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内源性胺类在豚鼠心室自律性调节中的生理作用

Physiological role of endogenous amines in the modulation of ventricular automaticity in the guinea-pig.

作者信息

Hume J, Katzung B G

出版信息

J Physiol. 1980 Dec;309:275-86. doi: 10.1113/jphysiol.1980.sp013508.

Abstract
  1. Current-clamp experiments were carried out with guinea-pig papillary muscles to determine the dependence of depolarization-induced automaticity on endogenous catecholamines. 2. Catecholamine depletion was produced by pre-treatment of animals with 6-hydroxydopamine and confirmed by fluorimetric assay of right ventricular tissue. Papillary muscles from depleted animals demonstrated a marked suppression of depolarization-induced automaticity for maximum diastolic potentials less negative than -55 mV. This suppression was completely reversed by noradrenaline but not by tyramine. 3. In normal tissue, noradrenaline and tyramine had much smaller effects on automaticity arising from maximum diastolic potentials negative to -55 mV than on repetitive activity arising positive to this level. 4. L-propranolol in concentrations of 2-3 x 10(-7) M reduced repetitive activity in the less negative range of maximum diastolic potential. No evidence of direct membrane depression was observed at these doses and the effect was reversed by application of noradrenaline. 5. D-propranolol, the isomer with much lower beta-receptor blocking potency, required twentyfold higher concentrations to depress automaticity and this was accompanied by evidence of direct membrane depression, i.e. reduction of upstroke velocity of action potentials. 6. These results show that automaticity induced in guinea-pig papillary muscles by depolarization positive to -55 mV is strongly dependent upon endogenous catecholamines. 7. The hypothesis that endogenous catecholamines facilitate depolarization-induced automaticity through an increase in calcium conductance was modelled using numerical techniques. It was found that changes in calcium conductance caused changes in the model which closely parallelled the experimental effects of catecholamine depletion and beta-blockade. The effects of changes in delayed rectification in the model did not accurately reproduce the experimental results.
摘要
  1. 采用豚鼠乳头肌进行电流钳实验,以确定去极化诱导的自律性对内源性儿茶酚胺的依赖性。2. 通过用6-羟基多巴胺预处理动物来产生儿茶酚胺耗竭,并通过对右心室组织进行荧光测定来证实。来自儿茶酚胺耗竭动物的乳头肌在最大舒张电位小于-55 mV时,去极化诱导的自律性受到明显抑制。这种抑制可被去甲肾上腺素完全逆转,但不能被酪胺逆转。3. 在正常组织中,去甲肾上腺素和酪胺对最大舒张电位为-55 mV负向时产生的自律性的影响,比对该水平正向时产生的重复活动的影响小得多。4. 浓度为2-3×10(-7) M的L-普萘洛尔可降低最大舒张电位较负范围内的重复活动。在这些剂量下未观察到直接膜抑制的证据,且该效应可通过应用去甲肾上腺素逆转。5. D-普萘洛尔,一种β受体阻断效力低得多的异构体,需要高20倍的浓度来抑制自律性,但这伴随着直接膜抑制的证据,即动作电位上升速度降低。6. 这些结果表明,豚鼠乳头肌中由大于-55 mV的去极化诱导的自律性强烈依赖于内源性儿茶酚胺。7. 利用数值技术对以下假设进行了建模:内源性儿茶酚胺通过增加钙电导促进去极化诱导的自律性。结果发现,钙电导的变化导致模型中的变化,这与儿茶酚胺耗竭和β受体阻断的实验效应密切平行。模型中延迟整流变化的效应不能准确再现实验结果。

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Optical isomers of propranolol.普萘洛尔的光学异构体。
Nature. 1966 Jun 25;210(5043):1336-8. doi: 10.1038/2101336a0.

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