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Updated: May 2, 2026

A Preclinical Model to Assess Brain Recovery After Acute Stroke in Rats
Published on: November 6, 2019
Alpha 1-antitrypsin therapy mitigated ischemic stroke damage in rats
Huong L Moldthan1, Aaron C Hirko2, Jeffrey S Thinschmidt2
1Department of Pharmaceutics, University of Florida College of Pharmacy, Gainesville, Florida.
Alpha-1 Antitrypsin (AAT) significantly reduced stroke damage and improved sensorimotor function in a rat model. This novel therapy shows promise for protecting against neurodegeneration after ischemic stroke.
Area of Science:
- Neuroscience
- Pharmacology
- Biochemistry
Background:
- Current acute ischemic stroke therapy relies on recombinant tissue plasminogen activator.
- Alpha-1 Antitrypsin (AAT) possesses anti-inflammatory, anti-apoptotic, and cytoprotective properties.
- AAT's potential therapeutic benefits in stroke warrant investigation.
Purpose of the Study:
- To evaluate the efficacy of AAT in improving outcomes following ischemic stroke.
- To test AAT's neuroprotective effects in a well-established rat stroke model.
Main Methods:
- Middle cerebral artery occlusion was induced in rats using endothelin-1.
- Rats received either intracranial or intravenous human AAT post-stroke.
- Sensorimotor function was assessed using cylinder and vibrissae tests.
- Infarct volumes were quantified using TTC assay or MRI.
Main Results:
- Human AAT treatment significantly reduced infarct volumes by 83% (local) and 63% (systemic) compared to controls.
- AAT administration led to significant improvements in sensorimotor deficits.
- P-values < .0001 and < .05 indicate statistical significance.
Conclusions:
- Human AAT demonstrates significant neuroprotective effects in a rat model of ischemic stroke.
- AAT effectively reduces infarct size and improves functional recovery.
- Further research is needed to explore AAT's mechanisms and efficacy in diverse models.
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