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. 2014 Jun;34(3):322-329.
doi: 10.1007/s11596-014-1277-1. Epub 2014 Jun 18.

Differential expression of alpha-adrenoceptor subtypes in rat dorsal root ganglion after chronic constriction injury

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Differential expression of alpha-adrenoceptor subtypes in rat dorsal root ganglion after chronic constriction injury

Hong-Ju Cheng et al. J Huazhong Univ Sci Technolog Med Sci. 2014 Jun.

Abstract

mRNAs of alpha-adrenoceptor (α-AR) subtypes are found in neurons in dorsal root ganglion (DRG) and change after peripheral nerve injury. In this study, the distribution of α-AR subtype proteins was studied in L5 DRG of normal rats and rats with chronic constriction injury of sciatic nerve (CCI). Using immunofluorescence technique, it was found that α1A-, α1B-, and α2A-AR proteins were expressed in large, medium, and small size neurons in normal DRG, and significantly increased in all size neurons 14 days after CCI. α1D- and α2C-AR was also expressed in all size neurons in normal DRG. However, α1D-AR was significantly increased and α2C-AR was decreased in small size neurons 14 days post CCI. α2B-AR neurons were not detectable in normal and CCI DRG. Co-expression of α1A- and α2A-AR in the same neuron was observed in normal DRG and increased post CCI. Collectively, these results indicated that there is distinct distribution of α-AR subtypes in DRG neurons, and the distribution and levels of expression of α-AR subtypes change differently after CCI. The up-regulation of α-AR subtypes in DRG neurons may play an important role in the process of generating and transmitting neuropathic pain.

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References

    1. Pain. 2005 Feb;113(3):386-394 - PubMed
    1. Neuroscience. 2013 Nov 12;252:512-25 - PubMed
    1. J Neurosci. 1997 Mar 1;17(5):1633-41 - PubMed
    1. J Huazhong Univ Sci Technolog Med Sci. 2005;25(4):371-4, 396 - PubMed
    1. J Comp Neurol. 2000 Dec 4;428(1):45-61 - PubMed

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