Up-regulation of endothelin (ETA and ETB) receptors and down-regulation of nitric oxide synthase in the detrusor of a rabbit model of partial bladder outlet obstruction

被引:32
作者
Khan, MA
Dashwood, MR
Thompson, CS
Mumtaz, FH
Mikhailidis, DP
Morgan, RJ
机构
[1] Royal Free Hosp, Dept Urol, London NW3 2QG, England
[2] UCL, Royal Free & Univ Coll Med Sch, Dept Mol Pathol & Clin Biochem, London WC1E 6BT, England
来源
UROLOGICAL RESEARCH | 1999年 / 27卷 / 06期
关键词
endothelin receptors; nitric oxide synthase; rabbit; bladder obstruction;
D O I
10.1007/s002400050134
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Bladder outlet obstruction (BOO) is associated with altered bladder structure and function. Endothelial (ET-1) has mitogenic and potent contractile properties. There are two ET receptors: ETA and ETB. Nitric oxide synthase (NOS) is the enzyme responsible for the synthesis of nitric oxide (NO) which is involved in smooth muscle relaxation. We investigated whether there are any changes in the density of ET-receptors and NOS in the detrusor and bladder neck in a rabbit model of BOG. Partial BOO was induced in adult male New Zealand White rabbits. Sham operated age-matched rabbits acted as controls. After six weeks the urinary bladders were excised and detrusor and bladder neck sections incubated with radioligands for ET-1, ETA and ETB receptors and with [H-3]-1-NOARG (a ligand for NOS). NADPH histochemistry was also performed. BOO bladder weights were significantly increased (P = 0.002). ET-1 binding and ETA receptor binding sites were significantly increased in the BOO detrusor smooth muscle (P = 0.03, P = 0.03 respectively) and urothelium (P = 0.002, P = 0.02 respectively). ETB receptor binding sites were also significantly increased in the BOO detrusor smooth muscle (P = 0.04). However, there was no change in the BOO bladder neck. NOS was significantly decreased in the detrusor smooth muscle (P = 0.003) and urothelium (P = 0.0002). In the bladder neck NOS was also significantly reduced in the urothelium (P = 0.003). NADPH staining was decreased in the detrusor and bladder neck. The up-regulation of ET receptorsalong with the down-regulation of NOS in the detrusor may contribute to the symptoms associated with BOO. Since ET-1 has a mitogenic role, especially via its ETA receptors, the increase in ETA receptors may also be involved in detrusor hyperplasia and hypertrophy in BOO. ET antagonists may therefore have a role in the treatment of patients with BOO.
引用
收藏
页码:445 / 453
页数:9
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