Substance P microinjected into the periaqueductal gray matter induces antinociception and is released following morphine administration

被引:44
|
作者
Rosén, A
Zhang, YX
Lund, I
Lundeberg, T
Yu, LC
机构
[1] Huddinge Hosp, Karolinska Inst, Dept Odontol, Div Oral & Maxillofacial Surg, SE-14104 Huddinge, Sweden
[2] Peking Univ, Dept Physiol, Coll Life Sci, Beijing 100872, Peoples R China
[3] Karolinska Inst, Dept Physiol & Pharmacol, Stockholm, Sweden
[4] Karolinska Hosp, Dept Rehabil Med, Stockholm, Sweden
关键词
hindpaw withdrawal latency; hot plate; microdialysis; periaqueductal gray; substance P;
D O I
10.1016/j.brainres.2003.11.060
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The aims of the present study were to investigate, in rats, the behavioral effects of substance P (SP) microinjected into the ventrolateral periaqueductal gray (PAG) and the effects of the neurokinin I (NK-1) receptor antagonist [D-Arg1, D-Trp7, 9, Leu11]-substance P (Spantide). The effect of morphine administration on the release of SP in the ventrolateral PAG was also investigated using microdialysis in awake rats.SP microinjected into the ventrolateral part of the PAG induced significant increases in the hindpaw withdrawal latencies (HWLs) to thermal and mechanical stimulation as an antinociceptive response. The NK-1 receptor antagonist blocked these effects but exhibited no antinociceptive effect alone. Subcutaneous administration of morphine increased basal SP-like immuno reactivity (SP-LI) release in the microdialysate obtained from the ventrolateral PAG of freely moving rats. Our results demonstrate that SP injected into the ventrolateral PAG induces an antinociceptive effect via activation of NK-1 receptors. Morphine administered systemically induces the release of SP in the ventrolateral PAG. We suggest that an increased release of SP in the PAG may contribute to opioid antinociception. (C) 2004 Elsevier B.V. All rights reserved.
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页码:87 / 94
页数:8
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