Evidence map›Paper›PMID 31912134›Full record

ArticleThe Journal of nutrition2020

Plasma Formate Is Greater in Fetal and Neonatal Rats Compared with Their Mothers.

Margaret E Brosnan, Garrett Tingley, Luke MacMillan, Brian Harnett, Theerawat Pongnopparat, Jenika D Marshall, John T Brosnan

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of nutrition, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. 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 1 institution in 1 country.

Margaret E BrosnanDepartment of Biochemistry, Memorial University of Newfoundland, St Johns, Newfoundland, Canada.
Garrett TingleyDepartment of Biochemistry, Memorial University of Newfoundland, St Johns, Newfoundland, Canada.
Luke MacMillanDepartment of Biochemistry, Memorial University of Newfoundland, St Johns, Newfoundland, Canada.
Brian HarnettDepartment of Biochemistry, Memorial University of Newfoundland, St Johns, Newfoundland, Canada.
Theerawat PongnopparatDepartment of Biochemistry, Memorial University of Newfoundland, St Johns, Newfoundland, Canada.
Jenika D MarshallDepartment of Biochemistry, Memorial University of Newfoundland, St Johns, Newfoundland, Canada.
John T BrosnanDepartment of Biochemistry, Memorial University of Newfoundland, St Johns, Newfoundland, Canada.
Memorial University of Newfoundland · CA

Funding

CIHR
6 · The paper itself

Abstract

backgroundFormate can be incorporated into 10-formyl-tetrahydrofolate (10-formyl-THF), which is a substrate for purine synthesis, and after further reduction of the one-carbon group, may be used as a substrate for thymidylate synthesis and for homocysteine remethylation.

objectiveWe examined plasma formate concentrations and the expression of genes involved in the production and utilization of formate in fetal and neonatal rats and in pregnant and virgin female rats.

methodsIn 1 experiment, plasma formate was measured by GC-MS in rats aged 1-56 d. In a second experiment, virgin female (adult) rats, 19-d pregnant rats (P) and their male and female fetuses (F), and 3-d-old (N) and 7-d-old (J) offspring had plasma and amniotic fluid analyzed for formate by GC-MS, mRNA abundance in liver and placenta by qPCR, and several plasma amino acids by HPLC.

resultsThe plasma formate concentration was significantly higher in fetuses at embryonic day 19 than in the mothers. It was also significantly higher in neonatal rats but slowly returned to adult concentrations by ∼3 wk. The abundance of mitochondrial monofunctional 10-formyl-tetrahydrofolate synthetase (Mthfd1l) mRNA was significantly higher in placenta (PP) and F liver than in liver of N or J. Expression of mitochondrial bifunctional NAD-dependent methylene-tetrahydrofolate dehydrogenase/methenyl-tetrahydrofolate cyclohydrolase (Mthfd2) was significantly enriched in PP and liver of P, intermediate in F liver, and much lower in liver of N and J, relative to PP. Serine hydroxymethyltransferase 2 (Shmt2), methylenetetrahydrofolate dehydrogenase 1 (Mthfd1), and glycine decarboxylase protein of the glycine cleavage system (Gldc) mRNA expression was significantly lower in PP compared with other groups. Cytoplasmic NAD(P)-dependent 10-formyl-tetrahydrofolate dehydrogenase (Aldh1/1) and mitochondrial NAD(P)-dependent 10-formyl-tetrahydrofolate dehydrogenase (Aldh1/2) , genes responsible for the catabolism of 10-formylTHF, were very weakly expressed in PP, low in livers of F and N, and reached the significantly higher adult levels in J. Serine, glycine, and methionine concentrations in plasma of F were significantly higher than in plasma of P.

conclusionsFormate metabolism is highly active in fetuses and in placenta of pregnant rats.

Indexed as

AgingAnimalsAnimals, NewbornFemaleFetusFormatesLiverMaternal-Fetal ExchangeMothersPlacentaPregnancyRatsRats, Sprague-DawleyFormatesformic acidfetusglycinemethioninemitochondriaone-carbon metabolismpregnancyserinetetrahydrofolate

Identifiers

PMID31912134
PMCPMC7198295
OpenAlexW2999294631

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.