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通过激活促肾上腺皮质激素受体、β-肾上腺素能受体和血管紧张素II受体促进去甲肾上腺素从交感神经释放。

Facilitation of noradrenaline release from sympathetic nerves through activation of ACTH receptors, beta-adrenoceptors and angiotensin II receptors.

作者信息

Costa M, Majewski H

机构信息

Department of Pharmacology, University of Melbourne, Victoria, Australia.

出版信息

Br J Pharmacol. 1988 Nov;95(3):993-1001. doi: 10.1111/j.1476-5381.1988.tb11730.x.

Abstract
  1. In rabbit pulmonary artery and left atrial strips previously incubated with [3H]-noradrenaline, the active fragment of adrenocorticotropic hormone (ACTH 1-24, 0.1 microM) significantly enhanced the stimulation-induced (S-I) outflow of radioactivity when a cocktail containing corticosterone (40 microM), cocaine (30 microM) and propranolol (4 microM) was present, but not in the absence of these drugs. In rabbit pulmonary artery a facilitatory effect of ACTH 1-24 (0.1 microM) was also observed when only cocaine (30 microM) was present. 2. ACTH 1-24 (0.1 microM) did not affect the S-I outflow of radioactivity from rat atria, rat pulmonary artery or guinea-pig pulmonary artery, either in the presence or in the absence of the cocktail containing corticosterone (40 microM), cocaine (30 microM) and propranolol (4 microM). These results suggest that the presence of facilitatory prejunctional ACTH receptors may be restricted to rabbit sympathetic nerve endings. 3. Angiotensin II (0.01 microM), but not isoprenaline (0.1 microM) or ACTH 1-24 (0.1 microM), significantly enhanced the S-I outflow of radioactivity from rabbit pulmonary artery. In the presence of phentolamine (1 microM) to block inhibitory alpha 2-adrenoceptors, the facilitatory effect of angiotensin II (0.01 microM) was significantly enhanced, and a significant facilitatory effect of isoprenaline (0.1 microM) and of ACTH 1-24 (0.1 microM) was then revealed. These results suggest that feedback inhibition of noradrenaline release, mediated through the prejunctional alpha 2-adrenoceptor mechanism, buffers increases in noradrenaline release during activation of facilitatory prejunctional receptors. 4. In rabbit pulmonary artery, two concentrations of 8-Br-cyclic AMP, (270 or 540 microM), enhanced the S-I outflow of radioactivity in the presence of phentolamine (1 microM) to a similar extent. In the presence of 8-Br-cyclic AMP (270 microM) and phentolamine, the facilitatory effects of isoprenaline (0.1 microM) and of ACTH,24 (0.1 microM) were blocked, whereas that of angiotensin II (0.01 microM) was not changed. These results suggest that both prejunctional beta-adrenoceptors and ACTH receptors enhance noradrenaline release by generating cyclic AMP. The mechanism by which angiotensin II facilitates noradrenaline release is probably independent of the cyclic AMP second messenger pathway.
摘要
  1. 在预先用[3H]-去甲肾上腺素孵育过的兔肺动脉和左心房肌条中,当存在含有皮质酮(40微摩尔)、可卡因(30微摩尔)和普萘洛尔(4微摩尔)的混合剂时,促肾上腺皮质激素(ACTH 1-24,0.1微摩尔)的活性片段显著增强了刺激诱导(S-I)的放射性流出,但在没有这些药物时则没有增强。在兔肺动脉中,当仅存在可卡因(30微摩尔)时,也观察到了ACTH 1-24(0.1微摩尔)的促进作用。2. 无论是否存在含有皮质酮(40微摩尔)、可卡因(30微摩尔)和普萘洛尔(4微摩尔)的混合剂,ACTH 1-24(0.1微摩尔)都不影响大鼠心房、大鼠肺动脉或豚鼠肺动脉的放射性S-I流出。这些结果表明,促进性节前ACTH受体的存在可能仅限于兔交感神经末梢。3. 血管紧张素II(0.01微摩尔),而非异丙肾上腺素(0.1微摩尔)或ACTH 1-24(0.1微摩尔),显著增强了兔肺动脉的放射性S-I流出。在存在酚妥拉明(1微摩尔)以阻断抑制性α2-肾上腺素能受体的情况下,血管紧张素II(0.01微摩尔)的促进作用显著增强,并且此时揭示出异丙肾上腺素(0.1微摩尔)和ACTH 1-24(0.1微摩尔)有显著的促进作用。这些结果表明,通过节前α2-肾上腺素能受体机制介导的去甲肾上腺素释放的反馈抑制,缓冲了促进性节前受体激活期间去甲肾上腺素释放的增加。4. 在兔肺动脉中,两种浓度的8-溴环磷酸腺苷(270或540微摩尔)在存在酚妥拉明(1微摩尔)的情况下,以相似的程度增强了放射性流出。在存在8-溴环磷酸腺苷(270微摩尔)和酚妥拉明时,异丙肾上腺素(0.1微摩尔)和ACTH 1-24(0.1微摩尔)的促进作用被阻断,而血管紧张素II(0.01微摩尔)的促进作用未改变。这些结果表明,节前β-肾上腺素能受体和ACTH受体均通过生成环磷酸腺苷来增强去甲肾上腺素释放。血管紧张素II促进去甲肾上腺素释放的机制可能独立于环磷酸腺苷第二信使途径。

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