# Bioactive Components of Parthenocissus quinquefolia with Antioxidant and Anti-Inflammatory Properties: A Systematic Review

**Authors:** Álvaro Becerra, Felipe Soto, Alejandro Vallejos, Daniela Millán, Juan José Valenzuela-Fuenzalida, Jose E. Leon-Rojas, Manuel E. Cortés

PMC · DOI: 10.3390/antiox15020169 · Antioxidants · 2026-01-27

## TL;DR

This paper reviews the antioxidant and anti-inflammatory compounds in Virginia creeper, highlighting its potential for natural therapies.

## Contribution

The study systematically characterizes the bioactive components of Parthenocissus quinquefolia with a focus on antioxidant and anti-inflammatory mechanisms.

## Key findings

- Phenolic compounds like flavonoids and stilbenes in P. quinquefolia show antioxidant activity via ROS scavenging and Nrf2/ARE activation.
- The plant's metabolites exhibit anti-inflammatory effects by downregulating NF-κB and inhibiting COX-2/iNOS expression.
- Consistent molecular responses suggest P. quinquefolia's potential for phytotherapeutic development targeting oxidative stress and inflammation.

## Abstract

Background: Parthenocissus quinquefolia (Virginia creeper), widely distributed and used in Chile, lacks a systematic characterization of its bioactive components. This study synthesizes the evidence on the phytochemical composition and biological activities of P. quinquefolia, with emphasis on metabolites involved in redox regulation and inflammation. Methods: A systematic review was conducted following PRISMA 2020 guidelines. Searches were performed across four electronic databases, including original studies reporting antioxidant and anti-inflammatory effects. Results: Of 665 records identified, 14 studies met the inclusion criteria. Phytochemical analyses revealed phenolic compounds, particularly flavonoids (e.g., catechin, epicatechin, gallocatechin, epigallocatechin, quercetin, rutin, isoquercitrin, myricetin, luteolin, naringin) and stilbenes (e.g., ε-viniferin, miyabenol C). These metabolites exhibit antioxidant activity through ROS scavenging, metal chelation, and Nrf2/ARE activation. Anti-inflammatory effects were attributed to the downregulation of NF-κB, AP-1, and MAPK signaling, inhibition of NLRP3 inflammasome activation, and suppression of COX-2/iNOS expression. Conclusions: P. quinquefolia is a rich source of phenolic metabolites with robust antioxidant and anti-inflammatory mechanisms. The consistency of molecular responses across studies highlights its potential as a promising candidate for phytotherapeutic development targeting oxidative stress and inflammatory pathways.

## Linked entities

- **Genes:** GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], are (Arylesterase) [NCBI Gene 59246804], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353], MAPK (mitogen activated kinase-like protein) [NCBI Gene 7446652], NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548], COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513], NOS2 (nitric oxide synthase 2) [NCBI Gene 4843]
- **Chemicals:** catechin (PubChem CID 1203), epicatechin (PubChem CID 1203), gallocatechin (PubChem CID 65084), epigallocatechin (PubChem CID 72277), quercetin (PubChem CID 5280343), rutin (PubChem CID 5280805), isoquercitrin (PubChem CID 5280804), myricetin (PubChem CID 5281672), luteolin (PubChem CID 5280445), naringin (PubChem CID 442428), miyabenol C (PubChem CID 46890011)
- **Species:** Parthenocissus quinquefolia (taxon 3607)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, FOSB (FosB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2354] {aka AP-1, G0S3, GOS3, GOSB}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, ISYNA1 (inositol-3-phosphate synthase 1) [NCBI Gene 51477] {aka INO1, INOS, IPS, IPS 1, IPS-1}, CAT (catalase) [NCBI Gene 847], JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, NOS3 (nitric oxide synthase 3) [NCBI Gene 4846] {aka EC-NOS, ECNOS, MYMY8, NOSIII, cNOS, eNOS}, NFKBIA (NFKB inhibitor alpha) [NCBI Gene 4792] {aka EDAID2, IKBA, MAD-3, NFKBI}
- **Diseases:** injury to (MESH:D014947), cardiovascular, metabolic and neurodegenerative diseases (MESH:D019636), -inflammatory (MESH:D007249), cancer (MESH:D009369), carcinogenesis (MESH:D063646), metabolic disease (MESH:D008659), polycystic ovary syndrome (MESH:D011085), endometrial cancer (MESH:D016889), miscarriage (MESH:D000022), gynecological disorders (MESH:D005831), infectious (MESH:D003141), tissue injury (MESH:D017695)
- **Chemicals:** epsilon-Viniferin (MESH:C091891), metal (MESH:D008670), Flavan-3-ols (MESH:C404987), flavonols (MESH:D044948), Rutin (MESH:D012431), DPPH (MESH:C004931), Stilbenes (MESH:D013267), miyabenol C (MESH:C585842), N. (MESH:D009584), Quercetin (MESH:D011794), polysaccharide (MESH:D011134), pectins (MESH:D010368), catechin (MESH:D002392), PGE2 (MESH:D015232), catechol (MESH:C034221), myricetin (MESH:C040015), kaempferol (MESH:C006552), resveratrol (MESH:D000077185), NO (MESH:D009614), branched rhamnogalacturonan I (-), naringin (MESH:C005274), parthenocissin M (MESH:C587278), isoquercitrin (MESH:C016527), callose (MESH:C048306), LPS (MESH:D008070), quercetin-3-O-alpha-L-rhamnoside (MESH:C012526), ABTS (MESH:C002502), lipid (MESH:D008055), polyphenols (MESH:D059808), ROS (MESH:D017382), glycosides (MESH:D006027), Flavonoids (MESH:D005419), epigallocatechin (MESH:C057580), luteolin (MESH:D047311), flavones (MESH:D047309)
- **Species:** Berberis microphylla (species) [taxon 186729], Aristotelia chilensis (species) [taxon 138855], Peumus boldus (species) [taxon 63812], Parthenocissus quinquefolia (Virginia creeper, species) [taxon 3607], Vitis heyneana (species) [taxon 345147], Homo sapiens (human, species) [taxon 9606], Parthenocissus tricuspidata (Boston-ivy, species) [taxon 345127], Vitis (genus) [taxon 3603]
- **Cell lines:** RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937967/full.md

## References

135 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937967/full.md

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Source: https://tomesphere.com/paper/PMC12937967