Skip to main content
Log in

Striatal dopamine depletion, tremors, and hypokinesia following the intracranial injection ofS-adenosylmethionine

A possible role of hypermethylation in parkinsonism

  • Original Articles
  • Published:
Molecular and Chemical Neuropathology

Abstract

The major symptoms of Parkinson disease (PD) are tremors, hypokinesia, rigidity, and abnormal posture, caused by the degeneration of dopamine (DA) neurons in the substantia nigra (SN) and deficiency of DA in the neostriatal DA terminals. Norepinephrine (NE) and serotonin (5-HT) levels in the neostriatum and tyrosine hydroxylase and melanin pigments in the substantia nigra are also decreased, and brain cholinergic activity is increased. The cause of PD is unknown, but PD is an age-related disorder, suggesting that changes that occur during the aging process may help to precipitate PD. Methylation increases in aging animals. Increased methylation can deplete DA, NE, and 5-HT; increase acetylcholine; and cause hypokinesia and tremors. These effects are similar to changes seen in PD, and interestingly also, they are similar to some of the changes that are associated with the aging process. It is suggested, therefore, that increased methylation may be an inducing factor in parkinsonism. Accordingly, the effects of an increase in methylation in the brain of rats were studied.S-adenosylmethionine (AdoMet), the limiting factor in the methylation process, was injected into the lateral ventricle of rats. Specific behavioral changes that resemble changes seen in PD were investigated. The results showed that AdoMet caused tremors, rigidity, hypokinesia, and depleted DA. The hypokinetic effects of a single dose of AdoMet lasted for about 90 min. AdoMet has a dose-dependent hypokinetic effect. A dose of 9.4 nmol reduced movement time (MT) by 68.9% and increased rest time (RT) by 20.7%, and a dose of 400 mnol reduced MT by 92.4% and increased RT by 27.6%. The normethyl analog of AdoMet,S-adenosylhomocysteine, did not cause hypokinesia or tremors, but it blocked the AdoMet-induced motor effects.l-dopa, the precursor of DA, also blocked the AdoMet-induced motor effects. These data suggest that the methyl group of AdoMet as well as DA depletion are involved in the AdoMet-induced motor effects. A dose of 0.65 μmol of AdoMet depleted DA in the ipsilateral caudate nucleus (CN) or neostriatum by 50.1%, and DA in the contralateral CN was reduced by 9.3%. Double the dose of AdoMet did not increase the depletion of DA on the ipsilateral CN, but DA in the contralateral CN was decreased by 26.3%. Taken together, the results suggest that increased methylation may contribute to the symptoms of PD.

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

  • Alvord E. C., Jr., Forno L. S., Kusske J. A., Kaufman R. J., Rhodes J. S., and Goetowski C. R. (1974) The pathology of parkinsonism: comparison of degeneration in cerebral cortex and brainstem.Adv. Neurol. 5, 175–193.

    PubMed  Google Scholar 

  • Baldessarini R. J. and Kopin I. J. (1966)S-adenosylmethionine in brain and other tissues.J. Neurochem. 13, 769–777.

    Article  PubMed  CAS  Google Scholar 

  • Barbeau A., Tetreault L., Morazain L., and Oliva L. (1965) Pharmacology of 3,4-dimethoxyphenylamine.Can. Med. Assoc. J. 92, 347.

    Google Scholar 

  • Barbeau A. (1968) Dopamine and dopamine metabolites in Parkinson’s disease— a review.Proc. Aust. Assoc. Neurol. 5, 95–100.

    PubMed  CAS  Google Scholar 

  • Blusztajn J. K., Zeisel S. H., and Wurtman R. J. (1979) Synthesis of lecithin (phosphatidylcholine) frm phosphatidylethanolamine in bovine brain.Brain Res. 179, 319–327.

    Article  PubMed  CAS  Google Scholar 

  • Blusztajn J. K. and Wurtman R. J. (1983) Choline and cholinergic neurons.Science 221, 614–620.

    Article  PubMed  CAS  Google Scholar 

  • Charlton C. G. and Way E. L. (1978) Tremor induced byS-adenosyl-L-methionine: possible relation tol-dopa effects.J. Pharma. Pharmacol. 30, 819–820.

    CAS  Google Scholar 

  • Charlton C. G. and Crowell B., Jr. (1990) Relationship between excessS-adenosylmethionine (SAM-dependent methylation) and Parkinson’s disease.Neurosci. Abstr. 16(1), 810.

    Google Scholar 

  • Charlton C. G. and Crowell B. Jr. (1992) Parkinson’s disease-like effects ofS-adenosyl-l-methionine: effects ofl-dopa.Pharm. Biochem. Behav. 43, 423–431.

    Article  CAS  Google Scholar 

  • Clarke S. (1992) Protein isoprenylation and methylation at carboxyl-terminal cysteine residues.Annu. Rev. Biochem. 61, 355–386.

    Article  PubMed  CAS  Google Scholar 

  • Collins M. A., Neafsey E. J., Matsubara K., Cobuzzi R. J., Jr., and Rollema H. (1992) Indole-N-methylated beta-carbolinium ions as potential brain-bioactivated neurotoxins.Brain Res. 570, 154–160.

    Article  PubMed  CAS  Google Scholar 

  • Coyle J. T. and Henry D. (1973) Catecholamines in fetal and newborn rat brain.J. Neurochem. 21, 61–67.

    Article  PubMed  CAS  Google Scholar 

  • Crowell B., Jr., Benson R., Shockley D., and Charlton C. G. (1993)S-adenosyl-l-methionine decreases motor activity in rat: similarity to Parkinson’s disease-like symptoms.Behav. Neural Biol. 59, 186–193.

    Article  PubMed  CAS  Google Scholar 

  • De Olivera Filgueiras O. M., Van Den Basselaar A. H. H. P., and Van Den Bosch H. (1979) Localization of lysophosphatidylcholine in bovine chromaffin granules.Biochim. Biophys. Acta 558, 73–84.

    Article  Google Scholar 

  • Diliberto E. J., Jr., and Axelrod J. (1976) Regional and subcellular distribution of protein carboxymethylase in brain and other tissues.J. Neurosci. 26, 1159–1165.

    CAS  Google Scholar 

  • Diliberto E. J., Jr., Viveros O. H., and Axelrod J. (1976) Subcellular distribution of protein carboxymethylase and its endogenous substrates in the adrenal medulla: possible role in excitation-secretion coupling.Proc. Natl. Acad. Sci. USA 73, 4050–4054.

    Article  PubMed  CAS  Google Scholar 

  • Eadie M. J. (1963) The pathology of certain medullary nuclei in parkinsonism.Brain 86, 781–790.

    Article  PubMed  CAS  Google Scholar 

  • Ernst A. M. (1962) Phenomena of the hypokinetic rigid type caused by O-methylation of dopamine in the para-position.Nature (Lond) 193, 178, 179.

    Article  CAS  Google Scholar 

  • Feuerstein C., Tauche M., Serre F., Gavend M., Pellat J., and Perret J. (1977) Does O-methylation play a role in levo-dopa-induced dyskinesias?Acta Neurol. Scand. 56, 79–82.

    Article  PubMed  CAS  Google Scholar 

  • Forno L. S. and Norvill R. L. (1976) Ultrastructure of Lewy bodies in the stellate ganglion.Acta Neuropathol. 34, 183–197.

    Article  PubMed  CAS  Google Scholar 

  • Gagnon C., Viveros O. H., Diliberto E. J., and Axelrod J. (1978) Enzymatic methylation of carboxyl groups of chromaffin granule membrane proteins.J. Biol. Chem. 253, 3778–3781.

    PubMed  CAS  Google Scholar 

  • Ganong W. F. (1991)Review of Medical Physiology. Appleton and Lange, San Francisco, CA.

    Google Scholar 

  • Gharib A., Sarda N., Chabannes B., Cronenberger L., and Pacheco H. (1982) The regional concentrations ofS-adenosyl-l-methionine,S-adenosyl-l-homocysteine and adenosine in rat brain.J. Neurochem. 38, 810–815.

    Article  PubMed  CAS  Google Scholar 

  • Goodman L. S. and Gilman A. (1981)The Pharmacological Basis of Therapeutics. Macmillan, New York.

    Google Scholar 

  • Hardie R. J., Lees A. J., and Stern G. M. (1986) Pharmacokinetics of levo-dopa and motor fluctuations.Adv. Neurol. 45, 487–492.

    Google Scholar 

  • Hirata F. and Axelrod J. (1978) Enzymatic methylation of phosphatidylethanolamine increases erythrocyte membrane fluidity.Nature 275, 219, 220.

    Article  PubMed  CAS  Google Scholar 

  • Jager D. H. and Bethlem J. (1960) The distribution of Lewy bodies in the central and autonomic nervous systems in idiopathic paralysis agitans.J. Neurol. Neurosurg. Psychiatr. 6, 283–290.

    Article  Google Scholar 

  • Jager W. A. den (1969) Sphingomyelin in Lewy inclusion bodies in Parkinson’s disease.Arch. Neurol. (Chicago) 21, 615–619.

    Google Scholar 

  • Jenner P. J. and Marsden C. D. (1988) MPTP-induced parkinsonism as an experimental model of Parkinson’s disease. In:Parkinson’s Disease and Movement Disorders (Jankovic J. and Tolosa E., eds.), pp. 37–48, Urban & Schwarzenberg, Baltimore-Munich.

    Google Scholar 

  • Knoll J. (1988) The striatal dopamine dependency of life span in male rats, longivity study with (−) deprenyl.Mech. Aging Dev. 46, 237–262.

    Article  PubMed  CAS  Google Scholar 

  • Langston J. W. and Forno L. S. (1978) The hypothalamus in Parkinson disease.Ann. Neurol. 3, 129–133.

    Article  PubMed  CAS  Google Scholar 

  • Maksem J., Jacobson N., and Neiderhiser D. H. (1984) Lysophosphatidylcholine-induced gastric injury and ulceration in the guinea pig.Am. J. Pathol. 115, 288–295.

    PubMed  CAS  Google Scholar 

  • Mays L. I., Borek E., and Finch C. E. (1973) Glycine N-methyltransferase is a regulatory enzyme which increases in aging animals.Nature 243, 411–413.

    Article  PubMed  CAS  Google Scholar 

  • Mena M. A., Murados V., Brazen E., Reiriz J., and De Yebenes J. G. (1977) Pharmacokinetics ofl-dopa in patients with Parkinson’s disease.Adv. Neurol. 45, 481–486.

    Google Scholar 

  • Muenter M. D., Sharpless N. S., and Tyce G. M. (1972) Plasma 3-O-methyldopa inl-dopa therapy of Parkinson’s disease.Mayo Clin. Proc. 47, 389–395.

    PubMed  CAS  Google Scholar 

  • Ohama E. and Ikuta F. (1976) Parkinson’s disease: distribution of Lewy bodies and monoamine neuron system.Acta Neuropathol. (Berl) 34, 311–319.

    Article  CAS  Google Scholar 

  • Phillips M. R., Pillinger M. H., Strand R., Volker C., Rosenfeld M. G., Weissman G., and Stock J. B. (1993) Carboxymethylation of Ras-related proteins during signal transduction in neurophils.Science 259, 977–980.

    Article  Google Scholar 

  • Rajput A. H. and Rozdisky B. (1970) Dysautonomia in parkinsonism: a clinico-pathological study.J. Neurol. Neurosurg. Psychiatr. 39, 1092–1100.

    Article  Google Scholar 

  • Schultz W. (1988) MPTP-induced parkinsonism in monkeys: mechanisms of action, selectivity and pathophysiology.Gen. Pharmacol. 19, 153–161.

    PubMed  CAS  Google Scholar 

  • Selby G. (1968) Cerebral atrophy in parkinsonismJ. Neurol. Sci. 6, 517–559.

    Article  PubMed  CAS  Google Scholar 

  • Sellinger O. Z., Kramer C. M., Conger A., and Duboff G. S. (1988) The carboxylmethylation of cerebral membrane-bound proteins increases with age.Mech. Aging Dev. 43, 161–173.

    Article  PubMed  CAS  Google Scholar 

  • Sharman D. F. (1976) The effect of drugs on dopamine in the striatum. In:Third Symposium on Parkinson’s Disease (Gillingham F. J. and Donaldson I. M. L., eds.), pp. 24–32, E and L Livingston, London.

    Google Scholar 

  • Slomiany B. L., Jerzy-Glass G. B., Kojima K., Banas-Gruszka Z., and Slomiany A. (1981) Effect of lysolecithin on the constitutents of gastric mucus. In:International Symposium on Mucus in Health and Disease (Chantler N., Elder J. B., and Elstein M., eds.), pp. 163–174, Plenum, New York.

    Google Scholar 

  • Stramentinoli G., Gualano M., Catto E., and Algeri S. (1977) Tissue levels ofS-adenosylmethionine in aging rats.J. Gerontol. 32, 392–394.

    PubMed  CAS  Google Scholar 

  • Taufek H. R. and Bone A. H. (1984) Influence of exogenousl-3,4-hydroxyphenylalanine (l-dopa) on methionine andS-adenosylmethionine concentrations in the brain and other tissues.Biochem. Soc. Trans. 8, 62–63.

    Google Scholar 

  • Tuomisto L. (1977) Ontogenesis and regional distribution of histamine and histamine-N-methyltransferase in the guinea pig brain.J. Neurochem. 28, 271–276.

    Article  PubMed  CAS  Google Scholar 

  • Vanderhaegen J. J., Poirier O., and Steronon J. E. (1970) Pathological findings in idiopathic orthostatic hypotension.Arch. Neurol. 22, 207–214.

    Google Scholar 

  • Volpe J. J. and Laster L. (1970) Trans-sulphuration in primate brain: regional distribution of methionine-activating enzyme in the brain of the Rhesus monkey at various stages of development.J. Neurochem. 17, 413–424.

    Article  PubMed  CAS  Google Scholar 

  • Weltzien H. U. (1979) Cytolytic and membrane perturbing properties of lysophosphatidylcholine.Biochim. Biophys. Acta 559, 259–287.

    PubMed  CAS  Google Scholar 

  • Wurtman R. J., Rose C. M., Matthysse S., Stephenson J., and Baldessarini R. J. (1970)l-dihydroxyphenylalanine: effect onS-adenosylmethionine in brain.Science 169, 395–397.

    Article  PubMed  CAS  Google Scholar 

  • Yahr M. D. and Bering E. A. (1968)Parkinson’s Disease: Present Status and Research Trends. Columbia University Press, New York.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Charlton, C.G., Crowell, B. Striatal dopamine depletion, tremors, and hypokinesia following the intracranial injection ofS-adenosylmethionine. Molecular and Chemical Neuropathology 26, 269–284 (1995). https://doi.org/10.1007/BF02815143

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02815143

Index Entries

Navigation