Background: Protocatechuic aldehyde (PA) extracts from S. miltiorrhiza, which anti-oxidative and antiinflammatory functions have been certified in diverse diseases. Nonetheless, the influence of PA in spinal cord injury (SCI) is still hazy. The research probed the function of PA in hydrogen peroxide (H 2 O 2)damaged PC12 cells. Methods: The disparate dosages of H 2 O 2 (0-400 mM) or PA (0-2 mM) were applied for stimulating PC12 cells, and subsequently cell viability, apoptosis, apoptosis-and autophagy-correlative factors were evaluated. After pc-MEG3 transfection, functions of MEG3 overexpression in H 2 O 2 and/or PA-managed PC12 cells were reassessed. Western blot was conducted to determine Wnt/b-catenin and PTEN/PI3K/ AKT pathways. Results: H 2 O 2 stimulation clearly triggered PC12 cell damage via prohibiting cell viability and accelerating apoptosis and autophagy. But, PA management mitigated H 2 O 2-triggered PC12 cells damage. Down-regulated MEG3 triggered by PA was presented in H 2 O 2-managed cells. What's more, overexpressed MEG3 dramatically overturned the influences of PA in H 2 O 2-damaged PC12 cells. Beyond that, PA activated Wnt/b-catenin and PTEN/PI3K/AKT via repression of MEG3 in H 2 O 2-managed PC12 cells. Conclusions: The results disclosed the protective impacts of PA on PC12 cells to resist H 2 O 2-provoked damage. MEG3, Wnt/b-catenin and PTEN/PI3K/AKT pathways joined in adjusting the activity of PA in H 2 O 2-damaged PC12 cells.