Abstract
Reducing post-stroke disability is the major goal of stroke therapy. Consequently, functional testing is essential in experimental stroke studies to increase the predictive value of animal models. We used several sensory and motor tests to assess functional disability in a mouse model of permanent distal middle cerebral artery occlusion (pdMCAO) that induced mainly cortical infarcts. Gait dynamics were transiently disturbed after pdMCAO as measured by different analysis techniques. Stance and brake duration were shorter after pdMCAO. Consistent with sensory and motor deficits the latency to move was prolonged up to 14 days after pdMCAO and the performance in the corner test and handedness were affected on day 1 or 2 after pdMCAO. Heart rate was decreased and heart rate variability were increased after pdMCAO indicating sympathetic-parasympathetic imbalance. In summary, pdMCAO-induced cortical infarcts lead to clinically relevant sensory, motor and cardiac autonomic dysfunction in mice. The present study provides a basis to explore the potential of functional testing for neuroprotection and neuroregeneration after stroke.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | Journal of Neuroscience Methods |
| Jahrgang | 184 |
| Ausgabenummer | 1 |
| Seiten (von - bis) | 95-103 |
| Seitenumfang | 9 |
| ISSN | 0165-0270 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 30.10.2009 |
Fördermittel
We thank Nadine Gehrig for help with histological techniques. This study was supported by a Deutsche Forschungsgemeinschaft grant to MS ( SCHW 416/5-1 ). TGH has ownership of Mouse Specifics Inc., a US corporation that has commercialized the DigiGait and ECGenie instrumentation that was applied in this study, and took part in data acquisition and analysis.
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
Strategische Forschungsbereiche und Zentren
- Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)
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