Abstract
The visual evoked potential (VEP) is an electronic potential recorded from the visual cortex in response to a visual stimulus. It provides a means to examine the function of the visual pathway from the retina to the occipital cortex. The most common animals employed in VEP laboratory studies are rats. In this chapter, we describe the basic ‘flash VEP’ recording protocol in rodents and discuss the practical aspects of the preparation including anaesthesia methods, electrode configuration, stimulus design, dark adaptation, filter settings and signal sampling with the authors’ personal experience. We also review the recent use of the VEP in laboratory researches in several optic nerve disease models, including glaucoma, ischemic optic neuropathy and optic neuritis.
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References
Creutzfeldt O, Maekawa K, Hosli L (1969) Forms of spontaneous and evoked postsynaptic potentials of cortical nerve cells. Prog Brain Res 31:265–273
Halliday A, McDonald W, Mushin J (1972) Delayed visual evoked response in optic neuritis. Lancet 1:982–985
Towle V, Moskowitz A, Sokol S, Schwartz B (1983) The visual evoked potential in glaucoma and ocular hypertension: effects of check size, field size, and stimulation rate. Invest Ophthalmol Vis Sci 24:175–183
Ridder W (2006) Visual evoked potentials in animals. In: Heckenlively JR, Arden GB (eds) Principles and practice of clinical electrophysiology of vision. The MIT Press, Cambridge, pp 935–947
Ridder W, Nusinowitz S (2006) The visual evoked potential in the mouse—origins and response characteristics. Vision Res 46:902–913
Creel D, Dustman R, Beck E (1973) Visually evoked responses in the rat, guinea pig, cat, monkey, and man. Exp Neurol 40:351–366
Creel D, Dustman RE, Beck EC (1974) Intensity of flash illumination and the visually evoked potential of rats, guinea pigs and cats. Vision Res 14:725–729
Heiduschka P, Schraermeyer U (2008) Comparison of visual function in pigmented and albino rats by electroretinography and visual evoked potentials. Graefes Arch Clin Exp Ophthalmol 246:1559–1573
Iwamura Y, Fujii Y, Kamei C (2003) The effects of certain H1-antagonists on visual evoked potential in rats. Brain Res Bull 61:393–398
Iwamura Y, Fujii Y, Kamei C (2004) The effects of selective serotonin-reuptake inhibitor on visual evoked potential in rats. J Pharmacol Sci 94:271–276
Miyake K-I, Yoshida M, Inoue Y, Hata Y (2007) Neuroprotective effect of transcorneal electrical stimulation on the acute phase of optic nerve injury. Invest Ophthalmol Vis Sci 48:2356–2361
Jehle T, Wingert K, Dimitriu C, Meschede W, Lasseck J, Bach M, Lagreze WA (2008) Quantification of ischemic damage in the rat retina: a comparative study using evoked potentials, electroretinography, and histology. Invest Ophthalmol Vis Sci 49:1056–1064
Papathanasiou ES, Peachey NS, Goto Y, Neafsey EJ, Castro AJ, Kartje GL (2006) Visual cortical plasticity following unilateral sensorimotor cortical lesions in the neonatal rat. Exp Neurol 199:122–129
Tomita H, Sugano E, Yawo H, Ishizuka T, Isago H, Narikawa S, Kugler S, Tamai M (2007) Restoration of visual response in aged dystrophic RCS rats using AAV-mediated channelopsin-2 gene transfer. Invest Ophthalmol Vis Sci 48:3821–3826
Onofrj M, Harnois C, Bodis-Wollner I (1985) The hemispheric distribution of the transient rat VEP: a comparison of flash and pattern stimulation. Exp Brain Res 59:427–433
Meeren H, Van Luijtelaar E, Coenen A (1998) Cortical and thalamic visual evoked potentials during sleep-wake states and spike-wave discharges in the rat. Electroencephalogr Clin Neurophysiol 108:306–319
Goto Y, Furuta A, Tobimatsu S (2001) Magnesium deficiency differentially affects the retina and visual cortex of intact rats. J Nutr 131:2378–2381
Yargicoglu P, Yaras N, Agar A, Gumuslu S, Bilmen S, Ozkaya G (2003) The effect of vitamin E on stress-induced changes in visual evoked potentials (VEPs) in rats exposed to different experimental stress models. Acta Ophthalmol Scand 81:181–187
Bernstein S, Guo Y, Kelman S, Flower R, Johnson M (2003) Functional and cellular responses in a noval rodent model of anterior ischemic optic neuropathy. Invest Ophthalmol Vis Sci 44:4153–4162
Herr D, Kim T, King D, Boyes W (1996) Possible confounding effects of strobe “clicks” on flash evoked potentials in rats. Physiol Behav 59:325–340
Green D, Herreros de Tejada P, Glover M (1994) Electrophysiological estimates of visual sensitivity in albino and pigmented mice. Vis Neurosci 11:919–925
Lopez L, Brusa A, Fadda A, Loizzo S, Martinangeli A, Sannita WG, Loizzo A (2002) Modulation of flash stimulation intensity and frequency: effects on visual evoked potentials and oscillatory potentials recorded in awake, freely moving mice. Brain Res 131:105–114
Mazzucchelli A, Conte S, D’Olimpio F, Ferlazzo F, Loizzo A, Palazzesi S, Renzi P (1995) Ultradian rhythms in the N1-P2 amplitude of the visual evoked potential in two inbred strains of mice: DBA/2J and C57BL/6. Behav Brain Res 67:81–84
Peachey NS, Roveri L, Messing A, McCall MA (1997) Functional consequences of oncogene-induced horizontal cell degeneration in the retinas of transgenic mice. Vis Neurosci 14:627–632
Porciatti V, Pizzourusso T, Maffei L (1999) The visual physiology of the wild type mouse determined with pattern VEPs. Vision Res 39:3071–3781
Peachey NS, Ball SL (2003) Electrophysiological analysis of visual function in mutant mice. Doc Ophthalmol 107:13–36
Henry K, Rhoades R (1978) Relation of albinism and drugs to the visual evoked potential of the mouse. J Comp Physiol Psychol 92:271–279
You Y, Klistorner A, Thie J, Graham S (2011) Latency delay of visual evoked potential is a real measurement of demyelination in a rat model of optic neuritis. Invest Ophthalmol Vis Sci 52:6911–6918
You Y, Klistorner A, Thie J, Graham S (2011) Improving reproducibility of VEP recording in rats: electrodes, stimulus source and peak analysis. Doc Ophthalmol 123:109–119
Castro-Junior J, Resende L, Bertotti M, Fonseca R, Zanchetta S, Schelp A (2005) Comparision of the effects of barbiturate, benzodiazepine and ketamine on visual evoked potentials in rabbits. Electromyogr Clin Neurophysiol 45:259–262
Anis N, Berry S, Burton N, Lodge D (1983) The dissociative anaesthetics, ketamine and phencyclidine, selectively reduce excitation of central mammalian neurones by N-methyl-aspartate. Br J Pharmacol 79:565–575
Virtanen R, Savola J, Saano V, Nyman L (1988) Characterization of the selectivity, specificity and potency of medetomidine as an alpha 2-adrenoceptor agonist. Eur J Pharmacol 150:9–14
Ridder W, Nusinowitz S, Heckenlively J (2002) Cause of cataract development in anesthetized mice. Exp Eye Res 75:365–370
Weymouth AE, Vingrys AJ (2008) Rodent electroretinography: methods for extraction and interpretation of rod and cone responses. Prog Retin Eye Res 27:1–44
Smith KJ, Waxman SG (2005) The conduction properties of demyelinated and remyelinated axons. In: Waxman SG (ed) Multiple sclerosis as a neuronal disease. Elsevier Academic Press, Amsterdam, pp 85–100
Boyes W, Padilla S, Dyer R (1985) Body temperature-dependent and independent actions of chlordimeform on visual evoked potentials and axonal transport in optic system of rat. Neuropharmacology 24:743–749
Hetzler B, Boyes W, Creason J, Dyer R (1988) Temperature-dependent changes in visual evoked potentials of rats. Electroencephalogr Clin Neurophysiol 70:137–154
Fahle M, Bach M (2006) Origin of the visual evoked potentials. In: Heckenlively J, Arden G (eds) Principles and practice of clinical electrophysiology of vision. MIT Press, Cambridge, pp 207–234
Leamey CA, Protti DA, Dreher B (2008) Comparative survey of the mammalian visual system with reference to the mouse. In: Chalupa LM, Williams RW (eds) Eye, retina, and visual system of the mouse. MIT Press, Cambridge, pp 35–60
Odom JV, Bach M, Brigell M, Holder GE, McCulloch DL, Tormene AP, Vaegan (2010) ISCEV standard for clinical visual evoked potentials (2009 update). Doc Ophthalmol 120:111–119
McCall M, Robinson S, Dreher B (1987) Differential retinal growth appears to be the primary factor producing the ganglion cell density gradient in the rat. Neurosci Lett 79:78–84
Shaw N (1992) The effects of low-pass filtering on the flash visual evoked potential of the albino rat. J Neurosci Methods 44:233–240
Narfstrom K, Ekesten B, Rosolen S, Spiess B, Percicot C, Ofri R (2002) Guidelines for clinical electroretinography in the dog. Doc Ophthalmol 105:83–92
Klistorner A, Crewther D, Crewther S (1997) Separate magnocellular and parvocellular contributions from temporal analysis of the multifocal VEP. Vision Res 37:2161–2169
Klistorner A, Graham S, Martins A, Grigg J, Arvind H, Kumar R, James A, Billson F (2007) Multifocal blue-on-yellow visual evoked potentials in early glaucoma. Ophthalmology 114:1613–1621
Klistorner A, Arvind H, Nguyen T, Garrick R, Paine M, Graham S, O’Day J, Grigg J, Billson F, Yiannikas C (2008) Axonal loss and myelin in early ON loss in postacute optic neuritis. Ann Neurol 64:325–331
Klistorner A, Graham S, Fraser C, Garrick R, Nguyen T, Paine M, O’Day J, Arvind H, Billson F (2007) Electrophysiological evidence for heterogeneity of lesions in optic neuritis. Invest Ophthalmol Vis Sci 48:4549–4556
Youl B, Turano G, Miller D, Towell A, MacManus D, Moore S, Jones S, Barrett G, Kendall B, Moseley I (1991) The pathophysiology of acute optic neuritis: an association of gadolinium leakage with clinical and electrophysiological deficits. Brain 114:2437–2450
Meyer R, Weissert R, Diem R, Storch MK, de Graaf KL, Kramer B, Bahr M (2001) Acute neuronal apoptosis in a rat model of multiple sclerosis. J Neurosci 21:6214–6220
Diem R, Demmer I, Boretius S, Merkler D, Schmelting B, Williams S, Sattler M, Bahr M, Michaelis T, Frahm J, Bruck W, Fuchs E (2008) Autoimmune optic neuritis in the common marmoset monkey: comparison of visual evoked potentials with MRI and histopathology. Invest Ophthalmol Vis Sci 49:3707–3714
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You, Y., Klistorner, A., Graham, S.L. (2013). Visual Evoked Potential Recording in Rodents. In: Pilowsky, P., Farnham, M., Fong, A. (eds) Stimulation and Inhibition of Neurons. Neuromethods, vol 78. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-233-9_16
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DOI: https://doi.org/10.1007/978-1-62703-233-9_16
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