Baicalin is known to exhibit neuroprotective effects during brain injury through its antioxidant and anti-inflammatory functions. Moreover, γ-enolase is specifically expressed in nerve cells and exhibits neuroprotective properties. In this study, we investigated whether baicalin regulates γ-enolase expression in an moddle cerebral artery occulsion (MCAO)-induced brain injury model. Adult male rats were intraperitoneally injected with baicalin (100 mg/kg) or phosphate-buffered saline (PBS) immediately after right MCAO surgery. Neurological behavior tests were performed 24 hours after surgery and brain water content was evaluated. Right cortical tissue was collected. Western blot analysis were conducted to elucidate γ-enolase expression in MCAO animals treated with baicalin. In addition, γ-enolase expression was analyzed using immunofluorescence staining. MCAO animals administered PBS displayed severe behavioral impairments and edema, whereas baicalin administration alleviated these disorders, demonstrating the protective effects of baicalin against ischemic damage. Western blot analysis results showed that MCAO-induced damage decreased γ-enolase expression, and baicalin treatment mitigated this reduction. These findings were confirmed through immunofluorescence staining. Since γ-enolase is known to contribute to neuroprotective effects, these results suggest that baicalin alleviates neurobehavioral impairments in stroke animals and exerts neuroprotective effects by attenuating the decline in γ-enolase expression caused by brain injury. In conclusion, we demonstrated that baicalin regulates γ-enolase expression during cerebral ischemic damage.