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相似文献

1
Cellular uptake of clindamycin and lincomycin.克林霉素和林可霉素的细胞摄取。
Br J Exp Pathol. 1984 Dec;65(6):725-30.
2
Different kinetic of enzymatic inactivation of lincomycin and clindamycin in Staphylococcus aureus.金黄色葡萄球菌中林可霉素和克林霉素酶促失活的不同动力学。
J Chemother. 1993 Aug;5(4):215-22. doi: 10.1080/1120009x.1993.11739235.
3
[In-vitro activity of clindamycin and lincomycin in the presence of Staphylococcus aureus].[金黄色葡萄球菌存在时克林霉素和林可霉素的体外活性]
Fortschr Med. 1984 Jun 7;102(21):603-4.
4
[Sensitivity of hospital strains of Staphylococcus aureus to lincomycin and clindamycin].[医院金黄色葡萄球菌菌株对林可霉素和克林霉素的敏感性]
Pol Tyg Lek. 1980 Feb 25;35(8):269-71.
5
Clindamycin as an anti-staphylococcal agent--indications and limitations.克林霉素作为一种抗葡萄球菌药物——适应证与局限性
Scand J Infect Dis Suppl. 1984;43:62-6.
6
[Antibacterial activity of clindamycin and lincomycin in broth, serum, and in combination with polymorphonuclear leukocytes against Staphylococcus aureus and Staphylococcus epidermidis].[克林霉素和林可霉素在肉汤、血清中以及与多形核白细胞联合对金黄色葡萄球菌和表皮葡萄球菌的抗菌活性]
Infection. 1984 Jul-Aug;12(4):280-5. doi: 10.1007/BF01645962.
7
Activity of antibiotics in chronic granulomatous disease leukocytes.抗生素在慢性肉芽肿病白细胞中的活性。
Pediatr Res. 1983 Nov;17(11):916-9. doi: 10.1203/00006450-198311000-00016.
8
Plasmid-mediated resistance to lincomycin by inactivation in Staphylococcus haemolyticus.溶血葡萄球菌中通过失活介导的对林可霉素的质粒抗性
Antimicrob Agents Chemother. 1985 Sep;28(3):421-4. doi: 10.1128/AAC.28.3.421.
9
Microbial kinetics of drug action against gram-positive and gram-negative organisms. III: Effect of lincomycin and clindamycin combinations on Staphylococcus aureus and Escherichia coli.针对革兰氏阳性菌和革兰氏阴性菌的药物作用的微生物动力学。III:林可霉素和克林霉素联合用药对金黄色葡萄球菌和大肠杆菌的影响。
J Pharm Sci. 1975 Oct;64(10):1621-6. doi: 10.1002/jps.2600641006.
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Two new types of resistance to lincomycin in pathogenic staphylococci from animals.动物致病性葡萄球菌中两种新的对林可霉素的耐药类型。
Ann Microbiol (Paris). 1980 Nov-Dec;131B(3):261-6.

引用本文的文献

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In vitro antibiotic activity against intraosteoblastic Staphylococcus aureus: a narrative review of the literature.骨内金黄色葡萄球菌的体外抗生素活性:文献综述。
J Antimicrob Chemother. 2021 Nov 12;76(12):3091-3102. doi: 10.1093/jac/dkab301.
2
Intracellular Penetration and Effects of Antibiotics on Inside Human Neutrophils: A Comprehensive Review.抗生素在人中性粒细胞内的穿透及作用:综述
Antibiotics (Basel). 2019 May 4;8(2):54. doi: 10.3390/antibiotics8020054.
3
Antimicrobial activity against intraosteoblastic Staphylococcus aureus.对成骨细胞内金黄色葡萄球菌的抗菌活性。
Antimicrob Agents Chemother. 2015 Apr;59(4):2029-36. doi: 10.1128/AAC.04359-14. Epub 2015 Jan 20.
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Penetration of brodimoprim into human neutrophils and intracellular activity.溴莫普明在人中性粒细胞中的渗透及细胞内活性。
Antimicrob Agents Chemother. 1996 Oct;40(10):2392-8. doi: 10.1128/AAC.40.10.2392.
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Optimum treatment of intracellular infection.细胞内感染的最佳治疗方法。
Drugs. 1996 Jul;52(1):45-59. doi: 10.2165/00003495-199652010-00004.
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Antimicrobial susceptibility of ileal symbiont intracellularis isolated from pigs with proliferative enteropathy.从患有增生性肠炎的猪中分离出的胞内艾美耳球虫回肠共生体的药敏性。
J Clin Microbiol. 1995 May;33(5):1314-7. doi: 10.1128/jcm.33.5.1314-1317.1995.
7
Uptake of ciprofloxacin by macrophages.巨噬细胞对环丙沙星的摄取。
J Clin Pathol. 1985 Apr;38(4):442-4. doi: 10.1136/jcp.38.4.442.
8
Evaluation of antibacterial agents in a high-volume bovine polymorphonuclear neutrophil Staphylococcus aureus intracellular killing assay.在一项高容量牛多形核中性粒细胞金黄色葡萄球菌细胞内杀伤试验中对抗菌剂的评估。
Antimicrob Agents Chemother. 1986 Apr;29(4):634-8. doi: 10.1128/AAC.29.4.634.
9
Reduction of wall degradability of clindamycin-treated staphylococci within macrophages.降低巨噬细胞内克林霉素处理的葡萄球菌的壁降解能力。
Infect Immun. 1990 Jan;58(1):197-204. doi: 10.1128/iai.58.1.197-204.1990.
10
Intracellular activity of tosufloxacin (T-3262) against Salmonella enteritidis and ability to penetrate into tissue culture cells of human origin.托氟沙星(T-3262)对肠炎沙门氏菌的细胞内活性及其渗透人源组织培养细胞的能力。
Antimicrob Agents Chemother. 1990 Jun;34(6):949-53. doi: 10.1128/AAC.34.6.949.

本文引用的文献

1
Antibiotic uptake by alveolar macrophages.肺泡巨噬细胞对抗生素的摄取。
J Lab Clin Med. 1980 Mar;95(3):429-39.
2
Antibiotic entry into human polymorphonuclear leukocytes.抗生素进入人多形核白细胞的过程。
Antimicrob Agents Chemother. 1982 Mar;21(3):373-80. doi: 10.1128/AAC.21.3.373.
3
Clindamycin uptake by human neutrophils.人中性粒细胞对克林霉素的摄取。
J Infect Dis. 1981 Nov;144(5):472-9. doi: 10.1093/infdis/144.5.472.

克林霉素和林可霉素的细胞摄取。

Cellular uptake of clindamycin and lincomycin.

作者信息

Easmon C S, Crane J P

出版信息

Br J Exp Pathol. 1984 Dec;65(6):725-30.

PMID:6498086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2040999/
Abstract

Neither clindamycin nor lincomycin killed intracellular Staphylococcus aureus over a 4-h period. Bio-assay of neutrophil sonicates after exposure to antibiotic showed the presence of active clindamycin at approximately 20 times the extracellular concentration. Clindamycin and lincomycin kill staphylococci relatively slowly, particularly in cell culture medium and balanced salt solution. This might account for their failure to kill intracellular staphylococci despite intracellular accumulation. The neutrophil experiments could not be extended to a time period (20 h) over which the antibiotics would kill S. aureus, as the presence of these bacteria within neutrophils for this length of time resulted in considerable cell lysis.

摘要

在4小时内,克林霉素和林可霉素均未杀死细胞内的金黄色葡萄球菌。对抗生素暴露后的中性粒细胞超声裂解物进行生物测定,结果显示活性克林霉素的存在量约为细胞外浓度的20倍。克林霉素和林可霉素杀死葡萄球菌的速度相对较慢,尤其是在细胞培养基和平衡盐溶液中。这可能解释了尽管它们在细胞内蓄积,但仍无法杀死细胞内葡萄球菌的原因。中性粒细胞实验无法延长至抗生素能够杀死金黄色葡萄球菌的时间段(20小时),因为中性粒细胞内存在这些细菌达此时长会导致大量细胞裂解。