Posterior Medial Frontal Cortex Regulates Sympathy: A TMS Study

2021 ◽  
Author(s):  
Colin Holbrook ◽  
Marco Iacoboni ◽  
Chelsea Gordon ◽  
Shannon Proksch ◽  
Harmony Makhfi ◽  
...  

Harm to some elicits greater sympathy than harm to others. Here, we examine the role of posterior medial frontal cortex (PMFC) in regulating sympathy, and explore the potential role of PMFC in the related phenomena of mentalizing and representing others as connected with oneself. We down-regulated either PMFC or a control region (middle temporal visual area), then assessed feelings of sympathy for and self-other overlap with two characters described as having suffered physical harm, and who were framed as adversarial or affiliative, respectively. We also measured mentalizing performance with regard to inferring the cognitive and affective states of the adversarial character. As hypothesized, down-regulating PMFC increased sympathy for both characters. Whereas we had predicted that down-regulating PMFC would decrease mentalizing ability given the postulated role of PMFC in the mentalizing network, participants in the PMFC down-regulation condition evinced greater second-order cognitive inference ability relative to controls. We observed no effect of the TMS manipulation on self-other overlap, although sympathy and self-other overlap were positively correlated. These findings are discussed as they may inform understanding of the functional role(s) of PMFC in regulating responses broadly linked with empathy.

2013 ◽  
Vol 25 (10) ◽  
pp. 1634-1648 ◽  
Author(s):  
Julie Duque ◽  
Etienne Olivier ◽  
Matthew Rushworth

Top–down control is critical to select goal-directed actions in changeable environments, particularly when several conflicting options compete for selection. In humans, this control system is thought to involve an inhibitory mechanism that suppresses the motor representation of unwanted responses to favor selection of the most appropriate action. Here, we aimed to evaluate the role of a region of the medial frontal cortex, the pre-SMA, in this form of inhibition by using a double coil TMS protocol combining repetitive TMS (rTMS) over the pre-SMA and a single-pulse TMS over the primary motor cortex (M1) during a visuomotor task that required participants to choose between a left or right button press according to an imperative cue. M1 stimulation allowed us to assess changes in motor excitability related to selected and nonselected (unwanted) actions, and rTMS was used to produce transient disruption of pre-SMA functioning. We found that when rTMS was applied over pre-SMA, inhibition of the nonselected movement representation was reduced. Importantly, this effect was only observed when the imperative cue produced a substantial amount of competition between the response alternatives. These results are consistent with previous studies pointing to a role of pre-SMA in competition resolution. In addition, our findings indicate that this function of pre-SMA involves the control of inhibitory influences directed at unwanted action representations.


NeuroImage ◽  
2000 ◽  
Vol 11 (5) ◽  
pp. S278
Author(s):  
Hope Benefield ◽  
Bruce Crosson ◽  
M. Allison Cato ◽  
Joseph R. Sadek ◽  
Kaundinya Gopinath ◽  
...  

2013 ◽  
Vol 59 (1) ◽  
pp. 25-50 ◽  
Author(s):  
A.V. Alessenko

The review discusses the functional role of sphingolipids in the pathogenesis of Alzheimer's disease. Certain evidence exist that the imbalance of sphingolipids such as sphingomyelin, ceramide, sphingosine, sphingosine-1-phosphate and galactosylceramide in the brain of animals and humans, in the cerebrospinal fluid and blood plasma of patients with Alzheimer's disease play a crucial role in neuronal function by regulating growth, differentiation and cell death in CNS. Activation of sphingomyelinase, which leads to the accumulation of the proapoptotic agent, ceramide, can be considered as a new mechanism for AD and may be a prerequisite for the treatment of this disease by using drugs that inhibit sphingomyelinase activity. The role of sphingolipids as biomarkers for the diagnosis of the early stage of Alzheimer's disease and monitoring the effectiveness of treatment with new drugs is discussed.


2010 ◽  
Vol 121 ◽  
pp. S224-S225
Author(s):  
T. Tsujii ◽  
S. Masuda ◽  
K. Sakatani ◽  
T. Akiyama ◽  
S. Watanabe

2020 ◽  
Vol 15 (12) ◽  
pp. 1361-1367
Author(s):  
Colin Holbrook ◽  
Marco Iacoboni ◽  
Chelsea Gordon ◽  
Shannon Proksch ◽  
Ramesh Balasubramaniam

Abstract Research indicates that the posterior medial frontal cortex (pMFC) functions as a ‘neural alarm’ complex broadly involved in registering threats and helping to muster relevant responses. Holbrook and colleagues investigated whether pMFC similarly mediates ideological threat responses, finding that downregulating pMFC via transcranial magnetic stimulation (TMS) caused (i) less avowed religious belief despite being reminded of death and (ii) less group bias despite encountering a sharp critique of the national in-group. While suggestive, these findings were limited by the absence of a non-threat comparison condition and reliance on sham rather than control TMS. Here, in a pre-registered replication and extension, we downregulated pMFC or a control region (MT/V5) and then primed participants with either a reminder of death or a threat-neutral topic. As mentioned previously, participants reminded of death reported less religious belief when pMFC was downregulated. No such effect of pMFC downregulation was observed in the neutral condition, consistent with construing pMFC as monitoring for salient threats (e.g. death) and helping to recruit ideological responses (e.g. enhanced religious belief). However, no effect of downregulating pMFC on group bias was observed, possibly due to reliance on a collegiate in-group framing rather than a national framing as in the prior study.


NeuroImage ◽  
2013 ◽  
Vol 83 ◽  
pp. 870-879 ◽  
Author(s):  
Chun-Yu Tse ◽  
Teemu Rinne ◽  
Kwun Kei Ng ◽  
Trevor B. Penney

2016 ◽  
Vol 7 ◽  
Author(s):  
Huan Xu ◽  
Pin Wang ◽  
Zhuo’er Ye ◽  
Xin Di ◽  
Guiping Xu ◽  
...  

2019 ◽  
Vol 132 ◽  
pp. 107124 ◽  
Author(s):  
Stephanie J. Wake ◽  
Ryuta Aoki ◽  
Kiyoshi Nakahara ◽  
Keise Izuma

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