Ischemic stroke is a leading cause of mortality and permanent disability in adults worldwide. Neurogenesis triggered by
ischemia in the adult mammalian brain may provide insights into
stroke treatment.
Morroniside is an active component of sarcocarp of C. officinalis that have shown
neuroprotective effects. The aim of the present study is to test whether
morroniside promotes neurogenesis via Wnt/β-
catenin signaling pathway for brain recovery in a rat model of focal
cerebral ischemia.
Morroniside was administered intragastrically once daily at the concentrations of 30, 90 and 270 mg/kg for 7 days post-
ischemia. Neurological functions were detected by Ludmila Belayev score tests. Endogenous neural stem cells responses were investigated with immunofluorescence staining of Ki-67 and
Nestin to identify the neurogenesis in the subventricular zone (SVZ). The expression of
proteins involved in and related to Wnt/β-
catenin signaling pathway was detected by western blotting analysis.
Morroniside significantly promoted neurogenesis for brain recovery 7 days post-
ischemia. Increased expression of Wnt 3a, β-
catenin and T-cell transcription factor-4 (Tcf-4), along with activation of downstream
transcription factors Pax6 and neurogenin2 (Ngn2), indicated that the neurorestorative effects of
morroniside may be associated with Wnt/β-
catenin signaling pathway. These data provide support for understanding the mechanisms of
morroniside in neurorestorative effects and suggest a potential new strategy for
ischemic stroke treatment.