PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of frontpsycholLink to Publisher's site
 
Front Psychol. 2017; 8: 2101.
Published online 2017 December 1. doi:  10.3389/fpsyg.2017.02101
PMCID: PMC5717539

Modulating Mimetic Preference with Theta Burst Stimulation of the Inferior Parietal Cortex

Abstract

We like an object more when we see someone else reaching for it. To what extent is action observation causally linked to object valuation? In this study, we set out to answer to this question by applying continuous theta burst stimulation (cTBS) over the left inferior parietal lobule (IPL). Previous studies pointed to this region as critical in the representation of others' actions and in tool manipulation. However, it is unclear to what extent IPL's involvement simply reflects action observation, rather than a casual role in objects' valuation. To clarify this issue, we measured cTBS-dependent modulations of participants' “mimetic preference ratings”, i.e., the difference between the ratings of pairs of familiar objects that were (vs. were not) reached out for by other individuals. Our result shows that cTBS increased mimetic preference ratings for tools, when compared to a control condition without stimulation. This effect was selective for items that were reached for or manipulated by another individual, whilst it was not detected in non-tool objects. Although preliminary, this finding suggests that the automatic and covert simulation of an observed action, even when there is no intention to act on an object, influences explicit affective judgments for objects. This work supports embodied cognition theories by substantiating that our subjective preference is grounded in action.

Keywords: action, observation, preference, tools, inferior parietal lobule, cTBS, objects, affective judgments

Introduction

In the last decades, research has shown that people commonly prefer objects that are the goal of others' actions, regardless of the objects' actual value(s) or their intrinsic properties (Gollwitzer and Moskowitz, 1996). For instance, on the playground children run after the same toy even when similar toys are readily available. In social cognition, this behavior has been termed mimetic desire (Girard, 1988) and it is recognized as a case of goal contagion (Aarts et al., 2004), for which objects that are the target of another individual tend to become the goal for the observer. A functional neuroimaging study (Lebreton et al., 2012), designed to uncover the neural mechanisms of this phenomenon, surprisingly found that object preference is influenced by the activity of motor-related areas, namely the ventral premotor and the inferior parietal cortices, belonging to the action observation–action execution network (which is active during motor act execution as well as the observation of motor acts performed by others; Rizzolatti and Craighero, 2004; Fabbri-Destro and Rizzolatti, 2008; Avenanti and Urgesi, 2011). In particular, the authors found that during the observation of goal-directed actions the activity of these parietofrontal areas modulated that of the ventral valuation system where the perceived value of objects is encoded (Rangel et al., 2008; Chib et al., 2009; Lebreton et al., 2009; Peters and Büchel, 2010). However, as the correlational nature of neuroimaging cannot provide a direct causal link between brain and function, it is an open question whether this activity is merely an epiphenomenon of action perception or whether it truly reflects a neurocomputational process functionally relevant for the expression of subjective preference for a particular object. The present experiment represents a preliminary approach aimed at deciding between these two alternatives.

In healthy participants, we used offline continuous theta burst stimulation (cTBS) to interfere with the neural activity of the left inferior parietal lobule (IPL). Among the numerous TMS stimulation protocols available (for a review, see Fitzgerald et al., 2006), we used cTBS as it is known to induce, after a short and tolerable stimulation (40 s), prolonged neural inhibition (>45 min; Huang et al., 2005; Franca et al., 2006) at stimulated loci, enough to last throughout our experimental sessions. The neuronal mechanisms related to the inhibitory (or excitatory) effects of brain stimulation are not fully understood, and they vary according to the type of stimulation (i.e., frequency, intensity, number of pulses). For instance, in the case of theta burst stimulation, previous investigations reported that the application of brief bursts resulted in a transient increase in cortical facilitation (Huang and Rothwell, 2004) whilst prolonged stimulation had the opposite effect (Di Lazzaro et al., 2005; Huang et al., 2005).

We targeted the IPL for two main reasons. First, in their imaging study, Lebreton and colleagues found that its activation correlated with an object's likability and represented the first node involved in translating action observation into preference (Lebreton et al., 2012). Second, IPL's activity codes for the agent–object relationship (reviewed in Gentilucci and Volta, 2008; Fernandino and Iacoboni, 2010). In other words, the IPL holds a higher-order representation of the goal of an observed action independently of the effector (e.g., hand or mouth) used to achieve it (Jastorff et al., 2010). On the contrary, activity in the ventral premotor cortex (i.e., the other node of the action observation–action execution network involved in mimetic desires) appears more clustered around the effector (e.g., specific muscle, joint, and digit movements) performing a motor act (Jastorff et al., 2010). Stimulation of the ventral premotor cortex is also more distressing as it activates superficial nerves and muscles in the “temporalis” muscle fascia.

In addition, it is well-established that the IPL has a functional role as an interface between perceptual and motor information. Indeed, it is pivotal in visuomotor transformations (Goodale and Milner, 1992; Jeannerod et al., 1995) converting the intrinsic properties (size and shape) of an object into a pattern of goal-directed movements to reach it such as grasping (Blakemore and Sirigu, 2003; Fogassi and Luppino, 2005) and translating visual information into motor programs to achieve imitations (Mühlau et al., 2005; Molenberghs et al., 2009). Further neuroimaging (Buccino et al., 2001; Chong et al., 2008; Jastorff et al., 2010), TMS (Cattaneo et al., 2010; Jacquet and Avenanti, 2015; for a review see Avenanti et al., 2013b), and lesion studies (e.g., Buxbaum et al., 2005; Kalénine et al., 2010; for a review see Urgesi et al., 2014) showed that the IPL is implicated in the representation of goals of observed actions (Fogassi et al., 2005) and in the internal simulation of an observed motor act (i.e., motor resonance; Gallese et al., 1996; Grafton, 2009) thus demonstrating its pivotal role in goal contagion. TMS (e.g., Ishibashi et al., 2011) and neuroimaging (Kellenbach et al., 2003; Boronat et al., 2005; Canessa et al., 2008) findings implicated the left IPL also in storing motor representations for using familiar tools, in accordance with the fact that damage in this area determines toll-use deficits as shown by apraxic patients (Buxbaum et al., 2000; Rosci et al., 2003).

We chose to stimulate the left IPL for two reasons. First, because IPL's activity is generally stronger in the left hemisphere (see Peeters et al., 2009; Jastorff et al., 2010). Second, because in our experiment the majority of the observed motor acts were carried out with the contralateral right hand (see Methods; research has shown hemispheric preference for contralateral effector movements, see Pelphrey et al., 2004; Shmuelof and Zohary, 2006).

Grounding our experiment on the evidence listed above, we hypothesized that targeting the IPL with cTBS would demonstrate the casual involvement of action perception in an objects' preference. We therefore looked for variations in mimetic preference ratings (obtained comparing participants' ratings of objects that were, vs. were not, reached for by others) for familiar tools and non-tool objects, when cTBS was (or was not) applied. Our prediction was that cTBS would interfere with covert simulation of observed actions, particularly those carried out on tools, and in turn this would reduce mimetic preferences for these items. Such result would support the existence of a causal link between one's motor experience and preferences for non-valence stimuli (i.e., without an inherent emotional content). It would also support embodied cognition theories (for a review, see Ping et al., 2009) in social behavior (Aarts et al., 2004) as well as in aesthetics (Freedberg and Gallese, 2007; Cross et al., 2011; Cross and Ticini, 2012; Ticini et al., 2014) postulating that subjective preference is influenced by others' behavior.

Methods

Participants and experimental protocol

This study was carried out in accordance with the recommendations of the Ethics committee of the Scientific Institute (IRCCS) Eugenio Medea with written informed consent from all subjects, in accordance with the Declaration of Helsinki. The experiment was carried out on 12 volunteers (aged 22.7 ± 4.6 years; four females; 11 right-handed and one mixed-handed, Briggs and Nebes, 1975), complying with what according to Sack et al. (2009) is thought to be sufficient to demonstrate a behavioral effect in case of TMS based on group Talairach coordinates.

We used 120 short videos (duration: 2–5 s; 640 × 480 pixels) from Lebreton et al. (2012) categorized in familiar tools (e.g., pen, lantern, comb, soap bottle) and non-tool objects (e.g., food, toys such as cards and teddy bear, clothes, flowers). In 60 videos, the objects were reached for by another agent (“Goal-objects”) who either moved them or not (Figure (Figure1A).1A). To remove the potential impact of eye gaze on the participant's judgment, the face of the agent was never visible (e.g., Bayliss et al., 2006). In 70% of the videos the action was executed with the right hand, in 6.7% with the left hand, in 15% with the mouth, and in 8.3% with other effectors (e.g., nose). The other 60 videos (“NoGoal-objects”; Figure Figure1B)1B) depicted the same objects but this time they were presented either statically (48% of the objects) or they were moved by a natural forces (e.g., wind or gravity with no human interaction; 20% of the objects) or a human agent was present but did not interact with the objects (32% of the objects). This allowed us to control for the confound that participants may prefer objects in Goal-objects conditions because of the presence of a human being or because of some movement in the video. The two objects within a pair (Goal- and NoGoal-objects) differed only by color and were otherwise identical. For instance, a green candy was the Goal-object for half the subjects, and the NoGoal-object for the other half. This allowed us to eliminate color preferences at the group level (cf. Lebreton et al., 2012).

Figure 1
The preference-rating task. (A) From left to right, the figure shows successive screens displayed in one trial. Participants rated the object (“How much do you like the object?”) featured in the video by moving a cursor along a scale. ...

Each trial started with a fixation cross (1.5 s) followed by one of the videos. After each video, the object reappeared (436 × 326 pixels) and participants were required to rate it (“How much do you like the object?”) by moving a cursor (randomized initial position) on a sliding scale with their right hand (from 0 or not liked, to 10 or highly liked). The question was focused on the object because we aimed at assessing whether observing object-directed actions increased the perceived value of the object. Moreover, previous research demonstrated that the precise formulation of the question (e.g., “How much do you like to use the object?” or “How much would you like to acquire the object?”) is not crucial (Lebreton et al., 2012). There were no time constraints and the video presentation (Goal-objects/NoGoal-objects, Tool/Non-tool stimuli) was randomized. Stimulus presentation was obtained by using the Cogent 2000 (Wellcome Trust Centre for NeuroImaging, London, UK) library of MatLab (Math-Works).

The experiment was run twice for a total of 240 videos. In one session (i.e., cTBS), participants were first positioned for the purpose of the experiment and then cTBS was administered (the experiment started immediately after cTBS). In the other (i.e., Non-cTBS), the TMS coil was never held against the participant's head. The order of the session was counterbalanced. Each of the two sessions lasted 10 min on average and both were run with the very same experimental setup and separated by an interval of 1 h. We applied cTBS over the left IPL (MNI coordinates −58, −32, 44; transformed in Talairach space for the use of the neuronavigation software SofTaxic Optic, E.M.S. s.r.l., Bologna, Italy) corresponding to the supramarginal and angular gyri as identified by Lebreton et al. (2012). cTBS consisted of trains of bursts of three pulses at 50 Hz repeated at 5 Hz and delivered uninterrupted for 40 s for a total of 600 pulses (Huang et al., 2005). It was delivered by an air-cooled figure-of-eight coil of 70 mm diameter attached to a Magstim Rapid2 stimulator, which was kept perpendicular to the underlying gyrus with the handle pointing upward and supported manually. The stimulation intensity was set at 45% of the maximal stimulator output (see for instance Stewart et al., 2001) for all participants. Exclusion criteria were the regular use of drugs or medications, any history of psychiatric or neurological disorders, and contra-indications to transcranial magnetic stimulation (e.g., pregnancy or metallic implants), all assessed by a standard questionnaire. All participants wore earplugs and no particular discomfort or other negative side effects were reported.

Analysis

We first conducted an omnibus repeated measured ANOVA, after having reduced the effect of inter-subject variability by normalizing (z scores) the preference ratings for each participants. We used “Stimulation” (cTBS, Non-cTBS) and “Action” (Goal, NoGoal-object) and “Object type” (Tool, Non-tool) as within subjects factors. Additionally, we computed the mimetic preference ratings (see Lebreton et al., 2012) as the difference in the original ratings between Goal vs. NoGoal conditions (preference for Goal-objects—preference for NoGoal-objects). This excluded effects associated with variations in preference scores among objects, as we postulated that the objects were non-valenced stimuli (i.e., without an inherent emotional content). We then used one-sample Bayesian t-tests to test the hypothesis that the population means for the mimetic preference in the four conditions (cTBS and No-cTBS for Tools and Non-tool objects) was not equal to zero. Bayesian t-tests (JASP; Love et al., 2015) employed default priors to estimate the Bayes Factors (BF; Rouder et al., 2012) and we used BF10 as it allows estimating the likelihood that the data fit a specified alternative hypothesis relative to the hypothesis of no effect (Rouder et al., 2012). A BF10 greater than 3 indicates substantial evidence for the alternative hypothesis (Wetzels and Wagenmakers, 2012), i.e., that the observed data favor the alternative hypothesis over the null hypothesis by a ratio of 3:1.

Results

The results of the ANOVA identified a statistically significant main effect of “Action” [F(1, 11) = 14.74, p = 0.003, ηp2 = 0.57] and a significant interaction between “Stimulation,” “Action,” and “Object type” [F(1, 11) = 5.1, p = 0.045, ηp2 = 0.32]. Non-specific effects of rTMS on the ratings [“Stimulation”: F(1, 11) = 1.3, p = 0.28, ηp2 = 0.1] and other factors or interaction (Fs < 2.74, ps > 0.12) were absent. We then broke the ANOVA for the factor “Object type” and run selected tests comparing the effects of stimulation within each “Object type” category. For the Tools category, we found a significant main effect of “Action” [F(1, 11) = 23.55, p < 0.001, ηp2 = 0.68] and a significant interaction between “Stimulation” and “Action” [F(1, 11) = 7.9, p = 0.017, ηp2 = 0.42]. Bonferroni-corrected post-hoc tests showed that the preference for Goal-objects was larger (ps < 0.001) when compared to NoGoal-objects in both cTBS (Goal-objects: 0.108 ± 0.054; NoGoal-objects: −0.211 ± 0.040; means ± S.E) and Non-cTBS conditions (Goal-objects: 0.024 ± 0.066; NoGoal-objects: −0.196 ± 0.056). Importantly, the preference scores between Goal-objects in cTBS were higher than those in Non-cTBS (p = 0.036). This indicated that cTBS selectively increased the preference for Goal-objects rather than decreasing that for NoGoal-objects. Instead, the means for NoGoal-objects did not differ between the two stimulation conditions (p > 0.99). As far as the Non-tools category is concerned, we found a significant main effect of “Action” [F(1, 11) = 8.48, p = 0.014, ηp2 = 0.43] confirming that in both cTBS and Non-cTBS conditions Goal-objects were preferred more than NoGoal-objects. No other results were significant (Fs < 2.8, ps > 0.12). A further omnibus ANOVA conducted on the judgements' response times revealed only a significant main effect of “Object type” [F(1, 11) = 5.17, p = 0.044, ηp2 = 0.32]: the time required to express the preference for Tools (1968.38 ± 203.04; ms ± S.E.) was longer than that for Non-tools objects (1931.97 ± 155.20). Other main effects and interactions were not significant (Fs < 1.96, ps > 0.19).

Table Table11 shows that all mean values of mimetic preference ratings (preference for Goal-objects—preference for NoGoal-objects) were significantly larger than the test value of zero (see Figure Figure2).2). This result was expected as previous experimental evidence (Lebreton et al., 2012) indicated higher preference for Goal-objects when compared to NoGoal-objects. Notably, the BF for Tools after cTBS was very large and indicated that the data favored the one-sided alternative hypothesis that the population mean was larger than the test value of zero by a ratio of 104.2: 1. One-way ANOVAs calculated in each condition (i.e., Tools Non-cTBS, Tools cTBS, etc.) indicated that the counterbalanced order of stimulation (i.e., whether participants begun the experiment with cTBS or Non-cTBS) did not influence the results (Fs < 5.6; ps > 0.16).

Table 1
Values of mimetic preference ratings measured across conditions.
Figure 2
(A) Comparison of mimetic preference ratings (difference in preference ratings between Goal- and NoGoal-objects) across participants for Tool and Non-Tools objects in the two stimulation conditions. Empty and filled bars represent mimetic preferences ...

A two-sample t-test (two-tailed) further showed that the mimetic preference for Tools after cTBS was significantly higher than that for Tools in the Non-cTBS conditions [t(11) = 2.8, p = 0.017, d = 0.81, C.I. 0.05 to 0.43]. The BF confirmed these results by indicating that the data favored the alternative hypothesis that the mimetic preference mean was higher in cTBS than in Non-cTBS by a ratio of 3.8: 1. This was clearly not the case for Non-tool objects [t(11) = −0.48, p = 0.64, d = −0.14; BF10 = 0.3; C.I. −0.31 to 0.19].

Discussion

In this study, we used non-invasive brain stimulation to test the embodied cognition's hypothesis that subjective preference is grounded in action, while we recorded the preference of healthy volunteers for objects that were (or were not) reached for or manipulated by other individuals. The result indicates that IPL stimulation, which is known to interfere with processing goal-related information (Cattaneo et al., 2010; Puzzo et al., 2013; for a review see Avenanti et al., 2013b) and tool manipulation (Ishibashi et al., 2011), led to a significant increase in mimetic preference ratings of tools. No effects were found on mimetic preferences of other familiar objects. We argue that, albeit preliminary, this result suggests a left IPL's contribution in integrating the representation of others' actions (Iacoboni et al., 1999; Grèzes et al., 2003; Johnson-Frey et al., 2003) with subjective preference for objects (Lebreton et al., 2009). We believe that the absence of an effect of the order of stimulation indicates that cTBS was not particularly disturbing per se (as people may rely more on others' choice in distressing situations) and did not induce arousal for objects (e.g., Dräger et al., 2004).

The present outcome prompts to question of why IPL's stimulation increased mimetic preference rather than the opposite, as we predicted. Indeed, previous research indicated that prolonged cTBS results in transient inhibitory effects (for a review, see Fitzgerald et al., 2006; Parkin et al., 2015). For instance, it determines a reduction in cortical excitability (or amplitude of motor-evoked potentials) when a testing single pulse of transcranial magnetic stimulation is applied over the primary motor cortex (Di Lazzaro et al., 2005; Huang et al., 2005). Although the mechanisms through which cTBS interferes with brain activity are not completely clear (Fitzgerald et al., 2006), some authors suggest that the change produced by cTBS may be related to a decreased effectiveness of synaptic connections recruited in the circuits that are involved in the generation of motor-evoked potentials (Huang et al., 2005).

In spite of the fact that some deemed irrelevant the direction of the behavioral effects when using TMS to empirically test the causal role of a brain area (Silvanto et al., 2008), two alternative explanations of our result are possible. On the one hand, cTBS may have increased the functional activation of the stimulated IPL (Siebner et al., 2001), thus permitting a better embodiment of the observed actions. In this regard, an interesting report indicated that interferential TMS over IPL improved recognition of emotional body movements (i.e., emotional expressions; Engelen et al., 2015). On the other, cTBS suppression of the IPL may have triggered compensatory activity in other sensorimotor areas with the result of facilitating the brain response to observed actions (e.g., Ubaldi et al., 2015). This apparently “paradoxical” facilitatory effect has been predicted and reported before (Kilner et al., 2007; Gazzola and Keysers, 2009; Friston et al., 2011; Schippers and Keysers, 2011; D'Ausilio et al., 2012; Arfeller et al., 2013; Avenanti et al., 2013a). In other words, disruptive cTBS over IPL may have increased motor resonance in frontal regions (Ubaldi et al., 2015) and in so doing facilitated the brain response to action observation (e.g., Avenanti et al., 2013a). In turn, as proposed by Lebreton et al. (2012), it is plausible that the increased activity in frontal areas would have engaged the ventral valuation system encoding the perceived value of objects (Rangel et al., 2008; Chib et al., 2009; Lebreton et al., 2009; Peters and Büchel, 2010). Obviously, the question of what are the underlying mechanisms associated to the spread of cTBS effects cannot be address in the current study as they would require, for instance, a combination of TMS and fMRI data in order to visualize compensatory processes. Another caveat (discussed below) is the absence of a control site. Overall, whether cTBS determined an increase or decrease of brain activity, our result seems to indicate that IPL belongs to a neural mechanism that translate the observation of goal-directed actions into preference ratings. We further believe that the pattern of our results rules out the possibility that the increase in mimetic preference toward tools was due to perceptual ease or fluency. This is observed when previous experience interacting with items affects one's own preference toward them (for a review, see Reber et al., 2004). Moreover, as the counterbalanced order of stimulation doesn't affect the pattern of results (see Results and Figure Figure2B),2B), we can also exclude that our measurements were affected by behavioral facilitation. This is observed when the modulation of baseline neural activity though adaptation to a stimulus leads to state-dependency TMS effects, i.e., the stimulation of functionally distinct neural populations within the targeted region (e.g., Cattaneo and Silvanto, 2008).

Additionally, we found that the time required to express the preference for tools was longer than for non-tool objects. This result could be explained, at least indirectly, by the fact that viewing tools automatically activates neural representations associated with their manipulation, which differ from that for other objects (Castiello, 2005; Proverbio et al., 2007, 2011, 2013; Cardellicchio et al., 2011). The integration of several complementary higher order relationships among action, affordance associated with tool manipulation, target and preference may require a longer processing time.

As mentioned above, a limitation of the current preliminary study is the absence of an active control stimulation site. The absence of control site means that we cannot exclude the possibility that cTBS applied elsewhere in the brain could cause similar effects on mimetic preference of tool objects. However, the choice of an “ideal” control site appears difficult when it comes to experiments requiring subjective judgements: TMS at different sites may influence participants' ratings in ways that cannot be always controlled for. For instance, TMS may cause diverse degrees of discomfort or distress associated with visual, acoustic, and tactile sensations or with activation of superficial nerves and muscles (e.g., when targeting the ventral premotor cortex through the “temporalis” muscle fascia). In addition, TMS of other sensorimotor areas (e.g., striate and extra-striate cortices, superior temporal sulcus) may interfere with the perception and processing of the visual stimuli per se (in our case, both Goal- and NoGoal-objects), and stimulation of prefrontal and posterior parietal cortices may modulate object likability (e.g., Cattaneo et al., 2014) independently of whether an object is the goal of an action or not. Overall, we believe that the stimulation of the IPL was meaningful to address the research question, as demonstrated by the pattern of our results, and we acknowledge the fact that future studies should include an appropriate active control site.

To conclude, our preliminary result demonstrates that an object's preference is contingent on the representation of others' behavior in the brain of the beholder. We believe that this outcome is relevant to our understanding of the neural mechanism that, through actions, allows conveying the value of items from individual to individual and automatically influence preference choices for the objects present in our environment.

Author contributions

CU, LT, and SK conceived the work, interpreted the data, draft and revised the manuscript. LT and CU acquired the data and LT analyzed them.

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We wish to thank Mathias Pessiglione for his assistance with the stimuli and an earlier draft of the manuscript, and Marco Poliaghi for helping during data acquisition. The research was supported by a research fund from The University of Manchester and grants from the Ministero Istruzione Università e Ricerca, Italy (Futuro In Ricerca, FIR 2012, Prot. N. RBFR12F0BD; to CU) and from Istituto di Ricovero e Cura a Carattere Scientifico (Ricerca Corrente 2014; to CU). The authors declare no competing financial interests.

References

  • Aarts H., Gollwitzer P. M., Hassin R. R. (2004). Goal contagion: perceiving is for pursuing. J. Pers. Soc. Psychol. 87, 23–37. 10.1037/0022-3514.87.1.23 [PubMed] [Cross Ref]
  • Arfeller C., Schwarzbach J., Ubaldi S., Ferrari P., Barchiesi G., Cattaneo L. (2013). Whole-brain haemodynamic after-effects of 1-Hz magnetic stimulation of the posterior superior temporal cortex during action observation. Brain Topogr. 26, 278–291. 10.1007/s10548-012-0239-9 [PubMed] [Cross Ref]
  • Avenanti A., Annella L., Candidi M., Urgesi C., Aglioti S. M. (2013a). Compensatory plasticity in the action observation network: virtual lesions of STS enhance anticipatory simulation of seen actions. Cereb. Cortex 23, 570–580. 10.1093/cercor/bhs040 [PubMed] [Cross Ref]
  • Avenanti A., Candidi M., Urgesi C. (2013b). Vicarious motor activation during action perception: beyond correlational evidence. Front. Hum. Neurosci. 7:185. 10.3389/fnhum.2013.00185 [PMC free article] [PubMed] [Cross Ref]
  • Avenanti A., Urgesi C. (2011). Understanding “what” others do: mirror mechanisms play a crucial role in action perception. Soc. Cogn. Affect. Neurosci. 6, 257–259. 10.1093/scan/nsr004 [PMC free article] [PubMed] [Cross Ref]
  • Bayliss A. P., Paul M. A., Cannon P. R., Tipper S. P. (2006). Gaze cuing and affective judgments of objects: i like what you look at. Psychon. Bull. Rev. 13, 1061–1066. 10.3758/BF03213926 [PubMed] [Cross Ref]
  • Blakemore S. J., Sirigu A. (2003). Action prediction in the cerebellum and in the parietal lobe. Exp. Brain Res. 153, 239–245. 10.1007/s00221-003-1597-z [PubMed] [Cross Ref]
  • Boronat C. B., Buxbaum L. J., Coslett H. B., Tang K., Saffran E. M., Kimberg D. Y., et al. . (2005). Distinctions between manipulation and function knowledge of objects: evidence from functional magnetic resonance imaging. Cogn. Brain Res. 23, 361–373. 10.1016/j.cogbrainres.2004.11.001 [PubMed] [Cross Ref]
  • Briggs G. G., Nebes R. D. (1975). Patterns of hand preference in a student population. Cortex 11, 230–238. 10.1016/S0010-9452(75)80005-0 [PubMed] [Cross Ref]
  • Buccino G., Binkofski F., Fink G. R., Fadiga L., Fogassi L., Gallese V., et al. . (2001). Action observation activates premotor and parietal areas in a somatotopic manner: an fMRI study. Eur. J. Neurosci. 13, 400–404. 10.1046/j.1460-9568.2001.01385.x [PubMed] [Cross Ref]
  • Buxbaum L. J., Johnson-Frey S. H., Bartlett-Williams M. (2005). Deficient internal models for planning hand–object interactions in apraxia. Neuropsychologia 43, 917–929. 10.1016/j.neuropsychologia.2004.09.006 [PubMed] [Cross Ref]
  • Buxbaum L. J., Veramonti T., Schwartz M. F. (2000). Function and manipulation tool knowledge in apraxia: knowing ‘what for’ but not ‘how’. Neurocase 6, 83–97. 10.1080/13554790008402763 [Cross Ref]
  • Canessa N., Borgo F., Cappa S. F., Perani D., Falini A., Buccino G., et al. . (2008). The different neural correlates of action and functional knowledge in semantic memory: an fMRI study. Cereb. Cortex 18, 740–751. 10.1093/cercor/bhm110 [PubMed] [Cross Ref]
  • Cardellicchio P., Sinigaglia C., Costantini M. (2011). The space of affordances: a TMS study. Neuropsychologia 49, 1369–1372. 10.1016/j.neuropsychologia.2011.01.021 [PubMed] [Cross Ref]
  • Castiello U. (2005). The neuroscience of grasping. Nat. Rev. Neurosci. 6, 726–736. 10.1038/nrn1744 [PubMed] [Cross Ref]
  • Cattaneo L., Sandrini M., Schwarzbach J. (2010). State-dependent TMS reveals a hierarchical representation of observed acts in the temporal, parietal, and premotor cortices. Cereb. Cortex 20, 2252–2258. 10.1093/cercor/bhp291 [PubMed] [Cross Ref]
  • Cattaneo Z., Lega C., Gardelli C., Merabet L. B., Cela-Conde C. J., Nadal M. (2014). The role of prefrontal and parietal cortices in esthetic appreciation of representational and abstract art: a TMS study. Neuroimage 99, 443–450. 10.1016/j.neuroimage.2014.05.037 [PubMed] [Cross Ref]
  • Cattaneo Z., Silvanto J. (2008). Investigating visual motion perception using the transcranial magnetic stimulation-adaptation paradigm. Neuroreport 19, 1423–1427. 10.1097/WNR.0b013e32830e0025 [PubMed] [Cross Ref]
  • Chib V. S., Rangel A., Shimojo S., O'Doherty J. P. (2009). Evidence for a common representation of decision values for dissimilar goods in human ventromedial prefrontal cortex. J. Neurosci. 29, 12315–12320. 10.1523/JNEUROSCI.2575-09.2009 [PubMed] [Cross Ref]
  • Chong T. T., Cunnington R., Williams M. A., Kanwisher N., Mattingley J. B. (2008). fMRI adaptation reveals mirror neurons in human inferior parietal cortex. Curr. Biol. 18, 1576–1580. 10.1016/j.cub.2008.08.068 [PMC free article] [PubMed] [Cross Ref]
  • Cross E. S., Kirsch L., Ticini L. F., Schütz-Bosbach S. (2011). The impact of aesthetic evaluation and physical ability on dance perception. Front. Hum. Neurosci. 5:102. 10.3389/fnhum.2011.00102 [PMC free article] [PubMed] [Cross Ref]
  • Cross E. S., Ticini L. F. (2012). Neuroaesthetics and beyond: new horizons in applying the science of the brain to the art of dance. Phenomenol. Cogn. Sci. 11, 5–16. 10.1007/s11097-010-9190-y [Cross Ref]
  • D'Ausilio A., Bufalari I., Salmas P., Fadiga L. (2012). The role of the motor system in discriminating normal and degraded speech sounds. Cortex 48, 882–887. 10.1016/j.cortex.2011.05.017 [PubMed] [Cross Ref]
  • Di Lazzaro V., Pilato F., Saturno E., Oliviero A., Dileone M., Mazzone P., et al. . (2005). Theta-burst repetitive transcranial magnetic stimulation suppresses specific excitatory circuits in the human motor cortex. J. Physiol. 565, 945–950. 10.1113/jphysiol.2005.087288 [PubMed] [Cross Ref]
  • Dräger B., Breitenstein C., Helmke U., Kamping S., Knecht S. (2004). Specific and nonspecific effects of transcranial magnetic stimulation on picture–word verification. Eur. J. Neurosci. 20, 1681–1687. 10.1111/j.1460-9568.2004.03623.x [PubMed] [Cross Ref]
  • Engelen T., de Graaf T. A., Sack A. T., de Gelder B. (2015). A causal role for inferior parietal lobule in emotion body perception. Cortex 73, 195–202. 10.1016/j.cortex.2015.08.013 [PubMed] [Cross Ref]
  • Fabbri-Destro M., Rizzolatti G. (2008). Mirror neurons and mirror systems in monkeys and humans. Physiology 23, 171–179. 10.1152/physiol.00004.2008 [PubMed] [Cross Ref]
  • Fernandino L., Iacoboni M. (2010). Are cortical motor maps based on body parts or coordinated actions? Implications for embodied semantics. Brain Lang. 112, 44–53. 10.1016/j.bandl.2009.02.003 [PubMed] [Cross Ref]
  • Fitzgerald P. B., Fountain S., Daskalakis Z. J. (2006). A comprehensive review of the effects of rTMS on motor cortical excitability and inhibition. Clin. Neurophysiol. 117, 2584–2596. 10.1016/j.clinph.2006.06.712 [PubMed] [Cross Ref]
  • Fogassi L., Ferrari P. F., Gesierich B., Rozzi S., Chersi F., Rizzolatti G. (2005). Parietal lobe: from action organization to intention understanding. Science 308, 662–667. 10.1126/science.1106138 [PubMed] [Cross Ref]
  • Fogassi L., Luppino G. (2005). Motor functions of the parietal lobe. Curr. Opin. Neurobiol. 15, 626–631. 10.1016/j.conb.2005.10.015 [PubMed] [Cross Ref]
  • Franca M., Koch G., Mochizuki H., Huang Y. Z., Rothwell J. C. (2006). Effects of theta burst stimulation protocols on phosphene threshold. Clin. Neurophysiol. 117, 1808–1813. 10.1016/j.clinph.2006.03.019 [PubMed] [Cross Ref]
  • Freedberg D., Gallese V. (2007). Motion, emotion and empathy in esthetic experience. Trends Cogn. Sci. 11, 197–203. 10.1016/j.tics.2007.02.003 [PubMed] [Cross Ref]
  • Friston K., Mattout J., Kilner J. (2011). Action understanding and active inference. Biol. Cybern. 104, 137–160. 10.1007/s00422-011-0424-z [PMC free article] [PubMed] [Cross Ref]
  • Gallese V., Fadiga L., Fogassi L., Rizzolatti G. (1996). Action recognition in the premotor cortex. Brain 119(Pt 2), 593–609. 10.1093/brain/119.2.593 [PubMed] [Cross Ref]
  • Gazzola V., Keysers C. (2009). The observation and execution of actions share motor and somatosensory voxels in all tested subjects: single-subject analyses of unsmoothed fMRI data. Cereb. Cortex 19, 1239–1255. 10.1093/cercor/bhn181 [PMC free article] [PubMed] [Cross Ref]
  • Gentilucci M., Volta R. D. (2008). Spoken language and arm gestures are controlled by the same motor control system. Q. J. Exp. Psychol. 61, 944–957. 10.1080/17470210701625683 [PubMed] [Cross Ref]
  • Girard R. (1988). Violence and the Sacred. London: Athlone.
  • Gollwitzer P. M., Moskowitz G. B. (1996). Goal effects on action and cognition, in Social Psychology: Handbook of Basic Principles, eds Higgins E. T., Kruglanski A. W., editors. (NewYork, NY: Guilford; ), 361–399.
  • Goodale M. A., Milner A. D. (1992). Separate visual pathways for perception and action. Trends Neurosci. 15, 20–25. 10.1016/0166-2236(92)90344-8 [PubMed] [Cross Ref]
  • Grafton S. T. (2009). Embodied cognition and the simulation of action to understand others. Ann. N. Y. Acad. Sci. 1156, 97–117. 10.1111/j.1749-6632.2009.04425.x [PubMed] [Cross Ref]
  • Grèzes J., Armony J. L., Rowe J., Passingham R. E. (2003). Activations related to ‘mirror’ and ‘canonical’ neurones in the human brain: an fMRI study. Neuroimage 18, 928–937. 10.1016/S1053-8119(03)00042-9 [PubMed] [Cross Ref]
  • Huang Y. Z., Edwards M. J., Rounis E., Bhatia K. P., Rothwell J. C. (2005). Theta burst stimulation of the human motor cortex. Neuron 45, 201–206. 10.1016/j.neuron.2004.12.033 [PubMed] [Cross Ref]
  • Huang Y. Z., Rothwell J. C. (2004). The effect of short-duration bursts of high-frequency, low-intensity transcranial magnetic stimulation on the human motor cortex. Clin. Neurophysiol. 115, 1069–1075. 10.1016/j.clinph.2003.12.026 [PubMed] [Cross Ref]
  • Iacoboni M., Woods R. P., Brass M., Bekkering H., Mazziotta J. C., Rizzolatti G. (1999). Cortical mechanisms of human imitation. Science 286, 2526–2528. 10.1126/science.286.5449.2526 [PubMed] [Cross Ref]
  • Ishibashi R., Ralph M. A. L., Saito S., Pobric G. (2011). Different roles of lateral anterior temporal lobe and inferior parietal lobule in coding function and manipulation tool knowledge: evidence from an rTMS study. Neuropsychologia 49, 1128–1135. 10.1016/j.neuropsychologia.2011.01.004 [PubMed] [Cross Ref]
  • Jacquet P. O., Avenanti A. (2015). Perturbing the action observation network during perception and categorization of actions' goals and grips: state-dependency and virtual lesion TMS effects. Cereb. Cortex 25, 598–608. 10.1093/cercor/bht242 [PubMed] [Cross Ref]
  • Jastorff J., Begliomini C., Fabbri-Destro M., Rizzolatti G., Orban G. A. (2010). Coding observed motor acts: different organizational principles in the parietal and premotor cortex of humans. J. Neurophysiol. 104, 128–140. 10.1152/jn.00254.2010 [PubMed] [Cross Ref]
  • Jeannerod M., Arbib M. A., Rizzolatti G., Sakata H. (1995). Grasping objects: the cortical mechanisms of visuomotor transformation. Trends Neurosci. 18, 314–320. 10.1016/0166-2236(95)93921-J [PubMed] [Cross Ref]
  • Johnson-Frey S. H., Maloof F. R., Newman-Norlund R., Farrer C., Inati S., Grafton S. T. (2003). Actions or hand-object interactions? Human inferior frontal cortex and action observation. Neuron 39, 1053–1058. 10.1016/S0896-6273(03)00524-5 [PubMed] [Cross Ref]
  • Kalénine S., Buxbaum L. J., Coslett H. B. (2010). Critical brain regions for action recognition: lesion symptom mapping in left hemisphere stroke. Brain 133, 3269–3280. 10.1093/brain/awq210 [PMC free article] [PubMed] [Cross Ref]
  • Kellenbach M. L., Brett M., Patterson K. (2003). Actions speak louder than functions: the importance of manipulability and action in tool representation. J. Cogn. Neurosci. 15, 30–46. 10.1162/089892903321107800 [PubMed] [Cross Ref]
  • Kilner J. M., Friston K. J., Frith C. D. (2007). Predictive coding: an account of the mirror neuron system. Cogn. Process. 8, 159–166. 10.1007/s10339-007-0170-2 [PMC free article] [PubMed] [Cross Ref]
  • Lebreton M., Jorge S., Michel V., Thirion B., Pessiglione M. (2009). An automatic valuation system in the human brain: evidence from functional neuroimaging. Neuron 64, 431–439. 10.1016/j.neuron.2009.09.040 [PubMed] [Cross Ref]
  • Lebreton M., Kawa S., Forgeot d'Arc B., Daunizeau J., Pessiglione M. (2012). Your goal is mine: unraveling mimetic desires in the human brain. J. Neurosci. 32, 7146–7157. 10.1523/JNEUROSCI.4821-11.2012 [PubMed] [Cross Ref]
  • Love J., Selker R., Marsman M., Jamil T., Verhagen A. J., Ly A., et al. (2015). JASP (Version 0.6.6) [Computer Software].
  • Molenberghs P., Cunnington R., Mattingley J. B. (2009). Is the mirror neuron system involved in imitation? A short review and meta-analysis. Neurosci. Biobehav. Rev. 33, 975–980. 10.1016/j.neubiorev.2009.03.010 [PubMed] [Cross Ref]
  • Mühlau M., Hermsdörfer J., Goldenberg G., Wohlschläger A. M., Castrop F., Stahl R., et al. . (2005). Left inferior parietal dominance in gesture imitation: an fMRI study. Neuropsychologia 43, 1086–1098. 10.1016/j.neuropsychologia.2004.10.004 [PubMed] [Cross Ref]
  • Parkin B. L., Ekhtiari H., Walsh V. F. (2015). Non-invasive human brain stimulation in cognitive neuroscience: a primer. Neuron 87, 932–945. 10.1016/j.neuron.2015.07.032 [PubMed] [Cross Ref]
  • Pelphrey K. A., Morris J. P., Mccarthy G. (2004). Grasping the intentions of others: the perceived intentionality of an action influences activity in the superior temporal sulcus during social perception. J. Cogn. Neurosci. 16, 1706–1716. 10.1162/0898929042947900 [PubMed] [Cross Ref]
  • Peeters R., Simone L., Nelissen K., Fabbri-Destro M., Vanduffel W., Rizzolatti G., et al. . (2009). The representation of tool use in humans and monkeys: common and uniquely human features. J. Neurosci. 29, 11523–11539. 10.1523/JNEUROSCI.2040-09.2009 [PubMed] [Cross Ref]
  • Peters J., Büchel C. (2010). Neural representations of subjective reward value. Behav. Brain Res. 213, 135–141. 10.1016/j.bbr.2010.04.031 [PubMed] [Cross Ref]
  • Ping R. M., Dhillon S., Beilock S. L. (2009). Reach for what you like: the body's role in shaping preferences. Emot. Rev. 1, 140–150. 10.1177/1754073908100439 [Cross Ref]
  • Proverbio A., Del Zotto M., Zani A. (2007). The emergence of semantic categorization in early visual processing: ERP indices of animal vs. artifact recognition. BMC Neurosci. 8:24. 10.1186/1471-2202-8-24 [PMC free article] [PubMed] [Cross Ref]
  • Proverbio A. M., Adorni R., D'Aniello G. E. (2011). 250 ms to code for action affordance during observation of manipulable objects. Neuropsychologia 9, 2711–2717. 10.1016/j.neuropsychologia.2011.05.019 [PubMed] [Cross Ref]
  • Proverbio A. M., Azzari R., Adorni R. (2013). Is there a left hemispheric asymmetry for tool affordance processing. Neuropsychologia 51, 2690–2701. 10.1016/j.neuropsychologia.2013.09.023 [PubMed] [Cross Ref]
  • Puzzo I., Cooper N. R., Cantarella S., Fitzgerald P. B., Russo R. (2013). The effect of rTMS over the inferior parietal lobule on EEG sensorimotor reactivity differs according to self-reported traits of autism in typically developing individuals. Brain Res. 1541, 33–41. 10.1016/j.brainres.2013.10.016 [PubMed] [Cross Ref]
  • Rangel A., Camerer C., Montague P. R. (2008). A framework for studying the neurobiology of value-based decision making. Nat. Rev. Neurosci. 9, 545–556. 10.1038/nrn2357 [PMC free article] [PubMed] [Cross Ref]
  • Reber R., Schwarz N., Winkielman P. (2004). Processing fluency and aesthetic pleasure: is beauty in the perceiver's processing experience? Pers. Soc. Psychol. Rev. 8, 364–382. 10.1207/s15327957pspr0804_3 [PubMed] [Cross Ref]
  • Rizzolatti G., Craighero L. (2004). The mirror-neuron system. Annu. Rev. Neurosci. 27, 169–192. 10.1146/annurev.neuro.27.070203.144230 [PubMed] [Cross Ref]
  • Rosci C., Chiesa V., Laiacona M., Capitani E. (2003). Apraxia is not associated to a disproportionate naming impairment for manipulable objects. Brain Cogn. 53, 412–415. 10.1016/S0278-2626(03)00156-8 [PubMed] [Cross Ref]
  • Rouder J. N., Morey R. D., Speckman P. L., Province J. M. (2012). Default Bayes factors for ANOVA designs. J. Math. Psychol. 56, 356–374. 10.1016/j.jmp.2012.08.001 [Cross Ref]
  • Sack A. T., Kadosh R. C., Schuhmann T., Moerel M., Walsh V., Goebel R. (2009). Optimizing functional accuracy of TMS in cognitive studies: a comparison of methods. J. Cogn. Neurosci. 21, 207–221. 10.1162/jocn.2009.21126 [PubMed] [Cross Ref]
  • Schippers M. B., Keysers C. (2011). Mapping the flow of information within the putative mirror neuron system during gesture observation. Neuroimage 57, 37–44. 10.1016/j.neuroimage.2011.02.018 [PubMed] [Cross Ref]
  • Shmuelof L., Zohary E. (2006). A mirror representation of others' actions in the human anterior parietal cortex. J. Neurosci. 26, 9736–9742. 10.1523/JNEUROSCI.1836-06.2006 [PubMed] [Cross Ref]
  • Siebner H. R., Takano B., Peinemann A., Schwaiger M., Conrad B., Drzezga A. (2001). Continuous transcranial magnetic stimulation during positron emission tomography: a suitable tool for imaging regional excitability of the human cortex. Neuroimage 14, 883–890. 10.1006/nimg.2001.0889 [PubMed] [Cross Ref]
  • Silvanto J., Cattaneo Z., Battelli L., Pascual-Leone A. (2008). Baseline cortical excitability determines whether TMS disrupts or facilitates behavior. J. Neurophysiol. 99, 2725–2730. 10.1152/jn.01392.2007 [PMC free article] [PubMed] [Cross Ref]
  • Stewart L. M., Walsh V., Rothwell J. C. (2001). Motor and phosphene thresholds: a transcranial magnetic stimulation correlation study. Neuropsychologia 39, 415–419. 10.1016/S0028-3932(00)00130-5 [PubMed] [Cross Ref]
  • Ticini L. F., Rachman L., Pelletier J., Dubal S. (2014). Enhancing aesthetic appreciation by priming canvases with actions that match the artist's painting style. Front. Hum. Neurosci. 8:391. 10.3389/fnhum.2014.00391 [PMC free article] [PubMed] [Cross Ref]
  • Ubaldi S., Barchiesi G., Cattaneo L. (2015). Bottom-up and top-down visuomotor responses to action observation. Cereb. Cortex 25, 1032–1041. 10.1093/cercor/bht295 [PubMed] [Cross Ref]
  • Urgesi C., Candidi M., Avenanti A. (2014). Neuroanatomical substrates of action perception and understanding: an anatomic likelihood estimation meta-analysis of lesion-symptom mapping studies in brain injured patients. Front. Hum. Neurosci. 8:344. 10.3389/fnhum.2014.00344 [PMC free article] [PubMed] [Cross Ref]
  • Wetzels R., Wagenmakers E. J. (2012). A default Bayesian hypothesis test for correlations and partial correlations. Psychon. Bull. Rev. 19, 1057–1064. 10.3758/s13423-012-0295-x [PMC free article] [PubMed] [Cross Ref]

Articles from Frontiers in Psychology are provided here courtesy of Frontiers Media SA