Protocol for in vivo recording of neural activity in deep structures of mice brain via gradient lenses by calcium imaging.

Abstract

Calcium (Ca²⁺) imaging is a viable approach for imaging neuronal activity patterns in local brain circuits in living animals. Here, we present a protocol for gradient lens implantation in deep brain structures followed by in vivo Ca²⁺ imaging. We describe in detail the steps for surgery preparation, followed by lens implantation, setup for awake head-fixed imaging, and the recording process. For complete details on the use and execution of this protocol, please refer to Cherepanov et al.¹.