Czackes W J, Wald H, Gutman Y
Res Commun Chem Pathol Pharmacol. 1977 May;17(1):133-43.
Microsomal ATPase isolated from rat kidney papilla was compared to that from kidney medulla. Microsomal Na, K-ATPase from papilla was more sensitive to inhibition by ouabain, Cad N-ethyl-maleimide, Hg++, Thiomerin, ethacrynic acid and Furosemide than the enzyme from the medulla. Mg-ATPase of the papilla was less sensitive than the medullary enzyme to inhibition by Ca++, Cd++, N-ethyl-maleimide, Hg++, ethacrynic acid and Furosemide. Papillary Mg-ATPase was less sensitive than papillary Na, K-ATPase to all the inhibitors mentioned. Medullary Mg-ATPase was more sensitive than medullary Na, K-ATPase to inhibition by ethacrynic acid and Furosemide but less sensitive than medullary Na, K-ATPase to all the other inhibitors. Papillary Na, K-ATPase is the most sensitive to inhibition and papillary Mg-ATPase is the most resistant to inhibition by various diuretic drugs. The possible significance of these characteristics is discussed.
将从大鼠肾乳头分离出的微粒体ATP酶与从肾髓质分离出的进行比较。与来自髓质的酶相比,来自乳头的微粒体钠钾ATP酶对哇巴因、N-乙基马来酰亚胺、汞离子、硫柳汞、依他尼酸和呋塞米的抑制作用更敏感。乳头的镁ATP酶对钙离子、镉离子、N-乙基马来酰亚胺、汞离子、依他尼酸和呋塞米抑制作用的敏感性低于髓质的酶。乳头的镁ATP酶对上述所有抑制剂的敏感性低于乳头的钠钾ATP酶。髓质的镁ATP酶对依他尼酸和呋塞米抑制作用的敏感性高于髓质的钠钾ATP酶,但对所有其他抑制剂的敏感性低于髓质的钠钾ATP酶。乳头的钠钾ATP酶对各种利尿药抑制作用最敏感,而乳头的镁ATP酶对其抑制作用最具抗性。讨论了这些特性的可能意义。