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Shapes and projections of neurons with immunoreactivity for gamma-aminobutyric acid in the guinea-pig small intestine

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Summary

The distribution of nerve cell bodies and fibres with immunoreactivity for γ-aminobutyric acid (GABA) has been studied in the guinea-pig small intestine. Cell bodies were common in myenteric ganglia but were extremely rare in the submucosa. Reactive fibres were numerous in the tertiary component of the myenteric plexus and in the circular muscle but they were rare in both myenteric and submucous ganglia. Reactive nerve fibres were absent from the mucosa. This distribution conforms to previous descriptions. Exposure to exogenous GABA, in vitro, was used to supplement endogenous stores of GABA. The morphology of cell bodies was better defined after this treatment. Nearly all cell bodies had type-I morphology, i.e., the cells had numerous short lamellar dendrites and one axon. Most axons ran anally. Some could be traced to the tertiary component of the myenteric plexus, others to the circular muscle. Removal of the myenteric plexus from a short length of intestine caused a loss of nerve fibres from the circular muscle beneath the site of operation and a decrease in fibre density in the circular muscle that extended anally from the lesion for about 1 mm. The nerve lesions caused no significant changes in the tertiary plexus. It is concluded that GABA is contained in motor neurons supplying the longitudinal and circular muscle, and that the neurons supplying the circular muscle may be inhibitory.

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References

  • Baetge G, Gershon MD (1986) GABA in the PNS: Demonstration in enteric neurons. Brain Res Bull 16:421–424

    Google Scholar 

  • Bornstein JC, Costa M, Furness JB, Lees GM (1984) Electrophysiology and enkephalin immunoreactivity of identified myenteric plexus neurons of guinea-pig small intestine. J Physiol (Lond) 351:313–325

    Google Scholar 

  • Bornstein JC, Costa M, Furness JB, Lang RJ (1986) Electrophysiological analysis of projections of enteric inhibitory motor neurones in the guinea-pig small intestine. J Physiol (Lond) 370:61–74

    Google Scholar 

  • Bywater RAR, Taylor GS (1986) Non-cholinergic excitatory and inhibitory junction potentials in the circular smooth muscle of the guinea-pig ileum. J Physiol (Lond) 374:153–164

    Google Scholar 

  • Davanger S, Ottersen OP, Storm-Mathisen J (1987) Immunocytochemical localization of GABA in cat myenteric plexus. Neurosci Lett 73:27–32

    Google Scholar 

  • Dogiel AS (1899) Über den Bau der Ganglien in den Geflechten des Darmes und der Gallenblase des Menschen und der Säugetiere. Arch Anat Physiol Leipzig, Ant Abt: 130–158

  • Erde SM, Sherman D, Gershon MD (1985) Morphology and serotonergic innervation of physiologically identified cells of the guinea pig's myenteric plexus. J Neurosci 5:617–633

    Google Scholar 

  • Furness JB, Costa M (1979) Projections of intestinal neurons showing immunoreactivity for vasoactive intestinal polypeptide are consistent with these neurons being the enteric inhibitory neurons. Neurosci Lett 15:199–203

    Google Scholar 

  • Furness JB, Llewellyn-Smith U, Bornstein JC, Costa M (1988) Neuronal circuitry in the enteric nervous system. In: Björklund A, Hökfelt T, Owman C (eds) Handbook of Chemical Neuroanatomy, vol 6. Eisevier, Amsterdam, pp 161–218

    Google Scholar 

  • Hills JM, Jessen KR, Mirsky R (1987) An immunohistochemical study of the distribution of enteric GABA-containing neurons in the rat and guinea-pig intestine. Neuroscience 22:301–312

    Google Scholar 

  • Hobbiger F (1958) Effects of γ-aminobutyric acid on the isolated mammalian ileum. J Physiol (Lond) 142:147–164

    Google Scholar 

  • Iyer V, Bornstein JC, Costa M, Furness JB, Takahashi Y, Iwanaga T (1988) Electrophysiology of guinea-pig myenteric neurons correlated with immunoreactivity for calcium binding proteins. J Autonom Nerv Syst 22:141–150

    Google Scholar 

  • Jessen KR, Hills JM, Dennison ME, Mirsky R (1983) γ-Aminobutyrate as an autonomic neurotransmitter: release and uptake of [3H]γ-aminobutyrate in guinea-pig large intestine and cultured enteric neurons using physiological methods and electron microscopic autoradiography. Neuroscience 10:1427–1442

    Google Scholar 

  • Jessen KR, Hills JM, Saffrey MJ (1986) Immunohistochemical demonstration of GABAergic neurons in the enteric nervous system. J Neurosci 6:1628–1634

    Google Scholar 

  • Jessen KR, Mirsky R, Hills JM (1987) GABA as an autonomic neurotransmitter: studies on intrinsic GABAergic neurons in the myenteric plexus of the gut. Trends Neurosci 10:255–262

    Google Scholar 

  • Katayama Y, Lees GM, Pearson GT (1986) Electrophysiology and morphology of vasoactive intestinal peptide immunoreactive neurones of the guinea-pig ileum. J Physiol (Lond) 378:1–11

    Google Scholar 

  • Kleinrok A, Kilbinger H (1983) γ-Aminobutyric acid and cholinergic transmission in the guinea-pig ileum. Naunyn Schmiedebergs Arch Pharmacol 322:216–220

    Google Scholar 

  • Krantis A, Kerr D (1981) Autoradiographic localisation of 3H-gamma aminobutyric acid in the myenteric plexus of the guineapig small intestine. Neurosci Lett 23:263–268

    Google Scholar 

  • Krantis A, Costa M, Furness J, Orbach J (1980) γ-Aminobutyric acid stimulates intrinsic inhibitory and excitatory nerves in the guinea-pig intestine. Eur J Pharmacol 67:461–468

    Google Scholar 

  • Krantis A, Kerr DIB, Dennis BJ (1986) Autoradiographic study of the distribution of [3H]γ-ammobutyrate-accumulating neural elements in guinea-pig intestine: evidence for a transmitter function of γ-aminobutyrate. Neuroscience 17:1243–1255

    Google Scholar 

  • Maley B, Newton B (1985) Immunohistochemistry of γ-aminobutyric acid in the cat nucleus tractus solitarius. Brain Res 330:364–368

    Google Scholar 

  • Ohkawa H (1987) Effects of γ-aminobutyric acid on the non-adrenergic inhibitory potentials in circular smooth muscle cells of the guinea-pig duodenum. Biomed Res 8(3):185–194

    Google Scholar 

  • Ong J, Kerr DIB (1983) GABAA- and GABAB-receptor-mediated modification of intestinal motility. Eur J Pharmacol 86:9–17

    Google Scholar 

  • Ong J, Kerr DIB (1984) Evidence for a physiological role of GABA in the control of guinea-pig intestinal motility. Neurosci Lett 50:339–343

    Google Scholar 

  • Ottersen OP, Storm-Mathisen J (1984) Glutamate- and GABAcontaining neurons in the mouse and rat brain, as demonstrated with a new immunocytochemical technique. J Comp Neurol 229:374–392

    Google Scholar 

  • Ottersen OP, Storm-Mathisen J, Madsen S, Skumlia S, Strømhaug J (1986) Evaluation of the immunocytochemical method for amino acids. Med Biol 64:147–158

    Google Scholar 

  • Saffrey MJ, Marcus N, Jessen KR, Burnstock (1983) Distribution of neurons with high-affinity uptake sites for GABA in the myenteric plexus of the guinea-pig, rat and chicken. Cell Tissue Res 234:231–235

    Google Scholar 

  • Saito N, Tanaka C (1986) Immunohistochemical demonstration of GABA containing neurons in the guinea pig ileum using purified GABA antiserum. Brain Res 376:78–84

    Google Scholar 

  • Smith TK, Furness JB, Costa M, Bornstein JC (1988) An electrophysiological study of the projections of motor neurones that mediate non-cholinergic excitation in the circular muscle of the guinea-pig small intestine. J Autonom Nerve Syst 22:115–128

    Google Scholar 

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Furness, J.B., Trussell, D.C., Pompolo, S. et al. Shapes and projections of neurons with immunoreactivity for gamma-aminobutyric acid in the guinea-pig small intestine. Cell Tissue Res. 256, 293–301 (1989). https://doi.org/10.1007/BF00218886

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