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Characteristics of the bradykinin-induced changes in intracellular calcium ion concentration of single bovine tracheal smooth muscle cells.

机译:缓激肽诱导的牛单支气管平滑肌细胞胞内钙离子浓度变化的特征。

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摘要

1. Single bovine tracheal smooth muscle (BTSM) cells were cultured and used to measure bradykinin-induced changes in [Ca2+]i by dynamic video imaging. 2. Bradykinin (10 pM-10 microM)-induced an increase in [Ca2+]i over basal levels (69 +/- 2 nM; n = 353) which was concentration-dependent (log EC50 = -8.7 M) in the presence of extracellular calcium ions (2 mM). The bradykinin B2 receptor antagonist, D-Arg[Hyp3,Thi5,8,D-Phe7]- bradykinin, produced a parallel shift to the right of the bradykinin concentration-response curve (log EC50 = -7.1 M and -5.8 M in the presence of 1 microM and 10 microM antagonist respectively) yielding an apparent KD of 26 nM. 3. In the absence of extracellular calcium ions (with 0.1 mM EGTA), bradykinin (10 pM-10 microM) produced a uniform increase in [Ca2+]i from a basal level of 33 +/- 2 nM (n = 140) to approximately 180 nM in BTSM cells indicating an 'all-or-nothing' release of intracellular calcium ions. In the presence of 10 microM D-Arg[Hyp3,Thi5,8,D-Phe7]-bradykinin no responses could be induced by bradykinin at concentrations below 100 nM. However, at 100 nM and 1 microM bradykinin there was no change in the uniform increase in [Ca2+]i in these cells previously observed. 4. In both the absence or presence of D-Arg[Hyp3,Thi5,8,D-Phe7]-bradykinin, there was a concentration-dependent increase in the percentage of cells responding to bradykinin (frequency) under calcium-rich or calcium-free conditions. Individual cells also demonstrated a difference in the sensitivity to any particular concentration of bradykinin.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.培养单个牛气管平滑肌(BTSM)细胞,并通过动态视频成像测量缓激肽诱导的[Ca2 +] i变化。 2.缓激肽(10 pM-10 microM)诱导[Ca2 +] i超过基础水平(69 +/- 2 nM; n = 353)的增加,该水平是浓度依赖性的(log EC50 = -8.7 M)细胞外钙离子(2 mM)。缓激肽B2受体拮抗剂D-Arg [Hyp3,Thi5,8,D-Phe7]-缓激肽在缓激肽浓度-反应曲线的右侧产生了一个平行位移(log EC50 = -7.1 M和-5.8 M在(分别存在1 microM和10 microM拮抗剂)产生的表观KD为26 nM。 3.在缺乏细胞外钙离子(含0.1 mM EGTA)的情况下,缓激肽(10 pM-10 microM)使[Ca2 +] i从基础水平的33 +/- 2 nM(n = 140)均匀增加至BTSM细胞中大约180 nM,表明细胞内钙离子“全部或全部释放”。在存在10 microM D-Arg [Hyp3,Thi5,8,D-Phe7]-缓激肽的情况下,缓激肽在低于100 nM的浓度下不会诱导应答。但是,在100 nM和1 microM缓激肽中,先前观察到的这些细胞中[Ca2 +] i的均匀增加没有变化。 4.在缺乏或存在D-Arg [Hyp3,Thi5,8,D-Phe7]-缓激肽的情况下,在富含钙或钙的情况下,响应缓激肽的细胞百分比(频率)呈浓度依赖性增加无条件。个别细胞还显示出对任何特定浓度的缓激肽敏感性的差异。(摘要截短为250字)

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    Marsh, K. A.; Hill, S. J.;

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  • 年度 1993
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