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[基于与氨氯吡咪相互作用的研究评估肠上皮细胞离子交换在阿莫西林肠道吸收中的作用]

[Assessment of the role of enterocyte ion exchange in the intestinal absorption of amoxicillin, based on a study of the interaction with amiloride].

作者信息

Westphal J F, Brogard J M, Jehl F, Carbon C

机构信息

Laboratoire de Pathologie Interne et Expérimentale, Clinique Médicale B, Strasbourg, France.

出版信息

Pathol Biol (Paris). 1995 Sep;43(7):590-5.

PMID:8570263
Abstract

Intestinal dipeptide carrier system has been shown in vitro to be involved in intestinal absorption of betalactam antibiotics. Given that efficiency of this transport system depends on a pH gradient (extracellular pH < intracellular pH) at the brush-border membrane of enterocytes, we assessed the effects of amiloride, a known inhibitor of the Na-H exchange, on the bioavilability of oral amoxicillin in eight normal volunteers. Following a single 10 mg oral dose of amiloride, the absolute bioavailability of oral amoxicillin turned out to decrease by 27% (p < 0.01). The extent of reduction of oral amoxicillin AUC appeared to significantly correlate (p = 0.005) with the extent of decrease in potassium renal excretion but not with variations in antibiotic renal clearance under amiloride effect. Such patterns seem to confirm in vivo the role of the Na-H exchange in betalactam absorption and to suggest the underlying regulatory function of intracellular Na concentration, the latter depending on the (NaK)-ATPase activity.

摘要

体外实验表明,肠道二肽载体系统参与β-内酰胺类抗生素的肠道吸收。鉴于该转运系统的效率取决于肠上皮细胞刷状缘膜处的pH梯度(细胞外pH < 细胞内pH),我们评估了钠-氢交换的已知抑制剂氨氯地平对8名正常志愿者口服阿莫西林生物利用度的影响。单次口服10 mg氨氯地平后,口服阿莫西林的绝对生物利用度降低了27%(p < 0.01)。口服阿莫西林AUC的降低程度似乎与肾脏钾排泄的降低程度显著相关(p = 0.005),但与氨氯地平作用下抗生素肾脏清除率的变化无关。这些模式似乎在体内证实了钠-氢交换在β-内酰胺吸收中的作用,并提示了细胞内钠浓度的潜在调节功能,后者取决于(钠钾)-ATP酶活性。

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