The DOI matches its Crossref record, with a small difference in title or year; 24 of the 24 references it cites were found in a registry or an index.
Breakdown of Neural Function under Isoflurane Anesthesia: In Vivo, Multineuronal Imaging in Caenorhabditis elegans
Open accessAbstract
Editor’s Perspective: What We Already Know about This Topic: What This Article Tells Us That Is New: Background: Previous work on the action of volatile anesthetics has focused at either the molecular level or bulk neuronal measurement such as electroencephalography or functional magnetic resonance imaging. There is a distinct gulf in resolution at the level of cellular signaling within neuronal systems. The authors hypothesize that anesthesia is caused by induced dyssynchrony in cellular signaling rather than suppression of individual neuron activity. Methods: Employing confocal microscopy and Caenorhabditis elegans expressing the calcium-sensitive fluorophore GCaMP6s in specific command neurons, the authors measure neuronal activity noninvasively and in parallel within the behavioral circuit controlling forward and reverse crawling. The authors compare neuronal dynamics and coordination in a total of 31 animals under atmospheres of 0, 4, and 8% isoflurane. Results: When not anesthetized, the interneurons controlling forward or reverse crawling occupy two possible states, with the activity of the “reversal” neurons AVA, AVD, AVE, and RIM strongly intercorrelated, and the “forward” neuron AVB anticorrelated. With exposure to 4% isoflurane and onset of physical quiescence, neuron activity wanders rapidly and erratically through indeterminate states. Neuron dynamics shift toward higher frequencies, and neuron pair correlations within the system are reduced. At 8% isoflurane, physical quiescence continues as neuronal signals show diminished amplitude with little correlation between neurons. Neuronal activity was further studied using statistical tools from information theory to quantify the type of disruption caused by isoflurane. Neuronal signals become noisier and more disordered, as measured by an increase in the randomness of their activity (Shannon entropy). The coordination of the system, measured by whether information exhibited in one neuron is also exhibited in other neurons (multiinformation), decreases significantly at 4% isoflurane ( P = 0.00015) and 8% isoflurane ( P = 0.0028). Conclusions: The onset of anesthesia corresponds with high-frequency randomization of individual neuron activity coupled with induced dyssynchrony and loss of coordination between neurons that disrupts functional signaling.
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“isoflurane was found to induce desynchronization of neuronal dynamics and reduced (surrogates of) information exchange [157], which is strikingly similar to EEG-based phenotypes in humans.”
From The Biology of General Anesthesia from Paramecium to Primate (2019) · cites this paper as [157]
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Ultrasensitive fluorescent proteins for imaging neuronal activity
Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474
The structure of the nervous system of the nematode Caenorhabditis elegans
White, J. G., Southgate, E., Thomson, J. N., & Brenner, S. (1986) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1986.0056 · Cited by 5,589
Consciousness as integrated information: a provisional manifesto
Tononi, G. (2008) · The Biological Bulletin · doi:10.2307/25470707 · Cited by 1,529
The neural circuit for touch sensitivity in Caenorhabditis elegans
Chalfie, M., Sulston, J., White, J., Southgate, E., Thomson, J., & Brenner, S. (1985) · The Journal of Neuroscience · doi:10.1523/jneurosci.05-04-00956.1985 · Cited by 1,093
A circuit for navigation in Caenorhabditis elegans
Gray, J. M., Hill, J. J., & Bargmann, C. I. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409009101 · Cited by 811
Global Brain Dynamics Embed the Motor Command Sequence of Caenorhabditis elegans
Kato, S., Kaplan, H. S., Schrödel, T., Skora, S., Lindsay, T. H., Yemini, E., Lockery, S. R., & Zimmer, M. (2015) · Cell · doi:10.1016/j.cell.2015.09.034 · Cited by 536
Numerical Differentiation of Noisy, Nonsmooth Data
Chartrand, R. (2011) · ISRN Applied Mathematics · doi:10.5402/2011/164564 · Cited by 476
Dietary choice behavior in Caenorhabditis elegans
Shtonda, B. B., & Avery, L. (2005) · Journal of Experimental Biology · doi:10.1242/jeb.01955 · Cited by 435
Disruption of frontal-parietal communication by ketamine, propofol, and sevoflurane
Lee, U., Ku, S., Noh, G., Baek, S., Choi, B., & Mashour, G. A. (2013) · Anesthesiology · doi:10.1097/aln.0b013e31829103f5 · Cited by 426
Whole-brain calcium imaging with cellular resolution in freely behaving Caenorhabditis elegans
Nguyen, J. P., Shipley, F. B., Linder, A. N., Plummer, G. S., Liu, M., Setru, S. U., Shaevitz, J. W., & Leifer, A. M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1507110112 · Cited by 398
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The Biology of General Anesthesia from Paramecium to Primate
Kelz, M. B., & Mashour, G. A. (2019) · Current Biology · doi:10.1016/j.cub.2019.09.071 · Cited by 151
Open Reimplementation of the BIS Algorithms for Depth of Anesthesia
Connor, C. W. (2022) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000006119 · Cited by 61
Self-citationWirak, G. S., Florman, J., Alkema, M. J., Connor, C. W., & Gabel, C. V. (2022) · eLife · doi:10.7554/elife.72135 · Cited by 37
Self-citationDivergent Neural Activity in the VLPO During Anesthesia and Sleep
Luo, M., Fei, X., Liu, X., Jin, Z., Wang, Y., & Xu, M. (2022) · Advanced Science · doi:10.1002/advs.202203395 · Cited by 37
Collapse of Global Neuronal States in Caenorhabditis elegans under Isoflurane Anesthesia
Awal, M. R., Wirak, G. S., Gabel, C. V., & Connor, C. W. (2020) · Anesthesiology · doi:10.1097/aln.0000000000003304 · Cited by 25
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Metadata
- Authors
- Awal, M. R., Austin, D., Florman, J., Alkema, M., Gabel, C. V., & Connor, C. W.
- Affiliations
- Boston University (US)
- Corresponding author
- Connor, Christopher W.
- Venue
- Anesthesiology
- Published
- 2018-10
- Volume
- 129
- Issue
- 4
- Pages
- 733-743
- ISSN
- 0003-3022 (ISSN-L)
- PMC
- PMC6148381
- OpenAlex
- W2883689126
- Cited by
- 22
- References
- 24
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 3 · 2023: 4 · 2022: 4 · 2021: 2 · 2020: 3 · 2019: 1 · 2018: 1
- FWCI
- 1.04
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Anesthesiology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- The Journal of the American Medical Association (JAMA) Network (American Medical Association) (submittedVersion)
- Funders
- National Institutes of Health (UL1TR001430)
- National Institute of General Medical Sciences (R01GM084491, R01GM121457)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Health Sciences › Medicine › Anesthesiology and Pain Medicine › Anesthesia and Sedative Agents
- Life Sciences › Neuroscience › Developmental Neuroscience › Anesthesia and Neurotoxicity Research
- Keywords
- isoflurane, volatile anesthetics, anesthetic mechanisms, neuronal signaling, dyssynchrony, Caenorhabditis elegans, crawling behavior, command neurons, Ava, AVE, RIM, GCaMP6s, Shannon entropy, information theory
- MeSH terms
- Animals, Female, Interneurons, Isoflurane, Male, Nerve Net, Neurons, Caenorhabditis elegans, Microscopy, Confocal, Anesthetics, Inhalation, Animals, Genetically Modified, Optical Imaging
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