Hu S J, Weng Z C, Jiang S J, Gu J W
Department of Physiology, Fourth Military Medical University, Xian.
Sheng Li Xue Bao. 1990 Oct;42(5):428-36.
By using a model of sustained discharges of polymodal nociceptors (PMN) due to injection of a compound algogenic substance into the skin in anesthetized rats, it was found that stimulation of the sciatic nerve inhibited or facilitated at first and then inhibited the PMN sustained discharges markedly. In a crossperfused preparation, stimulation of the sciatic nerve of donor rat caused the similar effects on sustained discharges of PMN of the recipient rat. Injection of the animal serum after stimulation of the sciatic nerve affected PMN activity obviously. The inhibitory course of most units could not be reversed by naloxone. In the animal tolerance to morphine, the effects of stimulation of the sciatic nerve could still be obtained. Preadministration of reserpine almost completely abolished the facilitatory effect. The results indicate that sustained activity of PMN could be modulated by some humoral factors due to somatic afferents. The inhibitory substances in the humoral factor seem to be both opioid and nonopioid in nature. The facilitatory substance seem to be a catecholamine.
通过在麻醉大鼠皮肤中注射复合致痛物质建立多模式伤害感受器(PMN)持续放电模型,发现刺激坐骨神经起初会抑制或易化PMN持续放电,随后显著抑制该放电。在交叉灌流制备中,刺激供体大鼠的坐骨神经对受体大鼠PMN的持续放电产生类似影响。刺激坐骨神经后注射动物血清对PMN活性有明显影响。大多数单位的抑制过程不能被纳洛酮逆转。在动物对吗啡产生耐受性时,仍可获得刺激坐骨神经的效应。预先给予利血平几乎完全消除了易化效应。结果表明,由于躯体传入神经,PMN的持续活动可被某些体液因素调节。体液因素中的抑制物质似乎既有阿片类性质又有非阿片类性质。易化物质似乎是一种儿茶酚胺。