Inhibition and Heart Rate Variability in Experimentally Induced Pain

References

• Craig A, Tran Y, Siddall P, et al. Developing a model of associations between chronic pain, depressive mood, chronic fatigue, and self-efficacy in people with spinal cord injury. J Pain. 2013;14(9):911–920. doi:10.1016/j.jpain.2013.03.002
   PubMed Web of Science ®Google Scholar
• Raja SN, Carr DB, Cohen M, et al. The revised international association for the study of pain definition of pain: concepts, challenges, and compromises. Pain. 2020;161(9):1976–1982. doi:10.1097/j.pain.0000000000001939
   PubMed Web of Science ®Google Scholar
• Koenig J, Jarczok MN, Ellis RJ, Hillecke TK, Thayer JF. Heart rate variability and experimentally induced pain in healthy adults: a systematic review. Eur J Pain. 2014;18(3):301–314. doi:10.1002/j.1532-2149.2013.00379.x
   PubMed Web of Science ®Google Scholar
• Melzack R. Evolution of the neuromatrix theory of pain. The Prithvi raj lecture: presented at the third world congress of world institute of pain, Barcelona 2004. Pain Pract. 2005;5(2):85–94. doi:10.1111/j.1533-2500.2005.05203.x
   PubMedGoogle Scholar
• Oosterman J, Derksen LC, van Wijck AJM, Kessels RPC, Veldhuijzen DS. Executive and attentional functions in chronic pain: does performance decrease with increasing task load? Pain Res Manag. 2012;17(3):159–165. doi:10.1155/2012/962786
   PubMed Web of Science ®Google Scholar
• Farmer MA, Baliki MN, Apkarian AV. A dynamic network perspective of chronic pain. Neurosci Lett. 2012;520(2):197–203. doi:10.1016/j.neulet.2012.05.001
   PubMed Web of Science ®Google Scholar
• Apkarian AV, Bushnell MC, Treede R-D, Zubieta J-K. Human brain mechanisms of pain perception and regulation in health and disease. Eur J Pain. 2005;9(4):463–484. doi:10.1016/j.ejpain.2004.11.001
   PubMed Web of Science ®Google Scholar
• Seminowicz DA, Davis KD. A re-examination of pain-cognition interactions: implications for neuroimaging. Pain. 2007;130(1–2):8–13. doi:10.1016/j.pain.2007.03.036
   PubMed Web of Science ®Google Scholar
• Gilbert SJ, Burgess PW. Executive function. Curr Biol. 2008;18(3):R110–4. doi:10.1016/j.cub.2007.12.014
   PubMed Web of Science ®Google Scholar
• Lorenz J, Minoshima S, Casey KL. Keeping pain out of mind: the role of the dorsolateral prefrontal cortex in pain modulation. Brain. 2003;126(Pt 5):1079–1091. doi:10.1093/brain/awg102
   PubMed Web of Science ®Google Scholar
• Oosterman JM, Dijkerman HC, Kessels RPC, Scherder EJA. A unique association between cognitive inhibition and pain sensitivity in healthy participants. Eur J Pain. 2010;14(10):1046–1050. doi:10.1016/j.ejpain.2010.04.004
   PubMed Web of Science ®Google Scholar
• Scherder EJA, Sergeant JA, Swaab DF. Pain processing in dementia and its relation to neuropathology. Lancet Neurol. 2003;2(11):677–686. doi:10.1016/s1474-4422(03)00556-8
   PubMed Web of Science ®Google Scholar
• Karsdorp PA, Geenen R, Vlaeyen JWS. Response inhibition predicts painful task duration and performance in healthy individuals performing a cold pressor task in a motivational context. Eur J Pain. 2014;18(1):92–100. doi:10.1002/j.1532-2149.2013.00348.x
   PubMed Web of Science ®Google Scholar
• Bunk S, Preis L, Zuidema S, Lautenbacher S, Kunz M. Executive functions and pain: a systematic review. Zeitschrift für Neuropsychol. 2019;30:169–196. doi:10.1024/1016-264X/a000264
   Web of Science ®Google Scholar
• Berryman C, Stanton TR, Bowering KJ, Tabor A, McFarlane A, Moseley GL. Do people with chronic pain have impaired executive function? A meta-analytical review. Clin Psychol Rev. 2014;34(7):563–579. doi:10.1016/j.cpr.2014.08.003
   PubMed Web of Science ®Google Scholar
• Thayer JF, Lane RD. A model of neurovisceral integration in emotion regulation and dysregulation. J Affect Disord. 2000;61(3):201–216. doi:10.1016/s0165-0327(00)00338-4
   PubMed Web of Science ®Google Scholar
• Benarroch EE. Pain-autonomic interactions: a selective review. Clin Auton Res off J Clin Auton Res Soc. 2001;11(6):343–349. doi:10.1007/BF02292765
   PubMed Web of Science ®Google Scholar
• Thayer JF, Ahs F, Fredrikson M, Sollers JJ, Wager TD. A meta-analysis of heart rate variability and neuroimaging studies: implications for heart rate variability as a marker of stress and health. Neurosci Biobehav Rev. 2012;36(2):747–756. doi:10.1016/j.neubiorev.2011.11.009
   PubMed Web of Science ®Google Scholar
• Smith TW, Deits-Lebehn C, Williams PG, Baucom BRW, Uchino BN. Toward a social psychophysiology of vagally mediated heart rate variability: concepts and methods in self-regulation, emotion, and interpersonal processes. Soc Personal Psychol Compass. 2020;14(3):e12516. doi:10.1111/spc3.12516
   Web of Science ®Google Scholar
• Forte G, Favieri F, Oliha EO, Marotta A, Casagrande M. Anxiety and attentional processes: the role of resting heart rate variability. Brain Sci. 2021;11(4):480. doi:10.3390/brainsci11040480
   PubMed Web of Science ®Google Scholar
• Forte G, Morelli M, Casagrande M. Heart Rate Variability and Decision-Making: autonomic Responses in Making Decisions. Brain Sci. 2021;11(2):243. doi:10.3390/brainsci11020243
   PubMed Web of Science ®Google Scholar
• Appelhans BM, Luecken LJ. Heart rate variability and pain: associations of two interrelated homeostatic processes. Biol Psychol. 2008;77(2):174–182. doi:10.1016/j.biopsycho.2007.10.004
   PubMed Web of Science ®Google Scholar
• Forte G, Favieri F, Casagrande M. Heart Rate Variability and Cognitive Function: a Systematic Review. Front Neurosci. 2019;13:13. doi:10.3389/fnins.2019.00710
   PubMedGoogle Scholar
• Hohenschurz-Schmidt DJ, Calcagnini G, Dipasquale O, et al. Linking pain sensation to the autonomic nervous system: the role of the anterior cingulate and periaqueductal gray resting-state networks. Front Neurosci. 2020;14:14. doi:10.3389/fnins.2020.00147
   PubMed Web of Science ®Google Scholar
• Thayer JF, Lane RD. Claude Bernard and the heart-brain connection: further elaboration of a model of neurovisceral integration. Neurosci Biobehav Rev. 2009;33(2):81–88. doi:10.1016/j.neubiorev.2008.08.004
   PubMed Web of Science ®Google Scholar
• Porcelli AJ. An alternative to the traditional cold pressor test: the cold pressor arm wrap. J Vis Exp. 2014;e50849. doi:10.3791/50849
   PubMed Web of Science ®Google Scholar
• Bjekić J, Živanović M, Purić D, Oosterman JM, Filipović SR. Pain and executive functions: a unique relationship between Stroop task and experimentally induced pain. Psychol Res. 2018;82(3):580–589. doi:10.1007/s00426-016-0838-2
   PubMed Web of Science ®Google Scholar
• Palmer AR, Distefano R, Leneman K, Berry D. Reliability of the BodyGuard2 (FirstBeat) in the detection of heart rate variability. Appl Psychophysiol Biofeedback. 2021;46(3):251–258. doi:10.1007/s10484-021-09510-6
   PubMed Web of Science ®Google Scholar
• Tarvainen MP, Niskanen J-P, Lipponen JA, Ranta-Aho PO, Karjalainen PA. Kubios HRV--heart rate variability analysis software. Comput Methods Programs Biomed. 2014;113(1):210–220. doi:10.1016/j.cmpb.2013.07.024
   PubMed Web of Science ®Google Scholar
• Pomeranz B, Macaulay RJ, Caudill MA, et al. Assessment of autonomic function in humans by heart rate spectral analysis. Am J Physiol. 1985;248(1 Pt 2):H151–3. doi:10.1152/ajpheart.1985.248.1.H151
   PubMed Web of Science ®Google Scholar
• Cossarizza A, Chang H-D, Radbruch A, et al. Guidelines for the use of flow cytometry and cell sorting in immunological studies. Eur J Immunol. 2019;49(10):1457–1973. doi:10.1002/eji.201970107
   PubMed Web of Science ®Google Scholar
• Weise F, Heydenreich F, Runge U. Contributions of sympathetic and vagal mechanisms to the genesis of heart rate fluctuations during orthostatic load: a spectral analysis. J Auton Nerv Syst. 1987;21(2):127–134. doi:10.1016/0165-1838(87)90015-4
   PubMedGoogle Scholar
• Saul JP, Rea RF, Eckberg DL, Berger RD, Cohen RJ. Heart rate and muscle sympathetic nerve variability during reflex changes of autonomic activity. Am J Physiol. 1990;258(3 Pt 2):H713–21. doi:10.1152/ajpheart.1990.258.3.H713
   PubMedGoogle Scholar
• Laborde S, Mosley E, Thayer JF. Heart rate variability and cardiac vagal tone in psychophysiological research—Recommendations for experiment planning, data analysis, and data reporting. Front Psychol. 2017;8:8. doi:10.3389/fpsyg.2017.00213
   PubMed Web of Science ®Google Scholar
• Porges SW. Respiratory Sinus Arrhythmia: physiological Basis, Quantitative Methods, and Clinical Implications. In: Grossman P, Janssen KHL, Vaitl D, editors. Cardiorespiratory and Cardiosomatic Psychophysiology. Springer; 1986:101–115. doi:10.1007/978-1-4757-0360-3_7
   Google Scholar
• Shaffer F, McCraty R, Zerr CL. A healthy heart is not a metronome: an integrative review of the heart’s anatomy and heart rate variability. Front Psychol. 2014;5:1040. doi:10.3389/fpsyg.2014.01040
   PubMed Web of Science ®Google Scholar
• Stroop JR. Studies of interference in serial verbal reactions. J Exp Psychol. 1935;18(6):643–662. doi:10.1037/h0054651
   Google Scholar
• Costantini AF, Hoving KL. The effectiveness of reward and punishment contingencies on response inhibition. J Exp Child Psychol. 1973;16(3):484–494. doi:10.1016/0022-0965(73)90009-X
   Web of Science ®Google Scholar
• Favieri F, Chen E, Casagrande M. Executive functions and body weight at different ages: a preliminary study. Nutrients. 2021;13(4). doi:10.3390/nu13041174
   PubMed Web of Science ®Google Scholar
• Marouf R, Caron S, Lussier M, Bherer L, Piche M, Rainville P. Reduced pain inhibition is associated with reduced cognitive inhibition in healthy aging. Pain. 2014;155(3):494–502. doi:10.1016/j.pain.2013.11.011
   PubMed Web of Science ®Google Scholar
• Zhou S, Kemp J, Despres O, Pebayle T, Dufour A. The association between inhibition and pain tolerance in the elderly: evidence from event-related potentials. Eur J Pain. 2015;19(5):669–676. doi:10.1002/ejp.588
   PubMed Web of Science ®Google Scholar
• Favieri F, Forte G, Pazzaglia M, Chen EY, Casagrande M. High-level executive functions: a possible role of sex and weight condition in planning and decision-making performances. Brain Sci. 2022;12(2):149. doi:10.3390/brainsci12020149
   PubMed Web of Science ®Google Scholar
• Bokura H, Yamaguchi S, Kobayashi S. Electrophysiological correlates for response inhibition in a Go/NoGo task. Clin Neurophysiol off J Int Fed Clin Neurophysiol. 2001;112(12):2224–2232. doi:10.1016/s1388-2457(01)00691-5
   Google Scholar
• Gonzalez-Rosa JJ, Inuggi A, Blasi V, et al. Response competition and response inhibition during different choice-discrimination tasks: evidence from ERP measured inside MRI scanner. Int J Psychophysiol off J Int Organ Psychophysiol. 2013;89(1):37–47. doi:10.1016/j.ijpsycho.2013.04.021
   PubMed Web of Science ®Google Scholar
• Kalanthroff E, Goldfarb L, Henik A. Evidence for interaction between the stop signal and the Stroop task conflict. J Exp Psychol Hum Percept Perform. 2013;39(2):579–592. doi:10.1037/a0027429
   PubMed Web of Science ®Google Scholar
• Langenecker SA, Nielson KA, Rao SM. fMRI of healthy older adults during Stroop interference. Neuroimage. 2004;21(1):192–200. doi:10.1016/j.neuroimage.2003.08.027
   PubMed Web of Science ®Google Scholar
• Zysset S, Schroeter ML, Neumann J, von Cramon DY. Stroop interference, hemodynamic response and aging: an event-related fMRI study. Neurobiol Aging. 2007;28(6):937–946. doi:10.1016/j.neurobiolaging.2006.05.008
   PubMed Web of Science ®Google Scholar
• Qiu J. Infant pain: does it hurt? Nature. 2006;444:143. doi:10.1038/444143a
   PubMed Web of Science ®Google Scholar
• Salomons TV, Johnstone T, Backonja -M-M, Shackman AJ, Davidson RJ. Individual differences in the effects of perceived controllability on pain perception: critical role of the prefrontal cortex. J Cogn Neurosci. 2007;19(6):993–1003. doi:10.1162/jocn.2007.19.6.993
   PubMed Web of Science ®Google Scholar
• Glass JM, Williams DA, Fernandez-Sanchez M-L, et al. Executive function in chronic pain patients and healthy controls: different cortical activation during response inhibition in fibromyalgia. J PAIN. 2011;12(12):1219–1229. doi:10.1016/j.jpain.2011.06.007
   PubMed Web of Science ®Google Scholar
• Schmidt-Wilcke T, Kairys A, Ichesco E, et al. Changes in clinical pain in fibromyalgia patients correlate with changes in brain activation in the cingulate cortex in a response inhibition task. Pain Med. 2014;15(8):1346–1358. doi:10.1111/pme.12460
   PubMed Web of Science ®Google Scholar
• Kyle BN, McNeil DW. Autonomic arousal and experimentally induced pain: a critical review of the literature. Pain Res Manag. 2014;19(3):159–167. doi:10.1155/2014/536859
   PubMed Web of Science ®Google Scholar
• Cooper SJ. from Claude Bernard to Walter Cannon. Emergence of the concept of homeostasis. Appetite. 2008;51(3):419–427. doi:10.1016/j.appet.2008.06.005
   PubMed Web of Science ®Google Scholar
• Leone M, Proietti Cecchini A, Mea E, Tullo V, Curone M, Bussone G. Neuroimaging and pain: a window on the autonomic nervous system. Neurol Sci off J Ital Neurol Soc Ital Soc Clin Neurophysiol. 2006;27:S134–7. doi:10.1007/s10072-006-0588-9
   Google Scholar
• Jänig W. Relationship between pain and autonomic phenomena in headache and other pain conditions. Cephalalgia. 2003;23(1):43–48. doi:10.1046/j.1468-2982.2003.00573.x
   PubMedGoogle Scholar
• Schlereth T, Birklein F. The sympathetic nervous system and pain. Neuromolecular Med. 2008;10(3):141–147. doi:10.1007/s12017-007-8018-6
   PubMed Web of Science ®Google Scholar
• Del paso GAR, Garrido S, Á P, Duschek S. Autonomic cardiovascular control and responses to experimental pain stimulation in fibromyalgia syndrome. J Psychosom Res. 2011;70(2):125–134. doi:10.1016/j.jpsychores.2010.09.012
   PubMed Web of Science ®Google Scholar
• Midenfjord I, Polster A, Sjovall H, Friberg P, Tornblom H, Simren M. Associations among neurophysiology measures in irritable bowel syndrome (IBS) and their relevance for IBS symptoms. Sci Rep. 2020;10(1). doi:10.1038/s41598-020-66558-w
   PubMed Web of Science ®Google Scholar
• Suarez-Roca H, Mamoun N, Sigurdson MI, Maixner W. Baroreceptor modulation of the cardiovascular system, pain, consciousness, and cognition. Compr Physiol. 2021;11(2):1373–1423. doi:10.1002/cphy.c190038
   PubMed Web of Science ®Google Scholar
• Balocchi R, Varanini M, Menicucci D, et al. Heart rate variability in subjects with different hypnotic susceptibility receiving nociceptive stimulation and suggestions of analgesia. In: 2005 27th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, Vols 1–7. Proceedings of Annual International Conference of the IEEE Engineering in Medicine and Biology Society; 2005:6996–6999. doi:10.1109/IEMBS.2005.1616116.
   Google Scholar
• DEl Paso GA R, Montoro C, Muñóz Ladrón de Guevara C, Duschek S, Jennings JR. The effect of baroreceptor stimulation on pain perception depends on the elicitation of the reflex cardiovascular response: evidence of the interplay between the two branches of the baroreceptor system. Biol Psychol. 2014;101:82–90. doi:10.1016/j.biopsycho.2014.07.004
   PubMed Web of Science ®Google Scholar
• Laborde S, Mosley E, Mertgen A. Vagal tank theory: the three rs of cardiac vagal control functioning – resting, reactivity, and recovery. Front Neurosci. 2018;12:12. doi:10.3389/fnins.2018.00458
   PubMed Web of Science ®Google Scholar
• Forte G, Troisi G, Pazzaglia M, Pascalis V, Casagrande M. Heart rate variability and pain: a systematic review. Brain Sci. 2022;12(2):153. doi:10.3390/brainsci12020153
   PubMed Web of Science ®Google Scholar
• Pollatos O, Füstös J, Critchley HD. On the generalised embodiment of pain: how interoceptive sensitivity modulates cutaneous pain perception. Pain. 2012;153(8):1680–1686. doi:10.1016/j.pain.2012.04.030
   PubMed Web of Science ®Google Scholar
• Terkelsen AJ, Molgaard H, Hansen J, Andersen OK, Jensen TS. Acute pain increases heart rate: differential mechanisms during rest and mental stress. Auton Neurosci. 2005;121(1–2):101–109. doi:10.1016/j.autneu.2005.07.001
   PubMed Web of Science ®Google Scholar
• Benarroch EE. The central autonomic network: functional organization, dysfunction, and perspective. Mayo Clin Proc. 1993;68(10):988–1001. doi:10.1016/s0025-6196(12)62272-1
   PubMed Web of Science ®Google Scholar
• Smith R, Thayer JF, Khalsa SS, Lane RD. The hierarchical basis of neurovisceral integration. Neurosci Biobehav Rev. 2017;75:274–296. doi:10.1016/j.neubiorev.2017.02.003
   PubMed Web of Science ®Google Scholar
• Benarroch EE. Pain-autonomic interactions. Neurol Sci off J Ital Neurol Soc Ital Soc Clin Neurophysiol. 2006;27:S130–3. doi:10.1007/s10072-006-0587-x
   Google Scholar
• Federico F, Marotta A, Adriani T, Maccari L, Casagrande M. Attention network test — the impact of social information on executive control, alerting and orienting. Acta Psychol. 2013;143(1):65–70. doi:10.1016/j.actpsy.2013.02.006
   PubMed Web of Science ®Google Scholar
• Spagna A, Martella D, Sebastiani M, Maccari L, Marotta A, Casagrande M. Efficiency and interactions of alerting, orienting and executive networks: the impact of imperative stimulus type. Acta Psychol. 2014;148:209–215. doi:10.1016/j.actpsy.2014.02.007
   PubMed Web of Science ®Google Scholar
• Spagna A, Martella D, Fuentes LJ, Marotta A, Casagrande M. Hemispheric modulations of the attentional networks. Brain Cogn. 2016;108:73–80. doi:10.1016/j.bandc.2016.07.002
   PubMed Web of Science ®Google Scholar