Loss of purinergic P2X3 and P2X5 receptor innervation in human detrusor from adults with urge incontinence

被引:61
作者
Moore, KH
Ray, FR
Barden, JA
机构
[1] Univ Sydney, Dept Anat & Histol, Sydney, NSW 2006, Australia
[2] Univ New S Wales, Detrusor Muscle Lab, Dept Urogynaecol, St George Hosp, Kogarah, NSW 2217, Australia
[3] Univ Sydney, Prot Struct Lab, Inst Biomed Res, Sydney, NSW 2006, Australia
关键词
purinergic P2X receptors; hypertonia; human urinary incontinence; detrusor instability; innervation; IDI bladder;
D O I
10.1523/JNEUROSCI.21-18-j0002.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activation of purinergic P2X receptors associated with the parasympathetic nerves that supply the human bladder smooth muscle (detrusor) is implicated in control of detrusor contractility. The relative abundance of all seven subtypes colocalized with synaptic vesicles on parasympathetic nerves was examined in specimens from normal adult bladder, infants, and in adults with overactive detrusor contractility and a diagnosis of idiopathic detrusor instability (IDI) to determine whether receptor distribution varied with age or in patients with incontinence. Alteration in control of detrusor innervation was examined with P2X subtype-specific antibodies and an antibody against synaptic vesicles, using immunofluorescence and confocal microscopy. Detrusor samples were taken from: controls, at cystectomy for cancer or cystoscopic biopsy for hematuria (n = 22; age 33-88), child bladder, at surgical correction of vesicoureteric reflux (n = 21; age 4 months to 2 years), and adults with detrusor instability at cystoscopy-cystodistension (n = 18; age 30-81). Adult specimens contained muscle with large varicosities (1.2 mum) along parasympathetic nerves with colocalized patches of all P2X(1-7) subtypes. Infant bladder revealed little evidence of P2X at age <9 months but approached adult levels at 2 years. Detrusor from IDI patients revealed selective absence of P2X(3) and P2X(5) beneath all the varicosities. This specific lack of P2X(3) and P2X(5) may impair control of detrusor contractility and contribute to the pathophysiology of urge incontinence.
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页数:6
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