Skip to main content

Advertisement

Log in

Effects of ageing on the content in sulfur-containing amino acids in rat brain

  • Full Papers
  • Published:
Journal of Neural Transmission / General Section JNT Aims and scope Submit manuscript

Summary

Concentrations of the sulfur-containing amino acids methionine, homocysteic acid, cysteic acid and taurine were measured in brain structures of young and old Wistar rats in an attempt to etablish a possible link between the increase in oxidative stress with ageing and changes in tissue levels of these amino acids. Contrary to data reported by others, in all brain structures of young and old rats homocysteic acid levels could not be quantified. Compared with young rats, in old animals taurine and methionine concentrations significantly decreased in striatum and cortex; decreased taurine levels were also found in nucleus accumbens and cerebellum and lower concentrations of methionine were found in midbrain, hippocampus and pons-medulla. Cysteic acid levels either did not change or significantly increased in cortex and hippocampus. These results are discussed taking into account the biosynthesis of sulfur-containing amino acids in rat brain and the decrease in glutathione in relation to oxidative stress with ageing.

Changes in aspartic acid, glutamic acid, serine, glutamine, glycine and GABA concentrations with ageing were also determined in the same brain structures and were in good agreement with those previously reported

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

H 2O2 :

hydrogen peroxide

MAO :

monoamine oxidase

GSHP :

glutathione peroxidase

PAPS :

3′-phosphoadenosine-5′-phosphosulfate

OPA :

O-phthaldialdehyde

HPLC :

high performance liquid chromatography

Asp :

aspartic acid

CA :

cysteic acid

CSA :

cysteine sulfinic acid

Cys :

cysteine

GABA :

γ-aminobutyric acid

Gln :

glutamine

Glu :

glutamic acid

Gly :

glycine

HCA :

homocysteic acid

Met :

methionine

Ser :

serine

Tau :

taurine

References

  • Aprison MH, Shank RP, Davidoff RA (1969) A comparison of the concentration of glycine, a transmitter suspect, in different areas of the brain and spinal cord in seven different vertebrates. Comp Biochem Physiol 28: 1345–1355

    PubMed  Google Scholar 

  • Benzi G, Pastoris O, Marzatico F, Villa RF (1988) Influence of aging and drug treatment on the cerebral glutathione system. Neurobiol Aging 9: 371–375

    PubMed  Google Scholar 

  • Cao Danh H, Strolin Benedetti M, Dostert P (1984) Differential changes in monoamine oxidase A and B activity in aging rat tissues. In: Tipton KF, Dostert P, Strolin Benedetti M (eds) Monoamine oxidase and disease. Prospects for therapy with reversible inhibitors. Academic Press, London, pp 301–317

    Google Scholar 

  • Cavallini D, Scandurra R, Duprè S, Federici G, Santoro L, Ricci G, Barra D (1976a) Alternative pathways of taurine biosynthesis. In: Huxtable R, Barbeau A (eds) Taurine. Raven Press, New York, pp 59–66

    Google Scholar 

  • Cavallini D, Scandurra R, Duprè S, Santoro L, Barra D (1976b) A new pathway of taurine biosynthesis. Physiol Chem Phys 8: 157–160

    PubMed  Google Scholar 

  • Cohen G (1990) Monoamine oxidase and oxidative stress at dopaminergic synapses. J Neural Transm [Suppl] 32: 229–238

    Google Scholar 

  • Cooper AJL (1983) Biochemistry of sulfur-containing amino acids. Ann Rev Biochem 52: 187–222

    PubMed  Google Scholar 

  • Curtis DR, Watkins JC (1960) The excitatory and depression of spinal neurones by structurally related amino acids. J Neurochem 6: 117–141

    PubMed  Google Scholar 

  • Curtis DR, Johnston GAR (1974) Amino acid transmitters in the mammalian central nervous system. Ergebn Physiol Biol Chem Exp Pharmakol 69: 94–188

    Google Scholar 

  • Damsma G, Boisvert DP, Mudrick LA, Wenkstern D, Fibiger HC (1990) Effects of transient forebrain ischaemia and pargyline on extracellular concentrations of dopamine, serotonin, and their metabolites in the rat striatum as determined by in vivo dialysis. J Neurochem 54: 801–808

    PubMed  Google Scholar 

  • De La Rosa J, Stipanuk MH (1985) Evidence for a rate-limiting role of cysteinesulfinate decarboxylase activity in taurine biosynthesis in vivo. Comp Biochem Physiol 81B: 565–571

    Google Scholar 

  • Do KQ, Herrling PL, Streit P, Cuénod M (1988) Release of neuroactive substances: homocysteic acid as an endogenous agonist of the NMDA receptor. J Neural Transm 72: 185–190

    PubMed  Google Scholar 

  • Farooqui MY, Day WW, Zamorano DM (1987) Glutathione and lipid peroxidation in the aging rat. Comp Biochem Physiol 88B: 177–180

    Google Scholar 

  • Fowler CJ, Strolin Benedetti M (1983) The metabolism of dopamine by both forms of monoamine oxidase in the rat brain and its inhibition by cimoxatone. J Neurochem 40: 1534–1541

    PubMed  Google Scholar 

  • Gaunt GL, De Duve C (1976) Subcellular distribution of D-amino acid oxidase and catalase in rat brain. J Neurochem 26: 749–759

    PubMed  Google Scholar 

  • Glowinski J, Iversen LL (1966) Regional studies of catecholamines in the rat brain. I. The disposition of [3H]norepinephrine, [3H]dopamine and [3H]DOPA in various regions of the brain. J Neurochem 13: 655–669

    PubMed  Google Scholar 

  • Guffroy C, Strolin Benedetti M (1987) Contribution of MAO B to lipid peroxidation in the brain of aging rats. Pharmacol Toxicol [Suppl 1]: 24

    Google Scholar 

  • Guffroy C, Strolin Benedetti M, Dostert P (1986) Induction or inhibition of lipid peroxidation in rat brain homogenates by biogenic and other amines. Abstracts of the 6th General Meeting of the ESN, Prague, p 369

  • Horn AS, Cuello AC, Miller RJ (1974) Dopamine in the mesolimbic system of the rat brain: endogenous levels and the effects of drugs on the uptake mechanism and stimulation of adenylate cyclase activity. J Neurochem 22: 265–270

    PubMed  Google Scholar 

  • Ida S, Kuriyama K (1983) Simultaneous determination of cysteine sulfinic acid and cysteic acid in rat brain by high-performance liquid chromatography. Anal Biochem 130: 95–101

    PubMed  Google Scholar 

  • Iwata H, Yamagami S, Baba A (1982) Cysteine sulfinic acid in the central nervous system: specific binding of [35S]cysteic acid to cortical synaptic membranes — An investigation of possible binding sites for cysteine sulfinic acid. J Neurochem 38: 1275–1279

    PubMed  Google Scholar 

  • Jacobsen JG, Thomas LL, Smith LH (1964) Properties and distribution of mammalian L-cysteine sulfinate carboxylases. Biochim Biophys Acta 85: 103–116

    PubMed  Google Scholar 

  • Jacobsen JG, Smith LH (1968) Biochemistry and physiology of taurine and taurine derivatives. Physiol Rev 48: 424–511

    PubMed  Google Scholar 

  • Jones BN, Gilligan JP (1983) o. Phthaldialdehyde precolumn derivatization and reversed-phase high-performance liquid chromatography of polypeptides hydrolysates and physiological fluids. J Chromatogr 266: 471–482

    PubMed  Google Scholar 

  • Kagan VE, Smirnov AV, Savov VM, Prilipko LL, Gorkin VZ (1983) Lipid peroxidation in mitochondrial membranes induced by enzymatic deamination of biogenic amines. Acta Physiol Pharmacol Bulg 9: 3–13

    Google Scholar 

  • Kilpatrick IC, Mozley LS (1986) An initial analysis of the regional distribution of excitatory sulphur-containing amino acids in the rat brain. Neurosci Lett 72: 189–193

    PubMed  Google Scholar 

  • Kuriyama K, Ida S, Ohkuma S (1984) Alteration of cerebral taurine biosynthesis in spontaneously hypertensive rats. J Neurochem 42: 1600–1606

    PubMed  Google Scholar 

  • Laplante M, Tran-Manh N (1973) L'étiologie et la pathogénèse de la forme idiopathique de la maladie de Parkinson: un modèle. Agressologie 14: 287–307

    PubMed  Google Scholar 

  • Legay F, Weise VK, Oertel WH, Tappaz ML (1987) Taurine biosynthesis in rat brain: a new specific and sensitive microassay of cysteine sulfinate decarboxylasec (CSDI) activity through selective immunotrapping and its use for distribution studies. J Neurochem 48: 345–351

    PubMed  Google Scholar 

  • Maker HS, Weiss C, Silides D, Cohen G (1981) Coupling of dopamine oxidation (monoamine oxide activity) to glutathione oxidation via the generation of hydrogen peroxide in rat brain homogenates. J Neurochem 36: 589–593

    PubMed  Google Scholar 

  • Mandel P, Mark J (1965) The influence of nitrogen deprivation on free amino acids in rat brain. J Neurochem 12: 987–992

    PubMed  Google Scholar 

  • Marnela K-M, Kontro P, Oja SS (1984) Effects of prolonged guanidinoethanesulfonate administration on taurine and other amino acids in rat tissues. Med Biol 62: 239–244

    PubMed  Google Scholar 

  • Martin WG, Truex CR, Tarka SM, Hill LJ, Gorby WG (1974) The synthesis of taurine from sulfate VIII. A constitutive enzyme in mammals (38387). Proc Soc Exp Biol Med 147: 563–565

    PubMed  Google Scholar 

  • Mewett KN, Oakes DJ, Olverman HJ, Smith DAS, Watkins JC (1983) Pharmacology of the excitatory actions of sulphonic and sulphinic amino acids. In: Mandel P, DeFeudis FV (eds) CNS receptors-from molecular pharmacology to behaviour. Raven Press, New York, pp 163–174

    Google Scholar 

  • Mussini E, Marcuccci F (1962) Free amino acids in brain after treatment with psychotropic drugs. In: Holden JT (ed) Amino acid pools. Elsevier, Amsterdam, pp 486–492

    Google Scholar 

  • Neubert D, Wojtczak AM, Lehninger AL (1962) Purification and enzymatic identity of mitochondrial contraction-factors I and II. Proc Natl Acad Sci USA 48: 1651–1658

    PubMed  Google Scholar 

  • Nordström C-H, Rehncrona S, Siesjö BK (1978) Effects of phenobarbital in cerebral ischaemia. Part II. Restitution of cerebral energy state, as well as glycolytic metabolites, citric acid cycle intermediates and associated amino acids after pronounced incomplete ischaemia. Stroke 9: 335–343

    PubMed  Google Scholar 

  • Oreland L, Hiraga Y, Jossan SS, Regland B, Gottfries CG (1990) Increased monoamine oxidase activity and vitamin B-12 deficiency in dementia disorders. In: Dostert P, Riederer P, Strolin Benedetti M, Roncucci R (eds) Early markers in Parkinson's and Alzheimer's diseases. Springer, Wien New York, pp 267–286

    Google Scholar 

  • Pulsinelli WA, Brierley JB, Plum F (1982) Temporal profile of neuronal damage in a model of transient forebrain ischaemia. Ann Neurol 11: 491–498

    PubMed  Google Scholar 

  • Rao AM, Drake MR, Stipanuk MH (1990) Role of the transulfuration pathway and of γ-cystathionase activity in the formation of cysteine and sulfate from methionine in rat hepathocytes. J Nutr 120: 837–845

    PubMed  Google Scholar 

  • Ravindranath V, Reed DJ (1990) Glutathione depletion and formation of glutathione-protein mixed disulfide following exposure of brain mitochondria to oxidative stress. Biochem Biophys Res Commun 169: 1075–1079

    PubMed  Google Scholar 

  • Richard C, Guichard JP, Strolin Benedetti M, Dostert P (1987) Effect of MAO inhibitors on in vivo lipid peroxidation. Pharmacol Toxicol 60 [Suppl 1]: 38

    Google Scholar 

  • Riederer P, Sofie E, Rausch W-D, Schmidt B, Reynolds GP, Jelliger K, Youdim MBH (1989) Transition metals, ferritin, glutathione, and ascorbic acid in parkinsonian brains. J Neurochem 52: 515–520

    PubMed  Google Scholar 

  • Seiler N, Bolkenius FN, Knödgen B, Mamont P (1980) Polyamine oxidase in rat tissues. Biochim Biophys Acta 615: 480–488

    PubMed  Google Scholar 

  • Sinet PM, Heikkila RE, Cohen G (1980) Hydrogen peroxide production by rat brain in vivo. J Neurochem 34: 1421–1428

    PubMed  Google Scholar 

  • Smith M-L, Auer RN, Siesjö BK (1984) The density and distribution of ischaemic brain injury in the rat following 2–10 min of forebrain ischaemia. Acta Neuropathol 64: 319–332

    PubMed  Google Scholar 

  • Strolin Benedetti M, Dostert P (1989a) Monoamine oxidase, brain ageing and degenerative diseases. Biochem Pharmacol 38: 555–561

    PubMed  Google Scholar 

  • Strolin Benedetti M, Dostert P (1989b) Effect of selective monoamine oxidase substrates and inhibitors on lipid peroxidation and their possible involvement in affective disorders. In: Lerer B, Gershom S (eds) New directions in affective disorders. Springer, New York, pp 156–160

    Google Scholar 

  • Strolin Benedetti M, Boucher T, Carlsson A, Fowler CJ (1983) Intestinal metabolism of tyramine by both forms of monoamine oxidase in the rat. Biochem Pharmacol 32: 47–52

    PubMed  Google Scholar 

  • Strolin Benedetti M, Cao Danh H, Dostert P (1986) Age-related changes in brain MAO and in enzymes involved in detoxication processes of MAO-generated compounds. In: Biggio G, Spano PF, Toffano G, Gessa GL (eds) Modulation of central and peripheral transmitter function. Liviano Press, Padova, pp 255–267

    Google Scholar 

  • Strolin Benedetti M, Cini M, Fusi R, Marrari P, Dostert P (1990a) The effects of aging on MAO activity and amino acid levels in rat brain. J Neural Transm [Suppl] 29: 259–268

    Google Scholar 

  • Strolin Benedetti M, Kettler R, Marrari P, Cini M, Da Prada M, Dostert P (1990b) The effects of lifelong treatment with MAO inhibitors on amino acid levels in rat brain. J Neural Transm [PD-Sect] 2: 239–248

    Google Scholar 

  • Sturman JA (1973) Taurine pool sizes in the rat: effects of vitamin B-6 deficiency and high taurine diet. J Nutr 103: 1566–1580

    PubMed  Google Scholar 

  • Szökö E, Bathory G, Magyar K (1990) Inhibition of lipid peroxidation by monoamine oxidase inhibitors. Acta Physiol Hung 75: 269–270

    PubMed  Google Scholar 

  • Van der Heyden JAM, Korf J (1978) Regional levels of GABA in the brain: rapid semiautomated assay and prevention of postmortem increase by 3-mercapto-propionic acid. J Neurochem 31: 197–203

    PubMed  Google Scholar 

  • Vitorica J, Machado A, Satrustegui J (1984) Age-dependent variations in peroxide-utilizing enzymes from rat brain mitochondria and cytoplasm. J Neurochem 42: 351–356

    PubMed  Google Scholar 

  • Westerink BHC, Korf J (1976) Comparison of effects of drugs on dopamine metabolism in the substantia nigra and the corpus striatum of rat brain. Eur J Pharmacol 40: 131–136

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Benedetti, M.S., Russo, A., Marrari, P. et al. Effects of ageing on the content in sulfur-containing amino acids in rat brain. J. Neural Transmission 86, 191–203 (1991). https://doi.org/10.1007/BF01250705

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01250705

Keywords

Navigation