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Mechanisms involved in cAMP mediated inhibition of the Ubiquitin‐Proteasome system

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.

The three-model screen

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All three models called this out of scope.

stratum: aff_core · design weight: 5595.24 (the sample is stratified; any rate computed without the weight is wrong)
Claude Opus 4.8OUT
genre: empirical
about Canada: no
confidence: high

Physiology study of cAMP-mediated inhibition of the ubiquitin-proteasome system in rat skeletal muscle.

GPT-5.6 (high)OUT
genre: empirical
about Canada: no
confidence: high

It studies cellular signaling and proteolysis in rat muscle, not research methods or the research system.

Grok 4.5OUT
genre: empirical
about Canada: no
confidence: high

Domain muscle physiology and UPS regulation in rats, not a study of research practice.

Abstract

Aim: This study was undertaken to investigate the role of beta‐2 adrenoceptors and cAMP in regulating the Ubiquitin‐proteasome system (UPS) in skeletal muscle from normal rats. Methods and results: The activity of UPS and the Akt/FoxO signaling pathway were measured in skeletal muscle from rats treated with clenbuterol (3 mg/kg wt; sc), a selective beta‐2 adrenergic agonist, for 3 days. In extensor digital longus (EDL) muscle, clenbuterol increased by 30% muscle weight, reduced by 45% the UPS activity and increased by 30% the phosphorylation of Akt and FoxO3. The addition of isobutylmethylxanthine (IBMX; 10 −3 M), a cAMP phosphodiesterase inhibitor, to the incubation medium increased cAMP levels (4‐fold) and decreased by 50% the UPS activity in isolated soleus and EDL muscles from normal rats. IBMX in vitro also reduced the levels of ubiquitin‐protein conjugated and the mRNA levels of the atrogin‐1/MAF bx (50%) and the E 2 ‐14KDa ubiquitin conjugating enzyme (30%) transcripts in muscles from normal rats. Ubiquitin and MuRF1 mRNA were not altered by IBMX in vitro. Conclusions: These data suggest that stimulation of beta‐2 adrenoceptors, through the activation of cAMP and Akt signaling pathways, inhibit ubiquitin‐proteasome proteolysis by increasing FoxO3 phosphorylation and suppressing atrogin‐1 mRNA expression in skeletal muscle from normal rats. Financial support: CNPq, CAPES, FAPESP

Stored with the screening record, where it is evidence for the labels above.

The record

Venue
The FASEB Journal
Topic
Pharmacological Effects and Assays
Field
Agricultural and Biological Sciences
Canadian institutions
McGill University
Funders
Conselho Nacional de Desenvolvimento Científico e TecnológicoCoordenação de Aperfeiçoamento de Pessoal de Nível SuperiorFundação de Amparo à Pesquisa do Estado de São Paulo
Keywords
IBMXClenbuterolUbiquitinInternal medicineEndocrinologyProtein kinase BProteasomeChemistrySkeletal musclePhosphorylationFOXO3MyocyteStimulationBiologyBiochemistryMedicineForskolin
Has abstract in OpenAlex
yes