Evidence mapPaperPMID 41956231Full record

ArticleJournal of ethnopharmacology2026

Modulation of TNF-α, IL-1β and myeloperoxidase contributes to the anti-inflammatory and analgesic effects of Paullinia pinnata Linn (Sapindaceae) extracts in complete Freund's adjuvant-induced mono-arthritis in rats.

Pius Pum Tseuguem, Christian Fofie Kuete, Sahar Mofidi Tabatabaei, Anny Treat, Benedict James Kolber, Kevin Joseph Tidgewell, Télesphore Benoît Nguelefack

Abstract read
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Article in Journal of ethnopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Pius Pum TseuguemResearch Unit of Animal Physiology and Phytopharmacology, Faculty of Sciences, University of Dschang, P.O. Box 67, Dschang, Cameroon; Laboratory of Applied Chemistry and Bioscience (LACB), Department of Chemistry and Biology, Faculty of Sciences, University of Bertoua, P.O. Box 416, Bertoua, Cameroon. Electronic address: piuspum@gmail.com.
Christian Fofie KueteDepartment of Neuroscience and Center for Advanced Pain Studies, The University of Texas at Dallas, 800 W. Campbell Road, Richardson, TX, 75080, USA. Electronic address: christian.kuetefofie@utdallas.edu.
Sahar Mofidi TabatabaeiDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY 40536, USA. Electronic address: sahar.mofidi@uky.edu.
Anny TreatDepartment of Neuroscience and Center for Advanced Pain Studies, The University of Texas at Dallas, 800 W. Campbell Road, Richardson, TX, 75080, USA. Electronic address: annytreat@gmail.com.
Benedict James KolberDepartment of Neuroscience and Center for Advanced Pain Studies, The University of Texas at Dallas, 800 W. Campbell Road, Richardson, TX, 75080, USA. Electronic address: benedict.kolber@utdallas.edu.
Kevin Joseph TidgewellDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY 40536, USA. Electronic address: kevin.tidgewell@uky.edu.
Télesphore Benoît NguelefackResearch Unit of Animal Physiology and Phytopharmacology, Faculty of Sciences, University of Dschang, P.O. Box 67, Dschang, Cameroon. Electronic address: nguelefack@yahoo.fr.

Funding

NCCIH NIH HHS R21 AT013164
6 · The paper itself

Abstract

ethnopharmacological relevancePaullinia pinnata Linn (Sapindaceae) is used in Cameroonian ethnomedicine for the treatment of arthritis. Its leafy aqueous (AEPP) and methanol (MEPP) extracts have shown potent preventive effects in mono-arthritis but their curative effects and their mechanism of action remain unknown.

aimThis work evaluates the effects of AEPP and MEPP on Complete Freund's Adjuvant (CFA)-induced septic mono-arthritis (SM-A) and their mechanism of action. MATERIALS AND

methodsSM-A was induced by intra-ankle injection of CFA (50 μl) in both male and female rats. On day 8 after, rats were administered orally with AEPP and MEPP (100 and 200 mg/kg/day) for 14 days. Methotrexate (250 μg/kg/day) was used as reference drug. Hyperalgesia and inflammation were monitored after a single (acute) or during the 14 days repeated (chronic) treatment. Thereafter, plasma samples were collected for TNF-α and IL-1β assays, and the synovial liquid of the injected ankle for myeloperoxidase (MPO) quantification. The in vitro analgesic potential of MEPP was evaluated on human induced pluripotent stem cell (hiPSC)-derived sensory neurons using a MEA system or via calcium imaging in mouse dorsal root ganglion neurons (DRGs), while its cytotoxicity was assayed in HEK-293 cells. The phytochemical investigations of MEPP were performed using high resolution MS/MS molecular networking.

resultsBoth single and repeated administration of AEPP or MEPP significantly reduced hyperalgesia (p < 0.001) and oedema induced by CFA, with up to 97.8% inhibition of pain and complete resorption of inflammation. AEPP and MEPP at the dose of 100 mg/kg/day, significantly (p < 0.01) inhibited plasma TNF-α by 51.5% while all the doses significantly (p < 0.001) reduced IL-1β by up to 88% and MPO by 90%. MEPP did not induce any detectable cytotoxicity in HEK-293 cells, significantly reduced neuronal firing (p < 0.05 to p < 0.0001) in hiPSC neurons, but the intracellular calcium concentration in mouse DRGs actually increased with higher doses of MEPP extract application. LC-MS/MS analysis identified 8 known compounds from the MEPP.

conclusionThese results show that P. pinnata's leaves possess restorative effects against CFA-induced SM-A. The inhibition of TNF-α, IL-1β and the reduction of inflammatory cells infiltration may contribute to these activities, together with the inhibition of cell firing. It remains unclear why MEPP increases calcium influx in mouse DRGs while reducing firing in human cells and reducing indices of pain in rats.

Indexed as

AnalgesicsAnti-Inflammatory AgentsArthritis, ExperimentalPlant ExtractsSapindaceaeAnimalsFemaleFreund's AdjuvantHEK293 CellsHumansHyperalgesiaInterleukin-1betaMalePeroxidaseRatsRats, WistarAnalgesicsAnti-Inflammatory AgentsFreund's AdjuvantInterleukin-1betaPeroxidasePlant ExtractsTumor Necrosis Factor-alphaAnti-arthritisCalcium imagingDRGhiPSCLC-MS/MSPaullinia pinnata

Identifiers

PMID41956231
PMCPMC13334538

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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 Socratic graph.