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ALDH2/SIRT1 Contributes to Type 1 and Type 2 Diabetes-Induced Retinopathy through Depressing Oxidative Stress.
- Source :
-
Oxidative medicine and cellular longevity [Oxid Med Cell Longev] 2021 Oct 23; Vol. 2021, pp. 1641717. Date of Electronic Publication: 2021 Oct 23 (Print Publication: 2021). - Publication Year :
- 2021
-
Abstract
- Clinical observations found vision-threatening diabetic retinopathy (DR) occurs in both type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus (T2DM) patients, but T1DM may perform more progressive retinal abnormalities at the same diabetic duration with or without clinical retinopathy. In the present study, T1DM and T2DM patients without manifestations of DR were included in our preliminary clinical retrospective observation study to investigate the differentiated retinal function at the preclinical stage. Then, T1DM and T2DM rat models with 12-week diabetic duration were constructed to explore the potential mechanism of the discrepancy in retinal disorders. Our data demonstrated T1DM patients presented a poor retinal function, a higher allele frequency for ALDH2GA/AA, and a depressed aldehyde dehydrogenase 2 (ALDH2) activity and silent information regulator 1 (SIRT1) level, compared to T2DM individuals. In line with this, higher amplitudes of neurovascular function-related waves of electroretinograms were found in T2DM rats. Furthermore, the retinal outer nuclear layers were reduced in T1DM rats. The levels of retinal oxidative stress biomarkers including total reactive oxygen species, NADPH oxidase 4 and mitochondrial DNA damage, and inflammatory indicators covering inducible/endothelial nitric acid synthase ratio, interleukin-1, and interleukin-6 were obviously elevated. Notably, the level of retinal ALDH2 and SIRT1 in T1DM rats was significantly diminished, while the expression of neovascularization factors was dramatically enhanced compared to T2DM. Together, our data indicated that the ALDH2/SIRT1 deficiency resulted in prominent oxidative stress and was in association with DR progression. Moreover, a differentiating ALDH2/SIRT1 expression may be responsible for the dissimilar severity of DR pathological processes in chronic inflammatory-related T1DM and T2DM.<br />Competing Interests: All authors have read the journal's policy on authorship agreement and conflict of interest. The authors have declared that no conflict of interest exists.<br /> (Copyright © 2021 Mengshan He et al.)
- Subjects :
- Adult
Aldehyde Dehydrogenase, Mitochondrial genetics
Animals
Diabetes Mellitus, Experimental enzymology
Diabetes Mellitus, Experimental genetics
Diabetes Mellitus, Type 1 enzymology
Diabetes Mellitus, Type 1 genetics
Diabetes Mellitus, Type 2 enzymology
Diabetes Mellitus, Type 2 genetics
Diabetic Retinopathy enzymology
Diabetic Retinopathy genetics
Disease Models, Animal
Disease Progression
Female
Humans
Male
Middle Aged
Rats, Sprague-Dawley
Retina pathology
Retrospective Studies
Rats
Aldehyde Dehydrogenase, Mitochondrial metabolism
Diabetes Mellitus, Experimental complications
Diabetes Mellitus, Type 1 complications
Diabetes Mellitus, Type 2 complications
Diabetic Retinopathy etiology
Oxidative Stress
Reactive Oxygen Species metabolism
Retina enzymology
Sirtuin 1 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1942-0994
- Volume :
- 2021
- Database :
- MEDLINE
- Journal :
- Oxidative medicine and cellular longevity
- Publication Type :
- Academic Journal
- Accession number :
- 34725563
- Full Text :
- https://doi.org/10.1155/2021/1641717