Evidence map›Paper›PMID 21871523›Full record

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

Liver toxicity and carcinogenicity in F344/N rats and B6C3F1 mice exposed to Kava Kava.

Mamta Behl, Abraham Nyska, Rajendra S Chhabra, Gregory S Travlos, Laurene M Fomby, Barney R Sparrow, Milton R Hejtmancik, Po C Chan

Open access · greenAbstract 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
6.5field-weighted citation impact, top 4% 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

6 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Journal of traditional and complementary medicine · 2022
    Article
  3. Review
  4. Hepatotoxicity Induced by "the 3Ks": Kava, Kratom and Khat.International journal of molecular sciences · 2016
    Review
  5. Article
  6. 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

8 authors at 3 institutions in 1 country.

Mamta BehlNational Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Abraham Nyska
Rajendra S Chhabra
Gregory S Travlos
Laurene M Fomby
Barney R Sparrow
Milton R Hejtmancik
Po C Chan
National Institute of Environmental Health Sciences · USBattelle · USIntegrated Laboratory Systems, Inc. · US

Funding

NTP DATABASE SUMMARIZATION AND EVALUATIONZ01ES045004 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI KISSLING, GRACE E · 1997 to 2008
$193k
Intramural NIH HHS Z01 ES045004Intramural NIH HHS Z99 ES999999NIEHS NIH HHS N01 ES065554
6 · The paper itself

Abstract

Kava Kava is an herbal supplement used as an alternative to antianxiety drugs. Although some reports suggest an association of Kava Kava with hepatotoxicity , it continues to be used in the United States due to lack of toxicity characterization. In these studies F344/N rats and B6C3F1 mice were administered Kava Kava extract orally by gavage in corn oil for two weeks, thirteen weeks or two years. Results from prechronic studies administered Kava Kava at 0.125 to 2g/kg body weight revealed dose-related increases in liver weights and incidences of hepatocellular hypertrophy. In the chronic studies, there were dose-related increases in the incidences of hepatocellular hypertrophy in rats and mice administered Kava Kava for up to 1g/kg body weight. This was accompanied by significant increases in incidences of centrilobular fatty change. There was no treatment- related increase in carcinogenic activity in the livers of male or female rats in the chronic studies. Male mice showed a significant dose-related increase in the incidence of hepatoblastomas. In female mice, there was a significant increase in the combined incidence of hepatocellular adenoma and carcinoma in the low and mid dose groups but not in the high dose group. These findings were accompanied by several nonneoplastic hepatic lesions.

Indexed as

Chemical and Drug Induced Liver InjuryAnimalsCarcinogenicity TestsDose-Response Relationship, DrugDrug Administration ScheduleFemaleKavaLiverMaleMiceMice, Inbred StrainsRatsRats, Inbred F344Sex Characteristics

Identifiers

PMID21871523
PMCPMC3190036
OpenAlexW2065844834

What OpenQuestion holds

Textmetadata
LicenceTDM
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.