Green Benedict T, Welch Kevin D, Gardner Dale R, Stegelmeier Bryan L, Pfister James A, Cook Daniel, Panter Kip E
Poisonous Plant Research Laboratory, Agricultural Research Service, USDA, Logan, UT 84321, USA.
Am J Vet Res. 2012 Aug;73(8):1318-24. doi: 10.2460/ajvr.73.8.1318.
To determine the toxicokinetics of N-(methylsuccinimido)anthranoyllycoctonine-type low larkspur alkaloids in beef cattle.
5 Black Angus steers and 35 Swiss Webster mice.
-Low larkspur (Delphinium andersonii) was collected, dried, ground, and administered to 5 steers via oral gavage to provide a dose of 12 mg of N-(methylsuccinimido)-anthranoyllycoctonine alkaloids/kg. Steers were housed in metabolism crates for 96 hours following larkspur administration; heart rate was monitored continuously, and blood samples were collected periodically for analysis of serum concentrations of 16-deacetylgeyerline, methyllycaconitine, geyerline, and nudicauline and assessment of kinetic parameters. The LD(50) of a total alkaloid extract from D andersonii was determined in Swiss Webster mice.
-The alkaloids were quickly absorbed, with a maximum serum concentration achieved within 18 hours after administration. Geyerline and nudicauline coeluted as 1 peak and were considered together for toxicokinetic analysis. Mean ± SD elimination half-life was 18.4 ± 4.4 hours, 15.6 ± 1.5 hours, and 16.5 ± 5.1 hours for 16-deacetylgeyerline, methyllycaconitine, and geyerline and nudicauline, respectively. There were significant differences in maximum serum concentration, amount absorbed, and distribution half-life among the 4 alkaloids. The mouse LD(50) was 9.8 mg/kg.
-Results suggested that clinical poisoning was likely to be most severe approximately 18 hours after exposure. Cattle should be closely monitored for at least 36 hours after initial exposure. Additionally, a withdrawal time of approximately 7 days would be required to clear > 99% of the toxic alkaloids from the serum of cattle that have ingested low larkspur.
测定N -(甲基琥珀酰亚胺基)邻氨基苯甲酰基牛扁碱型低飞燕草生物碱在肉牛体内的毒代动力学。
5头黑安格斯公牛和35只瑞士韦伯斯特小鼠。
采集、干燥、研磨低飞燕草(安德森氏翠雀花),通过口服灌胃给予5头公牛,剂量为12毫克N -(甲基琥珀酰亚胺基)-邻氨基苯甲酰基牛扁碱生物碱/千克。给予飞燕草后,将公牛置于代谢笼中96小时;持续监测心率,并定期采集血样,分析血清中16 -去乙酰基杰尔林、甲基牛扁碱、杰尔林和裸茎翠雀碱的浓度,并评估动力学参数。测定安德森氏翠雀花总生物碱提取物在瑞士韦伯斯特小鼠中的半数致死量(LD50)。
生物碱吸收迅速,给药后18小时内达到血清最大浓度。杰尔林和裸茎翠雀碱共洗脱为1个峰,在毒代动力学分析中一起考虑。16 -去乙酰基杰尔林、甲基牛扁碱、杰尔林和裸茎翠雀碱的平均消除半衰期分别为18.4±4.4小时、15.6±1.5小时和16.5±5.1小时。4种生物碱在最大血清浓度、吸收量和分布半衰期方面存在显著差异。小鼠的LD50为9.8毫克/千克。
结果表明,接触后约18小时临床中毒可能最为严重。初次接触后,应至少密切监测牛36小时。此外,摄入低飞燕草的牛血清中清除>99%的有毒生物碱大约需要7天的休药期。