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Association between alcohol-induced erythrocyte membrane alterations and hemolysis in chronic alcoholics
The present study aimed to understand the association between erythrocyte membrane alterations and hemolysis in chronic alcoholics. Study was conducted on human male volunteers aged between 35–45 years with a drinking history of 8–10 years. Results showed that plasma marker enzymes AST, ALT, ALP and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5281527/ https://www.ncbi.nlm.nih.gov/pubmed/28163384 http://dx.doi.org/10.3164/jcbn.16-16 |
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author | Bulle, Saradamma Reddy, Vaddi Damodara Padmavathi, Pannuru Maturu, Paramahamsa Puvvada, Pavan Kumar Nallanchakravarthula, Varadacharyulu |
author_facet | Bulle, Saradamma Reddy, Vaddi Damodara Padmavathi, Pannuru Maturu, Paramahamsa Puvvada, Pavan Kumar Nallanchakravarthula, Varadacharyulu |
author_sort | Bulle, Saradamma |
collection | PubMed |
description | The present study aimed to understand the association between erythrocyte membrane alterations and hemolysis in chronic alcoholics. Study was conducted on human male volunteers aged between 35–45 years with a drinking history of 8–10 years. Results showed that plasma marker enzymes AST, ALT, ALP and γGT were increased in alcoholic subjects. Plasma and erythrocyte membrane lipid peroxidation, erythrocyte lysate nitric oxide (NOx) levels were also increased significantly in alcoholics. Furthermore, erythrocyte membrane protein carbonyls, total cholesterol, phospholipid and cholesterol/phospholipid (C/P) ratio were increased in alcoholics. SDS-PAGE analysis of erythrocyte membrane proteins revealed that increased density of band 3, protein 4.2, 4.9, actin and glycophorins, whereas glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and glycophorin A showed slight increase, however, decreased ankyrin with no change in spectrins (α and β) and protein 4.1 densities were observed in alcoholics. Moreover, alcoholics red blood cells showed altered morphology with decreased resistance to osmotic hemolysis. Increased hemolysis showed strong positive association with lipid peroxidation (r = 0.703, p<0.05), protein carbonyls (r = 0.754, p<0.05), lysate NOx (r = 0.654, p<0.05) and weak association with C/P ratio (r = 0.240, p<0.05). Bottom line, increased lipid and protein oxidation, altered membrane C/P ratio and membrane cytoskeletal protein profile might be responsible for the increased hemolysis in alcoholics. |
format | Online Article Text |
id | pubmed-5281527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-52815272017-02-03 Association between alcohol-induced erythrocyte membrane alterations and hemolysis in chronic alcoholics Bulle, Saradamma Reddy, Vaddi Damodara Padmavathi, Pannuru Maturu, Paramahamsa Puvvada, Pavan Kumar Nallanchakravarthula, Varadacharyulu J Clin Biochem Nutr Original Article The present study aimed to understand the association between erythrocyte membrane alterations and hemolysis in chronic alcoholics. Study was conducted on human male volunteers aged between 35–45 years with a drinking history of 8–10 years. Results showed that plasma marker enzymes AST, ALT, ALP and γGT were increased in alcoholic subjects. Plasma and erythrocyte membrane lipid peroxidation, erythrocyte lysate nitric oxide (NOx) levels were also increased significantly in alcoholics. Furthermore, erythrocyte membrane protein carbonyls, total cholesterol, phospholipid and cholesterol/phospholipid (C/P) ratio were increased in alcoholics. SDS-PAGE analysis of erythrocyte membrane proteins revealed that increased density of band 3, protein 4.2, 4.9, actin and glycophorins, whereas glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and glycophorin A showed slight increase, however, decreased ankyrin with no change in spectrins (α and β) and protein 4.1 densities were observed in alcoholics. Moreover, alcoholics red blood cells showed altered morphology with decreased resistance to osmotic hemolysis. Increased hemolysis showed strong positive association with lipid peroxidation (r = 0.703, p<0.05), protein carbonyls (r = 0.754, p<0.05), lysate NOx (r = 0.654, p<0.05) and weak association with C/P ratio (r = 0.240, p<0.05). Bottom line, increased lipid and protein oxidation, altered membrane C/P ratio and membrane cytoskeletal protein profile might be responsible for the increased hemolysis in alcoholics. the Society for Free Radical Research Japan 2017-01 2016-10-05 /pmc/articles/PMC5281527/ /pubmed/28163384 http://dx.doi.org/10.3164/jcbn.16-16 Text en Copyright © 2017 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Bulle, Saradamma Reddy, Vaddi Damodara Padmavathi, Pannuru Maturu, Paramahamsa Puvvada, Pavan Kumar Nallanchakravarthula, Varadacharyulu Association between alcohol-induced erythrocyte membrane alterations and hemolysis in chronic alcoholics |
title | Association between alcohol-induced erythrocyte membrane alterations and hemolysis in chronic alcoholics |
title_full | Association between alcohol-induced erythrocyte membrane alterations and hemolysis in chronic alcoholics |
title_fullStr | Association between alcohol-induced erythrocyte membrane alterations and hemolysis in chronic alcoholics |
title_full_unstemmed | Association between alcohol-induced erythrocyte membrane alterations and hemolysis in chronic alcoholics |
title_short | Association between alcohol-induced erythrocyte membrane alterations and hemolysis in chronic alcoholics |
title_sort | association between alcohol-induced erythrocyte membrane alterations and hemolysis in chronic alcoholics |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5281527/ https://www.ncbi.nlm.nih.gov/pubmed/28163384 http://dx.doi.org/10.3164/jcbn.16-16 |
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