Department of Chemistry, Federal University of Amazonas (UFAM), Manaus 69080-900, AM, Brazil.
Gonçalo Moniz Institute, Oswaldo Cruz Foundation (IGM-FIOCRUZ/BA), Salvador 40296-710, BA, Brazil.
Molecules. 2022 Sep 2;27(17):5664. doi: 10.3390/molecules27175664.
Duguetia pycnastera Sandwith (Annonaceae) is a tropical tree that can be found in the Guyanas, Bolivia, Venezuela, and Brazil. In Brazil, it is popularly known as “ata”, “envira”, “envira-preta”, and “envira-surucucu”. In the present work, we investigated the in vitro and in vivo HepG2 cell growth inhibition capacity of D. pycnastera leaf essential oil (EO). The chemical composition of the EO was determined by GC−MS and GC−FID analyses. The alamar blue assay was used to examine the in vitro cytotoxicity of EO in cancer cell lines and non-cancerous cells. In EO-treated HepG2 cells, DNA fragmentation was measured by flow cytometry. The in vivo antitumor activity of the EO was assessed in C.B-17 SCID mice xenografted with HepG2 cells treated with the EO at a dosage of 40 mg/kg. Chemical composition analysis displayed the sesquiterpenes α-gurjunene (26.83%), bicyclogermacrene (24.90%), germacrene D (15.35%), and spathulenol (12.97%) as the main EO constituents. The EO exhibited cytotoxicity, with IC50 values ranging from 3.28 to 39.39 μg/mL in the cancer cell lines SCC4 and CAL27, respectively. The cytotoxic activity of the EO in non-cancerous cells revealed IC50 values of 16.57, 21.28, and >50 μg/mL for MRC-5, PBMC, and BJ cells, respectively. An increase of the fragmented DNA content was observed in EO-treated HepG2 cells. In vivo, EO displayed tumor mass inhibition activity by 47.76%. These findings imply that D. pycnastera leaf EO may have anti-liver cancer properties.
杜古拉毒木(番荔枝科)是一种热带乔木,分布于圭亚那、玻利维亚、委内瑞拉和巴西。在巴西,它通常被称为“ata”、“envira”、“envira-preta”和“envira-surucucu”。在本研究中,我们研究了杜古拉毒木叶精油(EO)对 HepG2 细胞的体外和体内生长抑制能力。采用 GC-MS 和 GC-FID 分析确定 EO 的化学成分。通过 alamar blue 法检测 EO 在癌细胞系和非癌细胞中的体外细胞毒性。通过流式细胞术测量 EO 处理的 HepG2 细胞中的 DNA 片段化。用荷 HepG2 细胞的 C.B-17 SCID 小鼠评估 EO 的体内抗肿瘤活性,EO 以 40mg/kg 剂量处理。化学成分分析显示,倍半萜烯 α-古巴烯(26.83%)、双环金合欢烯(24.90%)、大根香叶烯 D(15.35%)和斯巴醇(12.97%)是 EO 的主要成分。EO 在癌细胞系 SCC4 和 CAL27 中表现出细胞毒性,IC50 值分别为 3.28 至 39.39μg/mL。EO 在非癌细胞中的细胞毒性活性显示,MRC-5、PBMC 和 BJ 细胞的 IC50 值分别为 16.57、21.28 和>50μg/mL。在 EO 处理的 HepG2 细胞中观察到断裂的 DNA 含量增加。在体内,EO 对肿瘤质量的抑制活性为 47.76%。这些发现表明,杜古拉毒木叶 EO 可能具有抗肝癌特性。