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Cited 5 time in webofscience Cited 9 time in scopus
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Current clinical application of dantrolene sodiumopen access

Authors
Yang, Hong SeukChoi, Jae MoonIn, JunyongSung, Tae-yunKim, Yong BeomSultana, Shofina
Issue Date
Jul-2023
Publisher
대한마취통증의학회
Keywords
Adverse events; Dantrolene; Malignant hyperthermia; Pharmacology; Ryanodine receptor calcium release channel
Citation
Anesthesia & Pain Medicine, v.18, no.3, pp 220 - 232
Pages
13
Indexed
SCOPUS
KCI
Journal Title
Anesthesia & Pain Medicine
Volume
18
Number
3
Start Page
220
End Page
232
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/20044
DOI
10.17085/apm.22260
ISSN
1975-5171
2383-7977
Abstract
Dantrolene sodium (DS) was first introduced as an oral antispasmodic drug. However, in 1975, DS was demonstrated to be effective for managing malignant hyperthermia (MH) and was adopted as the primary therapeutic drug after intravenous administration. However, it is difficult to administer DS intravenously to manage MH. MH is life-threatening, pharmacog-enomically related, and induced by depolarizing neuromuscular blocking agents or inhalational anesthetics. All anesthesiologists should know the pharmacology of DS. DS suppresses Ca2+ release from ryanodine receptors (RyRs). RyRs are expressed in various tissues, although their distribution differs among subtypes. The anatomical and physiological functions of RyRs have also been demonstrated as effective therapeutic drugs for cardiac arrhythmias, Alzheimer’s disease, and other RyR-related diseases. Recently, a new formulation was introduced that enhanced the hydrophilicity of the lipophilic DS. The authors summarize the pharmacological properties of DS and comment on its indications, contraindications, adverse effects, and interactions with other drugs by reviewing reference articles. © the Korean Society of Anesthesiologists, 2023.
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