Xu X.-J., Wiesenfeld-Hallin Z., Villar M. J., Fahrenkrug J., Hökfelt T.
Department of Clinical Physiology, Section of Clinical Neurophysiology, Karolinska Institute, Huddinge University Hospital, S-141 86 Huddinge, Sweden.
Eur J Neurosci. 1990;2(9):733-743. doi: 10.1111/j.1460-9568.1990.tb00464.x.
The interaction of intrathecally (i.t.) applied galanin (GAL) with substance P (SP), calcitonin gene-related peptide (CGRP), vasoactive intestinal polypeptide (VIP), somatostatin (SOM) and C-fibre conditioning stimulation (CS) with regard to their effects on the spinal nociceptive flexor reflex was studied in decerebrate, spinalized, unanaesthetized rats with intact or sectioned sciatic nerves. SP, CGRP, VIP and SOM applied onto the surface of lumbar spinal cord or a brief CS train (1 Hz, 20 s) to the sural nerve facilitated the flexor reflex for several minutes in animals with intact or sectioned nerves. Pretreatment with GAL, which by itself had a biphasic effect on the flexor reflex in a dose-dependent manner, antagonized the reflex facilitation induced by sural CS before and after sciatic nerve section. SP-induced facilitation of the flexor reflex was antagonized by GAL in rats with intact sciatic nerves, but not after nerve section. In contrast, VIP-induced reflex facilitation was antagonized by GAL only after sectioning of the sciatic nerve. GAL was effective in antagonizing the facilitatory effect of CGRP under both situations, but had no effect on SOM-induced facilitation. A parallel immunohistochemical study revealed that after sciatic nerve section GAL-like immunoreactivity (LI) and VIP-LI are increased in the dorsal root ganglia and that these two peptides coexist in many cells. The present results indicate that GAL antagonizes the excitatory effect of some neuropeptides which exist in the spinal cord. This antagonism could explain the inhibitory effect of GAL on C-fibre CS-induced facilitation of the flexor reflex, which is presumably due to the release of some of these neuropeptides from the terminals of primary afferents. Furthermore, the interaction between GAL and other neuropeptides is altered by sciatic nerve section, paralleling changes in the levels of these neuropeptides in primary afferents and their pattern of coexistence after nerve section. It is proposed that SP and CGRP are important mediators of the spinal flexor reflex in intact rats. However, after axotomy VIP may replace SP in this capacity, paralleling the decrease in SP and marked increase in VIP levels. In general the study provides further support for involvement of peptides in sensory function.
在去大脑、脊髓横断、未麻醉且坐骨神经完整或切断的大鼠中,研究了鞘内(i.t.)注射甘丙肽(GAL)与P物质(SP)、降钙素基因相关肽(CGRP)、血管活性肠肽(VIP)、生长抑素(SOM)以及C纤维条件刺激(CS)之间的相互作用,及其对脊髓伤害性屈肌反射的影响。将SP、CGRP、VIP和SOM施加于腰段脊髓表面,或对腓肠神经进行短暂的CS刺激(1 Hz,20 s),在坐骨神经完整或切断的动物中,均可使屈肌反射增强数分钟。预先注射GAL,其本身对屈肌反射具有剂量依赖性的双相作用,可拮抗坐骨神经切断前后腓肠神经CS诱导的反射增强。在坐骨神经完整的大鼠中,GAL可拮抗SP诱导的屈肌反射增强,但在神经切断后则无此作用。相反,VIP诱导的反射增强仅在坐骨神经切断后被GAL拮抗。在两种情况下,GAL均能有效拮抗CGRP的促进作用,但对SOM诱导的促进作用无影响。一项平行的免疫组织化学研究显示,坐骨神经切断后,背根神经节中甘丙肽样免疫反应性(LI)和VIP-LI增加,且这两种肽在许多细胞中共存。本研究结果表明,GAL可拮抗脊髓中某些神经肽的兴奋作用。这种拮抗作用可以解释GAL对C纤维CS诱导的屈肌反射增强的抑制作用,这可能是由于这些神经肽从初级传入纤维末梢释放所致。此外,坐骨神经切断改变了GAL与其他神经肽之间的相互作用,与神经切断后初级传入纤维中这些神经肽水平及其共存模式的变化相一致。有人提出,在完整大鼠中,SP和CGRP是脊髓屈肌反射的重要介质。然而,轴突切断后,VIP可能会取代SP发挥这一作用,这与SP水平的降低和VIP水平的显著升高相一致。总的来说,该研究进一步支持了肽类参与感觉功能的观点。