Evidence map›Paper›PMID 31993312›Full record

ArticleActa pharmaceutica Sinica. B2020

Effects of total parenteral nutrition on drug metabolism gene expression in mice.

Christina Ferrucci-Da Silva, Le Zhan, Jianliang Shen, Bo Kong, Michael J Campbell, Naureen Memon, Thomas Hegyi, Lucy Lu, Grace L Guo

Open access · diamondAbstract read
In one paragraph

Article in Acta pharmaceutica Sinica. B, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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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 6 institutions in 1 country.

Christina Ferrucci-Da SilvaDivision of Neonatology, Department of Pediatrics, Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USA.
Le ZhanRutgers Cancer Institute of New Jersey, New Brunswick, NJ 08901, USA.
Jianliang ShenDepartment of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ 08854, USA.
Bo KongDepartment of Pharmacology and Toxicology, School of Pharmacy, Rutgers University, Piscataway, NJ 08854, USA.
Michael J CampbellDepartment of Pharmacology and Toxicology, School of Pharmacy, Rutgers University, Piscataway, NJ 08854, USA.
Naureen MemonMidAtlantic Neonatology Associates, Morristown, NJ 07960, USA.
Thomas HegyiDivision of Neonatology, Department of Pediatrics, Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USA.
Lucy LuSchool of Pharmacy, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Grace L GuoDepartment of Pharmacology and Toxicology, School of Pharmacy, Rutgers University, Piscataway, NJ 08854, USA.
Rutgers, The State University of New Jersey · USJohnson University · USEnvironmental and Occupational Health Sciences Institute · USRutgers Cancer Institute of New JerseyUniversity of Pittsburgh · USUrology Associates · US

Funding

Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI ROBERT John LAUMBACH · 1988 to 2026
$47.4M
TRAINING IN EVIRONMENTAL TOXICOLOGYT32ES007148 · NIEHS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI Lauren M Aleksunes · 1987 to 2026
$11.4M
Summer Research Training in Environmental Health SciencesR25ES020721 · NIEHS · RUTGERS, THE STATE UNIV OF N.J. · PI Lauren M Aleksunes, Debra L Laskin · 2011 to 2026
$1.2M
Gut bile acids, Fxr, & Fgf15 in total parenteral nutrition-associated cholestasisR01GM104037 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI GUO, GRACE L · 2013 to 2016
$1.1M
Differential roles of FXR and FGF15 in liver fibrosis developmentR21ES029258 · NIEHS · RUTGERS, THE STATE UNIV OF N.J. · PI GUO, GRACE L · 2018 to 2019
$426k
Role of Intestinal Bile Acid Signaling in Liver DiseasesI01BX002741 · VA · VA NEW JERSEY HEALTH CARE SYSTEM · PI GRACE L GUO · 2018 to 2026
–
BLRD VA I01 BX002741NIEHS NIH HHS P30 ES005022NIEHS NIH HHS R21 ES029258NIEHS NIH HHS R25 ES020721NIEHS NIH HHS T32 ES007148NIGMS NIH HHS R01 GM104037
6 · The paper itself

Abstract

Parenteral nutrition-associated liver disease (PNALD) is a liver dysfunction caused by various risk factors presented in patients receiving total parenteral nutrition (TPN). Omega-6 rich Intralipid® and omega-3 rich Omegaven® are two intravenous lipid emulsions used in TPN. TPN could affect the hepatic expression of genes in anti-oxidative stress, but it's unknown whether TPN affects genes in drug metabolism. In this study, either Intralipid®- or Omegaven®-based TPN was administered to mice and the expression of a cohort of genes involved in anti-oxidative stress or drug metabolism was analyzed, glutathione (GSH) levels were measured, and protein levels for two key drug metabolism genes were determined. Overall, the expression of most genes was downregulated by Intralipid®-based TPN (

Indexed as

CYP450, cytochrome p450Drug metabolismFAs, fatty acidsGADPH, glyceraldehyde 3-phosphate dehydrogenaseGclc: glutamate-cysteine ligase catalytic subunit, Gclm: glutamate-cysteine ligase modifier subunitGlutathioneGpx3, glutathione peroxidase 3GSH, glutathioneGSSG, GSH/glutathione disulfideGstm1, glutathione S-transferase, mu 1Gstm3, glutathione S-transferase, mu 3Gstm6, glutathione S-transferase, mu 6Gstp1, glutathione S-transferase, pi 1Ho-1, heme oxygenase 1LiverMt-1, metallothionein 1NQO1, NAD(P)H:quinone acceptor oxidoreductase 1Parenteral nutrition-associated liver diseasePNALD, parenteral nutrition-associated liver diseaseROS, reactive oxygen speciesTotal parenteral nutritionTPN, total parenteral nutrition

Identifiers

PMID31993312
PMCPMC6976970
OpenAlexW2984655285

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.