作者
Evan M. Gordon,Roselyne J. Chauvin,Andrew N. Van,Aishwarya Rajesh,Ashley N. Nielsen,Dillan J. Newbold,Charles J. Lynch,Nicole A. Seider,Samuel R. Krimmel,Kristen M. Scheidter,Julia Monk,Ryland L. Miller,Athanasia Metoki,David F. Montez,Annie Zheng,Immanuel Elbau,Thomas Madison,Tomoyuki Nishino,Michael J. Myers,Sydney Kaplan,Carolina Badke D’Andrea,Damion V. Demeter,Matthew Feigelis,Julian S.B. Ramirez,Ting Xu,Deanna M. Barch,Christopher D. Smyser,Cynthia Rogers,Jan Zimmermann,Kelly N. Botteron,John R. Pruett,Jon T. Willie,Peter Brunner,Joshua S. Shimony,Benjamin P. Kay,Scott Marek,Scott A. Norris,Caterina Gratton,Chad M. Sylvester,Jonathan D. Power,Conor Liston,Deanna J. Greene,Jarod L. Roland,Steven E. Petersen,Marcus E. Raichle,Timothy O. Laumann,Damien A. Fair,Nico U.F. Dosenbach
摘要
Abstract Motor cortex (M1) has been thought to form a continuous somatotopic homunculus extending down the precentral gyrus from foot to face representations 1,2 , despite evidence for concentric functional zones 3 and maps of complex actions 4 . Here, using precision functional magnetic resonance imaging (fMRI) methods, we find that the classic homunculus is interrupted by regions with distinct connectivity, structure and function, alternating with effector-specific (foot, hand and mouth) areas. These inter-effector regions exhibit decreased cortical thickness and strong functional connectivity to each other, as well as to the cingulo-opercular network (CON), critical for action 5 and physiological control 6 , arousal 7 , errors 8 and pain 9 . This interdigitation of action control-linked and motor effector regions was verified in the three largest fMRI datasets. Macaque and pediatric (newborn, infant and child) precision fMRI suggested cross-species homologues and developmental precursors of the inter-effector system. A battery of motor and action fMRI tasks documented concentric effector somatotopies, separated by the CON-linked inter-effector regions. The inter-effectors lacked movement specificity and co-activated during action planning (coordination of hands and feet) and axial body movement (such as of the abdomen or eyebrows). These results, together with previous studies demonstrating stimulation-evoked complex actions 4 and connectivity to internal organs 10 such as the adrenal medulla, suggest that M1 is punctuated by a system for whole-body action planning, the somato-cognitive action network (SCAN). In M1, two parallel systems intertwine, forming an integrate–isolate pattern: effector-specific regions (foot, hand and mouth) for isolating fine motor control and the SCAN for integrating goals, physiology and body movement.