Seo Young-Jun, Kwon Min-Soo, Shim Eon-Jeong, Park Soo-Hyun, Choi Ok-Sun, Suh Hong-Won
Department of Pharmacology and Institute of Natural Medicine, College of Medicine, Hallym University, 1 Okcheon-Dong, Chuncheon, Gangwon-Do 200-702, South Korea.
Brain Res Bull. 2006 Dec 11;71(1-3):279-86. doi: 10.1016/j.brainresbull.2006.09.012. Epub 2006 Oct 4.
In the present study, we examined the change of pain behaviors induced by formalin injected subcutaneously (s.c.) into the hind paw, or substance P (SP), glutamate, and pro-inflammatory cytokines (TNF-alpha, IL-1beta, and IFN-gamma) injected intrathecally (i.t.) in the mouse immobilization stress model. The mouse was restrained either once for 1h or five times for 5 days (once/day). In the formalin test, a single immobilization stress attenuated pain behaviors (licking, biting or scratching) in the second phase, while it had no effect on the pain behaviors revealed during the first phase. In addition, repeated immobilization stress attenuated pain behaviors revealed during the second phase but not in the first phase. A single as well as repeated immobilization stress decreased pain behaviors induced by substance P i.t. injection, but there were no significant changes in the glutamate test. In the pro-inflammatory cytokine pain model, a single immobilization stress decreased the pain behaviors induced by TNF-alpha, IL-1beta administered i.t. but not by IFN-gamma administered i.t. Moreover, a mouse applied with repeated immobilization stress did not show any changes in pain behaviors elicited by pro-inflammatory cytokines (TNF-alpha, IL-1beta and IFN-gamma) compared to the control group. These results suggest that a single and repeated immobilization stress differentially affects such nociceptive processing induced by formalin, SP, glutamate and pro-inflammatory cytokines in different manners.
在本研究中,我们检测了在小鼠制动应激模型中,皮下(s.c.)注射福尔马林至后爪或鞘内(i.t.)注射P物质(SP)、谷氨酸以及促炎细胞因子(肿瘤坏死因子-α、白细胞介素-1β和干扰素-γ)所诱导的疼痛行为变化。小鼠被制动一次,持续1小时,或连续5天每天制动一次,每次持续5小时。在福尔马林试验中,单次制动应激减轻了第二阶段的疼痛行为(舔、咬或抓挠),而对第一阶段所表现出的疼痛行为没有影响。此外,重复制动应激减轻了第二阶段而非第一阶段所表现出的疼痛行为。单次和重复制动应激均减少了鞘内注射P物质所诱导的疼痛行为,但在谷氨酸试验中没有显著变化。在促炎细胞因子疼痛模型中,单次制动应激减少了鞘内注射肿瘤坏死因子-α、白细胞介素-1β所诱导的疼痛行为,但对鞘内注射干扰素-γ所诱导的疼痛行为没有影响。此外,与对照组相比,施加重复制动应激的小鼠在促炎细胞因子(肿瘤坏死因子-α、白细胞介素-1β和干扰素-γ)所引发的疼痛行为上没有表现出任何变化。这些结果表明,单次和重复制动应激以不同方式对福尔马林、SP、谷氨酸和促炎细胞因子所诱导的伤害性处理产生不同影响。