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哇巴因对哺乳动物心室肌细胞间偶联和传导速度的作用。

The actions of ouabain on intercellular coupling and conduction velocity in mammalian ventricular muscle.

作者信息

Weingart R

出版信息

J Physiol. 1977 Jan;264(2):341-65. doi: 10.1113/jphysiol.1977.sp011672.

Abstract
  1. The effects of ouabain on the electrical coupling between cells and the conduction velocity, theta, were studied in ventricular muscle preparations from calf and cow hearts using a silicon-oil-chamber. 2. After 90 min of exposure to 2 X 10(-6) M ouabain, an increase of the inside longitudinal resistance, Ri, from 420 omega cm to 1032 omega CM was observed. Assuming a constant myoplasmic resistivity this presumably reflects a reduced electrical coupling between myocardial cells. 3. Concomitantly, theta was decreased from 50-3 to 29-4 cm/sec. This change could be explained by the observed alterations in the maximal rate of rise of the action potential, (dV/dt)max, the amplitude of the action potential Vp, the membrane capacity Cf, and the sum, respectively, of the inside and outside longitudinal resistance per unit distance (ri + ro). Quantitatively, about 60% of the decrease of theta could be accounted for by the experimentally determined increase of Ri. 4. Time course studies revealed a biphasic action of ouabain on Ri. An early dose-dependent drop in Ri, equivalent to an improvement of the intercellular coupling, was followed by a delayed massive increase in Ri, whose onset and magnitude were also concentration-dependent. 5. The delayed increase in Ri was associated with an increase of the diastolic tension. Toxic ouabain doses (2 X 10(-6) M) produced irreversible changes on both parameters, whereas thereapeutic doses (less than 5 X 10(-7) M) affected neither of them. Reversible effects on both parameters were observed at an intermediate drug concentration (10(-6) M). 6. The strong correlation between decoupling and contracture is consistent with the idea that the intracellular Ca concentration, [Ca]i, is involved in the control of the nexal conductance. This is supported by the finding that increasing the extracellular Ca concentration, [Ca]o, accelerated the ouabain-induced decoupling, whereas reducing [Ca]o retarded it. 7. If anything, the contracture slightly preceded the increase in Ri. From this it is concluded that the threshold [Ca]i for the electrical decoupling between cells must be somewhat larger than the threshold level for the tension activation. 8. The delayed increase in Ri is compatible with an inhibition of the Na pump which according to the Na-lag hypothesis predicts an increase of [Ca]i secondary to a Na-accumulation. The early drop in Ri can either be explained by a stimulation of the Na pump, or by a non-monotonic relationship between Ri and [Ca]i.
摘要
  1. 使用硅油室,研究了哇巴因对小牛和母牛心脏心室肌标本中细胞间电偶联和传导速度θ的影响。2. 在暴露于2×10⁻⁶ M哇巴因90分钟后,观察到内部纵向电阻Ri从420Ω·cm增加到1032Ω·cm。假设肌浆电阻率恒定,这大概反映了心肌细胞间电偶联的降低。3. 同时,θ从50 - 3 cm/sec降至29 - 4 cm/sec。这种变化可以用动作电位最大上升速率(dV/dt)max、动作电位幅度Vp、膜电容Cf以及每单位距离内外纵向电阻之和(ri + ro)的观察变化来解释。从数量上看,θ降低的约60%可由实验确定的Ri增加来解释。4. 时间进程研究揭示了哇巴因对Ri的双相作用。早期Ri呈剂量依赖性下降,相当于细胞间偶联的改善,随后是Ri的延迟大幅增加,其起始和幅度也呈浓度依赖性。5. Ri的延迟增加与舒张张力的增加有关。中毒剂量的哇巴因(2×10⁻⁶ M)对这两个参数产生不可逆变化,而治疗剂量(小于5×10⁻⁷ M)对它们均无影响。在中间药物浓度(10⁻⁶ M)下观察到对这两个参数的可逆作用。6. 去偶联与挛缩之间的强相关性与细胞内钙浓度[Ca]i参与连接电导控制的观点一致。细胞外钙浓度[Ca]o增加加速了哇巴因诱导的去偶联,而降低[Ca]o则使其延迟,这一发现支持了这一观点。7. 如果有什么不同的话,挛缩略先于Ri的增加。由此得出结论,细胞间电去偶联的[Ca]i阈值必须略大于张力激活的阈值水平。8. Ri的延迟增加与钠泵的抑制相一致,根据钠延迟假说,这预示着由于钠积累导致[Ca]i增加。Ri的早期下降要么可以用钠泵的刺激来解释,要么可以用Ri与[Ca]i之间的非单调关系来解释。

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