Mamiya N, Goldenring J R, Tsunoda Y, Modlin I M, Yasui K, Usuda N, Ishikawa T, Natsume A, Hidaka H
Department of Pharmacology, Nagoya University School of Medicine, Japan.
Biochem Biophys Res Commun. 1993 Sep 15;195(2):608-15. doi: 10.1006/bbrc.1993.2089.
A novel Ca2+/calmodulin-dependent protein kinase II (CaM Kinase II) inhibitor, KN-93 potently inhibits gastric acid secretion from parietal cells. As previously reported (1), treatment of parietal cells with a selective inhibitor of CaM kinase II, KN-62 resulted in the inhibition of cholinergic-stimulated rabbit parietal cell secretion, whereas it failed to inhibit the histamine and forskolin response. In contrast effects of carbachol, histamine and forskolin were significantly inhibited by KN-93 with an IC50 of 0.15, 0.3 and 1 microM, respectively; these effects occurred without any changes in intracellular cyclic AMP and Ca2+ levels. In the present study we investigated the mechanism by which KN-93 acts upon the acid-secreting machinery of gastric parietal cells. Neither redistribution of the proton pump activity nor the morphological transformation were affected by KN-93. The drug only weakly inhibited the H+, K(+)-ATPase activity but strongly dissipated the proton gradient formed in the gastric membrane vesicles and reduced the volume of luminal space. Thus KN-93 acts at pH gradient formation whereas KN-62 acts only at CaM Kinase II.
一种新型的钙/钙调蛋白依赖性蛋白激酶II(CaM激酶II)抑制剂KN-93能够有效抑制壁细胞分泌胃酸。如先前报道(1),用CaM激酶II的选择性抑制剂KN-62处理壁细胞会抑制胆碱能刺激的兔壁细胞分泌,但它无法抑制组胺和福斯高林反应。相比之下,卡巴胆碱、组胺和福斯高林的作用分别被KN-93显著抑制,其IC50分别为0.15、0.3和1微摩尔;这些作用发生时细胞内环磷酸腺苷和钙离子水平没有任何变化。在本研究中,我们探究了KN-93作用于胃壁细胞酸分泌机制的方式。质子泵活性的重新分布和形态转变均未受KN-93影响。该药物仅微弱抑制H⁺,K⁺-ATP酶活性,但强烈消散胃膜囊泡中形成的质子梯度并减小管腔空间体积。因此,KN-93作用于pH梯度形成,而KN-62仅作用于CaM激酶II。