MRI and histological evaluation of pulsed focused ultrasound and microbubbles treatment effects in the brain
Autor: | Joseph A. Frank, Scott R. Burks, Bobbi K. Lewis, Farhan Qureshi, Tsang-Wei Tu, Maggie Sundby, Neekita Jikaria, Zsofia I. Kovacs |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Pathology medicine.medical_specialty Central nervous system Medicine (miscellaneous) Hippocampus Blood–brain barrier Rats Sprague-Dawley pulsed focused ultrasound 03 medical and health sciences 0302 clinical medicine Cortex (anatomy) hyperphosphorylated Tau medicine Animals Longitudinal Studies Pharmacology Toxicology and Pharmaceutics (miscellaneous) Ultrasonography Cerebral Cortex Microbubbles medicine.diagnostic_test Microglia Histocytochemistry business.industry Magnetic resonance imaging blood-brain barrier medicine.disease Magnetic Resonance Imaging Astrogliosis 030104 developmental biology medicine.anatomical_structure sterile inflammation business 030217 neurology & neurosurgery Research Paper |
Zdroj: | Theranostics |
ISSN: | 1838-7640 |
DOI: | 10.7150/thno.24512 |
Popis: | Magnetic resonance imaging (MRI)-guided pulsed focused ultrasound (pFUS) combined with microbubbles (MB) contrast agent infusion has been shown to transiently disrupt the blood-brain barrier (BBBD), increasing the delivery of neurotherapeutics to treat central nervous system (CNS) diseases. pFUS interaction with the intravascular MB results in acoustic cavitation forces passing through the neurovascular unit (NVU), inducing BBBD detected on contrast-enhanced MRI. Multiple pFUS+MB exposures in Alzheimer's disease (AD) models are being investigated as a method to clear amyloid plaques by activated microglia or infiltrating immune cells. Since it has been reported that pFUS+MB can induce a sterile inflammatory response (SIR) [1-5] in the rat, the goal of this study was to investigate the potential long-term effects of SIR in the brain following single and six weekly sonications by serial high-resolution MRI and pathology. Methods: Female Sprague Dawley rats weighing 217±16.6 g prior to sonication received bromo-deoxyuridine (BrdU) to tag proliferating cells in the brain. pFUS was performed at 548 kHz, ultrasound burst 10 ms and initial peak negative pressure of 0.3 MPa (in water) for 120 s coupled with a slow infusion of ~460 µL/kg (5-8×107 MB) that started 30 s before and 30 s during sonication. Nine 2 mm focal regions in the left cortex and four regions over the right hippocampus were treated with pFUS+MB. Serial high-resolution brain MRIs at 3 T and 9.4 T were obtained following a single or during the course of six weekly pFUS+MB resulting in BBBD in the left cortex and the right hippocampus. Animals were monitored over 7 to 13 weeks and imaging results were compared to histology. Results: Fewer than half of the rats receiving a single pFUS+MB exposure displayed hypointense voxels on T2*-weighted (w) MRI at week 7 or 13 in the cortex or hippocampus without differences compared to the contralateral side on histograms of T2* maps. Single sonicated rats had evidence of limited microglia activation on pathology compared to the contralateral hemisphere. Six weekly pFUS+MB treatments resulted in pathological changes on T2*w images with multiple hypointense regions, cortical atrophy, along with 50% of rats having persistent BBBD and astrogliosis by MRI. Pathologic analysis of the multiple sonicated animals demonstrated the presence of metallophagocytic Prussian blue-positive cells in the parenchyma with significantly (p |
Databáze: | OpenAIRE |
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