细胞内
化学
部分
去甲肾上腺素
儿茶酚胺
神经递质
再摄取抑制剂
荧光
氢键
生物物理学
多巴胺
再摄取
立体化学
血清素
生物化学
受体
分子
有机化学
内科学
医学
生物
物理
量子力学
作者
Juan Qiao,Deyu Wu,Yuying Song,Wenliang Ji,Qingwei Yue,Lanqun Mao,Li Qi
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2021-10-28
卷期号:93 (44): 14743-14747
被引量:14
标识
DOI:10.1021/acs.analchem.1c03263
摘要
A long-standing challenge has been the simultaneous sensing of intracellular temperature and norepinephrine (NE) variations to explore signaling pathways and depression pathogeny. Here, we designed a fluorescent probe using poly(N-isopropylacrylamide) and 1-[4-(7-nitro-benzo [1,2,5]oxadiazol-4-yl)-piperazin-1-yl]-propenone (PNIPAm–AANBD) and (E)-1-(4-boronobenzyl)-2-(2-(1,3-dioxo-1H,3H-benzo[de]isochromen-6-yl)vinyl)pyridin-1-ium bromide (PHE) for simultaneously measuring the temperature and NE with high selectivity. The fluorescence intensity of the PNIPAm–AANBD moiety exhibited a good response to temperature changes. The PHE moiety could selectively sense NE due to the naphthalic anhydride group in PHE, which formed naphthalimide upon bonding with the primary amino group of NE. The hydroxyl-terminated ligand recognized the phenolic hydroxyl group of NE through the formation of hydrogen bonds. Using the proposed fluorescent probe, variations in the intracellular temperature and NE during NE reuptake could be simultaneously measured. It was first discovered that with the inhibition of antidepressant drugs, the intracellular temperature increased by 1.2–2.1 °C, and the NE reuptake decreased by about 21.5 μM. The measured variations in intracellular temperature and NE during neurotransmitter reuptake can shed light on the underlying mechanism of neurotransmitter signaling pathways, which may facilitate the treatment of depression.
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