Abstract

Generating spatially controlled, non-destructive changes in the interstitial spaces of the brain has a host of potential clinical applications, including enhancing the delivery of therapeutics, modulating biological features within the tissue microenvironment, altering fluid and pressure dynamics, and increasing the clearance of toxins, such as plaques found in Alzheimer’s disease. Recently we demonstrated that ultrasound can non-destructively enlarge the interstitial spaces of the brain ex vivo. The goal of the current study was to determine whether these effects could be reproduced in the living brain using non-invasive, transcranial MRI-guided focused ultrasound (MRgFUS). The left striatum of healthy rats was treated using MRgFUS. Computer simulations facilitated treatment planning, and targeting was validated using MRI acoustic radiation force impulse imaging. Following MRgFUS treatments, Evans blue dye or nanoparticle probes were infused to assess changes in the interstitial space. In MRgFUS-treated animals, enhanced dispersion was observed compared to controls for 70 nm (12.8 ± 0.9 mm3 vs. 10.6 ± 1.0 mm3, p = 0.01), 200 nm (10.9 ± 1.4 mm3 vs. 7.4 ± 0.7 mm3, p = 0.01) and 700 nm (7.5 ± 0.4 mm3 vs. 5.4 ± 1.2 mm3, p = 0.02) nanoparticles, indicating enlargement of the interstitial spaces. No evidence of significant histological or electrophysiological injury was identified. These findings suggest that transcranial ultrasound can safely and effectively modulate the brain interstitium and increase the dispersion of large therapeutic entities such as particulate drug carriers or modified viruses. This has the potential to expand the therapeutic uses of MRgFUS.

Highlights

  • 15–20% of the total volume of the brain is comprised of an anisotropic, narrow, and tortuous interstitial/extracellular space (ECS) [1]

  • We studied the distribution of a small molecule, Evans blue dye (EBD), as well as nanoparticle probes of different diameters in the living brain following MRI-guided focused ultrasound (MRgFUS) treatment

  • All focused ultrasound (FUS) treatments in this study were carried out using a commercial, MR-guided system designed to provide transcranial FUS exposures (Fig 1)

Read more

Summary

Introduction

15–20% of the total volume of the brain is comprised of an anisotropic, narrow, and tortuous interstitial/extracellular space (ECS) [1]. Movement of fluids and substances within the brain is determined in part by diffusion within the ECS as well as bulk flow through perivascular spaces. Alterations of the physical characteristics and microstructures of the brain ECS, including diameter (dECS) and tortuosity (λ), may affect a variety of physiological and pathophysiological processes. The diffusion of morphogens during embryogenesis [2], the movement of neurotransmitters during neuronal signaling [3,4,5], and the dispersion of therapeutic agents within the brain parenchyma may be limited by the narrow diameter and high tortuosity of the ECS [1]. Dysfunction of the GLS has been implicated in a number of neuro-degenerative conditions, including aging [10], Alzheimer’s disease [7, 11,12,13], and traumatic brain injury [14]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call