The preparation of the artery shown in both images is of unknown origin and the staining method is unknown as well.
A fluorescence image of an artery tissue as shown here is not usual. The preparation is more or less evenly green fluorescent colored, because the dye used has attached itself to the structural parts of the preparation. We see a fluorescence color image with details as you might encounter in bright field microscopy with dyes such as e.g. toluidine blue. Such dyes show more or less the same details in the preparation with ordinary bright field microscopy as is shown in the first image.
As mentioned before, visualizing a histological specimen completely by using a fluorescent substance is unusual, because here you apply only one color that shows no specific adhesion, except for proteins, because e.g. fat is uncolored in this preparation. With a normal hematoxylin and eosin staining you have more differentiation, namely in the cell core (DNA, dark blue) and proteins, cytoplasm (pink)
In histology, fluorescence is mainly used after a fluorescent substance has been chemically attached to a specific component present in the tissue.
On the fluorescent image of the preparation the parts of an artery can also be seen. The lumen is filled with green colored red blood cells, then there is a very thin (barely visible) layer of endothelium, the meandering lamina elastica interna (clearly visible) a layer of smooth muscle, the thinner lamina elastica externa (clearly visible), the adventitia (connective tissue) that turns into adipose (fat) tissue.
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