neurons at various concentrations (0.1, 1, 5 and 10 ng/mL) and the effects of 10 ng/mL interleukin-6 exposure to cortical neurons for various durations (2, 4, 8, 24 and 48 hours) by studying voltage-gated Na+ channels using a patch-clamp technique. Volt-age-clamp recording results demonstrated that interleukin-6 suppressed Na+ currents through its receptor in a time- and dose-dependent manner, but did not alter voltage-dependent activation and inactivation. Current-clamp recording results were consistent with voltage-clamp recording results. Interleukin-6 reduced the action potential amplitude of cortical neurons, but did not change the action potential threshold. The regulation of voltage-gated Na+channels in rat corti-cal neurons by interleukin-6 is time- and dose-dependent.
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These authors contributed equally to this work.
Author contributions: WX and GYP participated in experimental design, cell culture, electrophysiological experiments, fluorescent quantitative PCR, data collection and processing, and manuscript preparation. JTS was in charge of experimental design, electrophysiological experiments, fluorescent quantitative PCR, data collection and processing. FFZ participated in neuronal cultures and purity identification. JFG and WQC participated in experimental design, data collection and processing, wrote and modified the manuscript. All authors approved the final version of the paper.
ISSN:1673-5374
1876-7958
DOI:10.4103/1673-5374.155436