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Glucagon-like peptide-1 receptor expression in the human eye.
- Source :
-
Diabetes, obesity & metabolism [Diabetes Obes Metab] 2018 Sep; Vol. 20 (9), pp. 2304-2308. Date of Electronic Publication: 2018 May 24. - Publication Year :
- 2018
-
Abstract
- Semaglutide is a human glucagon-like peptide-1 (GLP-1) analogue that is in development for the treatment of type 2 diabetes. In the pre-approval cardiovascular outcomes trial SUSTAIN 6, semaglutide was associated with a significant increase in the risk of diabetic retinopathy (DR) complications vs placebo. GLP-1 receptor (GLP-1R) expression has previously been demonstrated in the retina in animals and humans; however, antibodies used to detect expression have been documented to be non-specific and fail to detect the GLP-1R using immunohistochemistry (IHC), a problem common for many G-protein coupled receptors. Using a validated GLP-1R antibody for IHC and in situ hybridization for GLP-1R mRNA in normal human eyes, GLP-1Rs were detected in a small fraction of neurons in the ganglion cell layer. In advanced stages of DR, GLP-1R expression was not detected at the protein or mRNA level. Specifically, no GLP-1R expression was found in the eyes of people with long-standing proliferative DR (PDR). In conclusion, GLP-1R expression is low in normal human eyes and was not detected in eyes exhibiting advanced stages of PDR.<br /> (© 2018 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.)
- Subjects :
- Adult
Aged
Diabetes Mellitus, Type 2 complications
Diabetic Retinopathy etiology
Female
Humans
Immunohistochemistry
In Situ Hybridization
Male
Middle Aged
RNA, Messenger metabolism
Diabetes Mellitus, Type 2 metabolism
Diabetic Retinopathy metabolism
Eye metabolism
Glucagon-Like Peptide-1 Receptor metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1463-1326
- Volume :
- 20
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Diabetes, obesity & metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 29707863
- Full Text :
- https://doi.org/10.1111/dom.13339