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Functional in vivo interaction between growth hormone and dopamine systems are correlated to changes in striatal somatostatin levels as detected by voltammetry

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Abstract

The effects of growth hormone (GH) and somatomedin C (SmC), as well as those of apomorphine, dopamine (DA) agonist, or haloperidol (DA antagonist), upon the size of striatal voltammetric peaks 2 and 5 were investigated. Local intrastriatal injections of GH or SmC were followed by an increase in the height of both peak 2 (corresponding to the oxidation of extracellular dihydro-phenylacetic acid, DOPAC, a metabolite of DA) and peak 5 (which may represent the oxidation of striatal extracellular somatostatin, SRIF). Treatment with haloperidol also increased the size of the striatal catechol peak but was responsible for a reduction of the neuropeptidergic signal. By contrast, apomorphine determined a decrease in striatal peak 2 (DOPAC) while increasing the levels of peak 5 (SRIF). The data further support the chemical identification of peak 5 at +800 mV as related to the in vivo oxidation of SRIF; in addition they indicate the presence of a functional relationship between this neuropeptide and the GH and DA systems in the striatum of anaesthetised rats.

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References

  • Abe H, Molitch M, Van Wyk J, Underwood L (1983) Human GH and somatomedin S suppress the spontaneous release of GH in unanaesthetised rats. Endocrinology 113: 1319–1324

    Google Scholar 

  • Beal M, Domesick V, Martin J (1983) Regional SRIF distribution in the rat striatum. Brain Res 278: 103–108

    Google Scholar 

  • Beal M, Martin J (1984a) Effects of neuroleptic drugs on brain somatostatin-like immunoreactivity. Neurosci Lett 47: 125–130

    Google Scholar 

  • Beal M, Martin J (1984b) Depletion of striatal somatostatin by local cysteamine injection. Brain Res 308: 319–324

    Google Scholar 

  • Bruni J, Hawkins R, Yen S (1982) Serotonergic mechanism in the control of β-endorphin and ACTH release in male rats. Life Sci 30: 1247–1254

    Google Scholar 

  • Chasselet M-F, Reisine T (1983) SRIF regulates DA release in rat striatal slices and cat caudate nuclei. J Neurosci 3: 232–236

    Google Scholar 

  • Chihara K, Minamitani N, Kaji H, Arimura A, Fujita T (1981) Intraventricularly injected GH stimulates SRIF release into rat hypophysial portal blood. Endocrinology 109: 2279–2281

    Google Scholar 

  • Crespi F (1986) Voltammetry in vivo with a single working electrode may permit detection of striatal DA-5HT interactions in anaesthetised and freely moving rats. Neurosci Lett 66: 1–6

    Google Scholar 

  • Crespi F (1990) In vivo voltammetry with micro-biosensors for analysis of neurotransmitter release and metabolism. J Neurosci Methods 34: 53–65

    Google Scholar 

  • Crespi F (1991) In vivo voltametric detection of neuropeptides with micro carbon fibre biosensors: possible selective detection of somatostatin. Anal Biochem 194: 69–76

    Google Scholar 

  • Crespi F, Marsden CA (1987) Can somatostatin be detected using in vivo voltammetry? Br J Pharmacol 92: 696P

  • Crespi F, Cespuglio R, Jouvet M (1982) Differential pulse voltammetry in brain tissue. Map of the rat serotonergic raphe nuclei by electrochemical detection of 5HIAA. Brain Res 270: 45–54

    Google Scholar 

  • Crespi F, Sharp T, Maidment N, Marsden C (1983) DPV in vivo — evidence that uric acid contributes to the indole oxidation peak. Neurosci Lett 43: 203–207

    Google Scholar 

  • Crespi F, Paret J, Keane P, Morre M (1984) An improved DP voltammetric technique allows the simultaneous analysis of DA and 5HT activities in vivo with a single carbon fibre electrode. Neurosci Lett 52: 159–164

    Google Scholar 

  • Crespi F, Paret J, Keane P, Coude FX, Morre M, Roncucci R (1985) Growth hormone-releasing factor modifies dopaminergic but not serotonergic activity in the arcuate nucleus of hypothalamus in the rat as recorded in vivo by differential pulse voltammetry. Brain Res 348: 367–370

    Google Scholar 

  • Crespi F, Martin KF, Marsden CA (1988) Nafion coated carbon fibre electrodes coated with differential pulse voltammetry measure serotonin release in vivo. Neuroscience 27: 885–896

    Google Scholar 

  • Crespi F, Martin K, Heal D, Buckett W, Sanghera M (1989) Measurement of 3-MT by in vivo voltammetry: evidence for differences in central dopamine functions in Balb/c and CBA mice. Brain Res 500: 241–246

    Google Scholar 

  • Crespi F, Garratt J, Sleight A, Marsden CA (1990) Simultaneous in vivo monitoring of 5HT and 5HIAA: evidence that 5HT cell firing and 5HT release are not necessarily reflected by changes in 5HT metabolism. Neuroscience 35: 139–144

    Google Scholar 

  • Crespi F, Baumeyer T, Möbius C, Dittrich J (1991) Simultaneous in vivo monitoring of dopamine and serotonin by differential pulse conditioning voltammetry with NA-CRO microbiosensors. Fresenius Z Anal Chem 341: 644

    Google Scholar 

  • Delitala G (1982) Neurotransmitter control of anterior pituitary hormone secretion and its implications in man. In: Besser GM, Martini L (eds) Clinical neuroendocrinology vol 2. Academic, New York, pp 62–123

    Google Scholar 

  • Finley J, Madernt J, Rogers L, Petrusz P (1981) The immunocytochemical localisation of SRIF-containing neurones in the rat CNS. Neuroscience 6: 2173–2192

    Google Scholar 

  • Fuller R (1981) Serotonergic stimulation of pituitary-adrenocortical function in rats. Neuroendocrinology 32: 118–124

    Google Scholar 

  • Geetinder K, Beal M (1987) Effect of cysteamine on SRIF and neuropeptide Y in rat striatum and cortical synaptosomes. Brain Res 401: 359–364

    Google Scholar 

  • Gonon F, Buda M, Cespuglio R, Jouvet M, Pujol JF (1980) In vivo electrochemical detection of catechols in the striatum of rats: dopamine or DOPAC? Nature 286: 902–904

    Google Scholar 

  • Hökfelt T, Lundberg J, Schulzberg M, Johanson O, Skirboll L, Anggard A, Fredholm B, Hamberger B, Pernow B, Rehfeld J, Goldstein M (1980) Cellular localisation of peptides in neural structures. Proc R Soc Lond [Biol] 210: 63–77

    Google Scholar 

  • Holmes M, Di Renzo G, Beckford U, Gillham B, Jones M (1982) Role of 5HT in the control of secretion of corticotropin releasing factor. J Endocrinol 93: 151–160

    Google Scholar 

  • Justice JB Jr (ed) (1987) Voltammetry in the neurosciences. Humana, Clifton

    Google Scholar 

  • Kiss J, Csaky A, Halasz B (1988) Demonstration of 5HT axon terminals on SRIF-immunoreactive neurons of the anterior periventricular nucleus of the rat hypothalamus. Brain Res 442: 23–32

    Google Scholar 

  • Kraicer J, Sheppard M, Luke J, Cowan J (1988) Effect of withdrawal of SRIF and growth hormone (GH)-releasing factor on GH release in vitro. Endocrinology 122: 1810–1815

    Google Scholar 

  • Manfridi A, Forloni A, Vezzani F, Fodritto F, Desimoni M (1991) Functional and histological consequences of quinolinic and kainic acid-induced seizures on hippocampal somatostatin neurons. Neuroscience 41: 127–135

    Google Scholar 

  • Martin J (1976) Brain regulation of GH secretion. Front Neuroendocrinol 4: 129–168

    Google Scholar 

  • Millard M, Sagar M, Badger T, Carr D, Kasting N, Martin J (1983) The effect of cysteamine on TRH and β-endorphin secretion in the rat. Endocrinology 112: 518–525

    Google Scholar 

  • Molitch M, Hlivyak L (1980) Growth hormone short-loop feedback: anatomic specificity of GH stimulation of hypothalamic SRIF concentration. Horm Metab Res 12: 559–560

    Google Scholar 

  • Nagy G, Gerhardt G, Oke A, Rice M, Adams R, Moore R, Martin C (1985) Ion exchange and transport of neurotransmitters in Nafion films on conventional and microelectrode surfaces. Electroanal Chem 188: 85–94

    Google Scholar 

  • Palkovits M, Browstein M, Eiden E, Arimura A, Szabo S (1982) Selective depletion of SRIF in rat brain by cysteamine. Brain Res 240: 178–180

    Google Scholar 

  • Paxinos G, Watson C (1987) The rat brain in stereotoxic coordinates. Academic Press, New York

    Google Scholar 

  • Peillon F, Liappi G, Gamier P (1988) In vitro secretion of SRIF from human GH-secreting adenomas. Relation with the GH release and regulation by TRH. CR Acad Sci Paris 306: 161–166

    Google Scholar 

  • Radke J, MacLennan A, Vincent S, Fibiger H (1988) Comparison between long and short-term haloperidol administration on SRIF and substance P conc. in the rat brain. Brain Res 445: 55–60

    Google Scholar 

  • Raghuramulu N, Jaya Rao K (1974) Growth hormone secretion in protein calorie malnutrition. J Clin Endocrinol Metab 38: 176–181

    Google Scholar 

  • Richardson S, Nguyen T, Hollander C (1981) Neurotransmitter modulation of SRIF release by the hypothalamus: possible mechanism for regulation of GH secretion (abstract) Clin Res 29: 564

    Google Scholar 

  • Rivier J, Burgus A (1979) Application of reverse phase high pressure liquid chromatography to peptides. Chromatogr Sci Ser 10: 147–161

    Google Scholar 

  • Sagar M, Laudry D, Millard W, Arnold M, Martin J (1982) Depletion of SRIF-like-immunoreactivity in the rat CNS by cysteamine. J Neurosci 2: 225–231

    Google Scholar 

  • Stachura E, Tyler J, Farmer P (1988) Combined effect of human GH-releasing factor-44 (GRF) and SRIF on post-SRIF rebound release of prolactin and GH: a model for GRF-SRIF modulation of secretion. Endocrinology 123: 1476–82

    Google Scholar 

  • Van Wyk J, Underwood L (1978) The somatomedins and their actions. In: Litwack G (ed) Biochemical actions of hormones. Academic, New York, p 101

    Google Scholar 

  • Williams T, Lelijam M, Crelin C, Downs R, Frohman L (1988) Differential effects of SRIF and a SRIF analog SMS 201–995 on the secretion of GH or thyroid-stimulating hormone in man. J Clin Endocrinol Metab 66: 39–45

    Google Scholar 

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Crespi, F. Functional in vivo interaction between growth hormone and dopamine systems are correlated to changes in striatal somatostatin levels as detected by voltammetry. Exp Brain Res 94, 363–370 (1993). https://doi.org/10.1007/BF00230196

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  • DOI: https://doi.org/10.1007/BF00230196

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