Usamma Amjad, Shreya Mahajan, Jiwon Choi, Ritesh Shrivastav, Raymond Murray, Abby Somich, Olivia Coyne, Helen N Schwerdt
{"title":"用于监测非人类灵长类动物电和化学神经活动的微创探针。","authors":"Usamma Amjad, Shreya Mahajan, Jiwon Choi, Ritesh Shrivastav, Raymond Murray, Abby Somich, Olivia Coyne, Helen N Schwerdt","doi":"10.1021/acschemneuro.5c00071","DOIUrl":null,"url":null,"abstract":"<p><p>We leveraged carbon fiber materials for creating sensors that provide dual neurochemical and electrical neural activity recording at microinvasive (10 μm) spatial footprints proximal to recording sites, and enabling these measurements from deep brain targets of primates with conventional cranial chambers. These shaft-assisted microinvasive probes (s-μIPs) are approximately 10 μm in diameter along the distal length (1-15 mm) immediately surrounding the targeted recording site. This microinvasive portion ensures that the recording site is isolated from tissue damage induced by the wider shaft portion of the device. The shaft (150-165 μm in diameter) within the device stiffens the remaining length of the probe (>100 mm), and provides compatibility with standard intracranial insertion protocols (e.g., guide tubes and chamber setups) that require a sufficiently rigid and long shaft for deep brain insertion in monkeys. The s-μIP was further expanded to provide dual-channel chemical and electrical neural activity recording with micrometer spatial resolution. Measurements of reward- and movement- related dopamine, spikes, and local field potentials were made from single and dual-channel s-μIPs implanted in task-performing monkeys. Recordings from chronically implanted s-μIPs display the capability of functional multimodal (chemical and electrical) neural activity measurements over 1-year postimplantation from microinvasive devices.</p>","PeriodicalId":13,"journal":{"name":"ACS Chemical Neuroscience","volume":" ","pages":"2237-2247"},"PeriodicalIF":3.9000,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12183687/pdf/","citationCount":"0","resultStr":"{\"title\":\"Microinvasive Probes for Monitoring Electrical and Chemical Neural Activity in Nonhuman Primates.\",\"authors\":\"Usamma Amjad, Shreya Mahajan, Jiwon Choi, Ritesh Shrivastav, Raymond Murray, Abby Somich, Olivia Coyne, Helen N Schwerdt\",\"doi\":\"10.1021/acschemneuro.5c00071\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We leveraged carbon fiber materials for creating sensors that provide dual neurochemical and electrical neural activity recording at microinvasive (10 μm) spatial footprints proximal to recording sites, and enabling these measurements from deep brain targets of primates with conventional cranial chambers. These shaft-assisted microinvasive probes (s-μIPs) are approximately 10 μm in diameter along the distal length (1-15 mm) immediately surrounding the targeted recording site. This microinvasive portion ensures that the recording site is isolated from tissue damage induced by the wider shaft portion of the device. The shaft (150-165 μm in diameter) within the device stiffens the remaining length of the probe (>100 mm), and provides compatibility with standard intracranial insertion protocols (e.g., guide tubes and chamber setups) that require a sufficiently rigid and long shaft for deep brain insertion in monkeys. The s-μIP was further expanded to provide dual-channel chemical and electrical neural activity recording with micrometer spatial resolution. Measurements of reward- and movement- related dopamine, spikes, and local field potentials were made from single and dual-channel s-μIPs implanted in task-performing monkeys. Recordings from chronically implanted s-μIPs display the capability of functional multimodal (chemical and electrical) neural activity measurements over 1-year postimplantation from microinvasive devices.</p>\",\"PeriodicalId\":13,\"journal\":{\"name\":\"ACS Chemical Neuroscience\",\"volume\":\" \",\"pages\":\"2237-2247\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-06-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12183687/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Chemical Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1021/acschemneuro.5c00071\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/30 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.5c00071","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Microinvasive Probes for Monitoring Electrical and Chemical Neural Activity in Nonhuman Primates.
We leveraged carbon fiber materials for creating sensors that provide dual neurochemical and electrical neural activity recording at microinvasive (10 μm) spatial footprints proximal to recording sites, and enabling these measurements from deep brain targets of primates with conventional cranial chambers. These shaft-assisted microinvasive probes (s-μIPs) are approximately 10 μm in diameter along the distal length (1-15 mm) immediately surrounding the targeted recording site. This microinvasive portion ensures that the recording site is isolated from tissue damage induced by the wider shaft portion of the device. The shaft (150-165 μm in diameter) within the device stiffens the remaining length of the probe (>100 mm), and provides compatibility with standard intracranial insertion protocols (e.g., guide tubes and chamber setups) that require a sufficiently rigid and long shaft for deep brain insertion in monkeys. The s-μIP was further expanded to provide dual-channel chemical and electrical neural activity recording with micrometer spatial resolution. Measurements of reward- and movement- related dopamine, spikes, and local field potentials were made from single and dual-channel s-μIPs implanted in task-performing monkeys. Recordings from chronically implanted s-μIPs display the capability of functional multimodal (chemical and electrical) neural activity measurements over 1-year postimplantation from microinvasive devices.
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