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

被引:118
作者
Aryal, Muna [1 ]
Fischer, Krisztina [1 ]
Gentile, Caroline [1 ,2 ]
Gitto, Salvatore [3 ]
Zhang, Yong-Zhi [1 ]
McDannold, Nathan [1 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA
[2] Harvard Univ, Dept Neurobiol, Cambridge, MA USA
[3] Univ Pavia, Dept Radiol, Pavia, Italy
关键词
MULTIDRUG-RESISTANCE; LIPOSOMAL DOXORUBICIN; GENE-EXPRESSION; SOLID TUMORS; DELIVERY; MODEL; CANCER; CELLS; PERMEABILITY; SYSTEM;
D O I
10.1371/journal.pone.0166061
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
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页数:15
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