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Endogenous digoxin-like immunoactivity and diabetes mellitus: facts and hypotheses
Substances with digoxin- and ouabain-like immunoactivity (DLIA) are specific inhibitors of Na +-K +-ATPase which increase the total amount of intracellular stored calcium (Ca 2+ i). In diabetic patients, DLIA levels have been reported to be increased. Although this increase is probably secondary to...
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Published in: | Medical hypotheses 1997-09, Vol.49 (3), p.271-275 |
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container_issue | 3 |
container_start_page | 271 |
container_title | Medical hypotheses |
container_volume | 49 |
creator | Martinka, E. Galajada, P. Ochodnicky, M. Lichardus, B. Straka, S. Mokan, M. |
description | Substances with digoxin- and ouabain-like immunoactivity (DLIA) are specific inhibitors of Na
+-K
+-ATPase which increase the total amount of intracellular stored calcium (Ca
2+
i). In diabetic patients, DLIA levels have been reported to be increased. Although this increase is probably secondary to sodium retention and volume expansion (induced in diabetic subjects by hyperinsulinemia and/or diabetic nephropathy), the question arises of whether it has pathophysiological consequences: namely, whether substances with DLIA, via their effect on Na
+-K
+-ATPase activity and Ca
2+
i stores, could in diabetic subjects facilitate development of hypertension and/or modulate insulin sensitivity or insulin secretion.
Clinical findings of correlations of DLIA to blood pressure, insulin levels and to degree of insulin resistance, together with experimental findings of decreased Na
+-K
+-ATPase activity, increased Ca
2+
i and decreased Mg
2+
i n both diabetic and hypertensioe subjects, support these hypotheses. However, the issue of whether or not these relations are causative and whether or not defects in intracellular milieu are primary or secondary to non-insulin-dependent diabetes mellitus has not been resolved yet. Moreover, pathogenesis of both diabetes mellitus and hypertension is multifactorial and includes many other factors. Therefore, further efforts should be made to elucidate the exact role of substances with DLIA in diabetes mellitus. |
doi_str_mv | 10.1016/S0306-9877(97)90212-7 |
format | article |
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+-K
+-ATPase which increase the total amount of intracellular stored calcium (Ca
2+
i). In diabetic patients, DLIA levels have been reported to be increased. Although this increase is probably secondary to sodium retention and volume expansion (induced in diabetic subjects by hyperinsulinemia and/or diabetic nephropathy), the question arises of whether it has pathophysiological consequences: namely, whether substances with DLIA, via their effect on Na
+-K
+-ATPase activity and Ca
2+
i stores, could in diabetic subjects facilitate development of hypertension and/or modulate insulin sensitivity or insulin secretion.
Clinical findings of correlations of DLIA to blood pressure, insulin levels and to degree of insulin resistance, together with experimental findings of decreased Na
+-K
+-ATPase activity, increased Ca
2+
i and decreased Mg
2+
i n both diabetic and hypertensioe subjects, support these hypotheses. However, the issue of whether or not these relations are causative and whether or not defects in intracellular milieu are primary or secondary to non-insulin-dependent diabetes mellitus has not been resolved yet. Moreover, pathogenesis of both diabetes mellitus and hypertension is multifactorial and includes many other factors. Therefore, further efforts should be made to elucidate the exact role of substances with DLIA in diabetes mellitus.</description><identifier>ISSN: 0306-9877</identifier><identifier>EISSN: 1532-2777</identifier><identifier>DOI: 10.1016/S0306-9877(97)90212-7</identifier><identifier>PMID: 9293472</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Biological and medical sciences ; Cardiotonic agents ; Cardiovascular system ; Diabetes Mellitus - physiopathology ; Diabetes Mellitus, Type 2 - physiopathology ; Diabetic Angiopathies - physiopathology ; Diabetic Nephropathies - physiopathology ; Digoxin - analysis ; Glucose - metabolism ; Humans ; Hyperinsulinism ; Hypertension - physiopathology ; Immunoassay ; Insulin - metabolism ; Insulin Secretion ; Medical sciences ; Models, Biological ; Ouabain - analysis ; Pharmacology. Drug treatments</subject><ispartof>Medical hypotheses, 1997-09, Vol.49 (3), p.271-275</ispartof><rights>1997</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-9bfec955d7f034e62afbb32045d2b8b88f94c9eab1b129c33a1b9201f868efbb3</citedby><cites>FETCH-LOGICAL-c389t-9bfec955d7f034e62afbb32045d2b8b88f94c9eab1b129c33a1b9201f868efbb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2777151$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9293472$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martinka, E.</creatorcontrib><creatorcontrib>Galajada, P.</creatorcontrib><creatorcontrib>Ochodnicky, M.</creatorcontrib><creatorcontrib>Lichardus, B.</creatorcontrib><creatorcontrib>Straka, S.</creatorcontrib><creatorcontrib>Mokan, M.</creatorcontrib><title>Endogenous digoxin-like immunoactivity and diabetes mellitus: facts and hypotheses</title><title>Medical hypotheses</title><addtitle>Med Hypotheses</addtitle><description>Substances with digoxin- and ouabain-like immunoactivity (DLIA) are specific inhibitors of Na
+-K
+-ATPase which increase the total amount of intracellular stored calcium (Ca
2+
i). In diabetic patients, DLIA levels have been reported to be increased. Although this increase is probably secondary to sodium retention and volume expansion (induced in diabetic subjects by hyperinsulinemia and/or diabetic nephropathy), the question arises of whether it has pathophysiological consequences: namely, whether substances with DLIA, via their effect on Na
+-K
+-ATPase activity and Ca
2+
i stores, could in diabetic subjects facilitate development of hypertension and/or modulate insulin sensitivity or insulin secretion.
Clinical findings of correlations of DLIA to blood pressure, insulin levels and to degree of insulin resistance, together with experimental findings of decreased Na
+-K
+-ATPase activity, increased Ca
2+
i and decreased Mg
2+
i n both diabetic and hypertensioe subjects, support these hypotheses. However, the issue of whether or not these relations are causative and whether or not defects in intracellular milieu are primary or secondary to non-insulin-dependent diabetes mellitus has not been resolved yet. Moreover, pathogenesis of both diabetes mellitus and hypertension is multifactorial and includes many other factors. Therefore, further efforts should be made to elucidate the exact role of substances with DLIA in diabetes mellitus.</description><subject>Biological and medical sciences</subject><subject>Cardiotonic agents</subject><subject>Cardiovascular system</subject><subject>Diabetes Mellitus - physiopathology</subject><subject>Diabetes Mellitus, Type 2 - physiopathology</subject><subject>Diabetic Angiopathies - physiopathology</subject><subject>Diabetic Nephropathies - physiopathology</subject><subject>Digoxin - analysis</subject><subject>Glucose - metabolism</subject><subject>Humans</subject><subject>Hyperinsulinism</subject><subject>Hypertension - physiopathology</subject><subject>Immunoassay</subject><subject>Insulin - metabolism</subject><subject>Insulin Secretion</subject><subject>Medical sciences</subject><subject>Models, Biological</subject><subject>Ouabain - analysis</subject><subject>Pharmacology. Drug treatments</subject><issn>0306-9877</issn><issn>1532-2777</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkctKxDAUhoMo43h5BKELEV1Uc2mbxo3I4A0GBC_rkKQnGu1lbNrBeXvTmTJbIZDF_52cc74gdELwJcEku3rFDGexyDk_F_xCYEpozHfQlKSMxpRzvoumW2QfHXj_hTEWCcsnaCKoYAmnU_RyVxfNB9RN76PCfTS_ro5L9w2Rq6q-bpTp3NJ1q0jVRciVhg58VEFZuq7315ENgF-Hn6tF032CB3-E9qwqPRyP9yF6v797mz3G8-eHp9ntPDYsF10stAUj0rTgFrMEMqqs1oziJC2oznWeW5EYAUoTTagwjCmiBcXE5lkOA3qIzjbvLtrmpwffycp5E0ZTNYR1JBfBQsZJANMNaNrG-xasXLSuUu1KEiwHl3LtUg6ipAhncCl5qDsZG_S6gmJbNcoL-emYK29UaVtVG-e32PAHJB3a32wwCDKWDlrpjYPaQOFaMJ0sGvfPIH-WMpI1</recordid><startdate>19970901</startdate><enddate>19970901</enddate><creator>Martinka, E.</creator><creator>Galajada, P.</creator><creator>Ochodnicky, M.</creator><creator>Lichardus, B.</creator><creator>Straka, S.</creator><creator>Mokan, M.</creator><general>Elsevier Ltd</general><general>Elsevier</general><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>19970901</creationdate><title>Endogenous digoxin-like immunoactivity and diabetes mellitus: facts and hypotheses</title><author>Martinka, E. ; Galajada, P. ; Ochodnicky, M. ; Lichardus, B. ; Straka, S. ; Mokan, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-9bfec955d7f034e62afbb32045d2b8b88f94c9eab1b129c33a1b9201f868efbb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Biological and medical sciences</topic><topic>Cardiotonic agents</topic><topic>Cardiovascular system</topic><topic>Diabetes Mellitus - physiopathology</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Diabetic Angiopathies - physiopathology</topic><topic>Diabetic Nephropathies - physiopathology</topic><topic>Digoxin - analysis</topic><topic>Glucose - metabolism</topic><topic>Humans</topic><topic>Hyperinsulinism</topic><topic>Hypertension - physiopathology</topic><topic>Immunoassay</topic><topic>Insulin - metabolism</topic><topic>Insulin Secretion</topic><topic>Medical sciences</topic><topic>Models, Biological</topic><topic>Ouabain - analysis</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martinka, E.</creatorcontrib><creatorcontrib>Galajada, P.</creatorcontrib><creatorcontrib>Ochodnicky, M.</creatorcontrib><creatorcontrib>Lichardus, B.</creatorcontrib><creatorcontrib>Straka, S.</creatorcontrib><creatorcontrib>Mokan, M.</creatorcontrib><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>Medical hypotheses</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martinka, E.</au><au>Galajada, P.</au><au>Ochodnicky, M.</au><au>Lichardus, B.</au><au>Straka, S.</au><au>Mokan, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endogenous digoxin-like immunoactivity and diabetes mellitus: facts and hypotheses</atitle><jtitle>Medical hypotheses</jtitle><addtitle>Med Hypotheses</addtitle><date>1997-09-01</date><risdate>1997</risdate><volume>49</volume><issue>3</issue><spage>271</spage><epage>275</epage><pages>271-275</pages><issn>0306-9877</issn><eissn>1532-2777</eissn><abstract>Substances with digoxin- and ouabain-like immunoactivity (DLIA) are specific inhibitors of Na
+-K
+-ATPase which increase the total amount of intracellular stored calcium (Ca
2+
i). In diabetic patients, DLIA levels have been reported to be increased. Although this increase is probably secondary to sodium retention and volume expansion (induced in diabetic subjects by hyperinsulinemia and/or diabetic nephropathy), the question arises of whether it has pathophysiological consequences: namely, whether substances with DLIA, via their effect on Na
+-K
+-ATPase activity and Ca
2+
i stores, could in diabetic subjects facilitate development of hypertension and/or modulate insulin sensitivity or insulin secretion.
Clinical findings of correlations of DLIA to blood pressure, insulin levels and to degree of insulin resistance, together with experimental findings of decreased Na
+-K
+-ATPase activity, increased Ca
2+
i and decreased Mg
2+
i n both diabetic and hypertensioe subjects, support these hypotheses. However, the issue of whether or not these relations are causative and whether or not defects in intracellular milieu are primary or secondary to non-insulin-dependent diabetes mellitus has not been resolved yet. Moreover, pathogenesis of both diabetes mellitus and hypertension is multifactorial and includes many other factors. Therefore, further efforts should be made to elucidate the exact role of substances with DLIA in diabetes mellitus.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>9293472</pmid><doi>10.1016/S0306-9877(97)90212-7</doi><tpages>5</tpages></addata></record> |
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source | ScienceDirect Journals |
subjects | Biological and medical sciences Cardiotonic agents Cardiovascular system Diabetes Mellitus - physiopathology Diabetes Mellitus, Type 2 - physiopathology Diabetic Angiopathies - physiopathology Diabetic Nephropathies - physiopathology Digoxin - analysis Glucose - metabolism Humans Hyperinsulinism Hypertension - physiopathology Immunoassay Insulin - metabolism Insulin Secretion Medical sciences Models, Biological Ouabain - analysis Pharmacology. Drug treatments |
title | Endogenous digoxin-like immunoactivity and diabetes mellitus: facts and hypotheses |
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