Effects of spasmolytic and/or non-steroidal antiinflammatory drugs on muscle hyperalgesia of ureteral origin in rats

Eur J Pharmacol. 1995 May 15;278(2):97-101. doi: 10.1016/0014-2999(95)00104-s.

Abstract

Rats with artificial calculosis of one ureter develop hyperalgesia in the ipsilateral oblique musculature as evidenced by decreased vocalization threshold to electrical muscle stimulation lasting over a week. The aim of the study was to evaluate the effect on this hyperalgesia of spasmolytic anticholinergic and/or non-steroidal antiinflammatory drugs, common therapies for colic pain in humans. Rats implanted with a unilateral ureteral stone were treated for 10 days with: (1) saline; (2) hyoscine-N-butylbromide (15 mg/kg/day i.p.); (3) ketoprofen (15 mg/kg/day); or (4) hyoscine-N-butylbromide + ketoprofen (15 + 15 mg/kg/day). Oblique muscle vocalization thresholds were measured daily for 3 days before and 10 days after operation. Ipsilateral thresholds decreased significantly after stone implantation on: (1) seven days (max. 32%) for saline; (2) one day (max. 20%) for hyoscine-N-butylbromide; (3) one day (max. 18%) for ketoprofen, but did not change significantly for hyoscine-N-butylbromide + ketoprofen. These results indicate a protective effect against muscle hyperalgesia of ureteral origin by spasmolytic and antiinflammatory drugs, maximal when the two treatments are combined.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Butylscopolammonium Bromide / therapeutic use
  • Electric Stimulation
  • Female
  • Hyperalgesia / drug therapy*
  • Hyperalgesia / etiology*
  • Hyperalgesia / pathology
  • Ketoprofen / therapeutic use
  • Muscular Diseases / drug therapy*
  • Muscular Diseases / etiology*
  • Muscular Diseases / pathology
  • Pain Measurement / drug effects
  • Pain Threshold / drug effects
  • Parasympatholytics / therapeutic use*
  • Rats
  • Rats, Sprague-Dawley
  • Ureteral Diseases / complications*
  • Ureteral Diseases / pathology

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Parasympatholytics
  • Butylscopolammonium Bromide
  • Ketoprofen