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抗生素的细胞内分布与活性

Intracellular distribution and activity of antibiotics.

作者信息

Tulkens P M

机构信息

Laboratory of Physiological Chemistry, Catholic University of Louvain, Brussels, Belgium.

出版信息

Eur J Clin Microbiol Infect Dis. 1991 Feb;10(2):100-6. doi: 10.1007/BF01964420.

Abstract

Intracellular penetration, accumulation and disposition are important parameters governing the activity of antibiotics against intracellular bacteria. Beta-lactams diffuse into but do not accumulate in phagocytes, probably because of their acidic character. Aminoglycosides are too polar to pass across membranes and are therefore only taken up slowly by endocytosis, which results in an exclusively lysosomal localization. Lincosaminides, macrolides and fluoroquinolones all accumulate in phagocytes, the two former classes of drugs showing both a cytosolic and a lysosomal localization. Fluoroquinolones appear to be entirely soluble in cells. Analysis of their activity in a model of Staphylococcus aureus-infected J774 macrophages has revealed low activity of clindamycin, whereas macrolides, and even more so fluoroquinolones, easily reduce the original inoculum.

摘要

细胞内渗透、积累和分布是决定抗生素对细胞内细菌活性的重要参数。β-内酰胺类抗生素可扩散进入吞噬细胞,但不会在其中积累,这可能是由于其酸性特性所致。氨基糖苷类抗生素极性太大,无法穿过细胞膜,因此只能通过内吞作用缓慢摄取,这导致其仅定位于溶酶体。林可酰胺类、大环内酯类和氟喹诺酮类抗生素都能在吞噬细胞中积累,前两类药物在细胞质和溶酶体中均有定位。氟喹诺酮类抗生素似乎完全可溶于细胞。在金黄色葡萄球菌感染的J774巨噬细胞模型中对它们的活性进行分析后发现,克林霉素的活性较低,而大环内酯类抗生素,尤其是氟喹诺酮类抗生素,能轻易减少初始接种量。

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