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Aging impairs Ca2+ sensitization pathways in gallbladder smooth muscle

机译:衰老损害胆囊平滑肌Ca 2 + 致敏途径

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摘要

Calcium sensitization is an important physiological process in agonist-induced contraction of smooth muscle. In brief, calcium sensitization is a pathway that leads to smooth muscle contraction independently of changes in [Ca2+]i by mean of inhibition of myosin light chain phosphatase. Aging has negative impacts on gallbladder contractile response due to partial impairment in calcium signaling and alterations in the contractile machinery. However, information regarding aging-induced alterations in calcium sensitization is scanty. We hypothesized that the calcium sensitization system is negatively affected by age. To investigate this, gallbladders were collected from adult (4 months old) and aged (22–24 months old) guinea pigs. To evaluate the contribution of calcium sensitization pathways we assayed the effect of the specific inhibitors Y-27632 and GF109203X on the “in vitro” isometric gallbladder contractions induced by agonist challenges. In addition, expression and phosphorylation (as activation index) of proteins participating in the calcium sensitization pathways were quantified by Western blotting. Aging reduced bethanechol- and cholecystokinin-evoked contractions, an effect associated with a reduction in MLC20 phosphorylation and in the effects of both Y-27632 and GF109203X. In addition, there was a drop in ROCK I, ROCK II, MYPT-1 and PKC expression and in the activation/phosphorylation of MYPT-1, PKC and CPI-17 in response to agonists. Interestingly, melatonin treatment for 4 weeks restored gallbladder contractile responses due to re-establishment of calcium sensitization pathways. These results demonstrate that age-related gallbladder hypocontractility is associated to alterations of calcium sensitization pathways and that melatonin treatment exerts beneficial effects in the recovery of gallbladder contractility.
机译:钙敏化是激动剂引起的平滑肌收缩的重要生理过程。简而言之,钙敏化是通过抑制肌球蛋白轻链磷酸酶而独立于[Ca 2 + ] i 的变化而导致平滑肌收缩的途径。由于钙信号传导的部分损伤和收缩机制的改变,衰老对胆囊的收缩反应具有负面影响。但是,关于衰老引起的钙敏化改变的信息很少。我们假设钙敏化系统受到年龄的负面影响。为了对此进行研究,从成年(4个月大)和成年(22-24个月大)豚鼠中收集胆囊。为了评估钙敏化途径的作用,我们分析了特定抑制剂Y-27632和GF109203X对激动剂激发引起的“体外”等距胆囊收缩的作用。另外,通过蛋白质印迹法定量了参与钙敏化途径的蛋白质的表达和磷酸化(作为活化指数)。衰老减少了乙二酚和胆囊收缩素引起的收缩,这是与MLC20磷酸化减少有关的影响,以及Y-27632和GF109203X的影响。另外,响应激动剂,ROCK I,ROCK II,MYPT-1和PKC的表达以及MYPT-1,PKC和CPI-17的激活/磷酸化都有所下降。有趣的是,由于钙敏化途径的重新建立,褪黑激素治疗4周恢复了胆囊收缩反应。这些结果表明,与年龄有关的胆囊收缩力降低与钙致敏途径的改变有关,褪黑激素治疗在恢复胆囊收缩力方面发挥有益作用。

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