不同抗生素给药途径对大鼠胫骨感染模型骨愈合抑制作用的比较研究。

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-02-28 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1529692
Xiaoyu Han, Wei Wang, Zengli Shen, Lisong Lv, Bingyuan Lin, Haiyong Ren, Yiyang Liu, Qiaofeng Guo, Huang Kai, Xiang Wang
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引用次数: 0

摘要

目的:本研究旨在通过大鼠胫骨感染模型,评估静脉注射与口服抗生素治疗在治疗骨感染,特别是骨髓炎方面的有效性。方法:采用皮质缺损部位注射金黄色葡萄球菌建立12周龄Wistar大鼠胫骨感染模型。6周后,给予万古霉素(静脉注射)、头孢唑林(静脉注射)、环丙沙星(口服)或环丙沙星联合利福平(口服)。采用微生物分析、血液促炎细胞因子分析、显微计算机断层扫描(μCT)、组织学分析和破骨细胞活性来评估每种治疗的疗效。结果:血液分析显示,静脉注射组白细胞计数和促炎细胞因子显著降低,尤其是万古霉素组。μCT成像显示,静脉给药组骨结构保存较好,而口服给药组骨结构恶化更为明显。微生物分析证实,与口服治疗相比,静脉注射组的细菌负荷较低,尤其是万古霉素。组织学分析显示,静脉注射组炎症减轻,纤维化减少,细菌存在最少。万古霉素和头孢唑林组破骨细胞活性明显降低,表明骨吸收控制较好。结论:与口服治疗相比,静脉给药万古霉素在控制骨感染、减轻炎症和保存骨结构方面具有更优越的疗效。虽然环丙沙星和环丙沙星-利福平联合用药有一定疗效,但效果不如静脉注射万古霉素,可能是由于生物利用度较低,药物在骨组织中的渗透不足。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative study of the inhibitory effects of different antibiotic administration routes on bone healing in a rat tibial infection model.

Objective: This study aimed to evaluate the effectiveness of intravenous versus oral antibiotic treatments in managing bone infections, particularly osteomyelitis, using a rat tibial infection model.

Methods: A tibial bone infection model was established in twelve-week-old Wistar rats via injection of Staphylococcus aureus at a cortical defect site. After six weeks, rats were treated with vancomycin (intravenous), cefazolin (intravenous), ciprofloxacin (oral), or ciprofloxacin combined with rifampin (oral). Microbial analysis, blood analysis for pro-inflammatory cytokines, micro-computed tomography (μCT), histological analysis, and osteoclast activity were used to assess the efficacy of each treatment.

Results: Blood analysis showed significant reductions in white blood cell count and pro-inflammatory cytokines in the intravenous treatment groups, especially with vancomycin. μCT imaging revealed better preservation of bone structure in intravenous treatment groups, while oral treatments resulted in more pronounced structural deterioration. Microbial analysis confirmed a lower bacterial load in the intravenous groups, particularly vancomycin, compared to oral treatments. Histological analysis revealed reduced inflammation, lower fibrosis, and minimal bacterial presence in intravenous groups. Osteoclast activity was notably reduced in the vancomycin and cefazolin groups, indicating better control of bone resorption.

Conclusion: Intravenous administration of vancomycin demonstrated superior efficacy in controlling bone infection, reducing inflammation, and preserving bone structure compared to oral treatments. While ciprofloxacin and the ciprofloxacin-rifampin combination showed some efficacy, they were less effective than intravenous vancomycin, likely due to lower bioavailability and insufficient drug penetration in bone tissue.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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