REFERENCES
- Andjelkovic A, Patcher JS. Central nervous system endothelium in neuroinflammatory, neuroinfectious and neurodegenerative disease. J Neurosci Res 1998; 51:423–430.
- Kapadia SE, de Lanerolle NC. Immunohistochemical and electron microscopic demonstration of vascular innervation in the mammalian brainstem. Brain Res 1984; 293: 33–39.
- Vaucher E, Hamel E. Cholinergic basal forebrain neurons project to cortical microvessels in the rat: electron-microscopic study with anterogradely transported Phaseolus vulgaris leucoagglutinin and choline acetyltransferase immunocytochemistry. J Neurosci 1995; 15: 427–441.
- Abbott N. Inflammatory mediators and modulation of blood brain barrier permeability. Cell Mol Neurobiol 2000; 20:2131–2147.
- Atlante A, Calissano P, Bobba A et al. Glutamate toxicity, oxidative stress and mitochondria. FEBS Lett 2001; 497: 1–5.
- Choi DW. Glutamate neurotoxicity and diseases of the nervous system. Neuron 1988; 1: 623–634.
- Rae C, Lawrance ML, Provis T, Bubb WA, Balcar VJ. Strategies for neurotoxic mechanisms involving deficient transport of L-glutamate: antisense knockout in rat brain in vivo and changes in the neurotransmitter metabolism following inhibition of glutamate transport in guinea pig brain slices. Brain Res Bu112000; 53: 373-381.
- Gottlieb M, Wang Y, Teichberg VI. Blood-mediated scavenging of cerebrospinal fluid glutamate. J Neurochem 2003; 87: 119–126.
- Koenig H, Trout JJ, Goldstone AD, Lu CY. Capillary NMDA receptors regulate blood-brain barrier function and breakdown. Brain Res 1992; 588:297–303.
- 'S'eastn9 F, 'S'kultétyová I, Pliss L, Jeiová D. Quinolinic acid enhances permeability of rat brain microvessels to plasma albumin. Brain Res Bull 2000; 53:415–420.
- 'S'eastny F, Schwendt M, Lis9 V, Jeiová D. Main subunits of ionotropic glutamate receptors are expressed in isolated rat brain microvessels. Neurol Res 2002; 24: 93–96.
- Parfenova H, Fedinec A, Leffler CW. Ionotropic glutamate receptors in cerebral microvascular endothelium are functionally linked to heme oxygenase. J Cereb Blood Flow Metab 2003; 23: 190–197.
- Mraulja BB, Mraulja BJ, Fujimoto T, Klatzo I, Spatz M. Isolation of brain capillaries: simplified techniques. Brain Res 1976; 110: 361–365.
- Lojda Z. Proteinases in pathology. Usefulness of histochemical methods. J Histochem Cytochem 1981; 29: 481–493.
- Seastny F, Hinoi E, Ogita K, Yoneda Y. Ferrous iron modulates quinolinate-mediated [3H]-MK-801 binding to rat brain synaptic membranes in the presence of glycine and spermidine. Neurosci Lett 1999; 262: 105–108.
- Santamaria A, Salvatierra-Sánchez R, Vazquez-Román B et al. Protective effects of the antioxidant selenium on quinolinic acid-induced neurotoxicity in rats: in vitro and in vivo studies. J Neurochem 2003; 86:479–488.
- Tsuzuki K, Iino M, Ozawa S. Ion channels activated by quinolinic acid in cultured rat hippocampal neurons. Brain Res 1989; 481:258–264.
- Lis' V, 'S'eastn9 F. Nitric oxide synthase inhibition and glutamate binding in quinolinate-lesioned rat hippocampus. Physiol Res 2002; 51:299–307.
- Santamaria A, Galván-Arzate S, Lisy V et al. Quinolinic acid induces oxidative stress in rat brain synaptosomes. Neuroreport 2001; 12: 871–874.
- PlAtemIc J, Stopka P, Vejrakka M, 'S'tipek S. Quinolinic acid-iron(II) complexes: slow autoxidation, but enhanced hydroxyl radical production in the Fenton reaction. Free Radic Res 2001; 34:445–459.
- Valle M, Price RW, Nilsson A, Heyes MP, Verrata D. CSF quinolinic acid levels are determined by local HIV infection: cross-sectional analysis and modelling of dynamics following antiretroviral therapy. Brain 2004; 127: 1047–1060.
- Beagles KE, Morrison PF, Heyes MP. Quinolinic acid in vivo synthesis rates, extracellular concentrations and intercompartmental distributions in normal and immune-activated brain as determined by multiple-isotope microdialysis. J Neurochem 1998; 70:281–291.
- Roberts RC, McCarthy KE, Du F, Okuno E, Schwarcz R. Immunocytochemical localization of the quinolinic acid synthesizing enzyme, 3-hydroxyanthranilic acid oxygenase, in the rat substantia nigra. Brain Res 1994; 650:229–238.
- Conti F, DeBiasi S, Minelli A, Melone M. Expression of NRI and NR2A/2B subunits of the NMDA receptor in cortical astrocytes. Glia 1996; 17: 254–258.
- Matute C, Gutiérrez-Igarza K, Rio C, Miledi R. Glutamate receptors in astrocytic end-feet. Neuroreport 1994; 5: 1205–1208.
- Hinoi E, Fujimori S, Nakamura Yet al. Constitutive expression of heterologous N-methyl-D-aspartate receptor subunits in rat adrenal medulla. J Neurosci Res 2002; 68:36–45.
- Bract K, Paemeleire K, D'Herde K, Sanderson MJ, L,eybaert L. Astrocyte-endothelial cell calcium signals conveyed by two signalling pathways. Eur J Neurosci 2001; 13: 79–91.
- Fiumana E, Parfenova H, Jaggar JH, Leffler CW. Carbon monoxide mediates vasodilator effects of glutamate in isolated pressurized cerebral arterioles of newborn pigs. Am J Physiol 2003; 284: H 1 073-H 1079.
- Zonta M, Angulo MC, Gobbo S et al. Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation. Nat Neurosci 2003; 6:43–50.
- Guillemin GJ, Smythe GA, Veas LA, Takikawa 0, Brew BJ. API, induces production of quinolinic acid by human macrophages and microglia. Neuroreport 2003; 14: 2311–2315.