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Development of in vitro microfluidic models to study endothelial responses to pulsatility with different mechanical circulatory support devices.
Wang, Xueying; Liang, Lixue; Giridharan, Guruprasad A; Sethu, Palaniappan; Wang, Yanxia; Qin, Kai-Rong; Qu, Peng; Wang, Yu.
Affiliation
  • Wang X; School of Optoelectronic Engineering and Instrumentation Science, Dalian University of Technology, Dalian 116024, Liaoning Province, P. R. China.
  • Liang L; School of Mechanical Engineering, Dalian University of Technology, Dalian 116024, Liaoning Province, P. R. China.
  • Giridharan GA; Department of Bioengineering, University of Louisville, Louisville, KY 40292, USA.
  • Sethu P; Department of Biomedical Engineering, School of Engineering, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Wang Y; School of Rehabilitation Medicine, Shandong Second Medical University, Weifang 261053, Shandong Province, P. R. China.
  • Qin KR; School of Biomedical Engineering, Faculty of Medicine, Dalian University of Technology, Dalian 116024, Liaoning Province, P. R. China. qupeng@dlut.edu.cn.
  • Qu P; School of Biomedical Engineering, Faculty of Medicine, Dalian University of Technology, Dalian 116024, Liaoning Province, P. R. China. qupeng@dlut.edu.cn.
  • Wang Y; School of Biomedical Engineering, Faculty of Medicine, Dalian University of Technology, Dalian 116024, Liaoning Province, P. R. China. qupeng@dlut.edu.cn.
Analyst ; 149(13): 3661-3672, 2024 Jun 24.
Article in En | MEDLINE | ID: mdl-38819086
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 Ca2+, 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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pulsatile Flow / Heart-Assist Devices Limits: Humans Language: En Journal: Analyst Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pulsatile Flow / Heart-Assist Devices Limits: Humans Language: En Journal: Analyst Year: 2024 Type: Article