Table of Contents Author Guidelines Submit a Manuscript
BioMed Research International
Volume 2015, Article ID 485709, 7 pages
http://dx.doi.org/10.1155/2015/485709
Research Article

Cholinergic Synaptic Transmissions Were Altered after Single Sevoflurane Exposure in Drosophila Pupa

1Department of Anesthesiology, Peking University Shenzhen Hospital, Shenzhen 518000, China
2Department of Anesthesiology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China
3Department of Anatomy and Neurobiology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou 510080, China
4Department of Rehabilitation, Shanghai First People’s Hospital, Shanghai 201620, China

Received 15 May 2014; Revised 6 November 2014; Accepted 6 November 2014

Academic Editor: Alfredo Conti

Copyright © 2015 Rongfa Chen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. X. Zhang, Z. Xue, and A. Sun, “Subclinical concentration of sevoflurane potentiates neuronal apoptosis in the developing C57BL/6 mouse brain,” Neuroscience Letters, vol. 447, no. 2-3, pp. 109–114, 2008. View at Publisher · View at Google Scholar · View at Scopus
  2. D. J. Culley, M. G. Baxter, R. Yukhananov, and G. Crosby, “Long-term impairment of acquisition of a spatial memory task following isoflurane -nitrous oxide anesthesia in rats,” Anesthesiology, vol. 100, no. 2, pp. 309–314, 2004. View at Publisher · View at Google Scholar · View at Scopus
  3. M. Satomoto, “Neonatal exposure to sevoflurane induces abnormal social behaviors and deficits in fear conditioning in mice,” Masui, vol. 59, pp. S196–S205, 2010. View at Google Scholar
  4. V. Jevtovic-Todorovic, R. E. Hartman, Y. Izumi et al., “Early exposure to common anesthetic agents causes widespread neurodegeneration in the developing rat brain and persistent learning deficits,” The Journal of Neuroscience, vol. 23, no. 3, pp. 876–882, 2003. View at Google Scholar · View at Scopus
  5. A. Fredriksson, E. Pontén, T. Gordh, and P. Eriksson, “Neonatal exposure to a combination of N-Methyl-D-aspartate and γ-aminobutyric acid type A receptor anesthetic agents potentiates apoptotic neurodegeneration and persistent behavioral deficits,” Anesthesiology, vol. 107, no. 3, pp. 427–436, 2007. View at Publisher · View at Google Scholar · View at Scopus
  6. Y. Shu, Z. Zhou, Y. Wan et al., “Nociceptive stimuli enhance anesthetic-induced neuroapoptosis in the rat developing brain,” Neurobiology of Disease, vol. 45, no. 2, pp. 743–750, 2012. View at Publisher · View at Google Scholar · View at Scopus
  7. G. K. Istaphanous, J. Howard, X. Nan et al., “Comparison of the neuroapoptotic properties of equipotent anesthetic concentrations of desflurane, isoflurane, or sevoflurane in neonatal mice,” Anesthesiology, vol. 114, no. 3, pp. 578–587, 2011. View at Publisher · View at Google Scholar · View at Scopus
  8. S. Bercker, B. Bert, P. Bittigau et al., “Neurodegeneration in newborn rats following propofol and sevoflurane anesthesia,” Neurotoxicity Research, vol. 16, no. 2, pp. 140–147, 2009. View at Publisher · View at Google Scholar · View at Scopus
  9. G. Liang, C. Ward, J. Peng, Y. Zhao, B. Huang, and H. Wei, “Isoflurane causes greater neurodegeneration than an equivalent exposure of sevoflurane in the developing brain of neonatal mice,” Anesthesiology, vol. 112, no. 6, pp. 1325–1334, 2010. View at Publisher · View at Google Scholar · View at Scopus
  10. G. Kostopanagiotou, K. Kalimeris, K. Kesidis et al., “Sevoflurane impairs post-operative olfactory memory but preserves olfactory function,” European Journal of Anaesthesiology, vol. 28, no. 1, pp. 63–68, 2011. View at Publisher · View at Google Scholar · View at Scopus
  11. J. Ishizeki, K. Nishikawa, K. Kubo, S. Saito, and F. Goto, “Amnestic concentrations of sevoflurane inhibit synaptic plasticity of hippocampal CA1 neurons through γ-aminobutyric acid-mediated mechanisms,” Anesthesiology, vol. 108, no. 3, pp. 447–456, 2008. View at Publisher · View at Google Scholar · View at Scopus
  12. R. Haseneder, S. Kratzer, L. von Meyer, M. Eder, E. Kochs, and G. Rammes, “Isoflurane and sevoflurane dose-dependently impair hippocampal long-term potentiation,” European Journal of Pharmacology, vol. 623, no. 1–3, pp. 47–51, 2009. View at Publisher · View at Google Scholar · View at Scopus
  13. M. T. Alkire, R. Gruver, J. Miller, J. R. McReynolds, E. L. Hahn, and L. Cahill, “Neuroimaging analysis of an anesthetic gas that blocks human emotional memory,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 5, pp. 1722–1727, 2008. View at Publisher · View at Google Scholar · View at Scopus
  14. A. P. A. S. Lima, K. Silva, C. M. Padovan, S. S. Almeida, and M. T. H. Fukuda, “Memory, learning, and participation of the cholinergic system in young rats exposed to environmental enrichment,” Behavioural Brain Research, vol. 259, pp. 247–252, 2014. View at Publisher · View at Google Scholar · View at Scopus
  15. M. Stepanichev, N. Lazareva, G. Tukhbatova, S. Salozhin, and N. Gulyaeva, “Transient disturbances in contextual fear memory induced by Aβ(25–35) in rats are accompanied by cholinergic dysfunction,” Behavioural Brain Research, vol. 259, pp. 152–157, 2014. View at Publisher · View at Google Scholar · View at Scopus
  16. Y.-S. Lee, A. Danandeh, J. Baratta, C.-Y. Lin, J. Yu, and R. T. Robertson, “Neurotrophic factors rescue basal forebrain cholinergic neurons and improve performance on a spatial learning test,” Experimental Neurology, vol. 249, pp. 178–186, 2013. View at Publisher · View at Google Scholar · View at Scopus
  17. M. Ng, R. D. Roorda, S. Q. Lima, B. V. Zemelman, P. Morcillo, and G. Miesenböck, “Transmission of olfactory information between three populations of neurons in the antennal lobe of the fly,” Neuron, vol. 36, no. 3, pp. 463–474, 2002. View at Publisher · View at Google Scholar · View at Scopus
  18. H. Gu and D. K. O'Dowd, “Whole cell recordings from brain of adult drosophila,” Journal of Visualized Experiments, no. 6, article e248, 2007. View at Publisher · View at Google Scholar · View at Scopus
  19. H. Gu and D. K. O'Dowd, “Cholinergic synaptic transmission in adult Drosophila Kenyon cells in situ,” Journal of Neuroscience, vol. 26, no. 1, pp. 265–272, 2006. View at Publisher · View at Google Scholar · View at Scopus
  20. T. Yokoyama, K. Minami, Y. Sudo et al., “Effects of sevoflurane on voltage-gated sodium channel Nav1.8, Nav1.7, and Nav1.4 expressed in Xenopus oocytes,” Journal of Anesthesia, vol. 25, no. 4, pp. 609–613, 2011. View at Publisher · View at Google Scholar · View at Scopus
  21. C. R. L. Simkus and C. Stricker, “The contribution of intracellular calcium stores to mEPSCs recorded in layer II neurones of rat barrel cortex,” Journal of Physiology, vol. 545, no. 2, pp. 521–535, 2002. View at Publisher · View at Google Scholar · View at Scopus
  22. J. Yang, L. An, Y. Yao, Z. Yang, and T. Zhang, “Melamine impairs spatial cognition and hippocampal synaptic plasticity by presynaptic inhibition of glutamatergic transmission in infant rats,” Toxicology, vol. 289, no. 2-3, pp. 167–174, 2011. View at Publisher · View at Google Scholar · View at Scopus
  23. B. R. Sastry and L. S. Bhagavatula, “Quantal release of transmitter at a central synapse,” Neuroscience, vol. 75, no. 4, pp. 987–992, 1996. View at Publisher · View at Google Scholar · View at Scopus
  24. S. A. Kushner, Y. Elgersma, G. G. Murphy et al., “Modulation of presynaptic plasticity and learning by the H-ras/extracellular signal-regulated kinase/synapsin I signaling pathway,” Journal of Neuroscience, vol. 25, no. 42, pp. 9721–9734, 2005. View at Publisher · View at Google Scholar · View at Scopus
  25. Y. Yang, G. J. Xiong, D. F. Yu et al., “Acute low-dose melamine affects hippocampal synaptic plasticity and behavior in rats,” Toxicology Letters, vol. 214, no. 1, pp. 63–68, 2012. View at Publisher · View at Google Scholar · View at Scopus
  26. D. Lee, H. Su, and D. K. O'Dowd, “GABA receptors containing Rdl subunits mediate fast inhibitory synaptic transmission in Drosophila neurons,” The Journal of Neuroscience, vol. 23, no. 11, pp. 4625–4634, 2003. View at Google Scholar · View at Scopus
  27. M. D. Amaral and L. Pozzo-Miller, “Intracellular Ca2+ stores and Ca2+ influx are both required for BDNF to rapidly increase quantal vesicular transmitter release,” Neural Plasticity, vol. 2012, Article ID 203536, 10 pages, 2012. View at Publisher · View at Google Scholar · View at Scopus