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光控心脏功能的光可切换毒蕈碱激动剂。

Optical Control of Cardiac Function with a Photoswitchable Muscarinic Agonist.

机构信息

Institute for Bioengineering of Catalonia (IBEC) , Barcelona Institute for Science and Technology (BIST) , Carrer de Baldiri Reixac 15-21 , 08028 Barcelona , Spain.

Network Biomedical Research Center in Bioengineering, Biomaterials, and Nanomedicine (CIBER-BBN) , 28029 Madrid , Spain.

出版信息

J Am Chem Soc. 2019 May 8;141(18):7628-7636. doi: 10.1021/jacs.9b03505. Epub 2019 Apr 26.

Abstract

Light-triggered reversible modulation of physiological functions offers the promise of enabling on-demand spatiotemporally controlled therapeutic interventions. Optogenetics has been successfully implemented in the heart, but significant barriers to its use in the clinic remain, such as the need for genetic transfection. Herein, we present a method to modulate cardiac function with light through a photoswitchable compound and without genetic manipulation. The molecule, named PAI, was designed by introduction of a photoswitch into the molecular structure of an M2 mAChR agonist. In vitro assays revealed that PAI enables light-dependent activation of M2 mAChRs. To validate the method, we show that PAI photoisomers display different cardiac effects in a mammalian animal model, and demonstrate reversible, real-time photocontrol of cardiac function in translucent wildtype tadpoles. PAI can also effectively activate M2 receptors using two-photon excitation with near-infrared light, which overcomes the scattering and low penetration of short-wavelength illumination, and offers new opportunities for intravital imaging and control of cardiac function.

摘要

光触发的生理功能可逆调节有望实现按需时空控制的治疗干预。光遗传学已成功应用于心脏,但在临床应用中仍存在重大障碍,例如需要基因转染。本文介绍了一种通过光开关化合物而无需遗传操作来调节心脏功能的方法。该分子命名为 PAI,是通过在 M2 mAChR 激动剂的分子结构中引入光开关而设计的。体外试验表明,PAI 能够实现光依赖性的 M2 mAChR 激活。为了验证该方法,我们表明 PAI 光异构体在哺乳动物动物模型中表现出不同的心脏效应,并在半透明的野生型蝌蚪中证明了心脏功能的可逆、实时光控。PAI 还可以使用近红外光的双光子激发有效地激活 M2 受体,这克服了短波长照明的散射和低穿透性,为活体成像和心脏功能控制提供了新的机会。

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