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Adaptive changes in the rat dopaminergic transmission following repeated lithium administration

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In the present study the alterations in the contents of dopamine (DA) and metabolites, as well as in the levels of mRNA coding for DA receptor D2, were determined in the rat striatum (STR) and nucleus accumbens septi (NAS), in correlation with the duration of lithium administration. Single or subchronic (3 days) administration of lithium produced less consistent effects as far as the levels of DA and metabolites are concerned; however, following 7 or 14 days of lithium administration, the DA release from terminals was significantly attenuated and the effect was more pronounced in NAS. After the same time of treatment, the increase in the levels of mRNA coding for the D2 receptor was increased; this might be interpreted as an adaptive change to the decreased dopaminergic transmission following the prolonged administration of lithium.

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References

  • Angulo JA, Corini H, Ledoux M, Schumacher M (1991) Regulation by dopaminergic neurotransmission of dopamine D2 mRNA and receptor levels in the striatum and nucleus accumbens of the rat. Mol Brain Res 11: 161–166

    Google Scholar 

  • Baptista T, Teneud L, Contreras Q, Burguera JL, Burguera M, Hernandez L (1993) Effects of acute and chronic lithium treatment on amphetamine-induced dopamine increase in the nucleus accumbens and prefrontal cortex in rats as studied by microdialysis. J Neural Transm [Gen Sect] 94: 75–89

    Google Scholar 

  • Bernard V, Le Moine C, Bloch B (1991) Striatal neurons express increased level of dopamine D2 receptor mRNA in response to haloperidol treatment: a quantitive in situ hybridization study. Neuroscience 45: 117–126

    Google Scholar 

  • Berggren U (1985) Effects of chronic lithium treatment on brain monoamine metabolism and amphetamine-induced locomotor stimulation in rats. J Neural Transm 64: 239–250

    Google Scholar 

  • Bliss EL, Ailion J (1970) The effect of lithium on brain neuroamines. Brain Res 24: 305–310

    Google Scholar 

  • Bloom FE, Baetge G, Deyo S, Ettenberg A, Koda L, Magistretti PJ, Shoemaker WJ, Staunton DA (1983) Chemical and physiological aspects of the action of lithium and antidepressant drugs. Neuropharmacology 22: 359–365

    Google Scholar 

  • Bowers MB, Rozitis A (1982) Dopamine metabolism and catalepsy after lithium and haloperidol. Eur J Pharmacol 78: 113–115

    Google Scholar 

  • Bunney WE, Garland BL (1983) Possible receptor effects of chronic lithium administration. Neuropharmacology 22: 367–372

    Google Scholar 

  • Bunney WE Jr, Brodie HKH, Murphy DL, Goodwin FK (1971) Studies of alpha-methyl-para-tyrosine, L-DOPA and L-tryptophan in depression and mania. Am J Psychiatry 127: 872–881

    Google Scholar 

  • Carli M, Anand-Srivastava MB, Molina-Holgado E, Dewar KM, Reader T (1994) Effects of chronic lithium treatments on central dopaminergic receptor systems: G proteins as a possible targets. Neurochem Int 24: 13–22

    Google Scholar 

  • Chen JF, Qin ZH, Szele F, Bai G, Weiss B (1991) Neuronal localization and modulation of the D2 dopamine receptor mRNA in brain of normal mice and mice lesioned with 6-hydroxydopamine. Neuropharmacology 30: 927–941

    Google Scholar 

  • Chen JF, Aloyo VJ, Weiss B (1993) Continuous treatment with the D2 dopamine receptor agonist quinpirole decreases D2 dopamine receptors, D2 dopamine receptor messenger RNA and proenkephalin messenger RNA, and increases mu opioid receptors in mouse striatum. Neuroscience 54: 669–680

    Google Scholar 

  • Coirini H, Schumacher M, Angulo J, McEwen B (1990) Increase in striatal dopamine D2 receptor mRNA after lesions or haloperidol treatment. Eur J Pharmacol 186: 369–371

    Google Scholar 

  • Corrodi H, Fuxe K, Schou M (1969) The effect of prolonged lithium administration on cerebral monoamine neurons in the rat. Life Sci 8: 643–651

    Google Scholar 

  • Dziedzicka-Wasylewska M, Rogoż R (1995) The effect of prolonged treatment with imipramine and electroconvulsive shock on the levels of endogenous enkephalins in the nucleus accumbens and the ventral tegmentum of the rat. J Neural Transm [Gen Sect] 102: 221–228

    Google Scholar 

  • Dziedzicka-Wasylewska M, Przewlocka B, Prezewlocki R (1995) The effect of prolonged lithium administration on the cAMP level in the rat striatum. Pol J Pharmacol 47: 115–120

    Google Scholar 

  • Friedman E, Gershon S (1973) Effect of lithium on brain dopamine. Nature 243: 520–521

    Google Scholar 

  • Garver DL, Davis JM (1979) Minireview: biogenic amine hypothesis of affective disorders. Life Sci 24: 383–394

    Google Scholar 

  • Gerfen C, Engber T, Mahan L, Susel Z, Chase T, Monsma F, Sibley D (1990) D1 and D2 dopamine receptor regulated gene expression of striatonigral and striatopallidal neurons. Science 250: 1429–1432

    Google Scholar 

  • Gerner RH, Post RMN, Bunney WE Jr (1976) A dopaminergic mechanism of mania. Am J Psychiatry 133: 1177–1180

    Google Scholar 

  • Gottberg E, Groudin I, Reader TA (1989) Acute effects of lithium on catecholamines, serotonin, and their major metabolites in discrete brain regions. J Neurosci Res 22: 338–345

    Google Scholar 

  • Ho AK, Loh HH, Cravevs F, Hitzemann RJ, Gershon S (1970) The effect of prolonged lithium treatment on the synthesis rate and turnover of monoamines in brain regions of rats. Eur J Pharmacol 10: 72–78

    Google Scholar 

  • Jaber M, Fournier MC, Bloch B (1992) Reserpine treatment stimulates enkephalin and D2 dopamine receptor gene expression in the rat striatum. Mol Brain Res 15: 189–194

    Google Scholar 

  • Jaber M, Tison F, Fournier MC, Bloch B (1994) Differential influence of haloperidol and sulpiride on dopamine receptors and peptide mRNA levels in the rat striatum and pituitary. Mol Brain Res 23: 14–20

    Google Scholar 

  • Li PP, Tam YK, Young LT, Warsh JJ (1991) Lithium decreases Gs, Gi-1 and Gi-2 α-subunit mRNA levels in rat cortex. Eur J Pharmacol 206: 165–166

    Google Scholar 

  • Lopez-Corcuera B, Gimenez C, Aragon C (1988) Change of synaptic membrane lipid composition and fluidity by chronic administration of lithium. Biochim Biophys Acta 939: 467–475

    Google Scholar 

  • Maj J (1986) Repeated treatment with antidepressant drugs: responses by brain dopamine receptors. In: Hippius H, Klerman GL, Matussek N (eds) New results in depression research. Springer, Berlin Heidelberg New York Tokyo, pp 90–98

    Google Scholar 

  • Mclntyre IM, Kuhn C, Demitriou S, Fucek FR, Stanley M (1983) Modulating role of lithium on dopamine turnover, prolactin release, and behavioral supersensitivity following haloperidol and reserpine. Psychopharmacology 81: 150–154

    Google Scholar 

  • Otero-Losada ME, Rubio MC (1985) Striatal dopamine and motor activity changes observed shortly after lithium administration. Naunyn Schmiedebergs Arch Pharmacol 330: 169–174

    Google Scholar 

  • Palkovits M, Brownstein MJ (1988) Maps and guide to microdissection of the rat brain. Elsevier, New York Amsterdam London

    Google Scholar 

  • Pert A, Rosenblatt JE, Sivit C, Pert CB, Bunney WE (1978) Long-term treatment with lithium prevents the development of dopamine receptor supersensitivity. Science 201: 171–173

    Google Scholar 

  • Pittman KJ, Jakubovic A, Fibiger HC (1984) The effects of chronic lithium on behavioral and biochemical indices of dopamine receptor supersensitivity in the rat. Psychopharmacology 82: 371–377

    Google Scholar 

  • Poitou P, Bohuon C (1975) catecholamine metabolism in the rat brain after short- and long-term lithium administration. J Neurochem 25: 535–537

    Google Scholar 

  • Post R (1989) Mood disorders: somatic treatment. In: Kaplan HI, Sadock BJ (eds) Comprehensive textbook of psychiatry. Williams and Wilkins, Baltimore, pp 913–931

    Google Scholar 

  • Pybus J, Bowers GN Jr (1970) Measurement of serum lithium by atomic absorption spectrometry. Clin Chem 16: 139–143

    Google Scholar 

  • Reches A, Jackson-Lewis V, Fahn S (1984) Chronic lithium administration has no effect on haloperidol-induced supersensitivity of pre- and postsynaptic dopamine receptors in rat brain. Brain Res 246: 172–177

    Google Scholar 

  • Roffler-Tarlov S, Sherman DF, Tergerdine P (1971) 3,4-Dihydroxyphenylacetic acid in the mouse striatum: a reflection of intra- and extraneuronal metabolism of dopamine? Br J Pharmacol 42: 343–351

    Google Scholar 

  • Schildkraut JJ (1965) The catecholamine hypothesis of affective disorders: a review of supporting evidence. Am J Psychiatry 122: 509–522

    Google Scholar 

  • Schubert J (1973) Effect of chronic lithium treatment on monoamine metabolism in rat brain. Psychopharmacology 32: 301–311

    Google Scholar 

  • Seeman P, Grigoriadis D (1987) Dopamine receptors in brain and periphery. Neurochem Int 1: 1–25

    Google Scholar 

  • Srivastava LK, Morency MA, Bajawa SB, Mishra RK (1990) Effect of haloperidol on expression of dopamine D2 receptor mRNAs in rat brain. J Mol Neurosci 2: 155–161

    Google Scholar 

  • Staunton DA, Magistretti PJ, Shoemaker WJ, Deyo SN, Bloom FE (1982) Effects of chronic lithium treatment on dopamine receptors in the rat corpus striatum. II. No effect on denervation or neuroleptic-induced supersensitivity. Brain Res 232: 401–412

    Google Scholar 

  • Wedzony K, Golembiowska K, Zazula M (1994) Differential effects of CGP 37849 and MK 801, competitive and noncompetitive NMDA antagonists, with respect to the modulation of sensorimotor gating and dopamine outflow in the prefrontal cortex in rats. Naunyn Schmiedebergs Arch Pharmacol 350: 555–562

    Google Scholar 

  • Westerink BHC (1985) Sequence and significance of dopamine metabolism in the rat brain. Neurochem Int 7: 221–227

    Google Scholar 

  • Wood PL, Altar CA (1988) Dopamine release in vivo from nigrostriatal, mesolimbic and mesocortical neurons: utility of 3-methoxytyramine measurements. Pharmacol Rev 40: 163–187

    Google Scholar 

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Dziedzicka-Wasylewska, M., Maćkowiak, M., Fijaτ, K. et al. Adaptive changes in the rat dopaminergic transmission following repeated lithium administration. J. Neural Transmission 103, 765–776 (1996). https://doi.org/10.1007/BF01273357

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  • DOI: https://doi.org/10.1007/BF01273357

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