Abstract: The present invention provides the visualization of the fiber architecture in the nervous tissue without staining. The major principle of the method is to make the neural tissue transparent in normal light, and to utilize the ability of neuronal fibers to deflect and deviate light directed from the side to render them visible. The method involves the preparation of thick sections (more than 200 mm) of the nervous tissue, their fixation in paraformaldehyde and dehydration in ethanol. Oil of wintergreen (methyl salicylate) is utilized to make the tissue transparent under normal (bright-field) light. Dark-field illumination is used to create illuminating rays of light arriving at an angle exceeding the collecting angle of the objective lens, thus causing only the axonal pathways to be visible as a bright silver silhouette against a dark background.

Abstract: The present invention provides the visualization of the fiber architecture in the nervous tissue without staining. The major principle of the method is to make the neural tissue transparent in normal light, and to utilize the ability of neuronal fibers to deflect and deviate light directed from the side to render them visible. The method involves the preparation of thick sections (more than 200 mm) of the nervous tissue, their fixation in paraformaldehyde and dehydration in ethanol. Oil of wintergreen (methyl salicylate) is utilized to make the tissue transparent under normal (bright-field) light. Dark-field illumination is used to create illuminating rays of light arriving at an angle exceeding the collecting angle of the objective lens, thus causing only the axonal pathways to be visible as a bright silver silhouette against a dark background.