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Updated: Feb 4, 2026

Rapid Determination of the Thermal Nociceptive Threshold in Diabetic Rats
Published on: May 17, 2012
ALDH2 attenuates early-stage STZ-induced aged diabetic rats retinas damage via Sirt1/Nrf2 pathway
Mengshan He1, Pan Long2, Weiming Yan2
1Department of Chinese Material Medical and Natural Medicines, Air Force Medical University, Xi'an, Shaanxi, China.
Aims:
Acetaldehyde dehydrogenase 2 (ALDH2) was reported for its protective properties on myocardial damage, stroke and neurodegeneration disease, but the effects and mechanisms of ALDH2 in the modulation of diabetic retinopathy remain unclear. The present study evaluated the protection effects of ALDH2 on streptozocin (STZ)-induced aged diabetic rats retinas damage.
Main Methods:
24 aged male diabetic Sprague-Dawley (SD) rats induced by a single intraperitoneal injection of STZ were randomly divided into Alda1-treated group and dimethylsulfoxide (DMSO) group. Rats were intraperitoneally injected with 10 mg/kg ALDH2 activator Alda1 (or DMSO) 3 days before STZ injection and 30 days afterwards. A series of detections on retinal structural, functional and molecular levels were applied at 1 d, 7 d and 30 d after aged diabetic rats model established.
Key Findings:
Optical coherence tomography (OCT) revealed that the thickness of outer nuclear layer (ONL) and whole retinas in Alda1-treated group were thicker than DMSO group. Full field electroretinograms (ffERG) showed a higher amplitude wave (dark-adaptation 3.0 and OPs) in Alda1-treated group. In addition, the levels of retinal tumor necrosis factor (TNF-α) and interleukin-6 (IL-6) from Alda1-treated group were lower whereas superoxide dismutase (SOD) activity was notably higher. Moreover, the expressions of ALDH2, silence information regulation factor 2 related enzyme I (Sirt1) and nuclear factor erythroid 2-related factor 2 (Nrf2) in Alda1-treated group retinas were significantly increased, while the expression of vascular endothelial growth factor (VEGF-α) was dramatically decreased.
Significance:
ALDH2 could ameliorate early-stage STZ-induced aged diabetic rats retinas damage possibly via increasing Sirt1 and Nrf2 expression.
Insights
Acetaldehyde dehydrogenase 2 (ALDH2) activation protected aged diabetic rat retinas from damage. This suggests ALDH2 may be a therapeutic target for diabetic retinopathy, potentially by increasing Sirt1 and Nrf2 expression.
Area of Science:
- Biochemistry
- Ophthalmology
- Pharmacology
Background:
- Acetaldehyde dehydrogenase 2 (ALDH2) is known for protective effects against myocardial damage, stroke, and neurodegeneration.
- The role of ALDH2 in modulating diabetic retinopathy remains largely unexplored.
- Diabetic retinopathy is a significant complication of diabetes, leading to vision loss.
Purpose of the Study:
- To evaluate the protective effects of ALDH2 on retinal damage in streptozocin (STZ)-induced aged diabetic rats.
- To investigate the underlying mechanisms by which ALDH2 influences diabetic retinal injury.
Main Methods:
- Aged male Sprague-Dawley rats were induced with diabetes using streptozocin (STZ).
- Rats were treated with the ALDH2 activator Alda1 or a vehicle control (DMSO).
- Retinal structural, functional, and molecular changes were assessed at 1, 7, and 30 days post-STZ injection.
Main Results:
- Alda1 treatment preserved retinal thickness and improved electroretinogram function.
- Alda1 reduced inflammatory markers (TNF-α, IL-6) and increased antioxidant activity (SOD).
- Alda1 upregulated ALDH2, Sirt1, and Nrf2 expression while decreasing VEGF-α levels.
Conclusions:
- ALDH2 activation ameliorates early-stage diabetic retinal damage in aged rats.
- The protective mechanism may involve the upregulation of Sirt1 and Nrf2 pathways.
- ALDH2 represents a potential therapeutic target for managing diabetic retinopathy.
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