Resumen
Due to the high possibility of mechanical damage to the underlying tissues attached to the rat skull during a craniectomy, previously described methods for visualization of the rat brain in vivo are limited to unilateral craniotomies and small cranial windows, often measuring 4?5 mm. Here, we introduce a novel method for producing bilateral craniectomies that encompass frontal, parietal, and temporal bones via sequential thinning of the skull while preserving the dura. This procedure requires the removal of a portion of the temporalis muscle bilaterally, which adds an additional 2?3 mm exposure within the cranial opening. Therefore, while this surgery can be performed in vivo, it is strictly non-survival. By creating large, bilateral craniectomies, this methodology carries several key advantages, such as the opportunity afforded to test innovate imaging modalities that require a larger field of view and also the use of the contralateral hemisphere as a control for neurophysiological studies.