Vowinkel Thorsten, Kalogeris Theodore J, Mori Mikiji, Krieglstein Christian F, Granger D Neil
Department of Molecular and Cellular Physiology, LSU Health Sciences Center, 1501 Kings Highway, Shreveport, Louisiana 71130-3932, USA.
Dig Dis Sci. 2004 Apr;49(4):556-64. doi: 10.1023/b:ddas.0000026298.72088.f7.
In dextran sulfate sodium (DSS)-induced inflammatory bowel disease in mice the relationship between the amount of ingested DSS and the severity of colitis has not been systematically investigated. We examined whether (1) the severity of colitis is DSS load-dependent, and (2) there is a critical DSS load required to reliably induce colitis. DSS load was calculated as: (drinking volume (ml) x [DSS (g)/100 ml])/body weight (g). A minimum DSS load > or = 30 mg/g body weight over 7 days resulted in a significantly elevated colonic myeloperoxidase (MPO) activity, compared to mice receiving less DSS and controls (P < 0.05). Histomorphologic data correlated with MPO activity and revealed significantly higher damage scores once the DSS load was > or = 30 mg/g body weight. Our findings demonstrate the importance of monitoring DSS load in this model of experimental colitis.
在葡聚糖硫酸钠(DSS)诱导的小鼠炎症性肠病中,摄入的DSS量与结肠炎严重程度之间的关系尚未得到系统研究。我们研究了:(1)结肠炎的严重程度是否依赖于DSS负荷;(2)可靠诱导结肠炎是否存在临界DSS负荷。DSS负荷计算如下:(饮水量(ml)×[DSS(g)/100 ml])/体重(g)。与接受较少DSS的小鼠和对照组相比,7天内最低DSS负荷≥30 mg/g体重会导致结肠髓过氧化物酶(MPO)活性显著升高(P<0.05)。组织形态学数据与MPO活性相关,且一旦DSS负荷≥30 mg/g体重,损伤评分显著更高。我们的研究结果表明,在这种实验性结肠炎模型中监测DSS负荷很重要。