Weng Te I, Chen Wen Jone, Wu Hsiao Yi, Liu Shing-Hwa
Department of Emergency Medicine, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, 10043, Taiwan.
J Infect Dis. 2006 Dec 15;194(12):1774-82. doi: 10.1086/509620. Epub 2006 Nov 8.
Uropathogenic Escherichia coli (UPEC) is a common cause of urinary-tract infection. The mechanisms by which bacteria cause the symptoms of cystitis remain unclear.
The contractions of isolated rat detrusor strips evoked by electrical field stimulations (EFS) or by exogenous agonists and immunoblotting for the detection of protein expression in the bladder were measured in the short (1 h) and long (24 h) term after the intravesical instillation of J96 (O4:K6) strain or UPEC isolated from patients with acute E. coli pyelonephritis or E. coli lipopolysaccharide (LPS).
One hour after the instillation of UPEC, the level of endothelial nitric oxide synthase (eNOS) and the contractile response, but not protein kinase C (PKC) and extracellular signal-regulated kinase (ERK)-1/2 activation, were higher. Twenty-four hours after UPEC treatment, detrusor contractions were decreased, and inducible (i) NOS protein expression and ERK1/2 phosphorylation, but not PKC activation, were observed. Both aminoguanidine and PD98059 treatment markedly reversed the decrease of EFS- and acetylcholine-evoked detrusor contractions induced by UPEC. The instillation of LPS triggered PKC activation but not ERK1/2 phosphorylation.
Short-term intravesical instillation of UPEC enhances detrusor contractions through an eNOS-related pathway, but iNOS-regulated ERK1/2 signaling may be involved in long-term UPEC treatment-induced responses. There are different mechanisms involved in the responses induced by UPEC and LPS.
尿路致病性大肠杆菌(UPEC)是尿路感染的常见病因。细菌引发膀胱炎症状的机制尚不清楚。
在膀胱内灌注J96(O4:K6)菌株、从急性大肠杆菌肾盂肾炎患者分离出的UPEC或大肠杆菌脂多糖(LPS)后的短期(1小时)和长期(24小时),测量电场刺激(EFS)或外源性激动剂诱发的离体大鼠逼尿肌条收缩,并通过免疫印迹法检测膀胱中的蛋白表达。
灌注UPEC1小时后,内皮型一氧化氮合酶(eNOS)水平和收缩反应升高,但蛋白激酶C(PKC)和细胞外信号调节激酶(ERK)-1/2的激活未升高。UPEC处理24小时后,逼尿肌收缩减弱,观察到诱导型(i)NOS蛋白表达和ERK1/2磷酸化,但PKC激活未出现。氨基胍和PD98059处理均显著逆转了UPEC诱导的EFS和乙酰胆碱诱发的逼尿肌收缩的降低。灌注LPS触发了PKC激活,但未触发ERK1/2磷酸化。
短期膀胱内灌注UPEC通过与eNOS相关的途径增强逼尿肌收缩,但iNOS调节的ERK1/2信号可能参与长期UPEC处理诱导的反应。UPEC和LPS诱导的反应涉及不同机制。