Voltage-Gated Ion Channels in Neuropathic Pain Signaling
Neuropathic pain is a chronic and debilitating disorder of the somatosensory system that affects a significant proportion of the population and is characterized by abnormal responses such as hyperalgesia and allodynia. Voltage-gated ion channels, including sodium (Na<sub>V</sub>), calciu...
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2025-05-01
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| author | Ricardo Felix Alejandra Corzo-Lopez Alejandro Sandoval |
| author_facet | Ricardo Felix Alejandra Corzo-Lopez Alejandro Sandoval |
| author_sort | Ricardo Felix |
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| description | Neuropathic pain is a chronic and debilitating disorder of the somatosensory system that affects a significant proportion of the population and is characterized by abnormal responses such as hyperalgesia and allodynia. Voltage-gated ion channels, including sodium (Na<sub>V</sub>), calcium (Ca<sub>V</sub>), and potassium (K<sub>V</sub>) channels, play a pivotal role in modulating neuronal excitability and pain signal transmission following nerve injury. This review intends to provide a comprehensive analysis of the molecular and cellular mechanisms by which dysregulation in the expression, localization, and function of specific Na<sub>V</sub> channel subtypes (mainly Na<sub>V</sub>1.7 and Na<sub>V</sub>1.8) and their auxiliary subunits contributes to aberrant neuronal activation, the generation of ectopic discharges, and sensitization in neuropathic pain. Likewise, special emphasis is placed on the crucial role of Ca<sub>V</sub> channels, particularly Ca<sub>V</sub>2.2 and the auxiliary subunit Ca<sub>V</sub>α<sub>2</sub>δ, whose overexpression increases calcium influx, neurotransmitter release, and neuronal hyperexcitability, thus maintaining persistent pain states. Furthermore, K<sub>V</sub> channels (particularly K<sub>V</sub>7 channels) function as brakes on neuronal excitability, and their dysregulation facilitates the development and maintenance of neuropathic pain. Therefore, targeting specific K<sub>V</sub> channel subtypes to restore their function is also a promising therapeutic strategy for alleviating neuropathic pain symptoms. On the other hand, recent advances in the development of small molecules as selective modulators or inhibitors targeting voltage-gated ion channels are also discussed. These agents have improved efficacy and safety profiles in preclinical and clinical studies by attenuating pathophysiological channel activity and restoring neuronal function. This review seeks to contribute to guiding future research and drug development toward more effective mechanism-based treatments by discussing the molecular mechanisms underlying neuropathic pain and highlighting translational therapeutic opportunities. |
| format | Article |
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| institution | Kabale University |
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| language | English |
| publishDate | 2025-05-01 |
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| series | Life |
| spelling | doaj-art-7e7d829168e44532b94429b2b306f6ae2025-08-20T03:27:19ZengMDPI AGLife2075-17292025-05-0115688810.3390/life15060888Voltage-Gated Ion Channels in Neuropathic Pain SignalingRicardo Felix0Alejandra Corzo-Lopez1Alejandro Sandoval2Department of Cell Biology, Centre for Research and Advanced Studies (Cinvestav), Mexico City 07360, MexicoSchool of Medicine FES Iztacala, National Autonomous University of Mexico (UNAM), Tlalnepantla 54090, MexicoSchool of Medicine FES Iztacala, National Autonomous University of Mexico (UNAM), Tlalnepantla 54090, MexicoNeuropathic pain is a chronic and debilitating disorder of the somatosensory system that affects a significant proportion of the population and is characterized by abnormal responses such as hyperalgesia and allodynia. Voltage-gated ion channels, including sodium (Na<sub>V</sub>), calcium (Ca<sub>V</sub>), and potassium (K<sub>V</sub>) channels, play a pivotal role in modulating neuronal excitability and pain signal transmission following nerve injury. This review intends to provide a comprehensive analysis of the molecular and cellular mechanisms by which dysregulation in the expression, localization, and function of specific Na<sub>V</sub> channel subtypes (mainly Na<sub>V</sub>1.7 and Na<sub>V</sub>1.8) and their auxiliary subunits contributes to aberrant neuronal activation, the generation of ectopic discharges, and sensitization in neuropathic pain. Likewise, special emphasis is placed on the crucial role of Ca<sub>V</sub> channels, particularly Ca<sub>V</sub>2.2 and the auxiliary subunit Ca<sub>V</sub>α<sub>2</sub>δ, whose overexpression increases calcium influx, neurotransmitter release, and neuronal hyperexcitability, thus maintaining persistent pain states. Furthermore, K<sub>V</sub> channels (particularly K<sub>V</sub>7 channels) function as brakes on neuronal excitability, and their dysregulation facilitates the development and maintenance of neuropathic pain. Therefore, targeting specific K<sub>V</sub> channel subtypes to restore their function is also a promising therapeutic strategy for alleviating neuropathic pain symptoms. On the other hand, recent advances in the development of small molecules as selective modulators or inhibitors targeting voltage-gated ion channels are also discussed. These agents have improved efficacy and safety profiles in preclinical and clinical studies by attenuating pathophysiological channel activity and restoring neuronal function. This review seeks to contribute to guiding future research and drug development toward more effective mechanism-based treatments by discussing the molecular mechanisms underlying neuropathic pain and highlighting translational therapeutic opportunities.https://www.mdpi.com/2075-1729/15/6/888voltage-gated ion channelsneuropathic paincalcium channelsCa<sub>V</sub> channelspotassium channelsK<sub>V</sub> channels |
| spellingShingle | Ricardo Felix Alejandra Corzo-Lopez Alejandro Sandoval Voltage-Gated Ion Channels in Neuropathic Pain Signaling Life voltage-gated ion channels neuropathic pain calcium channels Ca<sub>V</sub> channels potassium channels K<sub>V</sub> channels |
| title | Voltage-Gated Ion Channels in Neuropathic Pain Signaling |
| title_full | Voltage-Gated Ion Channels in Neuropathic Pain Signaling |
| title_fullStr | Voltage-Gated Ion Channels in Neuropathic Pain Signaling |
| title_full_unstemmed | Voltage-Gated Ion Channels in Neuropathic Pain Signaling |
| title_short | Voltage-Gated Ion Channels in Neuropathic Pain Signaling |
| title_sort | voltage gated ion channels in neuropathic pain signaling |
| topic | voltage-gated ion channels neuropathic pain calcium channels Ca<sub>V</sub> channels potassium channels K<sub>V</sub> channels |
| url | https://www.mdpi.com/2075-1729/15/6/888 |
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