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Increase of CGRP Expression in Motor Endplates Within Fore and Hind Limb Muscles of the Degenerating Muscle Mouse (Scn8admu)
Authors:Tadasu Sato  Yoshinaka Shimizu  Mitsuhiro Kano  Toshihiko Suzuki  Hiroyasu Kanetaka  Leona W. G. Chu  Patrice D. Côté  Hidetoshi Shimauchi  Hiroyuki Ichikawa
Affiliation:(1) Division of Periodontology and Endodontology, Tohoku University Graduate School of Dentistry, Sendai 980-8575, Japan;(2) Division of Oral Pathology, Tohoku University Graduate School of Dentistry, Sendai 980-8575, Japan;(3) Division of Oral and Craniofacial Anatomy, Tohoku University Graduate School of Dentistry, Sendai Miyagi, 980-8575, Japan;(4) Graduate School of Biomedical Engineering, Tohoku University, Sendai 980-8577, Japan;(5) Department of Biology and Neuroscience Institute, Life Sciences Center, Dalhousie University, Halifax, NS, B3H 4J1, Canada;(6) Department of Ophthalmology and Visual Sciences, QE II Health Sciences Centre, Halifax, NS, B3H 2Y9, Canada;
Abstract:The distribution of calcitonin gene-related peptide (CGRP) was examined in skeletal muscles of fore and hind limb as well as in oral and cranio-facial regions of the degenerating muscle (dmu) mouse, which harbours a null mutation in the voltage-gated sodium channel gene Scn8a. In limb, oral and cranio-facial muscles of wild type mice, only a few motor endplates contained CGRP-immunoreactivity. However, many CGRP-immunoreactive motor endplates appeared in the triceps brachii muscle, the biceps brachii muscle, the brachialis muscle, and the gastrocnemius muscle of dmu mice. CGRP-immunoreactive density of motor endplates in the skeletal muscles was also elevated by the mutation. In these muscles, the atrophy of muscle fibers could be detected and the density of cell nuclei in the musculature increased. In the flexor digitorum profundus muscle, the flexor digitorum superficialis muscle, and the soleus muscle as well as in oral and cranio-facial muscles, however, the distribution of CGRP-immunoreactivity was barely affected by the mutation. The morphology of muscle fibers and the distribution of cell nuclei within them were also similar in wild type and dmu mice. In the lumbar spinal cord of dmu mice, CGRP-immunoreactive density of spinal motoneurons increased. These findings suggest that the atrophic degeneration in some fore and hind limb muscles of dmu mice may increase CGRP expression in their motoneurons.
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