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Increased adrenergic contractility and decreased mRNA expression of NOS III in aging rat urinary bladders.

机译:在衰老的大鼠膀胱中,肾上腺素能收缩力增加,NOS III mRNA表达降低。

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Our objective was to study age-related changes in adrenergic contractility and gene expression profile in the rat urinary bladder. Young (3-month old), adult (10-month old) and senescent (30-month old) male WAG/Rij rats were used. Gene expression profile in the rat urinary bladder was defined using Atlas microarray technology. In vitro contractile responses induced by KCl, phenylephrine (PHE) and norepinephrine (NE) were compared in isolated urinary bladders dissected from young, adult and senescent rats. Among a total of 1176 genes present on the arrays, 15 genes showed an increase in expression and 10 genes a decrease with age. Four genes related to nerve growth factor were upregulated whereas NOS type III was downregulated in aging rats. Intrinsic contractility of isolated rat urinary bladders was not changed between adult and aging rats as judged by the response curves to KCl. In contrast, an age-related increase in the maximal contractile responses to NE, but not PHE, was noticed (13 +/- 1, 48 +/-2% and 59 +/- 2% at 3, 10 and 30 months, respectively). The alpha1D-adrenoceptor antagonist BMY7378 antagonized NE-induced contractions with low potency in both groups suggesting the involvement of the alpha1A-adrenoceptor subtype. This was confirmed by microarray, which demonstrated mRNA expression for the alpha1A-adrenoceptor subtype only. These results suggest that aging of the urinary bladder is associated with an increase in the maximal contractile response to NE which could be due to NO shortage resulting from downregulation of urothelial NOS III.
机译:我们的目的是研究大鼠膀胱中肾上腺素能收缩性和基因表达谱的年龄相关变化。使用年轻的(3个月大),成年的(10个月大)和衰老的(30个月大)雄性WAG / Rij大鼠。使用阿特拉斯微阵列技术定义了大鼠膀胱中的基因表达谱。比较了由KCl,去氧肾上腺素(PHE)和去甲肾上腺素(NE)诱导的体外收缩反应,该实验是从年轻,成年和衰老大鼠解剖的分离膀胱中进行的。在阵列上存在的总共1176个基因中,有15个基因显示表达增加,而10个基因随年龄下降。在衰老大鼠中,与神经生长因子相关的四个基因被上调,而第三型NOS被下调。根据对KCl的反应曲线判断,成年和成年大鼠之间离体大鼠膀胱的内在收缩力没有变化。相反,注意到与年龄相关的对NE的最大收缩反应增加,但对PHE则没有(在3、10和30个月时分别为13 +/- 1、48 +/- 2%和59 +/- 2%,分别)。在两组中,α1D-肾上腺素受体拮抗剂BMY7378拮抗NE诱导的收缩,但效能低下,提示α1A-肾上腺素受体亚型的参与。这由微阵列证实,其仅显示了α1A-肾上腺素受体亚型的mRNA表达。这些结果表明,膀胱的衰老与对NE的最大收缩反应的增加有关,这可能是由于尿路上皮NOS III下调引起的NO缺乏。

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