UPR de Chimie Organique, Département de Mathématiques, Physique et Chimie, UFR des Sciences Biologiques, Université Péléforo Gon Coulibaly, Korhogo BP 1328, Côte d'Ivoire.
Laboratoire de Constitution et Réaction de la Matière, UFR-SSMT, Université Félix Houphouët-Boigny, Abidjan BP 1328, Côte d'Ivoire.
Molecules. 2021 Oct 15;26(20):6228. doi: 10.3390/molecules26206228.
The chemical variability and the in vitro anti-inflammatory activity of the leaf essential oil from Ivorian were investigated for the first time. Forty-seven oil samples were analyzed using a combination of CC, GC(RI), GC-MS and C-NMR, thus leading to the identification of 113 constituents (90.8-98.9%). As the main components varied drastically from sample to sample, the 47 oil compositions were submitted to hierarchical cluster and principal components analyses. Three distinct groups, each divided into two subgroups, were evidenced. Subgroup I-A was dominated by ()-β-ocimene, β-eudesmol, germacrene D and ()-β-ocimene, while (10βH)-1β,8β-oxido-cadina-4-ene, santalenone, -α-bergamotene and -β-bergamotene were the main compounds of Subgroup I-B. The prevalent constituents of Subgroup II-A were germacrene B, ()-β-caryophyllene, (5αH,10βMe)-6,12-oxido-elema-1,3,6,11(12)-tetraene and γ-elemene. Subgroup II-B displayed germacrene B, germacrene D and ()-β-ocimene as the majority compounds. Germacrene D was the most abundant constituent of Group III, followed in Subgroup III-A by ()-β-caryophyllene, (10βH)-1β,8β-oxido-cadina-4-ene, germacrene D-8-one, and then in Subgroup III-B by ()-β-ocimene and ()-β-ocimene. The observed qualitative and quantitative chemical variability was probably due to combined factors, mostly phenology and season, then harvest site to a lesser extent. The lipoxygenase inhibition by a leaf oil sample was also evaluated. The oil IC (0.020 ± 0.005 mg/mL) was slightly higher than the non-competitive lipoxygenase inhibitor NDGA IC (0.013 ± 0.003 mg/mL), suggesting a significant in vitro anti-inflammatory potential.
首次对来自科特迪瓦的叶片精油的化学变异性和体外抗炎活性进行了研究。使用 CC、GC(RI)、GC-MS 和 C-NMR 的组合分析了 47 个油样,从而鉴定出 113 种成分(90.8-98.9%)。由于各样本中的主要成分差异很大,因此将 47 种油的组成进行了层次聚类和主成分分析。结果表明,有三个明显的组,每个组又分为两个亚组。亚组 I-A 以 ()-β-罗勒烯、β-桉叶醇、大根香叶烯 D 和 ()-β-罗勒烯为主,而 (10βH)-1β,8β-氧化-卡达烯-4-烯、檀香酮、-α-佛手柑烯和 -β-佛手柑烯则是亚组 I-B 的主要成分。亚组 II-A 的主要成分是大根香叶烯 B、()-β-丁香烯、(5αH,10βMe)-6,12-氧化-elema-1,3,6,11(12)-四烯和 γ-榄烯。亚组 II-B 表现出大根香叶烯 B、大根香叶烯 D 和 ()-β-罗勒烯为主要成分。大根香叶烯 D 是第 III 组中最丰富的成分,紧随其后的是亚组 III-A 中的 ()-β-丁香烯、(10βH)-1β,8β-氧化-卡达烯-4-烯、大根香叶烯 D-8-酮,然后是亚组 III-B 中的 ()-β-罗勒烯和 ()-β-罗勒烯。观察到的定性和定量化学变异性可能是由于多种因素造成的,主要是物候和季节,其次是收获地点。还评估了叶片油样对脂氧合酶的抑制作用。该油的 IC(0.020 ± 0.005 mg/mL)略高于非竞争性脂氧合酶抑制剂 NDGA 的 IC(0.013 ± 0.003 mg/mL),表明其具有显著的体外抗炎潜力。