Cell death/proliferation and alterations in glial morphology contribute to changes in diffusivity in the rat hippocampus after hypoxia-ischemia

. 2011 Mar ; 31 (3) : 894-907. [epub] 20100929

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid20877389

To understand the structural alterations that underlie early and late changes in hippocampal diffusivity after hypoxia/ischemia (H/I), the changes in apparent diffusion coefficient of water (ADC(W)) were studied in 8-week-old rats after H/I using diffusion-weighted magnetic resonance imaging (DW-MRI). In the hippocampal CA1 region, ADC(W) analyses were performed during 6 months of reperfusion and compared with alterations in cell number/cell-type composition, glial morphology, and extracellular space (ECS) diffusion parameters obtained by the real-time iontophoretic method. In the early phases of reperfusion (1 to 3 days) neuronal cell death, glial proliferation, and developing gliosis were accompanied by an ADC(W) decrease and tortuosity increase. Interestingly, ECS volume fraction was decreased only first day after H/I. In the late phases of reperfusion (starting 1 month after H/I), when the CA1 region consisted mainly of microglia, astrocytes, and NG2-glia with markedly altered morphology, ADC(W), ECS volume fraction and tortuosity were increased. Three-dimensional confocal morphometry revealed enlarged astrocytes and shrunken NG2-glia, and in both the contribution of cell soma/processes to total cell volume was markedly increased/decreased. In summary, the ADC(W) increase in the CA1 region underlain by altered cellular composition and glial morphology suggests that considerable changes in extracellular signal transmission might occur in the late phases of reperfusion after H/I.

Zobrazit více v PubMed

Alonso G. NG2 proteoglycan-expressing cells of the adult rat brain: possible involvement in the formation of glial scar astrocytes following stab wound. Glia. 2005;49:318–338. PubMed

Anderova M, Antonova T, Petrik D, Neprasova H, Chvatal A, Sykova E. Voltage-dependent potassium currents in hypertrophied rat astrocytes after a cortical stab wound. Glia. 2004;48:311–326. PubMed

Beilharz EJ, Williams CE, Dragunow M, Sirimanne ES, Gluckman PD. Mechanisms of delayed cell death following hypoxic-ischemic injury in the immature rat: evidence for apoptosis during selective neuronal loss. Brain Res Mol Brain Res. 1995;29:1–14. PubMed

Benesova J, Hock M, Butenko O, Prajerova I, Anderova M, Chvatal A. Quantification of astrocyte volume changes during ischemia in situ reveals two populations of astrocytes in the cortex of GFAP/EGFP mice. J Neurosci Res. 2009;87:96–111. PubMed

Busza AL, Allen KL, King MD, van Bruggen N, Williams SR, Gadian DG. Diffusion-weighted imaging studies of cerebral ischemia in gerbils. Potential relevance to energy failure. Stroke. 1992;23:1602–1612. PubMed

Chvatal A, Anderova M, Hock M, Prajerova I, Neprasova H, Chvatal V, Kirchhoff F, Sykova E. Three-dimensional confocal morphometry reveals structural changes in astrocyte morphology in situ. J Neurosci Res. 2007;85:260–271. PubMed

Dijkhuizen RM, Knollema S, van der Worp HB, Ter Horst GJ, De Wildt DJ, Berkelbach van der Sprenkel JW, Tulleken KA, Nicolay K. Dynamics of cerebral tissue injury and perfusion after temporary hypoxia-ischemia in the rat: evidence for region-specific sensitivity and delayed damage. Stroke. 1998;29:695–704. PubMed

Fortuna S, Pestalozza S, Lorenzini P, Bisso GM, Morelli L, Michalek H. Transient global brain hypoxia-ischemia in adult rats: neuronal damage, glial proliferation, and alterations in inositol phospholipid hydrolysis. Neurochem Int. 1997;31:563–569. PubMed

Frisen J, Johansson CB, Torok C, Risling M, Lendahl U. Rapid, widespread, and longlasting induction of nestin contributes to the generation of glial scar tissue after CNS injury. J Cell Biol. 1995;131:453–464. PubMed PMC

Gass A, Niendorf T, Hirsch JG. Acute and chronic changes of the apparent diffusion coefficient in neurological disorders—biophysical mechanisms and possible underlying histopathology. J Neurol Sci. 2001;186 (Suppl 1:S15–S23. PubMed

Gehrmann J, Bonnekoh P, Miyazawa T, Hossmann KA, Kreutzberg GW. Immunocytochemical study of an early microglial activation in ischemia. J Cereb Blood Flow Metab. 1992;12:257–269. PubMed

Goddard DR, Berry M, Kirvell SL, Butt AM. Fibroblast growth factor-2 induces astroglial and microglial reactivity in vivo. J Anat. 2002;200:57–67. PubMed PMC

Hirrlinger PG, Wurm A, Hirrlinger J, Bringmann A, Reichenbach A. Osmotic swelling characteristics of glial cells in the murine hippocampus, cerebellum, and retina in situ. J Neurochem. 2008;105:1405–1417. PubMed

Knollema S, Aukema W, Hom H, Korf J, ter Horst GJ. L-deprenyl reduces brain damage in rats exposed to transient hypoxia-ischemia. Stroke. 1995;26:1883–1887. PubMed

Kuan CY, Schloemer AJ, Lu A, Burns KA, Weng WL, Williams MT, Strauss KI, Vorhees CV, Flavell RA, Davis RJ, Sharp FR, Rakic P. Hypoxia-ischemia induces DNA synthesis without cell proliferation in dying neurons in adult rodent brain. J Neurosci. 2004;24:10763–10772. PubMed PMC

Li F, Liu KF, Silva MD, Meng X, Gerriets T, Helmer KG, Fenstermacher JD, Sotak CH, Fisher M. Acute postischemic renormalization of the apparent diffusion coefficient of water is not associated with reversal of astrocytic swelling and neuronal shrinkage in rats. AJNR Am J Neuroradiol. 2002;23:180–188. PubMed PMC

Lythgoe MF, Thomas DL, King MD, Pell GS, van der Weerd L, Ordidge RJ, Gadian DG. Gradual changes in the apparent diffusion coefficient of water in selectively vulnerable brain regions following brief ischemia in the gerbil. Magn Reson Med. 2005;53:593–600. PubMed

Lytle JM, Chittajallu R, Wrathall JR, Gallo V. NG2 cell response in the CNP-EGFP mouse after contusive spinal cord injury. Glia. 2009;57:270–285. PubMed PMC

Lytle JM, Wrathall JR. Glial cell loss, proliferation and replacement in the contused murine spinal cord. Eur J Neurosci. 2007;25:1711–1724. PubMed

Pforte C, Henrich-Noack P, Baldauf K, Reymann KG. Increase in proliferation and gliogenesis but decrease of early neurogenesis in the rat forebrain shortly after transient global ischemia. Neuroscience. 2005;136:1133–1146. PubMed

Ray SK, Karmakar S, Nowak MW, Banik NL. Inhibition of calpain and caspase-3 prevented apoptosis and preserved electrophysiological properties of voltage-gated and ligand-gated ion channels in rat primary cortical neurons exposed to glutamate. Neuroscience. 2006;139:577–595. PubMed

Risher WC, Andrew RD, Kirov SA. Real-time passive volume responses of astrocytes to acute osmotic and ischemic stress in cortical slices and in vivo revealed by two-photon microscopy. Glia. 2009;57:207–221. PubMed PMC

Sas K, Robotka H, Rozsa E, Agoston M, Szenasi G, Gigler G, Marosi M, Kis Z, Farkas T, Vecsei L, Toldi J. Kynurenine diminishes the ischemia-induced histological and electrophysiological deficits in the rat hippocampus. Neurobiol Dis. 2008;32:302–308. PubMed

Schmidt-Kastner R, Freund TF. Selective vulnerability of the hippocampus in brain ischemia. Neuroscience. 1991;40:599–636. PubMed

Schmidt-Kastner R, Szymas J, Hossmann KA. Immunohistochemical study of glial reaction and serum-protein extravasation in relation to neuronal damage in rat hippocampus after ischemia. Neuroscience. 1990;38:527–540. PubMed

Silva MD, Omae T, Helmer KG, Li F, Fisher M, Sotak CH. Separating changes in the intra- and extracellular water apparent diffusion coefficient following focal cerebral ischemia in the rat brain. Magn Reson Med. 2002;48:826–837. PubMed

Sizonenko SV, Camm EJ, Dayer A, Kiss JZ. Glial responses to neonatal hypoxic-ischemic injury in the rat cerebral cortex. Int J Dev Neurosci. 2008;26:37–45. PubMed

Sullivan SM, Bjorkman ST, Miller SM, Colditz PB, Pow DV. Structural remodeling of gray matter astrocytes in the neonatal pig brain after hypoxia/ischemia. Glia. 2010;58:181–194. PubMed

Sykova E, Nicholson C. Diffusion in brain extracellular space. Physiol Rev. 2008;88:1277–1340. PubMed PMC

Sykova E, Vorisek I, Mazel T, Antonova T, Schachner M. Reduced extracellular space in the brain of tenascin-R- and HNK-1-sulphotransferase deficient mice. Eur J Neurosci. 2005;22:1873–1880. PubMed

Tamura Y, Kataoka Y, Cui Y, Yamada H. Cellular proliferation in the cerebral cortex following neural excitation in rats. Neurosci Res. 2004;50:129–133. PubMed

van der Toorn A, Dijkhuizen RM, Tulleken CA, Nicolay K. T1 and T2 relaxation times of the major 1H-containing metabolites in rat brain after focal ischemia. NMR Biomed. 1995;8:245–252. PubMed

Vorisek I, Hajek M, Tintera J, Nicolay K, Sykova E. Water ADC, extracellular space volume, and tortuosity in the rat cortex after traumatic injury. Magn Reson Med. 2002;48:994–1003. PubMed

Vorisek I, Sykova E. Ischemia-induced changes in the extracellular space diffusion parameters, K+, and pH in the developing rat cortex and corpus callosum. J Cereb Blood Flow Metab. 1997;17:191–203. PubMed

Vorisek I, Sykova E. Measuring diffusion parameters in the brain: comparing the real-time iontophoretic method and diffusion-weighted magnetic resonance. Acta Physiol (Oxf) 2009;195:101–110. PubMed

Yokoyama A, Sakamoto A, Kameda K, Imai Y, Tanaka J. NG2 proteoglycan-expressing microglia as multipotent neural progenitors in normal and pathologic brains. Glia. 2006;53:754–768. PubMed

Zhao JW, Raha-Chowdhury R, Fawcett JW, Watts C. Astrocytes and oligodendrocytes can be generated from NG2+ progenitors after acute brain injury: intracellular localization of oligodendrocyte transcription factor 2 is associated with their fate choice. Eur J Neurosci. 2009;29:1853–1869. PubMed

Zoremba N, Homola A, Slais K, Vorisek I, Rossaint R, Lehmenkuhler A, Sykova E. Extracellular diffusion parameters in the rat somatosensory cortex during recovery from transient global ischemia/hypoxia. J Cereb Blood Flow Metab. 2008;28:1665–1673. PubMed

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

The absence of AQP4/TRPV4 complex substantially reduces acute cytotoxic edema following ischemic injury

. 2022 ; 16 () : 1054919. [epub] 20221208

On the Common Journey of Neural Cells through Ischemic Brain Injury and Alzheimer's Disease

. 2021 Sep 07 ; 22 (18) : . [epub] 20210907

Compromised Astrocyte Swelling/Volume Regulation in the Hippocampus of the Triple Transgenic Mouse Model of Alzheimer's Disease

. 2021 ; 13 () : 783120. [epub] 20220127

Ischemia-Triggered Glutamate Excitotoxicity From the Perspective of Glial Cells

. 2020 ; 14 () : 51. [epub] 20200319

Altered astrocytic swelling in the cortex of α-syntrophin-negative GFAP/EGFP mice

. 2014 ; 9 (11) : e113444. [epub] 20141126

Astrocytes and extracellular matrix in extrasynaptic volume transmission

Heterogeneity of astrocytes: from development to injury - single cell gene expression

. 2013 ; 8 (8) : e69734. [epub] 20130805

The increased activity of TRPV4 channel in the astrocytes of the adult rat hippocampus after cerebral hypoxia/ischemia

. 2012 ; 7 (6) : e39959. [epub] 20120627

Polydendrocytes display large lineage plasticity following focal cerebral ischemia

. 2012 ; 7 (5) : e36816. [epub] 20120510

Najít záznam

Citační ukazatele

Nahrávání dat ...

    Možnosti archivace