Comprehensive Assessment of Blood-Brain Barrier Opening and Sterile Inflammatory Response: Unraveling the Therapeutic Window.
Authors: Martinez P, Song JJ, Garay FG, Song KH, Mufford T, Steiner J, DeSisto J, Ellens N, Serkova NJ, Green AL, Borden M
Microbubbles (MBs) combined with focused ultrasound (FUS) have emerged as a promising noninvasive technique to permeabilize the blood-brain barrier (BBB) for drug delivery to the brain. However, the safety and biological consequences of BBB opening remain incompletely understood. This study investigates the effects of varying microbubble volume doses (MVD) and ultrasound mechanical indices (MI) on BBB opening and the sterile inflammatory response (SIR) using high-resolution ultra-high field MRI-guided FUS in mouse brains. The results demonstrate that both MVD and MI significantly influence the extent of BBB opening, with higher doses and mechanical indices leading to increased permeability. Moreover, RNA sequencing reveals upregulated inflammatory pathways and immune cell infiltration after BBB opening, suggesting the presence and extent of SIR. Gene set enrichment analysis identifies 12 gene sets associated with inflammatory responses that are upregulated at higher doses of MVD or MI. A therapeutic window is established between significant BBB opening and the onset of SIR, providing operating regimes for avoiding each three classes of increasing damage from stimulation of the NFκB pathway via TNFL signaling to apoptosis. This study contributes to the optimization and standardization of BBB opening parameters for safe and effective drug delivery to the brain and sheds light on the underlying molecular mechanisms of the sterile inflammatory response. The significance of this study lies in its comprehensive investigation of microbubble-facilitated focused ultrasound for blood-brain barrier (BBB) opening. By systematically exploring various combinations of microbubble volume doses and ultrasound mechanical indices, the study reveals their direct impact on the extent of BBB permeability and the induction of sterile inflammatory response (SIR). The establishment of a therapeutic window between significant BBB opening and the onset of SIR provides critical insights for safe and targeted drug delivery to the brain. These findings advance our understanding of the biological consequences of BBB opening and contribute to optimizing parameters for clinical applications, thus minimizing potential health risks, and maximizing the therapeutic potential of this technique.
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To determine how varying microbubble volume doses and ultrasound mechanical indices affect blood-brain barrier opening and the resulting sterile inflammatory response in mice.
Animal model / Human subject
Mouse (Mus musculus); strain: CD-1 IGS; age: 8-11 weeks old; sex: female
Disease model
Healthy
MRI or image guidance method
High-resolution ultra-high field MRI-guided FUS
Targeted brain region(s)
Striatum
Outcomes and Safety
Summary of Outcomes
Microbubble-facilitated focused ultrasound (FUS) produced dose-dependent BBB opening, higher exposure levels also caused strong sterile inflammatory responses. Moderate exposures produced BBB opening with minimal inflammatory activation.
Safety-related matter
Higher microbubble volume doses and mechanical indices increased BBB permeability and induced a sterile inflammatory response (upregulated inflammatory pathways and immune cell infiltration) that could progress through NFκB/TNF signaling to apoptosis; the authors established a therapeutic window to achieve BBB opening while avoiding SIR and associated tissue damage.
Brain Region
Ultrasound Parameters
Ultrasound instrument
Single-element, geometrically focused transducer driven by the RK-50 system (FUS Instruments, Toronto, Canada)
FUS Frequency
1.515 MHz
FUS Pressure
0.246, 0.492, 0.738 Mpa
FUS Mode
pulsed
Pulse duration
10 ms
Duration of a single FUS session
300 s
Focal Characteristics
Focal depth: None; Focal length: None; Aperture size: None
Treatment frequency
single session
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