Assessment of visceral pain-related pseudo-affective responses to colorectal distension in mice by intracolonic manometric recordings

被引:36
作者
Arvidsson, S [1 ]
Larsson, M [1 ]
Larsson, H [1 ]
Lindström, E [1 ]
Martinez, V [1 ]
机构
[1] AstraZeneca R&D, Dept Integrat Pharmacol GI Biol, SE-43183 Molndal, Sweden
关键词
colorectal distension; electromyography; manometry; mechanical recordings; mouse; visceral pain;
D O I
10.1016/j.jpain.2005.09.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Recently, a new manometric method has been proposed to quantify visceromotor responses (VMR) to colorectal distension (CRD) in rats. This method is based on monitoring pressure changes within the distending balloon during CRD. This study assesses the applicability of such a technique to the quantification of VMRs to CRD in mice. Electrical activity of the abdominal muscles and pressure changes within the distending balloon (mechanical response) were simultaneously recorded in conscious mice during CRD (phasic ascending, 10-80 mm Hg, or repetitive, 55 mm Hg). There was a clear stimulus-response relationship with a strong correlation between electrical and mechanical responses during the ascending (r(2) = 0.899, n = 7) or repetitive phasic CRD (r(2) = 0.926, n(8)). Repetitive phasic distensions (55 mm Hg) increased the mechanical and electrical responses by 71 +/- 20% and 42 +/- 16%, respectively (pulses 10-12 vs. 1-3; In = 8, both P < .01). Atropine (0.5 or 1 mg/kg, subcutaneously) did not affect the mechanical response to CRD. The mu-opioid agonist, fentanyl (0.05 mg/kg, subcutaneously), completely prevented the sensitizing response associated to repetitive distensions. These results show that noninvasive, surgery-free manometry of intracolonic pressure is a reliable method to assess VMRs to CRD in mice. The analgesic effect of compounds could be determined, indicating that the method can be used in pharmacologic studies. Perspective: The modelpresented to assess visceralpain in mice allows a broaduse of this species in pharmacological studies and will be of use in the characterization of potential targets and new drugs for the treatment of human pathologies with visceral pain arising from the gut as a significant component.
引用
收藏
页码:108 / 118
页数:11
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