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Study · Ex vivo tissue · rat · 2016

7 results

Effects of exogenous nicotinamide adenine dinucleotide (NAD+) in the rat heart are mediated by P2 purine receptors.

Kuzmin VS, Pustovit KB, Abramochkin DV

Journal of biomedical science27 Jun 2016Cited by 14 (Europe PMC)

Summary

BackgroundRecently, NAD+ has been considered as an essential factor, participating in nerve control of physiological functions and intercellular communication. NAD+ also has been supposed as endogenous activator of P1 and P2 purinoreceptors. Effects of extracellular NAD+ remain poorly investigated in cardiac tissue. This study aims to investigate the effects of extracellular NAD+ in different types of supraventricular and ventricular working myocardium from rat and their potential mechanisms.MethodsThe standard technique of sharp microelectrode action potential recording in cardiac multicellular preparations was used to study the effects of NAD+.ResultsExtracellular NAD+ induced significant changes in bioelectrical activity of left auricle (LA), right auricle (RA), pulmonary veins (PV) and right ventricular wall (RV) myocardial preparations. 10-100 μM NAD+ produced two opposite effects in LA and RA - quickly developing and transient prolongation of action potentials (AP) and delayed sustained AP shortening, which follows the initial positive effect. In PV and RV only AP shortening was observed in response to NAD+ application. In PV preparations AP shortening induced by NAD+ may be considered as a potential proarrhythmic effect. Revealed cardiotropic effects of NAD+ are likely to be mediated by P2 purine receptors, since P1 blocker DPCPX failed to affect them and P2 antagonist suramin abolished NAD + -induced alterations of electrical activity. P2X receptors may be responsible for NAD + -induced short-lasting AP prolongation, while P2Y receptors mediate persistent AP shortening. The latter effect is partially removed by PLC inhibitor U73122 showing the potential involvement of phosphoinositide signaling pathway in mediation of NAD+ cardiotropic effects.ConclusionsExtracellular NAD+ is supposed to be a novel regulator of cardiac electrical activity. P2 receptors represent the main target of NAD+ at least in the rat heart.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study7

4 results from studies that gave the peptide. No result from this study comes from people.

  1. 01LabEx vivo tissueActivity measurement

    In rat left and right auricular preparations, NAD+ caused rapid transient action potential prolongation.

    In plain wordsIn lab tests, NAD+ briefly prolonged action potentials in rat left and right auricular tissue.

    Outcome
    IncreaseAuricular transient AP prolongation
    Study

    ratn: not reported in source

    isolated myocardial preparations
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    10-100 μMAs given in this study (rat).

    Source sentences

    Summary
    10-100 μM NAD+ produced two opposite effects in LA and RA - quickly developing and transient prolongation of action potentials (AP) and delayed sustained AP shortening, which follows the initial positive effect.
    1 context sentence
    Summary · context
    The standard technique of sharp microelectrode action potential recording in cardiac multicellular preparations was used to study the effects of NAD+.
  2. 02LabEx vivo tissueActivity measurement

    In rat left and right auricular preparations, NAD+ caused delayed sustained action potential shortening after initial prolongation.

    In plain wordsIn lab tests, NAD+ shortened action potentials in rat auricular tissue after an initial brief prolongation.

    Outcome
    DecreaseAuricular sustained AP shortening
    Study

    ratn: not reported in source

    isolated myocardial preparations
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    10-100 μMAs given in this study (rat).

    Source sentences

    Summary
    10-100 μM NAD+ produced two opposite effects in LA and RA - quickly developing and transient prolongation of action potentials (AP) and delayed sustained AP shortening, which follows the initial positive effect.
    1 context sentence
    Summary · context
    The standard technique of sharp microelectrode action potential recording in cardiac multicellular preparations was used to study the effects of NAD+.
  3. 03LabEx vivo tissueActivity measurement

    In rat pulmonary vein preparations, NAD+ application produced only action potential shortening.

    In plain wordsIn lab tests, NAD+ shortened action potentials in rat pulmonary vein tissue.

    Outcome
    DecreasePulmonary vein AP shortening
    Study

    ratn: not reported in source

    isolated myocardial preparations
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In PV and RV only AP shortening was observed in response to NAD+ application.
    1 context sentence
    Summary · context
    The standard technique of sharp microelectrode action potential recording in cardiac multicellular preparations was used to study the effects of NAD+.
  4. 04LabEx vivo tissueActivity measurement

    In rat right ventricular preparations, NAD+ application produced only action potential shortening.

    In plain wordsIn lab tests, NAD+ shortened action potentials in rat right ventricular tissue.

    Outcome
    DecreaseRight ventricular AP shortening
    Study

    ratn: not reported in source

    isolated myocardial preparations
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In PV and RV only AP shortening was observed in response to NAD+ application.
    1 context sentence
    Summary · context
    The standard technique of sharp microelectrode action potential recording in cardiac multicellular preparations was used to study the effects of NAD+.

Studies that did not test the peptide alone3

In this study, NAD+ (nicotinamide adenine dinucleotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking NAD+ (nicotinamide adenine dinucleotide).

  1. 05LabNot a test of NAD+ (nicotinamide adenine dinucleotide) aloneEx vivo tissueMechanism

    In rat myocardial preparations, P1 blocker DPCPX did not affect NAD+-induced electrical effects.

    In plain wordsIn lab tests, DPCPX did not change NAD+-induced electrical effects compared with NAD+ without DPCPX.

    Outcome
    No significant changeP1 blockade of electrical effects
    Study

    ratn: not reported in source

    isolated myocardial preparations
    Comparator
    NAD+ effects without DPCPX
    Outcome group
    Heart function · Cardiovascular

    Source sentences

    Summary
    Revealed cardiotropic effects of NAD+ are likely to be mediated by P2 purine receptors, since P1 blocker DPCPX failed to affect them and P2 antagonist suramin abolished NAD + -induced alterations of electrical activity.
    1 context sentence
    Summary · context
    The standard technique of sharp microelectrode action potential recording in cardiac multicellular preparations was used to study the effects of NAD+.

    In this study, NAD+ (nicotinamide adenine dinucleotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking NAD+ (nicotinamide adenine dinucleotide).

  2. 06LabNot a test of NAD+ (nicotinamide adenine dinucleotide) aloneEx vivo tissueMechanism

    In rat myocardial preparations, P2 antagonist suramin abolished NAD+-induced electrical alterations.

    In plain wordsIn lab tests, suramin blocked NAD+-induced electrical changes compared with NAD+ without suramin.

    Outcome
    DecreaseP2 blockade of electrical effects
    Study

    ratn: not reported in source

    isolated myocardial preparations
    Comparator
    NAD+ effects without suramin
    Outcome group
    Heart function · Cardiovascular

    Source sentences

    Summary
    Revealed cardiotropic effects of NAD+ are likely to be mediated by P2 purine receptors, since P1 blocker DPCPX failed to affect them and P2 antagonist suramin abolished NAD + -induced alterations of electrical activity.
    1 context sentence
    Summary · context
    The standard technique of sharp microelectrode action potential recording in cardiac multicellular preparations was used to study the effects of NAD+.

    In this study, NAD+ (nicotinamide adenine dinucleotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking NAD+ (nicotinamide adenine dinucleotide).

  3. 07LabNot a test of NAD+ (nicotinamide adenine dinucleotide) aloneEx vivo tissueMechanism

    In rat myocardial preparations, PLC inhibitor U73122 partially removed NAD+-induced persistent action potential shortening.

    In plain wordsIn lab tests, U73122 partly reduced NAD+-induced action potential shortening compared with NAD+ without U73122.

    Outcome
    DecreasePLC inhibition of AP shortening
    Study

    ratn: not reported in source

    isolated myocardial preparations
    Comparator
    NAD+ effects without U73122
    Outcome group
    Heart function · Cardiovascular

    Source sentences

    Summary
    The latter effect is partially removed by PLC inhibitor U73122 showing the potential involvement of phosphoinositide signaling pathway in mediation of NAD+ cardiotropic effects.
    2 context sentences
    Summary · context
    P2X receptors may be responsible for NAD + -induced short-lasting AP prolongation, while P2Y receptors mediate persistent AP shortening.
    Summary · context
    The standard technique of sharp microelectrode action potential recording in cardiac multicellular preparations was used to study the effects of NAD+.

    In this study, NAD+ (nicotinamide adenine dinucleotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking NAD+ (nicotinamide adenine dinucleotide).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    14 Oct 2026, 05:02 UTC

    Study results updated

  2. Version 1

    14 Oct 2026, 01:46 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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