Eide K, Hole K
Department of Physiology, University of Bergen, Norway.
Pharmacol Toxicol. 1992 Jun;70(6 Pt 1):397-401. doi: 10.1111/j.1600-0773.1992.tb00496.x.
This study examined interactions between effects of the undecapeptide substance P and norepinephrine and the alpha-adrenoceptor agonist clonidine in the mouse spinal cord. All compounds were injected into the lumbar subarachnoid space, and effects on the tail-flick reflex and the behavioural response to intrathecal substance P were evaluated. The tail-flick response latencies were markedly increased 5-20 min. after intrathecal application of norepinephrine (0.0125-0.1 microgram) or clonidine (0.0125-0.1 microgram). The actions of both intrathecal norepinephrine (0.025 microgram) and intrathecal clonidine (0.025 microgram) were significantly attenuated when substance P (5 micrograms) was given intrathecally 55 and 45 min. before the agonists. There was a significant relationship between the tail-flick response latencies and the tail skin temperature. However, the tail-flick results were not due to changes in the skin temperature. Intrathecally applied substance P (10 ng) produced a response consisting of biting of the caudal part of the body and a few hindlimb scratches. The number of bites was significantly reduced 5 min. after injection of norepinephrine (0.1 micrograms) or clonidine (0.05-0.1 microgram), but the number of scratches was unchanged. The data show that increased stimulation of spinal alpha-adrenoceptors inhibits a spinal nociceptive reflex as well as the action of substance P in the spinal cord. Substance P modulates the action of alpha-adrenoceptor agonists on the tail-flick reflex, which may tentatively be explained by downregulation of alpha-adrenoceptors by substance P.
本研究检测了十一肽P物质、去甲肾上腺素的效应与α-肾上腺素能受体激动剂可乐定在小鼠脊髓中的相互作用。所有化合物均注入腰段蛛网膜下腔,并评估其对甩尾反射以及鞘内注射P物质后行为反应的影响。鞘内注射去甲肾上腺素(0.0125 - 0.1微克)或可乐定(0.0125 - 0.1微克)后5 - 20分钟,甩尾反应潜伏期显著延长。当在鞘内注射激动剂前55分钟和45分钟分别鞘内注射P物质(5微克)时,鞘内注射去甲肾上腺素(0.025微克)和鞘内注射可乐定(0.025微克)的作用均显著减弱。甩尾反应潜伏期与尾部皮肤温度之间存在显著关系。然而,甩尾结果并非由皮肤温度变化所致。鞘内注射P物质(10纳克)会引发包括咬身体尾部和后肢轻微抓挠的反应。注射去甲肾上腺素(0.1微克)或可乐定(0.05 - 0.1微克)5分钟后,咬的次数显著减少,但抓挠次数未变。数据表明,脊髓α-肾上腺素能受体刺激增加会抑制脊髓伤害性反射以及P物质在脊髓中的作用。P物质可调节α-肾上腺素能受体激动剂对甩尾反射的作用,这可能初步解释为P物质使α-肾上腺素能受体下调。