Table 1. The effects of RSV treatment on diabetes-related dementia.
Ref. No. | Study design | Treatment | Main findings |
---|---|---|---|
Tian et al. [59] | Male Sprague-Dawley rats (10–12 weeks old, 200–250 g), single dose of 60 mg/kg STZ (n = 15/group) | RSV (10 mg, 20 mg/kg), 8 weeks | • Improve cognitive performance (Morris water maze test) |
• Attenuate oxidative stress and inflammation | |||
• Inhibit synapse loss | |||
Tian et al. [60] | Male Sprague-Dawley rats (2 months old, 180–210 g), single dose of 60 mg/kg STZ (n = 15/group) | RSV (80 mg/kg), 4 weeks | • Improve cognitive deficit (Morris water maze test) |
• Reverse alterations in the protein expression of caspase-3, Bax, Bcl-2, NMDAR1 and BDNF | |||
Du et al. [62] | Male Sprague-Dawley rats (3 months old, 250 ± 20 g), ICV-STZ of 3 mg/kg, twice with an interval of 48 hours (n = 10/group) | RSV (30 mg/kg), 8 weeks | • Improve cognitive capability (Morris water maze test) |
• Reverse alterations ERK1/2 phosphorylation, tau phosphorylation, sirtuin 1 activity in hippocampus | |||
Schmatz et al. [61] | Male Wistar rats (70–90 days old, 250–270 g), single dose of 55 mg/kg STZ (n = 6–13/group) | RSV (10 mg/kg), 30 days | • Decrease acetylcholinesterase activity in blood and prevent memory impairment |
Wong et al. [63] | Thirty-six type 2 diabetes adults (40–80 years old) | Single doses of RSV (0, 75, 150, and 300 mg) | • Improve neurovascular coupling capacity and multi-tasking performance |
RSV, resveratrol; STZ, streptozotocin; NMDAR1, N-Methyl-D-aspartate receptor; BDNF, brain-derived neurotrophic factor; ICV, intracerebroventricular; ERK1/2, extracellular signal-regulated kinases 1 and 2.