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P物质对神经激肽-1受体的激活会触发培养的成年大鼠背根神经节神经元释放P物质。

Activation of the neurokinin-1 receptor by substance P triggers the release of substance P from cultured adult rat dorsal root ganglion neurons.

作者信息

Tang He-Bin, Li Yu-Sang, Arihiro Koji, Nakata Yoshihiro

机构信息

Department of Pharmacology, Graduate School of Biomedical Sciences, Hiroshima University, Kasumi 1-2-3, Minami-ku, Hiroshima 734-8553, Japan.

出版信息

Mol Pain. 2007 Dec 25;3:42. doi: 10.1186/1744-8069-3-42.

Abstract

BACKGROUND

Although substance P (SP) is an important primary afferent modulator in nociceptive processes, it is unclear whether SP regulates its own release from primary sensory neurons.

RESULTS

Using a highly sensitive radioimmunoassay for SP, we have demonstrated that the activation of neurokinin-1 receptor by SP or GR73632 (a potent neurokinin-1 receptor agonist) triggered an increase of SP release from cultured adult rat dorsal root ganglion (DRG) neurons depending on the dose and exposure time within 60 min, and thereafter, the SP release level gradually decreased over 360 min. Accompanying the SP release, a significant reduction in the percentage of neurons expressing neurokinin-1 receptor on their membranes during exposure to SP (200 pg/dish) occurred time dependently (56 +/- 5% and 32 +/- 2% at 180 and 360 min, respectively). The GR73632-evoked (10 nM, 60 min) SP release was attenuated by several inhibitors for mitogen-activated protein kinase kinase, p38 mitogen-activated protein (MAP) kinase and cyclooxygenase-2 (COX-2), protein kinase C (PKC), respectively. In contrast, a c-Jun NH2-terminal kinase inhibitor increased the GR73632-evoked SP release.

CONCLUSION

These results indicate that the neurokinin-1 receptor activation by its agonists regulates the SP release process involving the activation of MAP kinases, PKCs and COX-2 from cultured DRG neurons.

摘要

背景

尽管P物质(SP)是伤害性感受过程中一种重要的初级传入调质,但尚不清楚SP是否调节其自身从初级感觉神经元的释放。

结果

使用一种高度灵敏的SP放射免疫分析法,我们已证明,SP或GR73632(一种有效的神经激肽-1受体激动剂)对神经激肽-1受体的激活,在60分钟内,根据剂量和暴露时间,触发了培养的成年大鼠背根神经节(DRG)神经元中SP释放的增加,此后,SP释放水平在360分钟内逐渐下降。伴随着SP释放,在暴露于SP(200 pg/培养皿)期间,膜上表达神经激肽-1受体的神经元百分比出现了时间依赖性的显著降低(在180分钟和360分钟时分别为56±5%和32±2%)。GR73632诱发的(10 nM,60分钟)SP释放分别被几种丝裂原活化蛋白激酶激酶、p38丝裂原活化蛋白(MAP)激酶和环氧化酶-2(COX-2)、蛋白激酶C(PKC)抑制剂所减弱。相反,一种c-Jun氨基末端激酶抑制剂增加了GR73632诱发的SP释放。

结论

这些结果表明,激动剂对神经激肽-1受体的激活调节了培养的DRG神经元中涉及MAP激酶、PKC和COX-2激活的SP释放过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4171/2235838/5b30e4e715e1/1744-8069-3-42-1.jpg

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