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Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity
BACKGROUND: Diabetes-related eye disease is due in part to oxidative stress. Gamma-glutamyl transpeptidase (GGT) is a γ-glutamyl cycle enzyme that protects against oxidative stress via glutathione recapture. This study investigates corneal and Schirmer tears GGT activity in diabetic and non-diabetic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3548439/ https://www.ncbi.nlm.nih.gov/pubmed/23345964 http://dx.doi.org/10.2147/OPTH.S37546 |
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author | Burnham, Jordan M Sakhalkar, Monali Langford, Marlyn P Liang, Chanping Redens, Thomas B Jain, Sushil K |
author_facet | Burnham, Jordan M Sakhalkar, Monali Langford, Marlyn P Liang, Chanping Redens, Thomas B Jain, Sushil K |
author_sort | Burnham, Jordan M |
collection | PubMed |
description | BACKGROUND: Diabetes-related eye disease is due in part to oxidative stress. Gamma-glutamyl transpeptidase (GGT) is a γ-glutamyl cycle enzyme that protects against oxidative stress via glutathione recapture. This study investigates corneal and Schirmer tears GGT activity in diabetic and non-diabetic adults aged 50 to 83 years old. METHODS: GGT activity was determined by colorimetric assay on 50 corneas from 14 diabetic (without keratopathy) and 20 non-diabetic donors and on Schirmer type 1 test strips (no anesthesia) of 14 diabetic and 14 non-diabetic subjects. RESULTS: Type 1 (T1) diabetic cornea GGT activity was 40% lower than Type 2 (T2) diabetic cornea GGT activity (P = 0.04), but GGT activity was similar for corneas (without keratopathy) from diabetic and non-diabetic donors (P ≥ 0.44 for all). The number of endothelial cells/unit of GGT activity in diabetic corneas was 22% higher (P = 0.1) than in non-diabetic corneas. GGT activity per Schirmer strip and GGT activity per mm of tears were 36% and 50% higher (P ≤ 0.008 for all) for non-diabetic (tear volume dependent) than diabetic donors (tear volume independent), respectively. GGT activity per mm was 50% lower in T1 than T2 diabetics (P = 0.02). Higher tear GGT activity in non-diabetic than diabetic females (P ≤ 0.05) was due to higher GGT activity in the African American females. CONCLUSION: GGT activity was less in T1 than T2 diabetics, but comparable to non-diabetic corneas. Schirmer tear GGT activity in diabetic eyes was tear volume independent, less in T1 than T2, lower than in tear volume dependent, non-diabetic female eyes. Low cornea and tear GGT activity suggests loss of antioxidant potential and supports ocular antioxidant therapy for diabetic patients. |
format | Online Article Text |
id | pubmed-3548439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35484392013-01-23 Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity Burnham, Jordan M Sakhalkar, Monali Langford, Marlyn P Liang, Chanping Redens, Thomas B Jain, Sushil K Clin Ophthalmol Original Research BACKGROUND: Diabetes-related eye disease is due in part to oxidative stress. Gamma-glutamyl transpeptidase (GGT) is a γ-glutamyl cycle enzyme that protects against oxidative stress via glutathione recapture. This study investigates corneal and Schirmer tears GGT activity in diabetic and non-diabetic adults aged 50 to 83 years old. METHODS: GGT activity was determined by colorimetric assay on 50 corneas from 14 diabetic (without keratopathy) and 20 non-diabetic donors and on Schirmer type 1 test strips (no anesthesia) of 14 diabetic and 14 non-diabetic subjects. RESULTS: Type 1 (T1) diabetic cornea GGT activity was 40% lower than Type 2 (T2) diabetic cornea GGT activity (P = 0.04), but GGT activity was similar for corneas (without keratopathy) from diabetic and non-diabetic donors (P ≥ 0.44 for all). The number of endothelial cells/unit of GGT activity in diabetic corneas was 22% higher (P = 0.1) than in non-diabetic corneas. GGT activity per Schirmer strip and GGT activity per mm of tears were 36% and 50% higher (P ≤ 0.008 for all) for non-diabetic (tear volume dependent) than diabetic donors (tear volume independent), respectively. GGT activity per mm was 50% lower in T1 than T2 diabetics (P = 0.02). Higher tear GGT activity in non-diabetic than diabetic females (P ≤ 0.05) was due to higher GGT activity in the African American females. CONCLUSION: GGT activity was less in T1 than T2 diabetics, but comparable to non-diabetic corneas. Schirmer tear GGT activity in diabetic eyes was tear volume independent, less in T1 than T2, lower than in tear volume dependent, non-diabetic female eyes. Low cornea and tear GGT activity suggests loss of antioxidant potential and supports ocular antioxidant therapy for diabetic patients. Dove Medical Press 2013 2013-01-10 /pmc/articles/PMC3548439/ /pubmed/23345964 http://dx.doi.org/10.2147/OPTH.S37546 Text en © 2013 Burnham et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Burnham, Jordan M Sakhalkar, Monali Langford, Marlyn P Liang, Chanping Redens, Thomas B Jain, Sushil K Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity |
title | Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity |
title_full | Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity |
title_fullStr | Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity |
title_full_unstemmed | Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity |
title_short | Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity |
title_sort | diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3548439/ https://www.ncbi.nlm.nih.gov/pubmed/23345964 http://dx.doi.org/10.2147/OPTH.S37546 |
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