Biological Barriers and Severe Mental illness: Potential Novel Interventions
Research Article


DOI:
https://doi.org/10.58372/2835-6276.1334Keywords:
gut microbes, Membrane Lipid Replacement, Oscillations, EEG gamma waves, severe mental illnessAbstract
Life is dependent on the separation of body compartments from each other and the environment. The permeability of biological barriers, including the gastrointestinal and blood-brain, depends on the integrity of cell membranes and intercellular tight junctions.
Severe mental illness is characterized by premature cellular senescence and subsequent gray matter loss in the central nervous system. Senescence-induced gut barrier disruption enables microbial migration outside the gastrointestinal tract. Systemic immune responses to gut microorganisms or their molecules may lead to neuroinflammation and the subsequent pathology.
This review discusses cellular senescence and microbial migration outside of the gastrointestinal tract along with potential strategies for restoring the gut barrier homeostasis. These approaches include membrane lipid replacement, gamma wave entrainment, red light therapy, and pulsed electromagnetic field therapy.
References
Yu M, Wang Q, Ma Y, Li L, Yu K, Zhang Z, Chen G, Li X, Xiao W, Xu P, Yang H. Aryl Hydrocarbon Receptor Activation Modulates Intestinal Epithelial Barrier Function by Maintaining Tight Junction Integrity. Int J Biol Sci. 2018 Jan 11;14(1):69-77. doi: 10.7150/ijbs.22259.
Nacarino-Palma A, Rico-Leo EM, Campisi J, Ramanathan A, González-Rico FJ, Rejano-Gordillo CM, Ordiales-Talavero A, Merino JM, Fernández-Salguero PM. Aryl hydrocarbon receptor blocks aging-induced senescence in the liver and fibroblast cells. Aging (Albany NY). 2022 May 26;14(10):4281-4304. doi: 10.18632/aging.204103.
Greene C, Hanley N, Campbell M. Blood-brain barrier associated tight junction disruption is a hallmark feature of major psychiatric disorders. Transl Psychiatry. 2020 Nov 2;10(1):373. doi: 10.1038/s41398-020-01054-3.
Sienkiewicz M, Sroka K, Binienda A, Jurk D, Fichna J. A new face of old cells: An overview about the role of senescence and telomeres in inflammatory bowel diseases. Ageing Res Rev. 2023 Nov;91:102083. doi: 10.1016/j.arr.2023.102083.
Papanastasiou E, Gaughran F, Smith S. Schizophrenia as segmental progeria. J R Soc Med. 2011 Nov;104(11):475-84. doi: 10.1258/jrsm.2011.110051. PMID: 22048679
Sung KY, Zhang B, Wang HE, Bai YM, Tsai SJ, Su TP, Chen TJ, Hou MC, Lu CL, Wang YP, Chen MH. Schizophrenia and risk of new-onset inflammatory bowel disease: a nationwide longitudinal study. Aliment Pharmacol Ther. 2022 May;55(9):1192-1201. doi: 10.1111/apt.16856. E
Wiley CD, Velarde MC, Lecot P, Liu S, Sarnoski EA, Freund A, Shirakawa K, Lim HW, Davis SS, Ramanathan A, Gerencser AA, Verdin E, Campisi J. Mitochondrial Dysfunction Induces Senescence with a Distinct Secretory Phenotype. Cell Metab. 2016 Feb 9;23(2):303-14. doi: 10.1016/j.cmet.2015.11.011.
Marx W, McGuinness AJ, Rocks T, Ruusunen A, Cleminson J, Walker AJ, Gomes-da-Costa S, Lane M, Sanches M, Diaz AP, Tseng PT, Lin PY, Berk M, Clarke G, O'Neil A, Jacka F, Stubbs B, Carvalho AF, Quevedo J, Soares JC, Fernandes BS. The kynurenine pathway in major depressive disorder, bipolar disorder, and schizophrenia: a meta-analysis of 101 studies. Mol Psychiatry. 2021 Aug;26(8):4158-4178. doi: 10.1038/s41380-020-00951-9
Tao, Kai ; Yuan, Yanling ; Xie, Qinglian ; Dong, Zaiquan. Relationship between human oral microbiome dysbiosis and neuropsychiatric diseases: An updated overview Behavioural brain research, 2024-08, Vol.471, p.115111, Article 115111
Wood PL, Unfried G, Whitehead W, Phillipps A, Wood JA. Dysfunctional plasmalogen dynamics in the plasma and platelets of patients with schizophrenia. Schizophr Res. 2015 Feb;161(2-3):506-10. doi: 10.1016/j.schres.2014.11.032.
Nuss P, Tessier C, Ferreri F, De Hert M, Peuskens J, Trugnan G, Masliah J, Wolf C. Abnormal transbilayer distribution of phospholipids in red blood cell membranes in schizophrenia. Psychiatry Res. 2009 Sep 30;169(2):91-6. doi: 10.1016/j.psychres.2009.01.009. Epub 2009 Jul 30. PMID: 19646766.
Zhang Y, Yin J, Yan H, Yan L, Li Y, Zhang C, Li Y, Liu B, Lin J, Zhang L, Hu X, Song C. Correlations between omega-3 fatty acids and inflammatory/glial abnormalities: the involvement of the membrane and neurotransmitter dysfunction in schizophrenia. Front Cell Neurosci. 2023 Oct 23;17:1163764. doi: 10.3389/fncel.2023.1163764.
Bang S, Shin YH, Ma X, Park SM, Graham DB, Xavier RJ, Clardy J. A Cardiolipin from Muribaculum intestinale Induces Antigen-Specific Cytokine Responses. J Am Chem Soc. 2023 Nov 1;145(43):23422-23426. doi: 10.1021/jacs.3c09734.
Beaulieu JM, Zhang X, Rodriguiz RM, Sotnikova TD, Cools MJ, Wetsel WC, Gainetdinov RR, Caron MG. Role of GSK3 beta in behavioral abnormalities induced by serotonin deficiency. Proc Natl Acad Sci U S A. 2008 Jan 29;105(4):1333-8. doi: 10.1073/pnas.0711496105
Kimura AK, Kimura T. Phosphatidylserine biosynthesis pathways in lipid homeostasis: Toward resolution of the pending central issue for decades. FASEB J. 2021 Jan;35(1):e21177. doi: 10.1096/fj.202001802R.
Harayama T, Reizman H. Understanding the diversity of membrane lipid composition. Nat. Rev. Mol. Cell Biol. 2018; 19: 281-296.Nicolson, G.L. The Fluid—Mosaic Model of Membrane Structure: Still relevant to understanding the structure, function and dynamics of biological membranes after more than 40 years. Biochim. Biophys. Acta Biomembr. 2014; 1838: 1451–1466.
Nicolson, G.L.; Ferriera de Matos, G. A brief introduction to some aspects of the Fluid—Mosaic Model of cell membrane structure and its importance in Membrane Lipid Replacement. Membranes 2021; 11: 947.
Nicolson GL, Ferreira de Mattos G, Ash M, Settineri R, Escribá PV. Fundamentals of Membrane Lipid Replacement: A Natural Medicine Approach to Repairing Cellular Membranes and Reducing Fatigue, Pain, and Other Symptoms While Restoring Function in Chronic Illnesses and Aging. Membranes (Basel). 2021 Nov 29;11(12):944. doi: 10.3390/membranes11120944.
Jinling Wang, Xiufu Lin, Ningning Zhao, Guanping Dong, Wei Wu, Ke Huang, Junfen Fu. Effects of Mitochondrial Dynamics in the Pathophysiology of Obesity. Front. Biosci. (Landmark Ed) 2022, 27(3), 107. https://doi.org/10.31083/j.fbl2703107
Kim JA, Wei Y, Sowers JR. Role of mitochondrial dysfunction in insulin resistance. Circ Res. 2008 Feb 29;102(4):401-14. doi: 10.1161/CIRCRESAHA.107.165472.
Prasun P. Mitochondrial dysfunction in metabolic syndrome. Biochim Biophys Acta Mol Basis Dis. 2020 Oct 1;1866(10):165838. doi: 10.1016/j.bbadis.2020.165838.
Spinelli R, Baboota RK, Gogg S, Beguinot F, Blüher M, Nerstedt A, Smith U. Increased cell senescence in human metabolic disorders. J Clin Invest. 2023 Jun 15;133(12):e169922. doi: 10.1172/JCI169922. PMID: 37317964; PMCID: PMC10266774.
Zhang H, Zhou H, Shen X, Lin X, Zhang Y, Sun Y, Zhou Y, Zhang L, Zhang D. The role of cellular senescence in metabolic diseases and the potential for senotherapeutic interventions. Front Cell Dev Biol. 2023 Oct 6;11:1276707. doi: 10.3389/fcell.2023.1276707.
Palmer AK, Tchkonia T, Kirkland JL. Targeting cellular senescence in metabolic disease. Mol Metab. 2022 Dec;66:101601. doi: 10.1016/j.molmet.2022.101601.
Schafer MJ, Miller JD, LeBrasseur NK. Cellular senescence: Implications for metabolic disease. Mol Cell Endocrinol. 2017 Nov 5;455:93-102. doi: 10.1016/j.mce.2016.08.047.
Decker ST, Funai K. Mitochondrial membrane lipids in the regulation of bioenergetic flux. Cell Metab. 2024 Sep 3;36(9):1963-1978. doi: 10.1016/j.cmet.2024.07.024.
Oliveira MC, Yusupov M, Bogaerts A, Cordeiro RM. Lipid Oxidation: Role of Membrane Phase-Separated Domains. J Chem Inf Model. 2021 Jun 28;61(6):2857-2868. doi: 10.1021/acs.jcim.1c00104.
Zhuo C, Zhao F, Tian H, Chen J, Li Q, Yang L, Ping J, Li R, Wang L, Xu Y, Cai Z, Song X. Acid sphingomyelinase/ceramide system in schizophrenia: implications for therapeutic intervention as a potential novel target. Transl Psychiatry. 2022 Jun 23;12(1):260. doi: 10.1038/s41398-022-01999-7.
Adams JM 2nd, Pratipanawatr T, Berria R, Wang E, DeFronzo RA, Sullards MC, Mandarino LJ. Ceramide content is increased in skeletal muscle from obese insulin-resistant humans. Diabetes. 2004 Jan;53(1):25-31. doi: 10.2337/diabetes.53.1.25.
Fizíková I, Dragašek J, Račay P. Mitochondrial Dysfunction, Altered Mitochondrial Oxygen, and Energy Metabolism Associated with the Pathogenesis of Schizophrenia. Int J Mol Sci. 2023 Apr 28;24(9):7991. doi: 10.3390/ijms24097991.
Xia W, Veeragandham P, Cao Y, Xu Y, Rhyne TE, Qian J, Hung CW, Zhao P, Jones Y, Gao H, Liddle C, Yu RT, Downes M, Evans RM, Rydén M, Wabitsch M, Wang Z, Hakozaki H, Schöneberg J, Reilly SM, Huang J, Saltiel AR. Obesity causes mitochondrial fragmentation and dysfunction in white adipocytes due to RalA activation. Nat Metab. 2024 Feb;6(2):273-289. doi: 10.1038/s42255-024-00978-0.
Sentelle RD, Senkal CE, Jiang W, Ponnusamy S, Gencer S, Selvam SP, Ramshesh VK, Peterson YK, Lemasters JJ, Szulc ZM, Bielawski J, Ogretmen B. Ceramide targets autophagosomes to mitochondria and induces lethal mitophagy. Nat Chem Biol. 2012 Oct;8(10):831-8. doi: 10.1038/nchembio.1059. Erratum in: Nat Chem Biol. 2012 Dec;8(12):1008.
Mencarelli C, Martinez-Martinez P. Ceramide function in the brain: when a slight tilt is enough. Cell Mol Life Sci. 2013 Jan;70(2):181-203. doi: 10.1007/s00018-012-1038-x.
Schwarz E., Prabakaran S., Whitfield P., Major H., Leweke F. M., Keothe D., et al.. (2008). High troughput lipidomic profiling of schizophrenia and bipolar disorder brain tissue reveals alterations of free fatty acids, phosphatidylcolines and ceramides. J. Proteome Res. 7, 4266–4277. 10.1021/pr800188y
Bernal-Vega S, García-Juárez M, Camacho-Morales A. Contribution of ceramides metabolism in psychiatric disorders. J. Neurochem.2023; 164: 708-724.
Zhu, F., Ju, Y., Wang, W. et al. Metagenome-wide association of gut microbiome features for schizophrenia. Nat Commun 11, 1612 (2020). https://doi.org/10.1038/s41467-020-15457-9
Johnson, E.L., Heaver, S.L., Waters, J.L. et al. Sphingolipids produced by gut bacteria enter host metabolic pathways, impacting ceramide levels. Nat Commun 11, 2471 (2020). https://doi.org/10.1038/s41467-020-16274-w
Schugar RC, Shih DM, Warrier M, Helsley RN, Burrows A, Ferguson D, Brown AL, Gromovsky AD, Heine M, Chatterjee A, Li L, Li XS, et al. The TMAO-Producing Enzyme Flavin-Containing Monooxygenase 3 Regulates Obesity and the Beiging of White Adipose Tissue. Cell Rep. 2017 Jun 20;19(12):2451-2461. doi: 10.1016/j.celrep.2017.05.077. Erratum in: Cell Rep. 2017 Jul 5;20(1):279. doi: 10.1016/j.celrep.2017.06.053.
Liu Y, Dai M. Trimethylamine N-Oxide Generated by the Gut Microbiota Is Associated with Vascular Inflammation: New Insights into Atherosclerosis. Mediators Inflamm. 2020 Feb 17;2020:4634172. doi: 10.1155/2020/4634172.
Nguyen TT, Kosciolek T, Daly RE, Vázquez-Baeza Y, Swafford A, Knight R, Jeste DV. Gut microbiome in Schizophrenia: Altered functional pathways related to immune modulation and atherosclerotic risk. Brain Behav Immun. 2021 Jan;91:245-256. doi: 10.1016/j.bbi.2020.10.003.
de la Monte SM. Triangulated mal-signaling in Alzheimer's disease: roles of neurotoxic ceramides, ER stress, and insulin resistance reviewed. J Alzheimers Dis. 2012;30 Suppl 2(0 2):S231-49. doi: 10.3233/JAD-2012-111727.
Voronova O, Zhuravkov S, Korotkova E, Artamonov A, Plotnikov E. Antioxidant Properties of New Phenothiazine Derivatives. Antioxidants (Basel). 2022 Jul 14;11(7):1371. doi: 10.3390/antiox11071371.
Egbujor MC, Tucci P, Buttari B, Nwobodo DC, Marini P, Saso L. Phenothiazines: Nrf2 activation and antioxidant effects. J Biochem Mol Toxicol. 2024 Mar;38(3):e23661. doi: 10.1002/jbt.23661.
Zhou X, Long T, Haas GL, Cai H, Yao JK. Reduced Levels and Disrupted Biosynthesis Pathways of Plasma Free Fatty Acids in First-Episode Antipsychotic-Naïve Schizophrenia Patients. Front Neurosci. 2020 Jul 29;14:784. doi: 10.3389/fnins.2020.00784.
Almsherqi ZA. Potential Role of Plasmalogens in the Modulation of Biomembrane Morphology. Front Cell Dev Biol. 2021 Jul 21;9:673917. doi: 10.3389/fcell.2021.673917.
Schooneveldt YL, Paul S, Calkin AC, Meikle PJ. Ether Lipids in Obesity: From Cells to Population Studies. Front Physiol. 2022 Mar 3;13:841278. doi: 10.3389/fphys.2022.841278.
Thevaranjan N, Puchta A, Schulz C, Naidoo A, Szamosi JC, Verschoor CP, Loukov D, Schenck LP, Jury J, Foley KP, Schertzer JD, et al. Age-Associated Microbial Dysbiosis Promotes Intestinal Permeability, Systemic Inflammation, and Macrophage Dysfunction. Cell Host Microbe. 2017 Apr 12;21(4):455-466.e4. doi: 10.1016/j.chom.2017.03.002. Erratum in: Cell Host Microbe. 2018 Apr 11;23(4):570. doi: 10.1016/j.chom.2018.03.006.
Johnson EL, Heaver SL, Waters JL, Kim BI, Bretin A, Goodman AL, Gewirtz AT, Worgall TS, Ley RE. Sphingolipids produced by gut bacteria enter host metabolic pathways impacting ceramide levels. Nat Commun. 2020 May 18;11(1):2471. doi: 10.1038/s41467-020-16274-w.
Miwa S, Kashyap S, Chini E, von Zglinicki T. Mitochondrial dysfunction in cell senescence and aging. J Clin Invest. 2022 Jul 1;132(13):e158447. doi: 10.1172/JCI158447.
Guan A, Wang S, Huang A, Qiu C, Li Y, Li X, Wang J, Wang Q, Deng B. The role of gamma oscillations in central nervous system diseases: Mechanism and treatment. Front Cell Neurosci. 2022 Jul 29;16:962957. doi: 10.3389/fncel.2022.962957
Miller CJ, Nichol RC, Batuski DJ. Acoustic oscillations in the early universe and today. Science. 2001 Jun 22;292(5525):2302-3. doi: 10.1126/science.1060440. Epub 2001 May 24. PMID: 11375481.
Calamassi D, Lucicesare A, Pomponi GP, Bambi S. Music tuned to 432 Hz versus music tuned to 440 Hz for improving sleep in patients with spinal cord injuries: a double-blind cross-over pilot study. Acta Biomed. 2020 Nov 30;91(12-S):e2020008. doi: 10.23750/abm.v91i12-S.10755.
Hohneck A, Rodríguez ÁM, Weingärtner S, Merx K, Sarodnick F, von Gagern F, Mavratzas A, Burkholder I, Schumacher G, Hofmann WK, Hofheinz RD. Differential effects of sound interventions tuned to 432 Hz or 443 Hz on cardiovascular parameters in cancer patients: a randomized cross-over trial. BMC Complement Med Ther. 2025 Jan 22;25(1):18. doi: 10.1186/s12906-025-04758-5.
Nani A, Manuello J, Mancuso L, Liloia D, Costa T, Cauda F. The Neural Correlates of Consciousness and Attention: Two Sister Processes of the Brain. Front Neurosci. 2019 Oct 31;13:1169. doi: 10.3389/fnins.2019.01169.
Arnulfo G, Wang SH, Myrov V, Toselli B, Hirvonen J, Fato MM, Nobili L, Cardinale F, Rubino A, Zhigalov A, Palva S, Palva JM. Long-range phase synchronization of high-frequency oscillations in human cortex. Nat Commun. 2020 Oct 23;11(1):5363. doi: 10.1038/s41467-020-18975-8.
Wallmark Z, Deblieck C, Iacoboni M. Neurophysiological Effects of Trait Empathy in Music Listening. Front Behav Neurosci. 2018 Apr 6;12:66. doi: 10.3389/fnbeh.2018.00066.
Chawla G, Azharuddin M, Ahmad I, Hussain ME. Effect of Whole-body Vibration on Depression, Anxiety, Stress, and Quality of Life in College Students: A Randomized Controlled Trial. Oman Med J. 2022 Jul 31;37(4):e408. doi: 10.5001/omj.2022.72
Biel AL, Minarik T, Sauseng P. EEG cross-frequency phase synchronization as an index of memory matching in visual search. Neuroimage. 2021 Jul 15;235:117971. doi: 10.1016/j.neuroimage.2021.117971
Chao JY, Gutiérrez R, Legatt AD, Yozawitz EG, Lo Y, Adams DC, Delphin ES, Shinnar S, Purdon PL. Decreased Electroencephalographic Alpha Power During Anesthesia Induction Is Associated With EEG Discontinuity in Human Infants. Anesth Analg. 2022 Dec 1;135(6):1207-1216. doi: 10.1213/ANE.0000000000005864.
Melloni L, Molina C, Pena M, Torres D, Singer W, Rodriguez E. Synchronization of neural activity across cortical areas correlates with conscious perception. J Neurosci. 2007 Mar 14;27(11):2858-65. doi: 10.1523/JNEUROSCI.4623-06.2007.
Guan A, Wang S, Huang A, Qiu C, Li Y, Li X, Wang J, Wang Q, Deng B. The role of gamma oscillations in central nervous system diseases: Mechanism and treatment. Front Cell Neurosci. 2022 Jul 29;16:962957. doi: 10.3389/fncel.2022.962957.
Buzsáki G, Schomburg EW. What does gamma coherence tell us about inter-regional neural communication? Nat Neurosci. 2015 Apr;18(4):484-9. doi: 10.1038/nn.3952. Epub 2015 Feb 23. PMID: 25706474; PMCID: PMC4803441.
Angioletti L, Balconi M. EEG brain oscillations are modulated by interoception in response to a synchronized motor vs. cognitive task. Front Neuroanat. 2022 Sep 23;16:991522. doi: 10.3389/fnana.2022.991522.
Liberati G, Klöcker A, Algoet M, Mulders D, Maia Safronova M, Ferrao Santos S, Ribeiro Vaz JG, Raftopoulos C, Mouraux A. Gamma-Band Oscillations Preferential for Nociception can be Recorded in the Human Insula. Cereb Cortex. 2018 Oct 1;28(10):3650-3664. doi: 10.1093/cercor/bhx237.
Lehrer DS, Lorenz J. Anosognosia in schizophrenia: hidden in plain sight. Innov Clin Neurosci. 2014 May;11(5-6):10-7. PMID: 25152841; PMCID: PMC4140620.
Mahadevan V, Mitra A, Zhang Y, Yuan X, Peltekian A, Chittajallu R, Esnault C, Maric D, Rhodes C, Pelkey KA, Dale R, Petros TJ, McBain CJ. NMDARs Drive the Expression of Neuropsychiatric Disorder Risk Genes Within GABAergic Interneuron Subtypes in the Juvenile Brain. Front Mol Neurosci. 2021 Sep 14;14:712609. doi: 10.3389/fnmol.2021.712609.
Traikapi A, Konstantinou N. Gamma Oscillations in Alzheimer's Disease and Their Potential Therapeutic Role. Front Syst Neurosci. 2021 Dec 13;15:782399. doi: 10.3389/fnsys.2021.782399. PMID: 34966263; PMCID: PMC8710538.
Guerra A, Asci F, D'Onofrio V, Sveva V, Bologna M, Fabbrini G, Berardelli A, Suppa A. Enhancing Gamma Oscillations Restores Primary Motor Cortex Plasticity in Parkinson's Disease. J Neurosci. 2020 Jun 10;40(24):4788-4796. doi: 10.1523/JNEUROSCI.0357-20.2020.
McNally JM, McCarley RW. Gamma band oscillations: a key to understanding schizophrenia symptoms and neural circuit abnormalities. Curr Opin Psychiatry. 2016 May;29(3):202-10. doi: 10.1097/YCO.0000000000000244.
Pillmann F, Rohde A, Ullrich S, Draba S, Sannemüller U, Marneros A. Violence, criminal behavior, and the EEG: significance of left hemispheric focal abnormalities. J Neuropsychiatry Clin Neurosci. 1999 Fall;11(4):454-7. doi: 10.1176/jnp.11.4.454. PMID: 10570757.
De Carolis A, Cipollini V, Corigliano V, Comparelli A, Sepe-Monti M, Orzi F, Ferracuti S, Giubilei F. Anosognosia in people with cognitive impairment: association with cognitive deficits and behavioral disturbances. Dement Geriatr Cogn Dis Extra. 2015 Feb 17;5(1):42-50. doi: 10.1159/000367987. PMID: 25852731
Joseph B, Narayanaswamy JC, Venkatasubramanian G. Insight in schizophrenia: relationship to positive, negative and neurocognitive dimensions. Indian J Psychol Med. 2015 Jan-Mar;37(1):5-11. doi: 10.4103/0253-7176.150797.
Murray AJ, Rogers JC, Katshu MZUH, Liddle PF, Upthegrove R. Oxidative Stress and the Pathophysiology and Symptom Profile of Schizophrenia Spectrum Disorders. Front Psychiatry. 2021 Jul 22;12:703452. doi: 10.3389/fpsyt.2021.703452.
Wood PL, Unfried G, Whitehead W, Phillipps A, Wood JA. Dysfunctional plasmalogen dynamics in the plasma and platelets of patients with schizophrenia. Schizophr Res. 2015 Feb;161(2-3):506-10. doi: 10.1016/j.schres.2014.11.032.
Goodenowe DB, Haroon J, Kling MA, Zielinski M, Mahdavi K, Habelhah B, Shtilkind L, Jordan S. Targeted Plasmalogen Supplementation: Effects on Blood Plasmalogens, Oxidative Stress Biomarkers, Cognition, and Mobility in Cognitively Impaired Persons. Front Cell Dev Biol. 2022 Jul 6;10:864842. doi: 10.3389/fcell.2022.864842.
Schmitt CA, Tchkonia T, Niedernhofer LJ, Robbins PD, Kirkland JL, Lee S. COVID-19 and cellular senescence. Nat Rev Immunol. 2023 Apr;23(4):251-263. doi: 10.1038/s41577-022-00785-2. Epub 2022 Oct 5. PMID: 36198912; PMCID: PMC9533263.
Ursini F, Maiorino M. Lipid peroxidation and ferroptosis: The role of GSH and GPx4. Free Radic Biol Med. 2020 May 20;152:175-185. doi: 10.1016/j.freeradbiomed.2020.02.027. Epub 2020 Mar 9. PMID: 32165281.
Zhivaki D, Kagan JC. Innate immune detection of lipid oxidation as a threat assessment strategy. Nat Rev Immunol. 2022 May;22(5):322-330. doi: 10.1038/s41577-021-00618-8. Epub 2021 Sep 21.
Wen Q, Liu J, Kang R, Zhou B, Tang D. The release and activity of HMGB1 in ferroptosis. Biochem Biophys Res Commun. 2019 Mar 5;510(2):278-283. doi: 10.1016/j.bbrc.2019.01.090.
Sage C. The implications of non-linear biological oscillations on human electrophysiology for electrohypersensitivity (EHS) and multiple chemical sensitivity (MCS). Rev Environ Health. 2015;30(4):293-303. doi: 10.1515/reveh-2015-0007. PMID: 26368042
Cheong R, Levchenko A. Oscillatory signaling processes: the how, the why and the where. Curr Opin Genet Dev. 2010 Dec;20(6):665-9. doi: 10.1016/j.gde.2010.08.007
Bier M, Bakker BM, Westerhoff HV. How yeast cells synchronize their glycolytic oscillations: a perturbation analytic treatment. Biophys J. 2000 Mar;78(3):1087-93. doi: 10.1016/S0006-3495(00)76667-7. PMID: 10692299; PMCID: PMC1300712.
Martinez-Corral R, Liu J, Prindle A, Süel GM, Garcia-Ojalvo J. Metabolic basis of brain-like electrical signalling in bacterial communities. Philos Trans R Soc Lond B Biol Sci. 2019 Jun 10;374(1774):20180382. doi: 10.1098/rstb.2018.0382
Vislova A, Sosa OA, Eppley JM, Romano AE, DeLong EF. Diel Oscillation of Microbial Gene Transcripts Declines With Depth in Oligotrophic Ocean Waters. Front Microbiol. 2019 Sep 24;10:2191. doi: 10.3389/fmicb.2019.02191.
Başar E. Brain oscillations in neuropsychiatric disease. Dialogues Clin Neurosci. 2013 Sep;15(3):291-300. doi: 10.31887/DCNS.2013.15.3/ebasar.
Chan D, Suk HJ, Jackson B, Milman NP, Stark D, Beach SD, Tsai LH. Induction of specific brain oscillations may restore neural circuits and be used for the treatment of Alzheimer's disease. J Intern Med. 2021 Nov;290(5):993-1009. doi: 10.1111/joim.13329.
Stiefel KM, Ermentrout GB. Neurons as oscillators. J Neurophysiol. 2016 Dec 1;116(6):2950-2960. doi: 10.1152/jn.00525.2015.
Singer W. Neuronal oscillations: unavoidable and useful? Eur J Neurosci. 2018 Oct;48(7):2389-2398. doi: 10.1111/ejn.13796.
González J, Cavelli M, Mondino A, Rubido N, Bl Tort A, Torterolo P. Communication Through Coherence by Means of Cross-frequency Coupling. Neuroscience. 2020 Nov 21;449:157-164. doi: 10.1016/j.neuroscience.2020.09.019.
Grossberg S. Adaptive Resonance Theory: how a brain learns to consciously attend, learn, and recognize a changing world. Neural Netw. 2013 Jan;37:1-47. doi: 10.1016/j.neunet.2012.09.017.
Gourévitch B, Martin C, Postal O, Eggermont JJ. Oscillations in the auditory system and their possible role. Neurosci Biobehav Rev. 2020 Jun;113:507-528. doi: 10.1016/j.neubiorev.2020.03.030.
Martinez-Corral R, Liu J, Prindle A, Süel GM, Garcia-Ojalvo J. Metabolic basis of brain-like electrical signalling in bacterial communities. Philos Trans R Soc Lond B Biol Sci. 2019 Jun 10;374(1774):20180382. doi: 10.1098/rstb.2018.0382
Vislova A, Sosa OA, Eppley JM, Romano AE, DeLong EF. Diel Oscillation of Microbial Gene Transcripts Declines With Depth in Oligotrophic Ocean Waters. Front Microbiol. 2019 Sep 24;10:2191. doi: 10.3389/fmicb.2019.02191.
Spencer NJ, Hu H. Enteric nervous system: sensory transduction, neural circuits and gastrointestinal motility. Nat Rev Gastroenterol Hepatol. 2020 Jun;17(6):338-351. doi: 10.1038/s41575-020-0271-2.
Butt MF, Albusoda A, Farmer AD, Aziz Q. The anatomical basis for transcutaneous auricular vagus nerve stimulation. J Anat. 2020 Apr;236(4):588-611. doi: 10.1111/joa.13122.
Howland RH. Vagus Nerve Stimulation. Curr Behav Neurosci Rep. 2014 Jun;1(2):64-73. doi: 10.1007/s40473-014-0010-5.
Mogilevski T, Rosella S, Aziz Q, Gibson PR. Transcutaneous vagal nerve stimulation protects against stress-induced intestinal barrier dysfunction in healthy adults. Neurogastroenterol Motil. 2022 Oct;34(10):e14382. doi: 10.1111/nmo.14382.
Panagiotaropoulos TI, Deco G, Kapoor V, Logothetis NK. Neuronal discharges and gamma oscillations explicitly reflect visual consciousness in the lateral prefrontal cortex. Neuron. 2012 Jun 7;74(5):924-35. doi: 10.1016/j.neuron.2012.04.013. Erratum in: Neuron. 2012 Jun 21;74(6):1139. PMID: 22681695.
Dienel SJ, Fish KN, Lewis DA. The Nature of Prefrontal Cortical GABA Neuron Alterations in Schizophrenia: Markedly Lower Somatostatin and Parvalbumin Gene Expression Without Missing Neurons. Am J Psychiatry. 2023 Jul 1;180(7):495-507. doi: 10.1176/appi.ajp.20220676
Blanco-Duque C, Chan D, Kahn MC, Murdock MH, Tsai LH. Audiovisual gamma stimulation for the treatment of neurodegeneration. J Intern Med. 2024 Feb;295(2):146-170. doi: 10.1111/joim.13755.
Larsen ER, Licht RW, Nielsen RE, Lolk A, Borck B, Sørensen C, Christensen EM, Bizik G, Ravn J, Martiny K, Vinberg M, Jankuviené O, Jørgensen PB, Videbech P, Bech P. Transcranial pulsed electromagnetic fields for treatment-resistant depression: A multicenter 8-week single-arm cohort study. Eur Psychiatry. 2020 Feb 18;63(1):e18. doi: 10.1192/j.eurpsy.2020.3. PMID: 32093804; PMCID: PMC7315871.
Hattapoğlu E, Batmaz İ, Dilek B, Karakoç M, Em S, Çevik R. Efficiency of pulsed electromagnetic fields on pain, disability, anxiety, depression, and quality of life in patients with cervical disc herniation: a randomized controlled study. Turk J Med Sci. 2019 Aug 8;49(4):1095-1101. doi: 10.3906/sag-1901-65.
Cole JC, Green Bernacki C, Helmer A, Pinninti N, O'reardon JP. Efficacy of Transcranial Magnetic Stimulation (TMS) in the Treatment of Schizophrenia: A Review of the Literature to Date. Innov Clin Neurosci. 2015 Jul-Aug;12(7-8):12-9. PMID: 26351619; PMCID: PMC4558786.
Qiu K, Zou W, Fang H, Hao M, Mehta K, Tian Z, Guan JL, Zhang K, Huang T, Diao J. Light-activated mitochondrial fission through optogenetic control of mitochondria-lysosome contacts. Nat Commun. 2022 Jul 25;13(1):4303. doi: 10.1038/s41467-022-31970-5. PMID: 35879298; PMCID: PMC9314359.
Li JY, Zhang K, Xu D, Zhou WT, Fang WQ, Wan YY, Yan DD, Guo MY, Tao JX, Zhou WC, Yang F, Jiang LP, Han XJ. Mitochondrial Fission Is Required for Blue Light-Induced Apoptosis and Mitophagy in Retinal Neuronal R28 Cells. Front Mol Neurosci. 2018 Nov 27;11:432. doi: 10.3389/fnmol.2018.00432. PMID: 30538621; PMCID: PMC6277708.
Roopram SM, Burger AM, van Dijk DA, Enterman J, Haffmans J. A pilot study of bright light therapy in schizophrenia. Psychiatry Res. 2016 Nov 30;245:317-320. doi: 10.1016/j.psychres.2016.07.034. Epub 2016 Jul 19. PMID: 27568303.
Modena DAO, Soares CD, Martignago CCS, Almeida S, Cazzo E, Chaim EA. Effects of LED photobiomodulation therapy on the subcutaneous fatty tissue of obese individuals - histological and immunohistochemical analysis. J Cosmet Laser Ther. 2022 Nov 17;24(6-8):84-90. doi: 10.1080/14764172.2022.2109677. Epub 2022 Sep 8. PMID: 36074934.
Kheradmand A, Tabeie F, Seif P, Rezaei O, Yasamy MT. Effect of low-level laser therapy (LLLT) on cognitive impairment among patients with chronic schizophrenia: a double-blind randomized placebo-controlled clinical trial. Lasers Med Sci. 2022 Aug;37(6):2717-2725. doi: 10.1007/s10103-022-03545-9.
Dougall N, Maayan N, Soares-Weiser K, McDermott LM, McIntosh A. Transcranial magnetic stimulation (TMS) for schizophrenia. Cochrane Database Syst Rev. 2015 Aug 20;2015(8):CD006081. doi: 10.1002/14651858.CD006081.pub2
Agarwal SM, Shivakumar V, Bose A, Subramaniam A, Nawani H, Chhabra H, Kalmady SV, Narayanaswamy JC, Venkatasubramanian G. Transcranial direct current stimulation in schizophrenia. Clin Psychopharmacol Neurosci. 2013 Dec;11(3):118-25. doi: 10.9758/cpn.2013.11.3.118.
Grent-'t-Jong T, Brickwedde M, Metzner C, Uhlhaas PJ. 40-Hz Auditory Steady-State Responses in Schizophrenia: Toward a Mechanistic Biomarker for Circuit Dysfunctions and Early Detection and Diagnosis. Biol Psychiatry. 2023 Oct 1;94(7):550-560. doi: 10.1016/j.biopsych.2023.03.026. Epub 2023 Apr 21. PMID: 37086914.
Veit J, Hakim R, Jadi MP, Sejnowski TJ, Adesnik H. Cortical gamma band synchronization through somatostatin interneurons. Nat Neurosci. 2017 Jul;20(7):951-959. doi: 10.1038/nn.4562.
Choi KM, Im CH, Yang C, Lee HS, Kim S, Lee SH. Influence of inter-stimulus interval on 40-Hz auditory steady-state response in patients with schizophrenia. Schizophrenia (Heidelb). 2023 Jul 27;9(1):46. doi: 10.1038/s41537-023-00377-6.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 American Journal of Medical and Clinical Research & Reviews

This work is licensed under a Creative Commons Attribution 4.0 International License.