Evidence map›Paper›PMID 35016657›Full record

ArticleBMC complementary medicine and therapies2022

Euterpe oleracea fruit (Açai)-enriched diet suppresses the development of experimental cerebral malaria induced by Plasmodium berghei (ANKA) infection.

Karen Renata Herculano Matos Oliveira, Marjorie Lujan Marques Torres, Nayara Kauffmann, Brenda Jaqueline de Azevedo Ataíde, Nívia de Souza Franco Mendes, Larissa Medeiros Dos Anjos, Rosivaldo Dos Santos Borges, Carlomagno Pacheco Bahia, Luana Ketlen Reis Leão, Adelaide da Conceição Fonseca Passos and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. What We Know aboutNutrients · 2023
    Article
  5. Açaí (Food & nutrition research · 2022
    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

12 authors at 1 institution in 2 countries.

Karen Renata Herculano Matos OliveiraLaboratory of Experimental Neuropharmacology, Biological Science Institute, UFPa, Belém, PA, Brazil. oliveirakrm@gmail.com.
Marjorie Lujan Marques TorresLaboratory of Experimental Neuropharmacology, Biological Science Institute, UFPa, Belém, PA, Brazil.
Nayara KauffmannLaboratory of Experimental Neuropharmacology, Biological Science Institute, UFPa, Belém, PA, Brazil.
Brenda Jaqueline de Azevedo AtaídeLaboratory of Experimental Neuropharmacology, Biological Science Institute, UFPa, Belém, PA, Brazil.
Nívia de Souza Franco MendesLaboratory of Experimental Neuropharmacology, Biological Science Institute, UFPa, Belém, PA, Brazil.
Larissa Medeiros Dos AnjosLaboratory of Experimental Neuropharmacology, Biological Science Institute, UFPa, Belém, PA, Brazil.
Rosivaldo Dos Santos BorgesLaboratory of Pharmaceutical Chemistry, Health Science Institute, UFPa, Belém, PA, Brazil.
Carlomagno Pacheco BahiaLaboratory of Neuroplasticity, Health Science Institute, UFPa, Belém, PA, Brazil.
Luana Ketlen Reis LeãoLaboratory of Experimental Neuropharmacology, Biological Science Institute, UFPa, Belém, PA, Brazil.
Adelaide da Conceição Fonseca PassosLaboratory of Experimental Neuropharmacology, Biological Science Institute, UFPa, Belém, PA, Brazil.
Anderson Manoel HerculanoLaboratory of Experimental Neuropharmacology, Biological Science Institute, UFPa, Belém, PA, Brazil.
Evander de Jesus Oliveira BatistaLaboratory of Protozoology, Topical Medicine Nucleus, UFPa, Belém, PA, CEP: 66055-240, Brazil.
Center for Effective Philanthropy · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCerebral malaria is one of the most severe complications attributed to protozoal infection by Plasmodium falciparum, gaining prominence in children mortality rates in endemic areas. This condition has a complex pathogenesis associated with behavioral, cognitive and motor sequels in humans and current antimalarial therapies have shown little effect in those aspects. Natural products with antioxidant and anti-inflammatory properties have become a valuable alternative therapeutic option in the treatment of distinct conditions. In this context, this study investigated the neuroprotective effect of Euterpe oleracea (açai) enriched diet during the development of experimental cerebral malaria induced by the inoculation of Swiss albino mice with Plasmodium berghei ANKA strain.

methodsAfter Plasmodium infection, animals were maintained on a feeding with Euterpe oleracea enriched ration and parameters such as survival curve, parasitemia and body weight were routinely monitored. The present study has also evaluated the effect of açai-enriched diet on the blood-brain barrier leakage, histological alterations and neurocognitive impairments in mice developing cerebral malaria.

resultsOur results demonstrate that between 7th-19th day post infection the survival rate of the group treated with açai enriched ration was higher when compared with Plasmodium-infected mice in which 100% of mice died until the 11th days post-infection, demonstrating that açai diet has a protective effect on the survival of infected treated animals. The same was observed in the brain vascular extravasation, where Evans blue dye assays showed significantly less dye extravasation in the brains of Plasmodium-infected mice treated with açai enriched ration, demonstrating more preserved blood-brain barrier integrity. Açai-enriched diet also attenuate the histopathological alterations elicited by Plasmodium berghei infection. We also showed a decrease of the neurological impairments arising from the exposure of cerebral parenchyma in the group treated with açai diet, ameliorating motor and neuropsychiatric changes, analyzed through the SHIRPA protocol.

conclusionWith these results, we conclude that the treatment with açai enriched ration decreased the mortality of infected animals, as well as protected the blood-brain barrier and the neurocognitive deficits in Plasmodium-infected animals.

Indexed as

EuterpePhytotherapyAnimal FeedAnimalsBehavioral SymptomsBlood-Brain BarrierFemaleFruitMalaria, CerebralMaleMiceNeuroprotective AgentsPlants, MedicinalPlasmodium bergheiNeuroprotective AgentsAçai, natural productBlood-brain barrierCerebral malariaEuterpe oleraceaNeurobehavioral impairmentPlasmodium

Identifiers

PMID35016657
PMCPMC8751313
OpenAlexW4205731428

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.