Use of two-sided bifunctional liposomes in the study of a hypothalamic Na,K-ATPase inhibitor
- PMID: 7508028
- DOI: 10.1097/00005344-199322002-00017
Use of two-sided bifunctional liposomes in the study of a hypothalamic Na,K-ATPase inhibitor
Abstract
Two-sided bifunctional (ATP-filled) Na,K-ATPase liposomes have been developed as a result of knowledge about the average liposome diameter and volume, the liposome size distribution, the average number of Na,K-ATPase molecules reconstituted per liposome, and the orientation of the reconstituted Na,K-ATPase molecules. The addition of 5-10 microM external 86Rb to the liposomes containing 50 mM encapsulated ATP provoked an impressive 86Rb accumulation by the cell-like-oriented pumps. The successive addition of external ATP activated the pumps in the reversed orientation of the same liposome, leading to total extrusion of the previously accumulated 86Rb. An inhibitor extracted from bovine hypothalamus (hypothalamic inhibitory factor) inhibited the cell-like-oriented population, i.e., acted like an extracellular inhibitor at 30 nM. Conversely, at 75 nM, the reversed pump population was also blocked, indicating that the inhibitor either transversed the membrane or was able to act also at the intracellular enzyme side at a higher concentration. Thus, the side of action as well as the membrane permeability of structurally unknown endogenous Na,K-ATPase inhibitors can be determined simultaneously in a single suspension of two-sided bifunctional Na,K-ATPase liposomes.
Similar articles
-
Hypothalamic Na(+)-K(+)-ATPase inhibitor characterized in two-sided liposomes containing pure renal Na(+)-K(+)-ATPase.Am J Physiol. 1990 Jan;258(1 Pt 2):F144-53. doi: 10.1152/ajprenal.1990.258.1.F144. Am J Physiol. 1990. PMID: 2154124
-
Characterization of (Na+ + K+)-ATPase liposomes. I. Effect of enzyme concentration and modification on liposome size, intramembrane particle formation and Na+,K+-transport.Biochim Biophys Acta. 1984 Jun 27;773(2):253-61. doi: 10.1016/0005-2736(84)90089-0. Biochim Biophys Acta. 1984. PMID: 6329284
-
Mercury inhibits Na-K-ATPase primarily at the cytoplasmic side.Am J Physiol. 1992 May;262(5 Pt 2):F843-8. doi: 10.1152/ajprenal.1992.262.5.F843. Am J Physiol. 1992. PMID: 1317122
-
Na,K-ATPase characterized in artificial membranes. 2. Successive measurement of ATP-driven Rb-accumulation, ouabain-blocked Rb-flux and palytoxin-induced Rb-efflux.Mol Membr Biol. 1994 Oct-Dec;11(4):247-54. doi: 10.3109/09687689409160434. Mol Membr Biol. 1994. PMID: 7711834
-
Characterization of (Na+ + K+)-ATPase-liposomes. III. Controlled activation and inhibition of symmetric pumps by timed asymmetric ATP, RbCl, and cardiac glycoside addition.Biochim Biophys Acta. 1987 Jun 12;900(1):27-37. doi: 10.1016/0005-2736(87)90274-4. Biochim Biophys Acta. 1987. PMID: 2439119
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources