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Pulsed Radiofrequency Decreases pERK and Affects Intracellular Ca(2+) Influx, Cytosolic ATP Level, and Mitochondrial Membrane Potential in the Sensitized Dorsal Root Ganglion Neuron Induced by N-Methyl D-Aspartate

BACKGROUND: The molecular mechanism of pulsed radiofrequency (PRF) in chronic pain management is not fully understood. Chronic pain involves the activation of specific N-Methyl D-Aspartate receptors (NMDAR) to induce central sensitization. This study aims to determine the effect of PRF on central se...

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Autores principales: Laksono, Ristiawan Muji, Kalim, Handono, Rohman, Mohammad Saifur, Widodo, Nashi, Ahmad, Muhammad Ramli, Halim, Willy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216856/
https://www.ncbi.nlm.nih.gov/pubmed/37252110
http://dx.doi.org/10.2147/JPR.S409658
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author Laksono, Ristiawan Muji
Kalim, Handono
Rohman, Mohammad Saifur
Widodo, Nashi
Ahmad, Muhammad Ramli
Halim, Willy
author_facet Laksono, Ristiawan Muji
Kalim, Handono
Rohman, Mohammad Saifur
Widodo, Nashi
Ahmad, Muhammad Ramli
Halim, Willy
author_sort Laksono, Ristiawan Muji
collection PubMed
description BACKGROUND: The molecular mechanism of pulsed radiofrequency (PRF) in chronic pain management is not fully understood. Chronic pain involves the activation of specific N-Methyl D-Aspartate receptors (NMDAR) to induce central sensitization. This study aims to determine the effect of PRF on central sensitization biomarker phosphorylated extracellular signal-regulated kinase (pERK), Ca(2+) influx, cytosolic ATP level, and mitochondrial membrane potential (Δψm) of the sensitized dorsal root ganglion (DRG) neuron following NMDAR activation. METHODS: This study is a true experimental in-vitro study on a sensitized DRG neuron induced with 80 µM NMDA. There are six treatment groups including control, NMDA 80 µM, Ketamine 100 µM, PRF 2Hz, NMDA 80 µM + PRF 2 Hz, and NMDA 80 µM + PRF 2 Hz + ketamine 100 µM. We use PRF 2 Hz 20 ms for 360 seconds. Statistical analysis was performed using the One-Way ANOVA and the Pearson correlation test with α=5%. RESULTS: In the sensitized DRG neuron, there is a significant elevation of pERK. There is a strong correlation between Ca(2+), cytosolic ATP level, and Δψm with pERK intensity (p<0.05). PRF treatment decreases pERK intensity from 108.48 ± 16.95 AU to 38.57 ± 5.20 AU (p<0.05). PRF exposure to sensitized neurons also exhibits a Ca(2+) influx, but still lower than in the unexposed neuron. PRF exposure in sensitized neurons has a higher cytosolic ATP level (0.0458 ± 0.0010 mM) than in the unexposed sensitized neuron (0.0198 ± 0.0004 mM) (p<0.05). PRF also decreases Δψm in the sensitized neuron from 109.24 ± 6.43 AU to 33.21 ± 1.769 AU (p<0.05). CONCLUSION: PRF mechanisms related to DRG neuron sensitization are by decreasing pERK, altering Ca(2+) influx, increasing cytosolic ATP level, and decreasing Δψm which is associated with neuron sensitization following NMDAR activation.
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spelling pubmed-102168562023-05-27 Pulsed Radiofrequency Decreases pERK and Affects Intracellular Ca(2+) Influx, Cytosolic ATP Level, and Mitochondrial Membrane Potential in the Sensitized Dorsal Root Ganglion Neuron Induced by N-Methyl D-Aspartate Laksono, Ristiawan Muji Kalim, Handono Rohman, Mohammad Saifur Widodo, Nashi Ahmad, Muhammad Ramli Halim, Willy J Pain Res Original Research BACKGROUND: The molecular mechanism of pulsed radiofrequency (PRF) in chronic pain management is not fully understood. Chronic pain involves the activation of specific N-Methyl D-Aspartate receptors (NMDAR) to induce central sensitization. This study aims to determine the effect of PRF on central sensitization biomarker phosphorylated extracellular signal-regulated kinase (pERK), Ca(2+) influx, cytosolic ATP level, and mitochondrial membrane potential (Δψm) of the sensitized dorsal root ganglion (DRG) neuron following NMDAR activation. METHODS: This study is a true experimental in-vitro study on a sensitized DRG neuron induced with 80 µM NMDA. There are six treatment groups including control, NMDA 80 µM, Ketamine 100 µM, PRF 2Hz, NMDA 80 µM + PRF 2 Hz, and NMDA 80 µM + PRF 2 Hz + ketamine 100 µM. We use PRF 2 Hz 20 ms for 360 seconds. Statistical analysis was performed using the One-Way ANOVA and the Pearson correlation test with α=5%. RESULTS: In the sensitized DRG neuron, there is a significant elevation of pERK. There is a strong correlation between Ca(2+), cytosolic ATP level, and Δψm with pERK intensity (p<0.05). PRF treatment decreases pERK intensity from 108.48 ± 16.95 AU to 38.57 ± 5.20 AU (p<0.05). PRF exposure to sensitized neurons also exhibits a Ca(2+) influx, but still lower than in the unexposed neuron. PRF exposure in sensitized neurons has a higher cytosolic ATP level (0.0458 ± 0.0010 mM) than in the unexposed sensitized neuron (0.0198 ± 0.0004 mM) (p<0.05). PRF also decreases Δψm in the sensitized neuron from 109.24 ± 6.43 AU to 33.21 ± 1.769 AU (p<0.05). CONCLUSION: PRF mechanisms related to DRG neuron sensitization are by decreasing pERK, altering Ca(2+) influx, increasing cytosolic ATP level, and decreasing Δψm which is associated with neuron sensitization following NMDAR activation. Dove 2023-05-22 /pmc/articles/PMC10216856/ /pubmed/37252110 http://dx.doi.org/10.2147/JPR.S409658 Text en © 2023 Laksono et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Laksono, Ristiawan Muji
Kalim, Handono
Rohman, Mohammad Saifur
Widodo, Nashi
Ahmad, Muhammad Ramli
Halim, Willy
Pulsed Radiofrequency Decreases pERK and Affects Intracellular Ca(2+) Influx, Cytosolic ATP Level, and Mitochondrial Membrane Potential in the Sensitized Dorsal Root Ganglion Neuron Induced by N-Methyl D-Aspartate
title Pulsed Radiofrequency Decreases pERK and Affects Intracellular Ca(2+) Influx, Cytosolic ATP Level, and Mitochondrial Membrane Potential in the Sensitized Dorsal Root Ganglion Neuron Induced by N-Methyl D-Aspartate
title_full Pulsed Radiofrequency Decreases pERK and Affects Intracellular Ca(2+) Influx, Cytosolic ATP Level, and Mitochondrial Membrane Potential in the Sensitized Dorsal Root Ganglion Neuron Induced by N-Methyl D-Aspartate
title_fullStr Pulsed Radiofrequency Decreases pERK and Affects Intracellular Ca(2+) Influx, Cytosolic ATP Level, and Mitochondrial Membrane Potential in the Sensitized Dorsal Root Ganglion Neuron Induced by N-Methyl D-Aspartate
title_full_unstemmed Pulsed Radiofrequency Decreases pERK and Affects Intracellular Ca(2+) Influx, Cytosolic ATP Level, and Mitochondrial Membrane Potential in the Sensitized Dorsal Root Ganglion Neuron Induced by N-Methyl D-Aspartate
title_short Pulsed Radiofrequency Decreases pERK and Affects Intracellular Ca(2+) Influx, Cytosolic ATP Level, and Mitochondrial Membrane Potential in the Sensitized Dorsal Root Ganglion Neuron Induced by N-Methyl D-Aspartate
title_sort pulsed radiofrequency decreases perk and affects intracellular ca(2+) influx, cytosolic atp level, and mitochondrial membrane potential in the sensitized dorsal root ganglion neuron induced by n-methyl d-aspartate
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216856/
https://www.ncbi.nlm.nih.gov/pubmed/37252110
http://dx.doi.org/10.2147/JPR.S409658
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