Evidence map›Paper›PMID 28805659›Full record

ArticleThe Journal of clinical investigation2017

The atypical antipsychotic olanzapine causes weight gain by targeting serotonin receptor 2C.

Caleb C Lord, Steven C Wyler, Rong Wan, Carlos M Castorena, Newaz Ahmed, Dias Mathew, Syann Lee, Chen Liu, Joel K Elmquist

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

83 citing papers in PubMed, 161 citations in OpenAlex.

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  19. Innovation (Cambridge (Mass.)) · 2024
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23 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Caleb C LordDivision of Hypothalamic Research, Department of Internal Medicine, and.
Steven C WylerDivision of Hypothalamic Research, Department of Internal Medicine, and.
Rong WanDivision of Hypothalamic Research, Department of Internal Medicine, and.
Carlos M CastorenaDivision of Hypothalamic Research, Department of Internal Medicine, and.
Newaz AhmedDivision of Hypothalamic Research, Department of Internal Medicine, and.
Dias MathewDivision of Hypothalamic Research, Department of Internal Medicine, and.
Syann LeeDivision of Hypothalamic Research, Department of Internal Medicine, and.
Chen LiuDivision of Hypothalamic Research, Department of Internal Medicine, and.
Joel K ElmquistDivision of Hypothalamic Research, Department of Internal Medicine, and.
Southwestern Medical Center

Funding

ENDOCRINE &METABOLISM TRAINING GRANTT32DK007307 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI PHILIPP E SCHERER · 1986 to 2026
$5.4M
Hypothalamic Serotonin Receptors and Olanzapine-induced Metabolic SyndromeR01DK114036 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Chen Liu · 2017 to 2026
$4.2M
INTERACTIONS OF LEPTIN AND CENTRAL SEROTONIN SYSTEMSR01DK088423 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI ELMQUIST, JOEL K. · 2010 to 2019
$3.8M
Leptin Action and Central Melanocortin SystemsR37DK053301 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI ELMQUIST, JOEL K. · 2007 to 2016
$3.7M
Role of Serotonin Signaling in POMC Neurons to Regulate Lipid HomeostasisF32DK103449 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI LORD, CALEB C · 2014 to 2015
$106k
Uncovering a mechanism for SF-1 transcriptional activation in response to exerciseF32DK116427 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI WYLER, STEVEN C · 2017 to 2018
$103k
NIDDK NIH HHS F32 DK103449NIDDK NIH HHS F32 DK116427NIDDK NIH HHS R01 DK088423NIDDK NIH HHS R01 DK114036NIDDK NIH HHS R37 DK053301NIDDK NIH HHS T32 DK007307
6 · The paper itself

Abstract

Atypical antipsychotics such as olanzapine often induce excessive weight gain and type 2 diabetes. However, the mechanisms underlying these drug-induced metabolic perturbations remain poorly understood. Here, we used an experimental model that reproduces olanzapine-induced hyperphagia and obesity in female C57BL/6 mice. We found that olanzapine treatment acutely increased food intake, impaired glucose tolerance, and altered physical activity and energy expenditure in mice. Furthermore, olanzapine-induced hyperphagia and weight gain were blunted in mice lacking the serotonin 2C receptor (HTR2C). Finally, we showed that treatment with the HTR2C-specific agonist lorcaserin suppressed olanzapine-induced hyperphagia and weight gain. Lorcaserin treatment also improved glucose tolerance in olanzapine-fed mice. Collectively, our studies suggest that olanzapine exerts some of its untoward metabolic effects via antagonism of HTR2C.

Indexed as

AnimalsAntipsychotic AgentsBenzodiazepinesBody CompositionBody WeightDiabetes Mellitus, Type 2FemaleGlucoseGlucose Tolerance TestHyperphagiaMaleMiceMice, Inbred C57BLOlanzapineReceptor, Serotonin, 5-HT2CSerotonin AntagonistsAntipsychotic AgentsBenzodiazepinesGlucoseOlanzapineReceptor, Serotonin, 5-HT2CSerotonin Antagonists

Identifiers

PMID28805659
PMCPMC5669575
OpenAlexW2743028812

What OpenQuestion holds

Textmetadata
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.