Inhibition of propofol on single neuron and neuronal ensemble activity in prefrontal cortex of rats during working memory task

Behavioural Brain Research

Volumn 270, Issue , 2014, Pages 270-276

  Xu, Xinyu ^a   Tian, Yu ^a   Wang, Guolin ^a   Tian, Xin ^a  

^a TIANJIN MEDICAL UNIVERSITY   (China)

Author keywords

Neuron ensemble; Prefrontal cortex; Propofol; Single neuron; Working memory

Indexed keywords

PROPOFOL; INTRAVENOUS ANESTHETIC AGENT;

ACCURACY; ADULT; ANESTHESIA INDUCTION; ANIMAL BEHAVIOR; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN NERVE CELL; CONTROLLED STUDY; DRUG EFFECT; ELECTROENCEPHALOGRAM; MALE; MEMORY DISORDER; NERVE CELL; NERVE CELL EXCITABILITY; NEURONAL ENSEMBLE; NONHUMAN; PREFRONTAL CORTEX; PRIORITY JOURNAL; RAT; TASK PERFORMANCE; WORKING MEMORY IMPAIRMENT; ACTION POTENTIAL; ANIMAL; CYTOLOGY; DRUG EFFECTS; MAZE TEST; PHYSIOLOGY; REWARD; SHORT TERM MEMORY; SPRAGUE DAWLEY RAT; TIME;

ACTION POTENTIALS; ANESTHETICS, INTRAVENOUS; ANIMALS; BEHAVIOR, ANIMAL; MALE; MAZE LEARNING; MEMORY, SHORT-TERM; NEURONS; PREFRONTAL CORTEX; PROPOFOL; RATS; RATS, SPRAGUE-DAWLEY; REWARD; TIME FACTORS;

EID: 84901927334     PISSN: 01664328     EISSN: 18727549     Source Type: Journal    
DOI: 10.1016/j.bbr.2014.05.034     Document Type: Article

References (63)

1. Barr G., Anderson R.E., Owall A., Jakobsson J.G. Being awake intermittently during propofol-induced hypnosis: a study of BIS, explicit and implicit memory. Acta Anaesthesiol Scand 2001, 45:834-838.
2. Monk T.G., Weldon B.C., Garvan C.W., Dede D.E., van der Aa M.T., Heilman K.M., et al. Predictors of cognitive dysfunction after major noncardiac surgery. Anesthesiology 2008, 108:18-30.
3. Wilder R.T., Flick R.P., Sprung J., Katusic S.K., Barbaresi W.J., Mickelson C., et al. Early exposure to anesthesia and learning disabilities in a population-based birth cohort. Anesthesiology 2009, 110:796-804.
4. Erasso D.M., Chaparro R.E., Quiroga Del Rio C.E., Karlnoski R., Camporesi E.M., Saporta S. Quantitative assessment of new cell proliferation in the dentate gyrus and learning after isoflurane or propofol anesthesia in young and aged rats. Brain Res 2012, 1441:38-46.
5. Baddeley A. Working memory. Science 1992, 255:556-559.
6. Baddeley A. The episodic buffer: a new component of working memory. Trends Cogn Sci 2000, 4:417-423.
7. Ramos B.P., Birnbaum S.G., Lindenmayer I., Newton S.S., Duman R.S., Arnsten A.F. Dysregulation of protein kinase a signaling in the aged prefrontal cortex: new strategy for treating age-related cognitive decline. Neuron 2003, 40:835-845.
8. Bannerman D.M., Niewoehner B., Lyon L., Romberg C., Schmitt W.B., Taylor A., et al. NMDA receptor subunit NR2A is required for rapidly acquired spatial working memory but not incremental spatial reference memory. J Neurosci 2008, 28:3623-3630. (the official journal of the Society for Neuroscience).
9. Vann S.D. Gudden's ventral tegmental nucleus is vital for memory: re-evaluating diencephalic inputs for amnesia. Brain: J Neurol 2009, 132:2372-2384.
10. Kolb B. Animal models for human PFC-related disorders. Prog Brain Res 1990, 85:501-519.
11. Fuster J.M. Network memory. Trends Neurosci 1997, 20:451-459.
12. Fuster J.M., Alexander G.E. Neuron activity related to short-term memory. Science 1971, 173:652-654.
13. Kubota K., Niki H. Prefrontal cortical unit activity and delayed alternation performance in monkeys. J Neurophysiol 1971, 34:337-347.
14. Funahashi S., Bruce C.J., Goldman-Rakic P.S. Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex. J Neurophysiol 1989, 61:331-349.
15. Miller E.K., Erickson C.A., Desimone R. Neural mechanisms of visual working memory in prefrontal cortex of the macaque. J Neurosci 1996, 16:5154-5167. (the official journal of the Society for Neuroscience).
16. Hutzler M., Lambacher A., Eversmann B., Jenkner M., Thewes R., Fromherz P. High-resolution multitransistor array recording of electrical field potentials in cultured brain slices. J Neurophysiol 2006, 96:1638-1645.
17. Eytan D., Marom S. Dynamics and effective topology underlying synchronization in networks of cortical neurons. J Neurosci 2006, 26:8465-8476. (the official journal of the Society for Neuroscience).
18. Berdondini L., Imfeld K., Maccione A., Tedesco M., Neukom S., Koudelka-Hep M., et al. Active pixel sensor array for high spatio-temporal resolution electrophysiological recordings from single cell to large scale neuronal networks. Lab Chip 2009, 9:2644-2651.
19. Frey U., Egert U., Heer F., Hafizovic S., Hierlemann A. Microelectronic system for high-resolution mapping of extracellular electric fields applied to brain slices. Biosens Bioelectron 2009, 24:2191-2198.
20. Hochberg L.R., Serruya M.D., Friehs G.M., Mukand J.A., Saleh M., Caplan A.H., et al. Neuronal ensemble control of prosthetic devices by a human with tetraplegia. Nature 2006, 442:164-171.
21. Blanche T.J., Spacek M.A., Hetke J.F., Swindale N.V. Polytrodes: high-density silicon electrode arrays for large-scale multiunit recording. J Neurophysiol 2005, 93:2987-3000.
22. Miller E.K., Cohen J.D. An integrative theory of prefrontal cortex function. Annu Rev Neurosci 2001, 24:167-202.
23. Wang X.J. Synaptic reverberation underlying mnemonic persistent activity. Trends Neurosci 2001, 24:455-463.
24. DeCoteau W.E., Thorn C., Gibson D.J., Courtemanche R., Mitra P., Kubota Y., et al. Oscillations of local field potentials in the rat dorsal striatum during spontaneous and instructed behaviors. J Neurophysiol 2007, 97:3800-3805.
25. Devilbiss D.M., Berridge C.W. Cognition-enhancing doses of methylphenidate preferentially increase prefrontal cortex neuronal responsiveness. Biol Psychiatry 2008, 64:626-635.
26. Su Y.L., Huang J., Wang N., Wang J.Y., Luo F. The effects of morphine on basal neuronal activities in the lateral and medial pain pathways. Neurosci Lett 2012, 525:173-178.
27. Zhu L., Lai Y.C., Hoppensteadt F.C., He J. Characterization of neural interaction during learning and adaptation from spike-train data. Math Biosci Eng: MBE 2005, 2:1-23.
28. Bressler S.L., Seth A.K. Wiener-Granger causality: a well established methodology. NeuroImage 2011, 58:323-329.
29. Brovelli A., Ding M., Ledberg A., Chen Y., Nakamura R., Bressler S.L. Beta oscillations in a large-scale sensorimotor cortical network: directional influences revealed by Granger causality. Proc Nat Acad Sci USA 2004, 101:9849-9854.
30. Dhamala M., Rangarajan G., Ding M. Analyzing information flow in brain networks with nonparametric Granger causality. NeuroImage 2008, 41:354-362.
31. Seth A.K. A MATLAB toolbox for Granger causal connectivity analysis. J Neurosci Methods 2010, 186:262-273.
32. Bullmore E., Sporns O. Complex brain networks: graph theoretical analysis of structural and functional systems. Nat Rev Neurosci 2009, 10:186-198.
33. Chudasama Y., Robbins T.W. Functions of frontostriatal systems in cognition: comparative neuropsychopharmacological studies in rats, monkeys and humans. Biol Psychol 2006, 73:19-38.
34. Eichenbaum H. Hippocampus: cognitive processes and neural representations that underlie declarative memory. Neuron 2004, 44:109-120.
35. Lee M.G., Manns I.D., Alonso A., Jones B.E. Sleep-wake related discharge properties of basal forebrain neurons recorded with micropipettes in head-fixed rats. J Neurophysiol 2004, 92:1182-1198.
36. Vertes R.P. Interactions among the medial prefrontal cortex, hippocampus and midline thalamus in emotional and cognitive processing in the rat. Neuroscience 2006, 142:1-20.
37. Thierry A.M., Gioanni Y., Degenetais E., Glowinski J. Hippocampo-prefrontal cortex pathway: anatomical and electrophysiological characteristics. Hippocampus 2000, 10:411-419.
38. Zhang H.H., Wang M.Y. [Inhibitory effects of propofol on supraoptic nucleus neurons of rat hypothalamus in vitro]. Sheng Li Xue Bao 2012, 64:163-169.
39. Erasso D.M., Camporesi E.M., Mangar D., Saporta S. Effects of isoflurane or propofol on postnatal hippocampal neurogenesis in young and aged rats. Brain Res 2013, 1530:1-12.
40. Kaisti K.K., Metsahonkala L., Teras M., Oikonen V., Aalto S., Jaaskelainen S., et al. Effects of surgical levels of propofol and sevoflurane anesthesia on cerebral blood flow in healthy subjects studied with positron emission tomography. Anesthesiology 2002, 96:1358-1370.
41. Hentschke H., Schwarz C., Antkowiak B. Neocortex is the major target of sedative concentrations of volatile anaesthetics: strong depression of firing rates and increase of GABAA receptor-mediated inhibition. Eur J Neurosci 2005, 21:93-102.
42. Solt K., Forman S.A. Correlating the clinical actions and molecular mechanisms of general anesthetics. Curr Opin Anaesthesiol 2007, 20:300-306.
43. Lee I.H., Culley D.J., Baxter M.G., Xie Z., Tanzi R.E., Crosby G. Spatial memory is intact in aged rats after propofol anesthesia. Anesth Analg 2008, 107:1211-1215.
44. Johnson S.A., Young C., Olney J.W. Isoflurane-induced neuroapoptosis in the developing brain of nonhypoglycemic mice. J Neurosurg Anesthesiol 2008, 20:21-28.
45. Stratmann G., May L.D., Sall J.W., Alvi R.S., Bell J.S., Ormerod B.K., et al. Effect of hypercarbia and isoflurane on brain cell death and neurocognitive dysfunction in 7-day-old rats. Anesthesiology 2009, 110:849-861.
46. Murphy K.L., Baxter M.G. Long-term effects of neonatal single or multiple isoflurane exposures on spatial memory in rats. Front Neurol 2013, 4:87.
47. Lei X., Zhang W., Liu T., Xiao H., Liang W., Xia W., et al. Perinatal supplementation with omega-3 polyunsaturated fatty acids improves sevoflurane-induced neurodegeneration and memory impairment in neonatal rats. PLoS One 2013, 8:e70645.
48. Kodama M., Satoh Y., Otsubo Y., Araki Y., Yonamine R., Masui K., et al. Neonatal desflurane exposure induces more robust neuroapoptosis than do isoflurane and sevoflurane and impairs working memory. Anesthesiology 2011, 115:979-991.
49. Cattano D., Young C., Straiko M.M., Olney J.W. Subanesthetic doses of propofol induce neuroapoptosis in the infant mouse brain. Anesth Analg 2008, 106:1712-1714.
50. Kahraman S., Zup S.L., McCarthy M.M., Fiskum G. GABAergic mechanism of propofol toxicity in immature neurons. J Neurosurg Anesthesiol 2008, 20:233-240.
51. Whittington R.A., Virag L., Marcouiller F., Papon M.A., El Khoury N.B., Julien C., et al. Propofol directly increases tau phosphorylation. PLoS One 2011, 6:e16648.
52. Franks N.P., Lieb W.R. Molecular and cellular mechanisms of general anaesthesia. Nature 1994, 367:607-614.
53. Krasowski M.D., Harrison N.L. General anaesthetic actions on ligand-gated ion channels. Cell Mol Life Sci: CMLS 1999, 55:1278-1303.
54. Whittington M.A., Traub R.D. Interneuron diversity series: inhibitory interneurons and network oscillations in vitro. Trends Neurosci 2003, 26:676-682.
55. Mody I., Pearce R.A. Diversity of inhibitory neurotransmission through GABA(A) receptors. Trends Neurosci 2004, 27:569-575.
56. Fagiolini M., Fritschy J.M., Low K., Mohler H., Rudolph U., Hensch T.K. Specific GABAA circuits for visual cortical plasticity. Science 2004, 303:1681-1683.
57. Constantinidis C., Williams G.V., Goldman-Rakic P.S. A role for inhibition in shaping the temporal flow of information in prefrontal cortex. Nat Neurosci 2002, 5:175-180.
58. Swadlow H.A. Fast-spike interneurons and feedforward inhibition in awake sensory neocortex. Cereb Cortex 2003, 13:25-32.
59. Sonner J.M., Antognini J.F., Dutton R.C., Flood P., Gray A.T., Harris R.A., et al. Inhaled anesthetics and immobility: mechanisms, mysteries, and minimum alveolar anesthetic concentration. Anesth Analg 2003, 97:718-740.
60. + current and I(h) by an inhalational anaesthetic and neurotransmitters in rat brainstem motoneurones. J Physiol 2002, 541:717-729.
61. Robinson R.B., Siegelbaum S.A. Hyperpolarization-activated cation currents: from molecules to physiological function. Annu Rev Physiol 2003, 65:453-480.
62. + channels. Anesthesiology 2001, 95:1013-1021.
63. Westphalen R.I., Hemmings H.C. Effects of isoflurane and propofol on glutamate and GABA transporters in isolated cortical nerve terminals. Anesthesiology 2003, 98:364-372.