Liver ischemia increases the molecular order of microsomal membranes by increasing the cholesterol-to-phospholipid ratio
An accelerated degradation of phospholipid is the likely basis of irreversible cell injury in ischemia, and the membranes of the endoplasmic reticulum of the liver are a convenient system with which to study the effect of such a disturbance on the structure and function of cellular membranes. In the...
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Veröffentlicht in: | The Journal of biological chemistry 1984-11, Vol.259 (21), p.13217-13223 |
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description | An accelerated degradation of phospholipid is the likely basis of irreversible cell injury in ischemia, and the membranes of the endoplasmic reticulum of the liver are a convenient system with which to study the effect of such a disturbance on the structure and function of cellular membranes. In the present report, electron spin resonance spectroscopy has been used to evaluate changes in the molecular ordering of microsomal membrane phospholipids in the attempt to relate the loss of lipid to alterations in membrane structure. The order parameter, S, was calculated from spectra reflecting the anisotropic motion of 12-doxyl stearic acid incorporated into normal and 3-h ischemic microsomal membranes. Over the temperature range 4-40 degrees C, the molecular order (S) of ischemic membranes was increased by 8-10%. This increase was reproduced in the ordering of the phospholipids in liposomes prepared from total lipid extracts of the same membranes. In contrast, after removal of the neutral lipids, liposomes prepared from phospholipids of ischemic and control membranes had the same molecular order. There were no differences in the phospholipid species of control and ischemic membranes or in the fatty acid composition of the phospholipids. In the neutral lipid fraction of ischemic membranes, however, triglycerides and cholesterol were increased compared to control preparations. There were no free fatty acids. The total cholesterol content of the liver was unchanged after 3 h of ischemia. The cholesterol-to-phospholipid ratio of ischemic membranes, however, was increased by 22% from 0.258 to 0.315 as a consequence of the loss of phospholipid. Addition of cholesterol to the control total lipid extracts to give a cholesterol-to-phospholipid ratio the same as in ischemic membranes resulted in liposomes with order parameters similar to those of liposomes prepared from ischemic total lipids. It is concluded that the degradation of the phospholipids of the microsomal membrane results in a relative increase in the cholesterol-to-phospholipid ratio. This is accompanied, in turn, by an increased molecular order of the residual membrane phospholipids. |
doi_str_mv | 10.1016/S0021-9258(18)90680-0 |
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In the present report, electron spin resonance spectroscopy has been used to evaluate changes in the molecular ordering of microsomal membrane phospholipids in the attempt to relate the loss of lipid to alterations in membrane structure. The order parameter, S, was calculated from spectra reflecting the anisotropic motion of 12-doxyl stearic acid incorporated into normal and 3-h ischemic microsomal membranes. Over the temperature range 4-40 degrees C, the molecular order (S) of ischemic membranes was increased by 8-10%. This increase was reproduced in the ordering of the phospholipids in liposomes prepared from total lipid extracts of the same membranes. In contrast, after removal of the neutral lipids, liposomes prepared from phospholipids of ischemic and control membranes had the same molecular order. There were no differences in the phospholipid species of control and ischemic membranes or in the fatty acid composition of the phospholipids. In the neutral lipid fraction of ischemic membranes, however, triglycerides and cholesterol were increased compared to control preparations. There were no free fatty acids. The total cholesterol content of the liver was unchanged after 3 h of ischemia. The cholesterol-to-phospholipid ratio of ischemic membranes, however, was increased by 22% from 0.258 to 0.315 as a consequence of the loss of phospholipid. Addition of cholesterol to the control total lipid extracts to give a cholesterol-to-phospholipid ratio the same as in ischemic membranes resulted in liposomes with order parameters similar to those of liposomes prepared from ischemic total lipids. It is concluded that the degradation of the phospholipids of the microsomal membrane results in a relative increase in the cholesterol-to-phospholipid ratio. This is accompanied, in turn, by an increased molecular order of the residual membrane phospholipids.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/S0021-9258(18)90680-0</identifier><identifier>PMID: 6092367</identifier><identifier>CODEN: JBCHA3</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Cholesterol - analysis ; Cholesterol - metabolism ; Electron Spin Resonance Spectroscopy ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Intracellular Membranes - metabolism ; Ischemia - metabolism ; Kinetics ; Liver Circulation ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Medical sciences ; Membrane Lipids - metabolism ; Microsomes, Liver - metabolism ; Other diseases. Semiology ; Phospholipids - analysis ; Phospholipids - metabolism ; Rats ; Rats, Inbred Strains ; Thermodynamics</subject><ispartof>The Journal of biological chemistry, 1984-11, Vol.259 (21), p.13217-13223</ispartof><rights>1984 © 1984 ASBMB. 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In the present report, electron spin resonance spectroscopy has been used to evaluate changes in the molecular ordering of microsomal membrane phospholipids in the attempt to relate the loss of lipid to alterations in membrane structure. The order parameter, S, was calculated from spectra reflecting the anisotropic motion of 12-doxyl stearic acid incorporated into normal and 3-h ischemic microsomal membranes. Over the temperature range 4-40 degrees C, the molecular order (S) of ischemic membranes was increased by 8-10%. This increase was reproduced in the ordering of the phospholipids in liposomes prepared from total lipid extracts of the same membranes. In contrast, after removal of the neutral lipids, liposomes prepared from phospholipids of ischemic and control membranes had the same molecular order. There were no differences in the phospholipid species of control and ischemic membranes or in the fatty acid composition of the phospholipids. In the neutral lipid fraction of ischemic membranes, however, triglycerides and cholesterol were increased compared to control preparations. There were no free fatty acids. The total cholesterol content of the liver was unchanged after 3 h of ischemia. The cholesterol-to-phospholipid ratio of ischemic membranes, however, was increased by 22% from 0.258 to 0.315 as a consequence of the loss of phospholipid. Addition of cholesterol to the control total lipid extracts to give a cholesterol-to-phospholipid ratio the same as in ischemic membranes resulted in liposomes with order parameters similar to those of liposomes prepared from ischemic total lipids. It is concluded that the degradation of the phospholipids of the microsomal membrane results in a relative increase in the cholesterol-to-phospholipid ratio. This is accompanied, in turn, by an increased molecular order of the residual membrane phospholipids.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cholesterol - analysis</subject><subject>Cholesterol - metabolism</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Intracellular Membranes - metabolism</subject><subject>Ischemia - metabolism</subject><subject>Kinetics</subject><subject>Liver Circulation</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Medical sciences</subject><subject>Membrane Lipids - metabolism</subject><subject>Microsomes, Liver - metabolism</subject><subject>Other diseases. Semiology</subject><subject>Phospholipids - analysis</subject><subject>Phospholipids - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Thermodynamics</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS0EKkPhJ1TKAiFYpPgRJ_EKVRUvaSQWgMTO8uO6MbLHg50p9N_XmRmmy1qyvLjfuffcY4QuCL4kmPTvv2NMSSsoH9-S8Z3A_Yhb_AStCB5Zyzj59RStTshz9KKU37ieTpAzdNZjQVk_rNC_tb-F3PhiJoheNX5jMqgCpZknaGIKYHZB5SZlW7HkmuhNTiVFFZoIUWe1qay--y_0m5u90kxVWmbIKbRzardTKvUGv_W2yWr26SV65lQo8Or4nqOfnz7-uP7Srr99_np9tW5N1_O5pU5YDtwYx5ztGOs6YwkZLB-U6N1AxmHgxJlOdwysplowYawRzFKhjbacnaM3h77bnP7sqiUZ67IQQjWedkWOhOGBY1pBfgCX_UoGJ7fZR5XvJMFySVzuE5dLnJKMcp-4xFV3cRyw0xHsSXWMuNZfH-uqGBVcTcz4csIEGWvz8QGb_M3012eQ2qflUyTlQta5hFGydPtwwKBmdushy2I8bAzYKjGztMk_4vcekpGsDg</recordid><startdate>19841110</startdate><enddate>19841110</enddate><creator>Petrovich, D R</creator><creator>Finkelstein, S</creator><creator>Waring, A J</creator><creator>Farber, J L</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19841110</creationdate><title>Liver ischemia increases the molecular order of microsomal membranes by increasing the cholesterol-to-phospholipid ratio</title><author>Petrovich, D R ; Finkelstein, S ; Waring, A J ; Farber, J L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-2f9d5e5ccf3fd43344cd117d57a96f7187751fc4b43edb2b939cdc93d29bcbd53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cholesterol - analysis</topic><topic>Cholesterol - metabolism</topic><topic>Electron Spin Resonance Spectroscopy</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Intracellular Membranes - metabolism</topic><topic>Ischemia - metabolism</topic><topic>Kinetics</topic><topic>Liver Circulation</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Medical sciences</topic><topic>Membrane Lipids - metabolism</topic><topic>Microsomes, Liver - metabolism</topic><topic>Other diseases. Semiology</topic><topic>Phospholipids - analysis</topic><topic>Phospholipids - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Petrovich, D R</creatorcontrib><creatorcontrib>Finkelstein, S</creatorcontrib><creatorcontrib>Waring, A J</creatorcontrib><creatorcontrib>Farber, J L</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Petrovich, D R</au><au>Finkelstein, S</au><au>Waring, A J</au><au>Farber, J L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liver ischemia increases the molecular order of microsomal membranes by increasing the cholesterol-to-phospholipid ratio</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1984-11-10</date><risdate>1984</risdate><volume>259</volume><issue>21</issue><spage>13217</spage><epage>13223</epage><pages>13217-13223</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><coden>JBCHA3</coden><abstract>An accelerated degradation of phospholipid is the likely basis of irreversible cell injury in ischemia, and the membranes of the endoplasmic reticulum of the liver are a convenient system with which to study the effect of such a disturbance on the structure and function of cellular membranes. In the present report, electron spin resonance spectroscopy has been used to evaluate changes in the molecular ordering of microsomal membrane phospholipids in the attempt to relate the loss of lipid to alterations in membrane structure. The order parameter, S, was calculated from spectra reflecting the anisotropic motion of 12-doxyl stearic acid incorporated into normal and 3-h ischemic microsomal membranes. Over the temperature range 4-40 degrees C, the molecular order (S) of ischemic membranes was increased by 8-10%. This increase was reproduced in the ordering of the phospholipids in liposomes prepared from total lipid extracts of the same membranes. In contrast, after removal of the neutral lipids, liposomes prepared from phospholipids of ischemic and control membranes had the same molecular order. There were no differences in the phospholipid species of control and ischemic membranes or in the fatty acid composition of the phospholipids. In the neutral lipid fraction of ischemic membranes, however, triglycerides and cholesterol were increased compared to control preparations. There were no free fatty acids. The total cholesterol content of the liver was unchanged after 3 h of ischemia. The cholesterol-to-phospholipid ratio of ischemic membranes, however, was increased by 22% from 0.258 to 0.315 as a consequence of the loss of phospholipid. Addition of cholesterol to the control total lipid extracts to give a cholesterol-to-phospholipid ratio the same as in ischemic membranes resulted in liposomes with order parameters similar to those of liposomes prepared from ischemic total lipids. It is concluded that the degradation of the phospholipids of the microsomal membrane results in a relative increase in the cholesterol-to-phospholipid ratio. This is accompanied, in turn, by an increased molecular order of the residual membrane phospholipids.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>6092367</pmid><doi>10.1016/S0021-9258(18)90680-0</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Cholesterol - analysis Cholesterol - metabolism Electron Spin Resonance Spectroscopy Female Gastroenterology. Liver. Pancreas. Abdomen Intracellular Membranes - metabolism Ischemia - metabolism Kinetics Liver Circulation Liver. Biliary tract. Portal circulation. Exocrine pancreas Medical sciences Membrane Lipids - metabolism Microsomes, Liver - metabolism Other diseases. Semiology Phospholipids - analysis Phospholipids - metabolism Rats Rats, Inbred Strains Thermodynamics |
title | Liver ischemia increases the molecular order of microsomal membranes by increasing the cholesterol-to-phospholipid ratio |
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