Literature DB >> 16198528

Microelectrode array recordings of cardiac action potentials as a high throughput method to evaluate pesticide toxicity.

A Natarajan1, P Molnar, K Sieverdes, A Jamshidi, J J Hickman.   

Abstract

The threat of environmental pollution, biological warfare agent dissemination and new diseases in recent decades has increased research into cell-based biosensors. The creation of this class of sensors could specifically aid the detection of toxic chemicals and their effects in the environment, such as pyrethroid pesticides. Pyrethroids are synthetic pesticides that have been used increasingly over the last decade to replace other pesticides like DDT. In this study we used a high-throughput method to detect pyrethroids by using multielectrode extracellular recordings from cardiac cells. The data from this cell-electrode hybrid system was compared to published results obtained with patch-clamp electrophysiology and also used as an alternative method to further understand pyrethroid effects. Our biosensor consisted of a confluent monolayer of cardiac myocytes cultured on microelectrode arrays (MEA) composed of 60 substrate-integrated electrodes. Spontaneous activity of these beating cells produced extracellular field potentials in the range of 100 microV to nearly 1200 microV with a beating frequency of 0.5-4 Hz. All of the tested pyrethroids; alpha-Cypermethrin, Tetramethrin and Tefluthrin, produced similar changes in the electrophysiological properties of the cardiac myocytes, namely reduced beating frequency and amplitude. The sensitivity of our toxin detection method was comparable to earlier patch-clamp studies, which indicates that, in specific applications, high-throughput extracellular methods can replace single-cell studies. Moreover, the similar effect of all three pyrethroids on the measured parameters suggests, that not only detection of the toxins but, their classification might also be possible with this method. Overall our results support the idea that whole cell biosensors might be viable alternatives when compared to current toxin detection methods.

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Year:  2005        PMID: 16198528     DOI: 10.1016/j.tiv.2005.08.014

Source DB:  PubMed          Journal:  Toxicol In Vitro        ISSN: 0887-2333            Impact factor:   3.500


  15 in total

1.  Solving medical problems with BioMEMS.

Authors:  Erkin Seker; Jong Hwan Sung; Michael L Shuler; Martin L Yarmush
Journal:  IEEE Pulse       Date:  2011-11       Impact factor: 0.924

Review 2.  Using physiologically-based pharmacokinetic-guided "body-on-a-chip" systems to predict mammalian response to drug and chemical exposure.

Authors:  Jong Hwan Sung; Balaji Srinivasan; Mandy Brigitte Esch; William T McLamb; Catia Bernabini; Michael L Shuler; James J Hickman
Journal:  Exp Biol Med (Maywood)       Date:  2014-06-20

3.  Prototype for automatable, dielectrophoretically-accessed intracellular membrane-potential measurements by metal electrodes.

Authors:  Ulrich Terpitz; Vladimir L Sukhorukov; Dirk Zimmermann
Journal:  Assay Drug Dev Technol       Date:  2012-09-20       Impact factor: 1.738

Review 4.  Multiorgan Microphysiological Systems for Drug Development: Strategies, Advances, and Challenges.

Authors:  Ying I Wang; Carlos Carmona; James J Hickman; Michael L Shuler
Journal:  Adv Healthc Mater       Date:  2017-12-04       Impact factor: 9.933

Review 5.  Self-contained, low-cost Body-on-a-Chip systems for drug development.

Authors:  Ying I Wang; Carlota Oleaga; Christopher J Long; Mandy B Esch; Christopher W McAleer; Paula G Miller; James J Hickman; Michael L Shuler
Journal:  Exp Biol Med (Maywood)       Date:  2017-02-17

6.  Patterned cardiomyocytes on microelectrode arrays as a functional, high information content drug screening platform.

Authors:  Anupama Natarajan; Maria Stancescu; Vipra Dhir; Christopher Armstrong; Frank Sommerhage; James J Hickman; Peter Molnar
Journal:  Biomaterials       Date:  2011-03-31       Impact factor: 12.479

7.  Growth and electrophysiological properties of rat embryonic cardiomyocytes on hydroxyl- and carboxyl-modified surfaces.

Authors:  Anupama Natarajan; Changju Chun; James J Hickman; Peter Molnar
Journal:  J Biomater Sci Polym Ed       Date:  2008       Impact factor: 3.517

8.  Analysis of toxin-induced changes in action potential shape for drug development.

Authors:  Nesar Akanda; Peter Molnar; Maria Stancescu; James J Hickman
Journal:  J Biomol Screen       Date:  2009-12

9.  Rapid generation of spatially and temporally controllable long-range concentration gradients in a microfluidic device.

Authors:  Yanan Du; Jaesool Shim; Mahesh Vidula; Matthew J Hancock; Edward Lo; Bong Geun Chung; Jeffrey T Borenstein; Masoud Khabiry; Donald M Cropek; Ali Khademhosseini
Journal:  Lab Chip       Date:  2008-12-10       Impact factor: 6.799

10.  A new target for amyloid beta toxicity validated by standard and high-throughput electrophysiology.

Authors:  Kucku Varghese; Peter Molnar; Mainak Das; Neelima Bhargava; Stephen Lambert; Mark S Kindy; James J Hickman
Journal:  PLoS One       Date:  2010-01-08       Impact factor: 3.240

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