Department of Molecular Biosciences, School of Veterinary Medicine (R.Z., W.F., J.R.L., Y.D., G.C., I.N.P.), Department of Medicine and Epidemiology, The William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine (M.A., C.C.), and Department of Public Health Sciences, School of Medicine, School of Medicine (L.Q.), University of California, Davis, California
Department of Molecular Biosciences, School of Veterinary Medicine (R.Z., W.F., J.R.L., Y.D., G.C., I.N.P.), Department of Medicine and Epidemiology, The William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine (M.A., C.C.), and Department of Public Health Sciences, School of Medicine, School of Medicine (L.Q.), University of California, Davis, California.
Mol Pharmacol. 2020 Oct;98(4):351-363. doi: 10.1124/mol.120.119412. Epub 2020 Aug 6.
Ryanodine receptor () mutations confer stress-triggered malignant hyperthermia (MH) susceptibility. Dietary caffeine (CAF) is the most commonly consumed psychoactive compound by humans. CAF-triggered Ca release and its influences on skeletal muscle contractility are widely used as experimental tools to study RYR function/dysfunction and diagnose MH susceptibility. We hypothesize that dietary CAF achieving blood levels measured in human plasma exacerbates the penetrance of MH susceptibility mutations triggered by gaseous anesthetic, affecting both central and peripheral adverse responses. Heterozygous R163C-RYR1 (HET) MH susceptible mice are used to investigate the influences of dietary CAF on both peripheral and central responses before and after induction of halothane (HAL) maintenance anesthesia under experimental conditions that maintain normal core body temperature. HET mice receiving CAF (plasma CAF 893 ng/ml) have significantly shorter times to respiratory arrest compared with wild type, without altering blood chemistry or displaying hyperthermia or muscle rigor. Intraperitoneal bolus dantrolene before HAL prolongs time to respiratory arrest. A pilot electrographic study using subcutaneous electrodes reveals that dietary CAF does not alter baseline electroencephalogram (EEG) total power, but significantly shortens delay to isoelectric EEG, which precedes respiratory and cardiac arrest. CAF ± HAL are studied on RYR1 single-channel currents and HET myotubes to define molecular mechanisms of gene-by-environment synergism. Strong pharmacological synergism between CAF and HAL is demonstrated in both single-channel and myotube preparations. Central and peripheral nervous systems mediate adverse responses to HAL in a HET model of MH susceptibility exposed to dietary CAF, a modifiable lifestyle factor that may mitigate risks of acute and chronic diseases associated with mutations. SIGNIFICANCE STATEMENT: Dietary caffeine at a human-relevant dose synergizes adverse peripheral and central responses to anesthesia in malignant hyperthermia susceptible mice. Synergism of these drugs can be attributed to their actions at ryanodine receptors.
肌质网钙释放通道(RYR1)突变可导致应激性恶性高热(MH)易感性。咖啡因(CAF)是人类最常消费的精神活性化合物。CAF 触发的钙释放及其对骨骼肌收缩力的影响被广泛用作研究 RYR 功能障碍和诊断 MH 易感性的实验工具。我们假设,饮食中的 CAF 达到人类血浆中测量的水平会加剧气态麻醉剂引发的 MH 易感性突变的易感性,影响中枢和外周不良反应。杂合 R163C-RYR1(HET)MH 易感小鼠用于在实验条件下研究饮食 CAF 对诱导氟烷(HAL)维持麻醉前后的外周和中枢反应的影响,该实验条件维持正常核心体温。接受 CAF(血浆 CAF 893ng/ml)的 HET 小鼠与野生型相比,呼吸停止的时间明显缩短,而不改变血液化学性质,也不出现发热或肌肉僵硬。在 HAL 之前腹膜内推注丹曲林可延长呼吸停止时间。使用皮下电极进行的初步脑电图研究表明,饮食 CAF 不会改变脑电图(EEG)总功率的基线,但显著缩短等电 EEG 的延迟,这先于呼吸和心脏骤停。CAF±HAL 用于 RYR1 单通道电流和 HET 肌管研究基因-环境协同作用的分子机制。在单通道和肌管制剂中均证实 CAF 和 HAL 具有强烈的药理协同作用。在暴露于饮食 CAF 的 MH 易感性 RYR1 单基因突变小鼠模型中,中枢和周围神经系统介导 HAL 的不良反应,饮食 CAF 是一种可改变的生活方式因素,可能降低与突变相关的急性和慢性疾病的风险。意义声明:在易感性恶性高热的小鼠中,以与人类相关的剂量摄入咖啡因会协同麻醉的外周和中枢不良反应。这些药物的协同作用可归因于它们在肌质网钙释放通道上的作用。