Centrally Acting Skeletal Muscle Relaxants Sharing Molecular Targets with Drugs for Neuropathic Pain Management
Treatment of neuropathic pain (NP) remains a challenge in clinical practice because the current treatment approaches produce satisfactory pain alleviation in only 30% of patients. This necessitates developing novel drugs or repurposing existing medications intended to manage other diseases. When the repurposing intendance is chosen, similarity in the pharmacological properties should be hosted by the candidate drugs. Herein, this review sheds light on the mechanisms of certain centrally acting skeletal muscle relaxants (CMRs), specifically tolperisone. So far, data indicate that tolperisone displays voltage-gated sodium channel (VGSC) blocking properties with modulatory effect on voltage-gated calcium channels (VGCCs). These properties have led to recent preclinical research initiatives testing tolperisone in NP, resulting in positive outcomes. Furthermore, the review highlights the currently available VGSC blockers and proposes a strategy based on combining them with VGCC blockers that have been proven for the treatment of NP. This proposal is supported by the fact that tolperisone, in combination with pregabalin, has recently been shown to acutely halt NP.
Authors
- Kornél Király (ORCID: https://orcid.org/0000-0002-7252-0422)
- Anna Rita Galambos (ORCID: https://orcid.org/0009-0001-5539-9595)
- Tamás Tábi (ORCID: https://orcid.org/0000-0001-8273-1875)
- Éva Szökő (ORCID: https://orcid.org/0000-0003-1464-6403)
- Al-Khrasani Mahmoud
- Imre Boldizsár
- Dávid Árpád Karádi (ORCID: https://orcid.org/0000-0003-3159-6292)
- Sarah Kadhim Abbood (ORCID: https://orcid.org/0000-0001-5305-8730)
- Judit Mária Kirchlechner-Farkas
- Nariman Essmat
- Zoltán Patrik Lincmajer
Institutions
- Semmelweis University (HU)
- Zagazig University (EG)
Publication Details
- Journal
- Brain Sciences
- Published
- 2025-12-31
- DOI
- https://doi.org/10.3390/brainsci16010067
- Primary Topic
- Pain Mechanisms and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Semmelweis Egyetem
- Emberi Eroforrások Minisztériuma