Evidence map›Paper›PMID 19524129›Full record

ArticleMolecular and cellular endocrinology2009

Parathyroid hormone suppresses insulin signaling in adipocytes.

Eugene Chang, Shawn S Donkin, Dorothy Teegarden

Abstract read
In one paragraph

Article in Molecular and cellular endocrinology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 84 citations in OpenAlex.

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  10. Determinants of Bone Mineral Density in Iranian Women with Polycystic Ovary Syndrome.International journal of endocrinology and metabolism · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Eugene ChangInterdepartmental Nutrition Program, Purdue University, West Lafayette, IN 47907, USA.
Shawn S Donkin
Dorothy Teegarden
Purdue University West Lafayette · US

Funding

Dairy Product Intake Regulation of Energy MetabolismR01DK069965 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI TEEGARDEN, DOROTHY · 2005 to 2007
$789k
NIDDK NIH HHS DK069965NIDDK NIH HHS R01 DK069965
6 · The paper itself

Abstract

Previous reports suggest that parathyroid hormone (PTH) is associated with insulin resistance. This research investigated the effects of PTH on insulin signaling in differentiated 3T3-L1 adipocytes. PTH (10 nM, 24 h) treatment induced a reduction in insulin-stimulated glucose uptake, AKT activity (phosphorylated AKT/total AKT protein expression) and a decrease in GLUT4 and IRS-1 protein expression compared to vehicle treated controls in differentiated adipocytes. PTH treatment also induced increased phosphorylation of IRS-1 on serine 307, which suppresses insulin signaling. In addition, treatment of cells with adenyl cyclase inhibitor SQ52236 ameliorated the effects of PTH on insulin-stimulated glucose uptake, whereas inhibition of phospholipase C alpha (U73122) did not significantly alter the effects of PTH. Thus, PTH treatment of differentiated 3T3-L1 adipocytes suppresses insulin-stimulated glucose uptake and insulin signaling via cAMP pathway, potentially through the phosphorylation of IRS-1 at serine 307.

Indexed as

3T3-L1 CellsAdipocytesAnimalsGlucoseGlucose Transporter Type 1Glucose Transporter Type 4HumansInsulinInsulin Receptor Substrate ProteinsMiceParathyroid HormonePhosphorylationPhosphoserineProto-Oncogene Proteins c-aktReceptor, InsulinSignal TransductionGlucoseGlucose Transporter Type 1Glucose Transporter Type 4InsulinInsulin Receptor Substrate ProteinsParathyroid HormonePhosphoserineProto-Oncogene Proteins c-aktReceptor, Insulin

Identifiers

PMID19524129
PMCPMC2714196
OpenAlexW2068461520

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.