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去甲乌药碱:马的药理学、药代动力学及行为学效应

Hordenine: pharmacology, pharmacokinetics and behavioural effects in the horse.

作者信息

Frank M, Weckman T J, Wood T, Woods W E, Tai C L, Chang S L, Ewing A, Blake J W, Tobin T

机构信息

Kentucky Equine Drug Research Program, Graduate Center in Toxicology, University of Kentucky, Lexington 40506.

出版信息

Equine Vet J. 1990 Nov;22(6):437-41. doi: 10.1111/j.2042-3306.1990.tb04312.x.

DOI:10.1111/j.2042-3306.1990.tb04312.x
PMID:2269269
Abstract

Hordenine is an alkaloid occurring naturally in grains, sprouting barley, and certain grasses. It is occasionally found in post race urine samples, and therefore we investigated its pharmacological actions in the horse. Hordenine (2.0 mg/kg bodyweight [bwt]) was administered by rapid intravenous (iv) injection to 10 horses. Typically, dosed horses showed a flehmen response and defecated within 60 secs. All horses showed substantial respiratory distress. Respiratory rates increased about 250 per cent and heart rates were approximately double that of resting values. All animals broke out in a sweat shortly after iv injection, but basal body temperature was not affected. These effects were transient, and the animals appeared normal within 30 mins of dosing. Treated horses were tested in a variable interval responding apparatus 30 mins after dosing and no residual stimulation or depressant effects of hordenine were apparent. Animals dosed orally with 2.0 mg/kg bwt of hordenine showed no changes in heart rate, respiratory rate, basal body temperature or behaviour. After iv injection of hordenine, (2.0 mg/kg bwt) plasma reached a maximum value of about 1.0 micrograms/ml, and declined thereafter in a biexponential fashion. Kinetics of plasma concentration satisfied the concept of a two compartment open system, with an alpha-phase half-life of about 3 mins, and a beta-phase half-life of about 35 mins. Total urinary concentrations of hordenine (free and conjugated) peaked at about 400 micrograms/ml, and then declined exponentially to background levels by 24 h after dosing.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

去甲乌药碱是一种天然存在于谷物、发芽大麦和某些禾本科植物中的生物碱。它偶尔会在赛后尿液样本中被发现,因此我们研究了其在马身上的药理作用。将去甲乌药碱(2.0毫克/千克体重[bwt])通过快速静脉内(iv)注射给予10匹马。通常,给药的马匹会出现裂唇嗅反应,并在60秒内排便。所有马匹均表现出严重的呼吸窘迫。呼吸频率增加约250%,心率约为静息值的两倍。所有动物在静脉注射后不久就开始出汗,但基础体温未受影响。这些效应是短暂的,给药后30分钟内动物看起来正常。给药30分钟后,在可变间隔反应装置中对处理过的马匹进行测试,未发现去甲乌药碱有残留的兴奋或抑制作用。口服2.0毫克/千克体重去甲乌药碱的动物,其心率、呼吸频率、基础体温或行为均无变化。静脉注射去甲乌药碱(2.0毫克/千克体重)后,血浆达到约1.0微克/毫升的最大值,此后以双指数方式下降。血浆浓度动力学符合二室开放系统的概念,α相半衰期约为3分钟,β相半衰期约为35分钟。去甲乌药碱(游离和结合型)的总尿浓度在约400微克/毫升时达到峰值,给药后24小时后呈指数下降至背景水平。(摘要截断于250字)

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