Evidence map›Paper›PMID 17171556›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2007

Vatairea macrocarpa (Leguminosae) lectin activates cultured macrophages to release chemotactic mediators.

Nylane M N Alencar, Ana M S Assreuy, Alexandre Havt, Raquel G Benevides, Tales R de Moura, Romoaldo B de Sousa, Ronaldo A Ribeiro, Fernando Q Cunha, Benildo S Cavada

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Article in Naunyn-Schmiedeberg's archives of pharmacology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

  1. Lectin fromACS omega · 2025
    Article
  2. Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  3. Article
  4. A novel N-acetyl-glucosamine lectin of Lonchocarpus araripensis attenuates acute cellular inflammation in mice.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2016
    Article
  5. Correlation between proinflammatory role of a lectin from Typhonium giganteum Engl. and macrophage.International journal of clinical and experimental pathology · 2015
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

9 authors at 3 institutions in 1 country.

Nylane M N AlencarDepartamento de Fisiologia e Farmacologia, Universidade Federal do Ceará, Campus do Porangabuçu, Rua Coronel Nunes de Melo 1127, Fortaleza, Ceará, Brazil.
Ana M S Assreuy
Alexandre Havt
Raquel G Benevides
Tales R de Moura
Romoaldo B de Sousa
Ronaldo A Ribeiro
Fernando Q Cunha
Benildo S Cavada
Universidade Federal do Ceará · BRUniversidade de Ribeirão Preto · BRUniversidade Estadual do Ceará · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The lectin from the legume Vatairea macrocarpa is a galactose/N-acetylgalactosamine binding protein that induced cellular inflammatory response mediated by resident cells. This study investigated which inflammatory mediators would be released from lectin-activated cells. The intraperitoneal injection in rats of the supernatant from cultured macrophages, but not from mast cells, stimulated with lectin induced a time- and dose-dependent release of a neutrophil chemotactic factor, termed MNCF-VML. Pharmacological modulation with dexamethasone inhibited both the lectin-induced chemotactic activity in vivo and also the lectin-induced release of MNCF-VML into the supernatant of cultured macrophages. Cyclooxygenase and lipoxygenase metabolites are apparently not involved in the action of this factor or its release, since indomethacin or MK886 were unable to affect the lectin response. The molecular weight of MNCF-VML was found to be greater than 5 kDa, which led to the investigation of which cytokine(s) could be involved by the following approaches: (a) treatment of animals with antiserum to tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-1, or IL-8 before intraperitoneal injection of lectin and (b) addition of antiserum to TNF-alpha, IL-1, or IL-8 to the supernatant of lectin-stimulated macrophages before intraperitoneal administration. Antiserum to TNF-alpha, but not IL-1 nor IL-8, inhibited the neutrophil migration induced either by lectin or MNCF-VML. Our data suggest that neutrophil migration induced by V. macrocarpa lectin occurs via the release of cytokines such as TNF-alpha by macrophages. Thus, this lectin may represent an important tool to better understand pathological situations where an excess of leukocytes at inflammatory sites causes tissue injury.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalCells, CulturedChemotactic FactorsChemotaxis, LeukocyteChlorobenzenesDexamethasoneDose-Response Relationship, DrugFabaceaeFemaleIndolesIndomethacinInjections, IntraperitonealInterleukin-8Lipoxygenase InhibitorsMacrophagesAnti-Inflammatory Agents, Non-SteroidalChemotactic FactorsChlorobenzenesDexamethasoneIndolesIndomethacinInterleukin-8Lipoxygenase InhibitorsMK-886Plant LectinsTumor Necrosis Factor-alpha

Identifiers

PMID17171556
OpenAlexW2008907271

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.