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强啡肽A和乙基酮环唑新对心脏钠钾ATP酶活性的抑制作用。

Inhibition of cardiac Na+, K+-ATPase activity by dynorphin-A and ethylketocyclazocine.

作者信息

Maeda S, Nakamae J, Inoki R

机构信息

Department of Pharmacology, Faculty of Dentistry, Osaka University, Japan.

出版信息

Life Sci. 1988;42(4):461-8. doi: 10.1016/0024-3205(88)90085-9.

Abstract

The effect of various opioids on Na+, K+ -ATPase partially purified from rat heart was examined. Dynorphin-A (1-13), dynorphin-A (1-17) and ethylketocyclazocine (EKC), which are k-type opiate agonists, markedly inhibited the enzyme activity in a dose-dependent manner; IC50 values were 12 microM, 21 microM and 0.38 mM, respectively. Morphine (mu-type agonist), methionine- and leucine-enkephalin (delta-type agonist) at the concentration of 1 mM did not affect the enzyme activity. The effect of dynorphin-A (1-13) and EKC was not antagonized by naloxone. Dynorphin-A (1-13) mainly decreased Vmax value without the change of Km value in the activation of Na+, K+-ATPase by ATP, Na+ and K+. Dynorphin-A(1-13) inhibited the partial reactions of Na+, K+-ATPase at the different degree of the potency; the inhibition of K+-stimulated phosphatase was greater than that of Na+-dependent phosphorylation. The present study suggests that dynorphin-A and EKC have an effect on cardiovascular system which is mediated by the inhibition of Na+, K+-ATPase in the heart.

摘要

研究了各种阿片类药物对从大鼠心脏部分纯化的Na +,K + -ATP酶的影响。强啡肽A(1-13)、强啡肽A(1-17)和乙基酮环唑辛(EKC),这些κ型阿片激动剂,以剂量依赖性方式显著抑制该酶活性;IC50值分别为12μM、21μM和0.38 mM。浓度为1 mM的吗啡(μ型激动剂)、甲硫氨酸脑啡肽和亮氨酸脑啡肽(δ型激动剂)不影响该酶活性。强啡肽A(1-13)和EKC的作用不受纳洛酮拮抗。强啡肽A(1-13)主要降低Vmax值,而不改变ATP、Na +和K +对Na +,K + -ATP酶激活时的Km值。强啡肽A(1-13)在不同程度上抑制Na +,K + -ATP酶的部分反应;对K +刺激的磷酸酶的抑制作用大于对Na +依赖性磷酸化的抑制作用。本研究表明,强啡肽A和EKC对心血管系统有影响,这种影响是由抑制心脏中的Na +,K + -ATP酶介导的。

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