Medial Premotor Cortex Shows a Reduction in Inhibitory Markers and Mediates Recovery in a Mouse Model of Focal Stroke

• Published in: Stroke (1970) Vol. 44; no. 2; pp. 483 - 489
• Main Authors: ZEILER, Steven R, GIBSON, Ellen M, HOESCH, Robert E, LI, Ming Y, WORLEY, Paul F, O'BRIEN, Richard J, KRAKAUER, John W
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins 01.02.2013
• Subjects: Animals; Biological and medical sciences; Disease Models, Animal; Male; Medical sciences; Mice; Mice, Inbred C57BL; Motor Cortex - pathology; Motor Cortex - physiology; Motor Skills - physiology; Neural Inhibition - physiology; Neurology; Neuronal Plasticity - physiology; Neuropharmacology; Neuroprotective agent; Pharmacology. Drug treatments; Recovery of Function - physiology; Stroke - pathology; Stroke - physiopathology; Vascular diseases and vascular malformations of the nervous system; poststroke reorganization; Stroke; Nervous system diseases; premotor; Rodentia; Cardiovascular disease; inhibition; recovery; Cerebral disorder; Vascular disease; Vertebrata; Mammalia; Mouse; Animal; parvalbumin; Central nervous system disease; Premotor cortex; Cerebrovascular disease
• ISSN: 0039-2499; 1524-4628
• DOI: 10.1161/strokeaha.112.676940

Motor recovery after ischemic stroke in primary motor cortex is thought to occur in part through training-enhanced reorganization in undamaged premotor areas, enabled by reductions in cortical inhibition. Here we used a mouse model of focal cortical stroke and a double-lesion approach to test the idea that a medial premotor area (medial agranular cortex [AGm]) reorganizes to mediate recovery of prehension, and that this reorganization is associated with a reduction in inhibitory interneuron markers. C57Bl/6 mice were trained to perform a skilled prehension task to an asymptotic level of performance after which they underwent photocoagulation-induced stroke in the caudal forelimb area. The mice were then retrained and inhibitory interneuron immunofluorescence was assessed in prechosen, anatomically defined neocortical areas. Mice then underwent a second photocoagulation-induced stroke in AGm. Focal caudal forelimb area stroke led to a decrement in skilled prehension. Training-associated recovery of prehension was associated with a reduction in parvalbumin, calretinin, and calbindin expression in AGm. Subsequent infarction of AGm led to reinstatement of the original deficit. We conclude that with training, AGm can reorganize after a focal motor stroke and serve as a new control area for prehension. Reduced inhibition may represent a marker for reorganization or it is necessary for reorganization to occur. Our mouse model, with all of the attendant genetic benefits, may allow us to determine at the cellular and molecular levels how behavioral training and endogenous plasticity interact to mediate recovery.