Molecularly engineered supramolecular fluorescent chemodosimeter for measuring epinephrine dynamics

Accurately visualizing epinephrine (EP) activity is essential for understanding its physiological functions and pathological processes in brain. However, to the best of our knowledge, reliable, rapid, and specifical measurement of EP dynamics at cellular and in vivo level hasn't been previously reported. Herein, we report the probe for EP imaging and biosensing in neurons and living brain of freely behaving animals, based on creating a series of supramolecular fluorescent chemodosimeters through host-guest interaction. The optimized chemodosimeter enables real-time imaging and quantifying of EP with high specificity, sensitivity, signal-to-noise ratio, and rapid kinetics (~240 ms) in neurons, brain tissues and zebrafish. More significantly, we demonstrate real-time monitoring of EP in 26 regions within deep brain of freely behaving male mice, unraveling an augmented EP concentration in the amygdala, thalamus, hypothalamus, hippocampus and striatum under fear-induced stress. These findings highlight our chemodosimeter as a powerful tool for precise measurements of EP dynamics in diverse model organisms.

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Publication Details

Journal
Nature Communications
Published
2025-02-21
DOI
https://doi.org/10.1038/s41467-025-57100-5
Citations
12
Primary Topic
Photoreceptor and optogenetics research
Type
article
Field-Weighted Citation Impact
10.91

Funders

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article

Molecularly engineered supramolecular fluorescent chemodosimeter for measuring epinephrine dynamics

Yudan Zhao, Yang Tian, Yuxiao Mei, Zhichao Liu et al.
12 citations
Nature Communications
Photoreceptor and optogenetics research
10.91
article

Molecularly engineered supramolecular fluorescent chemodosimeter for measuring epinephrine dynamics

Yudan Zhao, Yang Tian, Yuxiao Mei, Zhichao Liu, Jing Sun
article en
12 citations

Abstract

Accurately visualizing epinephrine (EP) activity is essential for understanding its physiological functions and pathological processes in brain. However, to the best of our knowledge, reliable, rapid, and specifical measurement of EP dynamics at cellular and in vivo level hasn't been previously reported. Herein, we report the probe for EP imaging and biosensing in neurons and living brain of freely behaving animals, based on creating a series of supramolecular fluorescent chemodosimeters through host-guest interaction. The optimized chemodosimeter enables real-time imaging and quantifying of EP with high specificity, sensitivity, signal-to-noise ratio, and rapid kinetics (~240 ms) in neurons, brain tissues and zebrafish. More significantly, we demonstrate real-time monitoring of EP in 26 regions within deep brain of freely behaving male mice, unraveling an augmented EP concentration in the amygdala, thalamus, hypothalamus, hippocampus and striatum under fear-induced stress. These findings highlight our chemodosimeter as a powerful tool for precise measurements of EP dynamics in diverse model organisms.

Nature CommunicationsVol. 16(1)
East China Normal University (CN)
National Natural Science Foundation of China, Shanghai Municipal Education Commission, East China Normal University, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 1%
Photoreceptor and optogenetics research
10.91
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