Department of Clinical Neuroscience, Center for Psychiatry Research, Karolinska Institutet and Stockholm County Council, Stockholm, Sweden.
Department of Clinical Neuroscience, Center for Psychiatry Research, Karolinska Institutet and Stockholm County Council, Stockholm, Sweden.
Br J Anaesth. 2021 Jan;126(1):238-244. doi: 10.1016/j.bja.2020.08.052. Epub 2020 Oct 6.
The molecular actions underlying the clinical effects of inhaled anaesthetics such as sevoflurane and isoflurane are not fully understood. Unexpected observations in positron emission tomography (PET) studies with [C]AZD9272, a metabotropic glutamate receptor 5 (mGluR5) radioligand with possible affinity for monoamine oxidase-B (MAO-B), suggest that its binding is sensitive to anaesthesia with sevoflurane. The objective of the present study was to assess the effects of sevoflurane anaesthesia on the binding of [C]AZD9272 and of [C]L-deprenyl-D, a radioligand selective for MAO-B in non-human primates (NHPs).
Altogether, 12 PET measurements were conducted with a high-resolution research tomograph using the ligands [C]AZD9272 or [C]L-deprenyl-D in six cynomolgus monkeys anaesthetised with sevoflurane or ketamine/xylazine.
The specific binding of [C]AZD9272 and [C]L-deprenyl-D was markedly reduced during anaesthesia with sevoflurane compared with ketamine/xylazine. The reduction was 80-90% (n=3) for [C]AZD9272 and 77-80% (n=3) for [C]L-deprenyl-D.
Sevoflurane anaesthesia inhibited radioligand binding to MAO-B in the primate brain. The observation of lower MAO-B binding at clinically relevant concentrations of sevoflurane warrants further exploration of the potential role of MAO-B related mechanisms in regulation of systemic blood pressure during anaesthesia.
吸入麻醉剂(如七氟醚和异氟醚)的临床效应的分子作用机制尚未完全阐明。正电子发射断层扫描(PET)研究中使用[C]AZD9272(一种代谢型谷氨酸受体 5(mGluR5)放射性配体,可能与单胺氧化酶-B(MAO-B)有亲和力)的意外观察结果表明,其结合对七氟醚麻醉敏感。本研究的目的是评估七氟醚麻醉对[C]AZD9272结合的影响,以及在非人灵长类动物(NHP)中[C]L-deprenyl-D(一种针对 MAO-B 的放射性配体)的结合。
总共在六只使用七氟醚或氯胺酮/赛拉嗪麻醉的食蟹猴中进行了 12 次使用高分辨率研究断层扫描的 PET 测量,使用配体[C]AZD9272 或[C]L-deprenyl-D。
与氯胺酮/赛拉嗪相比,七氟醚麻醉时[C]AZD9272 和[C]L-deprenyl-D 的特异性结合明显减少。[C]AZD9272 减少 80-90%(n=3),[C]L-deprenyl-D 减少 77-80%(n=3)。
七氟醚麻醉抑制了灵长类动物大脑中 MAO-B 的放射性配体结合。在临床相关浓度的七氟醚下观察到 MAO-B 结合降低,进一步证明了 MAO-B 相关机制在麻醉期间调节全身血压的潜在作用。