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The Antinociceptive Effects of Tramadol and/or Gabapentin on Rat Neuropathic Pain Induced by a Chronic Constriction Injury.

Authors :
Corona-Ramos JN
De la O-Arciniega M
Déciga-Campos M
Medina-López JR
Domínguez-Ramírez AM
Jaramillo-Morales OA
Espinosa-Juárez JV
López-Muñoz FJ
Source :
Drug development research [Drug Dev Res] 2016 Aug; Vol. 77 (5), pp. 217-26. Date of Electronic Publication: 2016 Jun 14.
Publication Year :
2016

Abstract

Preclinical Research The current work evaluates the interaction between two commonly used drugs, tramadol (Tra) and gabapentin (Gbp). Dose-response curves (DRC) and isobolographic analysis were used to confirm their synergistic antihyperalgesic and anti-allodynic responses in a rat neuropathic pain model involving chronic constriction injury of the sciatic nerve and in von Frey and acetone tests. Tra and Gbp produced dose-dependent antihyperalgesic and anti-allodynic effects. Dose-response studies of combinations of Tra and Gbp in combination showed the DRC was leftward-shifted compared to the DRCs for each compound alone. One combination demonstrated both antihyperalgesic and anti-allodynic effects greater than those observed after individual administration. The remaining combinations demonstrated an additive effect. The Tra+Gbp combination demonstrated a potentiative effect with smaller doses of Tra. Additionally, it was determined lethal dose 50 (LD50 ) of Tra alone and tramadol + Gbp 10 using mice to 48 h post administration. The DRC (death) were similar for Tra alone and in Tra in combination, despite the improved effectiveness of Tra in the presence of GBP, 10 mg/kg. A combination of these drugs could be effective in neuropathic pain therapy because they can produce potentiative (at a low dose) or additive effects. Drug Dev Res 77 : 217-226, 2016.   © 2016 Wiley Periodicals, Inc.<br /> (© 2016 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1098-2299
Volume :
77
Issue :
5
Database :
MEDLINE
Journal :
Drug development research
Publication Type :
Academic Journal
Accession number :
27300150
Full Text :
https://doi.org/10.1002/ddr.21313