School of Life Science, Hubei University, Wuhan 430062, PR China.
School of Life Science, Hubei University, Wuhan 430062, PR China.
Pestic Biochem Physiol. 2017 Nov;143:111-115. doi: 10.1016/j.pestbp.2017.08.016. Epub 2017 Aug 30.
In order to search new local plant molluscicides for the control of the vectors of schistosomiasis, leaves of Macleaya cordata (Willd) R. Br. were used to extract and separate alkaloid components by thinner acid method and column chromatography, and the molluscicidal effect of alkaloid components against snail Oncomelania hupensis was determined by bioassay. The results showed that 7 alkaloid components (AN1-7) were obtained after extracting and separating alkaloids from the leaves of M. cordata, where AN2 was found being the most toxic against snail O. hupensis with 48h LC and LC values of AN2 of 6.35mg/L and 121.23mg/L, respectively. Responses of some critical enzymes to AN2, including activities of Alkaline phosphatase (ALP), Alanine aminotransferase (ALT), Aspartate transaminase (AST), Malic dehydrogenase (MDH) and Succinate dehydrogenase (SDH) in both cephalopodium and liver, were also detected through experiments, which also explored esterase isozyme (EST) exposed to AN2 in liver tissue. The results showed that AN2 significantly inhibited the activities of SDH, MDH and esterase isozyme, as AN2 significantly stimulated the activities of ALP, ALT and AST to increase at a low concentration (e.g. 25mg/L), while significantly inhibited the activities of these enzymes at a high concentration (100mg/L). These results indicated that AN2 not only inhibited protein synthesis, and respiratory chain oxidative phosphorylation, but also caused hepatocellular injury and reduced the detoxification ability of liver.
为了寻找新的用于控制血吸虫病传播媒介的本地植物性杀螺剂,我们使用博落回(Macleaya cordata(Willd.)R. Br.)叶通过薄酸法和柱层析提取和分离生物碱成分,并通过生物测定法测定生物碱成分对钉螺(Oncomelania hupensis)的杀螺效果。结果表明,从博落回叶中提取和分离生物碱后得到 7 种生物碱成分(AN1-7),其中 AN2 对钉螺 O. hupensis 的毒性最大,其 48hLC 和 LC 值分别为 6.35mg/L 和 121.23mg/L。实验还检测了一些关键酶对 AN2 的反应,包括碱性磷酸酶(ALP)、丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)、苹果酸脱氢酶(MDH)和琥珀酸脱氢酶(SDH)在头足类和肝脏中的活性,还探索了暴露于 AN2 的肝脏组织中的酯酶同工酶(EST)。结果表明,AN2 显著抑制 SDH、MDH 和酯酶同工酶的活性,而在低浓度(如 25mg/L)时,AN2 显著刺激 ALP、ALT 和 AST 的活性增加,而在高浓度(100mg/L)时,显著抑制这些酶的活性。这些结果表明,AN2 不仅抑制蛋白质合成和呼吸链氧化磷酸化,还导致肝细胞损伤和降低肝脏的解毒能力。