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Detrusor overactivity induced by intravesical application of adenosine 5'-triphosphate under different delivery conditions in rats.

机译:大鼠不同递送条件下膀胱内应用5'-三磷酸腺苷诱导的逼尿肌过度活动。

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OBJECTIVES: To investigate the effects of intravesical application of adenosine 5'-triphosphate (ATP) on bladder activity to elucidate the role of urothelial barrier function and ecto-ATPase activity in the ATP-mediated mechanism inducing detrusor overactivity. METHODS: Continuous cystometry by an intravesical catheter inserted from the bladder dome was performed in conscious female rats. RESULTS: ATP solutions adjusted to pH 6.0 did not elicit significant detrusor overactivity at a concentration of 60 mM. However, in bladders pretreated with protamine sulfate (10 mg/mL) to increase urothelial permeability, ATP solution (pH 6.0) induced detrusor overactivity by decreasing the intercontraction intervals. These irritant effects of ATP after protamine treatment were antagonized by P2X receptor antagonists, such as pyridoxal-5-phosphate-6-azophenyl-2',4'-disulfonic acid (70 micromol/kg) and 2',3'-O-(2,4,6, trinitrophenyl) ATP (30 micromol/kg). These were also suppressed in rats pretreated with systemic capsaicin (125 mg/kg subcutaneously). Alpha,beta-methylene ATP (5 mM, pH 6.0) or ATP (60 mM, pH6) after intravesical infusion of 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid (5 mM, pH 6.0), an ecto-ATPase inhibitor, induced detrusor overactivity without protamine pretreatment, but the reduction in intercontraction intervals was smaller compared with that with ATP after protamine treatment. CONCLUSIONS: Low permeability of bladder epithelium and ecto-ATPase activity can prevent ATP activation of subepithelial P2X receptors to induce bladder overactivity. Thus, enhanced penetration of endogenous ATP owing to urothelial damage may contribute to urinary frequency and bladder pain in hypersensitive bladder disorders such as interstitial cystitis.
机译:目的:探讨膀胱内应用5'-三磷酸腺苷(ATP)对膀胱活动的影响,以阐明尿路上皮屏障功能和体外ATP酶活性在ATP介导的诱导逼尿肌过度活动的机制中的作用。方法:在有意识的雌性大鼠中,通过从膀胱穹inserted插入的膀胱内导管进行连续膀胱测压。结果:调节至pH 6.0的ATP溶液在60 mM的浓度下不会引起明显的逼尿肌过度活跃。然而,在用硫酸鱼精蛋白(10 mg / mL)预处理以增加尿道上皮通透性的膀胱中,ATP溶液(pH 6.0)通过缩短收缩间隔来诱导逼尿肌过度活动。在鱼精蛋白处理后,ATP的这些刺激作用被P2X受体拮抗剂所拮抗,例如吡ido醛5-磷酸-6-6-偶氮苯基-2',4'-二磺酸(70 micromol / kg)和2',3'-O- (2,4,6,三硝基苯基)ATP(30 micromol / kg)。在全身性辣椒素(皮下注射125 mg / kg)预处理的大鼠中,这些也被抑制。膀胱内输注4,4'-二异硫氰基二苯乙烯-2,2'-二磺酸(5 mM,pH 6.0)的α,β-亚甲基ATP(5 mM,pH 6.0)或ATP(60 mM,pH6),外- ATPase抑制剂可在不进行鱼精蛋白预处理的情况下诱导逼尿肌过度活动,但与使用鱼精蛋白处理后的ATP相比,收缩间隔的减少较小。结论:膀胱上皮的低渗透性和胞外ATP酶活性可以阻止上皮下P2X受体的ATP活化,从而引起膀胱过度活动。因此,由于尿路上皮损伤而导致的内源性ATP穿透性增强可能会导致尿频和膀胱过敏,例如间质性膀胱炎。

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