Huang Cheng, Wang Yun, Han Ji-Sheng, Wan You
Neuroscience Research Institute, Peking University, 38 Xueyuan Road, Beijing 100083, China.
Brain Res. 2002 Jul 26;945(1):20-5. doi: 10.1016/s0006-8993(02)02503-9.
The present study was conducted to evaluate the characteristics of electroacupuncture (EA)-induced analgesia in mice. Three inbred strains of mice (DBA/2, C57BL/6J, BALB/c) and three outbred strains (ICR, LACA, NIH) were used in the experiment. Two pairs of metallic needles were inserted into acupoints ST 36 and SP 6 connected to an electric pulse generator. EA parameters were set as constant current output with alteration of a positive and negative square wave, 0.6 ms in pulse width for 2 Hz and 0.3 ms for 100 Hz. Tail-flick latencies evoked by radiant heat were measured before, during and after EA stimulation. We found that (1) DBA/2 mice showed a significantly more potent analgesic effect than the other five strains in response to both 100 and 2 Hz EA. In this case, the intensities were 1.0-2.0-2.0 mA, 10 min for each intensity totally 30 min. (2) EA analgesia increased as the intensity of stimulation increased from 0.5 to 2.0 mA, but it remained at this plateau when the intensity further increased from 2.0 to 3.0 mA. (3) 10.0 mg x kg(-1) naloxone was needed to block the analgesic effect induced by 2 Hz EA of 2.0 mA, but to block that by 100 Hz, 25.0 mg x kg(-1) was necessary. (4) A positive correlation was observed between analgesia induced by morphine at the dose of 5.0 mg x kg(-1) and by 100 Hz EA in two tested strains DBA/2 and C57BL/6J. In conclusion, EA induces reliable, strain-dependent analgesia in mice. The naloxone-reversibility of EA, a measure of whether it is opioid or non-opioid mediated, is dependent upon intensity and frequency.
本研究旨在评估电针(EA)诱导小鼠镇痛的特性。实验使用了三种近交系小鼠(DBA/2、C57BL/6J、BALB/c)和三种远交系小鼠(ICR、LACA、NIH)。将两对金属针插入与电脉冲发生器相连的穴位足三里(ST 36)和三阴交(SP 6)。EA参数设置为恒流输出,正负方波交替,脉宽2Hz时为0.6ms,100Hz时为0.3ms。在EA刺激前、刺激期间和刺激后测量辐射热诱发的甩尾潜伏期。我们发现:(1)在100Hz和2Hz EA刺激下,DBA/2小鼠的镇痛效果明显优于其他五个品系。在此情况下,强度分别为1.0 - 2.0 - 2.0mA,每种强度刺激10分钟,共30分钟。(2)EA镇痛效果随刺激强度从0.5mA增加到2.0mA而增强,但当强度从2.0mA进一步增加到3.0mA时,镇痛效果保持在该平台期。(3)需要10.0mg·kg⁻¹纳洛酮来阻断2.0mA、2Hz EA诱导的镇痛效果,但要阻断100Hz的镇痛效果,则需要25.0mg·kg⁻¹。(4)在两个受试品系DBA/2和C57BL/6J中,观察到5.0mg·kg⁻¹剂量的吗啡诱导的镇痛与100Hz EA诱导的镇痛之间存在正相关。总之,EA在小鼠中诱导出可靠的、品系依赖性的镇痛作用。EA的纳洛酮可逆性,作为其是否由阿片类或非阿片类介导的一种衡量指标,取决于强度和频率。