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摄取2在大鼠离体心房中神经源性去甲肾上腺素活性终止过程中的作用。

Involvement of uptake2 in the termination of activity of neurogenic noradrenaline in the rat isolated atrium.

作者信息

Bell C, Grabsch B

出版信息

J Physiol. 1976 Jan;254(1):203-12. doi: 10.1113/jphysiol.1976.sp011229.

Abstract
  1. An examination has been made of the relative effect of drugs which affect Uptake1 and Uptake2 on the mechanical responses to adrenergic nervous stimulation (0-5-5 Hz for 5 sec) in rat isolated atrium. 2. Inhibition of Uptake1 with desmethylimipramine (2 muM) prolonged by 50-90% the time taken for recovery of normal heart rate after a five sec train of nervous stimulation. Inhibition of Uptake2 with metanephrine (4 muM) prolonged by 20-40% the time taken for recovery of normal heart rate. 3. Neither desmethylimipramine nor metanephrine had any consistent effect on the time course of the inotropic response to stimulation or on the amplitudes of either inotropic or chronotropic responses. 4. After administration of desmethylimipramine, metanephrine had a somewhat greater effect on chronotropic responses than when given alone. After administration of metanephrine, desmethylimipramine still further prolonged chronotropic responses to low frequency stimulation (0-5, 1 Hz) but had no effect at 5 Hz. These results agree with the known affinities of each uptake process for different concentrations of noradrenaline in the rat heart. 5. It is concluded that both Uptake1 and Uptake2 participate in the termination of physiological activity of neurogenic noradrenaline in rat isolated atrium even at low frequencies of nervous activation. 6. No evidence was obtained to indicate that manipulation of circulating oestrogen levels by oöphorectomy and oestrogen-priming of female rats had any effect of the efficiency of the cardiac Uptake2 process.
摘要
  1. 已对影响摄取1和摄取2的药物对大鼠离体心房对肾上腺素能神经刺激(0 - 5 - 5赫兹,持续5秒)的机械反应的相对作用进行了研究。2. 用去甲丙咪嗪(2微摩尔)抑制摄取1,使5秒神经刺激序列后恢复正常心率所需的时间延长了50 - 90%。用间甲肾上腺素(4微摩尔)抑制摄取2,使恢复正常心率所需的时间延长了20 - 40%。3. 去甲丙咪嗪和间甲肾上腺素对刺激的变力反应的时间进程或变力性或变时性反应的幅度均无一致影响。4. 给予去甲丙咪嗪后,间甲肾上腺素对变时性反应的作用比单独给药时略大。给予间甲肾上腺素后,去甲丙咪嗪仍进一步延长了对低频刺激(0 - 5,1赫兹)的变时性反应,但对5赫兹刺激无影响。这些结果与大鼠心脏中每个摄取过程对不同浓度去甲肾上腺素的已知亲和力相符。5. 得出的结论是,即使在神经激活频率较低时,摄取1和摄取2都参与大鼠离体心房中神经源性去甲肾上腺素生理活性的终止。6. 未获得证据表明通过切除卵巢和对雌性大鼠进行雌激素预处理来操纵循环雌激素水平对心脏摄取2过程的效率有任何影响。

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