Evidence map›Paper›PMID 1832064›Full record

ArticleBritish journal of pharmacology1991

A novel anti-inflammatory peptide from human lipocortin 5.

M Perretti, C Becherucci, K G Mugridge, E Solito, S Silvestri, L Parente

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Article in British journal of pharmacology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

8 citing papers in PubMed, 33 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

6 authors.

M PerrettiSclavo Research Centre, Laboratory of Pharmacology, Siena, Italy.
C Becherucci
K G Mugridge
E Solito
S Silvestri
L Parente

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

1. A novel anti-inflammatory peptide (residues 204-212) of human recombinant lipocortin 5 (hrLC5) found on the high similarity region with uteroglobin is described. 2. Peptide 204-212 dose-dependently inhibited the contractions of rat isolated stomach strips elicited by porcine pancreatic phospholipase A2 (PLA2). Contractions caused by arachidonic acid (AA), prostaglandin E2 (PGE2) and 5-hydroxytryptamine were not affected. No direct enzyme inhibition was observed in a radiochemical assay. 3. PGE2 release by both human fibroblasts and rat macrophages was reduced by peptide 204-212 in a dose-dependent manner. 4. The development of carrageenin-induced oedema in rats was significantly inhibited by the local administration of peptide 204-212. 5. The pattern and potency of the biological effects of peptide 204-212 are similar to those of antiflammin 2, a lipocortin 1-derived peptide. 6. It is suggested that peptide 204-212 may represent the active site responsible for the anti-inflammatory properties of lipocortin 5.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalAmino Acid SequenceAnimalsAnnexin A5Calcium-Binding ProteinsCarrageenanDinoprostoneEdemaHumansMaleMolecular Sequence DataMuscle ContractionMuscle, SmoothPeptidesPhospholipases APhospholipases A2Annexin A5Anti-Inflammatory Agents, Non-SteroidalCalcium-Binding ProteinsCarrageenanDinoprostonePeptidesPhospholipases APhospholipases A2Pregnancy ProteinsRecombinant ProteinsUteroglobin

Identifiers

PMID1832064
PMCPMC1908345
OpenAlexW1985213145

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.