Fukuda Taeko, Furukawa Hajime, Hisano Setsuji, Toyooka Hidenori
Department of Anesthesiology, Institute of Clinical Medicine, Graduate School of Comprehensive Human Sciences, Tsukuba University, 1-1-1 Tennodai, Tsukuba 305-8575, Japan.
J Anesth. 2006;20(4):279-83. doi: 10.1007/s00540-006-0426-5.
In order to clarify the principal site for the antinociceptive effects of clonidine, we investigated the nociceptive behavior and neural activity (c-fos staining) of the dorsal horn (DH), locus ceruleus (LC), and A7 area after a formalin test in normal saline- or clonidine-injected rats.
Thirty-six rats were divided into 6 groups as follows: formalin test + saline (FS); formalin test + clonidine (1 mg.kg(-1)) (FC1); formalin test + clonidine (10 mg.kg(-1)) (FC10); saline (S); clonidine (1 mg.kg(-1)) (C1); and clonidine (10 mg.kg(-1)) (C10). Normal saline or clonidine was injected intraperitoneally 30 min before the formalin test. In the FS, FC1, and FC10 groups, 10% formalin was injected into the left rear paw. All rats were killed 2.5 h after normal saline or clonidine injection. Sections of the lumbar spinal cord, LC, and A7 area were processed for c-fos immunohistochemistry using the avidin-biotin peroxidase complex method. To evaluate the sedative effects of clonidine, we investigated the loss of righting reflex (LORR) for 90 min in 6 other rats as follows: clonidine (1 mg.kg(-1)) (n = 3) and clonidine (10 mg.kg(-1)) (n = 3).
The FC10 group showed fewer nociceptive behaviors and higher c-fos expression in the DH, but not in the A7 area, as well as lower c-fos expression in the LC than rats in the FS and FC1 groups (P < 0.05). The C10 group showed lower c-fos expression in the LC than that of rats in the S and C1 groups (P < 0.05). No rats exhibited LORR.
The antinociceptive effects of clonidine might be mediated primarily by neural activity in the DH.
为阐明可乐定的抗伤害感受作用的主要部位,我们研究了在注射生理盐水或可乐定的大鼠进行福尔马林试验后,其背角(DH)、蓝斑(LC)和A7区域的伤害感受行为及神经活动(c-fos染色)。
36只大鼠分为6组如下:福尔马林试验+生理盐水(FS)组;福尔马林试验+可乐定(1 mg·kg⁻¹)(FC1)组;福尔马林试验+可乐定(10 mg·kg⁻¹)(FC10)组;生理盐水(S)组;可乐定(1 mg·kg⁻¹)(C1)组;可乐定(10 mg·kg⁻¹)(C10)组。在福尔马林试验前30分钟腹腔注射生理盐水或可乐定。在FS、FC1和FC10组中,将10%福尔马林注射到左后爪。在注射生理盐水或可乐定后2.5小时处死所有大鼠。使用抗生物素蛋白-生物素过氧化物酶复合物法对腰段脊髓、LC和A7区域的切片进行c-fos免疫组织化学处理。为评估可乐定的镇静作用,我们在另外6只大鼠中观察了90分钟的翻正反射消失(LORR)情况如下:可乐定(1 mg·kg⁻¹)(n = 3)和可乐定(10 mg·kg⁻¹)(n = 3)。
与FS组和FC1组大鼠相比,FC10组在DH中表现出更少的伤害感受行为和更高的c-fos表达,但在A7区域未出现,并且在LC中c-fos表达更低(P < 0.05)。C10组在LC中的c-fos表达低于S组和C1组大鼠(P < 0.05)。没有大鼠出现LORR。
可乐定的抗伤害感受作用可能主要由DH中的神经活动介导。