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A somato-cognitive action network alternates with effector regions in motor cortex.

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 zones³ and maps of complex actions⁴. 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 action⁵ and physiological control⁶, arousal⁷, errors⁸ and pain⁹. 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 actions⁴ and connectivity to internal organs¹⁰ 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.

SUBMITTER: Gordon EM

PROVIDER: S-EPMC10172144 | biostudies-literature | 2023 May

REPOSITORIES: biostudies-literature

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A somato-cognitive action network alternates with effector regions in motor cortex.

Gordon Evan M EM Chauvin Roselyne J RJ Van Andrew N AN Rajesh Aishwarya A Nielsen Ashley A Newbold Dillan J DJ Lynch Charles J CJ Seider Nicole A NA Krimmel Samuel R SR Scheidter Kristen M KM Monk Julia J Miller Ryland L RL Metoki Athanasia A Montez David F DF Zheng Annie A Elbau Immanuel I Madison Thomas T Nishino Tomoyuki T Myers Michael J MJ Kaplan Sydney S Badke D'Andrea Carolina C Demeter Damion V DV Feigelis Matthew M Ramirez Julian S B JSB Xu Ting T Barch Deanna M DM Smyser Christopher D CD Rogers Cynthia E CE Zimmermann Jan J Botteron Kelly N KN Pruett John R JR Willie Jon T JT Brunner Peter P Shimony Joshua S JS Kay Benjamin P BP Marek Scott S Norris Scott A SA Gratton Caterina C Sylvester Chad M CM Power Jonathan D JD Liston Conor C Greene Deanna J DJ Roland Jarod L JL Petersen Steven E SE Raichle Marcus E ME Laumann Timothy O TO Fair Damien A DA Dosenbach Nico U F NUF

Nature 20230419 7960

Motor cortex (M1) has been thought to form a continuous somatotopic homunculus extending down the precentral gyrus from foot to face representations1,2, despite evidence for concentric functional zones3 and maps of complex actions4. 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, ha ...[more]

PMID: 37076628

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Project description:Several lines of evidence implicate serotonin (5-hydroxytryptamine, 5-HT)in regulating personality traits and mood control. Serotonergic neurons are classically thought to be tonic regular-firing, "clock-like" neurons. Neurotransmission by serotonin is tightly regulated by the serotonin transporter (SERT) and by autoreceptors (serotonin receptors expressed by serotonin neurons) through negative feedback inhibition at the cell bodies and dendrites (5-HT1A receptors) of the dorsal raphe nuclei or at the axon terminals (5-HT1B receptors). In dorsal raphe neurons, the release of serotonin from vesicles in the soma, dendrites, and/or axonal varicosities is independent of classical synapses and can be induced by neuron depolarization, by the stimulation of L-type calcium channels, by activation of glutamatergic receptors, and/or by activation of 5-HT2 receptors. The resulting serotonin release displays a slow kinetic and a large diffusion. This process called volume transmission may ultimately affect the rate of discharge of serotonergic neurons, and their tonic activity. The therapeutic effects induced by serotonin-selective reuptake inhibitor (SSRI) antidepressants are initially triggered by blocking SERT but rely on consequences of chronic exposure, i.e., a selective desensitization of somatodendritic 5-HT1A autoreceptors. Agonist stimulation of 5-HT2B receptors mimicked behavioral and neurogenic SSRI actions, and increased extracellular serotonin in dorsal raphe. By contrast, a lack of effects of SSRIs was observed in the absence of 5-HT2B receptors (knockout-KO), even restricted to serotonergic neurons (Htr2b5-HTKO mice). The absence of 5-HT2B receptors in serotonergic neurons is associated with a higher 5-HT1A-autoreceptor reactivity and thus a lower firing activity of these neurons. In agreement, mice with overexpression of 5-HT1A autoreceptor show decreased neuronal activity and increased depression-like behavior that is resistant to SSRI treatment. We propose thus that the serotonergic tone results from the opposite control exerted by somatodendritic (Gi-coupled) 5-HT1A and (Gq-coupled) 5-HT2B receptors on dorsal raphe neurons. Therefore, 5-HT2B receptors may contribute to SSRI therapeutic effects by their positive regulation of adult raphe serotonergic neurons. Deciphering the molecular mechanism controlling extrasynaptic release of serotonin, and how autoreceptors interact in regulating the tonic activity of serotonergic neurons, is critical to fully understand the therapeutic effect of SSRIs.

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A somato-cognitive action network alternates with effector regions in motor cortex.

Publications

A somato-cognitive action network alternates with effector regions in motor cortex.

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