À propos de cet article

Citez

Trevaskis NL, Kaminskas LM, Porter CJ. From sewer to saviour - targeting the lymphatic system to promote drug exposure and activity. Nat Rev Drug Discov. 2015;14(11):781-803. https://doi.org/10.1038/nrd4608 PMid:26471369 Search in Google Scholar

Jessen NA, Munk AS, Lundgaard I, Nedergaard M. The glymphatic system: A Beginner’s guide. Neurochem Res. 2015;40(12):2583-99. https://doi.org/10.1007/s11064-015-1581-6 PMid:25947369 Search in Google Scholar

Bacyinski A, Xu M, Wang W, Hu J. The paravascular pathway for brain waste clearance: Current understanding, significance and controversy. Front Neuroanat. 2017;11:101. https://doi.org/10.3389/fnana.2017.00101 PMid:29163074 Search in Google Scholar

McEwen BS. Protective and damaging effects of stress mediators: Central role of the brain. Dialogues Clin Neurosci. 2006;8(4):367-81. https://doi.org/10.31887/DCNS.2006.8.4/bmcewen PMid:17290796 Search in Google Scholar

Weller RO, Subash M, Preston SD, Mazanti I, Carare RO. Perivascular drainage of amyloid-beta peptides from the brain and its failure in cerebral amyloid angiopathy and Alzheimer’s disease. Brain Pathol. 2008;18(2):253-66. https://doi.org/10.1111/j.1750-3639.2008.00133.x PMid:18363936 Search in Google Scholar

Carare RO, Bernardes-Silva M, Newman TA, Page AM, Nicoll JA, Perry VH, et al. Solutes, but not cells, drain from the brain parenchyma along basement membranes of capillaries and arteries: Significance for cerebral amyloid angiopathy and neuroimmunology. Neuropathol Appl Neurobiol. 2008;34(2): 131-44. https://doi.org/10.1111/j.1365-2990.2007.00926.x PMid:18208483 Search in Google Scholar

Hawkes CA, Härtig W, Kacza J, Schliebs R, Weller RO, Nicoll JA, et al. Perivascular drainage of solutes is impaired in the aging mouse brain and in the presence of cerebral amyloid angiopathy. Acta Neuropathol. 2011;121(4):431-43. https://doi.org/10.1007/s00401-011-0801-7 PMid:21259015 Search in Google Scholar

Iliff JJ, Wang M, Liao Y, Plogg BA, Peng W, Gundersen GA, et al. A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid β. Sci Transl Med. 2012;4(147):147ra111. https://doi.org/10.1126/scitranslmed.3003748 PMid:22896675 Search in Google Scholar

Murtha LA, Yang Q, Parsons MW, Levi CR, Beard DJ, Spratt NJ, et al. Cerebrospinal fluid is drained primarily via the spinal canal and olfactory route in young and aged spontaneously hypertensive rats. Fluids Barriers CNS. 2014;11:12. https://doi.org/10.1186/2045-8118-11-12 PMid:24932405 Search in Google Scholar

Tarasoff-Conway JM, Carare RO, Osorio RS, Glodzik L, Butler T, Fieremans E, et al. Clearance systems in the brain-implications for Alzheimer disease. Nat Rev Neurol. 2015;11(8):457-70. https://doi.org/10.1038/nrneurol.2015.119 PMid:26195256 Search in Google Scholar

Simon MJ, Iliff JJ. Regulation of cerebrospinal fluid (CSF) flow in neurodegenerative, neurovascular and neuroinflammatory disease. Biochim Biophys Acta. 2016;1862(3):442-51. https://doi.org/10.1016/j.bbadis.2015.10.014 PMid:26499397 Search in Google Scholar

Lundgaard I, Lu ML, Yang E, Peng W, Mestre H, Hitomi E, et al. Glymphatic clearance controls state-dependent changes in brain lactate concentration. J Cereb Blood Flow Metab. 2017;37(6):2112-24. https://doi.org/10.1177/0271678X16661202 PMid:27481936 Search in Google Scholar

Iliff JJ, Chen MJ, Plog BA, Zeppenfeld DM, Soltero M, Yang L, et al. Impairment of glymphatic pathway function promotes tau pathology after traumatic brain injury. J Neurosci. 2014;34(49):16180-93. https://doi.org/10.1523/JNEUROSCI.3020-14.2014 PMid:25471560 Search in Google Scholar

Matsumae M, Atsumi H, Hirayama A, Hayashi N, Sano F, Taiozawa K, et al. A new look at cerebrospinal fluid motion. No Shinkei Geka. 2016;44:909-24. Search in Google Scholar

Achariyar TM, Li B, Peng W, Verghese PB, Shi Y, McConnell E, et al. Glymphatic distribution of CSF-derived apoE into brain is isoform specific and suppressed during sleep deprivation. Mol Neurodegener. 2016;11(1):74. Search in Google Scholar

Rangroo Thrane V, Thrane AS, Plog BA, Thiyagarajan M, Iliff JJ, Deane R, et al. Paravascular microcirculation facilitates rapid lipid transport and astrocyte signaling in the brain. Sci Rep. 2013;3:2582. https://doi.org/10.1038/srep02582 PMid:24002448 Search in Google Scholar

Kress BT, Iliff JJ, Xia M, Wang M, Wei HS, Zeppenfeld D, et al. Impairment of paravascular clearance pathways in the aging brain. Ann Neurol. 2014;76(6):845-61. https://doi.org/10.1002/ana.24271 PMid:25204284 Search in Google Scholar

Sullan MJ, Asken BM, Jaffee MS, DeKosky ST, Bauer RM. Glymphatic system disruption as a mediator of brain trauma and chronic traumatic encephalopathy. Neurosci Biobehav Rev. 2018;84:316-24. https://doi.org/10.1016/j.neubiorev.2017.08.016 PMid:28859995 Search in Google Scholar

Benveniste H, Liu X, Koundal S, Sanggaard S, Lee H, Wardlaw J. The glymphatic system and waste clearance with brain aging: A review. Gerontology. 2019;65(2):106-19. https://doi.org/10.1159/000490349 PMid:29996134 Search in Google Scholar

Wei F, Song J, Zhang C, Lin J, Xue R, Shan LD, et al. Chronic stress impairs the aquaporin-4-mediated glymphatic transport through glucocorticoid signaling. Psychopharmacology (Berl). 2019;236(4):1367-84. https://doi.org/10.1007/s00213-018-5147-6 PMid:30607477 Search in Google Scholar

Sapolsky RM, Romero LM, Munck AU. How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions. Endocr Rev. 2000;21(1):55-89. https://doi.org/10.1210/edrv.21.1.0389 PMid:10696570 Search in Google Scholar

Bernstein R. The Mind and Mental Health: How Stress Affects the Brain. California: Touro University Worldwide; 2016. Search in Google Scholar

McEwen BS, Bowles NP, Gray JD, Hill MN, Hunter RG, Karatsoreos IN, et al. Mechanisms of stress in the brain. Nat Neurosci. 2015;18(10):1353-63. https://doi.org/10.1038/nn.4086 PMid:26404710 Search in Google Scholar

Horner HC, Packan DR, Sapolsky RM. Glucocorticoids inhibit glucose transport in cultured hippocampal neurons and glia. Neuroendocrinology. 1990;52(1):57-64. https://doi.org/10.1159/000125539 PMid:2118608 Search in Google Scholar

Virgin CE Jr., Ha TP, Packan DR, Tombaugh GC, Yang SH, Horner HC, et al. Glucocorticoids inhibit glucose transport and glutamate uptake in hippocampal astrocytes: Implications for glucocorticoid neurotoxicity. J Neurochem. 1991;57(4):1422-8. https://doi.org/10.1111/j.1471-4159.1991.tb08309.x PMid:1680166 Search in Google Scholar

Doyle P, Guillaume-Gentil C, Rohner-Jeanrenaud F, Jeanrenaud B. Effects of corticosterone administration on local cerebral glucose utilization of rats. Brain Res. 1994; 645(1-2):225-30. https://doi.org/10.1016/0006-8993(94)91655-1 PMid:8062085 Search in Google Scholar

Sapolsky RM. Why stress is bad for your brain. Science. 1996;273(5276):749-50. https://doi.org/10.1126/science.273.5276.749 PMid:8701325 Search in Google Scholar

Newcomer JW, Craft S, Hershey T, Askins K, Bardgett ME. Glucocorticoid-induced impairment in declarative memory performance in adult humans. J Neurosci. 1994;14(4):2047-53. https://doi.org/10.1523/JNEUROSCI.14-04-02047.1994 PMid:8198631 Search in Google Scholar

Brady KT, Sonne SC. The role of stress in alcohol use, alcoholism treatment, and relapse. Alcohol Res Health. 1999;23(4):263-71. Search in Google Scholar

Lundgaard I, Wang W, Eberhardt A, Vinitsky HS, Reeves C, Peng S, et al. Beneficial effects of low alcohol exposure, but adverse effects of high alcohol intake on glymphatic function. Sci Rep. 2018;8(1):2246. https://doi.org/10.1038/s41598-018-20424-y PMid:29396480 Search in Google Scholar

Xie L, Kang H, Xu Q, Chen MJ, Liao Y, Thiyagarajan M, et al. Sleep drives metabolite clearance from the adult brain. Science. 2013;342(6156):373-7. https://doi.org/10.1126/science.1241224 PMid:24136970 Search in Google Scholar

Kalimo R, Tenkanen L, Härmä M, Poppius E, Heinsalmi P. Job stress and sleep disorders: Findings from the Helsinki Heart Study. Stress Med. 2000;16(2):65-75. Search in Google Scholar

Akerstedt T, Kecklund G, Axelsson J. Impaired sleep after bedtime stress and worries. Biol Psychol. 2007;76(3):170-3. https://doi.org/10.1016/j.biopsycho.2007.07.010 PMid:17884278 Search in Google Scholar

Bernardy NC, Friedman MJ. A Practical Guide to PTSD Treatment: Pharmacological and Psychotherapeutic Approaches. A Practical Guide to PTSD Treatment: Pharmacological and Psychotherapeutic Approaches. United States: American Psychological Association; 2014. Search in Google Scholar

Jansen AS, Van Nguyen X, Karpitskiy V, Mettenleiter TC, Loewy AD. Central command neurons of the sympathetic nervous system: Basis of the fight-or-flight response. Science. 1995;270(5236):644-6. Search in Google Scholar

McEwen BS. Protective and damaging effects of stress mediators. N Engl J Med. 1998;338(3):171-9. https://doi.org/10.1056/NEJM199801153380307 PMid:9428819 Search in Google Scholar

Lindquist TL, Beilin LJ, Knuiman MW. Influence of lifestyle, coping, and job stress on blood pressure in men and women. Hypertension. 1997;29(1 Pt 1):1-7. https://doi.org/10.1161/01.hyp.29.1.1 PMid:9039072 Search in Google Scholar

Kaplan JR, Manuck SB, Clarkson TB, Lusso FM, Taub DM, Miller EW. Social stress and atherosclerosis in normocholesterolemic monkeys. Science. 1983;220(4598):733-5. https://doi.org/10.1126/science.6836311 PMid:6836311 Search in Google Scholar

Dallman MF. Stress-induced obesity and the emotional nervous system. Trends Endocrinol Metab. 2010;21(3):159-65. https://doi.org/10.1016/j.tem.2009.10.004 PMid:19926299 Search in Google Scholar

Hammen C. Stress and depression. Annu Rev Clin Psychol. 2005;1:293-319. https://doi.org/10.1146/annurev.clinpsy.1.102803.143938 PMid:17716090 Search in Google Scholar

Goeders NE. The impact of stress on addiction. Eur Neuropsychopharmacol. 2003;13(6):435-41. https://doi.org/10.1016/j.euroneuro.2003.08.004 PMid:14636959 Search in Google Scholar

Shin LM, Liberzon I. The neurocircuitry of fear, stress, and anxiety disorders. Neuropsychopharmacology. 2010;35(1): 169-91. https://doi.org/10.1038/npp.2009.83 PMid:19625997 Search in Google Scholar

Berridge CW, Waterhouse BD. The locus coeruleusnoradrenergic system: Modulation of behavioral state and state-dependent cognitive processes. Brain Res Brain Res Rev. 2003;42(1):33-84. https://doi.org/10.1016/s0165-0173(03)00143-7 PMid:12668290 Search in Google Scholar

O’Donnell J, Ding F, Nedergaard M. Distinct functional states of astrocytes during sleep and wakefulness: Is norepinephrine the master regulator? Curr Sleep Med Rep. 2015;1(1):1-8. https://doi.org/10.1007/s40675-014-0004-6 PMid:26618103 Search in Google Scholar

Lee H, Xie L, Yu M, Kang H, Feng T, Deane R, et al. The Effect of body posture on brain glymphatic transport. J Neurosci. 2015;35(31):11034-44. https://doi.org/10.1523/JNEUROSCI.1625-15.2015 PMid:26245965 Search in Google Scholar

Akerstedt T. Psychosocial stress and impaired sleep. Scand J Work Environ Health 2006;32(6):493-501. Search in Google Scholar

Fu H, Hardy J, Duff KE. Selective vulnerability in neurodegenerative diseases. Nat Neurosci. 2018;21(10): 1350-8. https://doi.org/10.1038/s41593-018-0221-2 PMid:30250262 Search in Google Scholar

Ross CA, Poirier MA. Protein aggregation and neurodegenerative disease. Nat Med. 2004;10 Suppl: S10-7. http://doi.org/10.1038/nm1066 PMid:15272267 Search in Google Scholar

Hardy J, Allsop D. Amyloid deposition as the central event in the aetiology of Alzheimer’s disease. Trends Pharmacol Sci. 1991;12(10):383-8. https://doi.org/10.1016/0165-6147(91)90609-v PMid:1763432 Search in Google Scholar

Peng W, Achariyar TM, Li B, Liao Y, Mestre H, Hitomi E, et al. Suppression of glymphatic fluid transport in a mouse model of Alzheimer’s disease. Neurobiol Dis. 2016;93:215-25. https://doi.org/10.1016/j.nbd.2016.05.015 PMid:27234656 Search in Google Scholar

Zuroff L, Daley D, Black KL, Koronyo-Hamaoui M. Clearance of cerebral Aβ in Alzheimer’s disease: Reassessing the role of microglia and monocytes. Cell Mol Life Sci. 2017;74(12):2167-201. https://doi.org/10.1007/s00018-017-2463-7 PMid:28197669 Search in Google Scholar

Qi XM, Ma JF. The role of amyloid beta clearance in cerebral amyloid angiopathy: More potential therapeutic targets. Transl Neurodegener. 2017;6:22. https://doi.org/10.1186/s40035-017-0091-7 PMid:28824801 Search in Google Scholar

Wang LY, Murphy RR, Hanscom B, Li G, Millard SP, Petrie EC, et al. Cerebrospinal fluid norepinephrine and cognition in subjects across the adult age span. Neurobiol Aging. 2013;34(10):2287-92. https://doi.org/10.1016/j.neurobiolaging.2013.04.007 PMid:23639207 Search in Google Scholar

Szot P. Elevated cerebrospinal fluid norepinephrine in the elderly can link depression and a reduced glymphatic system as risk factors for Alzheimer’s Disease. J Aging Sci. 2016;4(2):158. Search in Google Scholar

Musiek ES, Xiong DD, Holtzman DM. Sleep, circadian rhythms, and the pathogenesis of Alzheimer’s disease. Exp Mol Med. 2015;47(3):e148. https://doi.org/10.1038/emm.2014.121 PMid:25766617 Search in Google Scholar

Rasmussen MK, Mestre H, Nedergaard M. The glymphatic pathway in neurological disorders. Lancet Neurol. 2018;17(11):1016-24. https://doi.org/10.1016/S1474-4422(18)30318-1 PMid:30353860 Search in Google Scholar

Mendelsohn AR, Larrick JW. Sleep facilitates clearance of metabolites from the brain: Glymphatic function in aging and neurodegenerative diseases. Rejuvenation Res. 2013;16(6):518-23. https://doi.org/10.1089/rej.2013.1530 PMid:24199995 Search in Google Scholar

Piantino J, Lim MM, Newgard CD, Iliff J. Linking traumatic brain injury, sleep disruption and post-traumatic headache: A potential role for glymphatic pathway dysfunction. Curr Pain Headache Rep. 2019;23(9):62. https://doi.org/10.1007/s11916-019-0799-4 PMid:31359173 Search in Google Scholar

Gaberel T, Gakuba C, Goulay R, De Lizarrondo SM, Hanouz JL, Emery E, et al. Impaired glymphatic perfusion after strokes revealed by contrast-enhanced MRI: A new target for fibrinolysis? Stroke. 2014;45(10):3092-6. https://doi.org/10.1161/STROKEAHA.114.006617 PMid:25190438 Search in Google Scholar

Back DB, Kwon KJ, Choi DH, Shin CY, Lee J, Han SH, et al. Chronic cerebral hypoperfusion induces post-stroke dementia following acute ischemic stroke in rats. J Neuroinflammation. 2017;14(1):216. https://doi.org/10.1186/s12974-017-0992-5 PMid:29121965 Search in Google Scholar

Bobela W, Aebischer P, Schneider BL. Alpha-synuclein as a mediator in the interplay between aging and Parkinson’s disease. Biomolecules. 2015;5(4):2675-700. https://doi.org/10.3390/biom5042675 PMid:26501339 Search in Google Scholar

Zou W, Pu T, Feng W, Lu M, Zheng Y, Du R, et al. Blocking meningeal lymphatic drainage aggravates Parkinson’s disease-like pathology in mice overexpressing mutated α-synuclein. Transl Neurodegener. 2019;8:7. https://doi.org/10.1186/s40035-019-0147-y PMid:30867902 Search in Google Scholar

Sundaram S, Hughes RL, Peterson E, Müller-Oehring EM, Brontë-Stewart HM, Poston KL, et al. Establishing a framework for neuropathological correlates and glymphatic system functioning in Parkinson’s disease. Neurosci Biobehav Rev. 2019;103:305-15. https://doi.org/10.1016/j.neubiorev.2019.05.016 PMid:31132378 Search in Google Scholar

Jiang Q, Zhang L, Ding G, Davoodi-Bojd E, Li Q, Li L, et al. Impairment of the glymphatic system after diabetes. J Cereb Blood Flow Metab. 2017;37(4):1326-37. https://doi.org/10.1177/0271678X16654702 PMid:27306755 Search in Google Scholar

Hirotsu C, Tufik S, Andersen ML. Interactions between sleep, stress, and metabolism: From physiological to pathological conditions. Sleep Sci. 2015;8(3):143-52. https://doi.org/10.1016/j.slsci.2015.09.002 PMid:26779321 Search in Google Scholar

Vasileva LV, Saracheva KE, Ivanovska MV, Petrova AP, Marchev AS, Georgiev MI, et al. Antidepressant-like effect of salidroside and curcumin on the immunoreactivity of rats subjected to a chronic mild stress model. Food Chem Toxicol. 2018;121:604-11. https://doi.org/10.1016/j.fct.2018.09.065 PMid:30268794 Search in Google Scholar

Dhabhar FS. Enhancing versus suppressive effects of stress on immune function: Implications for immunoprotection and immunopathology. Neuroimmunomodulation. 2009;16(5):300-17. https://doi.org/10.1159/000216188 PMid:19571591 Search in Google Scholar

Williams RB, Marchuk DA, Gadde KM, Barefoot JC, Grichnik K, Helms MJ, et al. Central nervous system serotonin function and cardiovascular responses to stress. Psychosom Med. 2001;63(2):300-5. https://doi.org/10.1097/00006842-200103000-00016 PMid:11292279 Search in Google Scholar

Lavi E, Cong L. Type I astrocytes and microglia induce a cytokine response in an encephalitic murine coronavirus infection. Exp Mol Pathol. 2020;115:104474. https://doi.org/10.1016/j.yexmp.2020.104474 PMid:32454103 Search in Google Scholar

Louveau A, Herz J, Alme MN, Salvador AF, Dong MQ, Viar KE, et al. CNS lymphatic drainage and neuroinflammation are regulated by meningeal lymphatic vasculature. Nat Neurosci 2018;21(10):1380-91. https://doi.org/10.1038/s41593-018-0227-9 PMid:30224810 Search in Google Scholar

Negi N, Das BK. CNS: Not an immunoprivilaged site anymore but a virtual secondary lymphoid organ. Int Rev Immunol. 2018;37(1): 57-68. https://doi.org/10.1080/08830185.2017.1357719 PMid:28961037 Search in Google Scholar

Yanev P, Poinsatte K, Hominick D, Khurana N, Zuurbier KR, Berndt M, et al. Impaired meningeal lymphatic vessel development worsens stroke outcome. J Cereb Blood Flow Metab. 2020;40(2):263-75. https://doi.org/10.1177/0271678X18822921 PMid:30621519 Search in Google Scholar

Chen J, He J, Ni R, Yang Q, Zhang Y, Luo L. Cerebrovascular injuries induce lymphatic invasion into brain parenchyma to guide vascular regeneration in zebrafish. Dev Cell. 2019;49(5): 697-710.e5. https://doi.org/10.1016/j.devcel.2019.03.022 PMid:31006646 Search in Google Scholar

Benakis C, Llovera G, Liesz A. The meningeal and choroidal infiltration routes for leukocytes in stroke. Ther Adv Neurol Disord. 2018;11:1756286418783708. https://doi.org/10.1177/1756286418783708 PMid:29977343 Search in Google Scholar

Rua R, McGavern DB. Advances in meningeal immunity. Trends Mol Med. 2018;24(6):542-59. https://doi.org/10.1016/j.molmed.2018.04.003 PMid:29731353 Search in Google Scholar

Mander BA, Winer JR, Walker MP. Sleep and human aging. Neuron. 2017;94(1):19-36. https://doi.org/10.1016/j.neuron.2017.02.004 PMid:28384471 Search in Google Scholar

Hablitz LM, Vinitsky HS, Sun Q, Stæger FF, Sigurdsson B, Mortensen KN, et al. Increased glymphatic influx is correlated with high EEG delta power and low heart rate in mice under anesthesia. Sci Adv. 2019;5(2):eaav5447. https://doi.org/10.1126/sciadv.aav5447 PMid:30820460 Search in Google Scholar

Tay TL, Savage JC, Hui CW, Bisht K, Tremblay M. Microglia across the lifespan: From origin to function in brain development, plasticity and cognition. J Physiol. 2017;595(6):1929-45. https://doi.org/10.1113/jp272134 Search in Google Scholar

Clarke LE, Liddelow SA, Chakraborty C, Münch AE, Heiman M, Barres BA. Normal aging induces A1-like astrocyte reactivity. Proc Natl Acad Sci U S A. 2018;115:E1896-905. https://doi.org/10.1073/pnas.1800165115 PMid:29437957 Search in Google Scholar

Cotrina ML, Nedergaard M. Astrocytes in the aging brain. J Neurosci Res. 2002;67(1):1-10. https://doi.org/10.1002/jnr.10121 PMid:11754075 Search in Google Scholar

Finch CE. Neurons, glia, and plasticity in normal brain aging. Neurobiol Aging. 2003;24(Suppl 1):S123-7. https://doi.org/10.1016/s0197-4580(03)00051-4 PMid:12829120 Search in Google Scholar

Campuzano O, Castillo-Ruiz MM, Acarin L, Castellano B, Gonzalez B. Increased levels of proinflammatory cytokines in the aged rat brain attenuate injury-induced cytokine response after excitotoxic damage. J Neurosci Res. 2009;87(11):2484-97. https://doi.org/10.1002/jnr.22074 PMid:19326443 Search in Google Scholar

Thrane VR, Thrane AS, Plog BA, Thiyagarajan M, Iliff JJ, Deane R, et al. Paravascular microcirculation facilitates rapid lipid transport and astrocyte signaling in the brain. Sci Rep. 2013;3:2582. https://doi.org/10.1038/srep02582 PMid:24002448 Search in Google Scholar

Profenno LA, Porsteinsson AP, Faraone SV. Meta-analysis of Alzheimer’s disease risk with obesity, diabetes, and related disorders. Biol Psychiatry. 2010;67(6):505-12. https://doi.org/10.1016/j.biopsych.2009.02.013 PMid:19358976 Search in Google Scholar

Gaede P, Vedel P, Larsen N, Jensen GV, Parving HH, Pedersen O, et al. Multifactorial intervention and cardiovascular disease in patients with Type 2 diabetes. N Engl J Med. 2003;348(5):383-93. https://doi.org/10.1056/NEJMoa021778 Search in Google Scholar

Seravalle G, Grassi G. Obesity and hypertension. Pharmacol Res. 2017;122:1-7. https://doi.org/10.1016/j.phrs.2017.05.013 PMid:28532816 Search in Google Scholar

Wysocki M, Luo X, Schmeidler J, Dahlman K, Lesser GT, Grossman H, et al. Hypertension is associated with cognitive decline in elderly people at high risk for dementia. Am J Geriatr Psychiatry. 2012;20(2):179-87. https://doi.org/10.1097/JGP.0b013e31820ee833 PMid:21814158 Search in Google Scholar

Kummer BR, Diaz I, Wu X, Aaroe AE, Chen ML, Iadecola C, et al. Associations between cerebrovascular risk factors and Parkinson disease. Ann Neurol. 2019;86(4):572-81. https://doi.org/10.1002/ana.25564 PMid:31464350 Search in Google Scholar

de Heus RA, Rikkert MG, Tully PJ, Lawlor BA, Claassen JA, NILVAD Study Group. Blood pressure variability and progression of clinical Alzheimer disease. Hypertension. 2019;74(5):1172-80. https://doi.org/10.1161/HYPERTENSIONAHA.119.13664 PMid:31542965 Search in Google Scholar

Mortensen KN, Sanggaard S, Mestre H, Lee H, Kostrikov S, Xavier AL, et al. Impaired glymphatic transport in spontaneously hypertensive rats. J Neurosci. 2019;39(32):6365-77. https://doi.org/10.1523/JNEUROSCI.1974-18.2019 PMid:31209176 Search in Google Scholar

Blair GW, Thrippleton MJ, Shi Y, Hamilton I, Stringer M, Chappell F, et al. Intracranial hemodynamic relationships in patients with cerebral small vessel disease. Neurology. 2020;94(21):e2258-69. https://doi.org/10.1212/WNL.0000000000009483 PMid:32366534 Search in Google Scholar

Geurts LJ, Zwanenburg JJ, Klijn CJ, Luijten PR, Biessels GJ. Higher pulsatility in cerebral perforating arteries in patients with small vessel disease related stroke, a 7T MRI Study. Stroke. 2019;50:62-8. Search in Google Scholar

Lorente-Cebrián S, Costa AG, Navas-Carretero S, Zabala M, Martínez JA, Moreno-Aliaga MJ. Role of omega-3 fatty acids in obesity, metabolic syndrome, and cardiovascular diseases: A review of the evidence. J Physiol Biochem. 2013;69(3): 633-51. https://doi.org/10.1007/s13105-013-0265-4 PMid:23794360 Search in Google Scholar

Bazinet RP, Layé S. Polyunsaturated fatty acids and their metabolites in brain function and disease. Nat Rev Neurosci. 2014;15(12):771-85. https://doi.org/10.1038/nrn3820 PMid:25387473 Search in Google Scholar

Ren H, Luo C, Feng Y, Yao X, Shi Z, Liang F, et al. Omega-3 polyunsaturated fatty acids promote amyloid-b clearance from the brain through mediating the function of the glymphatic system. FASEB J. 2017;31(1):282-93. https://doi.org/10.1096/fj.201600896 PMid:27789520 Search in Google Scholar

Zhang E, Wan X, Yang L, Wang D, Chen Z, Chen Y, et al. Omega-3 polyunsaturated fatty acids alleviate traumatic brain injury by regulating the glymphatic pathway in mice. Front Neurol. 2020;11:707. https://doi.org/10.3389/fneur.2020.00707 PMid:32765412 Search in Google Scholar

Chan JK, Trinder J, Colrain IM, Nicholas CL. The acute effects of alcohol on sleep electroencephalogram power spectra in late adolescence. Alcohol Clin Exp Res. 2015;39(2):291-9. https://doi.org/10.1111/acer.12621 PMid:25597245 Search in Google Scholar

eISSN:
1857-9388
Langue:
Anglais
Périodicité:
Volume Open
Sujets de la revue:
Medicine, Basic Medical Science, Immunology, Clinical Medicine, Laboratory Medicine