1. Academic Validation
  2. Astaxanthin inhibits oxidative stress and apoptosis in diabetic retinopathy

Astaxanthin inhibits oxidative stress and apoptosis in diabetic retinopathy

  • Acta Histochem. 2023 Jun 19;125(6):152069. doi: 10.1016/j.acthis.2023.152069.
Jian Fang 1 Wuxia Bai 2 Lina Yang 3
Affiliations

Affiliations

  • 1 Department of Ophthalmology, Xinchang County People's Hospital, Shaoxing City, Zhejiang Province 312500, China.
  • 2 School of Pharmacy, Hangzhou Medical College, Hangzhou City, Zhejiang Province 310059, China.
  • 3 Department of Ophthalmology, Xinchang County People's Hospital, Shaoxing City, Zhejiang Province 312500, China. Electronic address: lina.mango@163.com.
Abstract

Background: The pathophysiology of diabetic retinopathy (DR) is thought to be influenced by oxidative stress. Astaxanthin (ASX) is a natural product with antioxidant effect, but it is not clear whether its mechanism of inhibiting the development of DR is related to anti-oxidation.

Methods: Rats were intraperitoneally injected with streptozotocin (60 mg/kg) to create DR rat models followed by ASX (20 mg/kg) for 45 days. Retinal tissue was examined by Hematoxylin and Eosin staining. By using Enzyme-linked immunosorbent assay (ELISA), 2,7-Dichlorodrhydrofluorescein diace (DCFH-DA) probes, immunohistochemistry and western blot, it was feasible to evaluate the contents of inflammation-related factors (tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), IL-6 and macrophage inhibitory cytokine-1 (MIC-1)), oxidative stress-related indicators (glutathione (GSH), malonic dialdehyde (MDA), Glutathione Peroxidase (GPx), Reactive Oxygen Species (ROS) and Total antioxidant capacity (T-AOC)), antioxidant Enzymes (hemoxgenase-1(HO-1) and Quinone Oxidoreductase 1 (NQO1)), and apoptosis-related proteins (Bcl-2, Bcl2 Associated X Protein (Bax), and cleaved-caspase-3). Additionally, antioxidant proteins downstream of the nuclear factor E2 related factors (Nrf-2) pathway, expression levels of Nrf2/ Kelch-like ECH-associated protein 1(Keap 1) pathway-associated proteins, and nuclear and cytoplasmic levels of Nrf2 were assessed using immunohistochemistry, western blot, or quantitative real-time polymerase chain reaction (qRT-PCR).

Results: ASX alleviated retinal tissue damage by increasing overall retina thickness and ganglion cell layer (GCL) cell numbers and exerted the anti-inflammatory, anti-oxidative stress, and anti-apoptosis effects in DR rats. Additionally, ASX could inhibit the expression of Keap1, promote the transport of Nrf2 from cytoplasm to nucleus and facilitate the expressions of HO-1, NQO1, γ-glutamylcysteine synthetase, (γ-GCS) and GPx.

Conclusion: ASX exerted antioxidant effects through Nrf2/keap1 pathway, thereby alleviating Apoptosis, inflammation, and oxidative stress in retinal tissues of DR rats.

Keywords

Antioxidation; Astaxanthin; Diabetic retinopathy; Kelch-like ECH-associated protein; Nuclear factor erythroid 2-like 2.

Figures
Products