Evidence map›Paper›PMID 29170989›Full record

ArticleJournal of pharmacokinetics and pharmacodynamics2018

Modeling energy intake and body weight effects of a long-acting amylin analogue.

Annika Brings, Jens Markus Borghardt, Jolanta Skarbaliene, Tamara Baader-Pagler, Maria A Deryabina, Wolfgang Rist, Stefan Scheuerer

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of pharmacokinetics and pharmacodynamics, 2018. 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
0.5field-weighted citation impact, top 40% 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, 6 citations in OpenAlex.

  1. The long-acting amylin/calcitonin receptor agonist ZP5461 suppresses food intake and body weight in male rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  2. 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

7 authors at 2 institutions in 2 countries.

Annika BringsDrug Discovery Sciences, Boehringer Ingelheim Pharma GmbH & Co KG, 88397, Biberach, Germany.
Jens Markus BorghardtDrug Discovery Sciences, Boehringer Ingelheim Pharma GmbH & Co KG, 88397, Biberach, Germany.
Jolanta SkarbalieneZealand Pharma A/S, Glostrup, 2600, Copenhagen, Denmark.
Tamara Baader-PaglerCardiometabolic Diseases Research, Boehringer Ingelheim Pharma GmbH & Co KG, 88397, Biberach, Germany.
Maria A DeryabinaZealand Pharma A/S, Glostrup, 2600, Copenhagen, Denmark.
Wolfgang RistDrug Discovery Sciences, Boehringer Ingelheim Pharma GmbH & Co KG, 88397, Biberach, Germany.
Stefan ScheuererDrug Discovery Sciences, Boehringer Ingelheim Pharma GmbH & Co KG, 88397, Biberach, Germany. stefan.scheuerer@boehringer-ingelheim.com.ORCID 0000-0002-4417-098X
Boehringer Ingelheim (Germany) · DEZealand Pharma (Denmark) · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inhibitory effect of anti-obesity drugs on energy intake (EI) is counter-acted by feedback regulation of the appetite control circuit leading to drug tolerance. This complicates the design and interpretation of EI studies in rodents that are used for anti-obesity drug development. Here, we investigated a synthetic long-acting analogue of the appetite-suppressing peptide hormone amylin (LAMY) in lean and diet-induced obese (DIO) rats. EI and body weight (BW) were measured daily and LAMY concentrations in plasma were assessed using defined time points following subcutaneous administration of the LAMY at different dosing regimens. Overall, 6 pharmacodynamic (PD) studies including a total of 173 rats were considered in this evaluation. Treatment caused a dose-dependent reduction in EI and BW, although multiple dosing indicated the development of tolerance over time. This behavior could be adequately described by a population model including homeostatic feedback of EI and a turnover model describing the relationship between EI and BW. The model was evaluated by testing its ability to predict BW loss in a toxicology study and was utilized to improve the understanding of dosing regimens for obesity therapy. As such, the model proved to be a valuable tool for the design and interpretation of rodent studies used in anti-obesity drug development.

Indexed as

AnimalsAnti-Obesity AgentsBody WeightDiet, High-FatEnergy IntakeFemaleIslet Amyloid PolypeptideMaleObesityRatsRats, Sprague-DawleyRats, WistarAnti-Obesity AgentsIslet Amyloid PolypeptideAmylin analogueEnergy intakeModel-informed drug discoveryObesityTolerance

Identifiers

PMID29170989
OpenAlexW2768872330

What Socratic 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 Socratic graph.