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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" article-type="editorial">
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Explor Neurosci</journal-id>
<journal-id journal-id-type="publisher-id">EN</journal-id>
<journal-title-group>
<journal-title>Exploration of Neuroscience</journal-title>
</journal-title-group>
<issn pub-type="epub">2834-5347</issn>
<publisher>
<publisher-name>Open Exploration Publishing</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.37349/en.2025.1006101</article-id>
<article-id pub-id-type="manuscript">1006101</article-id>
<article-categories>
<subj-group>
<subject>Editorial</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Editorial: Neuropathic Pain</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3822-2923</contrib-id>
<name>
<surname>Varrassi</surname>
<given-names>Giustino</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/">Writing—original draft</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="I2">
<sup>2</sup>
</xref>
<xref ref-type="corresp" rid="cor1">
<sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9953-5635</contrib-id>
<name>
<surname>Farì</surname>
<given-names>Giacomo</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/">Writing—original draft</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3535-4023</contrib-id>
<name>
<surname>Al Alwany</surname>
<given-names>Ameen A.</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/">Writing—original draft</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5228-3733</contrib-id>
<name>
<surname>Leoni</surname>
<given-names>Matteo L.G.</given-names>
</name>
<xref ref-type="aff" rid="I4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="editor">
<name>
<surname>Hermann</surname>
<given-names>Dirk M.</given-names>
</name>
<role>Academic Editor</role>
<aff>University of Duisburg-Essen, Germany</aff>
</contrib>
</contrib-group>
<aff id="I1">
<sup>1</sup>Department of Research, Fondazione Paolo Procacci, 00193 Roma, Italy</aff>
<aff id="I2">
<sup>2</sup>College of Medicine, University of Baghdad, Baghdad 10071, Iraq</aff>
<aff id="I3">
<sup>3</sup>Department of Experimental Medicine, University of Salento, 73100 Lecce, Italy</aff>
<aff id="I4">
<sup>4</sup>Department of Medical and Surgical Sciences and Translational Medicine, Sapienza University of Roma, 00189 Roma, Italy</aff>
<author-notes>
<corresp id="cor1">
<bold>*Correspondence:</bold> Giustino Varrassi, Department of Research, Fondazione Paolo Procacci, 00193 Roma, Italy. <email>giuvarr@gmail.com</email></corresp>
</author-notes>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<pub-date pub-type="epub">
<day>23</day>
<month>07</month>
<year>2025</year>
</pub-date>
<volume>4</volume>
<elocation-id>1006101</elocation-id>
<history>
<date date-type="received">
<day>21</day>
<month>07</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>22</day>
<month>07</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>© The Author(s) 2025.</copyright-statement>
<license xlink:href="https://creativecommons.org/licenses/by/4.0/">
<license-p>This is an Open Access article licensed under a Creative Commons Attribution 4.0 International License (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.</license-p>
</license>
</permissions>
</article-meta>
</front>
<body>
<p id="p-1">Neuropathic pain (NP) arises from direct injury or disease affecting the somatosensory system and remains a substantial unmet clinical challenge [<xref ref-type="bibr" rid="B1">1</xref>]. Traditional pharmacotherapy often provides inadequate relief, fueling exploration into mechanism-based diagnostics and therapies. The papers in this special issue collectively advance understanding across three domains: diagnostic measures, mechanistic targets, and interventional strategies.</p>
<sec id="s1">
<title>Quantitative assessment of small-fiber dysfunction</title>
<p id="p-2">Berfelo et al. [<xref ref-type="bibr" rid="B2">2</xref>] investigated the utility of intra-epidermal electrical stimulation (IES) to assess nociceptive detection thresholds (NDT) and evoked potentials (EPs) in diabetic patients with (DMp) and without (DM) painful neuropathy. Their results demonstrated significant alterations in NDT and EP responses among patients with painful neuropathy, suggesting that IES-derived electrophysiological parameters can objectively capture small-fiber dysfunction. These findings support the use of IES as a valuable adjunctive tool in the diagnostic evaluation of painful diabetic polyneuropathy, offering a more precise and quantifiable assessment of sensory fiber impairment.</p>
</sec>
<sec id="s2">
<title>Mechanistic foundations supporting targeted treatment</title>
<sec id="t2-1">
<title>Sigma-1 receptor in diabetic neuropathy</title>
<p id="p-3">Peng et al. [<xref ref-type="bibr" rid="B3">3</xref>] conducted a comprehensive review of preclinical and early clinical studies implicating sigma-1 receptors (S1R)—endoplasmic reticulum-resident chaperones that modulate ion channel function and excitotoxic signaling—in the pathogenesis of painful diabetic neuropathy. They emphasize the relevance of endogenous ligands, such as neurosteroids (e.g., progesterone, DHEA) and hallucinogens (e.g., DMT), in modulating S1R activity. The authors propose that selective antagonism of S1R may reduce pathological neuronal excitability while preserving neuroprotective mechanisms, highlighting these receptors as promising targets for translational research. Accumulating evidence underscores the critical role of S1R in modulating pain perception and transmission [<xref ref-type="bibr" rid="B4">4</xref>–<xref ref-type="bibr" rid="B6">6</xref>].</p>
</sec>
<sec id="t2-2">
<title>Mechanism-based treatment framework</title>
<p id="p-4">Demartini et al. [<xref ref-type="bibr" rid="B7">7</xref>] advocate for a stratified therapeutic approach to NP, grounded in the identification of its underlying pathophysiological mechanisms—namely, peripheral deafferentation, central sensitization, or ectopic neuronal activity. By aligning specific mechanisms with corresponding targeted interventions, such as sodium channel blockers for neuronal hyperexcitability, ion channel modulators for ectopic discharges, and neuromodulation techniques for central dysrhythmias, the authors provide a compelling framework for personalized, mechanism-based management strategies aimed at enhancing treatment efficacy and clinical outcomes in NP patients.</p>
</sec>
</sec>
<sec id="s3">
<title>Novel pharmacological candidates</title>
<sec id="t3-1">
<title>1,4-naphthoquinones</title>
<p id="p-5">Kozlovskiy et al. [<xref ref-type="bibr" rid="B8">8</xref>] investigated the pharmacological properties of two synthetic 1,4-naphthoquinones (1,4-NQs) (U-286 and U-548), demonstrating their antagonistic activity at P<sub>2</sub>X<sub>7</sub> receptors. In vitro, both compounds significantly inhibited ATP-induced pore formation in macrophages and neuronal cells. In vivo, U-286 produced a marked anti-inflammatory effect, reducing carrageenan-induced inflammation by over 70% within four hours. These results support the potential of 1,4-NQs as dual anti-nociceptive and anti-inflammatory agents, meriting further pharmacodynamic and mechanistic evaluation.</p>
</sec>
<sec id="t3-2">
<title>Psychedelics and neuroplasticity</title>
<p id="p-6">Yasin et al. [<xref ref-type="bibr" rid="B9">9</xref>] reviewed current preclinical and clinical evidence on the potential role of serotonergic psychedelics, such as psilocybin and lysergic acid diethylamide (LSD), in the management of refractory chronic pain. They suggest that these compounds exert analgesic effects through 5-HT<sub>2A</sub> receptor activation, modulation of neuroinflammation, and enhancement of synaptic plasticity and cortical reorganization. Despite these promising mechanisms, the authors emphasize the need for rigorous clinical trials to establish optimal dosing, safety parameters, and long-term therapeutic efficacy.</p>
</sec>
</sec>
<sec id="s4">
<title>Interventional and device-based therapies</title>
<p id="p-7">Matejowsky et al. [<xref ref-type="bibr" rid="B10">10</xref>] present a comprehensive review of interventional strategies for managing refractory NP, encompassing spinal cord stimulation (SCS), intrathecal drug delivery systems (IDDS), peripheral nerve stimulation, and various ablative or destructive procedures. The authors synthesize evidence indicating that SCS and IDDS offer superior analgesic outcomes compared to conventional systemic pharmacotherapy, particularly in patients with treatment-resistant NP. They underscore the critical role of appropriate patient selection, interdisciplinary management, and systematic long-term outcome monitoring in maximizing therapeutic benefit. Safety remains a central concern in interventional pain management, and this is especially pertinent in the NP population, where invasive techniques carry specific risks and must be carefully balanced against potential benefits [<xref ref-type="bibr" rid="B11">11</xref>].</p>
<p id="p-8">This integrative, mechanism-targeted approach aligns with current clinical paradigms that prioritize individualized treatment strategies based on precise diagnostic phenotyping. However, the field still faces a major challenge in the rigorous validation of existing assessment tools. Addressing this gap, one study in this special issue validated the Chinese version of the painDETECT questionnaire, confirming its strong reliability, internal consistency, and discriminative accuracy for identifying NP. These findings support its clinical applicability as a culturally adapted screening instrument for Chinese-speaking populations [<xref ref-type="bibr" rid="B12">12</xref>]. Given that painDETECT is among the most widely utilized tools for the diagnosis of NP in both clinical and research contexts, its robust cross-cultural validation is of particular significance [<xref ref-type="bibr" rid="B13">13</xref>–<xref ref-type="bibr" rid="B15">15</xref>].</p>
</sec>
<sec id="s5">
<title>Challenges and future directions</title>
<p id="p-9">Despite substantial advances in the understanding and management of NP, several significant challenges remain unresolved. Translational research must effectively bridge the gap between preclinical discoveries and clinical implementation. For example, while IES offers promising objective measures of small-fiber function, normative reference data and validation across a range of NP phenotypes are essential for its broader clinical adoption. Similarly, the therapeutic potential of S1R modulators must be confirmed through clinical trials employing patient-centered endpoints to establish both efficacy and safety. Neuroplasticity-based treatments, particularly serotonergic psychedelics, show emerging promise but require rigorous randomized controlled trials with standardized protocols and long-term follow-up to determine their clinical utility. In parallel, the incorporation of neuromodulatory interventions such as SCS and IDDS into clinical practice necessitates additional high-quality evidence regarding their long-term effectiveness, cost-efficiency, appropriate patient selection criteria, and safety profile. Furthermore, while mechanism-based treatment algorithms offer a rational framework for individualized care, prospective validation in real-world settings is imperative to substantiate their clinical applicability and optimize treatment outcomes in diverse patient populations.</p>
</sec>
<sec id="s6">
<title>Conclusion</title>
<p id="p-10">The collective works presented in this special issue constitute a multi-dimensional advance in NP research. By integrating objective diagnostics, mechanism-based therapies, novel pharmacological modalities, and refined interventional techniques, they mark a substantial step toward personalized, effective, and durable NP management. Future efforts should prioritize rigorous clinical validation, multidisciplinary care models, and dynamic patient stratification to fully translate these insights into improved clinical outcomes.</p>
</sec>
</body>
<back>
<glossary>
<title>Abbreviations</title>
<def-list>
<def-item>
<term>1,4-NQs</term>
<def>
<p>1,4-naphthoquinones</p>
</def>
</def-item>
<def-item>
<term>EPs</term>
<def>
<p>evoked potentials</p>
</def>
</def-item>
<def-item>
<term>IDDS</term>
<def>
<p>intrathecal drug delivery systems</p>
</def>
</def-item>
<def-item>
<term>IES</term>
<def>
<p>intra-epidermal electrical stimulation</p>
</def>
</def-item>
<def-item>
<term>NDT</term>
<def>
<p>nociceptive detection thresholds</p>
</def>
</def-item>
<def-item>
<term>NP</term>
<def>
<p>neuropathic pain</p>
</def>
</def-item>
<def-item>
<term>S1R</term>
<def>
<p>sigma-1 receptors</p>
</def>
</def-item>
<def-item>
<term>SCS</term>
<def>
<p>spinal cord stimulation</p>
</def>
</def-item>
</def-list>
</glossary>
<sec id="s7">
<title>Declarations</title>
<sec id="t-7-1">
<title>Acknowledgments</title>
<p>The authors are grateful to the Fondazione Paolo Procacci for the support in the publication process.</p>
</sec>
<sec id="t-7-2">
<title>Author contributions</title>
<p>GV, GF, AAAA, and MLGL: Writing—original draft, Writing—review &amp; editing. All authors read and approved the submitted version.</p>
</sec>
<sec id="t-7-3" sec-type="COI-statement">
<title>Conflicts of interest</title>
<p>Giustino Varrassi, President of the Fondazione Paolo Procacci and the Associate Editor and Guest Editor of Exploration of Neuroscience, had no involvement in the decision-making or the review process of this manuscript. The other authors declare that they have no conflicts of interest.</p>
</sec>
<sec id="t-7-4">
<title>Ethical approval</title>
<p>Not applicable.</p>
</sec>
<sec id="t-7-5">
<title>Consent to participate</title>
<p>Not applicable.</p>
</sec>
<sec id="t-7-6">
<title>Consent to publication</title>
<p>Not applicable</p>
</sec>
<sec id="t-7-7" sec-type="data-availability">
<title>Availability of data and materials</title>
<p>Not applicable.</p>
</sec>
<sec id="t-7-8">
<title>Funding</title>
<p>Not applicable.</p>
</sec>
<sec id="t-7-9">
<title>Copyright</title>
<p>© The Author(s) 2025.</p>
</sec>
</sec>
<sec id="s8">
<title>Publisher’s note</title>
<p>Open Exploration maintains a neutral stance on jurisdictional claims in published institutional affiliations and maps. All opinions expressed in this article are the personal views of the author(s) and do not represent the stance of the editorial team or the publisher.</p>
</sec>
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