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在福尔马林试验后,全身性可乐定可激活脊髓背角神经元,但不激活蓝斑核(A6)或A7区:脊髓背角在可乐定抗伤害感受作用中的重要性。

Systemic clonidine activates neurons of the dorsal horn, but not the locus ceruleus (A6) or the A7 area, after a formalin test: the importance of the dorsal horn in the antinociceptive effects of clonidine.

作者信息

Fukuda Taeko, Furukawa Hajime, Hisano Setsuji, Toyooka Hidenori

机构信息

Department of Anesthesiology, Institute of Clinical Medicine, Graduate School of Comprehensive Human Sciences, Tsukuba University, 1-1-1 Tennodai, Tsukuba 305-8575, Japan.

出版信息

J Anesth. 2006;20(4):279-83. doi: 10.1007/s00540-006-0426-5.

Abstract

PURPOSE

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.

METHODS

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).

RESULTS

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.

CONCLUSION

The antinociceptive effects of clonidine might be mediated primarily by neural activity in the DH.

摘要

目的

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)。

方法

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)。

结果

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。

结论

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。

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