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Cited 2 time in webofscience Cited 2 time in scopus
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Effects of neuromuscular presynaptic muscarinic M-1 receptor blockade on rocuronium-induced neuromuscular blockade in immobilized tibialis anterior musclesopen access

Authors
Kim, Yong BeomYang, Hong-SeukKim, Ha JungChoi, Hey-RanIn, JunyongYoon, Soon-YoungRo, Young Jin
Issue Date
Dec-2018
Publisher
WILEY
Keywords
acetylcholine release; muscarinic acetylcholine receptors; muscle atrophy; neuromuscular junction; neuromuscular nondepolarizing agents; rocuronium
Citation
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, v.45, no.12, pp 1309 - 1316
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY
Volume
45
Number
12
Start Page
1309
End Page
1316
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/8847
DOI
10.1111/1440-1681.13012
ISSN
0305-1870
1440-1681
Abstract
This in vivo study tested the hypothesis that the modulation of acetylcholine (ACh) release by the M-1 muscarinic receptor (mAChR) in the neuromuscular junction of disused muscles may affect the tensions of the muscles during the neuromuscular monitoring of a rocuronium-induced neuromuscular block and compared the results with those obtained from normal muscles. A total of 20 C57BL/6 (wild-type) and 10 alpha 7 knock out (alpha 7KO) mice were used in this experiment. As a pre-experimental procedure, knee and ankle joints of right hind limbs were fixed by needle pinning at the 90 degrees flexed position. After 2 weeks, the main experiment was performed. Both tendons of the tibialis anterior (TA) muscles were obtained, and the muscle tensions were recorded while the dose-responses of rocuronium were measured three times in the same mouse by the serial administration of pirenzepine (0, 0.001 and 0.01 mu g/g). Weight losses were observed after 2 weeks of immobilization in both groups, and a decrease in the mass of TA muscles at the immobilized side was observed compared to those of the contralateral nonimmobilized side. Tension depression of the TA muscles at immobilized side of the alpha 7KO group was faster than those of the wild-type group, but these differences decreased after the administration of pirenzepine. The tension depressions were similar regardless of the pirenzepine doses at the same side in the group. Tension depression may become more rapid in the alpha 7 AChR-expressed disused muscles by the decreased release of ACh release upon neuronal firing by the blockade of facilitatory M-1 mAChR
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