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Orofacial inflammatory pain affects the expression of MT1 and NADPH-d in rat caudal spinal trigeminal nucleus and trigeminal ganglion 被引量:4

Orofacial inflammatory pain affects the expression of MT1 and NADPH-d in rat caudal spinal trigeminal nucleus and trigeminal ganglion
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摘要 Very little is known about the role of melatonin in the trigeminal system, including the function of melatonin receptor 1. In the present study, adult rats were injected with formaldehyde into the right vibrissae pad to establish a model of orofacial inflammatory pain. The distribution of melatonin re- ceptor 1 and nicotinamide adenine dinucleotide phosphate diaphorase in the caudal spinal trigeminal nucleus and trigeminal ganglion was determined with immunohistochemistry and histo- chemistry. The results show that there are significant differences in melatonin receptor 1 expression and nicotinamide adenine dinucleotide phosphate diaphorase expression in the trigeminal ganglia and caudal spinal nucleus during the early stage of orofacial inflammatory pain. Our findings sug- gest that when melatonin receptor 1 expression in the caudal spinal nucleus is significantly reduced, melatonin's regulatory effect on pain is attenuated. Very little is known about the role of melatonin in the trigeminal system, including the function of melatonin receptor 1. In the present study, adult rats were injected with formaldehyde into the right vibrissae pad to establish a model of orofacial inflammatory pain. The distribution of melatonin re- ceptor 1 and nicotinamide adenine dinucleotide phosphate diaphorase in the caudal spinal trigeminal nucleus and trigeminal ganglion was determined with immunohistochemistry and histo- chemistry. The results show that there are significant differences in melatonin receptor 1 expression and nicotinamide adenine dinucleotide phosphate diaphorase expression in the trigeminal ganglia and caudal spinal nucleus during the early stage of orofacial inflammatory pain. Our findings sug- gest that when melatonin receptor 1 expression in the caudal spinal nucleus is significantly reduced, melatonin's regulatory effect on pain is attenuated.
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2013年第32期2991-3002,共12页 中国神经再生研究(英文版)
基金 supported by the National Natural Science Foundation of China,No.81271166,81371107 the Natural Science Foundation of Guangdong Province in China,No.10451008901006145
关键词 neural regeneration pain melatonin nitric oxide maxillofacial pain caudal spinal trigeminalnucleus trigeminal ganglia mesencephalic trigeminal nucleus melatonin receptor 1 nicotinamideadenine dinucleotide phosphate diaphorase grants-supported paper NEUROREGENERATION neural regeneration pain melatonin nitric oxide maxillofacial pain caudal spinal trigeminalnucleus trigeminal ganglia mesencephalic trigeminal nucleus melatonin receptor 1 nicotinamideadenine dinucleotide phosphate diaphorase grants-supported paper neuroregeneration
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