Author: Hersh DS1, Nguyen BA2, Dancy JG1, Adapa AR1, Winkles JA3, Woodworth GF1, Kim AJ4, Frenkel V5
Affiliation:
1Department of Neurosurgery, University of Maryland School of Medicine, 22 S Greene St Suite 12D, Baltimore, MD 21201 (USA); Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, 22 S Greene St, Baltimore, MD 21201 (USA).
2Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, 419 W Redwood St Suite 110, Baltimore, MD 21201 (USA).
3Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, 22 S Greene St, Baltimore, MD 21201 (USA); Department of Surgery, University of Maryland School of Medicine, 22 S Greene St, Baltimore, MD 21201 (USA); Center for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, UMB BioPark One Room 210, 800 West Baltimore Street Baltimore, MD 21201 (USA).
4Department of Neurosurgery, University of Maryland School of Medicine, 22 S Greene St Suite 12D, Baltimore, MD 21201 (USA); Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, 22 S Greene St, Baltimore, MD 21201 (USA); Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, 20 Penn Street, HSFII Room 520, Baltimore, MD 21201 (USA); Center for Biomedical Engineering and Technology, University of Maryland School of Medicine, 111 S. Penn St. Suite 104, Baltimore, MD 21201 (USA). Electronic address: akim@smail.umaryland.edu.
5Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, 22 S Greene St, Baltimore, MD 21201 (USA); Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, 419 W Redwood St Suite 110, Baltimore, MD 21201 (USA). Electronic address: VFrenkel@som.umaryland.edu.
Conference/Journal: Brain Res.
Date published: 2016 Jun 28
Other:
Pages: S0006-8993(16)30464-4 , Special Notes: doi: 10.1016/j.brainres.2016.06.040. [Epub ahead of print] , Word Count: 220
Diffusion within the extracellular and perivascular spaces of the brain plays an important role in biological processes, therapeutic delivery, and clearance mechanisms within the central nervous system. Recently, ultrasound has been used to enhance the dispersion of locally administered molecules and particles within the brain, but ultrasound-mediated effects on the brain parenchyma remain poorly understood. We combined an electron microscopy-based ultrastructural analysis with high-resolution tracking of non-adhesive nanoparticles in order to probe changes in the extracellular and perivascular spaces of the brain following a non-destructive pulsed ultrasound regimen known to alter diffusivity in other tissues. Freshly obtained rat brain neocortical slices underwent sham treatment or pulsed, low intensity ultrasound for 5 minutes at 1MHz. Transmission electron microscopy revealed intact cells and blood vessels and evidence of enlarged spaces, particularly adjacent to blood vessels, in ultrasound-treated brain slices. Additionally, ultrasound significantly increased the diffusion rate of 100nm, 200nm, and 500nm nanoparticles that were injected into the brain slices, while 2000nm particles were unaffected. In ultrasound-treated slices, 91.6% of the 100nm particles, 20.7% of the 200nm particles, 13.8% of the 500nm particles, and 0% of the 2000nm particles exhibited diffusive motion. Thus, pulsed ultrasound can have meaningful structural effects on the brain extracellular and perivascular spaces without evidence of tissue disruption.
Copyright © 2016. Published by Elsevier B.V.
KEYWORDS: Diffusion; Extracellular space; Nanoparticle; Ultrasound
PMID: 27369449 DOI: 10.1016/j.brainres.2016.06.040
