Electrophysiological characteristics of IB4-negative TRPV1-expressing muscle afferent DRG neurons
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- Lin Yi-Wen
- College of Chinese Medicine, Graduate Institute of Acupuncture Science, China Medical University Research Center for Chinese Medicine & Acupuncture, China Medical University
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- Chen Chih-Cheng
- Institute of Biomedical Sciences, Academia Sinica Taiwan Mouse Clinic, Academia Sinica
抄録
Muscle afferent neurons that express transient receptor potential vanilloid type I (TRPV1) are responsible for muscle pain associated with tissue acidosis. We have previously found that TRPV1 of isolectin B4 (IB4)-negative muscle nociceptors plays an important role in the acid-induced hyperalgesic priming and the development of chronic hyperalgesia in a mouse model of fibromyalgia. To understand the electrophysiological properties of the TRPV1-expressing muscle afferent neurons, we used whole-cell patch clamp recording to study the acid responsiveness and action potential (AP) configuration of capsaicin-sensitive neurons innervating to gastrocnemius muscle. Here we showed that IB4-negative TRPV1-expressing muscle afferent neurons are heterogeneous in terms of cell size, resting membrane potential, AP configuration, tetrodotoxin (TTX)-resistance, and acid-induced current (Iacid), as well as capsaicin-induced current (Icap). TRPV1-expressing neurons were all acid-sensitive and could be divided into two acidsensitive groups depending on an acid-induced sustained current (type I) or an acid-induced biphasic ASIC3-like current (type II). Type I TRPV1-expressing neurons were distinguishable from type II TRPV1-expressing neurons in AP overshoot, afterhyperpolarization duration, and all Iacid parameters, but not in AP threshold, TTX-resistance, resting membrane potential, and Icap parameters. These differential biophysical properties of TRPV1-expressing neurons might partially annotate their different roles involved in the development and maintenance of chronic muscle pain.
収録刊行物
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- BIOPHYSICS
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BIOPHYSICS 11 (0), 9-16, 2015
日本生物物理学会
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詳細情報 詳細情報について
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- CRID
- 1390001205222017024
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- NII論文ID
- 130004940806
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- ISSN
- 13492942
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可