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氟烷类衍生物拮抗丙泊酚麻醉。

Antagonism of propofol anesthesia by alkyl-fluorobenzene derivatives.

机构信息

Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.

出版信息

Sci Rep. 2024 Jul 10;14(1):15943. doi: 10.1038/s41598-024-66672-z.

Abstract

Despite their frequent use across many clinical settings, general anesthetics are medications with lethal side effects and no reversal agents. A fluorinated analogue of propofol has previously been shown to antagonize propofol anesthesia in tadpoles and zebrafish, but little further investigation of this class of molecules as anesthetic antagonists has been conducted. A 13-member library of alkyl-fluorobenzene derivatives was tested in an established behavioral model of anesthesia in zebrafish at 5 days post fertilization. These compounds were examined for their ability to antagonize propofol and two volatile anesthetics, as well as their interaction with the anesthetic-binding model protein apoferritin. Two compounds provided significant antagonism of propofol, and when combined, were synergistic, suggesting more than one antagonist sensitive target site. These compounds did not antagonize the volatile anesthetics, indicating some selectivity amongst general anesthetics. For the compounds with the most antagonistic potency, similarities in structure and binding to apoferritin may be suggestive of competitive antagonism; however, this was not supported by a Schild analysis. This is consistent with multiple targets contributing to general anesthesia, but whether these are physiologic antagonists or are antagonists at only some subset of the many anesthetic potential targets remains unclear, and will require additional investigation.

摘要

尽管全身麻醉剂在许多临床环境中经常使用,但它们是具有致命副作用且没有逆转剂的药物。先前已经证明,丙泊酚的一种氟化类似物可拮抗蝌蚪和斑马鱼中的丙泊酚麻醉,但对这类分子作为麻醉拮抗剂的进一步研究却很少进行。在已建立的斑马鱼受精后 5 天麻醉行为模型中,测试了一个由 13 个烷基-氟苯衍生物组成的文库。这些化合物被检测是否能够拮抗丙泊酚和两种挥发性麻醉剂,以及它们与麻醉结合模型蛋白脱铁铁蛋白的相互作用。两种化合物对丙泊酚有显著的拮抗作用,联合使用时具有协同作用,表明存在不止一个敏感的拮抗作用靶位。这些化合物不能拮抗挥发性麻醉剂,表明在全身麻醉剂中存在一定的选择性。对于具有最强拮抗作用的化合物,结构上的相似性和与脱铁铁蛋白的结合可能提示竞争性拮抗作用;然而,这并没有 Schild 分析的支持。这与多个靶标共同参与全身麻醉一致,但这些靶标是生理拮抗剂还是仅在许多潜在麻醉靶标中的某些亚组中起拮抗剂作用尚不清楚,需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f34/11236999/d69e4cc781fe/41598_2024_66672_Fig1_HTML.jpg

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