Glenfatik Sistem

Ganong WF. The general and cellular basis of medical physiology, In: Review of Medical Physiology, Ganong WF(Ed.). Nineteenth Edition. Stamford Connecticut, USA: Appleton&Lange; 1999. pp. 1-46.

Liao S, Padera TP. Lymphatic function and immune regulation in health and disease. Lymphatic Research and Biology. 2013;11:136–43.

Gartner LP. Circulatory System, In: Textbook of Histology, Gartner LP(Ed.). Fourth Edition, Philadelphia, PA, USA: Elsevier; 2017. pp; 287-310.

Wang Z, Ying Z, Bosy-Westphal A, et al. Evaluation of specific metabolic rates of major organs and tissues: Comparison between nonobese and obese women. Obesity. 2012;20 (1), 95–100.

Taş F, Erdoğan E. Sıçan ependim hücrelerinde Aquaporin 4 kanallarının immünohistokimyasal dağılımı ve glimfatik sisteme etkisi. Ahi Evran Medical Journal. 2020;4(2), 41-47

Bucchieri F, Farina F, Zummo G, et al. Lymphatic vessels of the dura mater: A new discovery? Journal of Anatomy. 2015;227, 702–703.

Lecco V. Di una probabile modificazione delle fissure linfatiche della della parte dei seni venosi della dura madre. Archives Italian Otorhinolaringology. 1953;64, 287–96.

Sandrone S, Moreno-Zambrano D, Kipnis J, et al. A (delayed) history of the brain lymphatic system. Nature Medicine. 2019;25(4):538-540.

Diren F, Civelek E, Kabataş S. Beyin immünolojisi ve kafa travmalarında nöroinflamasyon. Türk Nöroşirurji Dergisi. 2020;30(2), 209-216.

Li J, Zhou J, Shi Y. Scanning electron microscopy of human cerebral meningeal stomata. Annals of Anatomy. 1996;178, 259–261.

Jessen NA, Munk AS, Lundgaard I, et al. The glymphatic system: a beginner’s guide. Neurochemical Research. 2015;40(12), 2583–2599.

Johanson CE, Duncan J, Klinge PM, et al. Multiplicity of cerebrospinal fluid functions: New challenges in health and disease. Cerebrospinal Fluid Research. 2008;5:10.

Thrane AS, Rangroo Thrane V, Nedergaard M. Drowning stars: reassessing the role of astrocytes in brain edema. Trends Neurosciences. 2014;37:620–628.

Johanson CE. Choroid plexus - Cerebrospinal fluid circulatory dynamics: Impact on brain growth, metabolism, and repair. Neuroscience in Medicine. 2008; pp:173-200

Keep RF, Jones HC. A morphometric study on the development of the lateral ventricle choroid plexus, choroid plexus capillaries and ventricular ependyma in the rat. Brain Research Developmental Brain Research. 1990;56, 47–53.

Rakunt C, Şahin C: Beyin omurilik sıvısı. Türkiye Klinikleri. 1987;7: 73-80.

Damkier HH, Brown PD, Praetorius J. Cerebrospinal fluid secretion by the choroid plexus. Physiological Reviews. 2013;93:1847–92.

Banizs B, Pike MM, Millican CL, et al. Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus. Development. 2005;132:5329–39.

Oshio K, Watanabe H, Song Y, et al. Reduced cerebrospinal fluid production and intracranial pressure in mice lacking choroid plexus water channel Aquaporin-1.FASEB Journal. 2005;19:76-78.

Papadopoulos MC, Verkman AS. Aquaporin water channels in the nervous system. Nature Reviews Neuroscience. 2013;14:265-277.

Brown P, Davies S, Speake T, et al. Molecular mechanisms of cerebrospinal fluid production. Neuroscience. 2004;129:957–70.

Davson H, Segal MB. The effects of some inhibitors and accelerators of sodium transport on the turnover of 22Na in the cerebrospinal fluid and the brain. The Journal Physiololgy. 1970;209:131–153.

Segal MB, Burgess AM. A combined physiological and morphological study of the secretory process in the rabbit choroid plexus. Jornal of Cell Science. 1974;14:339–350.

Praetorius J, Nielsen S. Distribution of sodium transporters and aquaporin-1 in the human choroid plexus. American Journal of Physiology Cell Physiology. 2006;291:C59–67.

Nielsen S, Smith BL, Christensen EI, et al. Distribution of the aquaporin CHIP in secretory and resorptive epithelia and capillary endothelia. Proceeding of the National Academy of Sciences of the United State America. 1993;90:7275–7279.

Prince E, Ahn S. Basic vascular neuroanatomy of the brain and spine: what the general interventional radiologist needs to know. Seminars in Interventional Radiology. 2013;30:234–9.

Zlokovic BV. Neurovascular pathways to neurodegeneration in Alzheimer's disease and other disorders. Nature Reviews Neuroscience. 2011;12:723–38.

Del Zoppo GJ, Moskowitz M, Nedergaard M: The Neurovascular Unit and Responses to Ischemia. Stroke. 2015:90-101

Yüncü M. Histobul. Adana: Çokurova Nobel Tıp Kitabevi; 2014. p. 135-37.

Colombo JA, Reisin HD. Interlaminar astroglia of the cerebral cortex: A marker of the primate brain. Brain Research. 2004;1006 (1), 126–131

Preston GM, Carroll TP, Guggino WB, et al. Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein. Science (New York, N.Y.). 1992;256, 5055, 385-7.

Bhattacharjee H, Carbrey J, Rosen BP. Drug uptake and pharmacological modulation of drug sensitivity in leukemia by AQP9. Biochemical and biophysical research communications. 2004;322, 3, 836-41.

Agre P, Kozono D. Aquaporin water channels: molecular mechanisms for human diseases. FEBS letters, 2003;555, 1, 72-8.

Iliff JJ, Wang M, Liao Y, Plogg BA, et al. 2012. A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid β. Science Translational Medicine. 2012;4, 147ra111.

Klose U, Strik C, Kiefer C. Detection of a relation between respiration and CSF pulsation with an echoplanar technique. Journal Magnetic Resonance Imaging. 2000;11:438–444.

Yamada S, Miyazaki M, Yamashita Y, et al. Influence of respiration on cerebrospinal fluid movement using magnetic resonance spin labeling. Fluids Barriers of the CNS. 2013;10:36.

Iliff JJ, Nedergaard M. Is there a cerebral lymphatic system?. Stroke. 2013;44:S93–5.

Iliff JJ, Wang M, Zeppenfeld DM, Venkataraman A, et al. Cerebral arterial pulsation drives paravascular CSF interstitial fluid exchange in the murine brain. The Journal of Neuroscience. 2013;33(46), 18190–18199.

Murtha LA, Yang Q, Parsons MW, 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.

Symss NP, Oi S. Theories of cerebrospinal fluid dynamics and hydrocephalus Historical trend. J Neurosurgery Pediatrics. 2013; 11:170- 177.

Aspelund A, Antila S, Proulx ST, et al. A dural lymphatic vascular system that drains brain interstitial fluid and macromolecules. ”The Jornal of Experimantal Medicine, 2015;212(7):991-999.

Madsen PL, Schmidt JF, Wildschiødtz G, et al. Cerebral O2 metabolism and cerebral blood flow in humans during deep and rapid-eye-movement sleep. Journal of Applied Physiology. 1991;70:2597–2601.

Xie L, Kang H, Xu Q, et al. Sleep drives metabolite clearance from the adult brain. Science. 2013;342:373–7

O'Donnell J, Zeppenfeld D, McConnell E, et al. 2012. Norepinephrine: a neuromodulator that boosts the function of multiple cell types to optimize CNS performance. Neurochemical Research. 2012; 37, 2496–2512.

Nilsson C, Lindvall-Axelsson M, Owman C. Neuroendocrine regulatory mechanisms in the choroid plexus-cerebrospinal fluid system. Brain Research Reviews. 1992;17:109–138.

Kress BT, Iliff JJ, Xia M, et al. Impairment of paravascular clearance pathways in the aging brain. Annals of Neurology. 2014:1–17

Sabbatini M, Barili P, Bronzetti E, et al. Age-related changes of glial fibrillary acidic protein immunoreactive astrocytes in the rat cerebellar cortex. Mechanisms Ageing and Development. 1999;108:165–172.

Nielsen S, King LS, Christensen BM, et al. Aquaporins in complex tissues. II. Subcellular distribution in respiratory and glandular tissues of rat. The American Journal Physiology. 1997; 273(5), C1549-C61.

Jiang Q, Zhang L, Ding G, et al. Impairment of the glymphatic system after diabetes. Journal of Cerebral Blood Flow and Metabolism. 2016; 37(4),1326- 37

Braak H, Braak E. Neuropathological staging of Alzheimer’s disease changes. Acta Neuropathologica. 1991;82:239-59.

Meraz-Rios MA, Lira-De Leon KI, Campos-Pena V, De Anda-Hernandez MA, Mena-Lopez R. Tau oligomers and aggregation in Alzheimer’s disease. J Neurochem 2010;112:1353-67.

Haass C, Selkoe DJ. Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer’s amyloid β-peptide. Nature reviews. 2007; 8:101-12.

Sjöberg MK, Shestakova E, Mansuroğlu Z, et al. Tau protein binds to pericentromeric DNA: a putative role for nuclear tau in nucleolar organisation. Journal of Cell Science. 2006;119:2025-34.

Ludolph AC, Kassubek J, Landwehrmeyer BG, et al. Reisenburg Working Group for Taupathies with Parkinsonis. Taupathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options. European Journal of Neurology. 2009;16:297-309.

Bero AW, Yan P, Roh JH, et al. Neuronal activity regulates the regional vulnerability to amyloid-beta deposition. Nature Neuroscience. 2011; 14:750–756.

Skaper SD, Evans NA, Rosin C, et al. Oligodendrocytes are a novel source of amyloid peptide generation. Neurochemical Research. 2009; 34:2243–2250.

Sagare AP, Bell RD, Zlokovic BV. Neurovascular dysfunction and faulty amyloid beta-peptide clearance in Alzheimer disease. Cold Spring Harbor Perspectives in Medicine. 2012; 2(10): a011452.

Ferrer I. Cognitive impairment of vascular origin: neuropathology of cognitive impairment of vascular origin. Journal of the Neurological Science. 2010;299:139–149.

Thal DR, Grinberg LT, Attems J. Vascular dementia: different forms of vessel disorders contribute to the development of dementia in the elderly brain. Experimental Gerontology. 2012;47:816–824.

Joutel A, Corpechot C, Ducros A, et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature. 1996;383:707–710.

Kuppers E, Gleiser C, Brito V, et al. AQP4 expression in striatal primary cultures is regulated by dopamine--implications for proliferation of astrocytes. The European journal of neuroscience. 2008;28, 11, 2173-82.

Li JY, Englund E, Holton JL, et al. Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation. Nature Medicine. 2008;14:501–503.

Foglio E, Rodella LF. Aquaporins and Neurodegenerative Diseases. Current Neuropharmacology. 2010;8, 2, 112-21.

Irimia A, Wang B, Aylward SR, et al. Neuroimaging of structural pathology and connectomics in traumatic brain injury: Toward personalized outcome prediction. Neuroimage Clinical. 2012;1:1–17.

Zemlan FP, Jauch EC, Mulchahey JJ, et al. C-tau biomarker of neuronal damage in severe brain injured patients: Association with elevated intracranial pressure and clinical outcome. Brain Researc. 2002;947:131–139.

Guo JL, Lee VM. Seeding of normal Tau by pathological Tau conformers drives pathogenesis of Alzheimer-like tangles. The Journal of Biological Chemistry. 2011;286:15317–15331.