PT - JOURNAL ARTICLE AU - Alexander Kraskov AU - Gita Prabhu AU - Marsha M. Quallo AU - Roger N. Lemon AU - Thomas Brochier TI - Ventral Premotor–Motor Cortex Interactions in the Macaque Monkey during Grasp: Response of Single Neurons to Intracortical Microstimulation AID - 10.1523/JNEUROSCI.0525-11.2011 DP - 2011 Jun 15 TA - The Journal of Neuroscience PG - 8812--8821 VI - 31 IP - 24 4099 - http://www.jneurosci.org/content/31/24/8812.short 4100 - http://www.jneurosci.org/content/31/24/8812.full SO - J. Neurosci.2011 Jun 15; 31 AB - Recent stimulation studies in monkeys and humans have shown strong interactions between ventral premotor cortex (area F5) and the hand area of primary motor cortex (M1). These short-latency interactions usually involve facilitation from F5 of M1 outputs to hand muscles, although suppression has also been reported. This study, performed in three awake macaque monkeys, sought evidence that these interactions could be mediated by short-latency excitatory and inhibitory responses of single M1 neurons active during grasping tasks. We recorded responses of these M1 neurons to single low-threshold (≤40 μA) intracortical microstimuli delivered to F5 sites at which grasp-related neurons were recorded. In 29 sessions, we tested 232 M1 neurons with stimuli delivered to between one and four sites in F5. Of the 415 responses recorded, 142 (34%) showed significant effects. The most common type of response was pure excitation (53% of responses), with short latency (1.8–3.0 ms) and brief duration (∼1 ms); purely inhibitory responses had slightly longer latencies (2–5 ms) and were of small amplitude and longer duration (5–7 ms). They accounted for 13% of responses, whereas mixed excitation then inhibition was seen in 34%. Remarkably, a rather similar set of findings applied to 280 responses of 138 F5 neurons to M1 stimulation; 109 (34%) responses showed significant effects. Thus, with low-intensity stimuli, the dominant interaction between these two cortical areas is one of short-latency, brief excitation, most likely mediated by reciprocal F5–M1 connections. Some neurons were tested with stimuli at both 20 and 40 μA; inhibition tended to dominate at the higher intensity.