短期服用戊酸前药引起肉毒碱耗竭的酮生功能受损

Abrahamsson K., Eriksson B.O., Holme E., Jodal U., Lindstedt S., Nordin I.
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引用次数: 37

摘要

长期服用戊酸前药会导致酮体生成受损。因此,研究短期治疗是否对脂肪酸氧化有影响是很有意义的。在这项研究中,6名健康男性每天服用1200毫克哌美西林,连续12天诱导肉毒碱缺乏。血清游离肉碱浓度由平均42.8 μmol/l(范围31 ~ 48)降至11.6 μmol/l(范围7.0 ~ 24),但肌肉肉碱浓度没有降低。在给药前后分别进行36小时空腹试验,研究对酮体生成的影响。治疗后,空腹结束时血清游离肉碱水平最低的两名受试者的生酮功能受损。这表明肝脏中的肉毒碱缺乏,这反映在血清中的游离肉毒碱浓度上,并且不能通过动员肌肉中的肉毒碱来补偿。我们得出的结论是,短期使用戊酸偶联药物治疗存在发生肉碱缺乏症和肝脏脂肪酸氧化受损的重大风险。
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Impaired Ketogenesis in Carnitine Depletion Caused by Short-Term Administration of Pivalic Acid Prodrug

Long-term treatment with pivalic acid prodrug results in impaired ketone-body production. Therefore, it was of interest to investigate whether short-term treatment had any influence on the fatty acid oxidation. In this study six healthy males were given 1200 mg per day of pivmecillinam for 12 days to induce carnitine deficiency. The concentration of free carnitine in serum was reduced from a mean of 42.8 μmol/liter (range, 31-48) to 11.6 μmol/liter (range, 7.0-24), but the muscle carnitine concentration was not reduced. A 36-h fasting test was performed before and after drug administration to study the effect on ketone-body production. After treatment, the two subjects with the lowest level of serum free carnitine at the end of the fasting period had impaired ketogenesis. This indicates a carnitine deficiency in the liver which was reflected in the free carnitine concentration in serum and which could not be compensated for by mobilization of muscle carnitine. We conclude that there is a substantial risk to develop carnitine deficiency and impaired fatty acid oxidation in the liver during short-term treatment with drugs conjugated with pivalic acid.

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