MacLean D B, Lewis S F
Brain Res. 1984 Jul 30;307(1-2):135-45. doi: 10.1016/0006-8993(84)90469-4.
The axoplasmic transport of somatostatin (SS) and substance P (SP) in the cervical vagus nerve was studied in the rat, guinea pig and cat. In preliminary studies, neuropeptide immunoreactivity (IR-SS and IR-SP) was evaluated in extracts of nodose ganglion and vagus nerve using gel and reverse-phase high-performance liquid chromatography (HPLC). In each species, a single immunoreactive form of SP co-eluted with the synthetic undecapeptide on a Bio-Gel P-10 column. More than 95% of transported vagal IR-SS co-eluted with synthetic SS-14. A small percentage in each species co-eluted with SS-28. No larger form, corresponding to a prosomatostatin, was identified in any of the 3 species. On HPLC, IR-SP and IR-SS co-eluted with their synthetic forms. To quantify neuropeptide transport, the vagus nerve was ligated distal to the nodose ganglion. 24 h later in each species, the content of IR-SS and IR-SP was more than 6 times greater in a 3-mm segment of nerve proximal to the ligature than in equal length segments distal to ligature or in the unligated contralateral nerve. In the proximal segment, the net content of IR-SP (pg/3-mm segment, mean +/- S.E.M.) was 366 +/- 45 in the rat, 2038 +/- 184 in the guinea pig, and 912 +/- 108 in the cat. The content of IR-SS in the same segment was 36 +/- 4, 66 +/- 13, and 575 +/- 59 pg/3-mm, respectively. The apparent transport velocities were similar for each peptide and among species. The contribution of the nodose ganglion to transported neuropeptide was estimated by crushing the vagus above the nodose ganglion and simultaneously ligating the nerve distal to the ganglion. The percent contribution of the ganglion to transported IR-SS following this procedure was 50% in the rat, 73% in the guinea pig, and 16% in the cat. Nodose ganglion contribution to IR-SP transport was 31%, 50% and 74%, respectively. Estimated turnover of IR-SS and IR-SP within the ganglion ranged from 4.1 to 6.8 times per 24 h in each species.(ABSTRACT TRUNCATED AT 400 WORDS)
在大鼠、豚鼠和猫中研究了生长抑素(SS)和P物质(SP)在颈迷走神经中的轴浆运输。在初步研究中,使用凝胶和反相高效液相色谱法(HPLC)对结节神经节和迷走神经提取物中的神经肽免疫反应性(IR-SS和IR-SP)进行了评估。在每个物种中,一种单一的SP免疫反应形式在Bio-Gel P-10柱上与合成的十一肽共洗脱。超过95%的运输性迷走神经IR-SS与合成的SS-14共洗脱。每个物种中有一小部分与SS-28共洗脱。在这3个物种中均未鉴定出与前生长抑素相对应的更大形式。在HPLC上,IR-SP和IR-SS与其合成形式共洗脱。为了量化神经肽运输,在结节神经节远端结扎迷走神经。24小时后,在每个物种中,结扎近端3毫米神经段中IR-SS和IR-SP的含量比结扎远端等长神经段或未结扎的对侧神经中的含量高6倍以上。在近端神经段中,IR-SP的净含量(pg/3毫米神经段,平均值±标准误)在大鼠中为366±45,在豚鼠中为2038±184,在猫中为912±108。同一神经段中IR-SS的含量分别为36±4、66±13和575±59 pg/3毫米。每种肽以及不同物种之间的表观运输速度相似。通过挤压结节神经节上方的迷走神经并同时结扎神经节远端的神经来估计结节神经节对运输的神经肽的贡献。在此操作后,神经节对运输的IR-SS的贡献百分比在大鼠中为50%,在豚鼠中为73%,在猫中为16%。神经节对IR-SP运输的贡献分别为31%、50%和74%。在每个物种中,神经节内IR-SS和IR-SP的估计周转率为每24小时4.1至6.8次。(摘要截断于400字)