Harkins J Daniel, Dirikolu Levent, Lehner Andreas F, Hughes Charlie, Schroedter Dwight, Mayer Brent, Bratton Calvert, Fisher Mitzi V, Tobin Thomas
Maxwell H. Gluck Equine Research Center and the Department of Veterinary Science, University of Kentucky, Lexington, KY 40546, USA.
Vet Ther. 2003 Summer;4(2):197-209.
Guanabenz (2,6-dichlorobenzylidene-amino-guanidine) is a centrally acting antihypertensive drug whose mechanism of action is via alpha2 adrenoceptors or, more likely, imidazoline receptors. Guanabenz is marketed as an antihypertensive agent in human medicine (Wytensin tablets, Wyeth Pharmaceuticals). Guanabenz has reportedly been administered to racing horses and is classified by the Association of Racing Commissioners International as a class 3 foreign substance. As such, its identification in a postrace sample may result in significant sanctions against the trainer of the horse. The present study examined liquid chromatographic/tandem quadrupole mass spectrometric (LC-MS/MS) detection of guanabenz in serum samples from horses treated with guanabenz by rapid i.v. injection at 0.04 and 0.2 mg/kg. Using a method adapted from previous work with clenbuterol, the parent compound was detected in serum with an apparent limit of detection of approximately 0.03 ng/ml and the limit of quantitation was 0.2 ng/ml. Serum concentrations of guanabenz peaked at approximately 100 ng/ml after the 0.2 mg/kg dose, and the parent compound was detected for up to 8 hours after the 0.04 mg/kg dose. Urine samples tested after administration of guanabenz at these dosages yielded evidence of at least one glucuronide metabolite, with the glucuronide ring apparently linked to a ring hydroxyl group or a guanidinium hydroxylamine. The LC-MS/MS results presented here form the basis of a confirmatory test for guanabenz in racing horses.
胍那苄(2,6 - 二氯亚苄基氨基胍)是一种作用于中枢的抗高血压药物,其作用机制是通过α2肾上腺素能受体,或者更有可能是通过咪唑啉受体。胍那苄作为一种抗高血压药物在人类医学中上市(商品名Wytensin片剂,惠氏制药公司生产)。据报道,胍那苄已被用于赛马,国际赛马委员协会将其列为3类外来物质。因此,在赛后样本中检测到胍那苄可能会对马匹的训练师实施重大制裁。本研究检测了快速静脉注射0.04和0.2mg/kg胍那苄后,马血清样本中胍那苄的液相色谱/串联四极杆质谱(LC-MS/MS)检测情况。采用一种改编自先前检测克伦特罗的方法,在血清中检测到母体化合物,其表观检测限约为0.03ng/ml,定量限为0.2ng/ml。0.2mg/kg剂量后,胍那苄的血清浓度在约100ng/ml时达到峰值,0.04mg/kg剂量后,母体化合物在长达8小时内均可检测到。在这些剂量下给予胍那苄后检测的尿液样本显示至少有一种葡萄糖醛酸代谢物,葡萄糖醛酸环显然与环羟基或胍基羟胺相连。本文给出的LC-MS/MS结果构成了赛马中胍那苄确证试验的基础。