Evidence map›Paper›PMID 33789505›Full record

ArticleBiological research for nursing2021

Olanzapine Administration Reduces Chemotherapy-Induced Nausea Behavior in Rats.

Rosario B Jaime-Lara, Tito Borner, Ruby A Holland, Evan Shaulson, Brianna Brooks, Bart C De Jonghe

Open access · greenAbstract read
In one paragraph

Article in Biological research for nursing, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. The antiemetic actions of GIP receptor agonism.American journal of physiology. Endocrinology and metabolism · 2024
    Review
  2. Article
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

6 authors at 4 institutions in 1 country.

Rosario B Jaime-LaraDepartment of Biobehavioral Health Sciences, 6572University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-5726-7529
Tito BornerDepartment of Biobehavioral Health Sciences, 6572University of Pennsylvania, Philadelphia, PA, USA.
Ruby A HollandDepartment of Biobehavioral Health Sciences, 6572University of Pennsylvania, Philadelphia, PA, USA.
Evan ShaulsonDepartment of Biobehavioral Health Sciences, 6572University of Pennsylvania, Philadelphia, PA, USA.
Brianna BrooksDepartment of Biobehavioral Health Sciences, 6572University of Pennsylvania, Philadelphia, PA, USA.
Bart C De JongheDepartment of Biobehavioral Health Sciences, 6572University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-6980-5355
University of Pennsylvania · USNational Institute of Nursing Research · USNational Institute on Alcohol Abuse and Alcoholism · USUniversity of Pittsburgh · US

Funding

Neural Mechanisms of Nausea, Vomiting, and Energy DysregulationR01DK112812 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Bart C DE JONGHE, MATTHEW R HAYES · 2017 to 2026
$4.4M
NIDDK NIH HHS R01 DK112812
6 · The paper itself

Abstract

Nausea and vomiting are consistently identified among the most distressing side effects of chemotherapy. In recent years, Olanzapine (OLZ) treatment was added to anti-emetic guidelines as a treatment for chemotherapy-induced nausea and vomiting (CINV), despite little available data supporting a mechanism behind the positive benefits of the drug. Here, we examine whether OLZ reduces cisplatin chemotherapy-induced side effects on food intake and pica behavior in rats (i.e., kaolin intake, a proxy for nausea/emesis). Behavioral experiments tested whether systemic or hindbrain administration of OLZ ameliorated cisplatin-induced pica, anorexia, and body weight loss in rats. We also tested whether systemic OLZ reduces cisplatin-induced neuronal activation in the dorsal vagal complex (DVC), a hindbrain region controlling emesis. Lastly, given their role in regulating feeding and emesis, circulating ghrelin levels and central mRNA expression levels of serotonin (HT) receptor subunits, including 5-HT2C, were measured in brain regions that regulate CINV and energy balance in an exploratory analysis to investigate potential mediators of OLZ action. Our results show that both systemic and hindbrain administration of OLZ attenuated cisplatin-induced kaolin intake and body weight loss, but not anorexia. Systemic OLZ decreased cisplatin-induced c-Fos immunofluorescence in the DVC and prevented cisplatin-induced reductions in circulating ghrelin levels. IP OLZ also blocked cisplatin-induced increases in

Indexed as

AntiemeticsAntineoplastic AgentsAnimalsCisplatinNauseaOlanzapineRatsVomitingAntiemeticsAntineoplastic AgentsCisplatinOlanzapineemesisnauseaolanzapinepicavomiting

Identifiers

PMID33789505
PMCPMC8726422
OpenAlexW3151180711

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.