Chaniad Prapaporn, Techarang Tachpon, Phuwajaroanpong Arisara, Na-Ek Prasit, Viriyavejakul Parnpen, Punsawad Chuchard
Department of Medical Sciences, School of Medicine, Walailak University, Nakhon Si Thammarat 80160, Thailand.
Department of Tropical Pathology, Faculty of Tropical Medicine, Mahidol University, Bangkok 10400, Thailand.
Evid Based Complement Alternat Med. 2021 Jul 1;2021:1270902. doi: 10.1155/2021/1270902. eCollection 2021.
To investigate the antimalarial effects and toxicity of the extracts of the flowers of L. and the leaves of (L.) Gaertn. in a mouse model.
To determine the antimalarial activity of the extracts, mice were intraperitoneally injected with the ANKA strain and then administered or extract daily for 4 days. Parasitemia was observed by light microscopy. For the detection of acute toxicity, the mice received a single dose of or extract and were observed for 14 days. Biochemical parameters of liver and kidney function and the histopathology of liver and kidney tissues of the acute toxicity group were then examined.
and crude extracts at a dose of 600 mg/kg body weight significantly suppressed parasitemia in malaria-infected mice by 65.65% and 62.65%, respectively. Mice treated with 400 mg/kg and crude extracts showed 50.82% and 57.67% suppression, and mice treated with 200 mg/kg displayed 26.33% and 38.57% suppression, respectively. Additionally, no symptoms of acute toxicity were observed in the and -treated groups. Moreover, no significant alterations in the biochemical parameters of liver and kidney function and no histological changes in the liver or kidney tissues were observed.
This study revealed that both and extracts have antimalarial properties with less toxic effects. Further studies are needed to elucidate the mechanisms of the active compounds from both plants.
在小鼠模型中研究[植物名称1]花提取物和[植物名称2]叶提取物的抗疟作用及毒性。
为测定提取物的抗疟活性,给小鼠腹腔注射ANKA株,然后连续4天每日给予[提取物1]或[提取物2]提取物。通过光学显微镜观察疟原虫血症。为检测急性毒性,小鼠接受单剂量的[提取物1]或[提取物2]提取物,并观察14天。然后检查急性毒性组小鼠的肝肾功能生化参数以及肝和肾组织的组织病理学。
体重600mg/kg剂量的[提取物1]和[提取物2]粗提物分别使疟疾感染小鼠的疟原虫血症显著抑制65.65%和62.65%。用400mg/kg[提取物1]和[提取物2]粗提物处理的小鼠分别表现出50.82%和57.67%的抑制率,用200mg/kg处理的小鼠分别表现出26.33%和38.57%的抑制率。此外,在[提取物1]和[提取物2]处理组中未观察到急性毒性症状。而且,未观察到肝肾功能生化参数有显著变化,肝或肾组织也无组织学改变。
本研究表明[提取物1]和[提取物2]提取物均具有抗疟特性且毒性较小。需要进一步研究以阐明这两种植物中活性化合物的作用机制。