Modulation of somatosensory evoked fields from SI and SII by acute GABAA-agonism and paired-pulse stimulation

NeuroImage

Volumn 40, Issue 2, 2008, Pages 427-434

  Huttunen, Juha ^a   Pekkonen, Eero ^a   Kivisaari, Reetta ^a,b   Autti, Taina ^b   Kähkönen, Seppo ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

^b HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

Author keywords

Cortical inhibition; Magnetoencephalography; Paired pulse; Somatosensory cortex

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR STIMULATING AGENT; LORAZEPAM; PLACEBO;

ADULT; ARTICLE; BRAIN DEPTH STIMULATION; DRUG MECHANISM; EVOKED SOMATOSENSORY RESPONSE; EXCITATORY POSTSYNAPTIC POTENTIAL; FEMALE; HUMAN; HUMAN EXPERIMENT; INHIBITORY POSTSYNAPTIC POTENTIAL; INTRACELLULAR RECORDING; MALE; MODULATION; NERVE STIMULATION; NORMAL HUMAN; PRIORITY JOURNAL; SOMATOSENSORY CORTEX;

ADULT; CEREBRAL CORTEX; CROSS-OVER STUDIES; DOUBLE-BLIND METHOD; ELECTRIC STIMULATION; EVOKED POTENTIALS, SOMATOSENSORY; FEMALE; GABA MODULATORS; HUMANS; LORAZEPAM; MALE;

EID: 40649107357     PISSN: 10538119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2007.12.024     Document Type: Article

References (37)

1. Cauller L.J., and Kulics A.T. The neural basis of the behaviourally relevant N1 component of the somatosensory evoked potential in SI cortex of awake monkeys: evidence that backward cortical projections signal conscious touch sensation. Exp. Brain Res. 84 (1991) 607-619
2. Creutzfeldt O. Neuronal basis of EEG waves. In: Remond A. (Ed). Handbook of Electroencephalography and Clinical Neurophysiology vol. 2 (1974.), Elsevier, Amsterdam 2C6-2C55
3. Davies C.H., and Collingridge G.L. Paired-pulse depression of monosynaptic GABA-mediated inhibitory postsynaptic responses in rat hippocampus. J. Physiol. 424 (1990) 513-531
4. Debanne D., Guerineau N.C., Gähwiler B.H., and Thompson S.M. Paired-pulse facilitation and depression at unitary synapses in rat hippocampus: quantal fluctuation affects subsequent release. J. Physiol. 491 (1996) 163-176
5. B-receptor mediated effects in human and rat neocortical neurones in vitro. Neuropharmacol 38 (1999) 1755-1766
6. Deisz R.A., and Prince D.A. Frequency-dependent depression of inhibition in guinea-pig neocortex in vitro by GABAB receptor feed-back on GABA release. J. Physiol. 412 (1989) 513-541
7. Farrant M., and Nusser Z. Variations on an inhibitory theme: phasic and tonic activations of GABA(A) receptors. Nat. Rev. Neurosci. 6 (2005) 215-229
8. Forss N., Hari R., Salmelin R., Ahonen A., Hämäläinen M., Kajola M., Knuutila J., and Simola J. Activation of the human posterior parietal cortex by median nerve stimulation. Exp. Brain Res. 99 (1994) 309-315
9. Gardner E.P., and Constanzo R.M. Temporal integration of multiple-point stimuli in primary somatosensory cortical receptive fields of awake monkeys. J. Neurophysiol. 43 (1980) 444-4468
10. Hari R., Reinikainen K., Kaukoranta E., Hämäläinen M., Ilmoniemi R., Penttinen A., Salminen J., and Teszner D. Somatosensory evoked cerebral magnetic fields from SI and SII in man. Electroenceph. Clin. Neurophysiol. 57 (1984) 254-263
11. Haueisen J., Heuer T., Nowak H., Liepert J., Weiller C., Okada Y., and Curio G. The influence of lorazepam on somatosensory-evoked fast frequency (600 Hz) activity in MEG. Brain Res. 874 (2000) 10-14
12. Hsu F.C., and Smith S.S. Progesterone withdrawal reduces paired-pulse inhibition in rat hippocampus: dependence on GABA(A) receptor alpha4 subunit upregulation. J. Neurophysiol. 89 (2003) 186-198
13. Huttunen J., Hari R., and Leinonen L. Cerebral magnetic responses to stimulation of ulnar and median nerves. Electroenceph. Clin. Neurophysiol. 66 (1987) 391-400
14. Huttunen J., Ahlfors S., and Hari R. Interaction of afferent impulses at the primary sensorimotor cortex. Electroenceph. Clin. Neurophysiol. 72 (1992) 332-339
15. Huttunen J., Komssi S., and Lauronen L. Spatial dynamics of population activities at S1 after median and ulnar nerve stimulation revisited: an MEG study. NeuroImage 32 (2006) 1024-1031
16. Hämäläinen M., Hari R., Ilmoniemi R., Knuutila J., and Lounasmaa O. Magnetoencephalography-theory, instrumentation, and applications to noninvasive studies of the working human brain. Rev. Mod. Phys. 65 (1993) 413-497
17. Ikeda H., Wang Y., and Okada Y.C. Origins of the somatic N20 and high-frequency oscillations evoked by trigeminal stimulation in the piglets. Clin. Neurophysiol. 116 (2005) 827-841
18. Inui K., Wang X., Tamura Y., Kaneoke Y., and Kakigi R. Serial processing in the human somatosensory system. Cereb. Cortex 14 (2004) 851-857
19. Korvenoja A., Huttunen J., Salli E., Pohjonen H., Martinkauppi S., Palva M., et al. Activation of multiple cortical areas in response to somatosensory stimulation: combined magnetoencephalographic and functional magnetic resonance imaging. Hum. Brain Map. 8 (1999) 13-27
20. Krnjevic K., and Schwartz S. The action of γ-aminobutyric acid on cortical neurones. Exp. Brain Res. 3 (1967) 320-336
21. Lauronen L., Huttunen J., Kirveskari E., Wikstrom H., Sainio K., Autti T., et al. Enlarged SI and SII somatosensory evoked responses in the CLN5 form of neuronal ceroid lipofuscinosis. Clin. Neurophysiol. 113 (2002) 1491-1500
22. Li L., Murphy T.H., Hayden M.R., and Raymond L.A. Enhanced striatal NR2B-containing N-methyl-d-aspartate receptor-mediated synaptic currents in a mouse model of Huntington disease. J. Neurophysiol. 92 (2004) 2738-2746
23. Manganotti P., Tamburin S., Zanette G., and Fiaschi A. Hyperexcitable cortical responses in progressive myoclonic epilepsy: a TMS study. Neurology 57 (2001) 1793-1799
24. Mennerick S., and Zorumski C.F. Paired-pulse modulation of fast excitatory synaptic currents in microcultures of rat hippocampal neurons. J. Physiol. 488 (1995) 85-101
25. Mima T., Nagamine T., Nakamura K., and Shibasaki H. Attention modulates both primary and second somatosensory cortical activities in humans: a magnetoencephalographic study. J. Neurophysiol. 80 (1998) 2215-2221
26. Mochizuki H., Machii K., Terao Y., Furubayashi T., Hanajima R., Enomoto H., et al. Recovery function of and effects of hyperventilation on somatosensory evoked high-frequency oscillation in Parkinson's disease and myoclonus epilepsy. Neurosci. Res. 46 (2003) 485-492
27. Nacimiento A.C., Lux H.D., and Creutzfeldt O.D. Postsynaptische Potentiale von Nervenzellen des motorischen Cortex nach elektrischer Reizung spezifischer und unspezifischer Thalamuskerne. Pfluegers Arch. 281 (1964) 152-169
28. Naylor D.E., and Wasterlain C.G. GABA synapses and the rapid loss of inhibition to dentate gyrus granule cells after brief perforant path stimulation. Epilepsia 46 Suppl. 5 (2005) 142-147
29. Nikouline V.V., Wikström H., Linkenkaer-Hansen K., Kesäniemi M., Ilmoniemi R.J., and Huttunen J. Somatosensory evoked magnetic fields, relation to prestimulus mu rhythm. Clin. Neurophysiol. 111 (2000) 1227-1233
30. Porter J.T., and Nieves D. Presynaptic GABAB receptors modulate thalamic excitation of inhibitory and excitatory neurons in the mouse barrel cortex. J. Neurophysiol. 92 (2004) 2762-2770
31. Sarter M., and Schneider H.H. High density of benzodiazepine binding sites in the substantia innominata of the rat. Pharmacol. Biochem. Behav. 30 (1988) 679-682
32. Tesche C.D., and Karhu J. Somatosensory evoked magnetic fields arising from sources in the human cerebellum. Brain Res. 744 (1997) 23-31
33. Torres-Escalante J.L., Barral J.A., Ibarra-Villa M.D., Perez-Burgos A., Gongora-Alfaro J.L., and Pineda J.C. 5-HT1A, 5-HT2A, and GABAB receptors interact to modulate neurotransmitter release probability in layer 2/3 somatosensory rat cortex as evaluated by the paired-pulse protocol. J. Neurosci Res. 78 (2004) 268-278
34. Usdin M.T., Shelbourne P.F., Myers R.M., and Madison D.V. Impaired synaptic plasticity in mice carrying the Huntington's disease mutation. Hum. Mol. Genet. 8 (1999) 839-846
35. Vanni S., Rockstroh B., and Hari R. Cortical sources of human short-latency somatosensory evoked fields to median and ulnar nerve stimulation. Brain Res. 737 (1996) 25-33
36. Volkow N.D., Wang G.J., Hitzemann R., Fowler J.S., Pappas N., Lowrimore P., et al. Depression of thalamic metabolism by lorazepam is associated with sleepiness. Neuropsychopharmacology 12 (1995) 123-132
37. Wikström H., Huttunen J., Korvenoja A., Virtanen J., Salonen O., and Ilmoniemi R.J. Effects of interstimulus interval on somatosensory evoked magnetic fields, a hypothesis concerning SEF generation at the primary sensorimotor cortex. Electroenceph. Clin. Neurophysiol. 100 (1996) 479-487