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长期给药后 ATP 的口服生物利用度。

Oral bioavailability of ATP after prolonged administration.

机构信息

Department of Epidemiology, Faculty of Health, Medicine and Life Sciences, Maastricht University, P.O. Box 616, 6200 MD Maastricht, The Netherlands.

出版信息

Br J Nutr. 2011 Feb;105(3):357-66. doi: 10.1017/S0007114510003570. Epub 2010 Dec 6.

Abstract

Purinergic receptors are important for the regulation of inflammation, muscle contraction, neurotransmission and nociception. Extracellular ATP and its metabolites are the main ligands for these receptors. Occasional reports on beneficial results of ATP administration in human and animal studies have suggested the bioavailability of oral ATP supplements. We investigated whether prolonged daily intake of oral ATP is indeed bioavailable. Thirty-two healthy subjects were randomised to receive 0, 250, 1250 or 5000 mg ATP per d for 28 d by means of enteric-coated pellets. In addition, on days 0 and 28, all thirty-two subjects received 5000 mg ATP to determine whether prolonged administration would induce adaptations in the bioavailability of ATP. ATP supplementation for 4 weeks did not lead to changes in blood or plasma ATP concentrations. Of all ATP metabolites, only plasma uric acid levels increased significantly after the administration of 5000 mg of ATP. Prolonged administration of ATP was safe as evidenced from liver and kidney parameters. We conclude that oral administration of ATP only resulted in increased uric acid concentrations. On the basis of these findings, we seriously question the claimed efficacy of oral ATP at dosages even lower than that used in the present study.

摘要

嘌呤能受体对于炎症、肌肉收缩、神经递质传递和痛觉感知的调节具有重要作用。细胞外 ATP 及其代谢物是这些受体的主要配体。在人类和动物研究中,偶尔有报道称 ATP 给药有有益效果,这表明口服 ATP 补充剂具有生物利用度。我们研究了长期每日口服 ATP 是否确实具有生物利用度。32 名健康受试者被随机分为 4 组,分别每天摄入 0、250、1250 或 5000 mg 肠溶包衣丸中的 ATP,持续 28 天。此外,在第 0 天和第 28 天,所有 32 名受试者均接受 5000 mg ATP 治疗,以确定长期给药是否会导致 ATP 生物利用度的适应性改变。4 周的 ATP 补充并未导致血液或血浆 ATP 浓度发生变化。在所有 ATP 代谢物中,只有在给予 5000 mg ATP 后,血浆尿酸水平显著升高。从肝肾功能参数来看,长期给予 ATP 是安全的。我们的结论是,口服 ATP 仅导致尿酸浓度升高。基于这些发现,我们严重质疑即使在比本研究中使用的剂量更低的情况下,口服 ATP 的声称功效。

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