Neuroinflammation increases oxygen extraction in a mouse model of Alzheimer's disease.

Alzheimer’s disease Cerebral oxygenation and hemodynamics Neuroinflammation Two-photon phosphorescence lifetime microscopy

Journal

Alzheimer's research & therapy
ISSN: 1758-9193
Titre abrégé: Alzheimers Res Ther
Pays: England
ID NLM: 101511643

Informations de publication

Date de publication:
10 Apr 2024
Historique:
received: 29 09 2023
accepted: 31 03 2024
medline: 11 4 2024
pubmed: 11 4 2024
entrez: 10 4 2024
Statut: epublish

Résumé

Neuroinflammation, impaired metabolism, and hypoperfusion are fundamental pathological hallmarks of early Alzheimer's disease (AD). Numerous studies have asserted a close association between neuroinflammation and disrupted cerebral energetics. During AD progression and other neurodegenerative disorders, a persistent state of chronic neuroinflammation reportedly exacerbates cytotoxicity and potentiates neuronal death. Here, we assessed the impact of a neuroinflammatory challenge on metabolic demand and microvascular hemodynamics in the somatosensory cortex of an AD mouse model. We utilized in vivo 2-photon microscopy and the phosphorescent oxygen sensor Oxyphor 2P to measure partial pressure of oxygen (pO2) and capillary red blood cell flux in cortical microvessels of awake mice. Intravascular pO2 and capillary RBC flux measurements were performed in 8-month-old APPswe/PS1dE9 mice and wildtype littermates on days 0, 7, and 14 of a 14-day period of lipopolysaccharide-induced neuroinflammation. Before the induced inflammatory challenge, AD mice demonstrated reduced metabolic demand but similar capillary red blood cell flux as their wild type counterparts. Neuroinflammation provoked significant reductions in cerebral intravascular oxygen levels and elevated oxygen extraction in both animal groups, without significantly altering red blood cell flux in capillaries. This study provides evidence that neuroinflammation alters cerebral oxygen demand at the early stages of AD without substantially altering vascular oxygen supply. The results will guide our understanding of neuroinflammation's influence on neuroimaging biomarkers for early AD diagnosis.

Sections du résumé

BACKGROUND BACKGROUND
Neuroinflammation, impaired metabolism, and hypoperfusion are fundamental pathological hallmarks of early Alzheimer's disease (AD). Numerous studies have asserted a close association between neuroinflammation and disrupted cerebral energetics. During AD progression and other neurodegenerative disorders, a persistent state of chronic neuroinflammation reportedly exacerbates cytotoxicity and potentiates neuronal death. Here, we assessed the impact of a neuroinflammatory challenge on metabolic demand and microvascular hemodynamics in the somatosensory cortex of an AD mouse model.
METHODS METHODS
We utilized in vivo 2-photon microscopy and the phosphorescent oxygen sensor Oxyphor 2P to measure partial pressure of oxygen (pO2) and capillary red blood cell flux in cortical microvessels of awake mice. Intravascular pO2 and capillary RBC flux measurements were performed in 8-month-old APPswe/PS1dE9 mice and wildtype littermates on days 0, 7, and 14 of a 14-day period of lipopolysaccharide-induced neuroinflammation.
RESULTS RESULTS
Before the induced inflammatory challenge, AD mice demonstrated reduced metabolic demand but similar capillary red blood cell flux as their wild type counterparts. Neuroinflammation provoked significant reductions in cerebral intravascular oxygen levels and elevated oxygen extraction in both animal groups, without significantly altering red blood cell flux in capillaries.
CONCLUSIONS CONCLUSIONS
This study provides evidence that neuroinflammation alters cerebral oxygen demand at the early stages of AD without substantially altering vascular oxygen supply. The results will guide our understanding of neuroinflammation's influence on neuroimaging biomarkers for early AD diagnosis.

Identifiants

pubmed: 38600598
doi: 10.1186/s13195-024-01444-5
pii: 10.1186/s13195-024-01444-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

78

Informations de copyright

© 2024. The Author(s).

Références

Weninger SC, Yankner BA. Inflammation and Alzheimer disease: the good, the bad, and the ugly. Nat Med. 2001;7(5):527–8.
pubmed: 11329045 doi: 10.1038/87839
Heneka MT, Carson MJ, Khoury JE, Landreth GE, Brosseron F, Feinstein DL, et al. Neuroinflammation in Alzheimer’s disease. Lancet Neurol. 2015;14(4):388–405.
pubmed: 25792098 pmcid: 5909703 doi: 10.1016/S1474-4422(15)70016-5
Calsolaro V, Edison P. Neuroinflammation in Alzheimer’s disease: current evidence and future directions. Alzheimers Dement. 2016;12(6):719–32.
pubmed: 27179961 doi: 10.1016/j.jalz.2016.02.010
Ransohoff RM. How neuroinflammation contributes to neurodegeneration. Science. 2016;353(6301):777–83.
pubmed: 27540165 doi: 10.1126/science.aag2590
Saijo K, Winner B, Carson CT, Collier JG, Boyer L, Rosenfeld MG, et al. A Nurr1/CoREST pathway in Microglia and astrocytes protects dopaminergic neurons from inflammation-Induced death. Cell. 2009;137(1):47–59.
pubmed: 19345186 pmcid: 2754279 doi: 10.1016/j.cell.2009.01.038
Sofroniew MV. Molecular dissection of reactive astrogliosis and glial scar formation. Trends Neurosci. 2009;32(12):638–47.
pubmed: 19782411 pmcid: 2787735 doi: 10.1016/j.tins.2009.08.002
Sofroniew MV, Vinters HV. Astrocytes: biology and pathology. Acta Neuropathol (Berl). 2010;119(1):7–35.
pubmed: 20012068 doi: 10.1007/s00401-009-0619-8
Boche D, Perry VH, Nicoll JaR, Review. Activation patterns of microglia and their identification in the human brain. Neuropathol Appl Neurobiol. 2013;39(1):3–18.
pubmed: 23252647 doi: 10.1111/nan.12011
Huber JD, Campos CR, Mark KS, Davis TP. Alterations in blood-brain barrier ICAM-1 expression and brain microglial activation after λ-carrageenan-induced inflammatory pain. Am J Physiol-Heart Circ Physiol. 2006;290(2):H732–40.
pubmed: 16199477 doi: 10.1152/ajpheart.00747.2005
Iadecola C. The neurovascular unit coming of age: a journey through neurovascular coupling in Health and Disease. Neuron. 2017;96(1):17–42.
pubmed: 28957666 pmcid: 5657612 doi: 10.1016/j.neuron.2017.07.030
Girouard H, Iadecola C. Neurovascular coupling in the normal brain and in hypertension, stroke, and Alzheimer disease. J Appl Physiol. 2006;100:328–35.
pubmed: 16357086 doi: 10.1152/japplphysiol.00966.2005
Korte N, Nortley R, Attwell D. Cerebral blood flow decrease as an early pathological mechanism in Alzheimer’s disease. Acta Neuropathol (Berl). 2020;140(6):793–810.
pubmed: 32865691 doi: 10.1007/s00401-020-02215-w
Daulatzai MA. Cerebral hypoperfusion and glucose hypometabolism: key pathophysiological modulators promote neurodegeneration, cognitive impairment, and Alzheimer’s disease: cerebral hypoperfusion and glucose hypometabolism promote cognitive dysfunction. J Neurosci Res. 2017;95(4):943–72.
pubmed: 27350397 doi: 10.1002/jnr.23777
Zlokovic BV. Neurovascular pathways to neurodegeneration in Alzheimer’s disease and other disorders. Nat Rev Neurosci. 2011;12(12):723–38.
pubmed: 22048062 pmcid: 4036520 doi: 10.1038/nrn3114
Zlokovic BV. Neurovascular mechanisms of Alzheimer’s neurodegeneration. Trends Neurosci. 2005;28(4):202–8.
pubmed: 15808355 doi: 10.1016/j.tins.2005.02.001
Heneka MT, Golenbock DT, Latz E. Innate immunity in Alzheimer’s disease. Nat Immunol. 2015;16(3):229–36.
pubmed: 25689443 doi: 10.1038/ni.3102
Butovsky O, Weiner HL. Microglial signatures and their role in health and disease. Nat Rev Neurosci. 2018;19(10):622–35.
pubmed: 30206328 pmcid: 7255106 doi: 10.1038/s41583-018-0057-5
Leng F, Edison P. Neuroinflammation and microglial activation in Alzheimer disease: where do we go from here? Nat Rev Neurol. 2021;17(3):157–72.
pubmed: 33318676 doi: 10.1038/s41582-020-00435-y
Cheataini F, Ballout N, Al Sagheer T. The effect of neuroinflammation on the cerebral metabolism at baseline and after neural stimulation in neurodegenerative diseases. J Neurosci Res. 2023;jnr.25198.
Van Horssen J, Van Schaik P, Witte M. Inflammation and mitochondrial dysfunction: a vicious circle in neurodegenerative disorders? Neurosci Lett. 2019;710:132931.
pubmed: 28668382 doi: 10.1016/j.neulet.2017.06.050
Lull ME, Block ML. Microglial activation and chronic neurodegeneration. Neurotherapeutics. 2010;7(4):354–65.
pubmed: 20880500 pmcid: 2951017 doi: 10.1016/j.nurt.2010.05.014
Wright AL, Zinn R, Hohensinn B, Konen LM, Beynon SB, Tan RP, et al. Neuroinflammation and neuronal loss Precede Aβ plaque deposition in the hAPP-J20 mouse model of Alzheimer’s Disease. PLoS ONE. 2013;8(4):e59586.
pubmed: 23560052 pmcid: 3613362 doi: 10.1371/journal.pone.0059586
Cuello AC. Early and late CNS inflammation in Alzheimer’s Disease: two extremes of a Continuum? Trends Pharmacol Sci. 2017;38(11):956–66.
pubmed: 28867259 doi: 10.1016/j.tips.2017.07.005
Wang WY, Tan MS, Yu JT, Tan L. Role of pro-inflammatory cytokines released from microglia in Alzheimer’s disease. Ann Transl Med. 2015;3(10):15.
Crumpler R, Roman RJ, Fan F, Capillary Stalling. A mechanism of decreased cerebral blood Flow in AD/ADRD. J Exp Neurol. 2021;2(4):149–53.
pubmed: 35028643 pmcid: 8754422
Tondo G, Iaccarino L, Caminiti SP, Presotto L, Santangelo R, Iannaccone S, et al. The combined effects of microglia activation and brain glucose hypometabolism in early-onset Alzheimer’s disease. Alzheimers Res Ther. 2020;12(1):50.
pubmed: 32354345 pmcid: 7193377 doi: 10.1186/s13195-020-00619-0
Takkinen JS, López-Picón FR, Al Majidi R, Eskola O, Krzyczmonik A, Keller T, et al. Brain energy metabolism and neuroinflammation in ageing APP/PS1-21 mice using longitudinal
pubmed: 27834284 doi: 10.1177/0271678X16677990
Kominsky DJ, Campbell EL, Colgan SP. Metabolic shifts in immunity and inflammation. J Immunol. 2010;184(8):4062–8.
pubmed: 20368286 doi: 10.4049/jimmunol.0903002
Edison P. Neuroinflammation, microglial activation, and glucose metabolism in neurodegenerative diseases. In: International Review of Neurobiology [Internet]. Elsevier; 2020 [cited 2023 Jun 7]. pp. 325–44. https://linkinghub.elsevier.com/retrieve/pii/S0074774220300489 .
Lauro C, Limatola C. Metabolic reprograming of Microglia in the regulation of the Innate Inflammatory Response. Front Immunol. 2020;11:493.
pubmed: 32265936 pmcid: 7099404 doi: 10.3389/fimmu.2020.00493
Liemburg-Apers DC, Willems PHGM, Koopman WJH, Grefte S. Interactions between mitochondrial reactive oxygen species and cellular glucose metabolism. Arch Toxicol. 2015;89(8):1209–26.
pubmed: 26047665 pmcid: 4508370 doi: 10.1007/s00204-015-1520-y
Holland R, McIntosh AL, Finucane OM, Mela V, Rubio-Araiz A, Timmons G, et al. Inflammatory microglia are glycolytic and iron retentive and typify the microglia in APP/PS1 mice. Brain Behav Immun. 2018;68:183–96.
pubmed: 29061364 doi: 10.1016/j.bbi.2017.10.017
Yang S, Qin C, Hu ZW, Zhou LQ, Yu HH, Chen M, et al. Microglia reprogram metabolic profiles for phenotype and function changes in central nervous system. Neurobiol Dis. 2021;152:105290.
pubmed: 33556540 doi: 10.1016/j.nbd.2021.105290
Cruz Hernández JC, Bracko O, Kersbergen CJ, Muse V, Haft-Javaherian M, Berg M, et al. Neutrophil adhesion in brain capillaries reduces cortical blood flow and impairs memory function in Alzheimer’s disease mouse models. Nat Neurosci. 2019;22(3):413–20.
pubmed: 30742116 pmcid: 6508667 doi: 10.1038/s41593-018-0329-4
El Amki M, Glück C, Binder N, Middleham W, Wyss MT, Weiss T, et al. Neutrophils obstructing brain capillaries are a Major cause of No-Reflow in ischemic stroke. Cell Rep. 2020;33(2):108260.
pubmed: 33053341 doi: 10.1016/j.celrep.2020.108260
Iadecola C. Neurovascular regulation in the normal brain and in Alzheimer’s disease. Nat Rev Neurosci. 2004;5:347–60.
pubmed: 15100718 doi: 10.1038/nrn1387
Wei Z, Xu J, Chen L, Hirschler L, Barbier EL, Li T, et al. Brain metabolism in tau and amyloid mouse models of Alzheimer’s disease: an MRI study. NMR Biomed. 2021;34(9):e4568.
pubmed: 34050996 pmcid: 9574887 doi: 10.1002/nbm.4568
Matsudaira T, Terada T, Obi T, Yokokura M, Takahashi Y, Ouchi Y. Coexistence of cerebral hypometabolism and neuroinflammation in the thalamo-limbic-brainstem region in young women with functional somatic syndrome. EJNMMI Res. 2020;10(1):29.
pubmed: 32198578 pmcid: 7083979 doi: 10.1186/s13550-020-00617-1
Sankar SB, Pybus AF, Liew A, Sanders B, Shah KJ, Wood LB et al. Low cerebral blood flow is a non-invasive biomarker of neuroinflammation after repetitive mild traumatic brain injury. Neurobiol Dis. 2018/12/25 ed. 2019;124:544–54.
Sardi F, Fassina L, Venturini L, Inguscio M, Guerriero F, Rolfo E, et al. Alzheimer’s disease, autoimmunity and inflammation. The good, the bad and the ugly. Autoimmun Rev. 2011;11(2):149–53.
pubmed: 21996556 doi: 10.1016/j.autrev.2011.09.005
Birch AM, Katsouri L, Sastre M. Modulation of inflammation in transgenic models of Alzheimer’s disease. J Neuroinflammation. 2014;11(1):25.
pubmed: 24490742 pmcid: 3922595 doi: 10.1186/1742-2094-11-25
Sakadžić S, Roussakis E, Yaseen MA, Mandeville ET, Srinivasan VJ, Arai K, et al. Two-photon high-resolution measurement of partial pressure of oxygen in cerebral vasculature and tissue. Nat Methods. 2010;7(9):755–9.
pubmed: 20693997 pmcid: 2932799 doi: 10.1038/nmeth.1490
Esipova TV, Barrett MJP, Erlebach E, Masunov AE, Weber B, Vinogradov SA. Oxyphor 2P: a high-performance probe for deep-tissue longitudinal oxygen imaging. Cell Metab. 2019;29(3):736–e7447.
pubmed: 30686745 pmcid: 6402963 doi: 10.1016/j.cmet.2018.12.022
Li B, Esipova TV, Sencan I, Kılıç K, Fu B, Desjardins M, et al. More homogeneous capillary flow and oxygenation in deeper cortical layers correlate with increased oxygen extraction. eLife. 2019;8:e42299.
pubmed: 31305237 pmcid: 6636997 doi: 10.7554/eLife.42299
Blinder P, Tsai PS, Kaufhold JP, Knutsen PM, Suhl H, Kleinfeld D. The cortical angiome: an interconnected vascular network with noncolumnar patterns of blood flow. Nat Neurosci. 2013;16(7):889–97.
pubmed: 23749145 pmcid: 4141079 doi: 10.1038/nn.3426
Sakadžić S, Mandeville ET, Gagnon L, Musacchia JJ, Yaseen MA, Yucel MA, et al. Large arteriolar component of oxygen delivery implies a safe margin of oxygen supply to cerebral tissue. Nat Commun. 2014;5(1):5734.
pubmed: 25483924 doi: 10.1038/ncomms6734
Weber B, Keller AL, Reichold J, Logothetis NK. The Microvascular System of the Striate and Extrastriate Visual cortex of the Macaque. Cereb Cortex. 2008;18(10):2318–30.
pubmed: 18222935 doi: 10.1093/cercor/bhm259
Wu J, Guo C, Chen S, Jiang T, He Y, Ding W, et al. Direct 3D analyses reveal barrel-specific vascular distribution and Cross-barrel branching in the mouse Barrel Cortex. Cereb Cortex. 2016;26(1):23–31.
pubmed: 25085882 doi: 10.1093/cercor/bhu166
De Kock CPJ, Bruno RM, Spors H, Sakmann B. Layer- and cell-type-specific suprathreshold stimulus representation in rat primary somatosensory cortex: sensory responses throughout barrel cortex. J Physiol. 2007;581(1):139–54.
pubmed: 17317752 pmcid: 2075227 doi: 10.1113/jphysiol.2006.124321
Hyder F, Rothman DL, Bennett MR. Cortical energy demands of signaling and nonsignaling components in brain are conserved across mammalian species and activity levels. Proc Natl Acad Sci. 2013;110(9):3549–54.
pubmed: 23319606 pmcid: 3587194 doi: 10.1073/pnas.1214912110
Hauss-Wegrzyniak B, Dobrzanski P, Stoehr JD, Wenk GL. Chronic neuroinflammation in rats reproduces components of the neurobiology of Alzheimer’s disease. Brain Res. 1998;780(2):294–303.
pubmed: 9507169 doi: 10.1016/S0006-8993(97)01215-8
Qin L, Wu X, Block ML, Liu Y, Breese GR, Hong JS, et al. Systemic LPS causes chronic neuroinflammation and progressive neurodegeneration. Glia. 2007;55(5):453–62.
pubmed: 17203472 pmcid: 2871685 doi: 10.1002/glia.20467
Batista CRA, Gomes GF, Candelario-Jalil E, Fiebich BL, de Oliveira ACP. Lipopolysaccharide-Induced Neuroinflammation as a bridge to Understand Neurodegeneration. Int J Mol Sci. 2019;20(9):2293.
pubmed: 31075861 pmcid: 6539529 doi: 10.3390/ijms20092293
Kealy J, Murray C, Griffin EW, Lopez-Rodriguez AB, Healy D, Tortorelli LS, et al. Acute inflammation alters Brain Energy Metabolism in mice and humans: role in suppressed spontaneous activity, impaired cognition, and Delirium. J Neurosci. 2020;40(29):5681–96.
pubmed: 32513828 pmcid: 7363463 doi: 10.1523/JNEUROSCI.2876-19.2020
Jung H, Lee D, You H, Lee M, Kim H, Cheong E, et al. LPS induces microglial activation and GABAergic synaptic deficits in the hippocampus accompanied by prolonged cognitive impairment. Sci Rep. 2023;13(1):6547.
pubmed: 37085584 pmcid: 10121592 doi: 10.1038/s41598-023-32798-9
Jankowsky JL, Fadale DJ, Anderson J, Xu GM, Gonzales V, Jenkins NA, et al. Mutant presenilins specifically elevate the levels of the 42 residue β-amyloid peptide in vivo: evidence for augmentation of a 42-specific γ secretase. Hum Mol Genet. 2004;13(2):159–70.
pubmed: 14645205 doi: 10.1093/hmg/ddh019
Kılıç K, Desjardins M, Tang J, Thunemann M, Sunil S, Erdener ŞE, et al. Chronic cranial Windows for Long Term Multimodal Neurovascular Imaging in mice. Front Physiol. 2021;11:612678.
pubmed: 33551837 pmcid: 7862556 doi: 10.3389/fphys.2020.612678
Goldey GJ, Roumis DK, Glickfeld LL, Kerlin AM, Reid RC, Bonin V, et al. Removable cranial windows for long-term imaging in awake mice. Nat Protoc. 2014;9(11):2515–38.
pubmed: 25275789 pmcid: 4442707 doi: 10.1038/nprot.2014.165
Holtmaat A, Bonhoeffer T, Chow DK, Chuckowree J, De Paola V, Hofer SB, et al. Long-term, high-resolution imaging in the mouse neocortex through a chronic cranial window. Nat Protoc. 2009;4(8):1128–44.
pubmed: 19617885 pmcid: 3072839 doi: 10.1038/nprot.2009.89
Kalmbach AS, Waters J. Brain surface temperature under a craniotomy. J Neurophysiol. 2012;108(11):3138–46.
pubmed: 22972953 pmcid: 3544864 doi: 10.1152/jn.00557.2012
Becker W, Bergmann A, Hink MA, König K, Benndorf K, Biskup C. Fluorescence lifetime imaging by time-correlated single-photon counting: fluorescence lifetime imaging by TCPSC. Microsc Res Tech. 2004;63(1):58–66.
pubmed: 14677134 doi: 10.1002/jemt.10421
Lecoq J, Parpaleix A, Roussakis E, Ducros M, Houssen YG, Vinogradov SA, et al. Simultaneous two-photon imaging of oxygen and blood flow in deep cerebral vessels. Nat Med. 2011;17(7):893–8.
pubmed: 21642977 pmcid: 3291110 doi: 10.1038/nm.2394
Grubbs FE. Procedures for detecting outlying observations in samples. Technometrics. 1969;11(1):1–21.
doi: 10.1080/00401706.1969.10490657
Uchida K, Reilly MP, Asakura T. Molecular Stability and function of Mouse Hemoglobins. Zoolog Sci. 1998;15(5):703–6.
doi: 10.2108/zsj.15.703
Lyons DG, Parpaleix A, Roche M, Charpak S. Mapping oxygen concentration in the awake mouse brain. eLife. 2016;5:e12024.
pubmed: 26836304 pmcid: 4775210 doi: 10.7554/eLife.12024
Rana R, Singhal R, Singh V. Analysis of repeated measurement data in the clinical trials. J Ayurveda Integr Med. 2013;4(2):77.
pubmed: 23930038 pmcid: 3737450 doi: 10.4103/0975-9476.113872
Wong-Riley MTT. Cytochrome oxidase: an endogenous metabolic marker for neuronal activity. Trends Neurosci. 1989;12(3):94–101.
pubmed: 2469224 doi: 10.1016/0166-2236(89)90165-3
Keller D, Erö C, Markram H. Cell densities in the mouse brain: a systematic review. Front Neuroanat. 2018;12:83.
pubmed: 30405363 pmcid: 6205984 doi: 10.3389/fnana.2018.00083
Şencan İ, Esipova T, Kılıç K, Li B, Desjardins M, Yaseen MA et al. Optical measurement of microvascular oxygenation and blood flow responses in awake mouse cortex during functional activation. J Cereb Blood Flow Metab. 2020;0271678X2092801.
Jespersen SN, Østergaard L. The roles of Cerebral Blood Flow, Capillary Transit Time heterogeneity, and Oxygen Tension in Brain Oxygenation and Metabolism. J Cereb Blood Flow Metab. 2012;32(2):264–77.
pubmed: 22044867 doi: 10.1038/jcbfm.2011.153
Lu X, Moeini M, Li B, Lu Y, Damseh R, Pouliot P, et al. A pilot study investigating changes in Capillary Hemodynamics and its modulation by Exercise in the APP-PS1 Alzheimer Mouse Model. Front Neurosci. 2019;13:1261.
pubmed: 31920472 pmcid: 6915102 doi: 10.3389/fnins.2019.01261
Lu X, Moeini M, Li B, de Montgolfier O, Lu Y, Bélanger S, et al. Voluntary exercise increases brain tissue oxygenation and spatially homogenizes oxygen delivery in a mouse model of Alzheimer’s disease. Neurobiol Aging. 2020;88:11–23.
pubmed: 31866158 doi: 10.1016/j.neurobiolaging.2019.11.015
Gutiérrez-Jiménez E, Angleys H, Rasmussen PM, West MJ, Catalini L, Iversen NK, et al. Disturbances in the control of capillary flow in an aged APPswe/PS1∆E9 model of Alzheimer’s disease. Neurobiol Aging. 2018;62:82–94.
pubmed: 29131981 doi: 10.1016/j.neurobiolaging.2017.10.006
Angleys H, Østergaard L, Jespersen SN. The effects of Capillary Transit Time heterogeneity (CTH) on Brain Oxygenation. J Cereb Blood Flow Metab. 2015;35(5):806–17.
pubmed: 25669911 pmcid: 4420854 doi: 10.1038/jcbfm.2014.254
Sasaki Y, Ohsawa K, Kanazawa H, Kohsaka S, Imai Y. Iba1 is an actin-cross-linking protein in Macrophages/Microglia. Biochem Biophys Res Commun. 2001;286(2):292–7.
pubmed: 11500035 doi: 10.1006/bbrc.2001.5388
von Boyen GBT. Proinflammatory cytokines increase glial fibrillary acidic protein expression in enteric glia. Gut. 2004;53(2):222–8.
doi: 10.1136/gut.2003.012625
François A, Rioux Bilan A, Quellard N, Fernandez B, Janet T, Chassaing D, et al. Longitudinal follow-up of autophagy and inflammation in brain of APPswePS1dE9 transgenic mice. J Neuroinflammation. 2014;11(1):139.
pubmed: 25158693 pmcid: 4154524 doi: 10.1186/s12974-014-0139-x
D’Angelo C, Costantini E, Salvador N, Marchioni M, Di Nicola M, Greig NH, et al. nAChRs gene expression and neuroinflammation in APPswe/PS1dE9 transgenic mouse. Sci Rep. 2021;11(1):9711.
pubmed: 33958667 pmcid: 8102527 doi: 10.1038/s41598-021-89139-x
Thomas BP, Sheng M, Tseng BY, Tarumi T, Martin-Cook K, Womack KB, et al. Reduced global brain metabolism but maintained vascular function in amnestic mild cognitive impairment. J Cereb Blood Flow Metab. 2017;37(4):1508–16.
pubmed: 27389176 doi: 10.1177/0271678X16658662
Jiang D, Lin Z, Liu P, Sur S, Xu C, Hazel K, et al. Brain oxygen extraction is differentially altered by Alzheimer’s and vascular diseases. J Magn Reson Imaging JMRI. 2020;52(6):1829–37.
pubmed: 32567195 doi: 10.1002/jmri.27264
Xie H, Guan J, Borrelli LA, Xu J, Serrano-Pozo A, Bacskai BJ. Mitochondrial alterations near amyloid plaques in an Alzheimer’s Disease Mouse Model. J Neurosci. 2013;33(43):17042–51.
pubmed: 24155308 pmcid: 3807029 doi: 10.1523/JNEUROSCI.1836-13.2013
Algamal M, Russ AN, Miller MR, Hou SS, Maci M, Munting LP, et al. Reduced excitatory neuron activity and interneuron-type-specific deficits in a mouse model of Alzheimer’s disease. Commun Biol. 2022;5(1):1323.
pubmed: 36460716 pmcid: 9718858 doi: 10.1038/s42003-022-04268-x
Klee JL, Kiliaan AJ, Lipponen A, Battaglia FP. Reduced firing rates of pyramidal cells in the frontal cortex of APP/PS1 can be restored by acute treatment with levetiracetam. Neurobiol Aging. 2020;96:79–86.
pubmed: 32950781 doi: 10.1016/j.neurobiolaging.2020.08.013
Hooijmans CR, Van der Zee CEEM, Dederen PJ, Brouwer KM, Reijmer YD, van Groen T, et al. DHA and cholesterol containing diets influence Alzheimer-like pathology, cognition and cerebral vasculature in APPswe/PS1dE9 mice. Neurobiol Dis. 2009;33(3):482–98.
pubmed: 19130883 doi: 10.1016/j.nbd.2008.12.002
DeFelipe J, Alonso-Nanclares L, Arellano JI. Microstructure of the neocortex: comparative aspects. J Neurocytol. 2002;31(3–5):299–316.
pubmed: 12815249 doi: 10.1023/A:1024130211265
Odoj K, Brawek B, Asavapanumas N, Mojtahedi N, Heneka MT, Garaschuk O. In vivo mechanisms of cortical network dysfunction induced by systemic inflammation. Brain Behav Immun. 2021;96:113–26.
pubmed: 34052361 doi: 10.1016/j.bbi.2021.05.021
Stellwagen D, Beattie EC, Seo JY, Malenka RC. Differential regulation of AMPA receptor and GABA receptor trafficking by tumor necrosis factor-alpha. J Neurosci off J Soc Neurosci. 2005;25(12):3219–28.
doi: 10.1523/JNEUROSCI.4486-04.2005
Mosili P, Maikoo S, Mabandla MV, Qulu L. The Pathogenesis of Fever-Induced Febrile seizures and its current state. Neurosci Insights. 2020;15:2633105520956973.
pubmed: 33225279 pmcid: 7649866 doi: 10.1177/2633105520956973
Pascual O, Ben Achour S, Rostaing P, Triller A, Bessis A. Microglia activation triggers astrocyte-mediated modulation of excitatory neurotransmission. Proc Natl Acad Sci [Internet]. 2012 Jan 24 [cited 2023 Jun 5];109(4). https://doi.org/10.1073/pnas.1111098109 .
Griton M, Konsman JP. Neural pathways involved in infection-induced inflammation: recent insights and clinical implications. Clin Auton Res. 2018;28(3):289–99.
pubmed: 29541878 doi: 10.1007/s10286-018-0518-y
Munshi S, Rosenkranz JA. Effects of Peripheral Immune Challenge on in vivo firing of basolateral amygdala neurons in adult male rats. Neuroscience. 2018;390:174–86.
pubmed: 30170159 doi: 10.1016/j.neuroscience.2018.08.017
Doenlen R, Krügel U, Wirth T, Riether C, Engler A, Prager G, et al. Electrical activity in rat cortico-limbic structures after single or repeated administration of lipopolysaccharide or staphylococcal enterotoxin B. Proc R Soc B Biol Sci. 2011;278(1713):1864–72.
doi: 10.1098/rspb.2010.2040
Kurki SN, Srinivasan R, Laine J, Virtanen MA, Ala-Kurikka T, Voipio J, et al. Acute neuroinflammation leads to disruption of neuronal chloride regulation and consequent hyperexcitability in the dentate gyrus. Cell Rep. 2023;42(11):113379.
pubmed: 37922309 doi: 10.1016/j.celrep.2023.113379
Giansante G, Marte A, Romei A, Prestigio C, Onofri F, Benfenati F, et al. Presynaptic L-Type Ca2 + channels increase glutamate release probability and excitatory strength in the Hippocampus during Chronic Neuroinflammation. J Neurosci off J Soc Neurosci. 2020;40(36):6825–41.
doi: 10.1523/JNEUROSCI.2981-19.2020
Atwell D, Laughlin SB. An Energy Budget for Signaling in the Grey Matter of the brain. J Cereb Blood Flow Metab. 2001;21:1133–45.
doi: 10.1097/00004647-200110000-00001
Varatharaj A, Galea I. The blood-brain barrier in systemic inflammation. Brain Behav Immun. 2017;60:1–12.
pubmed: 26995317 doi: 10.1016/j.bbi.2016.03.010
Erickson MA, Banks WA. Neuroimmune axes of the blood-brain barriers and blood-brain interfaces: bases for physiological regulation, Disease States, and pharmacological interventions. Pharmacol Rev. 2018;70(2):278–314.
pubmed: 29496890 pmcid: 5833009 doi: 10.1124/pr.117.014647
Erickson MA, Hansen K, Banks WA. Inflammation-induced dysfunction of the low-density lipoprotein receptor-related protein-1 at the blood-brain barrier: Protection by the antioxidant N-acetylcysteine. Brain Behav Immun. 2012;26(7):1085–94.
pubmed: 22809665 pmcid: 3434291 doi: 10.1016/j.bbi.2012.07.003
Vazquez AL, Masamoto K, Kim SG. Dynamics of oxygen delivery and consumption during evoked neural stimulation using a compartment model and CBF and tissue P
pubmed: 18504146 doi: 10.1016/j.neuroimage.2008.04.024
Tyrtyshnaia AA, Lysenko LV, Madamba F, Manzhulo IV, Khotimchenko MY, Kleschevnikov AM. Acute neuroinflammation provokes intracellular acidification in mouse hippocampus. J Neuroinflammation. 2016;13(1):283.
pubmed: 27809864 pmcid: 5094044 doi: 10.1186/s12974-016-0747-8
Nair S, Sobotka KS, Joshi P, Gressens P, Fleiss B, Thornton C, et al. Lipopolysaccharide-induced alteration of mitochondrial morphology induces a metabolic shift in microglia modulating the inflammatory response in vitro and in vivo. Glia. 2019;67(6):1047–61.
pubmed: 30637805 doi: 10.1002/glia.23587
Ganeshan K, Chawla A. Metabolic regulation of Immune responses. Annu Rev Immunol. 2014;32(1):609–34.
pubmed: 24655299 pmcid: 5800786 doi: 10.1146/annurev-immunol-032713-120236
Bernier LP, Brunner C, Cottarelli A, Balbi M. Location Matters: Navigating Regional Heterogeneity of the Neurovascular Unit. Front Cell Neurosci [Internet]. 2021 [cited 2023 Feb 7];15. https://www.frontiersin.org/articles/ https://doi.org/10.3389/fncel.2021.696540 .
Bernier LP, York EM, MacVicar BA. Immunometabolism in the brain: how metabolism shapes microglial function. Trends Neurosci. 2020;43(11):854–69.
pubmed: 32958333 doi: 10.1016/j.tins.2020.08.008
Thygesen C, Ilkjær L, Kempf SJ, Hemdrup AL, von Linstow CU, Babcock AA, et al. Diverse protein profiles in CNS myeloid cells and CNS tissue from lipopolysaccharide- and vehicle-injected APPSWE/PS1∆E9 transgenic mice implicate cathepsin Z in Alzheimer’s Disease. Front Cell Neurosci. 2018;12:397.
pubmed: 30459560 pmcid: 6232379 doi: 10.3389/fncel.2018.00397
Alasmari F, Alshammari MA, Alasmari AF, Alanazi WA, Alhazzani K. Neuroinflammatory Cytokines Induce Amyloid Beta Neurotoxicity through modulating amyloid precursor protein Levels/Metabolism. BioMed Res Int. 2018;2018:1–8.
doi: 10.1155/2018/3087475
Sheng J. Lipopolysaccharide-induced-neuroinflammation increases intracellular accumulation of amyloid precursor protein and amyloid β peptide in APPswe transgenic mice. Neurobiol Dis. 2003;14(1):133–45.
pubmed: 13678674 doi: 10.1016/S0969-9961(03)00069-X
Kitazawa M. Lipopolysaccharide-Induced inflammation exacerbates Tau Pathology by a cyclin-dependent kinase 5-Mediated pathway in a transgenic model of Alzheimer’s Disease. J Neurosci. 2005;25(39):8843–53.
pubmed: 16192374 pmcid: 6725603 doi: 10.1523/JNEUROSCI.2868-05.2005
Lee I, Hüttemann M. Energy crisis: the role of oxidative phosphorylation in acute inflammation and sepsis. Biochim Biophys Acta BBA - Mol Basis Dis. 2014;1842(9):1579–86.
doi: 10.1016/j.bbadis.2014.05.031
Yoo SM, Park J, Kim SH, Jung YK. Emerging perspectives on mitochondrial dysfunction and inflammation in Alzheimer’s disease. BMB Rep. 2020;53(1):35–46.
pubmed: 31818363 pmcid: 6999830 doi: 10.5483/BMBRep.2020.53.1.274
Brezzo G, Simpson J, Ameen-Ali KE, Berwick J, Martin C. Acute effects of systemic inflammation upon the neuro-glial-vascular unit and cerebrovascular function. Brain Behav Immun - Health. 2020;5:100074.
pubmed: 32685933 pmcid: 7357601 doi: 10.1016/j.bbih.2020.100074
Manouchehrian O, Ramos M, Bachiller S, Lundgaard I, Deierborg T. Acute systemic LPS-exposure impairs perivascular CSF distribution in mice. J Neuroinflammation. 2021;18(1):34.
pubmed: 33514389 pmcid: 7844902 doi: 10.1186/s12974-021-02082-6
Fruekilde SK, Bailey CJ, Lambertsen KL, Clausen BH, Carlsen J, Xu Nlong, et al. Disturbed microcirculation and hyperaemic response in a murine model of systemic inflammation. J Cereb Blood Flow Metab. 2022;0271678X:2211122.
Dash RK, Bassingthwaighte JB. Erratum to: blood HbO2 and HbCO2 dissociation curves at varied O2, CO2, pH, 2,3-DPG and temperature levels. Ann Biomed Eng. 2010;38(4):1683–701.
pubmed: 20162361 pmcid: 2862600 doi: 10.1007/s10439-010-9948-y
Dash RK, Korman B, Bassingthwaighte JB. Simple accurate mathematical models of blood HbO2 and HbCO2 dissociation curves at varied physiological conditions: evaluation and comparison with other models. Eur J Appl Physiol. 2016;116(1):97–113.
pubmed: 26298270 doi: 10.1007/s00421-015-3228-3
Bracko O, Cruz Hernández JC, Park L, Nishimura N, Schaffer CB. Causes and consequences of baseline cerebral blood flow reductions in Alzheimer’s disease. J Cereb Blood Flow Metab. 2021;41(7):1501–16.
pubmed: 33444096 pmcid: 8221770 doi: 10.1177/0271678X20982383
Walek KW, Stefan S, Lee JH, Puttigampala P, Kim AH, Park SW, et al. Near-lifespan longitudinal tracking of brain microvascular morphology, topology, and flow in male mice. Nat Commun. 2023;14(1):2982.
pubmed: 37221202 pmcid: 10205707 doi: 10.1038/s41467-023-38609-z
Krogh A. The number and distribution of capillaries in muscles with calculations of the oxygen pressure head necessary for supplying the tissue. J Physiol. 1919;52(6):409–15.
pubmed: 16993405 pmcid: 1402716 doi: 10.1113/jphysiol.1919.sp001839
Mächler P, Fomin-Thunemann N, Thunemann M, Sætra MJ, Desjardins M, Kılıç K, et al. Baseline oxygen consumption decreases with cortical depth. Das a, editor. PLOS Biol. 2022;20(10):e3001440.
pubmed: 36301995 pmcid: 9642908 doi: 10.1371/journal.pbio.3001440

Auteurs

Chang Liu (C)

Department of Bioengineering, Northeastern University, Boston, MA, 02115, USA.

Alfredo Cárdenas-Rivera (A)

Department of Bioengineering, Northeastern University, Boston, MA, 02115, USA.

Shayna Teitelbaum (S)

Department of Bioengineering, Northeastern University, Boston, MA, 02115, USA.

Austin Birmingham (A)

Department of Bioengineering, Northeastern University, Boston, MA, 02115, USA.

Mohammed Alfadhel (M)

Department of Bioengineering, Northeastern University, Boston, MA, 02115, USA.

Mohammad A Yaseen (MA)

Department of Bioengineering, Northeastern University, Boston, MA, 02115, USA. m.yaseen@northeastern.edu.

Classifications MeSH