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Cyclic nucleotide phosphodiesterases in rabbit detrusor smooth muscle.

机译:兔逼尿肌平滑肌中的环状核苷酸磷酸二酯酶。

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OBJECTIVES: To identify the phosphodiesterase (PDE) isoenzymes in the rabbit detrusor and to evaluate their roles in regulating detrusor muscular tone. Cyclic nucleotides are important secondary messengers involved in modulating the contractility of various smooth muscles. Cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) are synthesized by their respective cyclases and degraded by various PDEs. METHODS: PDE isoenzymes from male and female rabbit detrusor were isolated by the Mono-Q anion exchange column and identified with various inhibitors. Detrusor strips from both sexes were precontracted with carbachol and relaxed with PDE inhibitors and adenylate and guanylyl cyclase activators in a tissue bath. Cyclic nucleotide concentrations in strips from male rabbits were determined after the compound treatment. RESULTS: Similar results were obtained from both sexes in the experiments in which both sexes were used. The activities of PDE1, 2, 3, 4, and 5 were identified. Forskolin induced a dramatic rise in the cAMP levels and was the most effective relaxant. Papaverine generated moderate increases in the cAMP and cGMP levels and induced very good relaxation. Vinpocetine produced no detectable changes in the cyclic nucleotide levels but elicited good relaxation. Sildenafil caused an increase in the cGMP levels and had a similar relaxation effect as vinpocetine. Sodium nitroprusside induced some increase in cGMP and had no relaxation effect. Rolipram raised the cAMP levels significantly, yet had a moderate effect on relaxation. CONCLUSIONS: Our results demonstrated the presence of PDE1 through 5 in rabbit detrusor muscle and supported their involvement in regulating detrusor muscle tone. The relaxation of rabbit detrusor was mainly mediated by the cAMP pathway.
机译:目的:鉴定兔逼尿肌中的磷酸二酯酶(PDE)同工酶,并评估其在调节逼尿肌肌张力中的作用。环核苷酸是重要的二级信使,涉及调节各种平滑肌的收缩能力。环状腺苷单磷酸酯(cAMP)和环状鸟苷单磷酸酯(cGMP)由它们各自的环化酶合成,并被各种PDE降解。方法:通过Mono-Q阴离子交换柱分离雄性和雌性兔逼尿肌的PDE同工酶,并用各种抑制剂进行鉴定。将两性逼尿肌条与卡巴胆碱预收缩,并在组织浴中与PDE抑制剂,腺苷酸和鸟苷酸环化酶激活剂一起放松。复合处理后,测定雄性兔子试条中的环核苷酸浓度。结果:在使用两种性别的实验中,两种性别都获得了相似的结果。确定了PDE1、2、3、4和5的活动。福斯高林诱导cAMP水平急剧上升,是最有效的放松剂。罂粟碱使cAMP和cGMP水平适度增加,并引起非常良好的放松。长春西汀在环状核苷酸水平上未产生可检测的变化,但引起良好的松弛。西地那非引起cGMP水平升高,并具有与长春西汀类似的舒张作用。硝普钠可诱导cGMP升高,并且没有松弛作用。咯利普兰显着提高了cAMP的水平,但对放松有中等程度的作用。结论:我们的研究结果表明,兔逼尿肌中存在PDE1至5,并支持它们参与调节逼尿肌张力。兔逼尿肌的舒张主要由cAMP途径介导。

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