Use of transcutaneous spinal cord stimulation to explore inhibitory and facilitatory circuits in muscles of the human lower limb
The aim of this study was to explore the primary afferent depolarization mechanism, to determine whether the soleus transspinal evoked potential (TEP), elicited through transcutaneous spinal cord stimulation over the L1–L2 level, is modulated by presynaptic inhibition and heteronymous facilitation,...
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Published in | Experimental physiology |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Wiley-Blackwell
21.07.2025
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ISSN | 0958-0670 1469-445X 1469-445X |
DOI | 10.1113/EP093023 |
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Abstract | The aim of this study was to explore the primary afferent depolarization mechanism, to determine whether the soleus transspinal evoked potential (TEP), elicited through transcutaneous spinal cord stimulation over the L1–L2 level, is modulated by presynaptic inhibition and heteronymous facilitation, similar to the Hoffmann (H) reflex, elicited by posterior tibial nerve stimulation. Twenty subjects participated in two experiments. Experiment 1 assessed D 1 and D 2 inhibition by conditioning the H reflex and TEP with peroneal nerve stimulation at different interstimulus intervals (ISIs; ranging from 1 to 200 ms). Experiment 2 examined heteronymous facilitation of responses using femoral nerve conditioning stimulation (ISIs ranging from −1 to −10 ms). Conditioned responses (H PSI or TEP PSI and H FAC or TEP FAC ) were compared with unconditioned ones (H TEST or TEP TEST ). Concerning D 1 and D 2 inhibition, results did not reveal any significant difference between the two responses ( p = 0.89 and p = 0.51 for D 1 and D 2 , respectively). Inhibition was observed at all ISIs for D 1 and at the 100 and 200 ms ISIs for D 2 . Facilitation patterns were also comparable between the two responses. Moreover, a negative correlation was observed between the modulation of soleus TEP and tibialis anterior TEP (conditioning muscle during inhibition), whereas a positive correlation was obtained between soleus TEP and quadriceps TEP (conditioning muscle during facilitation). The similar modulations between the two responses suggest that TEP can be an alternative to the H reflex for studying spinal circuits, with the advantage of offering insight into the activity of multiple lower‐limb muscles.
What is the central question of this study? Is the transspinal evoked potential, elicited by transcutaneous spinal cord stimulation, sensitive to inhibitory and facilitatory circuits, similar to the H reflex evoked by peripheral nerve stimulation? What is the main finding and its importance? Both soleus H reflex and transspinal evoked potential are sensitive to D 1 and D 2 inhibition, mediated by activation of the antagonist tibialis anterior afferents, and to heteronymous facilitation, induced by projections of vastus lateralis afferents. These findings suggest that transcutaneous spinal cord stimulation is a valuable tool for investigating spinal circuits, offering the advantage of assessing multiple lower‐limb muscles simultaneously. |
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AbstractList | The aim of this study was to explore the primary afferent depolarization mechanism, to determine whether the soleus transspinal evoked potential (TEP), elicited through transcutaneous spinal cord stimulation over the L1–L2 level, is modulated by presynaptic inhibition and heteronymous facilitation, similar to the Hoffmann (H) reflex, elicited by posterior tibial nerve stimulation. Twenty subjects participated in two experiments. Experiment 1 assessed D1 and D2 inhibition by conditioning the H reflex and TEP with peroneal nerve stimulation at different interstimulus intervals (ISIs; ranging from 1 to 200 ms). Experiment 2 examined heteronymous facilitation of responses using femoral nerve conditioning stimulation (ISIs ranging from −1 to −10 ms). Conditioned responses (HPSI or TEPPSI and HFAC or TEPFAC) were compared with unconditioned ones (HTEST or TEPTEST). Concerning D1 and D2 inhibition, results did not reveal any significant difference between the two responses (p = 0.89 and p = 0.51 for D1 and D2, respectively). Inhibition was observed at all ISIs for D1 and at the 100 and 200 ms ISIs for D2. Facilitation patterns were also comparable between the two responses. Moreover, a negative correlation was observed between the modulation of soleus TEP and tibialis anterior TEP (conditioning muscle during inhibition), whereas a positive correlation was obtained between soleus TEP and quadriceps TEP (conditioning muscle during facilitation). The similar modulations between the two responses suggest that TEP can be an alternative to the H reflex for studying spinal circuits, with the advantage of offering insight into the activity of multiple lower-limb muscles. The aim of this study was to explore the primary afferent depolarization mechanism, to determine whether the soleus transspinal evoked potential (TEP), elicited through transcutaneous spinal cord stimulation over the L1-L2 level, is modulated by presynaptic inhibition and heteronymous facilitation, similar to the Hoffmann (H) reflex, elicited by posterior tibial nerve stimulation. Twenty subjects participated in two experiments. Experiment 1 assessed D and D inhibition by conditioning the H reflex and TEP with peroneal nerve stimulation at different interstimulus intervals (ISIs; ranging from 1 to 200 ms). Experiment 2 examined heteronymous facilitation of responses using femoral nerve conditioning stimulation (ISIs ranging from -1 to -10 ms). Conditioned responses (H or TEP and H or TEP ) were compared with unconditioned ones (H or TEP ). Concerning D and D inhibition, results did not reveal any significant difference between the two responses (p = 0.89 and p = 0.51 for D and D , respectively). Inhibition was observed at all ISIs for D and at the 100 and 200 ms ISIs for D . Facilitation patterns were also comparable between the two responses. Moreover, a negative correlation was observed between the modulation of soleus TEP and tibialis anterior TEP (conditioning muscle during inhibition), whereas a positive correlation was obtained between soleus TEP and quadriceps TEP (conditioning muscle during facilitation). The similar modulations between the two responses suggest that TEP can be an alternative to the H reflex for studying spinal circuits, with the advantage of offering insight into the activity of multiple lower-limb muscles. The aim of this study was to explore the primary afferent depolarization mechanism, to determine whether the soleus transspinal evoked potential (TEP), elicited through transcutaneous spinal cord stimulation over the L1-L2 level, is modulated by presynaptic inhibition and heteronymous facilitation, similar to the Hoffmann (H) reflex, elicited by posterior tibial nerve stimulation. Twenty subjects participated in two experiments. Experiment 1 assessed D1 and D2 inhibition by conditioning the H reflex and TEP with peroneal nerve stimulation at different interstimulus intervals (ISIs; ranging from 1 to 200 ms). Experiment 2 examined heteronymous facilitation of responses using femoral nerve conditioning stimulation (ISIs ranging from -1 to -10 ms). Conditioned responses (HPSI or TEPPSI and HFAC or TEPFAC) were compared with unconditioned ones (HTEST or TEPTEST). Concerning D1 and D2 inhibition, results did not reveal any significant difference between the two responses (p = 0.89 and p = 0.51 for D1 and D2, respectively). Inhibition was observed at all ISIs for D1 and at the 100 and 200 ms ISIs for D2. Facilitation patterns were also comparable between the two responses. Moreover, a negative correlation was observed between the modulation of soleus TEP and tibialis anterior TEP (conditioning muscle during inhibition), whereas a positive correlation was obtained between soleus TEP and quadriceps TEP (conditioning muscle during facilitation). The similar modulations between the two responses suggest that TEP can be an alternative to the H reflex for studying spinal circuits, with the advantage of offering insight into the activity of multiple lower-limb muscles.The aim of this study was to explore the primary afferent depolarization mechanism, to determine whether the soleus transspinal evoked potential (TEP), elicited through transcutaneous spinal cord stimulation over the L1-L2 level, is modulated by presynaptic inhibition and heteronymous facilitation, similar to the Hoffmann (H) reflex, elicited by posterior tibial nerve stimulation. Twenty subjects participated in two experiments. Experiment 1 assessed D1 and D2 inhibition by conditioning the H reflex and TEP with peroneal nerve stimulation at different interstimulus intervals (ISIs; ranging from 1 to 200 ms). Experiment 2 examined heteronymous facilitation of responses using femoral nerve conditioning stimulation (ISIs ranging from -1 to -10 ms). Conditioned responses (HPSI or TEPPSI and HFAC or TEPFAC) were compared with unconditioned ones (HTEST or TEPTEST). Concerning D1 and D2 inhibition, results did not reveal any significant difference between the two responses (p = 0.89 and p = 0.51 for D1 and D2, respectively). Inhibition was observed at all ISIs for D1 and at the 100 and 200 ms ISIs for D2. Facilitation patterns were also comparable between the two responses. Moreover, a negative correlation was observed between the modulation of soleus TEP and tibialis anterior TEP (conditioning muscle during inhibition), whereas a positive correlation was obtained between soleus TEP and quadriceps TEP (conditioning muscle during facilitation). The similar modulations between the two responses suggest that TEP can be an alternative to the H reflex for studying spinal circuits, with the advantage of offering insight into the activity of multiple lower-limb muscles. The aim of this study was to explore the primary afferent depolarization mechanism, to determine whether the soleus transspinal evoked potential (TEP), elicited through transcutaneous spinal cord stimulation over the L1–L2 level, is modulated by presynaptic inhibition and heteronymous facilitation, similar to the Hoffmann (H) reflex, elicited by posterior tibial nerve stimulation. Twenty subjects participated in two experiments. Experiment 1 assessed D 1 and D 2 inhibition by conditioning the H reflex and TEP with peroneal nerve stimulation at different interstimulus intervals (ISIs; ranging from 1 to 200 ms). Experiment 2 examined heteronymous facilitation of responses using femoral nerve conditioning stimulation (ISIs ranging from −1 to −10 ms). Conditioned responses (H PSI or TEP PSI and H FAC or TEP FAC ) were compared with unconditioned ones (H TEST or TEP TEST ). Concerning D 1 and D 2 inhibition, results did not reveal any significant difference between the two responses ( p = 0.89 and p = 0.51 for D 1 and D 2 , respectively). Inhibition was observed at all ISIs for D 1 and at the 100 and 200 ms ISIs for D 2 . Facilitation patterns were also comparable between the two responses. Moreover, a negative correlation was observed between the modulation of soleus TEP and tibialis anterior TEP (conditioning muscle during inhibition), whereas a positive correlation was obtained between soleus TEP and quadriceps TEP (conditioning muscle during facilitation). The similar modulations between the two responses suggest that TEP can be an alternative to the H reflex for studying spinal circuits, with the advantage of offering insight into the activity of multiple lower‐limb muscles. What is the central question of this study? Is the transspinal evoked potential, elicited by transcutaneous spinal cord stimulation, sensitive to inhibitory and facilitatory circuits, similar to the H reflex evoked by peripheral nerve stimulation? What is the main finding and its importance? Both soleus H reflex and transspinal evoked potential are sensitive to D 1 and D 2 inhibition, mediated by activation of the antagonist tibialis anterior afferents, and to heteronymous facilitation, induced by projections of vastus lateralis afferents. These findings suggest that transcutaneous spinal cord stimulation is a valuable tool for investigating spinal circuits, offering the advantage of assessing multiple lower‐limb muscles simultaneously. |
Author | Sordet, Julia Amiez, Nicolas Martin, Alain Papaiordanidou, Maria Quenot, Jean‐Pierre Amiridis, Ioannis |
Author_xml | – sequence: 1 givenname: Julia orcidid: 0009-0008-2866-4091 surname: Sordet fullname: Sordet, Julia organization: Université Bourgogne Europe, Inserm CAPS UMR 1093 Dijon France – sequence: 2 givenname: Maria orcidid: 0000-0002-4879-2065 surname: Papaiordanidou fullname: Papaiordanidou, Maria organization: Université Bourgogne Europe, Inserm CAPS UMR 1093 Dijon France – sequence: 3 givenname: Nicolas orcidid: 0000-0001-5175-5591 surname: Amiez fullname: Amiez, Nicolas organization: Laboratoire Interuniversitaire de Biologie de la Motricité (LIBM), Univ Lyon Université Claude Bernard Lyon 1 Villeurbanne France – sequence: 4 givenname: Ioannis orcidid: 0000-0003-3731-8998 surname: Amiridis fullname: Amiridis, Ioannis organization: Department of Physical Education and Sport Sciences at Serres Aristotle University of Thessaloniki Thessaloniki Greece – sequence: 5 givenname: Jean‐Pierre orcidid: 0000-0003-2351-682X surname: Quenot fullname: Quenot, Jean‐Pierre organization: Service de Médecine Intensive‐Réanimation CHU Dijon‐Bourgogne Dijon France – sequence: 6 givenname: Alain orcidid: 0000-0003-1335-912X surname: Martin fullname: Martin, Alain organization: Université Bourgogne Europe, Inserm CAPS UMR 1093 Dijon France |
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Cites_doi | 10.1016/j.xcrm.2024.101805 10.1113/JP276694 10.1155/2017/6751810 10.3390/jcm11133836 10.1152/japplphysiol.01128.2014 10.1113/jphysiol.1993.sp019652 10.1152/jn.00342.2022 10.1007/s00421-002-0577-5 10.1113/JP283706 10.1016/j.jneumeth.2009.03.006 10.1007/s00421-014-2969-8 10.1371/journal.pone.0102313 10.1515/bmt‐2013‐4010 10.1007/s00421-022-05119-7 10.1002/(SICI)1097-4598(199609)19:9<1110::AID-MUS5>3.0.CO;2-2 10.1002/bem.21808 10.1152/japplphysiol.00065.2022 10.1371/journal.pone.0192013 10.1017/CBO9780511545047 10.1002/mus.20700 10.1007/s00221-012-3258-6 10.3390/jcm10235543 10.1111/aor.12615 10.1177/1545968319893298 10.1136/jnnp.51.2.174 10.14814/phy2.16039 10.1016/j.neulet.2015.01.041 10.1007/s00421-023-05406-x 10.1007/BF00230681 10.1113/jphysiol.1987.sp016680 10.1113/jphysiol.1983.sp014638 10.1523/JNEUROSCI.19-01-00391.1999 10.1111/aor.12616 10.1093/brain/112.2.417 10.1038/s41593-022-01162-x 10.1113/jphysiol.2007.128447 10.1007/s002210050933 10.1371/journal.pone.0147479 10.1152/jn.1971.34.6.1010 10.1016/0301-0082(87)90007-4 10.1152/japplphysiol.00005.2021 10.1111/ejn.14321 10.3389/fpsyg.2017.00456 10.1016/0014-4886(78)90091-2 10.1371/journal.pone.0227057 10.1007/BF00230683 10.1371/journal.pone.0214818 |
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Keywords | posterior root muscle reflex presynaptic inhibition primary afferent depolarization heteronymous facilitation H reflex |
Language | English |
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References | Mizuno Y. (e_1_2_10_35_1) 1971; 34 Courtine G. (e_1_2_10_7_1) 2007; 582 Roy F. D. (e_1_2_10_41_1) 2012; 223 e_1_2_10_40_1 Ménard A. (e_1_2_10_30_1) 1999; 19 Zehr E. P. (e_1_2_10_50_1) 2002; 86 Vitry F. (e_1_2_10_49_1) 2021; 131 Maertens de Noordhout A. (e_1_2_10_28_1) 1988; 51 Bergmans J. (e_1_2_10_4_1) 1978; 60 Andrews J. C. (e_1_2_10_2_1) 2015; 589 Bakdash J. Z. (e_1_2_10_3_1) 2017; 8 Knikou M. (e_1_2_10_23_1) 2014; 9 Koceja J. (e_1_2_10_25_1) 2002; 42 Knikou M. (e_1_2_10_22_1) 2013; 34 Gravholt A. (e_1_2_10_13_1) 2024; 124 Papitsa A. (e_1_2_10_38_1) 2022; 133 Hofstoetter U. S. (e_1_2_10_19_1) 2022; 11 Hofstoetter U. S. (e_1_2_10_16_1) 2018; 13 Rudomin P. (e_1_2_10_42_1) 1999; 129 Saito A. (e_1_2_10_43_1) 2019; 14 Burke D. (e_1_2_10_6_1) 1989; 112 e_1_2_10_27_1 Binder V. E. (e_1_2_10_5_1) 2021; 10 Forget R. (e_1_2_10_12_1) 1989; 78 Hultborn H. (e_1_2_10_20_1) 1987; 389 Megía García A. (e_1_2_10_29_1) 2020; 34 Pierrot‐Deseilligny, & Burke (e_1_2_10_39_1) 2005 Metz K. (e_1_2_10_31_1) 2023; 601 Skiadopoulos A. (e_1_2_10_47_1) 2022; 128 Minassian K. (e_1_2_10_34_1) 2007; 35 Meunier S. (e_1_2_10_32_1) 1996; 19 Sayenko D. G. (e_1_2_10_44_1) 2015; 118 Theodosiadou A. (e_1_2_10_48_1) 2023; 123 Hofstoetter U. S. (e_1_2_10_18_1) 2015; 39 Hofstoetter U. S. (e_1_2_10_17_1) 2019; 14 Knikou M. (e_1_2_10_24_1) 2017; 2017 Krenn M. (e_1_2_10_26_1) 2015; 39 Grosprêtre S. (e_1_2_10_14_1) 2019; 597 Minassian K. (e_1_2_10_33_1) 2024; 5 El‐Tohamy A. (e_1_2_10_11_1) 1983; 337 Hari K. (e_1_2_10_15_1) 2022; 25 Doguet V. (e_1_2_10_10_1) 2014; 114 Crone C. (e_1_2_10_8_1) 1989; 78 Kitano K. (e_1_2_10_21_1) 2009; 180 Škarabot J. (e_1_2_10_46_1) 2019; 49 Schieppati M. (e_1_2_10_45_1) 1987; 28 Nakagawa K. (e_1_2_10_36_1) 2024; 12 Danner S. M. (e_1_2_10_9_1) 2016; 11 Nielsen J. (e_1_2_10_37_1) 1993; 464 |
References_xml | – volume: 5 issue: 11 year: 2024 ident: e_1_2_10_33_1 article-title: Article Transcutaneous spinal cord stimulation neuromodulates pre‐ and postsynaptic inhibition in the control of spinal spasticity Transcutaneous spinal cord stimulation neuromodulates pre‐ and postsynaptic inhibition in the control of spinal spasticity publication-title: Cell Reports Medicine doi: 10.1016/j.xcrm.2024.101805 – volume: 597 start-page: 921 issue: 3 year: 2019 ident: e_1_2_10_14_1 article-title: Spinal plasticity with motor imagery practice publication-title: The Journal of Physiology doi: 10.1113/JP276694 – volume: 2017 start-page: 1 year: 2017 ident: e_1_2_10_24_1 article-title: Spinal excitability changes after transspinal and transcortical paired associative stimulation in humans publication-title: Neural Plasticity doi: 10.1155/2017/6751810 – volume: 11 start-page: 3836 issue: 13 year: 2022 ident: e_1_2_10_19_1 article-title: Transcutaneous spinal cord stimulation: Advances in an emerging non‐invasive strategy for neuromodulation publication-title: Journal of Clinical Medicine doi: 10.3390/jcm11133836 – volume: 118 start-page: 1364 issue: 11 year: 2015 ident: e_1_2_10_44_1 article-title: Spinal segment‐specific transcutaneous stimulation differentially shapes activation pattern among motor pools in humans publication-title: Journal of Applied Physiology doi: 10.1152/japplphysiol.01128.2014 – volume: 464 start-page: 575 issue: 1 year: 1993 ident: e_1_2_10_37_1 article-title: The regulation of presynaptic inhibition during co‐contraction of antagonistic muscles in man publication-title: The Journal of Physiology doi: 10.1113/jphysiol.1993.sp019652 – volume: 128 start-page: 1641 issue: 6 year: 2022 ident: e_1_2_10_47_1 article-title: Physiological effects of cathodal electrode configuration for transspinal stimulation in humans publication-title: Journal of Neurophysiology doi: 10.1152/jn.00342.2022 – volume: 86 start-page: 455 issue: 6 year: 2002 ident: e_1_2_10_50_1 article-title: Considerations for use of the Hoffmann reflex in exercise studies publication-title: European Journal of Applied Physiology doi: 10.1007/s00421-002-0577-5 – volume: 601 start-page: 1925 issue: 10 year: 2023 ident: e_1_2_10_31_1 article-title: Post‐activation depression from primary afferent depolarization (PAD) produces extensor H‐reflex suppression following flexor afferent conditioning publication-title: The Journal of Physiology doi: 10.1113/JP283706 – volume: 180 start-page: 111 issue: 1 year: 2009 ident: e_1_2_10_21_1 article-title: Spinal reflex in human lower leg muscles evoked by transcutaneous spinal cord stimulation publication-title: Journal of Neuroscience Methods doi: 10.1016/j.jneumeth.2009.03.006 – volume: 114 start-page: 2509 issue: 12 year: 2014 ident: e_1_2_10_10_1 article-title: Reliability of H‐reflex in vastus lateralis and vastus medialis muscles during passive and active isometric conditions publication-title: European Journal of Applied Physiology doi: 10.1007/s00421-014-2969-8 – volume: 9 issue: 7 year: 2014 ident: e_1_2_10_23_1 article-title: Transpinal and transcortical stimulation alter corticospinal excitability and increase spinal output publication-title: PLoS ONE doi: 10.1371/journal.pone.0102313 – ident: e_1_2_10_27_1 doi: 10.1515/bmt‐2013‐4010 – volume: 123 start-page: 695 issue: 4 year: 2023 ident: e_1_2_10_48_1 article-title: Revisiting the use of Hoffmann reflex in motor control research on humans publication-title: European Journal of Applied Physiology doi: 10.1007/s00421-022-05119-7 – volume: 19 start-page: 1110 issue: 9 year: 1996 ident: e_1_2_10_32_1 article-title: Effects of femoral nerve stimulation on the electromyogram and reflex excitability of tibialis anterior and soleus publication-title: Muscle and Nerve doi: 10.1002/(SICI)1097-4598(199609)19:9<1110::AID-MUS5>3.0.CO;2-2 – volume: 34 start-page: 630 issue: 8 year: 2013 ident: e_1_2_10_22_1 article-title: Neurophysiological characterization of transpinal evoked potentials in human leg muscles publication-title: Bioelectromagnetics doi: 10.1002/bem.21808 – volume: 133 start-page: 1327 issue: 6 year: 2022 ident: e_1_2_10_38_1 article-title: Specific modulation of presynaptic and recurrent inhibition of the soleus muscle during lengthening and shortening submaximal and maximal contractions publication-title: Journal of Applied Physiology doi: 10.1152/japplphysiol.00065.2022 – volume: 13 issue: 1 year: 2018 ident: e_1_2_10_16_1 article-title: Common neural structures activated by epidural and transcutaneous lumbar spinal cord stimulation: Elicitation of posterior root‐muscle reflexes publication-title: PLoS ONE doi: 10.1371/journal.pone.0192013 – volume-title: The circuitry of the human spinal cord: Its role in motor control and movement disorders year: 2005 ident: e_1_2_10_39_1 doi: 10.1017/CBO9780511545047 – volume: 35 start-page: 327 issue: 3 year: 2007 ident: e_1_2_10_34_1 article-title: Posterior root‐muscle preflexes elicited by transcutaneous stimulation of the human lumbosacral cord publication-title: Muscle and Nerve doi: 10.1002/mus.20700 – volume: 223 start-page: 281 issue: 2 year: 2012 ident: e_1_2_10_41_1 article-title: Effect of percutaneous stimulation at different spinal levels on the activation of sensory and motor roots publication-title: Experimental Brain Research doi: 10.1007/s00221-012-3258-6 – volume: 10 start-page: 5543 issue: 23 year: 2021 ident: e_1_2_10_5_1 article-title: Influence of spine curvature on the efficacy of transcutaneous lumbar spinal cord stimulation publication-title: Journal of Clinical Medicine doi: 10.3390/jcm10235543 – volume: 39 start-page: E176 issue: 10 year: 2015 ident: e_1_2_10_18_1 article-title: Augmentation of voluntary locomotor activity by transcutaneous spinal cord stimulation in motor‐incomplete spinal cord‐injured individuals publication-title: Artificial Organs doi: 10.1111/aor.12615 – volume: 34 start-page: 3 issue: 1 year: 2020 ident: e_1_2_10_29_1 article-title: Transcutaneous spinal cord stimulation and motor rehabilitation in spinal cord injury: A systematic review publication-title: Neurorehabilitation and Neural Repair doi: 10.1177/1545968319893298 – volume: 51 start-page: 174 issue: 2 year: 1988 ident: e_1_2_10_28_1 article-title: Percutaneous electrical stimulation of lumbosacral roots in man publication-title: Journal of Neurology Neurosurgery and Psychiatry doi: 10.1136/jnnp.51.2.174 – volume: 12 issue: 9 year: 2024 ident: e_1_2_10_36_1 article-title: Reciprocal inhibition of the thigh muscles in humans: A study using transcutaneous spinal cord stimulation publication-title: Physiological Reports doi: 10.14814/phy2.16039 – volume: 589 start-page: 144 year: 2015 ident: e_1_2_10_2_1 article-title: Post‐activation depression in the human soleus muscle using peripheral nerve and transcutaneous spinal stimulation publication-title: Neuroscience Letters doi: 10.1016/j.neulet.2015.01.041 – volume: 124 start-page: 1821 issue: 6 year: 2024 ident: e_1_2_10_13_1 article-title: Do soleus responses to transcutaneous spinal cord stimulation show similar changes to H‐reflex in response to Achilles tendon vibration? publication-title: European Journal of Applied Physiology doi: 10.1007/s00421-023-05406-x – volume: 78 start-page: 10 issue: 1 year: 1989 ident: e_1_2_10_12_1 article-title: Facilitation of quadriceps motoneurones by group I afferents from pretibial flexors in man 1. Possible interneuronal pathway publication-title: Experimental Brain Research doi: 10.1007/BF00230681 – volume: 389 start-page: 729 issue: 1 year: 1987 ident: e_1_2_10_20_1 article-title: Assessing changes in presynaptic inhibition of la fibres: A study in man and the cat publication-title: The Journal of Physiology doi: 10.1113/jphysiol.1987.sp016680 – volume: 337 start-page: 497 year: 1983 ident: e_1_2_10_11_1 article-title: Spinal inhibition in man: Depression of the soleus H reflex by stimulation of the nerve to the antagonist muscle publication-title: The Journal of Physiology doi: 10.1113/jphysiol.1983.sp014638 – volume: 42 start-page: 159 issue: 3 year: 2002 ident: e_1_2_10_25_1 article-title: Assessment of motoneuron excitability using recurrent inhibition and paired reflex depression protocols: A test of reliability publication-title: Electromyography and Clinical Neurophysiology – volume: 19 start-page: 391 issue: 1 year: 1999 ident: e_1_2_10_30_1 article-title: The modulation of presynaptic inhibition in single muscle primary afferents during fictive locomotion in the cat publication-title: Journal of Neuroscience doi: 10.1523/JNEUROSCI.19-01-00391.1999 – ident: e_1_2_10_40_1 – volume: 39 start-page: 834 issue: 10 year: 2015 ident: e_1_2_10_26_1 article-title: Multi‐electrode array for transcutaneous lumbar posterior root stimulation publication-title: Artificial Organs doi: 10.1111/aor.12616 – volume: 112 start-page: 417 issue: 2 year: 1989 ident: e_1_2_10_6_1 article-title: The effects of voluntary contraction on the H reflex of human limb muscles publication-title: Brain doi: 10.1093/brain/112.2.417 – volume: 25 start-page: 1288 issue: 10 year: 2022 ident: e_1_2_10_15_1 article-title: GABA facilitates spike propagation through branch points of sensory axons in the spinal cord publication-title: Nature Neuroscience doi: 10.1038/s41593-022-01162-x – volume: 582 start-page: 1125 issue: 3 year: 2007 ident: e_1_2_10_7_1 article-title: Modulation of multisegmental monosynaptic responses in a variety of leg muscles during walking and running in humans publication-title: The Journal of Physiology doi: 10.1113/jphysiol.2007.128447 – volume: 129 start-page: 1 issue: 1 year: 1999 ident: e_1_2_10_42_1 article-title: Presynaptic inhibition in the vertebrate spinal cord revisited publication-title: Experimental Brain Research doi: 10.1007/s002210050933 – volume: 11 issue: 1 year: 2016 ident: e_1_2_10_9_1 article-title: Body position influences which neural structures are recruited by lumbar transcutaneous spinal cord stimulation publication-title: PLoS ONE doi: 10.1371/journal.pone.0147479 – volume: 34 start-page: 1010 issue: 6 year: 1971 ident: e_1_2_10_35_1 article-title: Reciprocal Group I Inhibition on Triceps Surae Motoneurons in Man publication-title: Journal of Neurophysiology doi: 10.1152/jn.1971.34.6.1010 – volume: 28 start-page: 345 issue: 4 year: 1987 ident: e_1_2_10_45_1 article-title: The hoffmann reflex: A means of assessing spinal reflex excitability and its descending control in man publication-title: Progress in Neurobiology doi: 10.1016/0301-0082(87)90007-4 – volume: 131 start-page: 1162 issue: 3 year: 2021 ident: e_1_2_10_49_1 article-title: Mechanisms modulating spinal excitability after nerve stimulation inducing extra torque publication-title: Journal of Applied Physiology doi: 10.1152/japplphysiol.00005.2021 – volume: 49 start-page: 1254 issue: 10 year: 2019 ident: e_1_2_10_46_1 article-title: Electrical stimulation of human corticospinal axons at the level of the lumbar spinal segments publication-title: European Journal of Neuroscience doi: 10.1111/ejn.14321 – volume: 8 start-page: 456 year: 2017 ident: e_1_2_10_3_1 article-title: Repeated measures correlation publication-title: Frontiers in Psychology doi: 10.3389/fpsyg.2017.00456 – volume: 60 start-page: 380 issue: 2 year: 1978 ident: e_1_2_10_4_1 article-title: Effects of low‐threshold muscular afferent fibers on different motoneuronal pools of the lower limb in man publication-title: Experiwental Neurology doi: 10.1016/0014-4886(78)90091-2 – volume: 14 issue: 12 year: 2019 ident: e_1_2_10_17_1 article-title: Recovery cycles of posterior root‐muscle reflexes evoked by transcutaneous spinal cord stimulation and of the H reflex in individuals with intact and injured spinal cord publication-title: PLoS ONE doi: 10.1371/journal.pone.0227057 – volume: 78 start-page: 28 issue: 1 year: 1989 ident: e_1_2_10_8_1 article-title: Experimental Brain Research Methodological implications of the post activation depression of the soleus H‐reflex in man publication-title: Experimental Brain Research doi: 10.1007/BF00230683 – volume: 14 issue: 4 year: 2019 ident: e_1_2_10_43_1 article-title: Repeatability of spinal reflexes of lower limb muscles evoked by transcutaneous spinal cord stimulation publication-title: PLoS ONE doi: 10.1371/journal.pone.0214818 |
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Title | Use of transcutaneous spinal cord stimulation to explore inhibitory and facilitatory circuits in muscles of the human lower limb |
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