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抗炎性有机硒化合物依布硒啉与分离的壁细胞中酸分泌及胃H⁺/K⁺-ATP酶的相互作用

Interaction of the anti-inflammatory seleno-organic compound ebselen with acid secretion in isolated parietal cells and gastric H+/K(+)-ATPase.

作者信息

Beil W, Staar U, Sewing K F

机构信息

Abteilung Allgemeine Pharmakologie, Medizinische Hochschule, Hannover, Federal Republic of Germany.

出版信息

Biochem Pharmacol. 1990 Nov 1;40(9):1997-2003. doi: 10.1016/0006-2952(90)90229-e.

Abstract

The effects of the anti-inflammatory seleno-organic compound ebselen on gastric H+/K(+)-ATPase, H+/K(+)-ATPase-mediated proton transport and on parietal cell HCl production was studied. Ebselen inhibited K(+)-stimulated ATPase activity in leaky gastric membranes (IC50:0.15 microM) and H+/K(+)-ATPase-mediated proton transport in intact gastric membrane vesicles (IC50:0.7 microM). Histamine- and dibutyryl-cAMP-stimulated HCl production in isolated and enriched guinea-pig parietal cells was inhibited with an IC50 value of 12 microM. The mercaptan dithioerythritol and the nucleotide ATP prevents the H+/K(+)-ATPase against inactivation and dithioerythritol was found to restore already inhibited enzyme activity and ATPase mediated H+ transport. Furthermore, dithioerythritol could prevent ebselen-induced inhibition of HCl production in the parietal cell preparation. It is concluded that ebselen inhibits acid secretion in the parietal cell by interference with SH groups of the gastric proton pump, the H+/K(+)-ATPase. Therefore ebselen can be regarded as an anti-inflammatory drug for which in vitro anti-secretory properties can be demonstrated.

摘要

研究了抗炎性有机硒化合物依布硒啉对胃H⁺/K⁺-ATP酶、H⁺/K⁺-ATP酶介导的质子转运以及壁细胞盐酸分泌的影响。依布硒啉抑制渗漏胃膜中K⁺刺激的ATP酶活性(IC50:0.15微摩尔)以及完整胃膜囊泡中H⁺/K⁺-ATP酶介导的质子转运(IC50:0.7微摩尔)。在分离和富集的豚鼠壁细胞中,组胺和二丁酰环磷腺苷刺激的盐酸分泌受到抑制,IC50值为12微摩尔。巯基二硫苏糖醇和核苷酸ATP可防止H⁺/K⁺-ATP酶失活,并且发现二硫苏糖醇可恢复已被抑制的酶活性和ATP酶介导的H⁺转运。此外,二硫苏糖醇可防止依布硒啉诱导的壁细胞制剂中盐酸分泌的抑制。得出的结论是,依布硒啉通过干扰胃质子泵H⁺/K⁺-ATP酶的SH基团来抑制壁细胞中的酸分泌。因此,依布硒啉可被视为一种能在体外证明具有抗分泌特性的抗炎药物。

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