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α1肾上腺素能受体降低兔心室肌细胞的背景钾电流。

Alpha 1-adrenoceptors reduce background K+ current in rabbit ventricular myocytes.

作者信息

Fedida D, Braun A P, Giles W R

机构信息

Department of Medical Physiology, University of Calgary, Alberta, Canada.

出版信息

J Physiol. 1991 Sep;441:673-84. doi: 10.1113/jphysiol.1991.sp018772.

Abstract
  1. Ventricular myocytes were isolated by enzymatic dispersion of adult rabbit hearts, and voltage clamped using the whole-cell variation of the patch clamp technique. Experiments were carried out at either 35 degrees C or room temperature (21-23 degrees C). 2. In the presence of 10(-3) M-4-aminopyridine to block the transient outward K+ current, and 10(-6) M-propranolol to block beta-adrenoceptors, the alpha 1-adrenergic agonist methoxamine produced action potential prolongation, and a small depolarization of the diastolic membrane potential. Under voltage clamp conditions, methoxamine decreased the magnitude of the inward rectifier K+ current, IK1, in both the inward and outward directions. This effect was dose dependent (10(-5)-10(-3) M) and fully reversible upon wash-out of the agonist. 3. The neurotransmitter noradrenaline (10(-6)-2 x 10(-5) M), in the presence of propranolol (10(-6) M), also reduced IK1 in ventricular cells, and this effect was blocked by the specific alpha 1-adrenoceptor antagonist prazosin. 4. The alpha 1-adrenoceptor-mediated decrease in IK1 in ventricular myocytes was not affected by pre-incubation of the cells with 0.5 micrograms/ml pertussis toxin (8-10 h, 30-32 degrees C). This result suggests that in rabbit ventricular cells, the alpha 1-modulation of IK1 occurs via a pertussis toxin-insensitive guanine nucleotide-binding regulatory protein. 5. These observations demonstrate that IK1 in ventricular myocytes can be modulated by cardiac alpha 1-adrenoceptors. The resulting changes in action potential repolarization and diastolic membrane potential may have significant effects on cardiac performance.
摘要
  1. 通过酶解法分散成年兔心脏来分离心室肌细胞,并使用膜片钳技术的全细胞模式进行电压钳制。实验在35℃或室温(21 - 23℃)下进行。2. 在存在10⁻³M 4 - 氨基吡啶以阻断瞬时外向钾电流以及10⁻⁶M普萘洛尔以阻断β - 肾上腺素能受体的情况下,α₁ - 肾上腺素能激动剂甲氧明使动作电位延长,并使舒张期膜电位出现小幅去极化。在电压钳制条件下,甲氧明在内向和外向两个方向上均降低了内向整流钾电流IK1的幅度。这种效应呈剂量依赖性(10⁻⁵ - 10⁻³M),并且在洗脱激动剂后完全可逆。3. 在存在普萘洛尔(10⁻⁶M)的情况下,神经递质去甲肾上腺素(10⁻⁶ - 2×10⁻⁵M)也降低了心室细胞中的IK1,并且这种效应被特异性α₁ - 肾上腺素能受体拮抗剂哌唑嗪阻断。4. 用0.5微克/毫升百日咳毒素对细胞进行预孵育(8 - 10小时,30 - 32℃),并不影响α₁ - 肾上腺素能受体介导的心室肌细胞IK1降低。该结果表明,在兔心室细胞中,IK1的α₁ - 调节是通过一种对百日咳毒素不敏感的鸟嘌呤核苷酸结合调节蛋白发生的。5. 这些观察结果表明,心室肌细胞中的IK1可被心脏α₁ - 肾上腺素能受体调节。动作电位复极化和舒张期膜电位的由此产生的变化可能对心脏功能有显著影响。

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