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豚鼠心室肌中肌动球蛋白 - ATP酶、Ca(2 +)-ATP酶和Na +,K(+)-ATP酶的能量消耗

The energy expenditure of actomyosin-ATPase, Ca(2+)-ATPase and Na+,K(+)-ATPase in guinea-pig cardiac ventricular muscle.

作者信息

Schramm M, Klieber H G, Daut J

机构信息

Physiologisches Insitut, Technischen Universität München, Germany.

出版信息

J Physiol. 1994 Dec 15;481 ( Pt 3)(Pt 3):647-62. doi: 10.1113/jphysiol.1994.sp020471.

DOI:10.1113/jphysiol.1994.sp020471
PMID:7707233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1155908/
Abstract
  1. The rate of heat production (heat rate) and isometric twitch tension of ventricular trabeculae isolated from guinea-pig heart were measured at 37 degrees C in order to determine the relative contributions of actomyosin-ATPase, Ca(2+)-ATPase and Na+,K(+)-ATPase to myocardial energy metabolism. 2. The increase in heat rate recorded during isometric contractions at optimal length (contraction-related heat production) was 19.1 +/- 1.2 mW cm-3 at a stimulation rate of 2 Hz. The tension-time integral of individual contractions measured under the same conditions was 147 +/- 15 mM s cm-2. 3. The heat production of the actomyosin-ATPase was determined by inhibiting the contractile proteins with 2,3-butanedione monoxime (BDM). Contraction-related heat production was reduced by 0.219 +/- 0.010 and the isometric tension-time integral was reduced by 0.288 +/- 0.016 in the presence of 1 mM BDM. From these data an estimate of 0.76 for the relative contribution of the actomyosin-ATPase to contraction-related heat production was derived. 4. The heat production related to actomyosin-ATPase plus Ca(2+)-ATPase was studied by blocking Ca2+ influx into the myocardial cells with a solution containing 100 microM Ca2+ and 400 microM Ni2+. In this solution contraction-related heat production was reduced by 0.907 +/- 0.012. Comparison of this value with the component attributable to the actomyosin-ATPase yields an estimate of 0.15 for the relative contribution of the Ca(2+)-ATPase to contraction related heat production. 5. The heat production related to the Na+,K(+)-ATPase in resting preparations was studied by blocking the sodium pump with 400 microM dihydro-ouabain (DHO). DHO produced a transient decrease in heat rate lasting 1-2 min, which was followed by a secondary increase. From the heat transient produced by DHO the heat rate related to the Na+,K(+)-ATPase in the steady state was extrapolated. The relative contribution of the sodium pump to resting heat production was estimated to be 0.17. 6. The heat production related to the Na+,K(+)-ATPase in contracting preparations was studied by first blocking Ca2+ influx with 100 microM Ca2+ and 400 microM Ni2+, and then inhibiting the sodium pump with 400 microM dihydro-ouabain (DHO). The relative contribution of the sodium pump to contraction-related heat production extrapolated from these data was 0.10, which agreed well with the fraction of contraction-related heat production persisting after blockage of actomyosin-ATPase and Ca(2+)-ATPase (0.09).(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 为了确定肌动球蛋白 - ATP酶、Ca(2 +)-ATP酶和Na +,K(+)-ATP酶对心肌能量代谢的相对贡献,在37摄氏度下测量了从豚鼠心脏分离出的心室小梁的产热速率(热率)和等长收缩张力。2. 在2赫兹的刺激频率下,等长收缩在最佳长度时记录到的热率增加(收缩相关产热)为19.1±1.2毫瓦/立方厘米。在相同条件下测量的单个收缩的张力 - 时间积分是147±15毫摩尔·秒/平方厘米。3. 用2,3 - 丁二酮一肟(BDM)抑制收缩蛋白来测定肌动球蛋白 - ATP酶的产热。在1毫摩尔BDM存在下,收缩相关产热降低了0.219±0.010,等长张力 - 时间积分降低了0.288±0.016。从这些数据得出,肌动球蛋白 - ATP酶对收缩相关产热的相对贡献估计为0.76。4. 用含有100微摩尔Ca2 +和400微摩尔Ni2 +的溶液阻断Ca2 +流入心肌细胞,研究与肌动球蛋白 - ATP酶加Ca(2 +)-ATP酶相关的产热。在这种溶液中,收缩相关产热降低了0.907±0.012。将该值与归因于肌动球蛋白 - ATP酶的部分进行比较,得出Ca(2 +)-ATP酶对收缩相关产热的相对贡献估计为0.15。5. 用400微摩尔二氢哇巴因(DHO)阻断钠泵,研究静息制剂中与Na +,K(+)-ATP酶相关的产热。DHO使热率短暂降低持续1 - 2分钟,随后是二次升高。从DHO产生的热瞬变推断出稳态下与Na +,K(+)-ATP酶相关的热率。钠泵对静息产热的相对贡献估计为0.17。6. 首先用100微摩尔Ca2 +和400微摩尔Ni2 +阻断Ca2 +流入,然后用400微摩尔二氢哇巴因(DHO)抑制钠泵,研究收缩制剂中与Na +,K(+)-ATP酶相关的产热。从这些数据推断出钠泵对收缩相关产热的相对贡献为0.10,这与肌动球蛋白 - ATP酶和Ca(2 +)-ATP酶被阻断后持续的收缩相关产热部分(0.09)非常吻合。(摘要截短为400字)
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b304/1155908/ce8308114dbf/jphysiol00335-0118-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b304/1155908/ce8308114dbf/jphysiol00335-0118-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b304/1155908/ce8308114dbf/jphysiol00335-0118-a.jpg

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