Evidence map›Paper›PMID 30849505›Full record

ArticleJournal of ethnopharmacology2019

Aqueous and methanol extracts of Paullinia pinnata L. (Sapindaceae) improve inflammation, pain and histological features in CFA-induced mono-arthritis: Evidence from in vivo and in vitro studies.

Pius Pum Tseuguem, Douglas Alphonse Mouga Ngangoum, Judith Manialeu Pouadjeu, Basile Nganmegne Piégang, Zacharie Sando, Benedict James Kolber, Kevin John Tidgewell, Télesphore Benoît Nguelefack

Open access · greenAbstract read
In one paragraph

Article in Journal of ethnopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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  6. Isolation of a novel isoprenylated phenolic compound and neuroprotective evaluation ofSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Article
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  11. Review
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  13. Aqueous and Methanol Extracts ofEvidence-based complementary and alternative medicine : eCAM · 2019
    Article
  14. 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

8 authors at 3 institutions in 2 countries.

Pius Pum TseuguemLaboratory of Animal Physiology and Phytopharmacology, Faculty of Sciences, University of Dschang, P.O.Box 67, Dschang, Cameroon. Electronic address: piuspum@gmail.com.
Douglas Alphonse Mouga NgangoumLaboratory of Animal Physiology and Phytopharmacology, Faculty of Sciences, University of Dschang, P.O.Box 67, Dschang, Cameroon. Electronic address: ngangoumdouglas@yahoo.com.
Judith Manialeu PouadjeuLaboratory of Animal Physiology and Phytopharmacology, Faculty of Sciences, University of Dschang, P.O.Box 67, Dschang, Cameroon. Electronic address: judithpouadjeu@yahoo.com.
Basile Nganmegne PiégangLaboratory of Animal Physiology and Phytopharmacology, Faculty of Sciences, University of Dschang, P.O.Box 67, Dschang, Cameroon. Electronic address: basilepiegang@yahoo.fr.
Zacharie SandoFaculty of Medicine and Biomedical Sciences, University of Yaoundé I, Cameroon. Electronic address: sandozac@yahoo.fr.
Benedict James KolberDepartment of Biological Sciences, Duquesne University, 600 Forbes Avenue, Pittsburgh, PA, 15282, USA. Electronic address: kolberb@duq.edu.
Kevin John TidgewellDivision of Medicinal Chemistry, Duquesne University, 600 Forbes Avenue, Pittsburgh, PA, 15282, USA. Electronic address: tidgewellk@duq.edu.
Télesphore Benoît NguelefackLaboratory of Animal Physiology and Phytopharmacology, Faculty of Sciences, University of Dschang, P.O.Box 67, Dschang, Cameroon. Electronic address: nguelefack@yahoo.fr.
Université de Dschang · CMDuquesne University · USUniversité de Yaoundé I · CM

Funding

Impact of Amygdala Lateralization on Processing and Modulation of Bladder PainR01DK115478 · NIDDK · UNIVERSITY OF TEXAS DALLAS · PI BENEDICT J KOLBER · 2018 to 2026
$4.3M
Cyanobacterial Natural Products to Treat Comorbid Pain and DepressionR15AT008060 · NCCIH · DUQUESNE UNIVERSITY · PI KOLBER, BENEDICT J, TIDGEWELL, KEVIN JOSEPH · 2014 to 2019
$905k
NCCIH NIH HHS R15 AT008060NIDDK NIH HHS R01 DK115478NIMH NIH HHS HHSN271200800025C
6 · The paper itself

Abstract

ethnopharmacological relevancePaullinia pinnata L. (Sapindaceae) is an African woody vine, traditionally used for the treatment of itch and pain-related conditions such as rheumatoid arthritis.

aimThis work evaluates, in vitro and in vivo, the anti-inflammatory and analgesic effects of aqueous (AEPP) and methanol (MEPP) extracts from Paullinia pinnata leaves.

methodsAEPP and MEPP (100, 200 and 300 mg/kg/day) were administered orally in monoarthritic rats induced by a unilateral injection of 50 μl of Complete Freund's Adjuvant (CFA) in the ankle joint. During the 14 days of treatment, pain and inflammation were evaluated alternatively in both ankle and paw of the CFA-injected leg. Malondialdehyde (MDA) and glutathione (GSH) levels were assessed in serum and spinal cord. Histology of soft tissue of the ankle was also analyzed. For in vitro studies, AEPP and MEPP (10, 30 and 100 μg/ml) were evaluated against nitric oxide (NO) production by macrophages that were either non-stimulated or stimulated with LPS, 8-Br-AMPc and the mixture of both substances after 8 h exposure. These extracts were also evaluated on TNF-α and IL-1β production in cells stimulated with LPS for 8 h. Finally, the ability of the extracts to bind to neuroactive receptors was evaluated in vitro using competitive binding assays with >45 molecular targets.

resultsAEPP and MEPP significantly reduced by 20-98% (p < 0.001) the inflammation and pain sensation in both the ankle and paw. AEPP significantly increased glutathione levels (p < 0.05) in serum. Both extracts reduced MDA production in serum and spinal cord (p < 0.001), and significantly improved tissue reorganization in treated arthritic rats. P. pinnata extracts did not affect NO production in non-stimulated macrophages but significantly reduced it by 47-88% in stimulated macrophages. AEPP and MEPP also significantly inhibited TNF-α (35-68%) and IL-1β (31-36%) production in LPS stimulated macrophages. No cytotoxic effect of plant extracts was observed. MEPP showed concentration-dependent affinity for Sigma 2 receptors with an IC

conclusionThese results demonstrate the analgesic and anti-inflammatory effects of P. pinnata extracts on monoarthritis and further support its traditional use for pain and inflammation. These activities are at least partly due to the ability of these extracts to inhibit the production of NO, TNF-α, IL-1β and to likely modulate Sigma 2 receptors.

Indexed as

AnalgesicsAnimalsAnkle JointAnti-Inflammatory AgentsArthralgiaArthritis, ExperimentalArthritis, RheumatoidDrug Evaluation, PreclinicalFemaleFreund's AdjuvantHumansMaleMedicine, African TraditionalMethanolNitric OxidePaulliniaAnalgesicsAnti-Inflammatory AgentsFreund's AdjuvantMethanolNitric OxidePlant ExtractsWaterAnalgesicAnti-inflammatoryCytokinesPaullinia pinnataRheumatoid arthritisSigma 2 receptor

Identifiers

PMID30849505
PMCPMC6484438
OpenAlexW2921622474

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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.