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Elimination of zinc-65 from the brain under kainate-induced seizures

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Abstract

On the basis of the previous evidence that 65Zn concentrations in the brain of EL (epilepsy) mice was affected by induction of seizures, 65Zn movement in the brain was quantitatively evaluated in ddY mice treated with kainate. Six days after intravenous injection of 65ZnCl2, mice were intraperitoneally injected with kainate (10 mg/kg ×6 times in 2 weeks). Myoclonic jerks were observed during treatment with kainate. Twenty days after 65Zn injection, 65Zn distribution in the brain was compared between the kainite-treated and control mice. 65Zn distribution in the brain of the kainate-treated mice was overall lower than in the control mice. 65Zn concentration was significantly decreased in the frontal cortex, hippocampal CA1, thalamus and hypothalamus by treatment with kainate. These results demonstrate that kainate-induced seizures are linked to decreased zinc concentrations in the brain.

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References

  • Assaf SY, Chung S-H. 1984 Release of endogeneous Zn2+ from brain tissue during activity. Nature 308, 734-735.

    Google Scholar 

  • Ben-Ari Y. 1985 Limbic seizure and brain damage produced by kainic acid: Mechanisms and relevance to human temporal lobe epilepsy. Neuroscience 14, 375-403.

    Google Scholar 

  • Buhl EH, Otis TS, Mody I. 1996 Zinc-induced collapse of augmented inhibition by GABA in a temporal lobe epilepsy model. Science 271, 369-373.

    Google Scholar 

  • Cole TB, Robbins CA, Wenzel HJ, Schwartzkroin PA, Palmiter RD. 2000 Seizures and neuronal damage in mice lacking vesicular zinc. Epilepsy Res 39, 153-169.

    Google Scholar 

  • During MJ, Ryder KM, Spencer DD. 1995 Hippocampal GABA transporter function in temporal-lobe epilepsy. Nature 376, 174-177.

    Google Scholar 

  • Ebadi M, Wilt S, Ramaley R, Swanson S, Mebus C. 1984 The role of zinc and zinc-binding proteins in regulation of glutamic acid decarboxylase in brain. In: Evangepoulous AE, ed. Chemical and biological aspects of vitamin B6 catalysis., New York: Liss; 255-275.

    Google Scholar 

  • Frederickson CJ. 1989 Neurobiology of zinc and zinc-containing neurons. Int Rev Neurobiol 31, 145-238.

    Google Scholar 

  • Frederickson CJ, Hernandez MD, Goik SA, Morton JD, McGinty JF. 1988 Loss of zinc staining from hippocampal mossy fibers during kainic acid induced seizures: A histofluorescence study. Brain Res 446, 383-386.

    Google Scholar 

  • Fukahori M, Itoh M, Oomagari K, Kawasaki H. 1988 Zinc content in discrete hippocampal and amygdaloid areas of the epilepsy (E1) mouse and normal mice. Brain Res 455, 381-384.

    Google Scholar 

  • Fukahori M, Itoh M. 1990 Effects of dietary zinc status on seizure susceptibility and hippocampal zinc content in the E1 (epilepsy) mouse. Brain Res 529, 16-22.

    Google Scholar 

  • Golub MS, Keen CL, Gershwin ME, Hendrickx AG. 1995 Developmental zinc deficiency and behavior. J Nutr 125, 2263-2271.

    Google Scholar 

  • Hirate M, Takeda A, Tamano H, Enomoto S, Oku N. 2002 Distribution of trace elements in the brain of EL (epilepsy) mice. Epilepsy Res 51, 109-116.

    Google Scholar 

  • Howell GA, Welch MG, Frederickson CJ. 1984 Stimulationinduced uptake and release of zinc in hippocampal slices. Nature 308, 736-738.

    Google Scholar 

  • Ojemann GA. 1987 Surgical therapy for medically intractable epilepsy. J Neurosurg 66, 489-499.

    Google Scholar 

  • Prohaska JR. 1987 Functions of trace elements in brain metabolism. Physiol Rev 67, 858-901.

    Google Scholar 

  • Sandstead HH, Frederickson CJ, Penland JG. 2000 History of zinc as related to brain function. J Nutr 130, 496S-502S.

    Google Scholar 

  • Sloviter RS. 1985 A selective loss of hippocampal mossy fiber Timm stain accompanies granule cell seizure activity induced by perforant path stimulation. Brain Res 330, 150-153.

    Google Scholar 

  • Sterman MB, Shouse MN, Fairchild MD, Belsito O. 1986 Kindled seizure induction alters and is altered by zinc absorption. Brain Res 383, 382-386.

    Google Scholar 

  • Sterman MB, Shouse MN, Fairchild MD. 1988 Zinc and seizure mechanisms. In: Morley JE, Sterman MB, Walsh JH, eds. Nutritional modulation of neural function. San Diego: Academic Press; 307-319.

    Google Scholar 

  • Takeda A. 2000 Movement of zinc and its functional significance in the brain. Brain Res Rev 34, 137-148.

    Google Scholar 

  • Takeda A. 2001 Zinc homeostasis and functions of zinc in the brain. BioMetals 14, 343-352.

    Google Scholar 

  • Takeda A, Sawashita J, Okada S. 1995 Biological half-lives of zinc and manganese in rat brain. Brain Res 695, 53-58.

    Google Scholar 

  • Takeda A, Hanajima T, Ijiro H, Ishige A, Iizuka S, Okada S, Oku N. 1999 Release of zinc from the brain of El (epilepsy) mice during seizure induction. Brain Res 828, 174-178.

    Google Scholar 

  • Takeda A, Hirate M, Tamano H, Oku N. 2003 Zinc movement in the brain under kainite-induced seizures. Epilepsy Res 54, 123-129.

    Google Scholar 

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Correspondence to Atsushi Takeda.

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Takeda, A., Hirate, M. & Oku, N. Elimination of zinc-65 from the brain under kainate-induced seizures. Biometals 17, 141–144 (2004). https://doi.org/10.1023/B:BIOM.0000018378.55494.d2

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  • DOI: https://doi.org/10.1023/B:BIOM.0000018378.55494.d2

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