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. 2008 Dec;140(3):465-471.
doi: 10.1016/j.pain.2008.09.027. Epub 2008 Nov 1.

Experimental muscle pain impairs descending inhibition

Affiliations

Experimental muscle pain impairs descending inhibition

Lars Arendt-Nielsen et al. Pain. 2008 Dec.

Abstract

In chronic musculoskeletal pain conditions, the balance between supraspinal facilitation and inhibition of pain shifts towards an overall decrease in inhibition. Application of a tonic painful stimulus results in activation of diffuse noxious inhibitory controls (DNIC). The aims of the present experimental human study were (1) to compare DNIC, evoked separately, by hypertonic saline (6%)-induced muscle pain (tibialis anterior) or cold pressor pain; (2) to investigate DNIC evoked by concomitant experimental muscle pain and cold pressor pain, and (3) to analyze for gender differences. Ten males and 10 age matched females participated in two sessions. In the first session unilateral muscle pain or unilateral cold pressor pain were induced separately; in the second session unilateral muscle pain and unilateral cold pressor pain were induced concomitantly. Pressure pain thresholds (PPT) were measured around the knee joint before, during, and after DNIC induction. Cold pressor pain increased PPT in both males and females with greater increases in males. Hypertonic saline-evoked muscle pain significantly increased PPT in males but not in females. When cold pressor and muscle pain were applied concomitantly the PPT increases were smaller when compared to the individual sessions. This study showed for the first time that two concurrent conditioning tonic pain stimuli (muscle pain and cold pressor pain) cause less DNIC compared with either of the conditioning stimuli given alone; and males showed greater DNIC than females. This may explain why patients with chronic musculoskeletal pain have impaired DNIC.

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Figures

Fig. 1
Fig. 1
PPT of test sites around both knees (R = Right, L = Left) before, during and after saline evoked pain for males and females. The five test sites were (1) 2 cm proximal to the superior lateral edge of patella, (2) 2 cm proximal to the superior edge of patella, (3) 2 cm proximal to the superior medial edge of patella, (4) 2 cm distal to the inferior lateral edge of patella, (5) 2 cm distal to the inferior medial edge of patella. *Significantly higher than before and after saline evoked pain.
Fig. 2
Fig. 2
PPT of test sites around both knees (R = Right, L = Left) before, during and after cold pain for males and females. The five test sites were (1) 2 cm proximal to the superior lateral edge of patella, (2) 2 cm proximal to the superior edge of patella, (3) 2 cm proximal to the superior medial edge of patella, (4) 2 cm distal to the inferior lateral edge of patella, (5) 2 cm distal to the inferior medial edge of patella. *Significantly higher than before and after cold pain.
Fig. 3
Fig. 3
PPT of test sites around both knees (R = Right, L = Left) before, during and after combined saline and cold pain for males and females. The five test sites were (1) 2 cm proximal to the superior lateral edge of patella, (2) 2 cm proximal to the superior edge of patella, (3) 2 cm proximal to the superior medial edge of patella, (4) 2 cm distal to the inferior lateral edge of patella, (5) 2 cm distal to the inferior medial edge of patella. *Significantly higher than before and after combined pain.
Fig. 4
Fig. 4
Increment of PPT of test sites during saline evoked muscle pain, cold pain, and combined saline/cold pain for males and females. *Significantly higher than females.
Fig. 5
Fig. 5
The VAS area under curve (arbitrary units) of males and females during saline evoked muscle pain, cold pain, and combined saline/cold pain. *Significantly higher than VAS area under curve during saline evoked muscle pain; +significantly higher VAS area during saline evoked muscle pain and cold pain.

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