Kuki Fumiko, Sugiyo Shinichi, Abe Tetsuya, Niwa Hitoshi, Takemura Motohide
Department of Dental Anesthesiology, Osaka University Graduate School of Dentistry, Osaka, Japan.
Pharmacology. 2014;93(1-2):10-7. doi: 10.1159/000356713. Epub 2014 Jan 8.
This study was designed to investigate the efficacy of a partial μ-opioid agonist, buprenorphine, against the formalin-induced hyperalgesia in the upper lip in chronically inferior alveolar nerve (IAN)-transected rats. Subcutaneous injection of diluted formalin into the upper lip in the IAN-transected rats showed an increased number of pain-related behavior (PRB; face-rubbing behavior) in every phase up to 45 min (p < 0.01) compared with that in the nontransected sham control rats. The numbers of c-Fos-immunoreactive (IR) cells in the superficial layers of the trigeminal nucleus caudalis (VcI/II) at the rostral (0-0.7 mm caudal to the obex) and middle levels (1.4-2.2 mm caudal to the obex) 2 h after the formalin injection in the IAN-transected rats were significantly increased compared with those in the control rats. The PRB in phases 1 and 2 (0-15 and 15-30 min after formalin injection) in rats with preadministration of morphine (3 mg/kg i.p.) or buprenorphine (100 µg/kg i.p.) was significantly (p < 0.05) smaller than those in the control rats. There was no significant difference in the efficacy between morphine and buprenorphine at these doses. The antinociceptive efficacy in phase 2 of buprenorphine (100 µg/kg) was higher (p < 0.05) than that of morphine (3 mg/kg) in the IAN-transected rats. The number of c-Fos-IR cells in the VcI/II at every level (0-3.6 mm caudal to the obex) after formalin injection was significantly decreased (p < 0.01) with preadministration of morphine (3 mg/kg) or buprenorphine (100 µg/kg) in the control rats. In the IAN-transected rats, the number of c-Fos-IR cells in the caudal VcI/II (2.2-3.6 mm caudal to the obex) after formalin injection was significantly decreased (p < 0.01) with preadministration of buprenorphine (100 µg/kg) but not so much (2.2-2.9 mm caudal to the obex, p < 0.05; 2.9-3.6 mm caudal to the obex, p > 0.05) with preadministration of morphine (3 mg/kg). These results indicate that IAN transection enhanced formalin-induced nocifensive responses in the upper lip, the dermatome of the intact nerve neighboring the IAN. Systemic preadministration of buprenorphine had more antinociceptive effects on the formalin-induced nocifensive behavior in the upper lip compared with morphine in the IAN-transected rats.
本研究旨在探讨部分μ-阿片受体激动剂丁丙诺啡对慢性下牙槽神经(IAN)横断大鼠上唇福尔马林诱导的痛觉过敏的疗效。与未横断的假手术对照大鼠相比,向IAN横断大鼠的上唇皮下注射稀释的福尔马林后,在长达45分钟的每个阶段,疼痛相关行为(PRB;擦脸行为)的数量均增加(p<0.01)。在IAN横断大鼠福尔马林注射后2小时,延髓头端(距闩尾端0 - 0.7 mm)和中间水平(距闩尾端1.4 - 2.2 mm)三叉神经尾侧核浅层(VcI/II)中c-Fos免疫反应性(IR)细胞的数量与对照大鼠相比显著增加。预先腹腔注射吗啡(3 mg/kg)或丁丙诺啡(100 μg/kg)的大鼠在福尔马林注射后第1和第2阶段(0 - 15和15 - 30分钟)的PRB显著(p<0.05)少于对照大鼠。在这些剂量下,吗啡和丁丙诺啡的疗效无显著差异。在IAN横断大鼠中,丁丙诺啡(100 μg/kg)在第2阶段的镇痛效果高于(p<0.05)吗啡(3 mg/kg)。在对照大鼠中,福尔马林注射前预先给予吗啡(3 mg/kg)或丁丙诺啡(100 μg/kg)后,各水平(距闩尾端0 - 3.6 mm)VcI/II中c-Fos-IR细胞的数量显著减少(p<0.01)。在IAN横断大鼠中,福尔马林注射前预先给予丁丙诺啡(100 μg/kg)后,尾侧VcI/II(距闩尾端2.2 - 3.6 mm)中c-Fos-IR细胞的数量显著减少(p<0.01),但预先给予吗啡(3 mg/kg)时减少程度较小(距闩尾端2.2 - 2.9 mm,p<0.05;距闩尾端2.9 - 3.6 mm,p>0.05)。这些结果表明,IAN横断增强了上唇福尔马林诱导的伤害性反应,上唇是与IAN相邻的完整神经的皮节。与吗啡相比,在IAN横断大鼠中,全身预先给予丁丙诺啡对福尔马林诱导的上唇伤害性行为具有更强的镇痛作用。