The Pineal Gland (PG) is a part of the human brain epithalamus that plays an important role in sleep, circadian rhythm, immunity, and reproduction. PG parenchyma is composed mainly of pinealocytes secreting melatonin.
The formation of concrements in human pineal gland (PG) is a physiological process. However, according to many researchers, it is associated with the involution of PG structures. The calcium deposits in PG can interfere with normal function of the organ and can be associated with different health disorders I ncluding serious neurological diseases.
XPCT imaging revealed high-resolution details of age-related PG alteration and noticeable degenerative change in both concrements and soft tissue of PGs with neuropathology. In particular, we observed a hollow core and separated layers as well as deep ragged cracks in PG concrements of Alzheimer’s disease and vascular dementia samples.
The mammalian olfactory bulb (OB) is a part of the forebrain involved in olfaction. It plays an essential role in the sense of smell. OB has a laminar structure.
XPCT offers sufficient resolution and contrast to identify single cells in large volumes of the brain. The numerous microanatomical structures detectable in XPCT image of the OB, however, greatly complicate the manual delineation of OB neuronal cell layers. To address the challenging problem of fully automated segmentation of XPCT images of human OB morphological layers convolutional neural networks (CNN) were used to segment XPCT image of native unstained human OB.
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