4.4 Article

Relationship between electrophysiological signature and defined sensory modality of trigeminal ganglion neurons in vivo

期刊

JOURNAL OF NEUROPHYSIOLOGY
卷 109, 期 3, 页码 749-757

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/jn.00693.2012

关键词

trigeminal ganglia; in vivo; electrophysiology; sensory neurons; nociceptors

资金

  1. Spanish Ministerio de Ciencia e Innovacion [BFU2008-04425, CSD2007-00023]
  2. Fundacion Carolina (Spain)

向作者/读者索取更多资源

Boada MD. Relationship between electrophysiological signature and defined sensory modality of trigeminal ganglion neurons in vivo. J Neurophysiol 109: 749-757, 2013. First published November 14, 2012; doi:10.1152/jn.00693.2012.-The trigeminal ganglia (TG) innervate a heterogeneous set of highly sensitive and exposed tissues. Weak, innocuous stimuli can evoke pain as a normal response in some areas such as the cornea. This observation implies, however, the capability of low-threshold mechanoreceptors, inducing pain in the normal condition. To clarify this matter, the present study correlates the electrical signature (both fiber conduction velocity and somatic electrical properties) with receptor field, mechanical threshold, and temperature responsiveness of sensory afferents innervating tissues with dissimilar sensitivity (skin vs. cornea) in the trigeminal domain. Intracellular recordings were obtained in vivo from 148 neurons of the left TG of 62 mice. In 111 of these neurons, the peripheral receptor field was successfully localized: 96 of them innervated the hairy skin, while the remaining 15 innervated the cornea. The electrical signature was defined and peripheral responses correlated with tissue target. No high threshold neurons were found in the cornea. Moreover, the electrical signature of corneal afferents resembles nociceptive neurons in the skin. TG skin afferents showed similar membrane electrical signature and sensory modality as skin afferents from dorsal root ganglion, although TG afferents exhibited a shorter duration of afterhyperpolarization then those previously described in dorsal root ganglion. These data suggest than new or different ways to classify and study TG sensory neurons may be required.

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