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Development of in vitro microfluidic models to study endothelial responses to pulsatility with different mechanical circulatory support devices.

Authors :
Wang, Xueying
Liang, Lixue
Giridharan, Guruprasad A.
Sethu, Palaniappan
Wang, Yanxia
Qin, Kai-rong
Qu, Peng
Wang, Yu
Source :
Analyst; 7/7/2024, Vol. 149 Issue 13, p3661-3672, 12p
Publication Year :
2024

Abstract

Continuous-flow ventricular assist devices (CFVAD) and counterpulsation devices (CPD) are used to treat heart failure (HF). CFVAD can diminish pulsatility, but pulsatile modes have been implemented to increase vascular pulsatility. The effects of CFVAD in a pulsatile mode and CPD support on the function of endothelial cells (ECs) are yet to be investigated. In this study, two in vitro microfluidic models for culturing ECs are proposed to reproduce blood pressure (BP) and wall shear stress (WSS) on the arterial endothelium while using these medical devices. The layout and parameters of the two microfluidic systems were optimized based on the principle of hemodynamic similarity to efficiently simulate physiological conditions. Moreover, the unique design of the double-pump and double afterload systems could successfully reproduce the working mode of CPDs in an in vitro microfluidic system. The performance of the two systems was verified by numerical simulations and in vitro experiments. BP and WSS under HF, CFVAD in pulsatile modes, and CPD were reproduced accurately in the systems, and these induced signals improved the expression of Ca<superscript>2+</superscript>, NO, and reactive oxygen species in ECs, proving that CPD may be effective in normalizing endothelial function and replacing CFVAD to a certain extent to treat non-severe HF. This method offers an important tool for the study of cell mechanobiology and a key experimental basis for exploring the potential value of mechanical circulatory support devices in reducing adverse events and improving outcomes in the treatment of HF in the future. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00032654
Volume :
149
Issue :
13
Database :
Complementary Index
Journal :
Analyst
Publication Type :
Academic Journal
Accession number :
178020079
Full Text :
https://doi.org/10.1039/d4an00507d