» Articles » PMID: 9243096

The Relationship Between Accumulation of Advanced Glycation End Products and Expression of Vascular Endothelial Growth Factor in Human Diabetic Retinas

Overview
Journal Diabetologia
Specialty Endocrinology
Date 1997 Jul 1
PMID 9243096
Citations 51
Authors
Affiliations
Soon will be listed here.
Abstract

Both advanced glycation end products and vascular endothelial growth factor are believed to play a role in the pathogenesis of diabetic retinopathy. It is known that vascular endothelial growth factor causes retinal neovascularization and a breakdown of the blood-retinal barrier; how advanced glycation end products affect the retina, however, remains largely unclear. The substance-Ne-(carboxymethyl)lysine is a major immunologic epitope, i.e. a dominant advanced glycation end products antigen. We generated an anti-Ne-(carboxymethyl)lysine antibody to investigate the relationship between the localization of advanced glycation end products and that of vascular endothelial growth factor in 27 human diabetic retinas by immunohistochemistry. Nine control retinas were also examined. In all 27 diabetic retinas, Ne-(carboxymethyl)lysine was located in the thickened vascular wall. In 19 of the 27 retinas, strand-shaped Ne-(carboxymethyl)lysine immunoreactivity was also observed around the vessels. In all 27 diabetic retinas, vascular endothelial growth factor revealed a distribution pattern similar to that of Ne-(carboxymethyl)lysine. Vascular endothelial growth factor was also located in the vascular wall and in the perivascular area. Neither Ne-(carboxymethyl)lysine nor vascular endothelial growth factor immunoreactivity was detected in the 9 control retinas. Vessels with positive immunoreactivity for Ne-(carboxymethyl)lysine and/or vascular endothelial growth factor were counted. A general association was noted between accumulation of Ne-(carboxymethyl)lysine and expression of vascular endothelial growth factor in the eyes with non-proliferative diabetic retinopathy (p < 0.01) and proliferative diabetic retinopathy (p < 0.05).

Citing Articles

Inhibition of Advanced Glycation End Products (AGEs) by Fermented Foods Using Lactic Acid Bacteria.

Nakashima Y, Kinoshita H Methods Mol Biol. 2024; 2851:135-141.

PMID: 39210178 DOI: 10.1007/978-1-0716-4096-8_12.


Glucoselysine, a unique advanced glycation end-product of the polyol pathway and its association with vascular complications in type 2 diabetes.

Yamaguchi H, Matsumura T, Sugawa H, Niimi N, Sango K, Nagai R J Biol Chem. 2024; 300(7):107479.

PMID: 38879006 PMC: 11283207. DOI: 10.1016/j.jbc.2024.107479.


Revisiting Retinal Degeneration Hallmarks: Insights from Molecular Markers and Therapy Perspectives.

Rosa J, Disner G, Pinto F, Lima C, Lopes-Ferreira M Int J Mol Sci. 2023; 24(17).

PMID: 37685886 PMC: 10488251. DOI: 10.3390/ijms241713079.


Changes in the AGE/Macrophage/TNF-α Pathway Affect Skin Dryness during KK-Ay/Tajcl Mice Aging.

Hiramoto K, Imai M, Tanaka S, Ooi K Life (Basel). 2023; 13(6).

PMID: 37374121 PMC: 10304917. DOI: 10.3390/life13061339.


Nε-(1-Carboxymethyl)-L-lysine, an advanced glycation end product, exerts malignancy on chondrosarcoma via the activation of cancer stemness.

Chang T, Lan K, Wu C, Sheu M, Yang R, Liu S Arch Toxicol. 2023; 97(8):2231-2244.

PMID: 37314482 DOI: 10.1007/s00204-023-03539-8.