Yüksel Cihan, Alıravcı Işıl D, Koşan Murat, Esen Sinem, Yenice Aktaş Sevinç, Kaya Terzi Neslihan, Berber Ahmet Ali, Alkan Sevil, Kaya Selçuk
Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Çanakkale Onsekiz Mart University, 17000 Çanakkale, Turkiye.
Department of Urology, Faculty of Medicine, Çanakkale Onsekiz Mart University, 17000 Çanakkale, Türkiye.
Antibiotics (Basel). 2025 Jun 16;14(6):611. doi: 10.3390/antibiotics14060611.
This study aimed to evaluate the therapeutic efficacy of intravesical tigecycline administration in a rat model of cystitis induced by a tigecycline-sensitive, extensively drug-resistant (XDR) strain.
Thirty-six female Wistar albino rats were inoculated intravesically with XDR to induce cystitis. Twenty-four rats that developed infection were divided into four groups: untreated control, saline irrigation, low-dose tigecycline (6.25 mg/kg), and high-dose tigecycline (25 mg/kg). Microbiological clearance was assessed via urine cultures on days 3 and 5. Bladder tissues were analyzed histopathologically and for genotoxicity using the Comet assay.
On day 5, microbiological clearance was significantly higher in tigecycline-treated groups compared to controls ( = 0.028). Histopathology revealed significantly more inflammation in the high-dose tigecycline group ( = 0.029). Genotoxicity was observed in both tigecycline groups, independent of dose ( < 0.05).
Intravesical tigecycline demonstrated microbiological efficacy against XDR -induced cystitis. However, its inflammatory and genotoxic potential necessitates further preclinical evaluation.
本研究旨在评估膀胱内给予替加环素对由一株对替加环素敏感的广泛耐药(XDR)菌株诱导的大鼠膀胱炎模型的治疗效果。
36只雌性Wistar白化大鼠经膀胱内接种XDR以诱导膀胱炎。将24只发生感染的大鼠分为四组:未治疗对照组、生理盐水冲洗组、低剂量替加环素组(6.25毫克/千克)和高剂量替加环素组(25毫克/千克)。在第3天和第5天通过尿培养评估微生物清除情况。使用彗星试验对膀胱组织进行组织病理学分析和遗传毒性分析。
在第5天,与对照组相比,替加环素治疗组的微生物清除率显著更高(P = 0.028)。组织病理学显示高剂量替加环素组的炎症明显更多(P = 0.029)。在两个替加环素组中均观察到遗传毒性,与剂量无关(P < 0.05)。
膀胱内给予替加环素对XDR诱导的膀胱炎显示出微生物学疗效。然而,其炎症和遗传毒性潜力需要进一步的临床前评估。