首页> 外文期刊>American Journal of Physiology >Effects of chronic hypoxia on Ca2+ mobilization and Ca2+ sensitivity of myofilaments in uterine arteries.
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Effects of chronic hypoxia on Ca2+ mobilization and Ca2+ sensitivity of myofilaments in uterine arteries.

机译:慢性低氧对子宫动脉肌丝Ca2 +动员和Ca2 +敏感性的影响。

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The effect of chronic hypoxia on free intracellular Ca2+ concentration ([Ca2+]i) and Ca2+ sensitivity of myofilaments during agonist stimulation was examined in uterine arteries obtained from normoxic and chronically hypoxic pregnant sheep maintained at high altitude (3,820 m) for approximately 110 days. Smooth muscle [Ca2+]i was measured simultaneously with muscle contraction in the same intact tissue. Whereas both KCl and 5-HT increased [Ca2+]i and tension simultaneously in the uterine artery, 5-HT produced significantly greater contractile tension (in g) than KCl at a given amount of [Ca2+]i as indicated by the ratio of fura 2 fluorescence intensity induced by excitation at 340 nm to that induced at 380 nm (29.8 +/- 6.9 vs. 16.9 +/- 4.0, P < 0.05). Chronic hypoxia did not change KCl-induced contractions, nor did it affect KCl-mediated increases in [Ca2+]i. In contrast, chronic hypoxia significantly inhibited 5-HT-induced contractions and decreased the 5-HT-stimulated increase in [Ca2+]i (pD2 7.46 +/- 0.18-->6.86 +/- 0.11, P < 0.05, where pD2 is -log half-maximal effective concentration) in uterine arteries. In addition, the slope (g tensionM [Ca2+]i) of the 5-HT-mediated [Ca2+]i-tension relationship was significantly decreased in chronically hypoxic arteries (0.024 +/- 0.002-->0.013 +/- 0.001, P < 0.01). The results suggest that chronic hypoxia suppresses agonist-mediated Ca2+ homeostasis in uterine arteries by inhibiting Ca2+ mobilization and the agonist-enhanced Ca2+ sensitivity of myofilaments.
机译:在维持高海拔(3,820 m)约110天的常氧和慢性低氧妊娠绵羊的子宫动脉中,研究了慢性低氧对激动剂刺激过程中肌丝游离细胞内Ca2 +浓度([Ca2 +] i)和Ca2 +敏感性的影响。在同一完整组织中同时测量平滑肌[Ca2 +] i和肌肉收缩。 KCl和5-HT会同时增加子宫动脉中的[Ca2 +] i和张力,而给定[Ca2 +] i量时,5-HT的收缩张力(以克为单位)比KCl大得多,如呋喃比所表明的2在340 nm处激发到380 nm处激发的荧光强度(29.8 +/- 6.9对16.9 +/- 4.0,P <0.05)。慢性缺氧既不改变KCl诱导的收缩,也不影响KCl介导的[Ca2 +] i的增加。相比之下,慢性低氧显着抑制了5-HT诱导的收缩,降低了5-HT刺激的[Ca2 +] i的增加(pD2 7.46 +/- 0.18-> 6.86 +/- 0.11,P <0.05,其中pD2为-log半数最大有效浓度)。此外,在慢性低氧动脉中,5-HT介导的[Ca2 +] i-张力关系的斜率(g张力/ nM [Ca2 +] i)显着降低(0.024 +/- 0.002-> 0.013 +/- 0.001 ,P <0.01)。结果表明,慢性低氧通过抑制Ca2 +的动员和肌丝的激动剂增强的Ca2 +敏感性来抑制激动剂介导的子宫动脉Ca2 +稳态。

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