The use of the microelectrode technique for recording extracellular neural signals in vivo has a long and valued tradition in neuroscience 1, 2. The ability to record electrical activity from many brain regions in freely behaving animals is, however, a more recent technology that is becoming increasingly common as the software packages for the acquisition, analysis and discrimination of neural signals becomes more sophisticated and user-friendly 3, 4. The technological advances on the software side have also been accompanied by reductions in the weight and bulk of the implantable devices, which have been scaled down sufficiently for recording in small mammals, such as mice. By using lightweight (mostly plastic) components, researchers are able to construct microdrives that allow for independent positioning of electrodes or tetrodes to target a wide variety of brain regions 5-7. Even deep brain structures, such as the amygdala 6 and the striatum 5, can be routinely targeted with the selection of an appropriately long drive screw. These recording techniques allow researchers to obtain high-fidelity neural signals and are in register with the electrical activity of single neurons recorded intracellularly 8, 9. Using these types of microdrives, we have successfully recorded single-units from mice for up to two months after implantation 10. In addition, the lightweight nature of the devices (approximately 1.5-2.0 g) has resulted in behavioral performance that is comparable to non-implanted mice in many behavioral tasks. In particular, we have demonstrated that implanted mice exhibit normal performance in the novel object recognition task 10 and the object place task (unpublished data).
The use of microdrives coupled to multiple tetrodes allows researchers to monitor and analyze neural activity at the network level while also recording from multiple single-units within the brain. Recording with these tetrodes has several major advantages for unit identification purposes and enables the high accuracy acquisition and discrimination of multiple single-units 11. We describe how to fabricate and gold-plate tetrode bundles and then subsequently load them into driveable electrode carriers. One type of drive carrier we describe is commercially available and the other is a simple, but easily expandable, drive design that can accommodate multiple carriers and tetrode arrangements without a significant investment of resources.
The overall goal of this procedure is to build a micro drive that can be used for brain recordings in mice while they move freely within an experimental chamber. This is accomplished by first preparing a bundle of four micro electrodes into a tede. The second step is to construct the base of the micro drive and assemble the drive components.
Next, the tetros are attached to the drive and are connected to gold pins. The final step is to gold plate the tip of the tetros to lower their impedance and ensure high signal to noise recordings. Ultimately, chronic micro drive arrays are used to record the neural activity of populations of neurons, as well as single neurons in awake behaving animals.
The main advantage of this technique is that it offers a fairly inexpensive and light wave solution for chronic brain recordings in mice and other small mammals. This technology can address key issues in the field of neuroscience, such as how neurons encode information during the performance of behavioral Tasks. We regularly employ this technique to record from neurons from the dorsal hippocampus and ulu, but have also used it to target deeper structures such as the amygdala.
Visual demonstration o