Holland Leland N, Goldstein Barry D
Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta, GA 30912 USA.
Pain. 1994 Mar;56(3):339-346. doi: 10.1016/0304-3959(94)90172-4.
Substance P (SP) has been suggested as a neuromediator of nociception in the dorsal horn. Following a single injection of SP onto the rat spinal cord, nociceptive reflexes are facilitated. Following successive administration of a high dose of SP, these responses are attenuated. We have administered multiple injections of SP onto the rat spinal cord in order to produce desensitization to the SP response. With this procedure, we have observed that phasic behaviors (short-term reflex) are attenuated for up to 150 min and are associated with a reduction in the number and affinity of SP-binding sites in the dorsal horn. This study was performed to examine the effect of SP-receptor desensitization in two well-established models of tonic (prolonged) nociception: the formalin test and the monosodium urate (MSU) test. Repeated intrathecal administration of SP (15 micrograms) reduced the first phase but did not alter the second phase of formalin-induced pain-related behavior. Similarly, repeated administration of SP did not alter MSU-induced pain-related behavior. In both tests, an analgesic dose of morphine administered in combination with SP did reduce the nociceptive behavior. These data show that alteration of SP-receptor activity in the dorsal horn does not alter responses to two longer acting agents considered to be nociceptive. These results suggest that SP in the dorsal horn does not directly mediate tonic nociception but rather may be involved in the expression of phasic pain-related behavior.
P物质(SP)被认为是脊髓背角伤害感受的神经介质。单次向大鼠脊髓注射SP后,伤害性反射增强。连续给予高剂量的SP后,这些反应减弱。我们向大鼠脊髓多次注射SP以产生对SP反应的脱敏作用。通过这个程序,我们观察到阶段性行为(短期反射)减弱长达150分钟,并且与脊髓背角中SP结合位点的数量和亲和力降低有关。本研究旨在检查SP受体脱敏在两种成熟的持续性(延长性)伤害感受模型中的作用:福尔马林试验和尿酸钠(MSU)试验。重复鞘内注射SP(15微克)减少了福尔马林诱导的疼痛相关行为的第一阶段,但没有改变第二阶段。同样,重复注射SP并没有改变MSU诱导的疼痛相关行为。在这两个试验中,与SP联合给予镇痛剂量的吗啡确实减少了伤害性反应。这些数据表明,脊髓背角中SP受体活性的改变不会改变对两种被认为是伤害性的长效药物的反应。这些结果表明,脊髓背角中的SP并不直接介导持续性伤害感受,而是可能参与阶段性疼痛相关行为的表达。