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雷诺丁揭示了血管平滑肌中的多种收缩和舒张机制:利用fura-2同步测量机械活性和细胞质游离钙离子水平。

Ryanodine reveals multiple contractile and relaxant mechanisms in vascular smooth muscle: simultaneous measurements of mechanical activity and of cytoplasmic free Ca2+ level with fura-2.

作者信息

Hisayama T, Takayanagi I, Okamoto Y

机构信息

Department of Chemical Pharmacology, Toho University School of Pharmaceutical Sciences, Chiba, Japan.

出版信息

Br J Pharmacol. 1990 Aug;100(4):677-84. doi: 10.1111/j.1476-5381.1990.tb14075.x.

DOI:10.1111/j.1476-5381.1990.tb14075.x
PMID:2119840
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917603/
Abstract
  1. The effects of ryanodine on changes in cytoplasmic Ca2+ level ([Ca2+]i) and muscle tension induced by maximum concentrations of phenylephrine (Phe; 1 microM), prostaglandin F2 alpha (PGF2 alpha, 10 microM), caffeine (Caf, 30 mM) and isoprenaline (Iso, 1 microM) were examined in rat aortic strips using fura-2. 2. In normal media, Phe and PGF2 alpha produced a phasic contraction, followed by a tonic one. Caf elicited only a transient contraction. When the preparation was treated with 10 microM ryanodine, an increase in [Ca2+]i was induced accompanied by a nicardipine (1 microM)-resistant contraction which was [Ca2+]o-dependent. 3. In Ca2(+)-free solution, the three stimulants elicited transient increases in [Ca2+]i. Transient contractions to Phe and Caf were accompanied by changes in [Ca2+]i. The transient increase in [Ca2+]i induced by PGF2 alpha was not accompanied by a corresponding contraction. 4. Sustained contractions were induced by Phe and PGF2 alpha in the absence of external Ca2+, while the increase in [Ca2+]i was reduced. A larger maximum contraction was induced by PGF alpha than by Phe. 5. Ryanodine abolished both the Caf- and Phe-induced [Ca2+]i transient increases and the corresponding contractions, but had no substantial effect on the PGF2 alpha-induced [Ca2+]i transient increase. Ryanodine had no influence on the sustained contractions induced by Phe and PGF2 alpha. 6. Iso relaxed both sustained contractions almost completely, without any detectable change in [Ca2+]i. Treatment of the preparation with ryanodine had no effect on the concentration-response curves for Iso in relaxing the 0.1 microM Phe- or 40 mM K(+)-induced precontraction. 7. It is suggested that Phe and Caf mobilize Ca2 + from a ryanodine-sensitive Ca2 + store and that PGF2 alpha. releases Ca2+ from a ryanodine-insensitive Ca2+ store. The former contributes to the transient contraction through a Ca2'-dependent process, while the latter seems not to be directly associated with the contraction. The sustained contraction under Ca2+-free conditions might involve a Ca2 '-independent process or a change in the sensitivity of the contractile filaments to Ca2 + 8. In addition to lowering cytoplasmic Ca2+ concentration, it is suggested that Iso counteracts the apparently Ca2 +-independent process. The ryanodine-sensitive Ca2+ store plays no substantial role in active relaxation by Iso, although it does play a major role in the maintenance of cytoplasmic Ca2+ in a quiescent muscle.
摘要
  1. 使用fura-2在大鼠主动脉条中检测了ryanodine对最大浓度的去氧肾上腺素(Phe;1微摩尔)、前列腺素F2α(PGF2α,10微摩尔)、咖啡因(Caf,30毫摩尔)和异丙肾上腺素(Iso,1微摩尔)诱导的细胞质Ca2+水平([Ca2+]i)变化和肌肉张力的影响。2. 在正常培养基中,Phe和PGF2α产生一个相性收缩,随后是一个强直性收缩。Caf仅引起一个短暂收缩。当制剂用10微摩尔ryanodine处理时,诱导[Ca2+]i增加,同时伴有硝苯地平(1微摩尔)抵抗性收缩,该收缩依赖于[Ca2+]o。3. 在无Ca2+溶液中,三种刺激物引起[Ca2+]i短暂增加。对Phe和Caf的短暂收缩伴有[Ca2+]i变化。PGF2α诱导的[Ca2+]i短暂增加不伴有相应收缩。4. 在无外部Ca2+时,Phe和PGF2α诱导持续性收缩,而[Ca2+]i增加减少。PGFα诱导的最大收缩比Phe大。5. Ryanodine消除了Caf和Phe诱导的[Ca2+]i短暂增加及相应收缩,但对PGF2α诱导的[Ca2+]i短暂增加无实质性影响。Ryanodine对Phe和PGF2α诱导的持续性收缩无影响。6. Iso几乎完全松弛了两种持续性收缩,[Ca2+]i无任何可检测到的变化。用ryanodine处理制剂对Iso松弛0.1微摩尔Phe或40毫摩尔K+诱导的预收缩的浓度 - 反应曲线无影响。7. 提示Phe和Caf从ryanodine敏感的Ca2+储存库中动员Ca2+,而PGF2α从ryanodine不敏感的Ca2+储存库中释放Ca2+。前者通过Ca2+依赖过程导致短暂收缩,而后者似乎与收缩无直接关联。无Ca2+条件下的持续性收缩可能涉及Ca2+非依赖过程或收缩细丝对Ca2+敏感性的变化。8. 除了降低细胞质Ca2+浓度外,提示Iso抵消了明显的Ca2+非依赖过程。ryanodine敏感的Ca2+储存库在Iso的主动松弛中不起实质性作用,尽管它在静息肌肉中细胞质Ca2+的维持中起主要作用。

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