Evidence map›Paper›PMID 19807154›Full record

ArticleJournal of agricultural and food chemistry2009

Endogenous levels of Echinacea alkylamides and ketones are important contributors to the inhibition of prostaglandin E2 and nitric oxide production in cultured macrophages.

Carlie A LaLone, Ludmila Rizshsky, Kimberly D P Hammer, Lankun Wu, Avery K S Solco, Manyu Yum, Basil J Nikolau, Eve S Wurtele, Patricia A Murphy, Meehye Kim and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of agricultural and food chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
10.3field-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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Echinacea for preventing and treating the common cold.The Cochrane database of systematic reviews · 2014
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Echinacea-induced cytosolic Ca2+ elevation in HEK293.BMC complementary and alternative medicine · 2010
    Article
  9. 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

11 authors at 1 institution in 2 countries.

Carlie A LaLoneCenter for Research on Dietary Botanical Supplements at Iowa State University, Iowa State University, Ames, Iowa 50011, USA.
Ludmila Rizshsky
Kimberly D P Hammer
Lankun Wu
Avery K S Solco
Manyu Yum
Basil J Nikolau
Eve S Wurtele
Patricia A Murphy
Meehye Kim
Diane F Birt
Iowa State University · US

Funding

THE PURIFICATION,STRUCTURE DETERMINATION AND SYNTHESIS OF BIOACTIVE COMPONENTSP01ES012020 · NIEHS · IOWA STATE UNIVERSITY · PI BIRT, DIANE FEICKERT · 2002 to 2006
$6.9M
SEPARATIONS/STRUCTURE/BIOAVAILABILITY/KRAUS, GEORGEP50AT004155 · NCCIH · IOWA STATE UNIVERSITY · PI BIRT, DIANE FEICKERT · 2007 to 2010
$4.5M
NCCIH NIH HHS 9P50AT004155-06NCCIH NIH HHS P50 AT004155NIEHS NIH HHS P01 ES012020
6 · The paper itself

Abstract

Because of the popularity of Echinacea as a dietary supplement, researchers have been actively investigating which Echinacea constituent or groups of constituents are necessary for immune-modulating bioactivities. Our prior studies indicate that alkylamides may play an important role in the inhibition of prostaglandin E2 (PGE(2)) production. High-performance liquid chromatography fractionation, employed to elucidate interacting anti-inflammatory constituents from ethanol extracts of Echinacea purpurea, Echinacea angustifolia, Echinacea pallida, and Echinacea tennesseensis, identified fractions containing alkylamides and ketones as key anti-inflammatory contributors using lipopolysaccharide-induced PGE(2) production in RAW264.7 mouse macrophage cells. Nitric oxide (NO) production and parallel cytotoxicity screens were also employed to substantiate an anti-inflammatory response. E. pallida showed significant inhibition of PGE(2) with a first round fraction, containing gas chromatography-mass spectrometry (GC-MS) peaks for Bauer ketones 20, 21, 22, 23, and 24, with 23 and 24 identified as significant contributors to this PGE(2) inhibition. Chemically synthesized Bauer ketones 21 and 23 at 1 microM each significantly inhibited both PGE(2) and NO production. Three rounds of fractionation were produced from an E. angustifolia extract. GC-MS analysis identified the presence of Bauer ketone 23 in third round fraction 3D32 and Bauer alkylamide 11 making up 96% of third round fraction 3E40. Synthetic Bauer ketone 23 inhibited PGE(2) production to 83% of control, and synthetic Bauer alkylamide 11 significantly inhibited PGE(2) and NO production at the endogenous concentrations determined to be present in their respective fraction; thus, each constituent partially explained the in vitro anti-inflammatory activity of their respective fraction. From this study, two key contributors to the anti-inflammatory properties of E. angustifolia were identified as Bauer alkylamide 11 and Bauer ketone 23.

Indexed as

AmidesAnimalsAnti-Inflammatory AgentsCell LineDinoprostoneEchinaceaGas Chromatography-Mass SpectrometryKetonesMacrophagesMiceNitric OxideAmidesAnti-Inflammatory AgentsDinoprostoneKetonesNitric Oxide

Identifiers

PMID19807154
PMCPMC2777644
OpenAlexW2032990219

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.