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雌性猪和人类尿道中的磷酸二酯酶5:形态学和功能方面

Phosphodiesterase 5 in the female pig and human urethra: morphological and functional aspects.

作者信息

Werkström Viktoria, Svensson Anna, Andersson Karl-Erik, Hedlund Petter

机构信息

Department of Clinical and Experimental Pharmacology, Institute for Laboratory Medicine, Lund University Hospital, Lund, Sweden.

出版信息

BJU Int. 2006 Aug;98(2):414-23. doi: 10.1111/j.1464-410X.2006.06217.x. Epub 2006 Apr 18.

Abstract

OBJECTIVE

To characterize the distribution of phosphodiesterase 5 (PDE-5), cGMP and cGMP-dependent protein kinase I (PKG1), and to evaluate the effect of pharmacological inhibition of PDE-5 in isolated preparations of pig and human urethra, as the nitric oxide (NO)/cGMP pathway generates the main inhibitory signals to reduce resistance in the bladder outlet and urethra during emptying of the bladder.

MATERIALS AND METHODS

After obtaining ethics committee approval, urethral specimens were obtained from three female patients during cystectomy, and from young female pigs. The specimens were prepared for immunohistochemical investigations and for functional studies in organ baths. Effects of sildenafil, vardenafil and tadalafil (1 nm to 30 microm) were studied in l-noradrenaline (1 microm)-activated or spontaneously contracted preparations, and on relaxations induced by electrical-field stimulation (EFS). Levels of cGMP were determined by radioimmunoassay.

RESULTS

After stimulation with the NO donor, DETA NONO-ate (1 mm), there was greater cGMP-immunoreactivity (IR) in urethral and vascular smooth muscles. There was a wide distribution of cGMP- and vimentin-positive interstitial cells between pig urethral smooth muscle bundles. There was also cGMP-IR within NO-synthase-IR endothelium. There was PDE-5 IR within the urethral and vascular smooth muscle cells, but also in vascular endothelial cells that expressed cGMP-IR. In pig and human sections, there was strong PKG1-IR in alpha-actin-IR urethral smooth muscle cells that also contained IR for cGMP. Sildenafil, vardenafil and tadalafil caused mean (sem) concentration-dependent relaxations of the pig urethra which, at 30 microm, were 80 (3)% (11 samples), 81 (5)% (12 samples) and 64 (4)% (10 samples) of the spontaneous tone. The relaxation of L-noradrenaline-contracted female human urethra was 100% in response to 10 microm sildenafil, and 85 (15)% and 47 (13)% for 30 microm of vardenafil and tadalafil, respectively (three samples). Vardenafil or sildenafil (30 microm) doubled cGMP levels in pig specimens. There were no effects on cGMP levels with tadalafil. EFS (1-32 Hz) caused l-NG-nitroarginine-sensitive relaxations of pig urethral muscle that were increased in amplitude and duration by PDE-5 inhibition. At 0.1 microm, sildenafil, vardenafil or tadalafil significantly prolonged the mean (sem) duration of the relaxation at 4 Hz by 55 (19)%, 45 (14)% and 51 (12)%, respectively.

CONCLUSIONS

PDE-5-, cGMP- and PKG1-IR is widely distributed in human and pig urethral tissues. Nerve-induced relaxations of urethral preparations were enhanced at low concentrations of sildenafil, vardenafil and tadalafil, whereas there were direct smooth muscle-relaxant actions of the PDE-5 inhibitors at high concentrations. Inhibition of PDE-5 might be an interesting option to facilitate cGMP-mediated relaxation of the outflow region.

摘要

目的

表征磷酸二酯酶5(PDE - 5)、环磷酸鸟苷(cGMP)和cGMP依赖性蛋白激酶I(PKG1)的分布,并评估在猪和人尿道分离制剂中对PDE - 5进行药理学抑制的效果,因为一氧化氮(NO)/cGMP途径在膀胱排空期间产生主要的抑制信号以降低膀胱出口和尿道的阻力。

材料与方法

获得伦理委员会批准后,在膀胱切除术期间从三名女性患者以及年轻雌性猪获取尿道标本。将标本制备用于免疫组织化学研究和器官浴中的功能研究。在1 - 去甲肾上腺素(1 μmol)激活或自发收缩的制剂中以及对电场刺激(EFS)诱导的舒张作用,研究西地那非、伐地那非和他达拉非(1 nM至30 μmol)的作用。通过放射免疫测定法测定cGMP水平。

结果

在用NO供体DETA NONO - 酯(1 mmol)刺激后,尿道和血管平滑肌中的cGMP免疫反应性(IR)增强。在猪尿道平滑肌束之间存在广泛分布的cGMP和波形蛋白阳性间质细胞。在NO合酶IR内皮内也存在cGMP - IR。在尿道和血管平滑肌细胞内存在PDE - 5 IR,但在表达cGMP - IR的血管内皮细胞中也存在。在猪和人切片中,在α - 肌动蛋白IR尿道平滑肌细胞中存在强PKG1 - IR,这些细胞也含有cGMP的IR。西地那非、伐地那非和他达拉非引起猪尿道平均(标准误)浓度依赖性舒张,在30 μmol时,分别为自发张力的80(3)%(11个样本)、81(5)%(12个样本)和64(4)%(10个样本)。对于10 μmol西地那非,L - 去甲肾上腺素收缩的女性人尿道舒张为100%,对于30 μmol伐地那非和他达拉非分别为85(15)%和47(13)%(三个样本)。伐地那非或西地那非(30 μmol)使猪标本中的cGMP水平加倍。他达拉非对cGMP水平无影响。EFS(1 - 32 Hz)引起猪尿道肌肉的L - NG - 硝基精氨酸敏感舒张,通过抑制PDE - 5,其幅度和持续时间增加。在0.1 μmol时,西地那非、伐地那非或他达拉非在4 Hz时分别使舒张的平均(标准误)持续时间显著延长55(19)%、45(14)%和51(12)%。

结论

PDE - 5、cGMP和PKG1 - IR广泛分布于人和猪尿道组织中。在低浓度西地那非、伐地那非和他达拉非时,神经诱导的尿道制剂舒张增强,而在高浓度时,PDE - 5抑制剂具有直接的平滑肌舒张作用。抑制PDE - 5可能是促进cGMP介导的流出区域舒张的一个有意义的选择。

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