» Articles » PMID: 28045902

Effects on P-Glycoprotein Expression After Blood-Brain Barrier Disruption Using Focused Ultrasound and Microbubbles

Overview
Journal PLoS One
Date 2017 Jan 4
PMID 28045902
Citations 66
Authors
Affiliations
Soon will be listed here.
Abstract

Many blood-borne substances attempting to pass through the luminal membrane of brain endothelial cells are acted upon by a variety of metabolizing enzymes or are actively expelled back into the capillary lumen by embedded efflux transporters, such as Permeability-glycoprotein (Pgp). Overexpression of this protein has also been linked to multidrug resistance in cancer cells. Previous studies have shown that focused ultrasound (FUS), when combined with a microbubble agent, has ability to temporarily disrupt blood-brain barrier (BBBD). In this work, we investigated whether modulation of Pgp expression is part of the FUS-induced effects. We found that ultrasound can temporarily suppress Pgp expression. When BBBD was produced at 0.55 MPa, Pgp was suppressed up to 48 hours and restored by 72 hours. At 0.81 MPa, suppression can last 72 hours or longer. These findings support the idea that microbubble-enhanced FUS disrupts the functional components of the BBB through suppression of drug efflux.

Citing Articles

Role of P ×  receptor during focused ultrasound induced blood brain barrier modulation.

Park J, Na Y, Lee J, Seo Y, Kim H, Han S Sci Rep. 2025; 15(1):965.

PMID: 39762398 PMC: 11704064. DOI: 10.1038/s41598-024-83913-3.


Focused Ultrasound Augments the Delivery and Penetration of Model Therapeutics into Cerebral Cavernous Malformations.

Fisher D, Hoch M, Gorick C, Huchthausen C, Breza V, Sharifi K bioRxiv. 2024; .

PMID: 39253521 PMC: 11383029. DOI: 10.1101/2024.08.27.609060.


Current Overview on the Use of Nanosized Drug Delivery Systems in the Treatment of Neurodegenerative Diseases.

Ozceylan O, Sezgin-Bayindir Z ACS Omega. 2024; 9(33):35223-35242.

PMID: 39184484 PMC: 11340000. DOI: 10.1021/acsomega.4c01774.


Current Progress in Magnetic Resonance-Guided Focused Ultrasound to Facilitate Drug Delivery across the Blood-Brain Barrier.

Meng Y, Kalia L, Kalia S, Hamani C, Huang Y, Hynynen K Pharmaceutics. 2024; 16(6).

PMID: 38931843 PMC: 11206305. DOI: 10.3390/pharmaceutics16060719.


Alzheimer's disease and drug delivery across the blood-brain barrier: approaches and challenges.

Iqbal I, Saqib F, Mubarak Z, Latif M, Wahid M, Nasir B Eur J Med Res. 2024; 29(1):313.

PMID: 38849950 PMC: 11161981. DOI: 10.1186/s40001-024-01915-3.


References
1.
Liu H, Hua M, Yang H, Huang C, Chu P, Wu J . Magnetic resonance monitoring of focused ultrasound/magnetic nanoparticle targeting delivery of therapeutic agents to the brain. Proc Natl Acad Sci U S A. 2010; 107(34):15205-10. PMC: 2930577. DOI: 10.1073/pnas.1003388107. View

2.
Pardridge W . Blood-brain barrier delivery. Drug Discov Today. 2007; 12(1-2):54-61. DOI: 10.1016/j.drudis.2006.10.013. View

3.
Schinkel . P-Glycoprotein, a gatekeeper in the blood-brain barrier. Adv Drug Deliv Rev. 2000; 36(2-3):179-194. DOI: 10.1016/s0169-409x(98)00085-4. View

4.
Kinoshita M, McDannold N, Jolesz F, Hynynen K . Noninvasive localized delivery of Herceptin to the mouse brain by MRI-guided focused ultrasound-induced blood-brain barrier disruption. Proc Natl Acad Sci U S A. 2006; 103(31):11719-23. PMC: 1544236. DOI: 10.1073/pnas.0604318103. View

5.
Nance E, Timbie K, Miller G, Song J, Louttit C, Klibanov A . Non-invasive delivery of stealth, brain-penetrating nanoparticles across the blood-brain barrier using MRI-guided focused ultrasound. J Control Release. 2014; 189:123-132. PMC: 4125545. DOI: 10.1016/j.jconrel.2014.06.031. View