3,5-Di-t-butyl catechol is a potent human ryanodine receptor 1 activator, not suitable for the diagnosis of malignant hyperthermia susceptibility

作者：Lacava Caterina; Michalek Sauberer Andrea; Kraft Birgit; Sgaragli Giampietro; Sipos Elisabeth; Hoeller Carmen; Kress Hans Georg; Fusi Fabio; Weigl Lukas G^*

来源：Pharmacological Research, 2012, 66(1): 80-87.

DOI：10.1016/j.phrs.2012.03.012

• Malignant hyperthermia
• Human skeletal muscle
• 3,5-Di-t-butyl catechol
• Ryanodine receptor
• In vitro contracture test

3,5-Di-t-butyl catechol (DTCAT) releases Ca2+ from rat skeletal muscle sarcoplasmic reticulum (SR) vesicles. Hence, it is a candidate for use as a substitute for halothane or caffeine in the in vitro contracture test for the diagnosis of susceptibility to malignant hyperthermia (MH). %26lt;br%26gt;To characterize the effect of DTCAT at cell level, Ca2+ release experiments were performed on cultured, human skeletal muscle myotubes using the fluorescent Ca2+ indicator fura2-AM. DTCAT was also assayed in the in vitro contracture test on human skeletal muscle bundles obtained from individuals diagnosed susceptible (MHS), normal (MHN) or equivocal for halothane (MHEH) and compared to the standard test substances caffeine and halothane. %26lt;br%26gt;DTCAT increased, in a concentration-dependent manner and with a higher efficacy as compared to caffeine, the free, intracellular Ca2+ levels of cultured MHN and MHS skeletal muscle myotubes. This effect was similar in both types of myotubes and involved the release of Ca2+ from SR stores as well as Ca2+-influx from the extracellular space. Inhibition of ryanodine receptors either with ryanodine or with ruthenium red markedly reduced DTCAT-induced increase in intracellular Ca2+ concentration while abolishing that induced by caffeine. In MHN skeletal muscle bundles, DTCAT induced contractures with an EC50 value of 160 +/- 91 mu M. However, the sensitivity of MHS or MHEH muscles to DTCAT was similar to that of MHN muscles. %26lt;br%26gt;In conclusion, DTCAT is not suitable for the diagnosis of MH susceptibility due to its failure to discriminate between MHN and MHS muscles.

• 出版日期2012-7