Evidence map›Paper›PMID 37490843›Full record

ArticleEndocrinology2023

The 16α-hydroxylated Bile Acid, Pythocholic Acid Decreases Food Intake and Increases Oleoylethanolamide in Male Mice.

Sei Higuchi, Courtney Wood, Raidah H Nasiri, Leela J Giddla, Valentina Molina, Rokia Diarra, Nicholas V DiPatrizio, Akira Kawamura, Rebecca A Haeusler

Open access · hybridAbstract read
In one paragraph

Article in Endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Bile acid metabolism in type 2 diabetes mellitus.Nature reviews. Endocrinology · 2025
    Review
  4. Review
  5. 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

9 authors at 4 institutions in 1 country.

Sei HiguchiDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY 11439, USA.ORCID 0000-0002-5134-8619
Courtney WoodDivision of Biomedical Sciences, School of Medicine, University of California, Riverside, CA 92521, USA.
Raidah H NasiriDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY 11439, USA.
Leela J GiddlaDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY 11439, USA.
Valentina MolinaDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY 11439, USA.
Rokia DiarraDepartment of Biological Sciences, St. John's University, Queens, NY 11439, USA.
Nicholas V DiPatrizioDivision of Biomedical Sciences, School of Medicine, University of California, Riverside, CA 92521, USA.ORCID 0000-0001-8423-0695
Akira KawamuraDepartment of Chemistry, Hunter College of CUNY, New York, NY 10065, USA.ORCID 0000-0002-1662-1093
Rebecca A HaeuslerNaomi Berrie Diabetes Center and Department of Pathology and Cell Biology, Columbia University, New York, NY 10032, USA.ORCID 0000-0002-6973-9845
St. John's University · USUniversity of California, Riverside · USColumbia University · USHunter College · US

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
RESEARCH TRAININGP30DK026687 · NIDDK · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI Anthony W Ferrante, DYMPNA GALLAGHER · 1986 to 2026
$33.0M
The Organoid and Cell Culture CoreP30DK132710 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Robert F. Schwabe · 2022 to 2026
$7.2M
Bile acids and insulin sensitivityR01DK115825 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Rebecca Anne Haeusler · 2018 to 2026
$5.4M
Insulin regulation of hepatic transportR01DK135298 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Rebecca Anne Haeusler · 2023 to 2026
$2.6M
Gut-brain endocannabinoid signaling in feeding behavior and obesityR01DK119498 · NIDDK · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI DIPATRIZIO, NICHOLAS VINCENT · 2019 to 2023
$1.7M
NCATS NIH HHS UL1 TR001873NIDDK NIH HHS P30 DK132710NIDDK NIH HHS R01 DK115825NIDDK NIH HHS R01 DK119498NIDDK NIH HHS R01 DK135298NIH HHS P30DK026687NIH HHS R01DK115825
6 · The paper itself

Abstract

Modulation of bile acid (BA) structure is a potential strategy for obesity and metabolic disease treatment. BAs act not only as signaling molecules involved in energy expenditure and glucose homeostasis, but also as regulators of food intake. The structure of BAs, particularly the position of the hydroxyl groups of BAs, impacts food intake partly by intestinal effects: (1) modulating the activity of N-acyl phosphatidylethanolamine phospholipase D, which produces the anorexigenic bioactive lipid oleoylethanolamide (OEA) or (2) regulating lipid absorption and the gastric emptying-satiation pathway. We hypothesized that 16α-hydroxylated BAs uniquely regulate food intake because of the long intermeal intervals in snake species in which these BAs are abundant. However, the effects of 16α-hydroxylated BAs in mammals are completely unknown because they are not naturally found in mammals. To test the effect of 16α-hydroxylated BAs on food intake, we isolated the 16α-hydroxylated BA pythocholic acid from ball pythons (Python regius). Pythocholic acid or deoxycholic acid (DCA) was given by oral gavage in mice. DCA is known to increase N-acyl phosphatidylethanolamine phospholipase D activity better than other mammalian BAs. We evaluated food intake, OEA levels, and gastric emptying in mice. We successfully isolated pythocholic acid from ball pythons for experimental use. Pythocholic acid treatment significantly decreased food intake in comparison to DCA treatment, and this was associated with increased jejunal OEA, but resulted in no change in gastric emptying or lipid absorption. The exogenous BA pythocholic acid is a novel regulator of food intake and the satiety signal for OEA in the mouse intestine.

Indexed as

Bile Acids and SaltsPhospholipase DAnimalsCholic AcidsEatingEndocannabinoidsEthanolamineMaleMammalsMiceOleic AcidsPhosphatidylethanolamines3,12,16-trihydroxycholan-24-oic acidBile Acids and SaltsCholic AcidsEndocannabinoidsEthanolamineOleic Acidsoleoylethanolamideoleoyl ethanolaminePhosphatidylethanolaminesPhospholipase Dbile acidsgastric emptyingNAPE-PLDOEApythocholic acid

Identifiers

PMID37490843
PMCPMC10407715
OpenAlexW4385231855

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.