Prion protein (PrP) is highly conserved and is expressed in most tissues in a developmental stage-specific manner. Glycosylated cellular prion protein (PrP) is found in most cells and subcellular areas as a physiological regulating molecule. On the other hand, the amyloid form of PrP, scrapie PrP (PrP), causes transmissible pathogenesis in the central nervous system and induces degeneration of the nervous system.
View Article and Find Full Text PDFCellular prion protein (PrP) encoded at gene is well-known to form a misfolded isoform, termed scrapie PrP (PrP) that cause transmissible degenerative diseases in central nervous system. The physiological role of PrP has been proposed by many studies, showing that PrP interacts with various intracellular, membrane, and extracellular molecules including mitochondrial inner membrane as a scaffold. PrP is expressed in most cell types including reproductive organs.
View Article and Find Full Text PDFPreviously, we showed that a chronic-low-dose nonylphenol (NP) exposure resulted in histological changes with sexually dimorphic pattern in rat adrenal glands. We hypothesized that such structural changes are closely related to the hormonal secretory patterns. To test this hypothesis, we developed the short-term adrenal incubation method, and measured the levels of catecholamines and cortical steroids using the high-performance liquid chromatography with electrochemical detection (HPLC-ECD) and specific enzyme-linked immunosorbent assay, respectively.
View Article and Find Full Text PDFJ Enzyme Inhib Med Chem
December 2023