Xylopic Acid Suppresses Adjuvant-induced Arthritis in Sprague Dawley Rats via Reduction in Serum Levels of IL-6 and TNF-alpha

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BACKGROUND: Xylopic acid (XA) is the principal constituent obtained from the biofractionation of the dried fruits of Xylopia aethiopica. Our initial reports have established the acute anti-inflammatory activity of this kaurene diterpene.

OBJECTIVE: Currently, we investigate the chronic anti-inflammatory activity of xylopic acid.

METHODS: The adjuvant-induced arthritis model in rats was employed in carrying out the study.

RESULTS: It was observed from the study that XA significantly (P < 0.05) suppressed the oedema associated with adjuvant arthritis while preventing associated joint deformation as identified from the radiographs. Histopathological analysis of joints of treated animals revealed signs of bone reformation and re-calcification following XA administration. From the haematological analysis, xylopic acid significantly decreased eosinophil sedimentation rate (ESR) while also decreasing white blood cells (WBC), which were increased after arthritis induction. Serum analysis showed the inhibitory effect of XA on serum expression of IL-6 and TNF-alpha in arthritic rats.

CONCLUSION: Our study demonstrates the anti-arthritic activity of orally administered XA while pointing to a possible mechanism of its anti-inflammatory action.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:21

Enthalten in:

Anti-inflammatory & anti-allergy agents in medicinal chemistry - 21(2022), 1 vom: 15., Seite 46-61

Sprache:

Englisch

Beteiligte Personen:

Osafo, Newman [VerfasserIn]
Antwi, Aaron O [VerfasserIn]
Otu-Boakye, Sarah [VerfasserIn]

Links:

Volltext

Themen:

Adjuvant-induced arthritis
Anti-Inflammatory Agents
Autoimmune disease
Diterpenes, Kaurane
Inflammation
Interleukin-6
Journal Article
Plant Extracts
Tumor Necrosis Factor-alpha
Tumour necrosis factor-alpha
Xylopic acid

Anmerkungen:

Date Completed 21.07.2022

Date Revised 22.07.2022

published: Print

Citation Status MEDLINE

doi:

10.2174/1871523021666220310094218

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM338034404