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首页> 外文期刊>Neurourology and urodynamics. >Changes in intracellular calcium concentration and P2X1 receptor expression in hypertrophic rat urinary bladder smooth muscle.
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Changes in intracellular calcium concentration and P2X1 receptor expression in hypertrophic rat urinary bladder smooth muscle.

机译:肥厚大鼠膀胱平滑肌细胞内钙浓度和P2X1受体表达的变化。

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摘要

AIMS: Contractile responses to purinergic activation in the urinary bladder are altered in outflow obstruction (O). We determined if the lowered contractile response to adenosine triphosphate (ATP) in obstructed rat urinary bladder was due to changes in calcium handling or in P2X1 purinoceptor density. MATERIALS AND METHODS: O was created in rat by partial ligature of the urethra, with non-obstructed rats as controls (C). Force and intracellular calcium were measured in bladder strips activated with ATP. Tissue was sectioned for light and electron microscopy and analyzed with Western blot using a P2X1 antibody. RESULTS: Bladder weight increased from 66 +/- 3 (C) to 206 +/- 17 mg (O) (n = 6). ATP gave a transient contractile response which was decreased in the obstructed strips (C: 161 +/- 20; O: 63 +/- 16% of high-K+ force). Intracellular calcium concentration after ATP activation in the obstructed bladder muscle was about 50% of that in the control preparations (C: 669 +/- 110; O: 335 +/- 59 nM). Half-time for calcium influx was increased in the O group. P2X1 immunoreactivity per unit bladder weight was similar in the two groups. Cell membrane area per unit wet weight was decreased in the O group. CONCLUSIONS: Attenuated contractile responses to ATP in obstructed rat urinary bladder are due to a lowered rate of calcium influx and maximal peak calcium concentration. This change in Ca2+transients is not due to a decrease in P2X1 receptor density in the smooth muscle cell membranes. Possibly, the increase in cell volume buffers the rapid and transient influx of Ca2+ following purinoceptor activation in the obstructed bladder.
机译:目的:对尿液中嘌呤能激活的收缩反应在流出道梗阻(O)中有所改变。我们确定阻塞的大鼠膀胱中对三磷酸腺苷(ATP)的收缩反应降低是否是由于钙处理或P2X1嘌呤受体密度的变化所致。材料与方法:O是通过尿道的部分结扎在大鼠中产生的,未阻塞的大鼠作为对照(C)。在用ATP激活的膀胱试纸中测量力和细胞内钙。将组织切片以进行光镜和电子显微镜检查,并使用P2X1抗体通过Western blot分析。结果:膀胱重量从66 +/- 3(C)增加到206 +/- 17 mg(O)(n = 6)。 ATP产生短暂的收缩反应,在阻塞的条带中降低(C:161 +/- 20; O:高K +力的63 +/- 16%)。 ATP激活后,梗阻性膀胱肌的细胞内钙浓度约为对照制剂的50%(C:669 +/- 110; O:335 +/- 59 nM)。 O组中钙渗透的半衰期增加。两组每单位膀胱重量的P2X1免疫反应性相似。 O组中每单位湿重的细胞膜面积减少。结论:梗阻大鼠膀胱对ATP的收缩反应减弱是由于钙流入速率降低和最大钙峰值浓度所致。 Ca2 +瞬态变化不是由于平滑肌细胞膜中P2X1受体密度降低所致。在阻塞性膀胱中嘌呤受体激活后,细胞体积的增加可能会缓冲Ca2 +的快速和短暂流入。

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