Sylvester C Ohadoma1 ,
Godwin C Akuodor2,
Lapah P Takem1,
Ekaette S Udoh1,
Arit Umoren1,
Ezechukwu I Nwokoma3
For correspondence:- Sylvester Ohadoma Email: chodraf@yahoo.com Tel:+234 8035081946
Received: 21 September 2024 Accepted: 14 February 2025 Published: 28 February 2025
Citation: Ohadoma SC, Akuodor GC, Takem LP, Udoh ES, Umoren A, Nwokoma EI. Inhibition and reversal of formaldehyde-induced inflammation in rats by active compounds isolated from leaf extract of Chikadoma plant (Duranta repens). Trop J Pharm Res 2025; 24(2):225-231 doi: 10.4314/tjpr.v24i2.10
© 2025 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Purpose: To investigate the anti-inflammatory activity of the leaf extracts of Duranta repens. Methods: Methanol, ethyl acetate, and hexane fractions from the methanol crude extract of Duranta repens leaves were obtained using gradient mixture elution in bioactivity-guided silica gel column chromatography. A mixture of spectrochemical, infrared (IR), nuclear magnetic resonance (NMR), and gas chromatographic/mass spectroscopic (GC/MS) investigations were used to clarify the structures of the identified active chemicals. A total of 50 Wistar rats randomized into 10 groups (n = 5) were given either 200 mg/kg of Hexane fraction (HFCP) or ethylacetate fraction (EAFCP) intraperitoneally. A subplantar injection of 0.1 mL 2.5 % formaldehyde solution was used to induce inflammation 1 h later, and this procedure was repeated on day three. After five days, the compounds were administered once daily, and then every other day for the next five days. Using a plethysmometer, the rat paw volume was measured every day following a 1 h drug delivery period. Diclofenac was used as the control. Results: Compounds isolated belong to the following groups: flavonol glycoside, stigmast steroid and triterpenehydroxyl acid. The molecules identified by their structures are ursolic acid, stigmastene 3, 6 dione, and tetrahydroxy flavone-3α-rhamnoside, respectively. In rats, the combination of these compounds showed significant (p < 0.05) biological action against formaldehyde-induced inflammation, exceeding the respective percentage inhibition of individual compounds (62.60, 82.60, and 62.60 %; p < 0.05). Conclusion: There is a significant anti-inflammatory activity of active compounds from the leaves of Chikadoma plant. The mechanism of this anti-inflammatory activity is through synergism. Clinical studies are necessary to advance the safety and toxicity profiles of these products.
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