Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity
Jordan M Burnham,1 Monali Sakhalkar,1 Marlyn P Langford,1 Chanping Liang,1 Thomas B Redens,1 Sushil K Jain21Department of Ophthalmology, 2Department of Pediatrics, Louisiana State University Health Sciences Center, Shreveport, LA, USABackground: Diabetes-related eye disease is due in part to oxidati...
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Dove Medical Press
2013
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oai:doaj.org-article:b8ad029b8f834b38a986b3bf570125d72021-12-02T00:15:25ZDiabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity1177-54671177-5483https://doaj.org/article/b8ad029b8f834b38a986b3bf570125d72013-01-01T00:00:00Zhttp://www.dovepress.com/diabetic-and-non-diabetic-human-cornea-and-tear-gamma-glutamyl-transpe-a11929https://doaj.org/toc/1177-5467https://doaj.org/toc/1177-5483Jordan M Burnham,1 Monali Sakhalkar,1 Marlyn P Langford,1 Chanping Liang,1 Thomas B Redens,1 Sushil K Jain21Department of Ophthalmology, 2Department of Pediatrics, Louisiana State University Health Sciences Center, Shreveport, LA, USABackground: 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.Keywords: cornea, diabetes, endothelium, epithelium, eye, γ-glutamyl transpeptidase, tear, oxidative stressBurnham JMSakhalkar MLangford MPLiang CRedens TBJain SKDove Medical PressarticleOphthalmologyRE1-994ENClinical Ophthalmology, Vol 2013, Iss default, Pp 99-107 (2013) |
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Ophthalmology RE1-994 Burnham JM Sakhalkar M Langford MP Liang C Redens TB Jain SK Diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity |
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Jordan M Burnham,1 Monali Sakhalkar,1 Marlyn P Langford,1 Chanping Liang,1 Thomas B Redens,1 Sushil K Jain21Department of Ophthalmology, 2Department of Pediatrics, Louisiana State University Health Sciences Center, Shreveport, LA, USABackground: 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.Keywords: cornea, diabetes, endothelium, epithelium, eye, γ-glutamyl transpeptidase, tear, oxidative stress |
format |
article |
author |
Burnham JM Sakhalkar M Langford MP Liang C Redens TB Jain SK |
author_facet |
Burnham JM Sakhalkar M Langford MP Liang C Redens TB Jain SK |
author_sort |
Burnham JM |
title |
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_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_sort |
diabetic and non-diabetic human cornea and tear γ-glutamyl transpeptidase activity |
publisher |
Dove Medical Press |
publishDate |
2013 |
url |
https://doaj.org/article/b8ad029b8f834b38a986b3bf570125d7 |
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