Lipid alterations in liver and kidney induced by normobaric hyperoxia: correlations with changes in microsomal membrane fluidity. 1987

C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio

The effects of normobaric hyperoxia on both microsomal membrane fluidity and mechanism of phospholipid synthesis in rabbit liver and kidney have been studied. Hyperoxia induces in both organs an impairment of de novo synthesis of glycerolipids which could be due to an inactivation of acyltransferase activities involved in the initial formation of phosphatidic acid. The ability to replace phospholipid fatty acids by reacylation mechanism decreases slightly in the hyperoxic kidney, while it does not change in the hyperoxic liver. Concerning the effect of high arterial pO2 on microsomal membrane fluidity, the hyperoxic liver shows a more fluid environment within the membrane core of microsomes; however, no difference was shown in that of microsomal membrane core of hyperoxic kidney. An insight into the lipid composition of microsomes indicates that liver microsomal membranes have lower cholesterol content and higher unsaturation degree of phospholipid fatty acids, whereas hyperoxic kidney microsomes become more saturated and did not show any difference in their cholesterol content. In both hyperoxic liver and kidney microsomes, phospholipid content decreases in agreement with the depression of phosphatidic acid biosynthesis. These results are discussed in relation to the values of microsomal membrane microviscosity obtained.

UI MeSH Term Description Entries
D007425 Intracellular Membranes Thin structures that encapsulate subcellular structures or ORGANELLES in EUKARYOTIC CELLS. They include a variety of membranes associated with the CELL NUCLEUS; the MITOCHONDRIA; the GOLGI APPARATUS; the ENDOPLASMIC RETICULUM; LYSOSOMES; PLASTIDS; and VACUOLES. Membranes, Intracellular,Intracellular Membrane,Membrane, Intracellular
D007668 Kidney Body organ that filters blood for the secretion of URINE and that regulates ion concentrations. Kidneys
D008243 1-Acylglycerophosphocholine O-Acyltransferase An enzyme localized predominantly within the plasma membrane of lymphocytes. It catalyzes the transfer of long-chain fatty acids, preferentially unsaturated fatty acids, to lysophosphatides with the formation of 1,2-diacylglycero-3-phosphocholine and CoA. EC 2.3.1.23. 1-Acylglycerophosphocholine Acyltransferase,Acyl CoA Lysolecithin Acyltransferase,Lysolecithin Acyltransferase,Acyl-CoA-1-Acylglycero-3-Phosphocholine-O-Acyltransferase,Lysophosphatidylcholine Acyltransferase,Lysophosphatidylcholine-Palmitoyl CoA Acyltransferase,Lysophospholipid Acyltransferase,1 Acylglycerophosphocholine Acyltransferase,1 Acylglycerophosphocholine O Acyltransferase,Acyl CoA 1 Acylglycero 3 Phosphocholine O Acyltransferase,Acyltransferase, 1-Acylglycerophosphocholine,Acyltransferase, Lysolecithin,Acyltransferase, Lysophosphatidylcholine,Acyltransferase, Lysophosphatidylcholine-Palmitoyl CoA,Acyltransferase, Lysophospholipid,CoA Acyltransferase, Lysophosphatidylcholine-Palmitoyl,Lysophosphatidylcholine Palmitoyl CoA Acyltransferase,O-Acyltransferase, 1-Acylglycerophosphocholine
D008297 Male Males
D008560 Membrane Fluidity The motion of phospholipid molecules within the lipid bilayer, dependent on the classes of phospholipids present, their fatty acid composition and degree of unsaturation of the acyl chains, the cholesterol concentration, and temperature. Bilayer Fluidity,Bilayer Fluidities,Fluidities, Bilayer,Fluidities, Membrane,Fluidity, Bilayer,Fluidity, Membrane,Membrane Fluidities
D008861 Microsomes Artifactual vesicles formed from the endoplasmic reticulum when cells are disrupted. They are isolated by differential centrifugation and are composed of three structural features: rough vesicles, smooth vesicles, and ribosomes. Numerous enzyme activities are associated with the microsomal fraction. (Glick, Glossary of Biochemistry and Molecular Biology, 1990; from Rieger et al., Glossary of Genetics: Classical and Molecular, 5th ed) Microsome
D008862 Microsomes, Liver Closed vesicles of fragmented endoplasmic reticulum created when liver cells or tissue are disrupted by homogenization. They may be smooth or rough. Liver Microsomes,Liver Microsome,Microsome, Liver
D010100 Oxygen An element with atomic symbol O, atomic number 8, and atomic weight [15.99903; 15.99977]. It is the most abundant element on earth and essential for respiration. Dioxygen,Oxygen-16,Oxygen 16
D010170 Palmitoyl-CoA Hydrolase Enzyme catalyzing reversibly the hydrolysis of palmitoyl-CoA or other long-chain acyl coenzyme A compounds to yield CoA and palmitate or other acyl esters. The enzyme is involved in the esterification of fatty acids to form triglycerides. EC 3.1.2.2. Acyl CoA Hydrolase,Fatty Acyl Thioesterase,Palmitoyl CoA Deacylase,Palmitoyl Coenzyme A Hydrolase,Palmitoyl Thioesterase,Long-Chain Fatty-Acyl-CoA Hydrolase,Oleoyl-CoA Acylhydrolase,Stearoyl CoA Hydrolase,Thioesterase I,Acylhydrolase, Oleoyl-CoA,CoA Deacylase, Palmitoyl,CoA Hydrolase, Acyl,CoA Hydrolase, Stearoyl,Deacylase, Palmitoyl CoA,Fatty-Acyl-CoA Hydrolase, Long-Chain,Hydrolase, Acyl CoA,Hydrolase, Long-Chain Fatty-Acyl-CoA,Hydrolase, Palmitoyl-CoA,Hydrolase, Stearoyl CoA,Long Chain Fatty Acyl CoA Hydrolase,Oleoyl CoA Acylhydrolase,Palmitoyl CoA Hydrolase,Thioesterase, Fatty Acyl,Thioesterase, Palmitoyl
D010313 Partial Pressure The pressure that would be exerted by one component of a mixture of gases if it were present alone in a container. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed) Partial Pressures,Pressure, Partial,Pressures, Partial

Related Publications

C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
May 1997, FEBS letters,
C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
February 1997, The Journal of surgical research,
C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
August 1987, The Biochemical journal,
C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
January 1982, Experimental gerontology,
C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
November 1994, Free radical biology & medicine,
C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
April 1990, Chemistry and physics of lipids,
C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
January 1986, The International journal of biochemistry,
C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
March 1998, The Journal of membrane biology,
C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
May 1999, Biology of the neonate,
C Casals, and M Gasset, and M C Méndez, and P García-Barreno, and A M Municio
August 1997, Journal of hypertension,
Copied contents to your clipboard!