Baicalin is an important medicinal herb purified from the dry roots of Scutellaria baicalensis Georgi. The present study was undertaken to evaluate the
neuroprotective effects of
baicalin in gerbils subjected to transient global cerebral ischemic-
reperfusion injury.
Baicalin at doses of 50, 100 and 200mg/kg was intraperitoneally injected into the gerbils immediately after
cerebral ischemia. Seven days after reperfusion,
hematoxylin and
eosin (HE) staining was performed to analyze hippocampal CA1 pyramidal damage histopathologically. In addition, in order to understand the potential protective mechanism of
baicalin, we examined anti-oxidative
enzymes, such
superoxide dismutase (SOD),
glutathione peroxidase (GSH-PX), non-enzymatic scavenger
glutathione (GSH) and measured the content of
malondialdehyde (MDA) in hippocampus. The
mRNA and
protein expressions of
BDNF were determined in ischemic hippocampus by real-time RT-PCR and Western blot, respectively. Evidence for neuronal apoptosis was detected by real-time RT-PCR, Western blot and
caspase-3 activity measurement. Histopathological examination showed that the administration of
baicalin by the dose of 100 and 200mg/kg significantly attenuated
ischemia-induced neuronal cell damage. Reduced level of MDA, obviously elevated activities of SOD and GSH as well as GSH-PX were also found in
baicalin-treated groups. Further investigation demonstrated that treatment with
baicalin remarkably promoted the expression of
BDNF and inhibited the expression of
caspase-3 at
mRNA and
protein levels by real-time RT-PCR and Western blot, respectively. Besides,
caspase-3 activity assay also elucidated that the administration of
baicalin could significantly suppress
caspase-3 in ischemic gerbils hippocampus. Theses findings suggest that
baicalin's neuroprotection appears to be associated with its anti-oxidative and anti-apoptotic properties in global
cerebral ischemia in the gerbils.