Luck M R, Münker M
Institute for Hormone and Fertility Research, Hamburg, Germany.
Reprod Fertil Dev. 1991;3(6):715-23. doi: 10.1071/rd9910715.
Bovine granulosa cells were treated in culture with alpha- and beta-adrenoceptor ligands to determine the receptor subtype mediating their response to catecholamines. The secretion of oxytocin by granulosa cells in serum-free medium was measured on the fourth day of culture (during the period of acquisition of a luteal phenotype). Cultures were performed in the presence of 0.5 mM ascorbic acid, which increased hormone output and potentiated the response to catecholamines. The effects of adrenaline and noradrenaline on oxytocin secretion were concentration-dependent; maximum stimulation was over 700% with adrenalin (EC50 92 nM) and 500% with noradrenaline (EC50 87 nM). The response to noradrenaline (10(-6) M) and adrenaline (10(-6) M) could be blocked by propranolol but not by phentolamine, suggesting that beta- rather than alpha-adrenoceptors were involved. Blockade by metoprolol and practolol (beta 1-adrenoceptor antagonists) was poor and dobutamine (beta 1-agonist) was weakly stimulatory. A concentration-dependent stimulatory response (EC50 200 nM) was obtained with salbutamol (beta 2-adrenoceptor agonist) and stimulation by adrenaline or salbutamol could be blocked by a selective beta 2-adrenoceptor antagonist (ICI 118,551). It is concluded that, during luteinization, the long-term response of bovine granulosa cells to stimulation induced by catecholamines is mediated through beta- rather than alpha-adrenoceptors. Although the beta 2-subtype is probably involved, the similar potencies of adrenaline and noradrenaline are uncharacteristic of beta 2-adrenoceptors and may be peculiar to the long-term response shown by these cells.
用α-和β-肾上腺素能受体配体处理培养的牛颗粒细胞,以确定介导其对儿茶酚胺反应的受体亚型。在培养的第四天(黄体表型形成期),测定无血清培养基中颗粒细胞催产素的分泌。培养在含有0.5 mM抗坏血酸的条件下进行,抗坏血酸可增加激素分泌并增强对儿茶酚胺的反应。肾上腺素和去甲肾上腺素对催产素分泌的影响呈浓度依赖性;肾上腺素(EC50 92 nM)的最大刺激超过700%,去甲肾上腺素(EC50 87 nM)的最大刺激为500%。普萘洛尔可阻断对去甲肾上腺素(10(-6) M)和肾上腺素(10(-6) M)的反应,而酚妥拉明则不能,这表明参与的是β-肾上腺素能受体而非α-肾上腺素能受体。美托洛尔和普拉洛尔(β1-肾上腺素能受体拮抗剂)的阻断作用较差,多巴酚丁胺(β1-激动剂)的刺激作用较弱。沙丁胺醇(β2-肾上腺素能受体激动剂)产生浓度依赖性刺激反应(EC50 200 nM),肾上腺素或沙丁胺醇的刺激可被选择性β2-肾上腺素能受体拮抗剂(ICI 118,551)阻断。得出结论,在黄体化过程中,牛颗粒细胞对儿茶酚胺诱导刺激的长期反应是通过β-肾上腺素能受体而非α-肾上腺素能受体介导的。虽然可能涉及β2-亚型,但肾上腺素和去甲肾上腺素的相似效力并非β2-肾上腺素能受体的特征,可能是这些细胞所显示的长期反应所特有的。