# Juniperus communis L. Needle Extract Modulates Oxidative and Inflammatory Pathways in an Experimental Model of Acute Inflammation

**Authors:** Dinu Bolunduț, Alina Elena Pârvu, Andra Diana Cecan, Anca Elena But, Florica Ranga, Marcel Pârvu, Iulia Ioana Morar, Ciprian Ovidiu Dalai

PMC · DOI: 10.3390/molecules31020247 · 2026-01-11

## TL;DR

This study shows that an extract from Juniperus communis needles has antioxidant and anti-inflammatory effects in an animal model of inflammation.

## Contribution

The study provides scientific validation for the traditional use of Juniperus communis in inflammation management through its polyphenol-rich extract.

## Key findings

- The extract showed strong antioxidant activity in multiple in vitro assays.
- In vivo administration reduced oxidative and nitrosative stress markers in rats.
- The extract suppressed inflammatory signaling by reducing NF-κB activity and cytokine levels.

## Abstract

Juniperus communis L. is a conifer widely used in traditional European medicine for the management of inflammatory disorders. However, its effects on oxidative stress and inflammation remain incompletely characterized. The present study investigated the antioxidant and anti-inflammatory potential of an ethanolic needle extract of J. communis using in vitro assays and an in vivo model of acute inflammation induced by turpentine oil in rats. Phytochemical profiling by HPLC–DAD–ESI–MS revealed a polyphenol-rich extract dominated by flavonols, flavanols, and hydroxybenzoic acids, with quercetin derivatives and taxifolin as major constituents. In vitro analyses demonstrated radical-scavenging and reducing capacities, exceeding or comparable to reference antioxidants in DPPH, hydrogen peroxide, ferric-reducing, and nitric oxide scavenging assays. In vivo, both therapeutic and prophylactic administration of the extract significantly attenuated oxidative and nitrosative stress, as evidenced by reductions in total oxidant status, oxidative stress index, malondialdehyde, advanced oxidation protein products, nitric oxide, 3-nitrotyrosine, and 8-hydroxy-2′-deoxyguanosine, alongside restoration of total antioxidant capacity and thiol levels. These effects were concentration-dependent. Concomitantly, inflammatory signaling was suppressed, with decreased NF-κB activity and reduced levels of interleukin-1β and interleukin-18. These results support the use of these extracts, whose benefits have been observed in traditional medicine, providing scientific support for the anti-inflammatory and antioxidant capacity of J. communis extract.

## Linked entities

- **Proteins:** NFKB1 (nuclear factor kappa B subunit 1), IL18 (interleukin 18)
- **Chemicals:** quercetin (PubChem CID 5280343), taxifolin (PubChem CID 471), malondialdehyde (PubChem CID 10964), nitric oxide (PubChem CID 145068), 3-nitrotyrosine (PubChem CID 65124), 8-hydroxy-2′-deoxyguanosine (PubChem CID 135406132)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** Acute (MESH:D000208), Inflammation (MESH:D007249)
- **Chemicals:** hydrogen peroxide (MESH:D006861), malondialdehyde (MESH:D008315), hydroxybenzoic acids (MESH:D062385), turpentine oil (MESH:D014425), taxifolin (MESH:C003377), DPPH (MESH:C004931), 3-nitrotyrosine (MESH:C002744), 8-hydroxy-2'-deoxyguanosine (MESH:D000080242), quercetin (MESH:D011794), flavonols (MESH:D044948), polyphenol (MESH:D059808), thiol (MESH:D013438), nitric oxide (MESH:D009569), J. communis extract (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Juniperus communis (common juniper, species) [taxon 58039]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12844129/full.md

---
Source: https://tomesphere.com/paper/PMC12844129