| Literature DB >> 27421861 |
Ryoji Nagai1, Jun-Ichi Shirakawa2, Rei-Ichi Ohno2, Kota Hatano2, Hikari Sugawa2, Shoutaro Arakawa2,3, Kenta Ichimaru2, Shoh Kinoshita2, Noriyuki Sakata4, Mime Nagai2.
Abstract
Advanced glycation end-products (AGEs) of the Maillard reaction were originally measured according to their fluorescent and browning properties. A subsequent study with instrumental analyses such as high-performance liquid chromatography and gas chromatography mass spectrometry more clearly demonstrated the involvement of each AGE structure in pathological conditions. Furthermore, immunochemical methods have also been developed to clarify the localization of AGEs in tissues and measurement of AGEs in multiple clinical samples. Although the involvement of AGEs in age-related diseases has progressed due to immunochemical techniques, the relationship between AGE structure and diseases has not been clear because little was known about the epitope structure of each anti-AGE antibody. However, the development of epitope-identified antibodies against AGEs has made it possible to clarify AGE structures involved in diseases. This review discusses not only the usability of anti-AGE antibodies to evaluate AGEs and disease pathology and screen AGE inhibitors, but also describes their usage.Entities:
Keywords: AGEs; Anti-AGEs antibody; Atherosclerosis; CML; Diabetes; Lifestyle-related diseases
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Year: 2016 PMID: 27421861 DOI: 10.1007/s10719-016-9708-9
Source DB: PubMed Journal: Glycoconj J ISSN: 0282-0080 Impact factor: 2.916