电生理学特性得到确定的大鼠脊髓背根神经节细胞内谷氨酸和P物质的共存

在离体灌流带脊髓和坐骨神经经的标本上,对脊髓背根神经节（ＤＲＧ）细胞的电生理学特性、对Ｐ物质（ＳＰ）受体激动剂的反应及谷氨酸（Ｇｌｕ）／ＳＰ共存的特点进行了研究。（１）对１３５个细胞进行了细胞内记录,并依纤维传导速度将其分为Ａα／β（〉１２ｍ／ｓ）和Ｃ（〈１．３ｍ／ｓ）两大类,它们的动作电位的快速后超极化（ｆＡＨＰ）有明显区别,Ｃ类的ｆＡＨＰ幅度小、时程长,Ａα／β类的ｆＡＨＰ幅度大、时程短;（２

Co-existence of glutamate and substance P in electrophysiologically identified dorsal root ganglion neurons of rats

Electrophysiological properties, reaction to substance P (SP) receptor agonist, and co-existence of glutamate (Glu) and SP in neurons of the spinal dorsal root ganglion (DRG) of the rat were investigated in vitro. The main results were: (1) According to the fiber conduction velocity, totally 135 intracellularly recorded DRG neurons were divided into A alpha/beta type (> 12 m/s) and C type (< 1.3 m/s). There were remarkable differences between the fast after hyperpolarization (fAHP) of action potential between the two types: fAHP of C type neurons had smaller amplititude and longer duration, whereas the fAHP of A alpha/beta type neurons had larger amplititude and shorter duration. (2) Among 22 DRG neurons of which overshoots of action potential appeared, specific SP receptor agonist Sar-SP induced depolorization in 42% (5/12) of the A alpha/beta type neurons and 80% (8/10) of the C type neurons. (3) Biocytin was intracellularly injected into the 22 Sar-SP administrated DRG neurons. After fixation and section, employing the immunofluorescent histochemical multi-staining technique for phosphate-activated glutaminase (PAG, a specific marker for glutamatergic neurons), SP and biocytin, 25% (3/12) of the A alpha/beta type neurons and 80% (8/10) of the C type neurons showed both PAG- and SP-like immunoreactivities. There was a great difference between the percentages of the PAG/SP co-existing A alpha/beta type neurons and C type neurons (P < 0.05). The present results indicated that there were some differences in chemicoanatomical and electrophysiological properties between A alpha/beta type and C type neurons, and SP might facilitate the discharge of DRG neurons through activating SP autoreceptors on their membrane.