Microglial interleukin-1β in the ipsilateral dorsal horn inhibits the development of mirror-image contralateral mechanical allodynia through astrocyte activation in a rat model of inflammatory pain

被引:46
作者
Choi, Hoon-Seong [1 ,2 ]
Roh, Dae-Hyun [3 ]
Yoon, Seo-Yeon [4 ,5 ]
Moon, Ji-Young [1 ,2 ]
Choi, Sheu-Ran [1 ,2 ]
Kwon, Soon-Gu [1 ,2 ]
Kang, Suk-Yun [6 ]
Han, Ho-Jae [1 ,2 ]
Kim, Hyun-Woo [7 ]
Beitz, Alvin J. [8 ]
Oh, Seog-Bae [4 ,5 ]
Lee, Jang-Herh [1 ,2 ]
机构
[1] Seoul Natl Univ, Res Inst Vet Sci, Dept Vet Physiol, PLUS Program Creat Vet Sci Res BK21, Seoul 151742, South Korea
[2] Seoul Natl Univ, Coll Vet Med, Seoul 151742, South Korea
[3] Kyung Hee Univ, Sch Dent, Dept Maxillofacial Tissue Regenerat, Seoul, South Korea
[4] Seoul Natl Univ, Sch Dent, Dent Res Inst, Coll Nat Sci,Pain Cognit Funct Res Ctr,Dept Brain, Seoul 151742, South Korea
[5] Seoul Natl Univ, Sch Dent, Dept Neurobiol & Physiol, Seoul 151742, South Korea
[6] Korea Inst Oriental Med, Dept Acupuncture Moxibust & Meridian Res, Div Med Res, Taejon, South Korea
[7] Chungnam Natl Univ, Sch Med, Inst Brain Res, Dept Physiol, Taejon, South Korea
[8] Univ Minnesota, Coll Vet Med, Dept Vet & Biomed Sci, St Paul, MN 55108 USA
基金
新加坡国家研究基金会;
关键词
Mirror-image pain; Microglia; Interleukin-1; beta; Astrocyte; GAP-JUNCTIONAL COMMUNICATION; SPINAL-CORD; NEUROPATHIC PAIN; GLIAL ACTIVATION; NERVE INJURY; INTRATHECAL INJECTION; CENTRAL SENSITIZATION; MURINE MODELS; TNF-ALPHA; P38; MAPK;
D O I
10.1097/j.pain.0000000000000148
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Damage on one side of the body can also result in pain on the contralateral unaffected side, called mirror-image pain (MIP). Currently, the mechanisms responsible for the development of MIP are unknown. In this study, we investigated the involvement of spinal microglia and interleukin-1 beta (IL-1 beta) in the development of MIP using a peripheral inflammatory pain model. After unilateral carrageenan injection, mechanical allodynia (MA) in both hind paws and the expression levels of spinal lba-1, IL-1 beta, and GFAP were evaluated. lpsilateral MA was induced beginning at 3 hours after carrageenan injection, whereas contralateral MA showed a delayed onset occurring 5 days after injection. A single intrathecal (it.) injection of minocycline, a tetracycline derivative that displays selective inhibition of microglial activation, or an interleukin-1 receptor antagonist (IL-1ra) on the day of carrageenan injection caused an early temporary induction of contralateral MA, whereas repeated i.t. treatment with these drugs from days 0 to 3 resulted in a long-lasting contralateral MA, which was evident in its advanced development. We further showed that IL-1 beta was localized to microglia and that minocycline inhibited the carrageenan-induced increases in spinal lba-1 and IL-1 beta expression. Conversely, minocycline or IL-1ra pretreatment increased GFAP expression as compared with that of control rats. However, it. pretreatment with fluorocitrate, an astrocyte inhibitor, restored minocycline- or IL-1ra-induced contralateral MA. These results suggest that spinal IL-1 beta derived from activated microglia temporarily suppresses astrocyte activation, which can ultimately prevent the development of contralateral MA under inflammatory conditions. These findings imply that microglial IL-1 beta plays an important role in regulating the induction of inflammatory MIP.
引用
收藏
页码:1046 / 1059
页数:14
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