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己酮可可碱和茶碱对儿茶酚胺刺激的大鼠脑ATP酶反应动力学的影响(作者译)

[The influence of pentifylline and theophylline on reaction kinetics on rat brain ATPase stimulatable by catecholamines (author's transl)].

作者信息

Porsche E, Stefanovich V

出版信息

Arzneimittelforschung. 1979;29(8):1089-92.

PMID:227424
Abstract

The effects of 1-hexyl-3,7-dimethyl-xanthine (pentifylline, Cosaldon) and theophylline on rat brain Na+-, K+-, Mg2+ ATPase activities were investigated in in vitro experiments. It was established that pentifylline inhibits catecholamine sensitive ATPase in a dose dependent manner. Theophylline was without effect. Pentifylline also inhibited the Mg2+-dependent portion of Na+, K+-, Mg2+-ATPase. The effect of pentifylline on the kinetic parameters of Na+-, K+-, Mg2+-ATPase of synaptosomes was studied in detail. It was shown by a Lineweaver-Burk plot under the influence of pentifylline that the Michaelis constant (Km) increases from 1.0 x 10(-4) mol/l to 6.7 x 10(-4) mol/l. Km by norepinephrine stimulated ATPase decreases from 3.7 x 10(-4) mol/l to 2.9 x 10(-4) mol/l. In both experimental situations a decrease of maximal reaction velocity (Vmax) was observed. At high concentration of potassium in incubation medium the ATPase of synaptosomes was significantly more sensitive to pentifylline than at low concentration of potassium. The inhibition of ATPase by pentifylline was not influenced by the change in Na+/K+ ratio in the incubation medium. In all these experiments, theophylline used as a standard xanthine, was virtually without effect on the reaction kinetic of Na+-, K+-ATPase.

摘要

在体外实验中研究了1-己基-3,7-二甲基黄嘌呤(己酮可可碱,Cosaldon)和茶碱对大鼠脑Na + -、K + -、Mg2 + -ATP酶活性的影响。已确定己酮可可碱以剂量依赖性方式抑制儿茶酚胺敏感的ATP酶。茶碱无作用。己酮可可碱还抑制Na + -、K + -、Mg2 + -ATP酶的Mg2 +依赖性部分。详细研究了己酮可可碱对突触体Na + -、K + -、Mg2 + -ATP酶动力学参数的影响。在己酮可可碱影响下通过Lineweaver-Burk图表明,米氏常数(Km)从1.0×10(-4)mol/L增加到6.7×10(-4)mol/L。去甲肾上腺素刺激的ATP酶的Km从3.7×10(-4)mol/L降低到2.9×10(-4)mol/L。在两种实验情况下均观察到最大反应速度(Vmax)降低。在孵育培养基中钾浓度高时,突触体的ATP酶对己酮可可碱的敏感性明显高于钾浓度低时。己酮可可碱对ATP酶的抑制不受孵育培养基中Na + /K +比值变化的影响。在所有这些实验中,用作标准黄嘌呤的茶碱实际上对Na + -、K + -ATP酶的反应动力学无作用。

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