Shibuta S, Mashimo T, Zhang P, Ohara A, Yoshiya I
Department of Anaesthesiology, Osaka University Medical School, Japan.
J Neurol Sci. 1996 Sep 15;141(1-2):1-5. doi: 10.1016/0022-510x(96)00102-5.
The utility of a new nitric oxide (NO) donor, NOC-18, and the contribution of the neurotransmitter NO to nociception in response to tissue injury in rats, were examined following the subcutaneous injection of formalin into the hindpaw. This model induces biphasic responses in pain-related behavior, such that C-fiber activation during the first phase triggers a state of central sensitization characterized by the second phase. Formalin-induced nociceptive behavior was facilitated by intracerebroventricular administration of NOC-18 in the second phase, but not the first phase. This enhancement was completely abolished by the soluble guanylate cyclase inhibitor, methylene blue. These findings indicate that NO causes nociception via the NO-cGMP pathway in the central nervous system and NOC-18 proved to be a convenient and useful tool for the investigation of nociception-related NO.
在大鼠后爪皮下注射福尔马林后,研究了一种新型一氧化氮(NO)供体NOC-18的效用以及神经递质NO对组织损伤所致伤害感受的作用。该模型在疼痛相关行为中引发双相反应,即第一阶段的C纤维激活触发以第二阶段为特征的中枢敏化状态。在第二阶段而非第一阶段,脑室内注射NOC-18可促进福尔马林诱导的伤害感受行为。可溶性鸟苷酸环化酶抑制剂亚甲蓝可完全消除这种增强作用。这些发现表明,NO通过中枢神经系统中的NO-环鸟苷酸途径引起伤害感受,并且NOC-18被证明是研究与伤害感受相关的NO的方便且有用的工具。