Involvement of peripheral P2Y1 receptors and potential interaction with IL-1 receptors in IL-1β-induced thermal hypersensitivity in rats

被引:9
作者
Kwon, Soon-Gu [1 ]
Roh, Dae-Hyun [4 ]
Yoon, Seo-Yeon [5 ]
Choi, Sheu-Ran [2 ,3 ]
Choi, Hoon-Seong [2 ,3 ]
Moon, Ji-Young [6 ]
Kang, Suk-Yun [6 ]
Beitz, Alvin J. [7 ]
Lee, Jang-Hern [2 ,3 ]
机构
[1] Neuracle Sci Co Ltd, Seoul 02841, South Korea
[2] Seoul Natl Univ, Dept Vet Physiol, PLUS Program Creat Vet Sci Res BK21, Res Inst Vet Sci, Seoul, South Korea
[3] Seoul Natl Univ, Coll Vet Med, Seoul 151742, South Korea
[4] Kyung Hee Univ, Sch Dent, Dept Maxillofacial Tissue Regenerat, Seoul, South Korea
[5] Seoul Natl Univ, Pain Cognit Funct Res Ctr, Dept Brain & Cognit Sci,Sch Dent, Coll Nat Sci,Dent Res Inst,Dept Neurobiol & Physi, Seoul, South Korea
[6] Korea Inst Oriental Med, KM Fundamental Res Div, Daejeon 305811, South Korea
[7] 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
Interleukin-1; beta; receptor; P2Y1; Thermal hypersensitivity; Inflammation; NEURONAL EXCITABILITY; INFLAMMATORY HYPERALGESIA; P2Y(1) RECEPTOR; SENSORY NEURONS; INTERLEUKIN-1-BETA; CYTOKINES; PAIN; PHOSPHORYLATION; EXPRESSION; NOCICEPTORS;
D O I
10.1016/j.brainresbull.2017.01.019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although interleuldn-1 beta (IL-1 beta) is a prototypical pro-inflammatory cytokine, the specific mechanisms underlying the role of its cognate receptor, the interleuldn-1 receptor (IL-1R) in peripheral sensitization remain to be investigated. Since emerging evidence in the literature indicates that IL-1 beta can modulate membrane-bound receptors, we decided to examine the involvement of P2Y1 receptor (P2Y1R) in IL-1 beta induced pain and the potential interaction of P2Y1Rs and IL-1Rs in both nave and carrageenan injected rats. Intraplantar (i.pl) injection of IL-1 beta dose-dependently produced mechanical and thermal hypersensitivity in nave rats. Pre-treatment with IL-lra (i.pl, 30 and 100 ng), an endogenous IL-1R antagonist, prevented the IL-1 beta induced mechanical and thermal hypersensitivity. Pre-treatment with MRS2500 (i.pl, 1 and 3 nmol), a specific P2Y1R antagonist, dose-dependently reduced IL-1 beta induced thermal hypersensitivity, but did not affect the development of mechanical hypersensitivity. Conversely coadministration of MRS2500 (i.pl, 0.1 nmol, sub-effective dose) together with IL-1ra (10 nmol, sub-effective dose) significantly reduced IL-1 beta induced thermal, but not mechanical hypersensitivity. We next used immunohistochemistry to demonstrate that P2Y1 and IL-1 type I receptors co-localize predominantly in small diameter neurons in the dorsal root ganglion. We also performed experiments to examine the interaction of P2Y1Rs and IL-1Rs under the inflammatory conditions induced by 2% carrageenan. Intraplantar coadministration of MRS2500 (3 nmol, sub-effective dose) and IL-lra (30 ng, sub-effective dose) significantly reduced inflammatory thermal, but not mechanical, hypersensitivity. These data indicate the involvement of P2Y1Rs in IL-1 beta mediated pain in both naive and carrageenan injected rats. There is a positive interaction between peripheral P2Y1Rs and IL-1Rs in both IL-1 beta and carrageenan-induced thermal hypersensitivity. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:165 / 172
页数:8
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