Skip to main content
Log in

Immunocytochemical localization of amino acid neurotransmitter candidates in the ventral horn of the cat spinal cord: a light microscopic study

  • Published:
Experimental Brain Research Aims and scope Submit manuscript

Abstract

The distribution of immunoreactivities to six amino acids, possibly related to synaptic function, was investigated in the motor nucleus of the cat L7 spinal cord (laminae VII and IX) using a postembedding peroxidase-antiperoxidase technique. Consecutive 0.5 μm transverse sections of plastic-embedded tissue were incubated with antisera raised against protein-glutaraldehyde conjugates of γ-aminobutyric acid (GABA), glycine, aspartate, glutamate, homocysteate, and taurine. This method allowed localization of the different immunoreactivities in individual cell profiles. The results showed that all these amino acids, except homocysteate, could be clearly detected in either neuronal or glial elements in the ventral horn. In cell bodies of neurons in lamina VII, immunoreactivity was observed for aspartate, glutamate, GABA, and glycine. Adjacent section analysis revealed that combinations of immunoreactivity for glycine/glutamate/aspartate, GABA/glycine/glutamate/aspartate and glutamate/aspartate, respectively, may occur in one and the same cell. In the motor nuclei (lamina IX), immunoreactivity to amino acids was observed in two types of neuron. Large cells, probably representing α-motoneurons, were harboring immunoreactivity to both glutamate and aspartate, while a few small neurons in this area displayed a colocalization of glycine, glutamate, and aspartate. Dendrites and axons in the motor nuclei cocontained glycine/glutamate/aspartate, GABA/glycine/glutamate/aspartate, and glutamate/aspartate immunoreactivities. In both laminae VII and IX, taurine-like immunoreactivity was absent in neuronal cell bodies, but highly concentrated in perivascular cells and small cells with a morphology resembling that of glial cells. A punctate immunolabeling, in all probability representing labeling of nerve terminals, could be demonstrated in the ventral horn for GABA, glycine, and glutamate, but not with certainty for aspartate or taurine. A quantitative estimate of the covering of cell bodies of α-motoneuron size by immunoreactive puncta revealed that glycine immunoreactive terminal-like structures were most abundant (covering 26–42% of the somatic membrane), while glutamate immunoreactive terminals were seen least frequently (5–9% covering). GABA-immunoreactive terminals covered from 10 to 24% of the soma surface. A colocalization of GABA and glycine immunoreactivities in putative nerve terminals could be shown both in the neuropil and in close relation to cell bodies of motoneurons. These results suggest that among the studied amino acids probably only three, namely GABA, glycine, and glutamate, can be considered to be neurotransmitter candidates in the ventral horn of the cat spinal cord.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Aprison MH, Nadi NS (1978) Glycine: inhibition from the sacrum to the medulla. In: Fonnum F (eds) Amino acids as chemical transmitters. Plenum, New York, pp 531–570

    Google Scholar 

  • Arvidsson U, Ulfhake B, Cullheim S, Bergstrand A, Theodorsson E, Hökfelt T (1991) Distribution of 125I-galanin binding sites, immunoreactive galanine, and its coexistence with 5-hydroxytryptamine in the cat spinal cord: biochemical, histochemical, and experimental studies at the light and electron microscopic level. J Comp Neurol 308:115–138

    Google Scholar 

  • Barber RP, Vaughn JE, Roberts E (1982) The cytoarchitecture of GABAergic neurons in the rat spinal cord. Brain Res 238:305–328

    Google Scholar 

  • Burger PM, Hell J, Mehl E, Krasel C, Lottspeich F, Jahn R (1991) GABA and glycine storage in synaptic vesicles: storage and transport characteristics. Neuron 7:287–293

    Google Scholar 

  • Burke RE (1990) Spinal cord: ventral horn. In: Shepherd GM (eds) The synaptic organization of the brain. Oxford University Press, Oxford, pp 88–132

    Google Scholar 

  • Burke RE, Bruggentage G ten (1971) Electrotonic characteristics of alpha motoneurons of varying size. J Physiol (Lond) 212:1–20

    Google Scholar 

  • Carlton SM, Hayes ES (1990) Light microscopic and ultrastructural analysis of GABA-immunoreactive profiles in the monkey spinal cord. J Comp Neurol 300:162–182

    Google Scholar 

  • Christensen H, Fonnum F (1990) Uptake of glycine, GABA and glutamate by synaptic vesicles isolated from different regions of rat CNS. Neurosci Lett 129:217–220

    Google Scholar 

  • Conradi S (1969) Ultrastructure and distribution of neuronal and glial elements on the motoneuron surface in the lumbar spinal cord of the adult cat. Acta Physiol Scand 332:5–48

    Google Scholar 

  • Conradi S, Kellerth J-O, Berthold C-H (1979) Electron microscopic studies on serially sectioned cat spinal α-motoneurons. II. A Method for the description of architecture and synaptology of the cell body and proximal dendritic segments. J Comp Neurol 184:741–754

    Google Scholar 

  • Cullheim S, Kellerth J-O (1978) A morphological study of the axons and recurrent axon collaterals of cat α-motoneurons supplying different hind-limb muscles. J Physiol (Lond) 281:285–289

    Google Scholar 

  • Cullheim S, Kellerth J-O (1981) Two kinds of recurrent inhibition of cat spinal alpha-motoneurones as differentiated pharmacologically. J Physiol (Lond) 312:209–224

    Google Scholar 

  • Cullheim S, Fleshman JM, Glenn LL, Burke RE (1987) Membrane area and dendritic structure in type-identified triceps surae alpha-motoneurons. J Comp Neurol 225:68–81

    Google Scholar 

  • Curtis DR, Watkins JC (1960) The excitation and depression of spinal neurons by structurally related amino acids. J Neurochem 6:117–141

    Google Scholar 

  • Dale N, Ottersen OP, Roberts A, Storm-Mathisen J (1986) Inhibitory neurons of a motor pattern generator in Xenopus revealed by antibodies to glycine. Nature 324:255–257

    Google Scholar 

  • Destombes J, Horcholle-Bossavit G, Thiesson D (1992) Distribution of glycinergic terminals on lumbar motoneurons of the adult cat: an ultrastructural study. Brain Res 559:353–360

    Google Scholar 

  • Eccles JC, Schmidt R, Willis WD (1963) Pharmacological studies on presynaptic inhibition. J Physiol (Lond) 168:500–530

    Google Scholar 

  • Fonnum F (1993) Regulation of the synthesis of the transmitter glutamate pool. Prog Biophys Mol Biol 59: (in press)

  • Fyffe REW (1991a) Glycine-like immunoreactivity in synaptic boutons of identified inhibitory interneurons in the mammalian spinal cord. Brain Res 547:175–179

    Google Scholar 

  • Fyffe REW (1991b) Spartial distribution of recurrent inhibitory synapses on spinal motoneurons in the cat. J Neurophysiol 65:1134–1149

    Google Scholar 

  • Graham LT Jr, Shank RP, Werman R, Aprison MH (1967) Distribution of some synaptic transmitter suspects in cat spinal cord: glutamic acid, aspartic acid, γ-aminobutyric acid, glycine, and glutamine. J Neurochem 14:465–472

    Google Scholar 

  • Headley PM, Grillner S (1990) Excitatory amino acids and synaptic transmission: the evidence for a physiological function. Trends Pharmacol Sci 11:205–211

    Google Scholar 

  • Holstege JC (1991) Utrastructural evidence for GABAergic brainstem projections to spinal motoneurons in the rat. J Neurosci 11:159–167

    Google Scholar 

  • Hökfelt T, Ljungdahl Å (1971) Light and electron microscopic autoradiography on spinal cord slices after incubation with labeled glycine. Brain Res 32:189–194

    Google Scholar 

  • Jankowska E, Lindström S (1971) Morphological identification of Renshaw cells. Acta Physiol Scand 81:428–430

    Google Scholar 

  • Jessel TM, Yoshika K, Jahr CE (1986) Amino acid receptor mediated transmission at primary afferent synapses in rat spinal cord. J Exp Biol 124:239–258

    Google Scholar 

  • Ji Z, Aas JE, Laake J, Walberg F, Ottersen OP (1991) An electron microscopic, immunogold analysis of glutamate and glutamine in terminals of rat spinocerebellar fibers. J Comp Neurol 307:296–310

    Google Scholar 

  • Kellerth J-O (1968) Aspect of the relative significance of preand postsynaptic inhibition in the spinal cord. In: Euler C von, Skoglund S, Söderberg U (eds) Structure and function of inhibitory neuronal mechanisms. Pergamon, Oxford, pp 197–212

    Google Scholar 

  • Kolston J, Osen KK, Hackney CM, Ottersen OP, Storm-Mathisen J (1992) An atlas of glycineand GABA-like immunoreactivity and colocalization in the cochlear nuclear complex of the guinea pig. Anat Embryol 186:443–465

    Google Scholar 

  • Lagerbäck PÅ, Kellerth J-O (1985) Light microscopic observations on cat Renshaw cells after intracellular staining with horseradish peroxidase. II. The cell bodies and dendrites. J Comp Neurol 240:368–376

    Google Scholar 

  • Lane BP, Europa DL (1965) Differential staining of ultrathin sections of Epon-embedded tissues for light microscopy. J Histochem Cytochem 13:579–582

    CAS  PubMed  Google Scholar 

  • Lee IS, Renno WM, Beitz AJ (1992) A quantitative light and electron microscopic analysis of taurine-like immunoreactivity in the dorsal horn of the rat spinal cord. J Comp Neurol 321:65–82

    Google Scholar 

  • Lewis CA, Faber DS (1993) GABA responses and their partial occlusion by glycine in cultured rat medullary neurons. Neuroscience 1:83–96

    Google Scholar 

  • Ljungdahl Å, Hökfelt T (1973) Autoradiographic uptake patterns of [3H]GABA and [3H]glycine in central nervous tissues with special references to the spinal cord. Brain Res 62:587–595

    Google Scholar 

  • Madsen S, Ottersen OP, Storm-Mathisen J (1990) Immunocytochemical localization of taurine: methodological aspects. Prog Clin Biol Res 351:37–44

    Google Scholar 

  • Maxwell DJ, Christie WM, Ottersen OP, Storm-Mathisen J (1990) Terminals of group Ia primary afferent fibres in Clarke's column are enriched with 1-glutamate-like immunoreactivity. Brain Res 510:346–350

    Google Scholar 

  • Mayer ML, Westbrook GL (1984) Mixed-agonist action of excitatory amino acids on mouse spinal cord neurons under voltage clamp. J Physiol (Lond) 354:29–53

    Google Scholar 

  • McLaughlin BJ, Barber RP, Saito K, Roberts E, Wu J-Y (1975) Immunocytochemical localization of glutamate decarboxylase in rat spinal cord. J Comp Neurol 167:305–322

    Google Scholar 

  • Örnung G, Shupliakov O, Cullheim S, Ulfhake B, Brodin L, Ottersen OP, Storm-Mathisen J (1992) Observations on the distriution of amino acid neurotransmitter candidates in the motor nucleus of the cat spinal cord. A light and electron microscopic study (abstract). Eur J Neurosci [Suppl] N5:286

    Google Scholar 

  • Ottersen OP (1987) Postembedding light and electron microscopic immunocytochemistry of amino acids: description of a new model system allowing identical conditions for specificity testing and tissue processing. Exp Brain Res 69:167–174

    Google Scholar 

  • Ottersen OP (1989) Postembedding immunogold labelling of fixed glutamate: an electron microscopic analysis of the relationship between gold particle density and antigen concentration. J Chem Neuroanat 2:57–66

    Google Scholar 

  • Ottersen OP, Storm-Mathisen J, Somogyi P (1988) Colocalization of glycine-like and GABA-like immunoreactivities in Golgi cell terminals in the rat cerebellum: a postembedding light and electron microscopic study. Brain Res 450:342–353

    Google Scholar 

  • Ottersen OP, Zhang N, Walberg F (1992) Metabolic compartmentation of glutamate and glutamine: morphological evidence obtained by quantitative immunocytochemistry in rat cerebellum. Neuroscience 46:519–534

    Article  CAS  PubMed  Google Scholar 

  • Palaigos G, Hertz L, Schousboe A (1989) Role of aspartate aminotransferase and mitochondrial dicarboxylate transport for release of endogenously and exogenously supplied neurotransmitter in glutamatergic neurons. Neurochem Res 14:359–366

    Google Scholar 

  • Palkovits M, Banay-Schwartz M, Lajtha A (1990) Taurine levels in brain nuclei of young adult and aging rats. In: Pasantes-Morales H, Martin DL, Shain W, Rio RM del (eds) Taurine: functional neurochemistry, physiology, and cardiology. Prog Clin Biol Res 351:45–52

  • Petrusz P, Van Eyck SL, Weinberg RJ, Rustioni A (1990) Antibodies to glutamate and aspartate recognize non-endogenous ligands for excitatory amino acid receptors. Brain Res 529:339–344

    Google Scholar 

  • Pol AN van den, Görcs T (1988) Glycine and glycine receptor imunoreactivity in brain and spinal cord. J Neurosci 8:472–492

    Google Scholar 

  • Rall W, Burke RE, Smith TG, Nelson PG, Frank K (1967) Dendritic location of synapses and possible mechanisms for the monosynaptic EPSP in motoneurons. J Neurophysiol 30:1169–1193

    Google Scholar 

  • Redman S (1990) Quantal analysis of synaptic potentials in the central nervous system. Physiol Rev 70:165–198

    Google Scholar 

  • Rexed B (1954) The cytoarchitectonic organization of the spinal cord in the cat. J Comp Neurol 96:415–496

    Google Scholar 

  • Rustioni A, Weinberg RJ (1992) Neurotransmission in primary afferents to superficial laminae of the dorsal horn. In: Willis WD Jr (eds) Hyperalgesia and allodynia. Raven, New York, pp 267–279

    Google Scholar 

  • Shupliakov O, Brodin L, Cullheim S, Ottersen OP, Storm-Mathisen J (1992) Immunogold quantification of glutamate in two types of excitatory synapses with different firing patterns. J Neurosci 12:3789–3803

    Google Scholar 

  • Snow H, Lowrie MB, Bennett JP (1992) A postsynaptic GABA transporter in rat spinal motor neurons. Neurosci Lett 143:119–122

    Google Scholar 

  • Somogyi P, Hodgson AJ (1985) Antiserum to γ-aminobutyric acid. III Demonstration of GABA in Golgi-impregnated neurons and in conventional electron microscopic sections of cat striate cortex. J Histochem Cytochem 33:249–257

    Google Scholar 

  • Somogyi P, Hodgson AJ, Smith AD, Nunzi AG, Gorio A, Wu Y-J (1984) Different populations of GABAergic neurons in the visual cortex and hippocampus of cat contain somatostatinor cholecystokinin-immunoreactive material. J Neurosci 4:2590–2603

    Google Scholar 

  • Sternberger, LA (1979) Immunocytochemistry. Wiley, New York

    Google Scholar 

  • Storm-Mathisen J, Leknes AK, Bore AT, Vaaland GL, Edminson P, Haug FM-S, Ottersen OP (1983) First visualization of glutamate and GABA in neurones by immunocytochemistry. Nature 301:517–520

    Google Scholar 

  • Todd AJ, Sullivan AC (1990) Light microscope study of the coexistence of GABA-like and glycine-like immunoreactivities in the spinal cord of the rat. J Comp Neurol 296:496–505

    Google Scholar 

  • Triller A, Cluzeaud F, Korn H (1987) Gamma-aminobutiric acidcontaining terminals can be apposed to glycine receptors at central synapses. J Cell Biol 104:947–956

    Google Scholar 

  • Ulfhake B, Cullheim S (1988) Postnatal development of the cat hind limb motoneurons. III. Changes in size of motoneurons supplyng the triceps surae muscle. J Comp Neurol 278:103–120

    Google Scholar 

  • Ulfhake B, Kellerth JO (1983) A quantitative morphological study of HRP-labelled cat alpha motoneurons supplying different hindlimb muscles. Brain Res 264:1–19

    Google Scholar 

  • Waller SJ, Kilpatrick IC, Chan MWJ, Evans RH (1991) The influence of assay conditions on measurement of excitatory dibasic sulphinic and sulphonic alpha-amino acids in nervous tissue. J Neurosci Meth 36:167–176

    Google Scholar 

  • Watkins JC (1986) Selective antagonists define subclasses of excitatory amino acid receptors. In: Iversen LL, Goodman E (eds) Fast and slow chemical signalling in the nervous system. Oxford Science, Oxford, pp 89–105

    Google Scholar 

  • Werman R, Davidoff RA, Aprison MH (1967) Inhibition of mooneurons by iontophoresis of glycine. Nature 214:680–683

    Google Scholar 

  • Wright CE, Tallan HH, Lin YY (1986) Taurine: biological update. Annu Rev Biochem 55:427–453

    Google Scholar 

  • Xu Q, Grant G (1988) Do certain spinocerebellar neurons in lamina IX at lumbosacral levels send collaterals to peripheral nerves? Arch Ital Biol 126:179–192

    Google Scholar 

  • Zhang N, Ottersen OP (1992) Different cellular distribution of two sulfur-containing amino acids in rat cerebellum. Exp Brain Res 90:11–20

    Google Scholar 

  • Zhang N, Walberg F, Laake JH, Meldrum BS, Ottersen OP (1990) Aspartate-like and glutamate-like immunoreactivities in the inferior olive and climbing fiber system: a light microscopic and semiquantitative electron microscopic study in rat and baboon (Papio anubis). Neuroscience 38:61–80

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Shupliakov, O., Örnung, G., Brodin, L. et al. Immunocytochemical localization of amino acid neurotransmitter candidates in the ventral horn of the cat spinal cord: a light microscopic study. Exp Brain Res 96, 404–418 (1993). https://doi.org/10.1007/BF00234109

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00234109

Key words

Navigation