AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (961.8 KB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Review Article | Open Access

Brain gamma rhythm and potential treatment of neurodegenerative disease

Jianhua Zhao1,2Ailin Du3,4Chengbiao Lu2,3,4( )
Department of Neurology, First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, Henan, China;
Henan Joint International Research Laboratory of Neurorestoratology for Senile Dementia / Henan Key Laboratory of Neurorestoratology, Weihui 453100, Henan, China;
Henan International Joint Laboratory for Non-invasive Brain Modulation / Key Laboratory for Brain Research of Henan Province, Xinxiang Medical University, Xinxiang 453003, Henan, China;
Department of Physiology and Neurophysiology, Xinxiang Medical University, Xinxiang 453003, Henan, China
Show Author Information

Abstract

In this mini-review, we illustrate the brain network oscillations in different brain areas, including the medial septal diagonal band complex (MSDB) and hippocampus, especially at gamma frequency bands (γ, 30–80 Hz) and theta frequency bands (θ, 4–12 Hz), and their induction and modulation by physical stimulation, such as light and sound, and pharmacological stimulation with agents such as agonists of the kainite subunit ionotropic glutamate receptor, metabotropic glutamate receptor, metabotropic cholinergic receptor, and nicotinic cholinergic receptor. Recent findings demonstrate that boosting gamma oscillations in specific brain areas appears to be able to restore cognitive function and reduce relative pathology in neurodegenerative diseases, such as Alzheimer’s disease. Thus, exploration of strategies to enhance or restore impaired gamma oscillations may be a new and effective method to improve the conditions in these devastating diseases.

References

[1]
A Fisahn, FG Pike, EH Buhl, et al. Cholinergic induction of network oscillations at 40 Hz in the hippocampus in vitro. Nature. 1998, 394(6689): 186-189.
[2]
G Buzsáki, A Draguhn. Neuronal oscillations in cortical networks. Science. 2004, 304(5679): 1926-1929.
[3]
T Womelsdorf, P Fries. The role of neuronal synchronization in selective attention. Curr Opin Neurobiol. 2007, 17(2): 154-160.
[4]
T Akam, DM Kullmann. Oscillatory multiplexing of population codes for selective communication in the mammalian brain. Nat Rev Neurosci. 2014, 15(2): 111-122.
[5]
J Csicsvari, B Jamieson, KD Wise, et al. Mechanisms of gamma oscillations in the hippocampus of the behaving rat. Neuron. 2003, 37(2): 311-322.
[6]
MF Carr, MP Karlsson, LM Frank. Transient slow gamma synchrony underlies hippocampal memory replay. Neuron. 2012, 75(4): 700-713.
[7]
H Pastoll, L Solanka, MC van Rossum, et al. Feedback inhibition enables θ-nested γ oscillations and grid firing fields. Neuron. 2013, 77(1): 141-154.
[8]
G Chen, Y Zhang, X Li, et al. Distinct inhibitory circuits orchestrate cortical beta and gamma band oscillations. Neuron. 2017, 96(6): 1403-1418.e6.
[9]
T Koenig, L Prichep, T Dierks, et al. Decreased EEG synchronization in Alzheimer’s disease and mild cognitive impairment. Neurobiol Aging. 2005, 26(2): 165-171.
[10]
U Smailovic, T Koenig, I Kåreholt, et al. Quantitative EEG power and synchronization correlate with Alzheimer’s disease CSF biomarkers. Neurobiol Aging. 2018, 63: 88-95.
[11]
G Fuggetta, MA Bennett, PA Duke, et al. Quantitative electroencephalography as a biomarker for proneness toward developing psychosis. Schizophr Res. 2014, 153(1–3): 68-77.
[12]
PJ Fitzgerald, BO Watson. Gamma oscillations as a biomarker for major depression: an emerging topic. Transl Psychiatry. 2018, 8(1): 177.
[13]
TH Zhou, NE Mueller, KM Spencer, et al. Auditory steady state response deficits are associated with symptom severity and poor functioning in patients with psychotic disorder. Schizophr Res. 2018, 201: 278-286.
[14]
HF Iaccarino, AC Singer, AJ Martorell, et al. Gamma frequency entrainment attenuates amyloid load and modifies microglia. Nature. 2017, 540(7632): 230.
[15]
AJ Martorell, AL Paulson, HJ Suk, et al. Multi- sensory gamma stimulation ameliorates Alzheimer’s- associated pathology and improves cognition. Cell. 2019, 177(2): 256-271.e22.
[16]
A Fisahn, A Contractor, RD Traub, et al. Distinct roles for the kainate receptor subunits GluR5 and GluR6 in kainate-induced hippocampal gamma oscillations. J Neurosci. 2004, 24(43): 9658-9668.
[17]
MO Cunningham, CH Davies, EH Buhl, et al. Gamma oscillations induced by kainate receptor activation in the entorhinal cortex in vitro. J Neurosci. 2003, 23(30): 9761-9769.
[18]
CB Lu, JG Jefferys, EC Toescu, et al. In vitro hippocampal gamma oscillation power as an index of in vivo CA3 gamma oscillation strength and spatial reference memory. Neurobiol Learn Mem. 2011, 95(3): 221-230.
[19]
CB Lu, Z Henderson. Nicotine induction of theta frequency oscillations in rodent hippocampus in vitro. Neuroscience. 2010, 166(1): 84-93.
[20]
Y Wang, Z Wang, J Wang, et al. The modulation of nicotinic acetylcholine receptors on the neuronal network oscillations in rat hippocampal CA3 area. Sci Rep. 2015, 5: 9493.
[21]
JG Wang, XL He, F Guo, et al. Multiple kinases involved in the nicotinic modulation of gamma oscillations in the rat hippocampal CA3 area. Front Cell Neurosci. 2017, 11: 57.
[22]
EH Buhl, G Tamás, A Fisahn. Cholinergic activation and tonic excitation induce persistent gamma oscillations in mouse somatosensory cortex in vitro. J Physiol. 1998, 513(1): 117-126.
[23]
RM Yoder, KC Pang. Involvement of GABAergic and cholinergic medial septal neurons in hippocampal theta rhythm. Hippocampus. 2005, 15(3): 381-392.
[24]
SE Rubio, VF Germán, M Albert, et al. Accelerated aging of the GABAergic septohippocampal pathway and decreased hippocampal rhythms in a mouse model of Alzheimer’s disease. FASEB J. 2012, 26(11): 4458-4467.
[25]
HL Garner, MA Whittington, Z Henderson. Induction by kainate of theta frequency rhythmic activity in the rat medial septum-diagonal band complex in vitro. J Physiol. 2005, 564(Pt 1): 83-102.
[26]
A Sirota, S Montgomery, S Fujisawa, et al. Entrainment of neocortical neurons and gamma oscillations by the hippocampal theta rhythm. Neuron. 2008, 60(4): 683-697.
[27]
Y Wang, J Wang, G Ouyang, et al. Co-activation of nAChR and mGluR induces γ oscillation in rat medial septum diagonal band of Broca slices. Acta Pharmacol Sin. 2014, 35(2): 175-184.
[28]
CB Lu, G Ouyang, Z Henderson, et al. Induction of theta-frequency oscillations in the rat medial septal diagonal band slice by metabotropic glutamate receptor agonists. Neuroscience. 2011, 177: 1-11.
[29]
CZ Li, ZY Guo, YL Wang, et al. A model of synaptic plasticity: activation of mGluR I induced long-term theta oscillations in medial septal diagonal band of rat brain slice. Neurol Sci. 2014, 35(4): 551-557.
Journal of Neurorestoratology
Pages 26-31
Cite this article:
Zhao J, Du A, Lu C. Brain gamma rhythm and potential treatment of neurodegenerative disease. Journal of Neurorestoratology, 2020, 8(1): 26-31. https://doi.org/10.26599/JNR.2020.9040002

855

Views

46

Downloads

5

Crossref

4

Web of Science

0

Scopus

Altmetrics

Received: 31 October 2019
Revised: 11 December 2019
Accepted: 08 January 2020
Published: 05 March 2020
© The authors 2020

This article is published with open access at http://jnr.tsinghuajournals.com

Return