Fate of Cerebrospinal Fluid‐Borne Amyloid β‐Peptide: Rapid Clearance into Blood and Appreciable Accumulation by Cerebral Arteries
Abstract
In Alzheimer's disease, the neuritic or senile amyloid plaques in hippocampus and association cortex, the diffuse plaques in brain areas such as the cerebellum and sensorimotor cortex, and the amyloid deposits in the walls of pial and parenchymal blood vessels are mainly composed of amyloid beta-peptides. In the present study, either soluble 40-residue amyloid beta-peptide radiolabeled with 125I (I-sAbeta) or [14C]polyethylene glycol ([14C]PEG, a reference material) was briefly infused into one lateral ventricle of normal rats. By 3.5 min, 30% of the I-sAbeta was cleared from ventricular CSF into blood; another 30% was removed over the next 6.5 min. No [14C]PEG was lost from the CSF-brain system during the first 5 min, and only 20% was cleared by 10 min. Much of the I-sAbeta that reached the subarachnoid space was retained by pial arteries and arterioles. Virtually no I-sAbeta was found in brain. The clearance of amyloid beta-peptides from the CSF-brain system, reported herein for normal rats, may be reduced in Alzheimer's disease, thus contributing to amyloid deposition in cerebral tissue and blood vessels.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
CSF Aβ has a high concentration relative to plasma Aβ and is normally cleared into blood.
“because CSF A, which has a high concentration relative to plasma A, is normally cleared into blood (Ghersi-Egea et al., 1996).”
From Age-Dependent Changes in Brain, CSF, and Plasma Amyloid β Protein in the Tg2576 Transgenic Mouse Model of Alzheimer's Disease (2001) · cites this paper as Ghersi-Egea et al., 1996
Cited by
Sorted by citations
Amyloid Beta: Structure, Biology and Structure-Based Therapeutic Development
Chen, G.-F., Xu, T.-H., Yan, Y., Zhou, Y.-R., Jiang, Y., Melcher, K., & Xu, H. E. (2017) · Acta Pharmacologica Sinica · doi:10.1038/aps.2017.28 · Cited by 1,965 · see citing works
RAGE mediates amyloid-β peptide transport across the blood-brain barrier and accumulation in brain
Deane, R., Du Yan, S., Submamaryan, R. K., LaRue, B., Jovanovic, S., Hogg, E., Welch, D., Manness, L., Lin, C., Yu, J., et al. (2003) · Nature Medicine · doi:10.1038/nm890 · Cited by 1,426 · see citing works
Self-citationShibata, M., Yamada, S., Kumar, S. R., Calero, M., Bading, J., Frangione, B., Holtzman, D. M., Miller, C. A., Strickland, D. K., Ghiso, J., et al. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10498 · Cited by 1,413 · see citing works
“Transport of Aβ out of the CSF was not associated with significant degradation of peptide in the CSF (29).”
BackgroundInfluentialSelf-citationCerebral Arterial Pulsation Drives Paravascular CSF–Interstitial Fluid Exchange in the Murine Brain
Iliff, J. J., Wang, M., Zeppenfeld, D. M., Venkataraman, A., Plog, B. A., Liao, Y., Deane, R., & Nedergaard, M. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1592-13.2013 · Cited by 1,319 · see citing works
“…veins (Iliff et al., 2012), presumably spilling solutes, such as A , into the subarachnoid CSF for subsequent elimination via the choroid plexus (Ghersi-Egea et al., 1996; Fujiyoshi et al., 2011), or through bulk CSF reabsorption through arachnoid granulations or cervical lymphatics (Johanson…”
BackgroundDeMattos, R. B., Bales, K. R., Cummins, D. J., Dodart, J.-C., Paul, S. M., & Holtzman, D. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.151261398 · Cited by 1,298 · see citing works
Kawarabayashi, T., Younkin, L. H., Saido, T. C., Shoji, M., Ashe, K. H., & Younkin, S. G. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-02-00372.2001 · Cited by 1,053 · see citing works
Cellular actions of beta-amyloid precursor protein and its soluble and fibrillogenic derivatives
Mattson, M. P. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.4.1081 · Cited by 1,006 · see citing works
A systemic view of Alzheimer disease — insights from amyloid-β metabolism beyond the brain
Wang, J., Gu, B. J., Masters, C. L., & Wang, Y.-J. (2017) · Nature Reviews Neurology · doi:10.1038/nrneurol.2017.111 · Cited by 808 · see citing works
Bell, R. D., Sagare, A. P., Friedman, A. E., Bedi, G. S., Holtzman, D. M., Deane, R., & Zlokovic, B. V. (2007) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600419 · Cited by 670 · see citing works
“However, the BBB bidirectional transport of exogenous soluble human Ab (Zlokovic et al, 1993; Maness et al, 1994; Ghilardi et al, 1996; Ghersi-Egea et al, 1996; Poduslo et al, 1997; Mackic et al, 1998b; Deane et al, 2003, 2004, 2005; Banks et al, 2003; LaRue et al, 2004) and the BBB influx of its…”
BackgroundAmyloid β protein forms ion channels: implications for Alzheimer's disease pathophysiology
LIN, H., Bhatia, R., & Lal, R. (2001) · The FASEB Journal · doi:10.1096/fj.01-0377com · Cited by 641 · see citing works
The role of brain barriers in fluid movement in the CNS: is there a ‘glymphatic’ system?
Abbott, N. J., Pizzo, M. E., Preston, J. E., Janigro, D., & Thorne, R. G. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1812-4 · Cited by 593 · see citing works
“However, it has also been suggested that this pattern of amyloid beta deposition could be due to abnormal perivascular amyloid beta entry and accumulation from the CSF into the brain [69, 137], consistent with reports that leptomeningeal arteries typically exhibit more cerebral amyloid angiopathy than penetrating cort…”
ResultBlood–Brain Barrier Dysfunction as a Cause and Consequence of Alzheimer's Disease
Erickson, M. A., & Banks, W. A. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.135 · Cited by 572 · see citing works
DeMattos, R. B., Bales, K. R., Cummins, D. J., Paul, S. M., & Holtzman, D. M. (2002) · Science · doi:10.1126/science.1067568 · Cited by 563 · see citing works
Plasma Aβ1–40 and Aβ1–42 and the risk of dementia: a prospective case-cohort study
van Oijen, M., Hofman, A., Soares, H. D., Koudstaal, P. J., & Breteler, M. M. (2006) · The Lancet Neurology · doi:10.1016/s1474-4422(06)70501-4 · Cited by 458 · see citing works
Ghersi-Egea, J.-F., Strazielle, N., Catala, M., Silva-Vargas, V., Doetsch, F., & Engelhardt, B. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1807-1 · Cited by 436 · see citing works
“The CSF circulation plays a role in amyloid beta distribution and clearance from the brain [49].”
BackgroundSelf-citationCerebral Amyloid Angiopathy: A Systematic Review
Biffi, A., & Greenberg, S. M. (2011) · Journal of Clinical Neurology · doi:10.3988/jcn.2011.7.1.1 · Cited by 444 · see citing works
Silverberg, G., Mayo, M., Saul, T., Rubenstein, E., & Mcguire, D. (2003) · Lancet Neurology · doi:10.1016/s1474-4422(03)00487-3 · Cited by 429 · see citing works
Calhoun, M. E., Burgermeister, P., Phinney, A. L., Stalder, M., Tolnay, M., Wiederhold, K.-H., Abramowski, D., Sturchler-Pierrat, C., Sommer, B., Staufenbiel, M., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.24.14088 · Cited by 410 · see citing works
Microglia and inflammatory mechanisms in the clearance of amyloid β peptide
Rogers, J., Strohmeyer, R., Kovelowski, C. J., & Li, R. (2002) · Glia · doi:10.1002/glia.10153 · Cited by 381 · see citing works
“, 2000), and that exogenous A is rapidly transported from CSF to plasma with an elimination half-life of some 30 min (Ghersi-Egea et al., 1996; Shibata et al., 2000).”
BackgroundKanai, M., Matsubara, E., Isoe, K., Urakami, K., Nakashima, K., Arai, H., Sasaki, H., Abe, K., Iwatsubo, T., Kosaka, T., et al. (1998) · Annals of Neurology · doi:10.1002/ana.410440108 · Cited by 340 · see citing works
Choroid Plexus in the Central Nervous System: Biology and Physiopathology
Strazielle, N., & Ghersi-Egea, J.-F. (2000) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/59.7.561 · Cited by 307 · see citing works
“Choroid plexuses also constitute a direct access to the ventricles, ependyma and subependymal tissue, leptomeninges, velae, outer layers of pial vessels, and perivascular spaces (39, 73).”
BackgroundSelf-citationStandardization of measurement of β-amyloid<sub>(1-42)</sub>in cerebrospinal fluid and plasma
Vanderstichele, H., Kerschaver, E. V., Hesse, C., Davidsson, P., Buyse, M.-A., Andreasen, N., Minthon, L., Wallin, A., Blennow, K., & Vanmechelen, E. (2000) · Amyloid · doi:10.3109/13506120009146438 · Cited by 301 · see citing works
Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies
Révész, T., Holton, J. L., Lashley, T., Plant, G. T., Frangione, B., Rostagno, A. A., & Ghiso, J. A. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0501-8 · Cited by 293 · see citing works
Self-citationJaeger, L. B., Dohgu, S., Sultana, R., Lynch, J. L., Owen, J. B., Erickson, M. A., Shah, G. N., Price, T. O., Fleegal-Demotta, M. A., Butterfiled, D. A., et al. (2009) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2009.01.017 · Cited by 281 · see citing works
“Ab is transported by RAGE (receptor for advanced glycation end products) into (Martel et al., 1996; Bell et al., 2006; Deane et al., 2003; Maness et al., 1994) and by LRP-1 (low density lipoprotein receptor-related protein-1) out of (Banks et al., 2003; Deane et al., 2004a; Shibata et al., 2000; Ghersi-Egea et al., 19…”
BackgroundDemattos, R. B., Bales, K. R., Parsadanian, M., O'Dell, M. A., Foss, E. M., Paul, S. M., & Holtzman, D. M. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.00889.x · Cited by 253 · see citing works
Fryer, J. D., Simmons, K., Parsadanian, M., Bales, K. R., Paul, S. M., Sullivan, P. M., & Holtzman, D. M. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.5170-04.2005 · Cited by 278 · see citing works
“…et al., 1993; Wisniewski et al., 1993; LaDu et al., 1994; Munson et al., 2000) and in vivo (Naslund et al., 1995; Wisniewski et al., 1995; Ghersi-Egea et al., 1996; Permanne et al., 1997; Russo et al., 1998; Shibata et al., 2000; Ji et al., 2001; DeMattos et al., 2004). apoE has also…”
BackgroundPizzo, M. E., Wolak, D. J., Kumar, N. N., Brunette, E., Brunnquell, C. L., Hannocks, M., Abbott, N. J., Meyerand, M. E., Sorokin, L., Stanimirovic, D. B., et al. (2018) · The Journal of Physiology · doi:10.1113/jp275105 · Cited by 272 · see citing works
“Much evidence suggests that bulk flow occurs in the PVS (Cserr et al. 1977, 1981; Rennels et al. 1985; Ichimura et al. 1991; Ghersi-Egea et al. 1996a; Proescholdt et al. 2000; Abbott, 2004; Hadaczek et al. 2006b), potentially driven by arterial pulsations (Rennels et al. 1985; Hadaczek et al.…”
BackgroundInfluentialZlokovic, B. V., Deane, R., Sagare, A. P., Bell, R. D., & Winkler, E. A. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07002.x · Cited by 261 · see citing works
Amyloid‐β efflux from the central nervous system into the plasma
Roberts, K. F., Elbert, D. L., Kasten, T. P., Patterson, B. W., Sigurdson, W. C., Connors, R., Ovod, V., Munsell, L. Y., Mawuenyega, K. G., Miller‐Thomas, M. M., et al. (2014) · Annals of Neurology · doi:10.1002/ana.24270 · Cited by 250 · see citing works
Age but Not Diagnosis Is the Main Predictor of Plasma Amyloid β-Protein Levels
Fukumoto, H., Tennis, M. K., Locascio, J. J., Hyman, B. T., Growdon, J. H., & Irizarry, M. C. (2003) · Archives of Neurology · doi:10.1001/archneur.60.7.958 · Cited by 258 · see citing works
Mackic, J. B., Stins, M., McComb, J. G., Calero, M., Ghiso, J., Kim, K. S., Yan, S. D., Stern, D., Schmidt, A. M., Frangione, B., et al. (1998) · Journal of Clinical Investigation · doi:10.1172/jci2029 · Cited by 242 · see citing works
“In the absence of significant brain-to-blood transport of sAb, rapid clearance of sAb1–40 from the CSF, as reported in rodents (43), could be important to maintaining low concentrations of sAb in brain extracellular fluids.”
BackgroundSelf-citationKuo, Y.-M., Kokjohn, T. A., Kalback, W., Luehrs, D., Galasko, D. R., Chevallier, N., Koo, E. H., Emmerling, M. R., & Roher, A. E. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2222 · Cited by 230 · see citing works
Biomarkers of Alzheimer disease in plasma
Irizarry, M. C. (2004) · NeuroRx · doi:10.1602/neurorx.1.2.226 · Cited by 269 · see citing works
“Nonetheless, animal studies indicate that A can pass between the CSF and plasma compartments.(21,22) Peripherally administered compounds with high-affinity binding to A increased the flux of A from the brain and CSF to the plasma in APP transgenic mice.”
BackgroundThe glymphatic hypothesis: the theory and the evidence
Hladky, S. B., & Barrand, M. A. (2022) · Fluids and Barriers of the CNS · doi:10.1186/s12987-021-00282-z · Cited by 271 · see citing works
“[216] found that when I125-amyloid-β was injected into a lateral ventricle of a rat it was rapidly cleared into blood.”
Systemic Catabolism of Alzheimer's Aβ40 and Aβ42
Ghiso, J., Shayo, M., Calero, M., Ng, D., Tomidokoro, Y., Gandy, S., Rostagno, A., & Frangione, B. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m407668200 · Cited by 209 · see citing works
Self-citationMehta, P. D., Pirttilä, T., Patrick, B. A., Barshatzky, M., & Mehta, S. P. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)01754-2 · Cited by 230 · see citing works
Amyloidosis and Alzheimer’s disease
Ghiso, J. A., & Frangione, B. (2002) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(02)00149-7 · Cited by 189 · see citing works
Self-citationCombination assay of CSF Tau, Aβ1-40 and Aβ1-42(43) as a biochemical marker of Alzheimer's disease
Shoji, M., Matsubara, E., Kanai, M., Watanabe, M., Nakamura, T., Tomidokoro, Y., Shizuka, M., Wakabayashi, K., Igeta, Y., Ikeda, Y., et al. (1998) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(98)00122-1 · Cited by 219 · see citing works
Amyloid efflux transporter expression at the blood-brain barrier declines in normal aging
Silverberg, G. D., Messier, A. A., Miller, M. C., Machan, J. T., Majmudar, S. S., Stopa, E. G., Donahue, J. E., & Johanson, C. E. (2010) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3181f46e25 · Cited by 191 · see citing works
Tight Junctions in Brain Barriers During Central Nervous System Inflammation
Coisne, C., & Engelhardt, B. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.3929 · Cited by 186 · see citing works
“…the major form of circulating A b that may interact with the BBB endothelium (127, 171) and be responsible for the cerebrovascular alteration, possibly through the production of ROS in BBB endothelial cells (110), in parallel to A b depositions observed in the CNS parenchyma during AD (43, 149).”
The Glymphatic Pathway: Waste Removal from the CNS via Cerebrospinal Fluid Transport
Benveniste, H., Lee, H., & Volkow, N. D. (2017) · The Neuroscientist · doi:10.1177/1073858417691030 · Cited by 203 · see citing works
Decreased β-amyloid 1-42 in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
Otto, M., Esselmann, H., Schulz‐Schaeffer, W., Neumann, M., Schröter, A., Ratzka, P., Cepek, L., Zerr, I., Steinacker, P., Windl, O., et al. (2000) · Neurology · doi:10.1212/wnl.54.5.1099 · Cited by 170 · see citing works
Fryer, J. D., Taylor, J. W., DeMattos, R. B., Bales, K. R., Paul, S. M., Parsadanian, M., & Holtzman, D. M. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-21-07889.2003 · Cited by 160 · see citing works
“Clearance of A 40 from the brain has been suggested to occur via active transport across the blood– brain barrier (Ghersi-Egea et al., 1996; Shibata et al., 2000; Ji et al., 2001) as well as along peri-arterial interstitial fluid drainage pathways into cervical lymph nodes and then into peripheral circulation (Weller…”
BackgroundBrain meets body: the blood-brain barrier as an endocrine interface.
Banks, W. (2012) · Endocrinology · doi:10.1210/en.2012-1435 · Cited by 159 · see citing works
Intrathecal delivery of protein therapeutics to the brain: a critical reassessment.
Calias, P., Banks, W., Begley, D., Scarpa, M., & Dickson, P. (2014) · Pharmacology and Therapeutics · doi:10.1016/j.pharmthera.2014.05.009 · Cited by 157 · see citing works
“Early human studies of proteins administered by the ICV route found that they were rapidly cleared from the CSF and brain into the blood, presumably failing to penetrate deeply into the brain parenchyma (Greene et al., 1969; Ghersi-Egea et al., 1996).”
Association of homocysteine with plasma amyloid β protein in aging and neurodegenerative disease
Irizarry, M., Gurol, M., Raju, S., Diaz-Arrastia, R., Locascio, J., Tennis, M., Hyman, B., Growdon, J., Greenberg, S., & Bottiglieri, T. (2005) · Neurology · doi:10.1212/01.wnl.0000183063.99107.5c · Cited by 157 · see citing works
Mechanism of Cerebral β-Amyloid Angiopathy: Murine and Cellular Models
Herzig, M. C., Nostrand, W. E. V., & Jucker, M. (2006) · Brain Pathology · doi:10.1111/j.1750-3639.2006.tb00560.x · Cited by 167 · see citing works
“In addition to perivascular drainage, Aβ is also cleared actively across the blood-brain barrier to the blood (62, 93, 183).”
BackgroundLanz, T. A., Himes, C. S., Pallante, G., Adams, L., Yamazaki, S., Amore, B., & Merchant, K. (2003) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.102.048280 · Cited by 147 · see citing works
Cabral, D., Beach, T. G., Vedders, L. J., Sue, L. I., Jacobson, S. A., Myers, K. W., & Sabbagh, M. N. (2011) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2010.12.008 · Cited by 155 · see citing works
Martel, C. L., Mackic, J. B., Matsubara, E., Governale, S., Miguel, C., Miao, W., McComb, J. G., Frangione, B., Ghiso, J., & Zlokovic, B. V. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.69051995.x · Cited by 149 · see citing works
Self-citationGiedraitis, V., Sundelöf, J. E., Irizarry, M. C., Gårevik, N., Hyman, B. T., Wahlund, L., Ingelsson, M., & Lannfelt, L. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.09.023 · Cited by 121 · see citing works
Holtzman, D. M. (2001) · Journal of Molecular Neuroscience · doi:10.1385/jmn:17:2:147 · Cited by 143 · see citing works
Blood Platelets in the Progression of Alzheimer’s Disease
Gowert, N. S., Donner, L., Chatterjee, M., Eisele, Y. S., Towhid, S. T., Münzer, P., Walker, B., Ogorek, I., Borst, O., Grandoch, M., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090523 · Cited by 142 · see citing works
Meta-Analysis of Plasma Amyloid-β levels in Alzheimer's Disease
Song, F., Poljak, A., Valenzuela, M., Mayeux, R. P., Smythe, G. A., & Sachdev, P. S. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-101977 · Cited by 151 · see citing works
Association of plasma amyloid β with risk of dementia
Lambert, J., Schraen-Maschke, S., Richard, F., Fiévet, N., Rouaud, O., Berr, C., Dartigues, J., Tzourio, C., Alpérovitch, A., Buée, L., et al. (2009) · Neurology · doi:10.1212/wnl.0b013e3181b78448 · Cited by 140 · see citing works
Siemers, E., Dean, R., Friedrich, S., Ferguson-Sells, L., Gonzales, C., Farlow, M., & May, P. (2007) · Clinical Neuropharmacology · doi:10.1097/wnf.0b013e31805b7660 · Cited by 140 · see citing works
“5 minutes; clearance of labeled polyethylene glycol by bulk flow was slower, with a loss of only 20% of label after 10 minutes.(18) After A" is transported from brain interstitial fluid or CSF to plasma, it is cleared rapidly, with a half-life of approximately 5 to 15 minutes in mice.”
BackgroundMackic, J. B., Weiss, M., Miao, W., Kirkman, E., Ghiso, J., Calero, M., Bading, J., Frangione, B., & Zlokovic, B. (1998) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1998.70010210.x · Cited by 140 · see citing works
Self-citationJaeger, L. B., Dohgu, S., Hwang, M. C., Farr, S., Murphy, M. P., Fleegal-DeMotta, M. A., Lynch, J. L., Robinson, S., Niehoff, M., Johnson, S. N., et al. (2009) · Journal of Alzheimer's Disease · doi:10.3233/jad-2009-1074 · Cited by 135 · see citing works
“A β is transported across the BBB in both the blood-to-brain and brain-to-blood directions by RAGE and LRP-1, respectively [40–43].”
Immunotherapy for Alzheimer's disease
Gélinas, D. S., Silva, K. D., Fenili, D., George‐Hyslop, P. S., & McLaurin, J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0404866101 · Cited by 156 · see citing works
González-Marrero, I., Giménez‐Llort, L., Johanson, C. E., Carmona-Calero, E. M., Castañeyra-Ruiz, L., Armas, J. M. B., Castañeyra-Perdomo, A., & Castro-Fuentes, R. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00017 · Cited by 140 · see citing works
“Aβ40 clears rapidly after i.c.v. injection (Ghersi-Egea et al., 1996; Ji et al., 2001), and may also be degraded faster in CP. Interestingly, in Tg mouse lines generating Aβ40 (APP47) and Aβ42 (APP48) in neurons, APP47 mice only show somatic Aβ granules consistent with a more rapid, complete…”
BackgroundThe Choroid Plexus Removes β-Amyloid from Brain Cerebrospinal Fluid
Crossgrove, J. S., Li, G. J., & Zheng, W. (2005) · Experimental Biology and Medicine · doi:10.1177/153537020523001011 · Cited by 130 · see citing works
EADI consortium, G. C., Lambert, J.-C., Grenier-Boley, B., Harold, D., Zelenika, D., Chouraki, V, Kamatani, Y., Sleegers, K., Ikram, M. A., Hiltunen, M., et al. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.14 · Cited by 129 · see citing works
Rickert, C. H., & Paulus, W. (2000) · Microscopy Research and Technique · doi:10.1002/1097-0029(20010101)52:1 · Cited by 160 · see citing works
Blood-Based Proteomic Biomarkers of Alzheimer’s Disease Pathology
Baird, A. L., Westwood, S., & Lovestone, S. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00236 · Cited by 118 · see citing works
Soluble Arctic amyloid β protein inhibits hippocampal long‐term potentiation in vivo
Klyubin, I. V., Walsh, D. M., Cullen, W. K., Fadeeva, J. V., Anwyl, R., Selkoe, D. J., & Rowan, M. J. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03389.x · Cited by 115 · see citing works
Circulating Biomarkers of Cognitive Decline and Dementia
Solfrizzi, V., D'Introno, A., Colacicco, A. M., Capurso, C., Todarello, O., Pellicani, V., Capurso, S. A., Pietrarossa, G., Santamato, V., Capurso, A., et al. (2006) · Clinica Chimica Acta · doi:10.1016/j.cca.2005.06.015 · Cited by 120 · see citing works
Neurotoxicology of the Brain Barrier System: New Implications
Zheng, W. (2001) · Journal of Toxicology Clinical Toxicology · doi:10.1081/clt-100108512 · Cited by 120 · see citing works
“Moreover, the BCB appears to play a cleansing role, removing Aβ from the CSF (41).”
BackgroundZhang, J., Wu, X., Qin, C., Jin, Q., Ma, S., Zhang, H., Kong, Q., Chen, D., Ba, D., & He, W. (2003) · Neurobiology of Disease · doi:10.1016/j.nbd.2003.07.005 · Cited by 102 · see citing works
Poduslo, J., Curran, G., Wengenack, T. M., Malester, B., & Duff, K. (2001) · Neurobiology of Disease · doi:10.1006/nbdi.2001.0402 · Cited by 111 · see citing works
Hu, N., Smith, I. M., Walsh, D. M., & Rowan, M. J. (2008) · Brain · doi:10.1093/brain/awn174 · Cited by 84 · see citing works
Links Between the Pathology of Alzheimer's Disease and Vascular Dementia
Sadowski, M., Pankiewicz, J., Scholtzova, H., Li, Y.-S., Quartermain, D., Duff, K., & Wisniewski, T. (2004) · Neurochemical Research · doi:10.1023/b:nere.0000023612.66691.e6 · Cited by 109 · see citing works
“It has been demonstrated that the clearance of A from the brain across the BBB is significantly influenced by its carrier protein (104).”
BackgroundMorley, J. E., & Banks, W. A. (2010) · Journal of Alzheimer's Disease · doi:10.3233/jad-2010-091576 · Cited by 108 · see citing works
Monro, O. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00317-7 · Cited by 107 · see citing works
Self-citationQuantification of cerebrospinal fluid transport across the cribriform plate into lymphatics in rats
Nagra, G., Koh, L., Zakharov, A., Armstrong, D., & Johnston, M. G. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00235.2006 · Cited by 107 · see citing works
“For instance, the half-lives in CSF of soluble amyloid peptide, sucrose, or PEG4000 were 8 min, 60 min, and 60 min, respectively (12, 13).”
BackgroundThe blood-brain barrier: connecting the gut and the brain
Banks, W. A. (2008) · Regulatory Peptides · doi:10.1016/j.regpep.2007.08.027 · Cited by 104 · see citing works
The unsolved relationship of brain aging and late-onset Alzheimer disease
Kern, A., & Behl, C. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2009.07.016 · Cited by 106 · see citing works
“Clearance experiments in rats depicted that after infusion of radiolabelled Aβ into the brain 30% of the injected peptides were found in blood and urine withinminutes andwere soon taken up by the liver or kidney [174].”
BackgroundEffect of Different Anti-Aβ Antibodies on Aβ Fibrillogenesis as Assessed by Atomic Force Microscopy
Legleiter, J. A., Czilli, D. L., Gitter, B. D., Demattos, R. B., Holtzman, D. M., & Kowalewski, T. (2003) · Journal of Molecular Biology · doi:10.1016/j.jmb.2003.11.019 · Cited by 104 · see citing works
The Blood–Brain Barrier in Alzheimer's Disease
Sharma, H. S., Castellani, R. J., Smith, M. A., & Sharma, A. (2012) · International review of neurobiology · doi:10.1016/b978-0-12-386986-9.00003-x · Cited by 102 · see citing works
Serum amyloid-beta levels are increased in patients with obstructive sleep apnea syndrome
Bu, X.-L., Liu, Y.-H., Wang, Q.-H., Jiao, S.-S., Zeng, F., Yao, X., Gao, D., Chen, J.-C., & Wang, Y.-J. (2015) · Scientific Reports · doi:10.1038/srep13917 · Cited by 98 · see citing works
Ji, Y., Permanne, B., Sigurdsson, E. M., Holtzman, D. M., & Wısnıewskı, T. (2001) · Journal of Alzheimer s Disease · doi:10.3233/jad-2001-3105 · Cited by 83 · see citing works
“We found that consistent with other studies [ 5 ], Aβ40 is rapidly cleared from the brain across the BBB; however, Aβ42 is cleared much less effectively.”
BackgroundMethodResultInfluentialHemin and related porphyrins inhibit β‐amyloid aggregation
Howlett, D., Cutler, P., Heales, S., & Camilleri, P. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)01290-8 · Cited by 95 · see citing works
Harnessing cerebrospinal fluid circulation for drug delivery to brain tissues
Naseri Kouzehgarani, G., Feldsien, T., Engelhard, H. H., Mirakhur, K. K., Phipps, C., Nimmrich, V., Clausznitzer, D., & Lefebvre, D. R. (2021) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2021.03.002 · Cited by 95 · see citing works
Boada, M., Anaya, F., Ortiz, P., Olazarán, J., Shua-Haim, J. R., Obisesan, T. O., Hernández, I., Muñoz, J., Buendia, M., Alegret, M., et al. (2017) · Journal of Alzheimer’s Disease · doi:10.3233/jad-160565 · Cited by 94 · see citing works
“Studies conducted in animal models showed that the elimination half-life of A between CSF and plasma is about 30 minutes [12, 15, 16].”
BackgroundPomeraniec, I. J., Bond, A. E., Lopes, M. B., & Jane, J. (2016) · Journal of Neurosurgery · doi:10.3171/2015.2.jns142318 · Cited by 94 · see citing works
“Neurofibrillary tangles 5 (6) 11 (41) <0.”
Plasma β Amyloid and the Risk of Alzheimer Disease and Dementia in Elderly Men
Sundelöf, J. E., Giedraitis, V., Irizarry, M. C., Sundström, J., Ingelsson, E., Rönnemaa, E., Ärnlöv, J., Gunnarsson, M. D., Hyman, B. T., Basun, H., et al. (2008) · Archives of Neurology · doi:10.1001/archneurol.2007.57 · Cited by 111 · see citing works
Amyloid β Levels in Human Red Blood Cells
Kiko, T., Nakagawa, K., Satoh, A., Tsuduki, T., Furukawa, K., Arai, H., & Miyazawa, T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049620 · Cited by 88 · see citing works
Seppälä, T. T., Herukka, S., Hänninen, T., Tervo, S., Hallikainen, M., Soininen, H. S., & Pirttilä, T. (2010) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2010.205757 · Cited by 95 · see citing works
The α5β1 Integrin Mediates Elimination of Amyloid-β Peptide and Protects Against Apoptosis
Matter, M. L., Zhang, Z., Nordstedt, C., & Ruoslahti, E. I. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.4.1019 · Cited by 97 · see citing works
“The a5b1 integrin may play a role in the rapid clearance of Ab that occurs in the normal brain ( Ghersi-Egea et al., 1996 ).”
BackgroundWu, D.-F., Yang, J. J., & Pardridge, W. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119708 · Cited by 91 · see citing works
“The absorption of Ab to meningeal vascular surfaces has also been demonstrated in vivo in the rat (36).”
BackgroundBading, J., Yamada, S., Mackic, J., Kirkman, L., Miller, C., Calero, M., Ghiso, J., Frangione, B., & Zlokovic, B. (2002) · Journal of drug targeting (Print) · doi:10.1080/10611860290031831 · Cited by 89 · see citing works
“Consistent with the prior work demonstrating that intact [125I]Ab40 was removed from the mouse brain (Shibata et al., 2000), rat CSF (Ghersi-Egea et al., 1996) and/or guinea pig CSF and brain (Monro et al., 2002), a spot chick analysis in one middle-aged and one old monkey indicated that at the end…”
BackgroundResultSelf-citationChoroid plexus and ageing in rats: a morphometric and ultrastructural study
Sérot, J., Foliguet, B., Béné, M., & Faure, G. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01693.x · Cited by 86 · see citing works
Homeostatic capabilities of the choroid plexus epithelium in Alzheimer's disease
Johanson, C. E., McMillan, P. N., Tavares, R., Spangenberger, A. G., Duncan, J., Silverberg, G. D., & Stopa, E. G. (2004) · Cerebrospinal Fluid Research · doi:10.1186/1743-8454-1-3 · Cited by 94 · see citing works
“Considerable evidence points to CP's ability to remove Aβ from CSF [71-73].”
Animal models of cerebral β-amyloid angiopathy
Walker, L. C. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00017-9 · Cited by 99 · see citing works
Fate of nanoparticles in the central nervous system after intrathecal injection in healthy mice
Householder, K. T., Dharmaraj, S., Sandberg, D. I., Wechsler-Reya, R. J., & Sirianni, R. W. (2019) · Scientific Reports · doi:10.1038/s41598-019-49028-w · Cited by 83 · see citing works
Nagaraja, T. N., Patel, P., Gorski, M., Gorevic, P. D., Patlak, C. S., & Fenstermacher, J. D. (2005) · Cerebrospinal Fluid Research · doi:10.1186/1743-8454-2-5 · Cited by 74 · see citing works
“The clearance of ~50% of it by 15 min and ~80% by 30 min is far faster than that of sucrose [14] or PEG4000 [13] which had no clearance over the first 5 min and apparent halflives ~60 min for both.”
BackgroundMethodResultInfluentialSelf-citationSystemic Amyloid Deposits in Familial British Dementia*
Ghiso, J., Holton, J., Miravalle, L., Calero, M., Lashley, T., Vidal, R., Houlden, H., Wood, N., Neubert, T., Rostagno, A., et al. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105956200 · Cited by 80 · see citing works
Self-citationUllah, R., Park, T. J., Huang, X., & Kim, M. O. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101451 · Cited by 78 · see citing works
“These findings indicate that the kidney may be a potential peripheral organ that participates in the physiological clearance of brain-derived Aβ peptides (Ghersi-Egea et al., 1996; Ghiso et al., 1997; Xiang et al., 2015).”
BackgroundApolipoprotein E influences amyloid-beta clearance from the murine periphery
Hone, E., Martins, I., Fonte, J., & Martins, R. N. (2003) · Journal of Alzheimer's Disease · doi:10.3233/jad-2003-5101 · Cited by 78 · see citing works
“There is accumulating evidence that factors regulating A β catabolism [1], aggregation[2] and clearance [3,4] also play significant roles in the majority of AD cases.”
Sagare, A. P., Deane, R., Zetterberg, H., Wallin, A., Blennow, K., & Zloković, B. V. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-101248 · Cited by 80 · see citing works
Cerebral Amyloid Angiopathy: A Common Cause of Cerebral Hemorrhage
Pezzini, A., Zotto, E. D., Volonghi, I., Giossi, A., Costa, P., & Padovani, A. (2009) · Current Medicinal Chemistry · doi:10.2174/092986709788682047 · Cited by 76 · see citing works
“In addition to perivascular drainage, A is also cleared actively across the blood-brain barrier to the blood [83-85].”
- Authors
- Ghersi‐Egea, J. ‐., Gorevic, P. D., Ghiso, J., Frangione, B., Patlak, C. S., & Fenstermacher, J. D.
- Affiliations
- Stony Brook University (US)
- NYU Langone Health (US)
- Henry Ford Hospital (US)
- Corresponding author
- Fenstermacher, J. D.
- Venue
- Journal of Neurochemistry
- Publisher
- Wiley
- Published
- 1996-08
- Volume
- 67
- Issue
- 2
- Pages
- 880-883
- ISSN
- 0022-3042 (ISSN-L)
- 1471-4159
- OpenAlex
- W2065410730
- Cited by
- 222
- References
- 0
- Citations by year
- 2025: 3 · 2024: 7 · 2023: 2 · 2022: 5 · 2021: 3 · 2020: 3 · 2019: 5 · 2018: 6 · 2017: 8 · 2016: 7 · 2015: 9 · 2014: 8 · 2013: 8 · 2012: 7
- FWCI
- 3.37
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Eli Lilly and Company
- National Institutes of Health (5r01ns026004-05, 5r29ag010593-05)
- National Institute on Aging (AG10593, AG05891)
- National Institute of Neurological Disorders and Stroke (NS-26004)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Cerebrospinal fluid and hydrocephalus
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Keywords
- amyloid-beta, cerebrospinal fluid, blood-CSF barrier, cerebral arteries, pial arteries, amyloid deposition, Alzheimer's disease, subarachnoid space
- MeSH terms
- Animals, Cerebral Arteries, Humans, Male, Metabolic Clearance Rate, Peptide Fragments, Amyloid beta-Peptides, Rats, Sprague-Dawley, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review