Evidence map›Paper›PMID 42703648›Full record

ArticleActa physiologica (Oxford, England)2026

ATP Release and Purinergic Signaling Potentiate β-Adrenergic Effects on Brown Adipocytes.

Marco Tozzi, Emilie B Berggreen, Rui Zhang, Anders Gudiksen, Wei Li, Mathias B Matz, Henriette Pilegaard, Jacob B Hansen, Ivana Novak

Abstract read
In one paragraph

Article in Acta physiologica (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Marco TozziSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-2576-0183
Emilie B BerggreenSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Rui ZhangSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Anders GudiksenSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0003-1800-4838
Wei LiSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-0279-0638
Mathias B MatzSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0009-0002-2246-7616
Henriette PilegaardSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-1071-0327
Jacob B HansenSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-5249-2586
Ivana NovakSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-8917-8010

Funding

Independent Research Fund Denmark 4002-00162BIndependent Research Fund Denmark 8020-00254B
6 · The paper itself

Abstract

aimBrown adipose tissue (BAT) specializes in energy consumption and thermogenesis in response to cold stress. Brown adipocytes (BA) express purinergic receptors, yet little is known about the source of extracellular ATP and the role of purinergic signaling, and the potential interaction with β-adrenergic signaling. We aimed at elucidating whether: BA could release extracellular ATP; ATP/purinergic signaling impacts β-adrenergic responses; and the expression of purinergic receptors in BAT of mice and cultured BA.

methodsReal-time ATP release was monitored in a mature BA cell model exposed to adrenergic agonists, insulin, glucose, and pharmacological inhibitors. Cellular assays included oxygen consumption, glycolysis, and lipolysis assays, and Ca

resultsWe show that β-adrenergic stimulation of BA causes ATP release through pannexin-1 in a cAMP-protein kinase A-dependent manner. ATP release is increased with glucose but decreased with insulin, the latter due to phosphodiesterase 3 activation. β-Adrenergic stimulation increases oxygen consumption, glycolysis, and lipolysis, while apyrase and pannexin-1 inhibitors decrease these effects. Both extracellular ATP and β-adrenergic stimulation induce Ca

conclusionsThe present study demonstrates that ATP is released from BA via pannexin-1 channels in response to β-adrenergic stimulation, that extracellular ATP, acting through P2 receptor signaling, potentiates β-adrenergic effects on BA function, and that expression of several purinergic receptors changes in response to β-adrenergic stimulation.

Indexed as

Adenosine TriphosphateAdipocytes, BrownAdrenergic beta-AgonistsReceptors, Adrenergic, betaReceptors, PurinergicSignal TransductionAnimalsCells, CulturedConnexinsMaleMiceMice, Inbred C57BLAdenosine TriphosphateAdrenergic beta-AgonistsConnexinsReceptors, Adrenergic, betaReceptors, Purinergicadipocytebrown adipose tissueextracellular ATPglycolysislipolysisoxygen consumptionP2X receptor expressionpannexin channelsthermogenesis

Identifiers

PMID42703648
PMCPMC13548067

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.