Haijun Yang, Ke Li, Tingfang Wang, Yi Zou, Guanyu Xu, Can Zhou, Zeying Liang, Yingqiu Wang, Jianguo Lin, Jian Yang
{"title":"新型双功能半姜黄素类似物作为阿尔茨海默病APP/PS1模型β-淀粉样蛋白成像的荧光和PET探针","authors":"Haijun Yang, Ke Li, Tingfang Wang, Yi Zou, Guanyu Xu, Can Zhou, Zeying Liang, Yingqiu Wang, Jianguo Lin, Jian Yang","doi":"10.1021/acschemneuro.4c00532","DOIUrl":null,"url":null,"abstract":"<p><p>Noninvasive imaging of β-amyloid <i>in vivo</i> is pivotal for the early diagnosis of Alzheimer's disease (AD). While single imaging methods have been extensively studied for detecting Aβ over the past decade, dual-modal probes have received scant attention. In this study, we synthesized and assessed a series of half-curcumin probes, among which <b>DiFboron-8</b> demonstrated a high affinity and selectivity for Aβ aggregates. <b>DiFboron-8</b> effectively served as a dual-functional fluorescent and positron emission tomography (PET) probe for imaging β-amyloid in an AD mouse model. Histological staining results underscored <b>DiFboron-8</b>'s potent staining capability for Aβ plaques in APP/PS1 brain slices, while <i>ex vivo</i> biodistribution studies highlighted its rapid clearance rate. <i>In vivo</i> imaging revealed that <b>[</b><sup><b>18</b></sup><b>F]-DiFboron-8</b> could penetrate the blood-brain barrier, displaying higher PET signals in the brains of APP/PS1 mice compared to wild-type mice just 3 min postinjection, a finding corroborated by autoradiography staining. Overall, we propose that <b>[</b><sup><b>18</b></sup><b>F]-DiFboron-8</b> represents an efficient fluorescent/PET dual-modal probe, offering promise for β-amyloid imaging in the early stages of AD.</p>","PeriodicalId":13,"journal":{"name":"ACS Chemical Neuroscience","volume":" ","pages":"365-373"},"PeriodicalIF":4.1000,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Novel Dual-Functional Half-Curcumin Analogues as a Fluorescent and PET Probe for β-Amyloid Imaging in the Alzheimer's Disease APP/PS1 Model.\",\"authors\":\"Haijun Yang, Ke Li, Tingfang Wang, Yi Zou, Guanyu Xu, Can Zhou, Zeying Liang, Yingqiu Wang, Jianguo Lin, Jian Yang\",\"doi\":\"10.1021/acschemneuro.4c00532\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Noninvasive imaging of β-amyloid <i>in vivo</i> is pivotal for the early diagnosis of Alzheimer's disease (AD). While single imaging methods have been extensively studied for detecting Aβ over the past decade, dual-modal probes have received scant attention. In this study, we synthesized and assessed a series of half-curcumin probes, among which <b>DiFboron-8</b> demonstrated a high affinity and selectivity for Aβ aggregates. <b>DiFboron-8</b> effectively served as a dual-functional fluorescent and positron emission tomography (PET) probe for imaging β-amyloid in an AD mouse model. Histological staining results underscored <b>DiFboron-8</b>'s potent staining capability for Aβ plaques in APP/PS1 brain slices, while <i>ex vivo</i> biodistribution studies highlighted its rapid clearance rate. <i>In vivo</i> imaging revealed that <b>[</b><sup><b>18</b></sup><b>F]-DiFboron-8</b> could penetrate the blood-brain barrier, displaying higher PET signals in the brains of APP/PS1 mice compared to wild-type mice just 3 min postinjection, a finding corroborated by autoradiography staining. Overall, we propose that <b>[</b><sup><b>18</b></sup><b>F]-DiFboron-8</b> represents an efficient fluorescent/PET dual-modal probe, offering promise for β-amyloid imaging in the early stages of AD.</p>\",\"PeriodicalId\":13,\"journal\":{\"name\":\"ACS Chemical Neuroscience\",\"volume\":\" \",\"pages\":\"365-373\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-02-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Chemical Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1021/acschemneuro.4c00532\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Chemical Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1021/acschemneuro.4c00532","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/17 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Novel Dual-Functional Half-Curcumin Analogues as a Fluorescent and PET Probe for β-Amyloid Imaging in the Alzheimer's Disease APP/PS1 Model.
Noninvasive imaging of β-amyloid in vivo is pivotal for the early diagnosis of Alzheimer's disease (AD). While single imaging methods have been extensively studied for detecting Aβ over the past decade, dual-modal probes have received scant attention. In this study, we synthesized and assessed a series of half-curcumin probes, among which DiFboron-8 demonstrated a high affinity and selectivity for Aβ aggregates. DiFboron-8 effectively served as a dual-functional fluorescent and positron emission tomography (PET) probe for imaging β-amyloid in an AD mouse model. Histological staining results underscored DiFboron-8's potent staining capability for Aβ plaques in APP/PS1 brain slices, while ex vivo biodistribution studies highlighted its rapid clearance rate. In vivo imaging revealed that [18F]-DiFboron-8 could penetrate the blood-brain barrier, displaying higher PET signals in the brains of APP/PS1 mice compared to wild-type mice just 3 min postinjection, a finding corroborated by autoradiography staining. Overall, we propose that [18F]-DiFboron-8 represents an efficient fluorescent/PET dual-modal probe, offering promise for β-amyloid imaging in the early stages of AD.
期刊介绍:
ACS Chemical Neuroscience publishes high-quality research articles and reviews that showcase chemical, quantitative biological, biophysical and bioengineering approaches to the understanding of the nervous system and to the development of new treatments for neurological disorders. Research in the journal focuses on aspects of chemical neurobiology and bio-neurochemistry such as the following:
Neurotransmitters and receptors
Neuropharmaceuticals and therapeutics
Neural development—Plasticity, and degeneration
Chemical, physical, and computational methods in neuroscience
Neuronal diseases—basis, detection, and treatment
Mechanism of aging, learning, memory and behavior
Pain and sensory processing
Neurotoxins
Neuroscience-inspired bioengineering
Development of methods in chemical neurobiology
Neuroimaging agents and technologies
Animal models for central nervous system diseases
Behavioral research