Ilsa Hunaifi, Andi Kurnia Bintang, Jumraini Tammasse, Isra Wahid, Rizka Vidya Lestari, Triana Dyah Cahyawati, Iman Surya Pratama
Background: Ischemia causes neuronal death and releases Neuron-Specific Enolase (NSE). Thrombolysis is a standard therapy for ischemic stroke, but only 10-20 percent of patients receive thrombolysis. It is necessary to develop a treatment to increase neuroprotection by administering MLC 901 to influence NSE levels. Objectives: The study investigates the efficacy of MLC 901 on NSE levels, functional outcome and infarct volume in the stroke model of rats. Methods: Male Wistar rats were divided into acute ischemic stroke with MLC 901 43.2 mg/body weight, acute ischemic stroke with MLC 901 21.6 mg/body weight and acute ischemic stroke with CMC-Na for placebo-all treatment for 14 days. The NSE level was determined by ELISA, functional outcome determined by motoric score and infarct volume using NIH Image J. Results: NSE level increased at 24 hours after stroke. There was no difference in administering the dose of MLC 901 to improve functional outcome and reduce cerebral infarct volume. Conclusion: MLC 901 improved functional outcomes and reduced the volume of cerebral infarction in acute ischemic stroke but did not affect NSE levels.
Acute ischemic stroke
Functional outcome
Infarction volume
MLC 901
Neuron-specific enolase