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无氮低亲和力配体3',4'-二羟基-α-甲基苯丙酮(U-0521)对心肌β-肾上腺素能受体的激活作用。

Activation of myocardial beta-adrenoceptors by the nitrogen-free low affinity ligand 3',4'-dihydroxy-alpha-methylpropiophenone (U-0521).

作者信息

Kaumann A J, Wittmann R, Birnbaumer L, Hoppe B H

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1977 Feb;296(3):217-28. doi: 10.1007/BF00498688.

Abstract

The effect of 3',4'-dihydroxy-alpha-methylpropiophenone (U-0521) on the rate of spontaneously contracting cultured rat heart cells and right atria of rats and kittens was investigated. The action of U-0521 on the cellular content of cyclic AMP and on the adenylyl cyclase of heart membrane particels was also studied. 1. U-0521 caused positive chronotropic effects on single cultured heart cells and right atria of the rat. U-0521 was about 10(5) times less potent than (--)-isoprenaline. The maximum effect of U-0521 was smaller than the maximum effect of (--)-isoprenaline. A small positive chronotropic effect of U-0521 was also observed on kitten atria. 2. The beta-adrenoceptor blocker (--)-bupranolol antagonized the positive chronotropic effects of U-0521 to the same extent as the effects of (--)-isoprenaline on single cells and atria of the rat. The effects of both U-0521 and (--)-isoprenaline appear therefore mediated through the same beta-adrenoceptors. The positive chronotropic effects of U-0521 on kitten atria were also blocked by (--)-bupranolol. 3. Up to 0.1 mM U-0521 did not block the effects of (--)-isoprenaline on rat atria, not even in the presence of corticosterone or hydrocortisone. 4. 1 min incubations with equieffective (increase in cellular beating rate) concentrations of U-0521 (0.1 mM) and (--)-isoprenaline (1 nM) caused a significant increase in the cellular content of cAMP; this effect of both drugs was antagonized by 10 nM (--)-bupranolol. 5. 0.1--3.3 mM U-0521 did not stimulate the adenylyl cyclase of cell-free membrane particles of kitten ventricles. The cyclase was depressed by 10 mM U-0521. 3.3 mM U-0521 caused a 20% decrease of the maximum cyclase-stimulating effect of (--)-isoprenaline and a 1.6-fold increase of its apparent Km. 6. The results with U-0521 suggest that beta-adrenoceptors can be activated by agonists devoid of nitrogen. However, the affinity of U-0521 for the beta-adrenoceptor is very low (KU-0521 approximately 5.5 mM). The concentration of U-0521 (0.1 mM) causing maximal increases in beating rate of cultured cells probably occupies less than 7% of the available beta-adrenoceptors.

摘要

研究了3',4'-二羟基-α-甲基苯丙酮(U-0521)对培养的大鼠心脏细胞以及大鼠和小猫右心房自发收缩速率的影响。还研究了U-0521对环磷酸腺苷(cAMP)细胞含量以及心脏膜颗粒腺苷酸环化酶的作用。1. U-0521对单个培养的心脏细胞和大鼠右心房产生正性变时作用。U-0521的效力比(-)-异丙肾上腺素低约10^5倍。U-0521的最大效应小于(-)-异丙肾上腺素的最大效应。在小猫心房上也观察到U-0521有轻微的正性变时作用。2. β-肾上腺素能受体阻滞剂(-)-布普萘洛尔对U-0521正性变时作用的拮抗程度与对大鼠单细胞和心房上(-)-异丙肾上腺素作用的拮抗程度相同。因此,U-0521和(-)-异丙肾上腺素的作用似乎都是通过相同的β-肾上腺素能受体介导的。(-)-布普萘洛尔也阻断了U-0521对小猫心房的正性变时作用。3. 高达0.1 mM的U-0521不会阻断(-)-异丙肾上腺素对大鼠心房的作用,即使在存在皮质酮或氢化可的松的情况下也是如此。4. 用等效(细胞搏动率增加)浓度的U-0521(0.1 mM)和(-)-异丙肾上腺素(1 nM)孵育1分钟,导致cAMP细胞含量显著增加;两种药物的这种作用都被10 nM的(-)-布普萘洛尔拮抗。5. 0.1 - 3.3 mM的U-0521不会刺激小猫心室无细胞膜颗粒的腺苷酸环化酶。10 mM的U-0521会抑制该环化酶。3.3 mM的U-0521使(-)-异丙肾上腺素的最大环化酶刺激效应降低20%,并使其表观Km增加1.6倍。6. 关于U-0521的结果表明,β-肾上腺素能受体可被不含氮的激动剂激活。然而,U-0521对β-肾上腺素能受体的亲和力非常低(KU-0521约为5.5 mM)。导致培养细胞搏动率最大增加的U-0521浓度(0.1 mM)可能占据不到7%的可用β-肾上腺素能受体。

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