Assay of therapeutic ultrasound induced-antinociception in experimental trigeminal neuropathic pain

• Published in: Journal of neuroscience research 2012-08, Vol.90 (8), p.1639-1645
• Main Authors: Savernini, Átila, Savernini, Natascha, de Amaral, Flávio Almeida, Romero, Thiago Roberto Lima, Duarte, Igor Dimitri Gama, de Castro, Maria Salete Abreu
• Format: Article
• Language: English
• Subjects: Animals; Cell Movement - physiology; chronic constriction injury; Disease Models, Animal; heat nociception; Hyperalgesia - diagnostic imaging; infraorbital nerve; Male; Neutrophils - diagnostic imaging; Nociception - physiology; Pain Threshold; Rats; Rats, Wistar; therapeutic ultrasound; Trigeminal Neuralgia - diagnostic imaging; trigeminal neuropathic pain; Ultrasonography
• ISSN: 0360-4012; 1097-4547
• DOI: 10.1002/jnr.23056

Trigeminal neuralgia is considered one of the most painful conditions, and pharmacological treatment can be as debilitating as the pathology itself. The aim of this work was to evaluate the effectiveness of pulsed therapeutic ultrasound (TU) on an experimental rat model of trigeminal neuropathic nociception (chronic constriction injury—infraorbital nerve; CCI‐ION). To evaluate facial thermonociception, an apparatus that measured the reaction time for head withdrawal was constructed. After surgery, a gradual reduction in reaction time was observed until day 15 post‐CCI, when the values became constant. Three ipsilateral applications of TU to post‐CCI rats promoted an increase in latency time. This antinociceptive effect was evident even after the first TU application, reaching maximal values at 24 hr. The magnitude of this effect was proportional to ultrasonic wave intensity (0.3 and 0.4 W/cm2). Posttreatment with naltrexone (5 mg/kg, s.c.) completely blocked the hypoalgesic effect of TU. Pretreatment with an opioid antagonist was unable to block the antinociceptive effect during the first 8 hr, suggesting that opioids are involved only in the latter phase of the TU effects. Myeloperoxidase (MPO) levels in the infraorbital nerve were not increased by TU use, indicating that TU causes no injury or is at least insufficient to induce neutrophil migration. In conclusion, TU is an effective resource in a model of trigeminal neuropathic pain, with a mechanism involving opioid receptor activation, confirming its potential usefulness in the treatment of trigeminal neuralgia. © 2012 Wiley Periodicals, Inc.