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Effects of manganese oxide on monkeys as revealed by a combined neurochemical, histological and neurophysiological evaluation

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Abstract

Four monkeys were exposed to a total of 8 g each of manganese as oxide by repetitive subcutaneous injections during 5 months, after which they were left for 1 week to 6 months before they were sacrificed. All animals developed hyperactive behaviour after about 2 months. About 5 months after the start of the exposure the animals became hypoactive with an unsteady gait, and subsequently an action tremor appeared in some of the animals. The animals lost power in both upper and lower limbs and the movements of the hands and feet were very clumsy. The serum content of manganese rose 10–40 times during the exposure time and the content in brain was generally increased more than 10 times, with the highest content found in globus pallidus and putamen. The observed neurochemical effects were also largest in globus pallidus and putamen. In these regions there was a considerable depletion of dopamine and 3,4-dihydroxyphenylacetic acid, while the homovanillic acid content remained almost unchanged. A severe neuronal cell loss was observed in globus pallidus but not in other regions. This is in accordance with results from the most recent neuropathological study of a human suffering from chronic manganese poisoning [Yamada et al. (1986) Acta Neuropathol 70: 273–278] where globus pallidus was devoid of neuronal cells while the content of pigmented cells in substantia nigra was normal. Our data suggest a reduction in number of dopaminergic nerve terminals, as the activity of the dopamine synthesizing enzyme DOPA-decarboxylase was also lowered. In addition to the effects on the dopaminergic system, a reduced content of 5-hydroxyindole acetic acid was observed in the putamen and globus pallidus. Moreover neurotensin, a neuropeptide with functional connection to the dopaminergic system, was found to be reduced in the putamen. It was remarkable that all the neurochemical effects seen in the putamen were more or less absent from the caudate nucleus. These observations are discussed in relation to what has been found in Parkinsonian and MPTP-lesioned brains.

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References

  • Aquilonius S-M, Hartvig P (1986) A Swedish county with unexpectedly high utilization of anti-Parkinsonian drugs. Acta Neurol Scand 74: 379–382

    Google Scholar 

  • Autissier N, Rochette L, Dumas P, Beley A, Loireau A, Bralet J (1982) Dopamine and norepinephrine turnover in various regions of the rat brain after chronic manganese chloride administration. Toxicology 24: 175–182

    Google Scholar 

  • Barbeau A (1984) Manganese and extrapyramidal disorders. Neurotoxicology 5: 13–36

    Google Scholar 

  • Bernheimer H, Birkmayer W, Hornykiewicz O, Jellinger K, Seitelberger F (1973) Brain dopamine and the syndromes of Parkinson and Huntington — clinical, morphological and neurochemical correlations. J Neurol Sci 20: 415–425

    Google Scholar 

  • Bird ED, Anton AH, Bullock B (1984) The effect of manganese inhalation on basal ganglia dopamine concentrations in Rhesus monkey. Neurotoxicology 5: 59–66

    Google Scholar 

  • Bissette G, Jennes L, Prange AJ, Breese GR, Nemeroff CB (1983) Neurotensin and dopamine are not co-localized in rat brain. Soc Neurosci Abstr 9: 290

    Google Scholar 

  • Broch OJ, Fonnum F (1972) The regional and subcellular distribution of catechol-0-methyl transferase in the rat brain. J Neurochem 19: 2049–2055

    Google Scholar 

  • Burns RS, Chiueh CC, Markey SP, Ebert MH, Jacobowitz DM, Kopin IJ (1983) A primate model of parkinsonism: Selective destruction of dopaminergic neurons in the pars compacta of the substantia nigra by N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. Proc Natl Acad Sci (USA) 80: 4546–4550

    Google Scholar 

  • Chandra SV, Shukla GS, Srivastava RS (1981) An explorative study of manganese exposure to welders. Clin Toxicol 18: 407–416

    Google Scholar 

  • Cook DG, Fahn S, Brait KA (1974) Chronic manganese intoxication. Arch Neurol 30: 59–64

    Google Scholar 

  • Deskin R, Bursian SJ, Edens FW (1980) An investigation into the effects of manganese and other divalent cations on tyrosine hydroxylase activity. Neurotoxicology 2: 75–81

    Google Scholar 

  • Donaldson J, LaBella FS, Gesser D (1981) Enhanced autoxidation of dopamine as a possible basis of manganese neurotoxicology. Neurotoxicology 2: 53–64

    Google Scholar 

  • Donaldson J, Barbeau A (1985) Manganese neurotoxicity: Possible clues to the etiology of human brain disorders. In: Gabay S, Harris J, Ho BT (eds) Neurology and neurobiology, vol. 15. Metal ions in neurology and psychiatry, Alan R Liss Inc, New York, pp 259–285

    Google Scholar 

  • Eriksson H, Heilbronn E (1983) Changes in the redox state of neuroblastoma cells after manganese exposure. Arch Toxicol 54: 53–59

    Google Scholar 

  • Eriksson H, Lenngren S, Heilbronn E (1987) Effects of long-term administration of manganese on biogenic amine levels in discrete striatal regions of rat brain. Arch Toxicol 59: 426–431

    Google Scholar 

  • Fonnum F (1975) A rapid radiochemical method for determination of choline acetyltransferase. J Neurochem 24: 407–409

    Google Scholar 

  • Fonnum F, Storm-Mathisen J, Walberg F (1970) GAD inhibitory neurons. A study of the enzyme in Purkinje cell axons. Brain Res 20: 259–275

    Google Scholar 

  • Gianutsos G, Seltzer MD, Saymeh R, Wu M-LW, Michel RG (1985) Brain manganese accumulation following systemic administration of different forms. Arch Toxicol 57: 272–275

    Google Scholar 

  • Graham DG (1984) Catecholamine toxicity: A proposal for the molecular pathogenesis of manganese neurotoxicity and Parkinson's disease. Neurotoxicology 5: 83–96

    Google Scholar 

  • Gupta SK, Murthy RC, Chandra SV (1980) Neuromelanin in manganese-exposed primates. Toxicol Lett 6: 17–20

    Google Scholar 

  • Heilbronn E, Eriksson H, Häggblad J (1982) Neurotoxic effects of manganese: Studies on cell cultures, tissue homogenates and intact animals. Neurobehav Toxicol Teratol 4: 655–658

    Google Scholar 

  • Hill JM, Switzer RC (1984) The regional distribution and cellular localization of iron in the rat brain. Neuroscience 11: 595–603

    Google Scholar 

  • Hornykiewicz O (1979) Brain dopamine in Parkinson's disease and other neurogical disturbances. In: AS Horn, J Korf, BHC Westerink (eds) The neurobiology of dopamine, Academic Press, London, pp 633–654

    Google Scholar 

  • Kristensson K, Eriksson H, Lundh B, Plantin LO, WachtmeisterL, El-Azazi M, Morath C, Heilbronn E (1986) Studies on the effects of manganese chloride on the rat developing nervous system. Acta Pharmacol Toxicol 59: 345–348

    Google Scholar 

  • Lai JCK, Leung TKC, Lim L (1981) Brain regional distribution of glutamic acid decarboxylase, choline acetyltransferase, and acetylcholinesterase in the rat: Effects of chronic manganese chloride administration after two years. J Neurochem 36: 1443–1448

    Google Scholar 

  • Mustafa SJ, Chandra SV (1971) Levels of 5-hydroxytryptamine, dopamine and norepinephrine in whole brain of rabbits in chronic manganese toxicity. J Neurochem 18: 931–933

    Google Scholar 

  • Neff NH, Barret RE, Costa E (1969) Selective depletion of caudate nucleus dopamine and serotonin during chronic manganese dioxide administration to squirrel monkeys. Experientia 25: 1140–1141

    Google Scholar 

  • Nemeroff CB, Cain ST (1985) Neurotensin-dopamine interactions in the CNS. TIPS 8: 201–205

    Google Scholar 

  • Pentschew A, Ebner FF, Kovatch RM (1963) Experimental manganese encephalopathy in monkeys. A preliminary report. J Neuropath Exp Neurol 22: 488–499

    Google Scholar 

  • Perry TL, Godin DV, Hansen S (1982) Parkinson's disease: A disorder due to nigral glutathione deficiency? Neurosci Lett 33: 305–308

    Google Scholar 

  • Plantin LO (1972) A method for determination of Mn, Cu, Zn, K and Na in small tissue biopsies by neutron activation analysis. J Radioanal Chem 12: 441–449

    Google Scholar 

  • Prasad KN, Nayak M, Edward-Prasad J, Cummings S, Pattisapu K (1980) Modification of glutamate effects on neuroblastoma cells in culture by heavy metals. Life Sci 27: 2251–2259

    Google Scholar 

  • Rodier J (1955) Manganese poisoning in maroccan miners. Br J Ind Med 12: 21–35

    Google Scholar 

  • Scheuhammer AM, Cherian MG (1985) Binding of manganese in human and rat plasma. Biochem Biophys Acta 840: 163–169

    Google Scholar 

  • Sommer JH, O'Hara PB, Jonah CD, Bersohn R (1982) Relative reducibilities of complexes of Fe(III), Co(III), Mn(III) and Cu(II) with apotransferrin using e eq and CO 2 . Biochim Biophys Acta 703: 62–68

    Google Scholar 

  • Suzuki Y, Mouri T, Suzuki Y, Nishiyama K, Fujii N, Yano H (1975) Study of subacute toxicity of manganese dioxide in monkeys. Tokushima J Exp Med 22: 5–10

    Google Scholar 

  • Theodorsson-Norheim E (1983) Immunochemical and chromatographic studies on neurotensin-like immunoreactivity in plasma. PhD thesis. Karolinska Institute, Stockholm, Sweden

    Google Scholar 

  • Theodorus PM, Akerboom PM, Sies H (1981) Assay of glutathione, glutathione disulfide, and glutathione mixed disulfides in biological samples. In: WB Jakoby (ed) Methods in enzymology, vol 77. Academic Press, New York, pp 373–382

    Google Scholar 

  • Whitlock CM, Amuso SJ, Bittenbender JB (1966) Chronic neurological disease in two manganese steel workers. Am Ind Hyg Assoc J 27: 454–459

    Google Scholar 

  • WHO report (1981) Manganese. Environmental Health Criteria 17, pp 12–14 and pp 63–72

  • Yamada M, Ohno S, Okayasu I, Okeda R, Hatakeyama S, Watanabe H, Ushio K, Tsukagoshi H (1986) Chronic manganese poisoning: A neuropathological study with determination of manganese distribution in the brain. Acta neuropathol (Berl) 70: 273–278

    Google Scholar 

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Eriksson, H., Mägiste, K., Plantin, LO. et al. Effects of manganese oxide on monkeys as revealed by a combined neurochemical, histological and neurophysiological evaluation. Arch Toxicol 61, 46–52 (1987). https://doi.org/10.1007/BF00324547

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  • DOI: https://doi.org/10.1007/BF00324547

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