神经解剖学杂志
神經解剖學雜誌
신경해부학잡지
CHINESE JOURNAL OF NEUROANATOMY
2006年
3期
267-274
,共8页
林芮禾%李瑞锡%王劼%钱琼英%高璐%吴丽如%彭裕文
林芮禾%李瑞錫%王劼%錢瓊英%高璐%吳麗如%彭裕文
림예화%리서석%왕할%전경영%고로%오려여%팽유문
疼痛调节%GABAB受体%背根神经节%脊髓背角%大鼠
疼痛調節%GABAB受體%揹根神經節%脊髓揹角%大鼠
동통조절%GABAB수체%배근신경절%척수배각%대서
pain regulation%GABAB receptor%dorsal root ganglion%spinal dorsal horn%rat
已知痛觉传递调制途径之一是通过背根神经节中的小型神经元的突触前代谢型GABAB受体介导.为了探讨肽能和非肽能2个亚群的小型背根神经节(DRG)神经元是否在痛觉调制过程中发挥同等作用,本实验用免疫荧光组织化学法和激光共聚焦显微镜技术观察了DRG内肽能和非肽能2个亚群的小型神经元中GABAB受体的表达.结果显示:92%的肽能和90%的非肽能亚群的小型神经元均表达GABAB受体,这些受体存在于2个亚群的胞体及其分布在脊髓背角特定板层的中枢突中.该结果表明在痛觉调制过程中,肽能和非肽能2个亚群的小型DRG内神经元在脊髓水平发挥类似作用,但作用于脊髓背角的不同板层.
已知痛覺傳遞調製途徑之一是通過揹根神經節中的小型神經元的突觸前代謝型GABAB受體介導.為瞭探討肽能和非肽能2箇亞群的小型揹根神經節(DRG)神經元是否在痛覺調製過程中髮揮同等作用,本實驗用免疫熒光組織化學法和激光共聚焦顯微鏡技術觀察瞭DRG內肽能和非肽能2箇亞群的小型神經元中GABAB受體的錶達.結果顯示:92%的肽能和90%的非肽能亞群的小型神經元均錶達GABAB受體,這些受體存在于2箇亞群的胞體及其分佈在脊髓揹角特定闆層的中樞突中.該結果錶明在痛覺調製過程中,肽能和非肽能2箇亞群的小型DRG內神經元在脊髓水平髮揮類似作用,但作用于脊髓揹角的不同闆層.
이지통각전체조제도경지일시통과배근신경절중적소형신경원적돌촉전대사형GABAB수체개도.위료탐토태능화비태능2개아군적소형배근신경절(DRG)신경원시부재통각조제과정중발휘동등작용,본실험용면역형광조직화학법화격광공취초현미경기술관찰료DRG내태능화비태능2개아군적소형신경원중GABAB수체적표체.결과현시:92%적태능화90%적비태능아군적소형신경원균표체GABAB수체,저사수체존재우2개아군적포체급기분포재척수배각특정판층적중추돌중.해결과표명재통각조제과정중,태능화비태능2개아군적소형DRG내신경원재척수수평발휘유사작용,단작용우척수배각적불동판층.
It has been reported that the small type of neurons in the dorsal root ganglion (DRG) play an important role in pain regulation by a presynaptic mechanism via the metabotropic type-B γ-aminobutyric acid receptors ( GABABR ). In order to understand whether the 2populations of the small type of the neurons, peptidergic and nonpeptidergic, in DRG share the same role, immunoflourescent histochemical methods and confocal laser scanning microscope were employed to investigate the expression of the GABABR in the peptidergic and nonpeptidergic small DRG neurons. The results revealed that 92% of the peptidergic and 90% of nonpeptidergic small DRG neurons express GABABR in their perikarya and central processes, which distribute in the various laminae of the spinal dorsal horn. These results suggest both the peptidergic and nonpeptidergic populations of the small neurons in the DRG share similar role in pain modulation via presynaptic mechanisms but in given laminae of the spinal dorsal horn.