Sitton N G, Dixon J S, Astbury C, Francis R J, Bird H A, Wright V
Clinical Pharmacology Unit, Royal Bath Hospital, Harrogate.
Ann Rheum Dis. 1988 Jan;47(1):48-52. doi: 10.1136/ard.47.1.48.
To investigate the cause of low serum histidine in rheumatoid arthritis (RA) single oral and intravenous doses of L-histidine were administered to patients with active RA, and to an equal number of age and sex matched control subjects. In the first study 13 patients and their controls received a 100 mg kg-1 dose of L-histidine as an aqueous slurry. Significant differences were seen in body weight, predose baseline serum histidine concentration, Cmax, t1/2, and area under curve, AUC0-infinity. In a second study six patients and six controls each received a 50 mg kg-1 dose of L-histidine both orally and intravenously on two separate occasions. The patients with RA had a lower baseline serum histidine concentration, a lower volume of distribution, and a shorter plasma half life than the controls, but these differences were not statistically significant. No difference was seen in bioavailability or clearance. Low serum histidine in RA is unlikely to be due to malabsorption from the gut, uptake by abnormal gut flora, or increased metabolism.
为了探究类风湿关节炎(RA)患者血清组氨酸水平低的原因,对活动期RA患者以及年龄和性别匹配的同等数量对照受试者分别口服和静脉注射单剂量L-组氨酸。在第一项研究中,13例患者及其对照接受了100 mg/kg剂量的L-组氨酸水悬液。在体重、给药前基线血清组氨酸浓度、Cmax、t1/2以及曲线下面积(AUC0-∞)方面观察到显著差异。在第二项研究中,6例患者和6例对照分别在两个不同时间口服和静脉注射50 mg/kg剂量的L-组氨酸。与对照相比,RA患者的基线血清组氨酸浓度较低、分布容积较小且血浆半衰期较短,但这些差异无统计学意义。在生物利用度或清除率方面未观察到差异。RA患者血清组氨酸水平低不太可能是由于肠道吸收不良、异常肠道菌群摄取或代谢增加所致。