Mapping neuronal activity by imaging intrinsic optical signals

Neuroscientist

Volumn 3, Issue 6, 1997, Pages 381-388

  Macvicar, Brian A ^a  

^a UNIVERSITY OF CALGARY   (Canada)

Author keywords

Cellular swelling; Imaging; Intrinsic optical signals; Light reflectance; Light scattering

Indexed keywords

EID: 0012027275     PISSN: 10738584     EISSN: None     Source Type: Journal    
DOI: 10.1177/107385849700300611     Document Type: Review

References (39)

1. Hill DK, Keynes RD. Opacity changes in stimulated nerve. J Physiol (Lond) 1949;108:278-281.
2. Frostig RD, Lieke EE, Ts'o DY, Grinvald A. Cortical functional architecture and local coupling between neuronal activity and the microcirculation revealed by in vivo high-resolution optical imaging of intrinsic signals. Proc Natl Acad Sci U S A 1990;87: 6082-6086.
3. Grinvald A, Lieke E, Frostig RD, Gilbert CD, Wiesel TN. Functional architecture of cortex revealed by optical imaging of intrinsic signals. Nature 1986;324:361-364.
4. Ts'o DY, Frostig RD, Lieke EE, Grinvald A. Functional organization of primate visual cortex revealed by high resolution optical imaging. Science 1990;249:417-420.
5. Federico P, MacVicar BA. Imaging the induction and spread of seizure activity in the isolated brain of the guinea pig: The roles of GABA and glutamate receptors. J Neurophysiol 1996;76: 3471-3492.
6. Federico P, Borg SG, Salkauskus AG, MacVicar BA. Mapping patterns of neuronal activity and seizure propagation by imaging intrinsic optical signals in the isolated whole brain of the guinea-pig. Neuroscience 1994;58:461-480.
7. Andrew RD, MacVicar BA. Imaging cell volume changes and neuronal excitation in the hippocampal slice. Neuroscience 1994;62:371-383.
8. MacVicar BA, Hochman D. Imaging of synaptically evoked intrinsic optical signals in hippocampal slices. J Neurosci 1991;11: 1458-1469.
9. Stepnoski RA, LaPorta A, Raccuia-Behling F, Blonder GE, Slusher RE, Kleinfeld D. Noninvasive detection of changes in membrane potential in cultured neurons by light scattering. Proc Natl Acad Sci U S A 1991;88:9382-9386.
10. Cohen LB. Changes in neuron structure during action potential propagation and synaptic transmission. Physiol Rev 1973;53: 373-418.
11. Obaid AL, Flores R, Salzberg BM. Calcium channels that are required for secretion from intact nerve terminals of vertebrates are sensitive to omega-conotoxin and relatively insensitive to dihydropyridines. optical studies with and without voltage-sensitive dyes. J Gen Physiol 1989;93:715-729.
12. Salzberg BM, Obaid AL, Gainer H. Large and rapid changes in light scattering accompany secretion by nerve terminals in the mammalian neurohypophysis. J Gen Physiol 1985;86:395-411.
13. Rector D, Harper R. Imaging of hippocampal neural activity in freely behaving animals. Behav Brain Res 1991;42:143-149.
14. Rector DM, Poe GR, Kristensen MP, Harper RM. Imaging the dorsal hippocampus: light reflectance relationships to electroencephalographic patterns during sleep. Brain Res 1995;696:151-160.
15. Lipton P. Effects of membrane depolarization on light scattering by cerebral cortical slices. J Physiol (Lond) 1973;231:365-383.
16. MacVicar BA. Infrared video microscopy to visualize neurons in the in vitro brain slice preparation. J Neurosci Methods 1984;12: 133-139.
17. Andrew RD. Seizure and acute osmotic change: clinical and neurophysiological aspects. J Neurol Sci 1991;101:7-18.
18. Dietzel I, Heineman U, Hofmeier O, Lux HD. Transient changes in the size of the extracellular space in the sensorimotor cortex of cats in relation to stimulus induced changes in potassium concentration. Exp Brain Res 1980;40:432-439.
19. Dietzel I, Heinemann U, Lux HD. Relations between slow extracellular potential changes, glial potassium buffering, and electrolyte and cellular volume changes during neuronal hyperactivity in cat brain. Glia 1989;2:25-44.
20. Strange K. Regulation of solute and water balance and cell volume in the central nervous system. J Am Soc Nephrol 1992;3:12-27.
21. Krizaj D, Rice ME, Wardle RA, Nicholson C. Water compartmentalization and extracellular tortuosity after osmotic changes in cerebellum of Trachemys scripta. J Physiol (Lond) 1996;492(Pt 3):887-896.
22. McBain CJ, Traynelis SF, Dingledine R. Regional variation of extracellular space in the hippocampus. Science 1990;249:674-677.
23. Ransom BR, Yamate CL, Connors BW. Activity-dependent shrinkage of extracellular space in rat optic nerve: a developmental study. J Neurosci 1985;5:532-535.
24. Holtoff K, Witte OW. Intrinsic optical signals in rat neocortical slices measured with near-infrared dark-field microscopy reveal changes in extracellular space. J Neurosci 1996;16:2749.
25. Kimelberg HK, Jalonen T, Walz W. Regulation of the brain microenvironment: transmitters and ions. In: Murphy S, editor. Astrocytes: pharmacology and function. New York: Academic; 1993. p. 193-228.
26. Kimelberg HK, Ransom BR. Physiological and pathological aspects of astrocyte swelling. In: Federoff S, Vernadalis A, editors. Astrocytes: cell biology and pathology of astrocytes. New York: Academic; 1986. p. 129-166.
27. Serve G, Endres W, Grafe P. Continuous electrophysiological measurements of changes in cell volume of motoneurons in the isolated frog spinal cord. Pflugers Arch 1988;411:410-415.
28. Walz W, Hertz L. Intense furosemide-sensitive potassium accumulation in astrocytes in the presence of pathologically high extracellular K levels. J Cereb Blood Flow Metab 1984;4:301-304.
29. Walz W, Hinks EC. Carrier-mediated KCl accumulation accompanied by water movements is involved in the control of physiological K levels by astrocytes. Brain Res 1986;368:226-232.
30. Malonek D, Grinvald A. Interactions between electrical activity and cortical microcirculation revealed by imaging spectroscopy: implications for functional brain mapping. Science 1996;272: 551-554.
31. Chance B, Williams GR. A method for the localization of sites from oxidative phosphorylation. Nature 1955;176:250-254.
32. Chance B, Cohen P, Jobsis F, Schoener B. Intracellular oxidation-reduction states in vivo. Science 1962;137:499-507.
33. LaManna JC, Sick TJ, Pikarsky SM, Rosenthal M. Detection of an oxidizable fraction of cytochrome oxidase in intact rat brain. Am J Physiol 1987;253:C477-C483.
34. Blasdel GG, Salama G. Voltage-sensitive dyes reveal a modular organization in monkey striate cortex. Nature 1986;321:579-585.
35. Arieli A, Shoham D, Hildesheim R, Grinvald A. Coherent spatio-temporal patterns of ongoing activity revealed by real-time optical imaging coupled with single-unit recording in the cat visual cortex. J Neurophysiol 1995;73:2072-2093
36. MacVicar BA, Watson TWJ, Le Blanc FE, Borg SG, Federico P. Mapping of neuronal activity patterns using intrinsic optical signals: from isolated brain slices to the intact human brain. In: Dirnagl U, Villringer A, Einhaeufl KM, editors. Optical imaging of brain function and metabolism. New York: Plenum; 1993. p. 71-79.
37. MacVicar BA, Watson TWJ, Hochman D. Optical imaging system for neurosurgery. US patent 5,215,095. 1993.
38. Haglund MM, Ojemann GA, Hochman DW. Optical imaging of epileptiform and functional activity in human cerebral cortex. Nature 1992;358:668-671.
39. Menon RS, Ogawa S, Hu X, Strupp JP, Anderson P, Ugurbil K. BOLD based functional MRI at 4 Tesla includes a capillary bed contribution: echo-planar imaging correlates with previous optical imaging using intrinsic signals. Magn Reson Med 1995;33:453-459.