Mizumura K, Sato J, Kumazawa T
Pflugers Arch. 1987 May;408(6):565-72. doi: 10.1007/BF00581157.
An in vitro testis-superior spermatic nerve preparation was used to evaluate the effects of chemical agents applied in the bathing solution. Both directly evoked discharges and responses to algesic solutions [bradykinin (BK) 9 X 10(-8) M, hypertonic saline 616 mM and high K+ solution 60 mM] of polymodal receptors were studied. Prostaglandin (PG)-E2 (1.4 X 10(-6)-1.4 X 10(-5) M) and serotonin (5-HT) (1.1 X 10(-6) to 1.4 X 10(-4) M) had only a weak excitatory effect. However, test responses to algesic substances were regularly greatly increased by PG-E2, -I2 and 5-HT. Concentrations of PG-E2 of 1.4 X 10(-8) M or greater augmented BK responses; higher concentrations and/or longer applications were needed to enhance responses to algesic salt solutions. Effective concentrations for the PGs and 5-HT were near those reported for inflamed tissues and exudate. Aspirin (ASA) (5.5 X 10(-4) M or greater, for more than 4 min) suppressed the responses to BK but not those evoked by hypertonic saline. The ASA effect on the BK response was largely restored by an addition of PG-E2. Substance P also had a weak excitatory effect on some polymodal receptors, but no significant enhancement of the response to BK was noted. These results further support a role of polymodal receptors in transmitting nociceptive information, of inflammatory origin.
采用体外睾丸-精索上神经制备方法来评估浴液中所施加化学试剂的作用。研究了多模式感受器的直接诱发放电以及对致痛溶液[缓激肽(BK)9×10⁻⁸M、高渗盐水616mM和高钾溶液60mM]的反应。前列腺素(PG)-E2(1.4×10⁻⁶ - 1.4×10⁻⁵M)和5-羟色胺(5-HT)(1.1×10⁻⁶至1.4×10⁻⁴M)仅有微弱的兴奋作用。然而,PG-E2、-I2和5-HT可使对致痛物质的测试反应经常显著增强。1.4×10⁻⁸M或更高浓度的PG-E2可增强BK反应;增强对致痛盐溶液的反应则需要更高浓度和/或更长时间的应用。PG和5-HT的有效浓度接近报道的炎症组织和渗出液中的浓度。阿司匹林(ASA)(5.5×10⁻⁴M或更高,作用超过4分钟)可抑制对BK的反应,但不抑制高渗盐水诱发的反应。添加PG-E2可在很大程度上恢复ASA对BK反应的影响。P物质对一些多模式感受器也有微弱的兴奋作用,但未观察到对BK反应有显著增强。这些结果进一步支持了多模式感受器在传递炎症源性伤害性信息中的作用。