Evidence map›Paper›PMID 33889948›Full record

ArticleBiology of reproduction2021

Tauroursodeoxycholic acid/TGR5 signaling promotes survival and early development of glucose-stressed porcine embryos†.

Naomi Dicks, Karina Gutierrez, Luke Currin, Mariana P de Macedo, Werner G Glanzner, Rafael G Mondadori, Marek Michalak, Luis B Agellon, Vilceu Bordignon

Open access · greenAbstract read
In one paragraph

Article in Biology of reproduction, 2021. 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
1.8field-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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  3. Cross-Species Insights intoAntioxidants (Basel, Switzerland) · 2025
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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

9 authors at 3 institutions in 2 countries.

Naomi DicksDepartment of Animal Science, McGill University, Quebec, Canada.
Karina GutierrezDepartment of Animal Science, McGill University, Quebec, Canada.
Luke CurrinDepartment of Animal Science, McGill University, Quebec, Canada.
Mariana P de MacedoDepartment of Animal Science, McGill University, Quebec, Canada.
Werner G GlanznerDepartment of Animal Science, McGill University, Quebec, Canada.
Rafael G MondadoriDepartment of Animal Science, McGill University, Quebec, Canada.
Marek MichalakDepartment of Biochemistry, University of Alberta, Edmonton, Alberta, Canada.
Luis B AgellonSchool of Human Nutrition, McGill University, Quebec, Canada.
Vilceu BordignonDepartment of Animal Science, McGill University, Quebec, Canada.
McGill University · CAUniversidade Federal de Pelotas · BRUniversity of Alberta · CA

Funding

CIHR MOP-15291
6 · The paper itself

Abstract

Conditions of impaired energy and nutrient homeostasis, such as diabetes and obesity, are associated with infertility. Hyperglycemia increases endoplasmic reticulum stress as well as oxidative stress and reduces embryo development and quality. Oxidative stress also causes deoxyribonucleic acid damage, which impairs embryo quality and development. The natural bile acid tauroursodeoxycholic acid reduces endoplasmic reticulum stress and rescues developmentally incompetent late-cleaving embryos, as well as embryos subjected to nuclear stress, suggesting the endoplasmic reticulum stress response, or unfolded protein response, and the genome damage response are linked. Tauroursodeoxycholic acid acts via the Takeda-G-protein-receptor-5 to alleviate nuclear stress in embryos. To evaluate the role of tauroursodeoxycholic acid/Takeda-G-protein-receptor-5 signaling in embryo unfolded protein response, we used a model of glucose-induced endoplasmic reticulum stress. Embryo development was impaired by direct injection of tauroursodeoxycholic acid into parthenogenetically activated oocytes, whereas it was improved when tauroursodeoxycholic acid was added to the culture medium. Attenuation of the Takeda-G-protein-receptor-5 precluded the positive effect of tauroursodeoxycholic acid supplementation on development of parthenogenetically activated and fertilized embryos cultured under standard conditions and parthenogenetically activated embryos cultured with excess glucose. Moreover, attenuation of tauroursodeoxycholic acid/Takeda-G-protein-receptor-5 signaling induced endoplasmic reticulum stress, oxidative stress and cell survival genes, but decreased expression of pluripotency genes in parthenogenetically activated embryos cultured under excess glucose conditions. These data suggest that Takeda-G-protein-receptor-5 signaling pathways link the unfolded protein response and genome damage response. Furthermore, this study identifies Takeda-G-protein-receptor-5 signaling as a potential target for mitigating fertility issues caused by nutrient excess-associated blastomere stress and embryo death.

Indexed as

AnimalsBlastomeresCholagogues and CholereticsEmbryo, MammalianEmbryonic DevelopmentEndoplasmic Reticulum StressGlucoseOxidative StressReceptors, G-Protein-CoupledSus scrofaTaurochenodeoxycholic AcidUnfolded Protein ResponseCholagogues and CholereticsGlucoseReceptors, G-Protein-CoupledTaurochenodeoxycholic Acidursodoxicoltaurineembryo developmentER stressGPBAR1TUDCAUPR

Identifiers

PMID33889948
PMCPMC8256098
OpenAlexW3156633656

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.