Hassiba Metrouh-Amir1 
,
Nadir Amir2,3
For correspondence:- Hassiba Metrouh-Amir Email: hassiba.metrouh@univ-bejaia.dz
Accepted: 2 August 2024 Published: 31 August 2024
Citation: Metrouh-Amir H, Amir N. In vivo acute toxicity, analgesic and anti-inflammatory activities of phenolic extract of Matricaria pubescens. Trop J Pharm Res 2024; 23(8):1283-1290 doi: 10.4314/tjpr.v23i8.7
© 2024 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 evaluate the in vivo acute toxicity, analgesic and anti-inflammatory proprieties of the phenolic extract of Matricaria pubescens (Desf.) Schultz (Asteraceae).
Methods: Acute toxicity assessment was carried out on 18 mice that were divided equally into three groups and treated orally with saline, 2500 and 5000 mg/kg of M. pubescens extract, respectively. The evaluation of peripheral analgesic activity was done by applying acetic acid-induced contortion test on 40 mice. The mice were divided into 5 equal groups of 8 mice each. Negative and positive control groups were treated orally with saline (1 %) and acetylsalicylic acid (200 mg/kg), respectively. Other groups were treated with 50, 100 and 200 mg/kg of M. pubescens extract. Study groups were administered saline, diclofenac potassium (10 mg/kg) and M. pubescens extract orally at 50, 100, and 200 mg/kg. Central analgesic activity was carried out using the tail immersion test. The distribution and treatment of the mice was similar to the analgesic model. Anti-inflammatory effect was evaluated by carrageenan-induced mice paw edema.
Results: Acute toxicity results showed that the LD50 of M. pubescens phenolic extract is above 5000 mg/kg, which means that this extract is safe. Peripheral and central analgesic data revealed that different doses of extract significantly inhibited abdominal contractions and reduced pain caused by heat compared to control (p ? 0.05). Anti-inflammatory activity data indicate significant inhibition of inflammatory edema at various doses compared to diclofenac potassium (p ? 0.05).
Conclusion: The phenolic extract of M. pubescens exerts significant peripheral, central analgesic and anti-inflammatory activities in mice. However, further investigations are required to ascertain the potentials of the extract for its clinical development.
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