Evidence map›Paper›PMID 36635416›Full record

ArticleJournal of natural medicines2023

Ergot alkaloids in sclerotia collected in Japan: synthetic profiles and induction of apoptosis by Clavine-type compounds.

Yuji Doi, Daigo Wakana, Satoshi Kitaoka, Fumiaki Sato, Eiji Tanaka, Hisashi Takeda, Tomoo Hosoe

Abstract read
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In one paragraph

Article in Journal of natural medicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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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

7 authors at 3 institutions in 1 country.

Yuji DoiFaculty of Pharmaceutical Sciences, Hoshi University, Shinagawa, Tokyo, Japan.
Daigo WakanaFaculty of Pharmaceutical Sciences, Hoshi University, Shinagawa, Tokyo, Japan.
Satoshi KitaokaFaculty of Pharmacy and Pharmaceutical Sciences, Josai University, Sakado, Saitama, Japan.
Fumiaki SatoFaculty of Pharmaceutical Sciences, Hoshi University, Shinagawa, Tokyo, Japan.
Eiji TanakaDepartment of Environmental Science, Ishikawa Prefectural University, Nonoichi, Ishikawa, Japan.
Hisashi TakedaFaculty of Pharmaceutical Sciences, Hoshi University, Shinagawa, Tokyo, Japan.
Tomoo HosoeFaculty of Pharmaceutical Sciences, Hoshi University, Shinagawa, Tokyo, Japan. hosoe@hoshi.ac.jp.ORCID http://orcid.org/0000-0002-0877-6263
Hoshi University · JPIshikawa Prefectural University · JPJosai University · JP

Funding

Japan Society for the Promotion of Science 16K07238
6 · The paper itself

Abstract

The genus Claviceps (Clavicipitaceae) is famous for producing ergot alkaloids (EAs) in sclerotia. EAs can cause ergotism, resulting in convulsions and necrosis when ingested, making these compounds a serious concern for food safety. Agroclavine (2), a typical Clavine-type EA, is a causative agent of ergotism and is listed as a compound to be monitored by the European Food Safety Authority. Clavine-type EAs are known to cause cytotoxicity, but the mechanism has not been elucidated. We performed annexin V and PI double-staining followed by flow cytometric analysis to detect apoptosis in HepG2 and PANC-1 cells after exposure to Clavine-type EAs. Clavine-type EAs reduced cell viability and induced apoptosis in both cell lines. We then performed LC-MS analysis of EAs from 41 sclerotia samples of Claviceps collected in Japan. 24 out of 41 sclerotia extracts include peptide-type EAs (ergosine/inine: 4/4', ergotamine: 5, ergocornine/inine: 6/6', α-ergocryptine/inine: 8/8', and ergocristine/inine: 9/9') and 19 sclerotia extracts among 24 sclerotia detected peptide type EAs include Clavine-type EAs (pyroclavine: 1, agroclavine: 2, festuclavine: 3) by LC-MS. We then performed a metabolomic analysis of the EAs in the sclerotia using principal component analysis (PCA). The PCA score plots calculated for EAs suggested the existence of four groups with different EA production patterns. One of the groups was formed by the contribution of Clavine-type EAs. These results suggest that Clavine-type EAs are a family of compounds requiring attention in food safety and livestock production in Japan.

Indexed as

ClavicepsErgot AlkaloidsErgotismApoptosisHumansJapanPeptidesErgot AlkaloidsPeptidesApoptosisClavicepsErgotErgot alkaloids

Identifiers

PMID36635416
OpenAlexW4315707114

What OpenQuestion holds

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Registered trials

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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.