The video demonstrates how to set up a counterbalance system for a microdrive implanted in a mouse. It involves connecting a PVC pipe, positioning arms above the cage, attaching the microdrive with a corresponding weight, and ensuring proper access for the mouse while securing the setup to the electronic interface board.

recovery after micro-drive implantation

Микродрайвовый имплантат для записи ежедневной нейронной активности у молодых мышей

The brain undergoes large-scale changes during the critical developmental windows of childhood and adolescence1,2,3. Many neurologic and psychiatric diseases, including autism and schizophrenia, first manifest behaviorally and biologically during this period of juvenile and adolescent brain development4,5,6. While much is known regarding the cellular, synaptic, and genetic changes that occur across early development, comparatively little is known regarding how circuit- or network-level processes change throughout this time window. Importantly, circuit-level brain function, which ultimately underlies complex behaviors, memory, and cognition, is a non-predictable, emergent property of cellular and synaptic function7,8,9,10. Thus, to fully understand network-level brain function, it is necessary to directly study neural activity at the level of an intact neural circuit. In addition, to identify how brain activity is altered throughout the progression of neuropsychiatric disorders, it is critical to examine network activity in a valid disease model during the specific temporal window when the behavioral phenotypes of the disease manifest and to track the observed changes as they persist into adulthood.
One of the most common and powerful scientific model organisms is the mouse, with large numbers of unique genetic strains that model neurodevelopmental disorders with age-dependent onset of the behavioral and/or mnemonic phenotypes11,12,13,14,15,16,17,18,19,20,21. While it is challenging to correlate precise developmental time points between the brains of humans and mice, morphological and behavioral comparisons indicate that p20-p21 mice represent the human ages of 2-3 years old, and p25-p35 mice represent the human ages of 11-14 years old, with mice likely reaching the developmental equivalent of a human 20 year old adult by p603,22. Thus, to better understand how the juvenile brain develops and to identify how the neural networks of the brain become dysfunctional in diseases like autism or schizophrenia, it would be ideal to directly monitor brain activity in vivo in mice across the ages of 20 days to 60 days old.
However, a fundamental challenge in monitoring brain activity across early development in mice is the small size and relative weakness of juvenile mice. The chronic implantation of electrodes, which is necessary for longitudinal studies of brain development, typically requires large, bulky housing to protect the fine electrode wires and interface boards23,24, and the implants must be firmly attached to the mouse skull, which is thinner and less rigid in young mice due to reduced ossification. Thus, virtually all studies of in vivo rodent physiology have been performed in adult subjects due to their relative size, strength, and skull thickness. To date, most studies exploring in vivo juvenile rodent brain physiology have been performed in wild-type juvenile rats, which necessarily limits the ability to experimentally monitor juvenile brain function in a freely behaving model of a human disorder25,26,27,28,29,30.
This manuscript describes novel implant housing, a surgical implantation procedure, and a post-surgery recovery strategy to chronically study the long-term (up to 4 or more weeks) in vivo brain function of juvenile mice across a developmentally critical time window (p20 to p60 and beyond). The implantation procedure allows for the reliable, permanent affixation of the electrodes to the skulls of juvenile mice. Furthermore, the micro-drive design is lightweight, as this micro-drive weighs ~4-6 g when fully assembled, and due to the minimal counterbalancing required to offset the weight of the implant, it does not impact the behavioral performance of juvenile mice during typical behavioral paradigms.

В центре внимания автора: Легкий имплант привода для записи хронических тетродов у молодых мышей  

Легкий имплантат привода для хронической записи тетрода у молодых мышей

We're interested in understanding how the brain operates at a network level. This method is our attempt to explore the development of brain networks to identify developmental alterations in age dependent diseases like autism, schizophrenia or bipolar disorder. The silicon probe technology provides a simpler, more consistent method to record network activity in vivo.But despite this, chronic tetra recordings do offer some advantages over silicon probes, such as simultaneously recording over a broader spatial distribution of brain regions. Chronic recordings pose a unique challenge to in vivo electrophysiology due to several factors, including gliosis at the recording sites, movement of the recording site over time or failure of the attachment method. Our recent work demonstrated that the sweeps encoded by the theta oscillation of the hippocampus during active movement of the animal every hundred milliseconds or so iteratively cycle forward, prospectively evaluating possible future states and backwards retrospectively evaluating prior actions.Performing these in vivo recordings in juvenile mice poses several engineering challenges due to the small size of the mice, their relative weakness and the lack of development in their skull. Our methodology overcomes these limitations and allows us to chronically record network level activity daily in the developing mouse brain. Besides recording chronically in juvenile mice, our method allows us to record from up to 16 distinct bilateral brain regions irrespective of the spatial relationship of those regions.These developments will allow us to identify how networks establish functional communication across developments, both in the healthy brain and in mouse models of neurodevelopmental disorders, like autism spectrum disorders.

Watch this Scientific Journal Video about Recovery after Micro-Drive Implantation at JoVE.com

Recovery after Micro-Drive Implantation  

Восстановление после имплантации микропривода

Для начала настройте систему противовеса, подключив трубу из ПВХ диаметром 0,75 дюйма. Вставьте один рычаг системы через отверстия в крышке клетки. Поместите второй рычаг поверх крышки клетки, а третий рычаг вытяните над клеткой и за ее пределы.Закончите, закрыв самую верхнюю руку. После имплантации микропривода на цель мыши прикрепите микропривод к системе противовесов с помощью противовеса, равного весу микропривода и костных винтов. Закрепите прочную нить или леску от платы электронного интерфейса к противовесу, который висит над самым верхним рычагом.Наконец, убедитесь, что противовес надежно подключен к электронной интерфейсной плате микропривода и что мышь имеет полный доступ к клетке.

Research

JoVE Journal

Neuroscience

Recovery after Micro-Drive Implantation

315 Views.  UT Southwestern Medical Center. Для начала настройте систему противовеса, подключив трубу из ПВХ диаметром 0,75 дюйма. Вставьте один рычаг системы через отверстия в крышке клетки. Поместите второй рычаг поверх крышки клетки, а третий рычаг вытяните над клеткой и за ее пределы.Закончите, закрыв самую ?...

Video: Recovery after Micro-Drive Implantation  

A Lightweight Drive Implant for Chronic Tetrode Recordings in Juvenile Mice

In vivo electrophysiology provides unparalleled insight into the sub-second-level circuit dynamics of the intact brain and represents a method of particular importance for studying mouse models of human neuropsychiatric disorders. However, such methods often require large cranial implants, which cannot be used in mice at early developmental time points. As such, virtually no studies of in vivo physiology have been performed in freely behaving infant or juvenile mice, despite the fact that a better understanding of neurological development in this critical window would likely provide unique insights into age-dependent developmental disorders such as autism or schizophrenia. Here, a micro-drive design, surgical implantation procedure, and post-surgery recovery strategy are described that allow for chronic field and single-unit recordings from multiple brain regions simultaneously in mice as they age from postnatal day 20 (p20) to postnatal day 60 (p60) and beyond, a time window roughly corresponding to the human ages of 2 years old through to adulthood. The number of recording electrodes and final recording sites can be easily modified and expanded, thus allowing flexible experimental control of the in vivo monitoring of behavior- or disease-relevant brain regions across development.

Here, we describe a micro-drive design, surgical implantation procedure, and post-surgery recovery strategy that allow for chronic field and single-unit recordings from multiple brain regions simultaneously in juvenile and adolescent mice across a critical developmental window from postnatal day 20 (p20) to postnatal day 60 (p60) and beyond.

In vivo electrophysiology provides unparalleled insight into the sub-second-level circuit dynamics of the intact brain and represents a method of ...

Micro-Drive Design and Construction

After digitally designing and printing the micro drive, attach two screw attachments to each tetrode advancing screw one above and one below the ridge. Hold the screw attachments together with gel cyanoacrylate. Ensure that the screw attachments do not move in the longitudinal axis of the screw, but can rotate freely with minimal resistance.Extend each polyamide section through the output holes on the micro drive cannula by a few millimeters. Secure the polyamide to the cannula using a clean 30 gauge needle in small amounts of liquid cyanoacrylate, being careful not to let it enter the inside of the polyamide tube. Retrieve the large polyamide tubes from the top of the micro drive cannula and pass them through the large polyamide holes in the micro drive body.Gently push the micro drive cannula and micro drive body together until they are adjacent and the cannula body attachment tabs interlock. Secure the micro drive body and the micro drive cannula with cyanoacrylate. Using a new sharp razor blade, severe the large polyamide tube ends extruding from the bottom of the cannula output holes, ensuring the cut is precisely at the cannula's base, making the tubes and cannula bottom flush.With sharp scissors, cut the large polyamide tubing just above the edge of the inner rim of the drive body at a 45 degree angle. Cut small polyamide tubing into four centimeter long sections. Pass the small polyamide sections through the large polyamide tubing already mounted in the micro drive and ensure that excess small polyamide tubing protrudes from the top and bottom.Secure the small polyamide tubes to the screw attachments with cyanoacrylate. Avoid letting any cyanoacrylate enter the large or small polyamide tubes. Using a new sharp razor blade, sever the small polyamide tube ends extruding from the bottom of the cannula holes.Ensure the cut is at the cannula's base and clean with nothing blocking the polyamide tube hole. Then use sharp scissors to cut the top of the small polyamide. a few millimeters above the top of the screw attachment at a 45 degree angle, ensuring the cut is clean.Using ceramic or rubber tipped forceps, carefully pass a tetrode through one of the small polyamide tubes, leaving approximately two centimeters protruding from the top of the small polyamide tube. Secure the tetrode to the top of the small polyamide tube with liquid cyanoacrylate. Retract the screw until it is near the top of the drive.Grab the tetrode wire protruding from the bottom of the drive and gently kink it at the point where it emerges from the cannula. Fully advance the screw into the drive. Using sharp scissors, cut the tetrode wire just above the kink.Then inspect it under a microscope to ensure the cut is clean and the metal of all four tetrodes is exposed. Finally, connect each electrode of each tetrode to the appropriate port on the electronic interface board. Tightly wind one bone screw with a thin, highly conductive wire that will be ground and attached to the electronic interface board.

Проектирование и строительство микроприводов

Surgical Implantation of the Micro-Drive on the Mouse Skull

After preparing the mouse for surgery and exposing the skull, place the bone screws in the extreme lateral, rostral or caudal portions of the skull where the bone is thickest and the bone screws are sufficiently far away from the micro drive implant. Use a scalpel blade or drill bit to score the skull near the bone screw hole locations, providing a rough surface for the liquid cyanoacrylate to bind. Then thread each bone screw into place, careful not to pierce the underlying dura.Using a sterile 30-gauge needle, apply liquid cyanoacrylate around each bone screw, thickening the skull where the bone screws have been attached. Ensure that no cyanoacrylate enters the exposed dura above the recording sites.

Хирургическая имплантация микронакопителя на череп мыши

To begin, set up the counterbalance system by connecting a 0.75-inch-diameter PVC pipe. Insert one arm of the system through the holes in the cage lid. Place the second arm on top of the cage lid, and extend the third arm above and beyond the cage.Finish by capping the top-most arm. After implanting the microdrive on the mouse goal, attach the microdrive to the counterbalance system using a counterbalance weight equal to the weight of the microdrive and bone screws. Secure a strong thread or fishing line from the electronic interface board to the counterbalance weight which hangs over the top-most arm.Finally, ensure the counterbalance is firmly connected to the microdrive electronic interface board and that the mouse has full access to the cage.