Bian J T, Sun M Z, Han J S
Department of Physiology, Beijing Medical University, PR China.
Int J Neurosci. 1993 Sep;72(1-2):15-29. doi: 10.3109/00207459308991620.
Two varieties of neurons were found in nucleus parafascicularis (pf) of the rat: one responds to noxious stimuli with an increase in firing (pain-excited neuron, PEN), the other with a decrease in firing (pain-inhibited neuron, PIN). Electroacupuncture (EA) has been shown to suppress PEN and excite PIN, which can be taken as an electrophysiological index for EA analgesia. This effect of EA subsided after prolonged (6 h) EA stimulation, suggesting the development of tolerance to EA. Intracerebroventricular (icv) injection of CCK-8 antiserum aiming at neutralizing endogenously released CCK-8 resulted in a complete restoration of the EA effect. Normal rabbit serum was not effective. CCK-8 antiserum per se did not affect the firing pattern of the PEN or PIN in nontolerant rat. The results obtained from single neuron recording in anesthetized animals thus confirmed those obtained in intact animals using the tail flick as the end point, implying that an excess of endogenously released CCK-8 may constitute one of the mechanisms for the development of EA tolerance.
在大鼠的束旁核(pf)中发现了两种神经元:一种对伤害性刺激产生放电增加的反应(痛兴奋神经元,PEN),另一种则产生放电减少的反应(痛抑制神经元,PIN)。电针(EA)已被证明可抑制PEN并兴奋PIN,这可作为电针镇痛的电生理指标。在长时间(6小时)电针刺激后,电针的这种效应减弱,提示对电针产生了耐受性。脑室内(icv)注射CCK - 8抗血清以中和内源性释放的CCK - 8,导致电针效应完全恢复。正常兔血清则无效。CCK - 8抗血清本身并不影响未产生耐受性大鼠的PEN或PIN的放电模式。因此,在麻醉动物中通过单神经元记录获得的结果证实了在完整动物中以甩尾为终点所获得的结果,这意味着内源性释放的CCK - 8过量可能是电针耐受性产生的机制之一。