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Using a near-infrared (NIR) light flood-illumination imager equipped with a high-speed (120 Hz) CCD camera, we demonstrated optical imaging of stimulus-evoked retinal activity in isolated, but intact, frog eye. Both fast and slow transient intrinsic optical signals (IOSs) were observed. Fast optical response occurred immediately after the stimulus onset, could reach peak magnitude within 100 ms, and correlated tightly with ON and OFF edges of the visible light stimulus; while slow optical response lasted a relatively long time (many seconds). High-resolution images revealed both positive (increasing) and negative (decreasing) IOSs, and dynamic optical change at individual CCD pixels could often exceed 10% of the background light intensity. Our experiment on isolated eye suggests that further development of fast, high (sub-cellular) resolution fundus imager will allow robust detection of fast IOSs in vivo, and thus allow noninvasive, three-dimensional evaluation of retinal neural function.

In vivo fiber photometry is a powerful technique to analyze the dynamics of population neurons during functional study of neuroscience. Here, we introduced a detailed protocol for fiber photometry-based calcium recording in freely moving mice, covering from virus injection, fiber stub insertion, optogenetical stimulation to data procurement and analysis. Furthermore, we applied this protocol to explore neuronal activity of mice lateral-posterior (LP) thalamic nucleus in response to optogenetical stimulation of primary visual cortex (V1) neurons, and explore axon clusters activity of optogenetically evoked V1 neurons. Final confirmation of virus-based protein expression in V1 and precise fiber insertion indicated that the surgery procedure of this protocol is reliable for functional calcium recording. The scripts for data analysis and some tips in our protocol are provided in details. Together, this protocol is simple, low-cost, and effective for neuronal activity detection by fiber photometry, which will help neuroscience researchers to carry out functional and behavioral study in vivo.

Neural activity that occur during motor movement, speech, thought, and various other events can be observed in the form of brainwaves composed of synchronized electrical pulses emitted from adjoining communicative neurons. Observations of these brainwaves have been made possible through neurodevices, which can detect changes in electrical and/or mechanical parameters. For decades, the field of neuroscience has been enriched by the utilization of neurotechnologies at the microscale, which has begun to gain further enhancement with the introduction of nanotechnology. For example, microelectrodes were initially used for only extracellular measurements, but over the past decade, developments have been made to also record intracellular signals. Likewise, nanoknives, which gained popularity due to their versatility, can now be used for both fabricating bio-Micro-Electro-Mechanical Systems (MEMS) and also as a neurosurgery tool. Thus, considerable efforts have been made over the years to make micro- and nanosystems reliable, accurate, and sensitive to neural activity. In the late 20th century, several sophisticated technologies, including magnetic resonance imaging (MRI), computed tomography (CT), and intracranial pressure (ICP) monitoring have been integrated with MEMS. Furthermore, existing biotechnologies are being miniaturized at both the system and component level. For example, there is a remarkable interest in the field of neuroscience to utilize microfluidic technology as a diagnostic tool using specimens such as cerebrospinal fluid (CSF). Microfluidic devices are also employed as biocompatible drug delivery systems to target cells, tissues, and organs. This paper summarizes the recent developments in micro- and nano-scale neurotechnologies, including devices, fabrication processes, detection methods, their implementation challenges, in neural stimulation, monitoring, and drug delivery.

This review discusses recent developments in micro and nanotechnologies, fabrication methods, and their implementation in neuroimaging, neurostimulation, monitoring of neural activities, and neural drug delivery.