Identification of a fluorescent general anesthetic, 1-aminoanthracene

被引:46
作者
Butts, Christopher A. [2 ]
Xi, Jin [1 ]
Brannigan, Grace [3 ]
Saad, Abdalla A. [4 ,5 ]
Venkatachalan, Srinivasan P. [4 ,5 ]
Pearce, Robert A. [4 ,5 ]
Klein, Michael L. [3 ]
Eckenhoff, Roderic G. [1 ]
Dmochowski, Ivan J. [2 ]
机构
[1] Univ Penn, Sch Med, Dept Anesthesiol & Crit Care, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
[3] Univ Penn, Ctr Mol Modeling, Philadelphia, PA 19104 USA
[4] Univ Wisconsin, Dept Anesthesiol, Madison, WI 53711 USA
[5] Univ Wisconsin, Dept Physiol, Madison, WI 53711 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
ferritin; probe; GABA; propofol; imaging; ODORANT-BINDING PROTEIN; RAT-BRAIN; VOLATILE ANESTHETICS; HIGH-RESOLUTION; METABOLISM; HALOTHANE; NEURODEGENERATION; AUTORADIOGRAPHY; SPECTROSCOPY; ISOFLURANE;
D O I
10.1073/pnas.0810590106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
We identified a fluorophore, 1-aminoanthracene (1-AMA), that is anesthetic, potentiates GABAergic transmission, and gives an appropriate dissociation constant, K-d approximate to 0.1 mM, for binding to the general anesthetic site in horse spleen apoferritin (HSAF). 1-AMA fluorescence is enhanced when bound to HSAF. Thus, displacement of 1-AMA from HSAF by other anesthetics attenuates the fluorescence signal and allows determination of K-d, as validated by isothermal titration calorimetry. This provides a unique fluorescence assay for compound screening and anesthetic discovery. Additional electrophysiology experiments in isolated cells indicate that 1-AMA potentiates chloride currents elicited by GABA, similar to many general anesthetics. Furthermore, 1-AMA reversibly immobilizes stage 45-50 Xenopus laevis tadpoles (EC50 = 16 mu M) and fluorescence micrographs show 1-AMA localized to brain and olfactory regions. Thus, 1-AMA provides an unprecedented opportunity for studying general anesthetic distribution in vivo at the cellular and subcellular levels.
引用
收藏
页码:6501 / 6506
页数:6
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