Pharmacological interactions of sulforaphane and gabapentin in a murine fibromyalgia-like pain model

Therapeutic management of a chronic painful syndrome such as fibromyalgia (FM) lacks effective and safe single or combined analgesics. Current medications such as gabapentin (GPB) or pregabalin are moderately effective but in the presence of several adverse effects. Natural products derived from cruciferous vegetables such as sulforaphane (SFN) produce neuroprotective effects due to their potent antioxidant and anti-inflammatory properties. However, it is unknown whether positive or negative pharmacological interactions may occur when GBP and SFN are combined. The aim of this study was to estimate the pharmacological interaction of GBP and SFN in FM-like pain induced in rats. Time course curves of antiallodynic and antihyperalgesic effects were constructed for both SFN (3.16, 31.6, and 100 mg/kg, i.p.) and GBP (10, 31.6, and 100 mg/kg, i.p.) by recording behavioral responses every 30 min and up to 4 h afterward, from which dose-response effects were also obtained to decide the dosage combination. An electrocorticographic (ECoG) recording in mice and docking analysis were also explored to explain the pharmacological interaction. Our results demonstrated significant and dose-dependent antiallodynic and antihyperalgesic effects in their individual administration. While a combination of intermediate doses of these drugs enhanced their effects producing the same level as that obtained by using only 1/3 of the individual dose in each case. The ECoG recording and docking analysis suggest that calcium channels could be partly involved in the drug interaction. This study provides preclinical evidence that SFN alone and in combination with GBP may be beneficial for relieving FM-like pain at certain doses.

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Publication Details

Journal
Biomedicine & Pharmacotherapy
Published
2025-02-18
DOI
https://doi.org/10.1016/j.biopha.2025.117929
Citations
3
Primary Topic
Fibromyalgia and Chronic Fatigue Syndrome Research
Type
article
Field-Weighted Citation Impact
4.41

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article

Pharmacological interactions of sulforaphane and gabapentin in a murine fibromyalgia-like pain model

Fernando Narváez-González, Alberto Hernández-León, María Eva González-Trujano, Rosa Ventura‐Martínez et al.
3 citations
Biomedicine & Pharmacotherapy
Fibromyalgia and Chronic Fatigue Syndrome Research
4.41
article

Pharmacological interactions of sulforaphane and gabapentin in a murine fibromyalgia-like pain model

Fernando Narváez-González, Alberto Hernández-León, María Eva González-Trujano, Rosa Ventura‐Martínez, Gabriel Fernando Moreno-Pérez, David Martı́nez-Vargas, Francisco Javier López‐Muñoz, Francisco Pellicer, Ik-Yahalcab Zamora-Díaz
article en
3 citations

Abstract

Therapeutic management of a chronic painful syndrome such as fibromyalgia (FM) lacks effective and safe single or combined analgesics. Current medications such as gabapentin (GPB) or pregabalin are moderately effective but in the presence of several adverse effects. Natural products derived from cruciferous vegetables such as sulforaphane (SFN) produce neuroprotective effects due to their potent antioxidant and anti-inflammatory properties. However, it is unknown whether positive or negative pharmacological interactions may occur when GBP and SFN are combined. The aim of this study was to estimate the pharmacological interaction of GBP and SFN in FM-like pain induced in rats. Time course curves of antiallodynic and antihyperalgesic effects were constructed for both SFN (3.16, 31.6, and 100 mg/kg, i.p.) and GBP (10, 31.6, and 100 mg/kg, i.p.) by recording behavioral responses every 30 min and up to 4 h afterward, from which dose-response effects were also obtained to decide the dosage combination. An electrocorticographic (ECoG) recording in mice and docking analysis were also explored to explain the pharmacological interaction. Our results demonstrated significant and dose-dependent antiallodynic and antihyperalgesic effects in their individual administration. While a combination of intermediate doses of these drugs enhanced their effects producing the same level as that obtained by using only 1/3 of the individual dose in each case. The ECoG recording and docking analysis suggest that calcium channels could be partly involved in the drug interaction. This study provides preclinical evidence that SFN alone and in combination with GBP may be beneficial for relieving FM-like pain at certain doses.

Biomedicine & PharmacotherapyVol. 184
Universidad Autónoma de la Ciudad de México (MX), Centro Cultural Universitario de Ciudad Juarez (MX), Hospital de Especialidades (MX), Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz (MX), Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (MX), Universidad Nacional Autónoma de México (MX)
Consejo Nacional de Ciencia y Tecnología
Zero hunger
Openalex Percentile: Top 7%
Fibromyalgia and Chronic Fatigue Syndrome Research
4.41
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