Lipopolysaccharide-Induced Delirium-like Behaviour in a Rat Model of Chronic Cerebral Hypoperfusion Is Associated with Increased Indoleamine 2,3-Dioxygenase Expression and Endotoxin Tolerance

Indoleamine 2,3-dioxygenase (IDO) and the tryptophan–kynurenine pathway (TRP-KP) are upregulated in ageing and could be implicated in the pathogenesis of delirium. This study evaluated the role of IDO/KP in lipopolysaccharide (LPS)-induced delirium in an animal model of chronic cerebral hypoperfusion (CCH), a proposed model for delirium. CCH was induced by a permanent bilateral common carotid artery ligation (BCCAL) in Sprague Dawley rats to trigger chronic neuroinflammation-induced neurodegeneration. Eight weeks after permanent BCCAL, the rats were treated with a single systemic LPS. The rats were divided into three groups: (1) post-BCCAL rats treated with intraperitoneal (i.p.) saline, (2) post-BCCAL rats treated with i.p. LPS 100 μg/kg, and (3) sham-operated rats treated with i.p. LPS 100 μg/kg. Each group consisted of 10 male rats. To elucidate the LPS-induced delirium-like behaviour, natural and learned behaviour changes were assessed by a buried food test (BFT), open field test (OFT), and Y-maze test at 0, 24-, 48-, and 72 h after LPS treatment. Serum was collected after each session of behavioural assessment. The rats were euthanised after the last serum collection, and the hippocampi and cerebral cortex were collected. The TRP-KP neuroactive metabolites were measured in both serum and brain tissues using ELISA. Our data show that LPS treatment in CCH rats was associated with acute, transient, and fluctuated deficits in natural and learned behaviour, consistent with features of delirium. These behaviour deficits were mild compared to the sham-operated rats, which exhibited robust behaviour impairments. Additionally, heightened hippocampal IDO expression in the LPS-treated CCH rats was associated with reduced serum KP activity together with a decrease in the hippocampal quinolinic acid (QA) expression compared to the sham-operated rats, suggested for the presence of endotoxin tolerance through the immunomodulatory activity of IDO in the brain. These data provide new insight into the underlying mechanisms of delirium, and future studies should further explore the role of IDO modulation and its therapeutic potential in delirium.

[1]  Zachary J. Kunicki,et al.  Six-Year Cognitive Trajectory in Older Adults Following Major Surgery and Delirium. , 2023, JAMA internal medicine.

[2]  S. Makpol,et al.  Altered Tryptophan-Kynurenine Pathway in Delirium: A Review of the Current Literature , 2023, International journal of molecular sciences.

[3]  Dan Zeng,et al.  The role of indoleamine 2,3-dioxygenase 1 in early-onset post-stroke depression , 2023, Frontiers in Immunology.

[4]  R. de Cabo,et al.  Preclinical and translational models for delirium: Recommendations for future research from the NIDUS delirium network , 2023, Alzheimer's & dementia : the journal of the Alzheimer's Association.

[5]  M. Ohnishi,et al.  Indoleamine 2, 3-dioxygenase is responsible for low stress tolerance after intracerebral hemorrhage , 2023, PloS one.

[6]  Hye-Min Kang,et al.  Cerebral chronic hypoperfusion in mice causes premature aging of the cerebrovasculature , 2023, Brain Research Bulletin.

[7]  L. Baccalá,et al.  Autoregulation of blood flow drives early hypotension in a rat model of systemic inflammation induced by bacterial lipopolysaccharide , 2023, PNAS nexus.

[8]  P. Wei,et al.  Aryl hydrocarbon receptor: The master regulator of immune responses in allergic diseases , 2022, Frontiers in Immunology.

[9]  D. Fuchs,et al.  Indoleamine 2,3-dioxygenase 1 activation in mature cDC1 promotes tolerogenic education of inflammatory cDC2 via metabolic communication , 2022, Immunity.

[10]  Qilei Chen,et al.  Protective effects of endotoxin tolerance on peripheral lipopolysaccharide-induced neuroinflammation and dopaminergic neuronal injury , 2022, Immunopharmacology and immunotoxicology.

[11]  Sang-Woo Lee,et al.  Selective neurodegeneration of the hippocampus caused by chronic cerebral hypoperfusion: F-18 FDG PET study in rats , 2022, PloS one.

[12]  A. Salminen Role of indoleamine 2,3-dioxygenase 1 (IDO1) and kynurenine pathway in the regulation of the aging process , 2022, Ageing Research Reviews.

[13]  S. Klöppel,et al.  Associations of delirium with urinary tract infections and asymptomatic bacteriuria in adults aged 65 and older: A systematic review and meta‐analysis , 2021, Journal of the American Geriatrics Society.

[14]  S. Bhatia,et al.  The Footprint of Kynurenine Pathway in Neurodegeneration: Janus-Faced Role in Parkinson’s Disorder and Therapeutic Implications , 2021, International journal of molecular sciences.

[15]  J. O'Connor,et al.  Neuroinflammation and the Kynurenine Pathway in CNS Disease: Molecular Mechanisms and Therapeutic Implications , 2021, Cells.

[16]  O. Bugiani Why is delirium more frequent in the elderly? , 2021, Neurological Sciences.

[17]  S. Abate,et al.  Global prevalence and predictors of postoperative delirium among non-cardiac surgical patients: A systematic review and meta-analysis , 2021 .

[18]  A. Kuhad,et al.  IDO-1 inhibition protects against neuroinflammation, oxidative stress and mitochondrial dysfunction in 6-OHDA induced murine model of Parkinson's disease. , 2021, Neurotoxicology.

[19]  B. Salim,et al.  Incidence and risk factors of delirium in surgical intensive care unit , 2021, Trauma Surgery & Acute Care Open.

[20]  A. MacLullich,et al.  Delirium , 2020, Nature Reviews Disease Primers.

[21]  S. Inouye,et al.  Delirium in Older Patients With COVID-19 Presenting to the Emergency Department , 2020, JAMA network open.

[22]  Lei Jiang,et al.  The Effect of IDO on Neural Progenitor Cell Survival Under Oxygen Glucose Deprivation , 2020, Frontiers in Cellular Neuroscience.

[23]  N. Egorova,et al.  Microstructural degeneration and cerebrovascular risk burden underlying executive dysfunction after stroke , 2020, Scientific Reports.

[24]  M. Diao,et al.  A retrospective study of sepsis-associated encephalopathy: epidemiology, clinical features and adverse outcomes , 2020, BMC Emergency Medicine.

[25]  G. Caplan,et al.  A call to action for delirium research: Meta-analysis and regression of delirium associated mortality , 2020, BMC Geriatrics.

[26]  T. Jin,et al.  Risk factors and outcomes of sepsis-associated delirium in intensive care unit patients: A secondary data analysis. , 2020, Intensive & critical care nursing.

[27]  Neel S. Singhal,et al.  Resilience to Injury: A New Approach to Neuroprotection? , 2020, Neurotherapeutics.

[28]  T. Morimoto,et al.  Incidence, risk factors, and outcomes for sepsis-associated delirium in patients with mechanical ventilation: A sub-analysis of a multicenter randomized controlled trial. , 2019, Journal of critical care.

[29]  Deepak Kanojia,et al.  GCN2 is essential for CD8+ T cell survival and function in murine models of malignant glioma , 2019, Cancer Immunology, Immunotherapy.

[30]  M. Ihara,et al.  Animal Models of Chronic Cerebral Hypoperfusion: From Mouse to Primate , 2019, International journal of molecular sciences.

[31]  D. Weaver,et al.  Effects of the Novel IDO Inhibitor DWG-1036 on the Behavior of Male and Female 3xTg-AD Mice , 2019, Front. Pharmacol..

[32]  Sang-Woo Lee,et al.  The effect of chronic cerebral hypoperfusion on the pathology of Alzheimer's disease: A positron emission tomography study in rats , 2019, Scientific Reports.

[33]  K. Rockwood,et al.  The consistent burden in published estimates of delirium occurrence in medical inpatients over four decades: a systematic review and meta-analysis study , 2019, medRxiv.

[34]  D. McMillan,et al.  The effect of anesthesia on the postoperative systemic inflammatory response in patients undergoing surgery: A systematic review and meta-analysis , 2019, Surgery open science.

[35]  Mal-Soon Shin,et al.  Preischemic treadmill exercise improves short-term memory by inhibiting hypoperfusion-induced disruption of blood-brain barrier after bilateral common carotid arteries occlusion , 2019, Journal of exercise rehabilitation.

[36]  N. Hattori,et al.  The Effects of Astrocyte and Oligodendrocyte Lineage Cell Interaction on White Matter Injury under Chronic Cerebral Hypoperfusion , 2019, Neuroscience.

[37]  Farzaneh A. Sorond,et al.  Role of age-related alterations of the cerebral venous circulation in the pathogenesis of vascular cognitive impairment. , 2019, American journal of physiology. Heart and circulatory physiology.

[38]  R. Dijkhuizen,et al.  Effect of bilateral carotid occlusion on cerebral hemodynamics and perivascular innervation: An experimental rat model , 2019, The Journal of comparative neurology.

[39]  R. Kalaria,et al.  White matter capillaries in vascular and neurodegenerative dementias , 2019, Acta Neuropathologica Communications.

[40]  N. Arsenijević,et al.  Role of indoleamine 2,3-dioxygenase in pathology of the gastrointestinal tract , 2018, Therapeutic advances in gastroenterology.

[41]  Z. Hassan,et al.  Cholinergic modulation of hippocampal long-term potentiation in chronic cerebral hypoperfused rats , 2018, Neuroscience Research Notes.

[42]  A. Badawy Hypothesis kynurenic and quinolinic acids: The main players of the kynurenine pathway and opponents in inflammatory disease. , 2018, Medical hypotheses.

[43]  B. Malnic,et al.  Buried Food-seeking Test for the Assessment of Olfactory Detection in Mice. , 2018, Bio-protocol.

[44]  Rong Zhang,et al.  Cerebral blood flow in normal aging adults: cardiovascular determinants, clinical implications, and aerobic fitness , 2018, Journal of neurochemistry.

[45]  B. Caramelli,et al.  Hypertension, mitral valve disease, atrial fibrillation and low education level predict delirium and worst outcome after cardiac surgery in older adults , 2018, BMC Anesthesiology.

[46]  D. Cao,et al.  Common Carotid Arteries Occlusion Surgery in Adult Rats as a Model of Chronic Cerebral Hypoperfusion. , 2018, Bio-protocol.

[47]  Xiao-Guang Luo,et al.  Peripheral immune tolerance alleviates the intracranial lipopolysaccharide injection-induced neuroinflammation and protects the dopaminergic neurons from neuroinflammation-related neurotoxicity , 2017, Journal of Neuroinflammation.

[48]  R. Kuswardhani,et al.  Factors Related to the Severity of Delirium in the Elderly Patients With Infection , 2017, Gerontology & geriatric medicine.

[49]  S. E. Rooij,et al.  Pathophysiological and behavioral effects of systemic inflammation in aged and diseased rodents with relevance to delirium: A systematic review , 2017, Brain, Behavior, and Immunity.

[50]  A. Ghaemmaghami,et al.  The role of indoleamine 2,3-dioxygenase-aryl hydrocarbon receptor pathway in the TLR4-induced tolerogenic phenotype in human DCs , 2017, Scientific Reports.

[51]  C. Hopf,et al.  The stress kinase GCN2 does not mediate suppression of antitumor T cell responses by tryptophan catabolism in experimental melanomas , 2016, Oncoimmunology.

[52]  T. Aiba,et al.  Prevalence, determinants, and prognostic significance of delirium in patients with acute heart failure. , 2016, International journal of cardiology.

[53]  F. Abelha,et al.  Postoperative delirium: age and low functional reserve as independent risk factors. , 2016, Journal of clinical anesthesia.

[54]  Mian Peng,et al.  Battery of behavioral tests in mice to study postoperative delirium , 2016, Scientific Reports.

[55]  M. Moro,et al.  The Kynurenine Pathway in the Acute and Chronic Phases of Cerebral Ischemia. , 2016, Current pharmaceutical design.

[56]  P. Stella,et al.  Incidence, Predictive Factors, and Effect of Delirium After Transcatheter Aortic Valve Replacement. , 2016, JACC. Cardiovascular interventions.

[57]  M. Halliday,et al.  PERK inhibition prevents tau-mediated neurodegeneration in a mouse model of frontotemporal dementia , 2015, Acta Neuropathologica.

[58]  Yiwen Ruan,et al.  Chronic cerebral hypoperfusion induces vascular plasticity and hemodynamics but also neuronal degeneration and cognitive impairment , 2015, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[59]  M. L. Seibenhener,et al.  Use of the Open Field Maze to measure locomotor and anxiety-like behavior in mice. , 2015, Journal of visualized experiments : JoVE.

[60]  J. Kobayashi,et al.  Preoperative brain magnetic resonance imaging and postoperative delirium after off-pump coronary artery bypass grafting: a prospective cohort study , 2015, Canadian Journal of Anesthesia/Journal canadien d'anesthésie.

[61]  Adam Linder,et al.  An Endotoxin Tolerance Signature Predicts Sepsis and Organ Dysfunction at Initial Clinical Presentation , 2014, EBioMedicine.

[62]  M. Boustani,et al.  The DSM-5 criteria, level of arousal and delirium diagnosis: inclusiveness is safer , 2014, BMC Medicine.

[63]  M. Geffard,et al.  Aryl hydrocarbon receptor control of a disease tolerance defence pathway , 2014, Nature.

[64]  D. Munn,et al.  Activation of the STING Adaptor Attenuates Experimental Autoimmune Encephalitis , 2014, The Journal of Immunology.

[65]  E. Sampson,et al.  Risk factors for incident delirium among older people in acute hospital medical units: a systematic review and meta-analysis , 2014, Age and ageing.

[66]  Chun-ling Dai,et al.  Chronic cerebral hypoperfusion causes decrease of O-GlcNAcylation, hyperphosphorylation of tau and behavioral deficits in mice , 2014, Front. Aging Neurosci..

[67]  W. Breitbart,et al.  The Phenomenology of Delirium: Presence, Severity, and Relationship between Symptoms , 2014 .

[68]  C. del Fresno,et al.  Pathophysiology of endotoxin tolerance: mechanisms and clinical consequences , 2013, Critical Care.

[69]  A. Yoshitake,et al.  Pre-existing cerebral infarcts as a risk factor for delirium after coronary artery bypass graft surgery. , 2013, Interactive cardiovascular and thoracic surgery.

[70]  F. Bihel,et al.  The neuroprotector kynurenic acid increases neuronal cell survival through neprilysin induction , 2013, Neuropharmacology.

[71]  J. Godbout,et al.  Review: Microglia of the aged brain: primed to be activated and resistant to regulation , 2013, Neuropathology and applied neurobiology.

[72]  Chad E. Wagner,et al.  Delirium in the Cardiovascular ICU: Exploring Modifiable Risk Factors* , 2013, Critical care medicine.

[73]  P. Beaune,et al.  Tryptophan Depletion and the Kinase GCN2 Mediate IFN-γ–Induced Autophagy , 2012, The Journal of Immunology.

[74]  S. Rapoport,et al.  Bilateral Common Carotid Artery Ligation Transiently Changes Brain Lipid Metabolism in Rats , 2012, Neurochemical Research.

[75]  J. Rawlins,et al.  Systemic inflammation induces acute working memory deficits in the primed brain: relevance for delirium , 2012, Neurobiology of Aging.

[76]  V. Gebski,et al.  Tryptophan metabolism to kynurenine is a potential novel contributor to hypotension in human sepsis* , 2011, Critical care medicine.

[77]  M. Weller,et al.  An endogenous tumour-promoting ligand of the human aryl hydrocarbon receptor , 2011, Nature.

[78]  A. Kiss,et al.  The relationship between indoleamine 2,3-dioxygenase activity and post-stroke cognitive impairment , 2011, Journal of Neuroinflammation.

[79]  S. Antonia,et al.  Indoleamine 2,3-Dioxygenase: Is It an Immune Suppressor? , 2010, Cancer journal.

[80]  C. J. Omiecinski,et al.  Kynurenic acid is a potent endogenous aryl hydrocarbon receptor ligand that synergistically induces interleukin-6 in the presence of inflammatory signaling. , 2010, Toxicological sciences : an official journal of the Society of Toxicology.

[81]  Pierre Tattevin,et al.  Enhanced indoleamine 2,3-dioxygenase activity in patients with severe sepsis and septic shock. , 2010, The Journal of infectious diseases.

[82]  K. Kurz,et al.  Accelerated Tryptophan Degradation Predicts Poor Survival in Trauma and Sepsis Patients , 2010, International journal of tryptophan research : IJTR.

[83]  A. Hara,et al.  Marked increases in hippocampal neuron indoleamine 2, 3-dioxygenase via IFN-γ-independent pathway following transient global ischemia in mouse , 2009, Neuroscience Research.

[84]  Norbert Schuff,et al.  Subcortical Lacunes Are Associated With Executive Dysfunction in Cognitively Normal Elderly , 2008, Stroke.

[85]  F. Bari,et al.  Permanent, bilateral common carotid artery occlusion in the rat: A model for chronic cerebral hypoperfusion-related neurodegenerative diseases , 2007, Brain Research Reviews.

[86]  Á. Kelly,et al.  Lipopolysaccharide impairs long-term potentiation and recognition memory and increases p75NTR expression in the rat dentate gyrus , 2007, Brain Research.

[87]  J. Seibyl,et al.  Cerebral perfusion changes in older delirious patients using 99mTc HMPAO SPECT. , 2006, The journals of gerontology. Series A, Biological sciences and medical sciences.

[88]  M. Adib-Conquy,et al.  Bench-to-bedside review: Endotoxin tolerance as a model of leukocyte reprogramming in sepsis , 2006, Critical care.

[89]  M. Minami,et al.  Endotoxin Preconditioning Prevents Cellular Inflammatory Response During Ischemic Neuroprotection in Mice , 2004, Stroke.

[90]  T. B. Paiva,et al.  Different mechanism of LPS‐induced vasodilation in resistance and conductance arteries from SHR and normotensive rats , 2002, British journal of pharmacology.

[91]  M. Weiner,et al.  Executive dysfunction in subcortical ischaemic vascular disease , 2002, Journal of neurology, neurosurgery, and psychiatry.

[92]  A. Terashi,et al.  [Measurement of regional cerebral blood flow and glucose utilization in rat brain under chronic hypoperfusion conditions following bilateral carotid artery occlusion. Analyzed by autoradiographical methods]. , 1997, Nihon Ika Daigaku zasshi.

[93]  S. Inouye,et al.  Precipitating Factors for Delirium in Hospitalized Elderly Persons: Predictive Model and Interrelationship With Baseline Vulnerability , 1996 .

[94]  Teresa A. Victor,et al.  Putative Neuroprotective and Neurotoxic Kynurenine Pathway Metabolites Are Associated with Hippocampal and Amygdalar Volumes in Subjects with Major Depressive Disorder , 2015, Neuropsychopharmacology.

[95]  J. Korf,et al.  The role of indoleamine 2,3-dioxygenase in a mouse model of neuroinflammation-induced depression. , 2012, Journal of Alzheimer's disease : JAD.

[96]  O. Takikawa,et al.  Indoleamine 2,3-Dioxygenase Expression and Regulation in Chronic Periodontitis , 2009 .