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肌浆网在雪貂和大鼠心肌对酸中毒反应中的作用。

The role of the sarcoplasmic reticulum in the response of ferret and rat heart muscle to acidosis.

作者信息

Orchard C H

机构信息

Laboratory for Cardiovascular Studies, National Institutes of Health, Baltimore, MD 21224.

出版信息

J Physiol. 1987 Mar;384:431-49. doi: 10.1113/jphysiol.1987.sp016462.

Abstract
  1. The photoprotein aequorin was micro-injected into papillary muscles from the right ventricle of ferrets and rats. Tension and aequorin light (a function of intracellular [Ca2+]) were monitored. 2. In stimulated ferret papillary muscles, increasing the [CO2] of the bicarbonate-buffered superfusate from 5% (pH 7.35) to 20% (pH 6.8) led to a rapid decrease of developed tension, with no significant change in the size of the intracellular Ca2+ transient which accompanies contraction. There was then a small brief recovery of tension which was accompanied by a large brief increase in the size of the Ca2+ transient. Tension then declined again before recovering more slowly, with no significant change in the size of the Ca2+ transient. 3. The time course of the Ca2+ transient was prolonged on exposure to the acid solution, but shortened on continued exposure to the acid solution. Relaxation of twitch tension became faster on exposure to the acid solution, but slowed again on continued exposure to the acid solution. 4. In the presence of 10 mM-caffeine the size of the Ca2+ transient increased during the initial decline of developed tension, the short-lived recovery of tension was abolished, and the Ca2+ transient became smaller during the slower recovery of developed tension. 2 microM-ryanodine had similar effects on developed tension. 5. Addition of 10 mM-lactic acid to the superfusate produced changes similar to those described in 2 and 3 above. 6. An intracellular acidosis, produced by the addition and subsequent withdrawal of 20 mM-NH4Cl from the superfusate also caused changes similar to those described above. In the presence of caffeine, withdrawal of NH4Cl produced changes similar to those described in 4 above. 7. In unstimulated ferret papillary muscles, increasing superfusate [CO2] produced an increase of aequorin light when the bathing [Ca2+] was increased or in the presence of ouabain (10 microM). This increase was not inhibited by verapamil (5 microM), carbonyl cyanide p-trifluoromethoxyphenylhydrazone (1 microM) and oligomycin (2.5 microM), but was reduced by ryanodine (2 microM). 8. Rat papillary muscles showed responses which were quantitatively different from those observed in ferret papillary muscles: the initial recovery of tension developed more slowly, and sarcoplasmic reticulum (s.r.) inhibitors had a greater inhibitory effect on the recovery of tension. 9. It is concluded that the early decline of developed tension observed during acidosis is due to a decrease in Ca2+ release by the s.r. and a decrease in Ca2+ binding by the myofilaments.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 将光蛋白水母发光蛋白微量注射到雪貂和大鼠右心室的乳头肌中。监测张力和水母发光蛋白发出的光(细胞内[Ca2+]的一种功能)。2. 在受刺激的雪貂乳头肌中,将碳酸氢盐缓冲灌流液的[CO2]从5%(pH 7.35)增加到20%(pH 6.8)会导致所产生的张力迅速下降,而伴随收缩的细胞内Ca2+瞬变大小无显著变化。随后张力有一小段短暂的恢复,同时Ca2+瞬变大小有一大段短暂的增加。然后张力再次下降,之后恢复得更慢,Ca2+瞬变大小无显著变化。3. 暴露于酸性溶液时Ca2+瞬变的时间进程延长,但持续暴露于酸性溶液时缩短。暴露于酸性溶液时抽搐张力的松弛变快,但持续暴露于酸性溶液时又变慢。4. 在存在10 mM咖啡因的情况下,在张力最初下降期间Ca2+瞬变大小增加,短暂的张力恢复消失,并且在张力较慢恢复期间Ca2+瞬变变小。2 microM的兰尼碱对所产生的张力有类似作用。5. 向灌流液中添加10 mM乳酸产生的变化与上述2和3中描述的相似。6. 通过向灌流液中添加并随后去除20 mM氯化铵产生的细胞内酸中毒也引起与上述相似的变化。在存在咖啡因的情况下,去除氯化铵产生的变化与上述4中描述的相似。7. 在未受刺激的雪貂乳头肌中,当浴液[Ca2+]增加或存在哇巴因(10 microM)时,增加灌流液[CO2]会使水母发光蛋白发出的光增加。这种增加不受维拉帕米(5 microM)、羰基氰对三氟甲氧基苯腙(1 microM)和寡霉素(2.5 microM)的抑制,但被兰尼碱(2 microM)降低。8. 大鼠乳头肌表现出与在雪貂乳头肌中观察到的在数量上不同的反应:张力的初始恢复发展得更慢,并且肌浆网(s.r.)抑制剂对张力恢复的抑制作用更大。9. 得出结论,酸中毒期间观察到的所产生张力的早期下降是由于肌浆网Ca2+释放减少和肌丝Ca2+结合减少。(摘要截短至400字)

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