Table 2.
Summary of in vivo animal studies on eye and AST.
| Study type | Animals | AST dose | Referred ocular disease | Biological effects | Related genes | References |
|---|---|---|---|---|---|---|
| In vivo | C57BL/6J mice | 1/0.1/0.01 ng/ml by eye drop | Phototoxic keratitis | Increase corneal thickness, antiapoptosis, reduce ROS and NF-κB | NF-κB | [44] |
| In vivo | C57BL/6J mice | 6mg | Phototoxic keratitis | Improve corneal epithelial thickness | NF-κB , caspase-3, CD45, COX-2, TNF-α,IκB | [13] |
| Antiapoptosis | ||||||
| Inhibit activity of NF-κB | ||||||
| Decrease proinflammatory factors and ROS | ||||||
| In vivo | Chicken embryo model | 50/80/100 mg/ml | Cataract | Inhibit HC-induced cataract | — | [54] |
| Reduced GSH levels | ||||||
| In vivo | Sprague Dawley rat | 16/80 mg/kg | Cataract | Delay progress of cataract | AGEs, SOD, GSH, CAT, MDA | [51] |
| Protect epithelium of lens | ||||||
| Decrease antioxidant levels | ||||||
| In vivo | Db/db rats | 25/5 mg/kg by oral gavage | Type 2 diabetes mellitus | Decrease levels of oxidative stress marker | MDA, 8-OHdG, SOD | [16] |
| Inhibit apoptosis | ||||||
| In vivo | Psammomys obesus | 10 mg/kg | Type 2 diabetes mellitus | Increase HO-1 expression | HO-1, glial markers (GFAP, CRALBP, and GS) | [55] |
| Attenuates glial dysfunction | ||||||
| In vivo | Wistar rats | 0.6/3 mg/kg | Type 1 diabetes mellitus | Decrease oxidative stress and inflammatory mediators and inhibit activity of NF-κB | 8-OHdG, NO, acrolein, ICAM-1, MCP-1 | [56] |
| Increase antioxidant enzyme | ||||||
| In vivo | ddY mice | 100 mg/kg | Retina ischemia (AMD, DR, glaucoma | Protect retinal functional and histological damage | — | [53] |
| Decrease RGCs death | ||||||
| In vivo | C57BL/6J mice | 10/100 ng/μL | Pathological retinal angiogenesis | Antiproliferation and antiapoptosis of endothelial cells | — | [57] |
| In vivo | C57BL/6J mice | 1/10/100 mg/kg | AMD | Suppress CNV and macrophage infiltration | ICAM-1, MCP-1, IL-6, VEGF, VEGFR-1, VEGFR-2, IκB | [15] |
| Decrease expression of inflammatory and angiogenic molecules | ||||||
| Inhibit activity of NF-κB | ||||||
| In vivo | ddY mice | 100 mg/kg | AMD/RP | Increase GCL and INL | 8-OHdG, 4-HNE | [58] |
| Inhibit oxidative DNA damage and lipid peroxidation damage | ||||||
| Antiapoptosis | ||||||
| In vivo | ddY mice | 100 mg/kg | AMD/RP | Ameliorate retinal dysfunction and histological damage | 8-OHdG, ROS | [48] |
| Antiapoptosis | ||||||
| In vivo | Glast ± mice and C57BL/6J mice | 10/30/60 mg/kg | Normal intraocular glaucoma (NTG) | Suppress RGCs loss | 4-HNE, pIκB, IκB | [59] |
| In vivo | C57BL/6J mice | 50 mg/kg | Glaucoma | Protect retinal tissues and RGCs from oxidative stress | Bax, Bcl-2, Nrf2. HO-1, ROS | [11] |
| Inhibit apoptosis of RGCs | ||||||
| Active nrf2/HO-1 pathway | ||||||
| In vivo | Sprague Dawley rat | 25/75 mg/kg | Retinal toxicity | Prevent retinal toxicity by CIS | GSH, MDA | [60] |