Development and validation of an animal model of prostate inflammation-induced chronic pelvic pain: evaluating from inflammation of the prostate to pain behavioral modifications

PLoS One. 2014 May 13;9(5):e96824. doi: 10.1371/journal.pone.0096824. eCollection 2014.

Abstract

Background: Chronic prostatitis/Chronic pelvic pain syndrome (CP/CPPS) is the most common type of prostatitis. Due to the lack of a suitable animal model partly, the pathogenesis for this condition is obscure. In the current study we developed and validated an animal model for nonbacterial prostatitis and prostate inflammation-induced chronic pelvic pain in rats with the use of intraprostatic injection of λ-carrageenan.

Methods: Male Sprague-Dawley rats weighing 250-350 g were used for the experiments. After intraprostatic injection of 3% λ-carrageenan, at different time points(after 24 h, 7 d, 14 d and 30 d of injection), radiant heat and von Frey filaments were applied to the scrotum of rats to measure the heat and mechanical thresholds respectively. Then the prostate was removed for histology, and cyclooxygenase (COX) 2 protein expression was determined by Western-blot. Evans blue(50 mg/kg) was also injected intravenously to assess for plasma protein extravasation at different time points after injection of λ-carrageenan.

Results: Compared to control group, inflamed animals showed a significant reduction in mechanical threshold (mechanical allodynia) at 24 h and 7d(p = 0.022,0.046, respectively), and a significant reduction in heat threshold (thermal hyperalgesia) at 24 h, 7d and 14 d(p = 0.014, 0.018, 0.002, respectively) in the scrotal skin. Significant increase of inflammatory cell accumulation, COX2 expression and Evans blue extravasation were observed at 24 h, 7d and 14 d after injection.

Conclusions: Intraprostatic λ-carrageenan injection induced neurogenic prostatitis and prostate inflammation pain, which lasted at least 2 weeks. The current model is expected to be a valuable preclinical tool to study the neurobiological mechanisms of male chronic pelvic pain.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Animals
  • Behavior, Animal / physiology
  • Cyclooxygenase 2 / metabolism
  • Disease Models, Animal
  • Hyperalgesia / etiology
  • Hyperalgesia / metabolism
  • Hyperalgesia / physiopathology*
  • Male
  • Pain Threshold / physiology*
  • Pelvic Pain / etiology
  • Pelvic Pain / metabolism
  • Pelvic Pain / physiopathology*
  • Prostate / metabolism
  • Prostate / physiopathology*
  • Prostatitis / chemically induced
  • Prostatitis / complications
  • Prostatitis / physiopathology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Cyclooxygenase 2

Grants and funding

The authors' study was supported by the National Natural Science Foundation of China (No. 81200549), and the freedom explore Program of Central South University (2011QNZT136). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.