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Localization of l-glutamate decarboxylase immunoreactivity in the major pelvic ganglion and in the coeliac-superior mesenteric ganglion complex of the rat

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Summary

The localization of l-glutamate decarboxylase (GAD), the GABA-synthesizing enzyme, was studied in the rat major pelvic ganglion and in the coeliac-superior mesenteric ganglion complex by indirect immunofluorescence technique with a specific antiserum raised in rabbits. GAD immunoreactivity was demonstrated in small cells of these ganglia. The GAD-immunoreactive small cells were 10–20 μm in diameter and formed clusters or occured as solitary cells. The principal neurons were non-reactive but they were surrounded by immunoreactive processes. Studies on colocalization of GAD with tyrosine hydroxylase (TH), the rate-limiting enzyme of the catecholamine synthesis, in the major pelvic ganglion and in the coeliac-superior mesenteric ganglion complex indicated that all GAD-immunoreactive small cells were also labelled with TH. In the major pelvic ganglion all TH-immunoreactive SIF cells were also immunoreactive for GAD. However, in the coeliac-superior mesenteric ganglion complex there occured TH-immunoreactive small cells which showed no immunoreactivity to GAD. It is suggested that the small GAD-immunoreactive cells represent small intensely fluorescent (SIF) cells.

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References

  • Bertilsson L, Suria A, Costa E (1976) γ-Aminobutyric acid in rat superior cervical ganglion. Nature 260:540–541

    Google Scholar 

  • Chan-Palay V, Wu J-Y, Palay SL (1979) Immunocytochemical localization of γ-aminobutyric acid transaminase at cellular and ultrastructural levels. Proc Natl Acad Sci USA 76:2067–2071

    Google Scholar 

  • Coons AH (1958) Fluorescent antibody methods. In: Danielli JF (ed) General cytochemical methods. Academic Press, New York pp 399–422

    Google Scholar 

  • Dail WG, Evan AP, Eason HR (1975) The major pelvic ganglion in the pelvic plexus of the male rat: A histochemical and ultrastructural study. Cell Tissue Res 159:49–62

    Google Scholar 

  • De Groat WC (1970) The actions of γ-aminobutyric acid and related amino acids on mammalian autonomic ganglia. J Pharmacol Exp Ther 172:384–396

    Google Scholar 

  • Eränkö O, Eränkö L (1971) Small, intensely fluorescent granulecontaining cells in the sympathetic gangion of the rat. Prog Brain Res 34:39–45

    Google Scholar 

  • Eränkö O, Härkönen M (1963) Histochemical demonstration of fluorogenic amines in the cytoplasm of sympathetic ganglion cells of the rat. Acta Physiol Scand 58:285–286

    Google Scholar 

  • Eränkö O, Pickel VM, Härkönen M, Eränkö L, Joh T, Reis DJ (1982) Effect of hydrocortisone and catecholamines and the enzymes synthesizing them in the developing sympathetic ganglion. Histochem J 14:461–478

    Google Scholar 

  • Erdö SL (1985) Peripheral GABAergic mechanisms. TIPS 6:205–208

    Google Scholar 

  • Häppölä O, Päivärinta H, Soinila S, Wu J-Y, Panula P (1987) Localization of l-glutamate decarboxylase and GABA transaminase immunoreactivity in the sympathetic ganglia of the rat. Neuroscience 21:271–281

    Google Scholar 

  • Jessen KR, Mirsky R, Dennison ME, Burnstock G (1979) GABA may be a neurotransmitter in the vertebrate peripheral nervous system. Nature 281:71–74

    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. TINS 10:255–262

    Google Scholar 

  • Joh TH, Geegham C, Reis DJ (1973) Immunochemical demonstration of increased tyrosine hydroxylase protein in sympathetic ganglia and adrenal medulla elicited by reserpine. Proc Natl Acad Sci USA 70:2767–2773

    Google Scholar 

  • Kanazawa I, Iversen LL, Kelly JS (1976) Glutamate decarboxylase activity in the rat posterior pituitary, pineal gland, dorsal root ganglion and superior cervical ganglion. J Neurochem 27:1267–1269

    Google Scholar 

  • Kataoka Y, Gutman Y, Guidotti A, Panula P, Wroblewski J, Cosenza-Murphy D, Wu J-Y, Costa E (1984) Intrinsic GABAergic system of adrenal chromaffin cells. Proc Natl Acad Sci USA 81:3218–3222

    Google Scholar 

  • Kenny SL, Ariano MA (1986) The immunofluorescence localization of glutamate decarboxylase in the rat superior cervical ganglion. J Auton Nerv Syst 17:211–215

    Google Scholar 

  • Landis SC, Pattersson PH (1981) Neural crest cell lineages. Trends Neurosci 4:172–175

    Google Scholar 

  • Maggi CA, Santicioli P, Grimaldi G, Meli A (1983) The effect of peripherally administered GABA on spontaneous contractions of rat urinary bladder in vivo. Gen Pharmacol 14:455–458

    Google Scholar 

  • Maggi CA, Santicioli P, Meli A (1985) GABA inhibits neurotransmission in rat pelvic ganglia. J Pharm Pharmacol 37:349–351

    Google Scholar 

  • Stanton HC (1963) Mode of action of GABA on the cardiovascular system. Arch Int Pharmacodyn Ther 143:195–204

    Google Scholar 

  • Tanaka C (1985) Minireview: γ-aminobutyric acid in peripheral tissues, pp 175–183. Life Sci 37:2221–2235

    Google Scholar 

  • Taniyama K, Tanaka C (1986) GABAergic mechanisms and their functional relevance in the urinary bladder. In: Erdö SL, Bowery NG (eds) GABAergic mechanisms in the mammalian periphery. Raven Press, New York, pp 175–183

    Google Scholar 

  • Tramu G, Pillez A, Leonardelli J (1978) An efficient method of antibody elution for the successive or simultaneous localization of two antigens by immunocytochemistry. J Histochem Cytochem 26:322–324

    Google Scholar 

  • Waniewski RA, Suria A (1977) Alterations in γ-aminobutyric acid content in the rat superior cervical ganglion and pineal gland. Life Sci 21:1129–1142

    Google Scholar 

  • Wolff JR, Joó F, Kása P, Storm-Mathisen J, Toldi J, Balcar VJ (1986) Presence of neurons with GABA-like immunoreactivity in the superior cervical ganglion of the rat. Neurosci Lett 71:157–162

    Google Scholar 

  • Wu J-Y (1976) Purification and properties of l-glutamate decarboxylase (GAD) and GABA-aminotransferase (GABA-T). In: Roberts E, Chase T, Tower D (eds) GABA in nervous system function. Raven Press, New York, pp 7–55

    Google Scholar 

  • Wu J-Y, Matsuda T, Roberts E (1973) Purification and characterization of glutamate decarboxylase from mouse brain. J Biol Chem 248:3029–3034

    Google Scholar 

  • Wu J-Y, Su Y, Lam D, Schousboe A, Chude O (1981) Assay methods, purification and characterization of L-glutamate decarboxylase and GABA-transaminase. Res Methods Neurochem 5:129–177

    Google Scholar 

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Karhula, T., Häppölä, O., Joh, T. et al. Localization of l-glutamate decarboxylase immunoreactivity in the major pelvic ganglion and in the coeliac-superior mesenteric ganglion complex of the rat. Histochemistry 90, 255–260 (1988). https://doi.org/10.1007/BF00495968

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