Striated muscle action potential assessment as an indicator of cellular energetic state

Action potentials of striated muscle are created through movement of ions through membrane ion channels. ATP-sensitive potassium (KATP) channels are the only known channels that are gated by the intracellular energetic level ([ATP]/[ADP] ratio). KATP channels are...

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Main Author: Burnett, Colin Michael-Lee
Other Authors: Hodgson-Zingman, Denice M.
Format: Others
Language:English
Published: University of Iowa 2012
Subjects:
Online Access:https://ir.uiowa.edu/etd/2830
https://ir.uiowa.edu/cgi/viewcontent.cgi?article=3200&context=etd
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spelling ndltd-uiowa.edu-oai-ir.uiowa.edu-etd-32002019-10-13T04:53:19Z Striated muscle action potential assessment as an indicator of cellular energetic state Burnett, Colin Michael-Lee Action potentials of striated muscle are created through movement of ions through membrane ion channels. ATP-sensitive potassium (KATP) channels are the only known channels that are gated by the intracellular energetic level ([ATP]/[ADP] ratio). KATP channels are both effectors and indicators of cellular metabolism as part of a negative feedback system. Decreased intracellular energetic level alters the gating of KATP channels, which is reflected in alterations of the action potential morphology. These changes protect the cell from exhaustion or injury by altering energy-consuming processes that are driven by membrane potential. Assessing the effects of KATP channel activation on resting membrane potential and action potential morphology, and the relationship to cellular stress is important to the understanding of normal cellular function. To better understand how muscle cells adapt to energetic stress, the monophasic action potential (MAP) electrode and floating microelectrode were used to record action potentials in intact hearts and skeletal muscles, respectively. Intact organs provide a more physiological environment for the study of energetics and membrane electrical phenomena. Utilizing these techniques, a stress on the intracellular energetic state resulted in greater and faster shortening of the duration of cardiac action potentials, and hyperpolarization of the membrane of skeletal muscle in a KATP channel dependent manner. Motion artifacts are a limitation to studying transmembrane action potentials, but the MAP and floating microelectrode techniques uniquely allow for reading of action potential morphology uncoupled from motion artifacts. The use of the floating microelectrode in skeletal muscles is a novel approach that provides previously unavailable data on skeletal muscle membrane potentials in situ. 2012-05-01T07:00:00Z thesis application/pdf https://ir.uiowa.edu/etd/2830 https://ir.uiowa.edu/cgi/viewcontent.cgi?article=3200&context=etd Copyright 2012 Colin Michael-Lee Burnett Theses and Dissertations eng University of IowaHodgson-Zingman, Denice M. action potential cardiac muscle floating microelectrode KATP channel membrane potential skeletal muscle Biomedical Engineering and Bioengineering
collection NDLTD
language English
format Others
sources NDLTD
topic action potential
cardiac muscle
floating microelectrode
KATP channel
membrane potential
skeletal muscle
Biomedical Engineering and Bioengineering
spellingShingle action potential
cardiac muscle
floating microelectrode
KATP channel
membrane potential
skeletal muscle
Biomedical Engineering and Bioengineering
Burnett, Colin Michael-Lee
Striated muscle action potential assessment as an indicator of cellular energetic state
description Action potentials of striated muscle are created through movement of ions through membrane ion channels. ATP-sensitive potassium (KATP) channels are the only known channels that are gated by the intracellular energetic level ([ATP]/[ADP] ratio). KATP channels are both effectors and indicators of cellular metabolism as part of a negative feedback system. Decreased intracellular energetic level alters the gating of KATP channels, which is reflected in alterations of the action potential morphology. These changes protect the cell from exhaustion or injury by altering energy-consuming processes that are driven by membrane potential. Assessing the effects of KATP channel activation on resting membrane potential and action potential morphology, and the relationship to cellular stress is important to the understanding of normal cellular function. To better understand how muscle cells adapt to energetic stress, the monophasic action potential (MAP) electrode and floating microelectrode were used to record action potentials in intact hearts and skeletal muscles, respectively. Intact organs provide a more physiological environment for the study of energetics and membrane electrical phenomena. Utilizing these techniques, a stress on the intracellular energetic state resulted in greater and faster shortening of the duration of cardiac action potentials, and hyperpolarization of the membrane of skeletal muscle in a KATP channel dependent manner. Motion artifacts are a limitation to studying transmembrane action potentials, but the MAP and floating microelectrode techniques uniquely allow for reading of action potential morphology uncoupled from motion artifacts. The use of the floating microelectrode in skeletal muscles is a novel approach that provides previously unavailable data on skeletal muscle membrane potentials in situ.
author2 Hodgson-Zingman, Denice M.
author_facet Hodgson-Zingman, Denice M.
Burnett, Colin Michael-Lee
author Burnett, Colin Michael-Lee
author_sort Burnett, Colin Michael-Lee
title Striated muscle action potential assessment as an indicator of cellular energetic state
title_short Striated muscle action potential assessment as an indicator of cellular energetic state
title_full Striated muscle action potential assessment as an indicator of cellular energetic state
title_fullStr Striated muscle action potential assessment as an indicator of cellular energetic state
title_full_unstemmed Striated muscle action potential assessment as an indicator of cellular energetic state
title_sort striated muscle action potential assessment as an indicator of cellular energetic state
publisher University of Iowa
publishDate 2012
url https://ir.uiowa.edu/etd/2830
https://ir.uiowa.edu/cgi/viewcontent.cgi?article=3200&context=etd
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