Evidence map›Paper›PMID 21802472›Full record

ArticleFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association2011

Assessment of usnic acid toxicity in rat primary hepatocytes using ¹³C isotopomer distribution analysis of lactate, glutamate and glucose.

Bakary J Sonko, Thomas C Schmitt, Lei Guo, Qiang Shi, Laszlo G Boros, Julian E A Leakey, Richard D Beger

Abstract read
In one paragraph

Article in Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
8.0field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 37 citations in OpenAlex.

  1. Natural product as a lead for impairing mitochondrial respiration in cancer cells.Journal of enzyme inhibition and medicinal chemistry · 2025
    Article
  2. Article
  3. Review
  4. Toxicity of Usnic Acid: A Narrative Review.Journal of toxicology · 2022
    Review
  5. Article
  6. (+)-Usnic Acid Inhibits Migration of c-KIT Positive Cells in Human Colorectal Cancer.Evidence-based complementary and alternative medicine : eCAM · 2018
    Article
  7. Endoplasmic Reticulum Stress and Store-Operated Calcium Entry Contribute to Usnic Acid-Induced Toxicity in Hepatic Cells.Toxicological sciences : an official journal of the Society of Toxicology · 2015
    Article
  8. The role of autophagy in usnic acid-induced toxicity in hepatic cells.Toxicological sciences : an official journal of the Society of Toxicology · 2014
    Article
  9. Article
  10. Autophagy in drug-induced liver toxicity.Journal of food and drug analysis · 2014
    Article
  11. Article
  12. Article
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 1 country.

Bakary J SonkoDivision of Systems Biology, National Center for Toxicological Research, US FDA, Jefferson, AR 72079, USA.
Thomas C Schmitt
Lei Guo
Qiang Shi
Laszlo G Boros
Julian E A Leakey
Richard D Beger
National Center for Toxicological Research · USUniversity of California, Los Angeles · US

Funding

Intramural FDA HHS FD999999PHS HHS IAG 224-07-007 NCTR/NTP
6 · The paper itself

Abstract

The lichen metabolite usnic acid (UA) has been promoted as a dietary supplement for weight loss, although cases of hepatotoxicity have been reported. Here we evaluated UA-associated hepatotoxicity in vitro using isolated rat hepatocytes. We measured cell viability and ATP content to evaluate UA induced cytotoxicity and applied (13)C isotopomer distribution measuring techniques to gain a better understanding of glucose metabolism during cytotoxicity. The cells were exposed to 0, 1, 5 or 10 μM UA concentrations for 2, 6 or 24h. Aliquots of media were collected at the end of these time periods and the (13)C mass isotopomer distribution determined for CO(2), lactate, glucose and glutamate. The 1 μM UA exposure did not appear to cause significant change in cell viability compared to controls. However, the 5 and 10 μM UA concentrations significantly reduced cell viability as exposure time increased. Similar results were obtained for ATP depletion experiments. The 1 and 5 μM UA doses suggest increased oxidative phosphorylation. Conversely, oxidative phosphorylation and gluconeogenesis were dramatically inhibited by 10 μM UA. Augmented oxidative phosphorylation at the lower UA concentrations may be an adaptive response by the cells to compensate for diminished mitochondrial function.

Indexed as

AnimalsBenzofuransCarbonCarbon IsotopesCells, CulturedCell SurvivalDose-Response Relationship, DrugGlucoseGlutamic AcidHepatocytesLactic AcidLichensMitochondria, LiverRatsRats, Sprague-DawleyBenzofuransCarbonCarbon IsotopesGlucoseGlutamic AcidLactic Acidusnic acid

Identifiers

PMID21802472
PMCPMC5753584
OpenAlexW2056350697

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.