Evidence map›Paper›PMID 25771926›Full record

ArticleInternational journal of obesity (2005)2015

Novel lipidized analogs of prolactin-releasing peptide have prolonged half-lives and exert anti-obesity effects after peripheral administration.

L Maletínská, V Nagelová, A Tichá, J Zemenová, Z Pirník, M Holubová, A Špolcová, B Mikulášková, M Blechová, D Sýkora and 4 more

Abstract read
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In one paragraph

Article in International journal of obesity (2005), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 67 citations in OpenAlex.

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  20. Prolactin-Releasing Peptide: Physiological and Pharmacological Properties.International journal of molecular sciences · 2019
    Review
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

14 authors at 3 institutions in 1 country.

L MaletínskáAntiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic.
V NagelováAntiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic.
A TicháAntiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic.
J Zemenová1] Antiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic [2] Department of Analytical Chemistry, University of Chemistry and Technology, Prague, Czech Republic.
Z Pirník1] Antiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic [2] Laboratory of Functional Neuromorphology, Institute of Experimental Endocrinology, SAS, Bratislava, Slovak Republic [3] Department of Human and Clinical Pharmacology, University of Veterinary Medicine, Košice, Slovak Republic.
M HolubováAntiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic.
A ŠpolcováAntiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic.
B Mikulášková1] Antiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic [2] Institute of Physiology, AS CR, Prague, Czech Republic.
M BlechováAntiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic.
D SýkoraDepartment of Analytical Chemistry, University of Chemistry and Technology, Prague, Czech Republic.
Z LacinováThird Department of Medicine, Charles University in Prague, Prague, Czech Republic.
M HaluzíkThird Department of Medicine, Charles University in Prague, Prague, Czech Republic.
B ŽeleznáAntiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic.
J Kuneš1] Antiobesity Peptides, Institute of Organic Chemistry and Biochemistry, AS CR, Prague, Czech Republic [2] Institute of Physiology, AS CR, Prague, Czech Republic.
Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry · CZCharles University · CZUniversity of Chemistry and Technology, Prague · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesObesity is a frequent metabolic disorder but an effective therapy is still scarce. Anorexigenic neuropeptides produced and acting in the brain have the potential to decrease food intake and ameliorate obesity but are ineffective after peripheral application. We have designed lipidized analogs of prolactin-releasing peptide (PrRP), which is involved in energy balance regulation as demonstrated by obesity phenotypes of both PrRP- and PrRP-receptor-knockout mice.

resultsLipidized PrRP analogs showed binding affinity and signaling in PrRP receptor-expressing cells similar to natural PrRP. Moreover, these analogs showed high binding affinity also to anorexigenic neuropeptide FF-2 receptor. Peripheral administration of myristoylated and palmitoylated PrRP analogs to fasted mice induced strong and long-lasting anorexigenic effects and neuronal activation in the brain areas involved in food intake regulation. Two-week-long subcutaneous administration of palmitoylated PrRP31 and myristoylated PrRP20 lowered food intake, body weight and improved metabolic parameters, and attenuated lipogenesis in mice with diet-induced obesity.

conclusionsOur data suggest that the lipidization of PrRP enhances stability and mediates its effect in central nervous system. Strong anorexigenic and body-weight-reducing effects make lipidized PrRP an attractive candidate for anti-obesity treatment.

Indexed as

AnimalsAnti-Obesity AgentsAppetite RegulationEatingEnergy MetabolismHalf-LifeLipidsMaleMiceMice, Inbred C57BLObesityProlactin-Releasing HormoneSignal TransductionAnti-Obesity AgentsLipidsProlactin-Releasing Hormone

Identifiers

PMID25771926
OpenAlexW2048660711

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.