Effects of Remimazolam and Propofol on Ca²⁺ Regulation by Ryanodine Receptor 1 with Malignant Hyperthermia Mutation.

ABSTRACT:

Background

We investigated the potential safety of remimazolam and propofol in malignant hyperthermia- (HM-) susceptible patients using ryanodine receptor 1- (RYR1-) expressing human embryonic kidney- (HEK-) 293 cells.

Methods

We compared the enhanced responsiveness of HEK-293 cells expressing wild-type RYR1 with that of mutant RYR1 to caffeine following perfusion with remimazolam or propofol. Furthermore, we investigated whether RYR1 enhanced the responsiveness of cells to remimazolam or propofol and compared the median effective concentration (EC₅₀; i.e., the concentration required to reach half-maximal activation) using an unpaired two-tailed t-test while a P < 0.05 was considered significant.

Results

Remimazolam and propofol did not promote the caffeine-induced increase in intracellular Ca²⁺ levels in HEK-293 cells expressing mutant RYR1 even with exposure to approximately 100-fold the clinically used concentration. In wild-type RYR1, EC₅₀ values of remimazolam following refusion vs. nonperfusion were 2.86?mM vs. 2.75?mM (P = 0.76) while for propofol perfusion vs. nonperfusion, they were 2.76?mM vs. 2.75?mM, respectively (P = 0.83). In mutant RYR1, EC₅₀ values of remimazolam refusion vs. nonperfusion were 1.58?mM vs. 1.71?mM, respectively (P = 0.63) while for propofol perfusion vs. nonperfusion, they were 1.65?mM vs. 1.71?mM, respectively (P = 0.73). Remimazolam and propofol increased intracellular Ca²⁺ levels in a concentration-dependent manner, but the effect was not enhanced by RYR1. EC₅₀ values of remimazolam with non-RYR1 vs. wild-type RYR1 were 1.00?mM vs. 0.92?mM, respectively (P = 0.91) while those of propofol were 1.09?mM vs. 1.05?mM, respectively (P = 0.84).

Conclusions

The increase in intracellular Ca²⁺ concentration caused by remimazolam or propofol was not considered an RYR1-mediated reaction. We conclude that remimazolam and propofol can be safely used as an anesthetic in MH-susceptible patients with RYR1-mutation without causing MH and may be safely substituted for an MH-triggering anesthetic when RYR1-mediated MH occurs.

SUBMITTER: Watanabe T 

PROVIDER: S-EPMC7801102 | biostudies-literature | 2021

REPOSITORIES: biostudies-literature