Infrared inhibition impacts on locally initiated and propagating action potentials and the downstream synaptic transmission

Significance: Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic applications and offer critical insights into IR light modulation of complex neural networks. Aim: We explore the IR-mediated inhibition of...

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Published inNeurophotonics (Print) Vol. 7; no. 4; p. 045003
Main Authors Zhu, Xuedong, Lin, Jen-Wei, Sander, Michelle Y
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Abstract Significance: Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic applications and offer critical insights into IR light modulation of complex neural networks. Aim: We explore the IR-mediated inhibition of action potentials (APs) that either propagate along single axons or are initiated locally and their downstream synaptic transmission responses. Approach: APs were evoked locally by two-electrode current clamp or at a distance for propagating APs. The neuromuscular transmission was recorded with intracellular electrodes in muscle cells or macro-patch pipettes on terminal bouton clusters. Results: IR light pulses completely and reversibly terminate the locally initiated APs firing at low frequencies, which leads to blocking of the synaptic transmission. However, IR light pulses only suppress but do not block the amplitude and duration of propagating APs nor locally initiated APs firing at high frequencies. Such suppressed APs do not influence the postsynaptic responses at a distance. While the suppression of AP amplitude and duration is similar for propagating and locally evoked APs, only the former exhibits a 7% to 21% increase in the maximum time derivative of the AP rising phase. Conclusions: The suppressed APs of motor axons can resume their waveforms after passing the localized IR light illumination site, leaving the muscular and synaptic responses unchanged. IR-mediated modulation on propagating and locally evoked APs should be considered as two separate models for axonal and somatic modulations.
AbstractList Significance: Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic applications and offer critical insights into IR light modulation of complex neural networks. Aim: We explore the IR-mediated inhibition of action potentials (APs) that either propagate along single axons or are initiated locally and their downstream synaptic transmission responses. Approach: APs were evoked locally by two-electrode current clamp or at a distance for propagating APs. The neuromuscular transmission was recorded with intracellular electrodes in muscle cells or macro-patch pipettes on terminal bouton clusters. Results: IR light pulses completely and reversibly terminate the locally initiated APs firing at low frequencies, which leads to blocking of the synaptic transmission. However, IR light pulses only suppress but do not block the amplitude and duration of propagating APs nor locally initiated APs firing at high frequencies. Such suppressed APs do not influence the postsynaptic responses at a distance. While the suppression of AP amplitude and duration is similar for propagating and locally evoked APs, only the former exhibits a 7% to 21% increase in the maximum time derivative of the AP rising phase. Conclusions: The suppressed APs of motor axons can resume their waveforms after passing the localized IR light illumination site, leaving the muscular and synaptic responses unchanged. IR-mediated modulation on propagating and locally evoked APs should be considered as two separate models for axonal and somatic modulations.
Significance: Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic applications and offer critical insights into IR light modulation of complex neural networks. Aim: We explore the IR-mediated inhibition of action potentials (APs) that either propagate along single axons or are initiated locally and their downstream synaptic transmission responses. Approach: APs were evoked locally by two-electrode current clamp or at a distance for propagating APs. The neuromuscular transmission was recorded with intracellular electrodes in muscle cells or macro-patch pipettes on terminal bouton clusters. Results: IR light pulses completely and reversibly terminate the locally initiated APs firing at low frequencies, which leads to blocking of the synaptic transmission. However, IR light pulses only suppress but do not block the amplitude and duration of propagating APs nor locally initiated APs firing at high frequencies. Such suppressed APs do not influence the postsynaptic responses at a distance. While the suppression of AP amplitude and duration is similar for propagating and locally evoked APs, only the former exhibits a 7% to 21% increase in the maximum time derivative of the AP rising phase. Conclusions: The suppressed APs of motor axons can resume their waveforms after passing the localized IR light illumination site, leaving the muscular and synaptic responses unchanged. IR-mediated modulation on propagating and locally evoked APs should be considered as two separate models for axonal and somatic modulations.Significance: Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic applications and offer critical insights into IR light modulation of complex neural networks. Aim: We explore the IR-mediated inhibition of action potentials (APs) that either propagate along single axons or are initiated locally and their downstream synaptic transmission responses. Approach: APs were evoked locally by two-electrode current clamp or at a distance for propagating APs. The neuromuscular transmission was recorded with intracellular electrodes in muscle cells or macro-patch pipettes on terminal bouton clusters. Results: IR light pulses completely and reversibly terminate the locally initiated APs firing at low frequencies, which leads to blocking of the synaptic transmission. However, IR light pulses only suppress but do not block the amplitude and duration of propagating APs nor locally initiated APs firing at high frequencies. Such suppressed APs do not influence the postsynaptic responses at a distance. While the suppression of AP amplitude and duration is similar for propagating and locally evoked APs, only the former exhibits a 7% to 21% increase in the maximum time derivative of the AP rising phase. Conclusions: The suppressed APs of motor axons can resume their waveforms after passing the localized IR light illumination site, leaving the muscular and synaptic responses unchanged. IR-mediated modulation on propagating and locally evoked APs should be considered as two separate models for axonal and somatic modulations.
Significance: Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic applications and offer critical insights into IR light modulation of complex neural networks. Aim: We explore the IR-mediated inhibition of action potentials (APs) that either propagate along single axons or are initiated locally and their downstream synaptic transmission responses. Approach: APs were evoked locally by two-electrode current clamp or at a distance for propagating APs. The neuromuscular transmission was recorded with intracellular electrodes in muscle cells or macro-patch pipettes on terminal bouton clusters. Results: IR light pulses completely and reversibly terminate the locally initiated APs firing at low frequencies, which leads to blocking of the synaptic transmission. However, IR light pulses only suppress but do not block the amplitude and duration of propagating APs nor locally initiated APs firing at high frequencies. Such suppressed APs do not influence the postsynaptic responses at a distance. While the suppression of AP amplitude and duration is similar for propagating and locally evoked APs, only the former exhibits a 7% to 21% increase in the maximum time derivative of the AP rising phase. Conclusions: The suppressed APs of motor axons can resume their waveforms after passing the localized IR light illumination site, leaving the muscular and synaptic responses unchanged. IR-mediated modulation on propagating and locally evoked APs should be considered as two separate models for axonal and somatic modulations.
Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic applications and offer critical insights into IR light modulation of complex neural networks. We explore the IR-mediated inhibition of action potentials (APs) that either propagate along single axons or are initiated locally and their downstream synaptic transmission responses. APs were evoked locally by two-electrode current clamp or at a distance for propagating APs. The neuromuscular transmission was recorded with intracellular electrodes in muscle cells or macro-patch pipettes on terminal bouton clusters. IR light pulses completely and reversibly terminate the locally initiated APs firing at low frequencies, which leads to blocking of the synaptic transmission. However, IR light pulses only suppress but do not block the amplitude and duration of propagating APs nor locally initiated APs firing at high frequencies. Such suppressed APs do not influence the postsynaptic responses at a distance. While the suppression of AP amplitude and duration is similar for propagating and locally evoked APs, only the former exhibits a 7% to 21% increase in the maximum time derivative of the AP rising phase. The suppressed APs of motor axons can resume their waveforms after passing the localized IR light illumination site, leaving the muscular and synaptic responses unchanged. IR-mediated modulation on propagating and locally evoked APs should be considered as two separate models for axonal and somatic modulations.
Significance: Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic applications and offer critical insights into IR light modulation of complex neural networks.Aim: We explore the IR-mediated inhibition of action potentials (APs) that either propagate along single axons or are initiated locally and their downstream synaptic transmission responses.Approach: APs were evoked locally by two-electrode current clamp or at a distance for propagating APs. The neuromuscular transmission was recorded with intracellular electrodes in muscle cells or macro-patch pipettes on terminal bouton clusters.Results: IR light pulses completely and reversibly terminate the locally initiated APs firing at low frequencies, which leads to blocking of the synaptic transmission. However, IR light pulses only suppress but do not block the amplitude and duration of propagating APs nor locally initiated APs firing at high frequencies. Such suppressed APs do not influence the postsynaptic responses at a distance. While the suppression of AP amplitude and duration is similar for propagating and locally evoked APs, only the former exhibits a 7% to 21% increase in the maximum time derivative of the AP rising phase.Conclusions: The suppressed APs of motor axons can resume their waveforms after passing the localized IR light illumination site, leaving the muscular and synaptic responses unchanged. IR-mediated modulation on propagating and locally evoked APs should be considered as two separate models for axonal and somatic modulations.
Author Lin, Jen-Wei
Sander, Michelle Y
Zhu, Xuedong
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  surname: Sander
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Cites_doi 10.1117/1.NPh.4.2.025001
10.1117/1.3257230
10.1103/PhysRevX.8.011043
10.1007/BF00213750
10.1096/fj.201903049R
10.1364/BOE.8.004568
10.1088/1741-2560/9/3/036003
10.1117/1.NPh.6.4.040501
10.1016/j.neuroimage.2013.08.040
10.1117/1.JBO.21.6.060505
10.1152/jn.00424.2011
10.1529/biophysj.107.104786
10.1002/lsm.23139
10.1113/jphysiol.1974.sp010641
10.1117/1.NPh.2.1.015007
10.1007/s10827-012-0436-2
10.1016/j.heares.2010.06.021
10.1117/1.NPh.1.1.011010
10.1152/jn.00857.2011
10.1117/1.2121772
10.1038/s41467-017-00435-5
10.1109/JSTQE.2007.910119
10.1117/12.2508996
10.1088/1741-2552/ab131b
10.1364/OL.30.000504
10.1152/jn.00253.2014
10.1016/j.bpj.2014.03.008
10.1109/TBME.2012.2194146
10.1113/jphysiol.1989.sp017684
10.1002/mus.1084
10.1038/srep02600
10.1364/BOE.10.006580
10.1126/sciadv.aau7046
10.1152/jn.00123.2009
10.1002/lsm.20522
10.1117/1.NPh.3.4.040501
10.1016/j.jneumeth.2007.03.016
10.1088/1741-2560/11/1/016001
10.1002/jbio.201700020
10.1113/jphysiol.1985.sp015877
10.1113/jphysiol.2010.198804
10.1016/j.ceca.2014.01.004
10.1117/12.2249521
10.1097/MLG.0b013e318074ec00
10.1088/1741-2552/aa795f
10.1016/j.heares.2014.03.008
10.1117/1.NPh.5.4.045002
10.1038/ncomms1742
10.1002/jbio.201800403
10.1002/jbio.201100134
10.1038/s41598-017-03374-9
10.1117/1.NPh.1.1.011011
10.1016/j.neuroimage.2011.03.084
10.1002/lpor.200900044
10.1088/1741-2560/9/6/066006
10.1038/nrn2148
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Issue 4
Keywords infrared nerve inhibition
action potential initiation
synaptic transmission
photothermal effect
action potential propagation
neural modulation
Language English
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References r2
r3
r4
r5
r6
r7
r8
r9
r50
r52
r51
r10
r54
r53
r12
r56
r11
r55
r14
r13
r16
r15
r18
r17
r19
r21
r20
r23
r22
r25
r24
r27
r26
r29
r28
r30
r32
r31
r34
r33
r36
r35
r38
r37
r39
r41
r40
r43
r42
r45
r44
r47
r46
r49
r48
r1
References_xml – ident: r29
  doi: 10.1117/1.NPh.4.2.025001
– ident: r52
  doi: 10.1117/1.3257230
– ident: r17
  doi: 10.1103/PhysRevX.8.011043
– ident: r40
  doi: 10.1007/BF00213750
– ident: r28
  doi: 10.1096/fj.201903049R
– ident: r31
  doi: 10.1364/BOE.8.004568
– ident: r54
  doi: 10.1088/1741-2560/9/3/036003
– ident: r24
  doi: 10.1117/1.NPh.6.4.040501
– ident: r8
  doi: 10.1016/j.neuroimage.2013.08.040
– ident: r36
  doi: 10.1117/1.JBO.21.6.060505
– ident: r25
  doi: 10.1152/jn.00424.2011
– ident: r13
  doi: 10.1529/biophysj.107.104786
– ident: r35
  doi: 10.1002/lsm.23139
– ident: r41
  doi: 10.1113/jphysiol.1974.sp010641
– ident: r12
  doi: 10.1117/1.NPh.2.1.015007
– ident: r38
  doi: 10.1007/s10827-012-0436-2
– ident: r4
  doi: 10.1016/j.heares.2010.06.021
– ident: r34
  doi: 10.1117/1.NPh.1.1.011010
– ident: r39
  doi: 10.1152/jn.00857.2011
– ident: r46
  doi: 10.1117/1.2121772
– ident: r15
  doi: 10.1038/s41467-017-00435-5
– ident: r11
  doi: 10.1109/JSTQE.2007.910119
– ident: r56
  doi: 10.1117/12.2508996
– ident: r23
  doi: 10.1088/1741-2552/ab131b
– ident: r45
  doi: 10.1364/OL.30.000504
– ident: r27
  doi: 10.1152/jn.00253.2014
– ident: r16
  doi: 10.1016/j.bpj.2014.03.008
– ident: r22
  doi: 10.1109/TBME.2012.2194146
– ident: r42
  doi: 10.1113/jphysiol.1989.sp017684
– ident: r55
  doi: 10.1002/mus.1084
– ident: r20
  doi: 10.1038/srep02600
– ident: r19
  doi: 10.1364/BOE.10.006580
– ident: r9
  doi: 10.1126/sciadv.aau7046
– ident: r44
  doi: 10.1152/jn.00123.2009
– ident: r50
  doi: 10.1002/lsm.20522
– ident: r32
  doi: 10.1117/1.NPh.3.4.040501
– ident: r47
  doi: 10.1016/j.jneumeth.2007.03.016
– ident: r53
  doi: 10.1088/1741-2560/11/1/016001
– ident: r30
  doi: 10.1002/jbio.201700020
– ident: r43
  doi: 10.1113/jphysiol.1985.sp015877
– ident: r26
  doi: 10.1113/jphysiol.2010.198804
– ident: r6
  doi: 10.1016/j.ceca.2014.01.004
– ident: r18
  doi: 10.1117/12.2249521
– ident: r48
  doi: 10.1097/MLG.0b013e318074ec00
– ident: r10
  doi: 10.1088/1741-2552/aa795f
– ident: r2
  doi: 10.1016/j.heares.2014.03.008
– ident: r5
  doi: 10.1117/1.NPh.5.4.045002
– ident: r14
  doi: 10.1038/ncomms1742
– ident: r33
  doi: 10.1002/jbio.201800403
– ident: r49
  doi: 10.1002/jbio.201100134
– ident: r21
  doi: 10.1038/s41598-017-03374-9
– ident: r3
  doi: 10.1117/1.NPh.1.1.011011
– ident: r7
  doi: 10.1016/j.neuroimage.2011.03.084
– ident: r1
  doi: 10.1002/lpor.200900044
– ident: r51
  doi: 10.1088/1741-2560/9/6/066006
– ident: r37
  doi: 10.1038/nrn2148
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Snippet Significance: Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic...
Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic applications...
Significance: Systematic studies of the physiological outputs induced by infrared (IR)-mediated inhibition of motor nerves can provide guidance for therapeutic...
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StartPage 045003
SubjectTerms Electrodes
Light
Localization
Motor neurons
Muscle contraction
Nerves
Nervous system
Neural networks
Neuromuscular junctions
Physiology
Research Papers
Synaptic transmission
Temperature
Therapeutic applications
Title Infrared inhibition impacts on locally initiated and propagating action potentials and the downstream synaptic transmission
URI http://www.dx.doi.org/10.1117/1.NPh.7.4.045003
https://www.ncbi.nlm.nih.gov/pubmed/33094124
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Volume 7
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