首页> 美国卫生研究院文献>Journal of Cellular and Molecular Medicine >Modulation of adenylyl cyclase activity in young and adult rat brain cortex. Identification of suramin as a direct inhibitor of adenylyl cyclase
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Modulation of adenylyl cyclase activity in young and adult rat brain cortex. Identification of suramin as a direct inhibitor of adenylyl cyclase

机译:年轻和成年大鼠大脑皮质中腺苷酸环化酶活性的调节。确定苏拉明为腺苷酸环化酶的直接抑制剂

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摘要

Adenylyl cyclase (AC) in brain cortex from young (12‐day‐old) rats exhibits markedly higher activity than in adult (90‐day‐old) animals. In order to find some possibly different regulatory features of AC in these two age groups, here we modulated AC activity by dithiothreitol (DTT), Fe2+, ascorbic acid and suramin. We did not detect any substantial difference between the effects of all these tested agents on AC activity in cerebrocortical membranes from young and adult rats, and the enzyme activity was always about two‐fold higher in the former preparations. Nevertheless, several interesting findings have come out of these investigations. Whereas forskolin‐ and Mn2+‐stimulated AC activity was significantly enhanced by the addition of DTT, increased concentrations of Fe2+ ions or ascorbic acid substantially suppressed the enzyme activity. Lipid peroxidation induced by suitable combinations of DTT/Fe2+ or by ascorbic acid did not influence AC activity. We have also observed that PKC‐ or protein tyrosine kinase‐mediated phosphorylation apparently does not play any significant role in different activity of AC determined in cerebrocortical preparations from young and adult rats. Our experiments analysing the presumed modulatory role of suramin revealed that this pharmacologically important drug may act as a direct inhibitor of AC. The enzyme activity was diminished to the same extent by suramin in membranes from both tested age groups. Our present data show that AC is regulated similarly in brain cortex from both young and adult rats, but its overall activity is much lower in adulthood.
机译:年轻(12日龄)大鼠大脑皮质中的腺苷酸环化酶(AC)表现出比成年(90日龄)动物明显更高的活性。为了找到这两个年龄组中AC的一些可能不同的调节特征,我们在这里通过二硫苏糖醇(DTT),Fe 2 + ,抗坏血酸和苏拉明来调节AC活性。我们没有发现所有这些测试试剂对幼年和成年大鼠的大脑皮质膜中AC活性的影响之间没有任何实质性差异,并且在以前的制剂中,酶活性始终高出约两倍。然而,从这些调查中得出了一些有趣的发现。加入DTT可以显着增强福斯高林和Mn 2 + 刺激的AC活性,而增加的Fe 2 + 离子或抗坏血酸的浓度则明显抑制了酶的活性。 DTT / Fe 2 + 的适当组合或抗坏血酸引起的脂质过氧化作用不会影响AC活性。我们还观察到,PKC或蛋白酪氨酸激酶介导的磷酸化作用显然在年轻和成年大鼠的大脑皮层制剂中测定的AC的不同活性中没有任何重要作用。我们的实验分析了苏拉明的调节作用,发现该药理学上重要的药物可能是AC的直接抑制剂。苏拉明在两个测试年龄组的膜中的酶活性都以相同的程度降低。我们目前的数据表明,幼鼠和成年大鼠的大脑皮层中的AC受到类似的调节,但成年后其总体活性要低得多。

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