Edaravone attenuates HO or glutamate-induced toxicity in hippocampal neurons and improves AlCl/D-galactose induced cognitive impairment in mice.

Edaravone (Eda) is a free radical scavenger used in clinical trials for the treatment of ischemic stroke and amyotrophic lateral sclerosis. However, how Eda exerts its neuroprotective effects remains to be elucidated. We investigated the neuroprotective effects of Eda in cultured hippocampal neurons and in a mouse model of AlCl/D-galactose-induced cognitive impairment.

Ginsenoside Rg1 ameliorates the cognitive deficits in D-galactose and AlCl-induced aging mice by restoring FGF2-Akt and BDNF-TrkB signaling axis to inhibit apoptosis.

Ginsenoside Rg1 is the main active ingredient of with the activity of neuroprotective, antioxidant and strengthening the immune system. Therefore, we hypothesized that Rg1 may afford anti-aging effects although the mechanism remains to be elucidated. In this study, chemically induced aging mice were established by consecutive administration of D-galactose and AlCl.

Edaravone protects rat astrocytes from oxidative or neurotoxic inflammatory insults by restoring Akt/Bcl-2/Caspase-3 signaling axis.

Astrocytes are the major glia cells in the central nervous system (CNS). Increasing evidence indicates that more than to be safe-guard and supporting cells for neurons, astrocytes play a broad spectrum of neuroprotective and pathological functions. Thus, they are compelling models to decipher mechanistic insights of glia cells to CNS insults and for the development of drugs.

2,3,5,4'-Tetrahydroxystilbene-2-O-β-d-glucoside attenuates MPP+/MPTP-induced neurotoxicity in vitro and in vivo by restoring the BDNF-TrkB and FGF2-Akt signaling axis and inhibition of apoptosis.

The major bioactive ingredient THSG of Polygonum multiflorum is well established for its anti-oxidation, anti-aging and anti-inflammation properties. Increasing evidence supports the capacity of THSG to ameliorate the biochemistry of neurotrophins and their downstream signaling axis in mouse models to attenuate neurodegenerative diseases such as Alzheimer's and Parkinson's disease. In this study, the neuroprotective effects of THSG were studied in vitro and in vivo.

[Effects of root-excision on trunk hydraulic traits and growth status of Ginkgo biloba].

The roots of 8-year-old Ginkgo biloba saplings were partially excised to three degrees to study the effects of root-excision on the trunk hydraulic traits and growth status of the saplings. The three degrees were severe, medium, and light (8:1, 10:1, and 12:1 of excised root diameter to base diameter of tree trunk, respectively). Physiological parameters including trunk ultrasound acoustic emission (UAE) signal, branch percentage loss of hydraulic conductance (PLC), sap flow flux, and leaf stomatal conductance, transpiration rate and water potential were measured periodically after root-excision.