Table 4:
Study type | Model | Treatment | Main findings | Reference |
---|---|---|---|---|
In vitro | Rat PC12 neuronal cell model of AD | Phlorotannin extracted from Ecklonia radiata for 48 h | Inhibits in vitro Aβ1–42 aggregation by 90% | Alghazwi et al. (2020) |
Reduces Aβ1–42-induced apoptosis threefold | ||||
Murine N2a-sw neuronal cell model of AD | Unsaturated mannuronate oligosaccharide (1 mg/ml) for 24 h | Decreases Aβ1–42 production as measured by downregulated APP and BACE1 expression | Bi et al. (2021) | |
Animal | MPTP-induced C57BL/6J mouse model of PD | Oral administration of polymannuronic acid (30 mg/kg) for 4 weeks | Improves motor functions as measured by increased survival of TH-IR neurons in SNpc | Dong et al. (2020) |
Exhibits anti-inflammatory effect in CNS as measured by suppressed IL-6 and TNF-α mRNA expression | ||||
Enhances integrity of BBB and intestinal barrier as demonstrated by increased expression of occludin and ZO-1 | ||||
MPTP-induced C57BL/6J mouse model of PD | Oral administration of polymannuronic acid (30 mg/kg) for 4 weeks prior to MPTP | Increases survival of TH-IR neurons in the SNpc | Du et al. (2021) | |
Improves motor function in pole test | ||||
Increases striatal levels of serotonin and its metabolite 5-hydroxyindole acetic acid | ||||
5XFAD transgenic mouse model of AD | Oral administration of GV-971 (100 mg/kg) for 1 month | Normalizes fecal and blood phenylalanine and isoleucine concentrations | Wang et al. (2019) | |
Decreases Th1 cells, reactive microglia, Aβ plaque deposition, and tau phosphorylation in the brain | ||||
APP/PS1 mouse model of AD | Oral administration of GV-971 (50 or 100 mg/kg) for 3 months | Improves cognitive functions as measured by enhanced spatial learning and memory performance | Wang et al. (2019) | |
Human clinical trials | Phase III clinical trial of patients with mild to moderate AD | Oral administration of GV-971 (450 mg) twice a day for 36 weeks | Improves ADAS-Cog12 score compared to baseline and patients who took a placebo | Xiao et al. (2021) |
AD, Alzheimer’s disease; ADAS-Cog12, Alzheimer’s Disease Assessment Scale; APP, amyloid precursor protein; Aβ, amyloid β; BACE1, β-site APP cleaving enzyme 1; BBB, blood–brain barrier; CNS, central nervous system; IL, interleukin; MPTP, 1-methyl-4-phenyl-1,2,3,4-tetrahydropyridine; PD, Parkinson’s disease; PS1, presenilin 1; SNpc, substantia nigra pars compacta; Th1, type 1 T helper; TNF-α, tumor necrosis factor α; and ZO, zonula occludens.