» Articles » PMID: 30286191

A Control Mechanism for Intra-mural Peri-arterial Drainage Via Astrocytes: How Neuronal Activity Could Improve Waste Clearance from the Brain

Overview
Journal PLoS One
Date 2018 Oct 5
PMID 30286191
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

The mechanisms behind the clearance of soluble waste from deep within the parenchyma of the brain remain unclear. Experimental evidence reveals that one pathway for clearance of waste, termed intra-mural peri-arterial drainage (IPAD), is the rapid drainage of interstitial fluid along basement membranes (BM) of the smooth muscle cells of cerebral arteries; failure of IPAD is closely associated with the pathology of Alzheimer's disease (AD), but its driving mechanism remains unclear. We have previously shown that arterial pulsations generated by the heart beat are not strong enough to drive IPAD. Here we present computational evidence for a mechanism for clearance of waste from the brain that is driven by functional hyperaemia, that is, the dilatation of cerebral arterioles as a consequence of increased nutrient demand from neurons. This mechanism is based on our model for the flow of fluid through the vascular BM. It accounts for clearance rates observed in mouse experiments, and aligns with pathological observations and recommendations to lower the individual risk of AD, such as mental and physical activity. Thus, our neurovascular hypothesis should act as the new working hypothesis for the driving force behind IPAD.

Citing Articles

Attentional failures after sleep deprivation represent moments of cerebrospinal fluid flow.

Yang Z, Williams S, Beldzik E, Anakwe S, Schimmelpfennig E, Lewis L bioRxiv. 2024; .

PMID: 39605725 PMC: 11601381. DOI: 10.1101/2024.11.15.623271.


Cellular and molecular mechanisms of the blood-brain barrier dysfunction in neurodegenerative diseases.

Chen T, Dai Y, Hu C, Lin Z, Wang S, Yang J Fluids Barriers CNS. 2024; 21(1):60.

PMID: 39030617 PMC: 11264766. DOI: 10.1186/s12987-024-00557-1.


Approaches for Increasing Cerebral Efflux of Amyloid-β in Experimental Systems.

Loeffler D J Alzheimers Dis. 2024; 100(2):379-411.

PMID: 38875041 PMC: 11307100. DOI: 10.3233/JAD-240212.


Neuroimmunology of Cardiovascular Disease.

Zarate S, Kirabo A, Hinton Jr A, Santisteban M Curr Hypertens Rep. 2024; 26(7):339-347.

PMID: 38613621 PMC: 11199253. DOI: 10.1007/s11906-024-01301-8.


The Neurovascular Unit as a Locus of Injury in Low-Level Blast-Induced Neurotrauma.

Elder G, Gama Sosa M, De Gasperi R, Perez Garcia G, Perez G, Abutarboush R Int J Mol Sci. 2024; 25(2).

PMID: 38256223 PMC: 10816929. DOI: 10.3390/ijms25021150.


References
1.
Smith J, Nielson K, Woodard J, Seidenberg M, Durgerian S, Hazlett K . Physical activity reduces hippocampal atrophy in elders at genetic risk for Alzheimer's disease. Front Aging Neurosci. 2014; 6:61. PMC: 4005962. DOI: 10.3389/fnagi.2014.00061. View

2.
Haydon P, Carmignoto G . Astrocyte control of synaptic transmission and neurovascular coupling. Physiol Rev. 2006; 86(3):1009-31. DOI: 10.1152/physrev.00049.2005. View

3.
Gomez-Pinilla F, Hillman C . The influence of exercise on cognitive abilities. Compr Physiol. 2013; 3(1):403-28. PMC: 3951958. DOI: 10.1002/cphy.c110063. View

4.
Black J, Waxman S . Specialization of astrocytic membrane at glia limitans in rat optic nerve: freeze-fracture observations. Neurosci Lett. 1985; 55(3):371-8. DOI: 10.1016/0304-3940(85)90464-1. View

5.
Fratiglioni L, Paillard-Borg S, Winblad B . An active and socially integrated lifestyle in late life might protect against dementia. Lancet Neurol. 2004; 3(6):343-53. DOI: 10.1016/S1474-4422(04)00767-7. View