Evidence map›Paper›PMID 42199596›Full record

ArticleCureus2026

Eucalyptol Ameliorates Neuroendocrine Stress-Aggravated Rheumatoid Arthritis Through Anti-inflammatory, Antioxidant, and Chondroprotective Mechanisms Associated with NF-κB and MAPK Signaling Pathways.

Lavkush Tiwari, Nitu Nigam, Urmila Dhakad, Suyog Sindhu, Puneet Kumar, Ch V Rao, Shubha Shukla, Suresh Babu

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lavkush TiwariCentre for Advanced Research, King George's Medical University, Lucknow, IND.
Nitu NigamCentre for Advanced Research, King George's Medical University, Lucknow, IND.
Urmila DhakadDepartment of Rheumatology, King George's Medical University, Lucknow, IND.
Suyog SindhuDepartment of Pharmacology, King George's Medical University, Lucknow, IND.
Puneet KumarDepartment of Rheumatology, King George's Medical University, Lucknow, IND.
Ch V RaoPharmacology Division, CSIR-National Botanical Research Institute, Lucknow, IND.
Shubha ShuklaDivision of Neuroscience, CSIR-Central Drug Research Institute (CDRI), Lucknow, IND.
Suresh BabuDepartment of Pathology, King George's Medical University, Lucknow, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA) is a lingering autoimmune disorder typified by synovial inflammation, oxidative imbalance, and advanced articular damage. Psychological and physical stress are known to exacerbate disease progression by enhancing inflammatory signaling and disrupting redox homeostasis. Although methotrexate remains a first-line therapy, its long-term use is accompanied by adverse effects, necessitating safer adjunctive strategies. Eucalyptol (1,8-cineole), a naturally occurring monoterpene, has demonstrated anti-inflammatory and antioxidant potential; however, its role in stress-aggravated RA remains inadequately explored.

objectiveTo evaluate the protective effects of eucalyptol in restraint stress-augmented Complete Freund's Adjuvant (CFA)-induced arthritis and to investigate its underlying mechanisms, both as monotherapy and in combination with methotrexate. METHODOLOGY: Experimental arthritis was induced in Wistar rats using CFA, followed by chronic restraint stress for 28 days. Animals were treated with eucalyptol (50, 100, or 200 mg/kg), methotrexate (1 mg/kg), or their combination. Disease progression was assessed using clinical scoring, functional parameters, biochemical assays, cytokine profiling, nuclear factor-kappa B (NF-κB) and mitogen-activated protein kinase (MAPK) pathway analysis, gene expression studies, and histopathological evaluation.

resultsRestraint stress significantly aggravated arthritic severity, resulting in increased oxidative and nitrosative stress, elevated pro-inflammatory cytokines, activation of NF-κB/MAPK signaling, and enhanced joint damage. Eucalyptol treatment produced significant dose-dependent improvements across these parameters. Notably, it reduced tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) levels while restoring antioxidant defenses. Combination therapy demonstrated the most pronounced therapeutic effect, with near normalization of multiple disease indicators.

conclusionsEucalyptol attenuates stress-exacerbated RA through integrated anti-inflammatory and antioxidant mechanisms. Its enhanced efficacy in combination with methotrexate highlights its potential as a complementary therapeutic strategy in RA management. Serum NF-κB and MAPK levels were used as surrogate markers of pathway involvement.

Indexed as

autoimmune synovitisneuroendocrine stress responsenf-kb signaling pathwayrestraint stress: rheumatoid arthritis

Identifiers

PMID42199596
PMCPMC13200764

What OpenQuestion 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 OpenQuestion graph.