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禁食对阿苯达唑及其代谢产物在犊牛体内药代动力学行为的影响。

Fasting-induced changes to the pharmacokinetic behaviour of albendazole and its metabolites in calves.

作者信息

Sánchez S F, Alvarez L I, Lanusse C E

机构信息

Departamento de Fisiopatología, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro, Tandil, Argentina.

出版信息

J Vet Pharmacol Ther. 1997 Feb;20(1):38-47. doi: 10.1046/j.1365-2885.1997.00810.x.

Abstract

The influence of fasting on the bioavailability and disposition kinetics of albendazole (ABZ) and its metabolites in cattle was investigated. ABZ (10 mg/ kg) was given by intraruminal (i.r.) (Experiment 1) and intravenous (i.v.) (Experiment 2) administration to Holstein calves either fed ad libitum (control) or subjected to a 48 h fasting period (fasted group) prior to treatment. The rate of passage of digesta through the gastrointestinal (GI) tract was evaluated by measurement of cobalt faecal excretion following the oral administration of the sodium-cobalt-ethylendiamine-tetracetic acid complex to calves subjected to the feeding conditions above described. Jugular blood and abomasal fluid (via cannula) samples were collected over 120 h post-treatment; samples were analysed by high performance liquid chromatography (HPLC) for ABZ, ABZ sulphoxide (ABZSO) and ABZ sulphone (ABZSO2). Fasting the animals prior to the i.r. treatment resulted in pronounced modifications to the plasma and abomasal fluid disposition kinetics of ABZ and its metabolites. A greater extent of GI absorption with significantly higher CmaX (150%) and AUC (310%) values for ABZSO in plasma, was observed in fasted compared to fed animals following the i.r. administration of ABZ. Extended detection of ABZ metabolites resulting in significantly longer plasma t 1/2el and MRT was also obtained in fasted compared to fed calves. These results correlated with the substantially enhanced availability of ABZ and its metabolites (AUCs over 200% greater) in the abomasal fluid of the fasted animals. Fasting did not induce changes to the plasma disposition of either ABZ or its metabolites after the i.v. treatment. The digesta passage rate, measured by the amount of cobalt excreted in faeces, was significantly lower in fasted compared to animals fed ad libitum. A delayed GI transit time that decreases the rate of passage of the drug down the digestive tract, may have accounted for enhanced ABZ dissolution and absorption in fasted compared to fed calves. The findings reported in this article show that fasting prior to treatment notably affects the bioavailability and disposition kinetics of ABZ and its metabolites in cattle.

摘要

研究了禁食对阿苯达唑(ABZ)及其代谢产物在牛体内的生物利用度和处置动力学的影响。分别通过瘤胃内(i.r.)(实验1)和静脉内(i.v.)(实验2)给药,给荷斯坦犊牛服用ABZ(10mg/kg),这些犊牛在治疗前要么自由采食(对照组),要么经历48小时禁食期(禁食组)。通过给上述饲养条件下的犊牛口服钴-乙二胺四乙酸钠络合物后,测量钴的粪便排泄量,评估消化物通过胃肠道(GI)的速率。在治疗后120小时内采集颈静脉血和皱胃液(通过插管)样本;通过高效液相色谱法(HPLC)分析样本中的ABZ、阿苯达唑亚砜(ABZSO)和阿苯达唑砜(ABZSO2)。在瘤胃内给药治疗前禁食动物,导致ABZ及其代谢产物在血浆和皱胃液中的处置动力学发生显著改变。与自由采食动物相比, 禁食动物在瘤胃内给予ABZ后,胃肠道吸收程度更大,血浆中ABZSO的CmaX(150%)和AUC(310%)值显著更高。与自由采食的犊牛相比,禁食的犊牛对ABZ代谢产物的检测时间延长,导致血浆t1/2el和MRT显著延长。这些结果与禁食动物皱胃液中ABZ及其代谢产物的可用性大幅提高(AUC超过200%)相关。静脉给药治疗后,禁食并未引起ABZ及其代谢产物的血浆处置发生变化。通过粪便中钴的排泄量测量的消化物通过率,禁食动物显著低于自由采食动物。与自由采食的犊牛相比,禁食犊牛的胃肠道转运时间延迟,降低了药物在消化道中的通过速率,这可能是ABZ溶解和吸收增加的原因。本文报道的研究结果表明,治疗前禁食显著影响ABZ及其代谢产物在牛体内的生物利用度和处置动力学。

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