Chemical Profiling and Assessment of Analgesic and Anti-Inflammatory Activity of Ammoides verticillata Essential Oil: In Vitro, In Vivo, and In Silico Studies

<b>Background/Objectives</b>: Essential oils are increasingly recognized for their therapeutic potential, yet <i>Ammoides verticillata</i> essential oil (AVEO) remains relatively unexplored, particularly for its anti-inflammatory and analgesic properties. This study aimed to profile AVEO's chemical composition and evaluate its antioxidant, anti-inflammatory, and analgesic effects, with a focus on its novel pharmacological actions. <b>Methods</b>: The chemical composition of AVEO was determined using GC-MS analysis, and antioxidant capacity was assessed through in vitro assays. Furthermore, the anti-inflammatory potential was investigated using a carrageenan-induced paw edema model in rats, complemented by the inhibition assays of cyclooxygenase (COX) enzymes. The analgesic effects were evaluated through acetic acid-induced writhing and tail immersion tests. Additionally, a computational study was performed to explore the binding affinity of AVEO's major constituents to COX-2. <b>Results</b>: GC-MS analysis revealed a rich monoterpene profile dominated by carvacrol (32.51%). It was found that AVEO exhibited significant antioxidant activity. Similarly, in vivo, AVEO showed significant anti-inflammatory effects, achieving a percentage inhibition of 52.23% at 200 mg/kg, comparable to diclofenac, along with potent COX-2 inhibition observed (IC<sub>50</sub> = 1.51 ± 0.20, SI = 5.56). Moreover, analgesic tests demonstrated dose-dependent pain relief, in which the dose of 200 mg/kg significantly prolonged tail latency to 14.00 ± 1.45 s and markedly reduced abdominal constriction to 21.17 ± 1.62. Computational analysis further corroborated the high binding affinity of carvacrol and thymol with COX-2 (-7.381 and -6.939 Kcal/mol, respectively). <b>Conclusions</b>: These findings underscore AVEO's potential as a promising therapeutic agent for managing inflammation and pain.

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Journal
Pharmaceuticals
Published
2025-04-27
DOI
https://doi.org/10.3390/ph18050635
Primary Topic
Essential Oils and Antimicrobial Activity
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article
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article

Chemical Profiling and Assessment of Analgesic and Anti-Inflammatory Activity of Ammoides verticillata Essential Oil: In Vitro, In Vivo, and In Silico Studies

Alain Muselli, Mohammed Esseddik Toumi, Fethi Benbelaïd, Abdennacer Boudah et al.
Pharmaceuticals
Essential Oils and Antimicrobial Activity
article

Chemical Profiling and Assessment of Analgesic and Anti-Inflammatory Activity of Ammoides verticillata Essential Oil: In Vitro, In Vivo, and In Silico Studies

Alain Muselli, Mohammed Esseddik Toumi, Fethi Benbelaïd, Abdennacer Boudah, Luc Jasmin, Kebaili Fethi Farouk, Leila Bellebcir, Redouane Rebai, Salsabil Mebarki, Imene Derardja
article en

Abstract

<b>Background/Objectives</b>: Essential oils are increasingly recognized for their therapeutic potential, yet <i>Ammoides verticillata</i> essential oil (AVEO) remains relatively unexplored, particularly for its anti-inflammatory and analgesic properties. This study aimed to profile AVEO's chemical composition and evaluate its antioxidant, anti-inflammatory, and analgesic effects, with a focus on its novel pharmacological actions. <b>Methods</b>: The chemical composition of AVEO was determined using GC-MS analysis, and antioxidant capacity was assessed through in vitro assays. Furthermore, the anti-inflammatory potential was investigated using a carrageenan-induced paw edema model in rats, complemented by the inhibition assays of cyclooxygenase (COX) enzymes. The analgesic effects were evaluated through acetic acid-induced writhing and tail immersion tests. Additionally, a computational study was performed to explore the binding affinity of AVEO's major constituents to COX-2. <b>Results</b>: GC-MS analysis revealed a rich monoterpene profile dominated by carvacrol (32.51%). It was found that AVEO exhibited significant antioxidant activity. Similarly, in vivo, AVEO showed significant anti-inflammatory effects, achieving a percentage inhibition of 52.23% at 200 mg/kg, comparable to diclofenac, along with potent COX-2 inhibition observed (IC<sub>50</sub> = 1.51 ± 0.20, SI = 5.56). Moreover, analgesic tests demonstrated dose-dependent pain relief, in which the dose of 200 mg/kg significantly prolonged tail latency to 14.00 ± 1.45 s and markedly reduced abdominal constriction to 21.17 ± 1.62. Computational analysis further corroborated the high binding affinity of carvacrol and thymol with COX-2 (-7.381 and -6.939 Kcal/mol, respectively). <b>Conclusions</b>: These findings underscore AVEO's potential as a promising therapeutic agent for managing inflammation and pain.

PharmaceuticalsVol. 18(5)
University Frères Mentouri Constantine 1 (DZ), Centre National de la Recherche Scientifique (FR), Université de Corse Pascal Paoli (FR), University of California, San Francisco (US), University of Biskra (DZ), University of Abou Bekr Belkaïd (DZ), Higher National Veterinary School (DZ), Université de ain Témouchent (DZ)
Openalex Percentile: Top 89%
Essential Oils and Antimicrobial Activity
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