Multiphoton imaging of the monosachharide induced formation of fluorescent advanced glycation end products in tissues

Author:

Lin Chih‐Ju1ORCID,Mondal Sohidul1ORCID,Lee Sheng‐Lin1,Kang Jeon‐Woong2,So Peter T. C.234,Dong Chen Yuan1ORCID

Affiliation:

1. Department of Physics National Taiwan University Taipei Taiwan, ROC

2. Laser Biomedical Research Center, G. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology Cambridge Massachusetts USA

3. Department of Mechanical Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA

4. Department of Biological Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA

Abstract

AbstractWe studied the in vitro rate of fluorescent advanced glycation end products (fAGEs) formation with multiphoton microscopy in different porcine tissues (aorta, cornea, kidney, dermis, and tendon). These tissues were treated with d‐glucose, d‐galactose, and d‐fructose, three primary monosaccharides found in human diets. We found that the use of d‐fructose resulted in the highest glycation rate, followed by d‐galactose and then d‐glucose. Moreover, compared to non‐collagen tissue constituents such as elastic fibers and cells, the rate of tissue glycation was consistently higher in collagen, suggesting that collagen is a more sensitive target for fAGE formation. However, we also found that collagen in different tissues exhibits different rates of fAGE formation, with slower rates observed in tightly packed tissues such as cornea and tendon. Our study suggests that for fAGE to be developed into a long‐term glycemic biomarker, loosely organized collagen tissues located in the proximity of vasculature may be the best targets.

Funder

Ministry of Science and Technology, Taiwan

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,General Biochemistry, Genetics and Molecular Biology,General Materials Science,General Chemistry

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1. Multiphoton imaging of the formation of fluorescent advanced glycation end products in tissues;Multiphoton Microscopy in the Biomedical Sciences XXIV;2024-03-12

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