Effects of gabapentin on experimental somatic pain and temporal summation

被引:52
作者
Arendt-Nielsen, Lars
Frokjær, Jens Brondum
Staahl, Camilla
Graven-Nielsen, Thomas
Huggins, John P.
Smart, Trevor S.
Drewes, Asbjorn Mohr
机构
[1] Aalborg Univ, Ctr Sensory Motor Interact, Lab Human Expt Pain Res, DK-9220 Aalborg E, Denmark
[2] Aalborg Univ, Dept Hlth Sci & Technol, Aalborg, Denmark
[3] Univ Hosp Aalborg, Dept Gastroenterol, Aalborg, Denmark
[4] Univ Hosp Aalborg, Ctr Visceral Biomech & Pain, Aalborg, Denmark
[5] Pfizer Ltd, Sandwich CT13 9NJ, Kent, England
关键词
drug profiling; experimental pain; gabapentin;
D O I
10.1016/j.rapm.2007.05.002
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background and objectives: Gabapentin is used for treatment of neuropathic pain, but its effect on different somatic pain modalities and integrative mechanisms are not completely understood. The aim of this double-blind, placebo-controlled experimental pain study, conducted on 20 healthy volunteers, was to examine the effect of a single dose of 1200 mg gabapentin on multi-modal experimental cutaneous and muscle pain models. Methods: The following pain models were applied: (1) pain thresholds to single and repeated cutaneous and intramuscular electrical stimulation (temporal sununation to 5 stimuli delivered at 2 Hz); (2) stimulus-response function relating pain intensity scores (visual analog scale, VAS) to increasing current intensities for electrical skin and muscle stimuli (single and repeated, determined at baseline); and (3) the pain intensity (VAS) and pain areas after intramuscular injection of hypertonic saline. Pain assessments were performed prior to, and at 4, 6, and 8 hours after medication. Results: When responses were averaged across the post-dose times, gabapentin: (1) significantly increased the temporal summation pain threshold in skin compared with placebo (P =.03); (2) significantly reduced the area under the pain intensity curve to hypertonic saline injections in the muscle (P =.02); and (3) significantly reduced the area of pain evoked by hypertonic saline (P =.03). Conclusions: Gabapentin reduces temporal summation of skin stimuli at pain threshold intensities; this may have potential as a biomarker for drugs with efficacy on neurogenic pain. The data also suggest that tonic muscle pain is responsive to gabapentin treatment and suggest further clinical studies.
引用
收藏
页码:382 / 388
页数:7
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