Bosscha K, Nieuwenhuijs V B, Gooszen A W, van Duijvenbode-Beumer H, Visser M R, Verweij W R, Akkermans L M
Department of Surgery, University Hospital Utrecht, The Netherlands.
Eur J Surg. 2000 Dec;166(12):963-7. doi: 10.1080/110241500447146.
To develop a standardised and reproducible model of intra-abdominal infection and abscess formation in rats.
Experimental study.
University hospital, The Netherlands.
36 adult male Wistar rats.
In 32 rats, peritonitis was produced using two different concentrations of Escherichia coli (E. coli) and Bacteroides fragilis (B. fragilis) incorporated in fibrin clots (E. coii 1 x 10(5) colony forming units (CFU)/ml or 1 x 10(8) CFU/ml, B. fragilis: 1 x 10(8) CFU/ml). Four rats with fibrin clots without bacteria served as uninfected controls.
Macroscopy and bacterial counts in peritoneal fluid, blood, and fibrin clots after 24 hours, 4 days, 7 days, and 4 weeks.
Macroscopically, there were signs of intra-abdominal infection and abscesses. With the higher starting concentration of E. coli, macroscopic signs were more pronounced and in nearly all rats bacterial counts in peritoneal fluid and fibrin clots showed persistently high numbers of E. coli and B. fragilis for at least 7 days (E. coli = 2 x 10(3) to 1 x 10(6) CFU/ml and 5 x 10(7) to 9 x 10(8) CFU/clot; B. fragilis = 1 x 10(3) to 1 x 10(6) CFU/ml and 5 x 10(7) to 6 x 10(8) CFU/clot).
This standardised and reproducible model of intra-abdominal infection and abscess formation seems well suited for further use and development in experiments on the pathophysiology of intra-abdominal infection and abscesses.
建立一种标准化且可重复的大鼠腹腔内感染和脓肿形成模型。
实验研究。
荷兰大学医院。
36只成年雄性Wistar大鼠。
在32只大鼠中,使用两种不同浓度的大肠杆菌(E. coli)和脆弱拟杆菌(B. fragilis)掺入纤维蛋白凝块中来诱发腹膜炎(大肠杆菌:1×10⁵菌落形成单位(CFU)/毫升或1×10⁸CFU/毫升,脆弱拟杆菌:1×10⁸CFU/毫升)。4只植入不含细菌的纤维蛋白凝块的大鼠作为未感染对照。
24小时、4天、7天和4周后腹腔液、血液和纤维蛋白凝块的宏观检查及细菌计数。
宏观上,有腹腔内感染和脓肿的迹象。随着大肠杆菌起始浓度的升高,宏观迹象更明显,几乎所有大鼠腹腔液和纤维蛋白凝块中的细菌计数显示,至少7天内大肠杆菌和脆弱拟杆菌数量持续居高(大肠杆菌 = 2×10³至1×10⁶CFU/毫升和5×10⁷至9×10⁸CFU/凝块;脆弱拟杆菌 = 1×10³至1×10⁶CFU/毫升和5×10⁷至6×10⁸CFU/凝块)。
这种标准化且可重复的腹腔内感染和脓肿形成模型似乎非常适合在腹腔内感染和脓肿病理生理学实验中进一步使用和开发。