Kusman Irfan Taufik, Pradini Gita Widya, Ma'ruf Ilma Fauziah, Fauziah Nisa, Berbudi Afiat, Achadiyani Achadiyani, Wiraswati Hesti Lina
Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.
Department of Biomedical Science, Faculty of Medicine, Universitas Padjadjaran, Jatinangor, 45363, Jawa Barat, Indonesia.
Infect Drug Resist. 2023 Nov 7;16:7109-7138. doi: 10.2147/IDR.S433328. eCollection 2023.
Malaria is a life-threatening disease prevalent in tropical and subtropical regions. Artemisinin combination therapy (ACT) used as an antimalarial treatment has reduced efficacy due to resistance, not only to the parasite but also to the vector. Therefore, it is important to find alternatives to overcome malaria cases through medicinal plants such as and other related plants within family.
This review summarizes the antimalarial and insecticidal activities of and other plants belonging to family.
Google Scholar, PubMed, Science Direct, and Springer link.
Online databases were used to retrieve journals using specific keywords combined with Boolean operators. The inclusion criteria were articles with experimental studies either in vivo or in vitro, in English or Indonesian, published after 1st January 2000, and full text available for inclusion in this review.
The antimalarial activity, insecticidal activity, and structure of the isolated compounds were retrieved from the selected studies.
Antimalarial in vitro study showed that the dichloromethane extract was the most widely studied with an IC50 value <10 μg/mL. Among 84 isolated active compounds, 2-hydroxymethyl-non-3-ynoic acid 2-[2,2']-bithiophenyl-5- ethyl ester, a bithienyl compound from the plant show the smallest IC50 with value 0.01 and 0.02 µg/mL in MRC-pf-2 and MRC-pf-56, respectively. In vivo studies showed that the aqueous extract of showed the best activity, with a 98.8% inhibition percentage using a 100 mg/kg dose of (NK65 Strain). (Z)- γ-Bisabolene from showed very good insecticidal activity against and with LC50 values of 2.04 μg/mL and 4.05 μg/mL.
and other plants of family are promising reservoirs of natural compounds that exert antimalarial or insecticidal activity.
疟疾是一种在热带和亚热带地区流行的危及生命的疾病。由于对寄生虫和媒介均产生了耐药性,作为抗疟治疗方法的青蒿素联合疗法(ACT)的疗效有所降低。因此,寻找通过药用植物(如[植物名称])及[植物所属科名]科内其他相关植物来克服疟疾病例的替代方法非常重要。
本综述总结了[植物名称]及[植物所属科名]科其他植物的抗疟和杀虫活性。
谷歌学术、PubMed、科学Direct和施普林格链接。
使用在线数据库通过特定关键词结合布尔运算符检索期刊。纳入标准为2000年1月1日后发表的、以英文或印尼文撰写的、具有体内或体外实验研究的文章,且全文可供纳入本综述。
从所选研究中检索抗疟活性、杀虫活性及分离化合物的结构。
体外抗疟研究表明,二氯甲烷提取物研究最为广泛,其IC50值<10μg/mL。在84种分离出的活性化合物中,来自[植物名称]植物的一种联噻吩化合物2-羟甲基-壬-3-炔酸2-[2,2']-联噻吩-5-乙酯在MRC-pf-2和MRC-pf-56中分别显示出最小的IC50值,为0.01和0.02μg/mL。体内研究表明,[植物名称]的水提取物活性最佳,使用100mg/kg剂量的[植物名称](NK65菌株)时抑制率达98.8%。来自[植物名称]的(Z)-γ-红没药烯对[蚊虫名称1]和[蚊虫名称2]显示出非常好的杀虫活性,LC50值分别为2.04μg/mL和4.05μg/mL。
[植物名称]及[植物所属科名]科的其他植物有望成为具有抗疟或杀虫活性的天然化合物的来源。