Evidence map›Paper›PMID 28624479›Full record

ArticlePhysiology & behavior2018

Food restriction-induced changes in motivation differ with stages of the estrous cycle and are closely linked to RFamide-related peptide-3 but not kisspeptin in Syrian hamsters.

Noah A Benton, Kim A Russo, Jeremy M Brozek, Ryan J Andrews, Veronica J Kim, Lance J Kriegsfeld, Jill E Schneider

Open access · hybridAbstract read
In one paragraph

Article in Physiology & behavior, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Noah A BentonDepartment of Biological Sciences, Lehigh University, Bethlehem, PA 18015, United States.
Kim A RussoDepartment of Psychology and The Helen Wills Neuroscience Institute, University of California, Berkeley, CA 94720, United States.
Jeremy M BrozekDepartment of Biological Sciences, Lehigh University, Bethlehem, PA 18015, United States.
Ryan J AndrewsDepartment of Psychology and The Helen Wills Neuroscience Institute, University of California, Berkeley, CA 94720, United States.
Veronica J KimDepartment of Psychology and The Helen Wills Neuroscience Institute, University of California, Berkeley, CA 94720, United States.
Lance J KriegsfeldDepartment of Psychology and The Helen Wills Neuroscience Institute, University of California, Berkeley, CA 94720, United States.
Jill E SchneiderDepartment of Biological Sciences, Lehigh University, Bethlehem, PA 18015, United States. Electronic address: js0v@lehigh.edu.
University of California, Berkeley · USLehigh University · US

Funding

The role of kisspeptin and RFRP-3 in the neuroendocrine control of female reproductionR01HD050470 · NICHD · UNIVERSITY OF CALIFORNIA BERKELEY · PI KRIEGSFELD, LANCE J · 2007 to 2022
$5.0M
NICHD NIH HHS R01 HD050470
6 · The paper itself

Abstract

We tested the hypothesis that the effects of food restriction on behavioral motivation are mediated by one or both of the RFamide peptides, RFamide-related peptide-3 (RFRP-3) and kisspeptin (Kp) in female Syrian hamsters (Mesocricetus auratus). Female hamsters fed ad libitum and given a choice between food and adult male hamsters are highly motivated to visit males instead of food on all four days of the estrous cycle, but after 8days of mild food restriction (75% of ad libitum intake) they shift their preference toward food every day of the estrous cycle until the day of estrus, when they shift their preference back toward the males. In support of a role for RFRP-3 in these behavioral changes, the preference for food and the activation of RFRP-3-immunoreactive (Ir) cells in the dorsomedial hypothalamus (DMH) showed the same estrous cycle pattern in food-restricted females, but no association was observed between behavior and the activation of Kp cells in the hypothalamic arcuate nucleus or preoptic area. Next, we tested the hypothesis that food-restriction-induced activation of RFRP-3-Ir cells is modulated by high levels of ovarian steroids at the time of estrus. In support of this idea, on nonestrous days, mild food restriction increased activation of RFRP-3-Ir cells, but failed to do so on the day of estrus even though this level of food restriction did not significantly decrease circulating concentrations of estradiol or progesterone. Furthermore, in ovariectomized females, food-restriction-induced increases in activation of RFRP-3-Ir cells were blocked by systemic treatment with progesterone alone, estradiol plus progesterone, but not estradiol alone. Central infusion with RFRP-3 in ad libitum-fed females significantly decreased sexual motivation and produced significant increases in 90-minute food hoarding, in support of the hypothesis that elevated central levels of RFRP-3 are sufficient to create the shift in behavioral motivation in females fed ad libitum. Together, these results are consistent with the hypothesis that high levels of ingestive motivation are promoted during the nonfertile phase of the estrous cycle by elevated activation of RFRP-3-Ir cells, and RFRP-3-Ir cellular activation is modulated by ovarian steroids around the time of estrus, thereby diverting attention away from food and increasing sexual motivation.

Indexed as

AnimalsCaloric RestrictionCricetinaeEstradiolEstrous CycleFemaleFood DeprivationHypothalamusKisspeptinsMaleMesocricetusMicroinjectionsMotivationNeuropeptidesOvariectomyProgesteroneEstradiolKisspeptinsNeuropeptidesProgesteroneRFamide peptideEstradiolFood hoardingGnIHIngestive behaviorKpLeptinMale preferenceProgesteroneProgesterone receptorRFRP-3Sex behavior

Identifiers

PMID28624479
PMCPMC5732085
OpenAlexW2625407478

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.