Prevention of processes coupled with free radical formation prevents also the development of calcium-resistance in the diabetic heart
Recently it was shown that besides their negative role in pathogenesis of diabetes, reactive oxygen species (ROS) and particularly the products of non-enzymatic glycation of proteins (NEGP) may also participate in some processes of adaptation of the myocardium to diabetes, such as in the mechanism o...
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Veröffentlicht in: | Life sciences (1973) 1999-10, Vol.65 (18), p.1999-2001 |
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creator | Ziegelhöffer, A. Styk, J. Ravingerová, T. Šeboková, J. Volkovová, K. Waczulíková, I. Čársky, J. Džurba, A. Dočolomanský, P. |
description | Recently it was shown that besides their negative role in pathogenesis of diabetes, reactive oxygen species (ROS) and particularly the products of non-enzymatic glycation of proteins (NEGP) may also participate in some processes of adaptation of the myocardium to diabetes, such as in the mechanism of development of calcium resistance of the heart. Our study revealed that the hearts of rats with experimentally induced diabetes (single dose of streptozotocin, 45 mg/kg i.V., 6 U/kg insulin daily) develop considerable resistance against calcium overload (induced by means of Ca-paradox). On the day 63 after the beginning of experiment, when the diabetic cardiomyopathy became fully developed but the hearts were still not failing, their calcium resistance was increased to 83.33 %. Our results provide evidence that, when applied in a special regimen, resorcylidene aminoguanidine (RAG, 4 mg/kg) prevented both, the formation of fructosamine (a source of ROS generation), and also that of the advanced Maillard products, in the heart sarcolemma of diabetic rats. The effect of RAG was accompanied by a decrease in calcium resistance in the group of rats with chronic diabetes (63 days) from 83.3 to 46.7 %. It is concluded that NEGP and ROS formation are inevitably needed for development of calcium resistance in the diabetic hearts. |
doi_str_mv | 10.1016/S0024-3205(99)00464-6 |
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Our study revealed that the hearts of rats with experimentally induced diabetes (single dose of streptozotocin, 45 mg/kg i.V., 6 U/kg insulin daily) develop considerable resistance against calcium overload (induced by means of Ca-paradox). On the day 63 after the beginning of experiment, when the diabetic cardiomyopathy became fully developed but the hearts were still not failing, their calcium resistance was increased to 83.33 %. Our results provide evidence that, when applied in a special regimen, resorcylidene aminoguanidine (RAG, 4 mg/kg) prevented both, the formation of fructosamine (a source of ROS generation), and also that of the advanced Maillard products, in the heart sarcolemma of diabetic rats. The effect of RAG was accompanied by a decrease in calcium resistance in the group of rats with chronic diabetes (63 days) from 83.3 to 46.7 %. It is concluded that NEGP and ROS formation are inevitably needed for development of calcium resistance in the diabetic hearts.</description><identifier>ISSN: 0024-3205</identifier><identifier>EISSN: 1879-0631</identifier><identifier>DOI: 10.1016/S0024-3205(99)00464-6</identifier><identifier>PMID: 10576454</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Animals ; Antioxidants - pharmacology ; Calcium - metabolism ; calcium resistance ; Diabetes Mellitus, Experimental - metabolism ; diabetic heart ; Free Radicals - metabolism ; fructosamine ; Glycoproteins - metabolism ; Guanidines - pharmacology ; Male ; Myocardium - metabolism ; non-enzymatic protein glycation ; Rats ; Rats, Wistar ; reactive oxygen species ; Reactive Oxygen Species - metabolism ; resorcylidene aminoguanidine ; Sarcolemma - drug effects ; Sarcolemma - metabolism</subject><ispartof>Life sciences (1973), 1999-10, Vol.65 (18), p.1999-2001</ispartof><rights>1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-4939d96b8e12b3433e9154a924aaf9d25009c8224be2551f094f3115d7fd870b3</citedby><cites>FETCH-LOGICAL-c392t-4939d96b8e12b3433e9154a924aaf9d25009c8224be2551f094f3115d7fd870b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0024-3205(99)00464-6$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10576454$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ziegelhöffer, A.</creatorcontrib><creatorcontrib>Styk, J.</creatorcontrib><creatorcontrib>Ravingerová, T.</creatorcontrib><creatorcontrib>Šeboková, J.</creatorcontrib><creatorcontrib>Volkovová, K.</creatorcontrib><creatorcontrib>Waczulíková, I.</creatorcontrib><creatorcontrib>Čársky, J.</creatorcontrib><creatorcontrib>Džurba, A.</creatorcontrib><creatorcontrib>Dočolomanský, P.</creatorcontrib><title>Prevention of processes coupled with free radical formation prevents also the development of calcium-resistance in the diabetic heart</title><title>Life sciences (1973)</title><addtitle>Life Sci</addtitle><description>Recently it was shown that besides their negative role in pathogenesis of diabetes, reactive oxygen species (ROS) and particularly the products of non-enzymatic glycation of proteins (NEGP) may also participate in some processes of adaptation of the myocardium to diabetes, such as in the mechanism of development of calcium resistance of the heart. Our study revealed that the hearts of rats with experimentally induced diabetes (single dose of streptozotocin, 45 mg/kg i.V., 6 U/kg insulin daily) develop considerable resistance against calcium overload (induced by means of Ca-paradox). On the day 63 after the beginning of experiment, when the diabetic cardiomyopathy became fully developed but the hearts were still not failing, their calcium resistance was increased to 83.33 %. Our results provide evidence that, when applied in a special regimen, resorcylidene aminoguanidine (RAG, 4 mg/kg) prevented both, the formation of fructosamine (a source of ROS generation), and also that of the advanced Maillard products, in the heart sarcolemma of diabetic rats. The effect of RAG was accompanied by a decrease in calcium resistance in the group of rats with chronic diabetes (63 days) from 83.3 to 46.7 %. It is concluded that NEGP and ROS formation are inevitably needed for development of calcium resistance in the diabetic hearts.</description><subject>Animals</subject><subject>Antioxidants - pharmacology</subject><subject>Calcium - metabolism</subject><subject>calcium resistance</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>diabetic heart</subject><subject>Free Radicals - metabolism</subject><subject>fructosamine</subject><subject>Glycoproteins - metabolism</subject><subject>Guanidines - pharmacology</subject><subject>Male</subject><subject>Myocardium - metabolism</subject><subject>non-enzymatic protein glycation</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>resorcylidene aminoguanidine</subject><subject>Sarcolemma - drug effects</subject><subject>Sarcolemma - metabolism</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2KFTEQhYM4ONfRR1CyknHRmt_OzUpkGH9gQEFdh3RS4Ua6O22SHvEB5r3NvT2Iu1kVFN85RZ2D0AtK3lBC-7ffCGGi44zIS61fEyJ60fWP0I7ule5Iz-ljtPuHnKOnpfwkhEip-BN0TolUvZBih-6-ZriFucY04xTwkpODUqBgl9ZlBI9_x3rAIQPgbH10dsQh5cmeBMumLdiOJeF6AOzbYkzL1LZHu4a7uE5dhhJLtbMDHOcNjHaAGh0-gM31GToLzQOe388L9OPD9ferT93Nl4-fr97fdI5rVjuhufa6H_ZA2cAF56CpFFYzYW3QnklCtNszJgZgUtJAtAicUulV8HtFBn6BXm2-7c9fK5RqplgcjKOdIa3F9JqTFq56EKSKayUVa6DcQJdTKRmCWXKcbP5jKDHHosypKHNswWhtTkWZvule3h9Yhwn8f6qtmQa82wBoedxGyKa4CC1BHzO4anyKD5z4C1ATpEk</recordid><startdate>19991001</startdate><enddate>19991001</enddate><creator>Ziegelhöffer, A.</creator><creator>Styk, J.</creator><creator>Ravingerová, T.</creator><creator>Šeboková, J.</creator><creator>Volkovová, K.</creator><creator>Waczulíková, I.</creator><creator>Čársky, J.</creator><creator>Džurba, A.</creator><creator>Dočolomanský, P.</creator><general>Elsevier Inc</general><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>7QP</scope><scope>7X8</scope></search><sort><creationdate>19991001</creationdate><title>Prevention of processes coupled with free radical formation prevents also the development of calcium-resistance in the diabetic heart</title><author>Ziegelhöffer, A. ; Styk, J. ; Ravingerová, T. ; Šeboková, J. ; Volkovová, K. ; Waczulíková, I. ; Čársky, J. ; Džurba, A. ; Dočolomanský, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-4939d96b8e12b3433e9154a924aaf9d25009c8224be2551f094f3115d7fd870b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Antioxidants - pharmacology</topic><topic>Calcium - metabolism</topic><topic>calcium resistance</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>diabetic heart</topic><topic>Free Radicals - metabolism</topic><topic>fructosamine</topic><topic>Glycoproteins - metabolism</topic><topic>Guanidines - pharmacology</topic><topic>Male</topic><topic>Myocardium - metabolism</topic><topic>non-enzymatic protein glycation</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>resorcylidene aminoguanidine</topic><topic>Sarcolemma - drug effects</topic><topic>Sarcolemma - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ziegelhöffer, A.</creatorcontrib><creatorcontrib>Styk, J.</creatorcontrib><creatorcontrib>Ravingerová, T.</creatorcontrib><creatorcontrib>Šeboková, J.</creatorcontrib><creatorcontrib>Volkovová, K.</creatorcontrib><creatorcontrib>Waczulíková, I.</creatorcontrib><creatorcontrib>Čársky, J.</creatorcontrib><creatorcontrib>Džurba, A.</creatorcontrib><creatorcontrib>Dočolomanský, P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ziegelhöffer, A.</au><au>Styk, J.</au><au>Ravingerová, T.</au><au>Šeboková, J.</au><au>Volkovová, K.</au><au>Waczulíková, I.</au><au>Čársky, J.</au><au>Džurba, A.</au><au>Dočolomanský, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevention of processes coupled with free radical formation prevents also the development of calcium-resistance in the diabetic heart</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>1999-10-01</date><risdate>1999</risdate><volume>65</volume><issue>18</issue><spage>1999</spage><epage>2001</epage><pages>1999-2001</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>Recently it was shown that besides their negative role in pathogenesis of diabetes, reactive oxygen species (ROS) and particularly the products of non-enzymatic glycation of proteins (NEGP) may also participate in some processes of adaptation of the myocardium to diabetes, such as in the mechanism of development of calcium resistance of the heart. Our study revealed that the hearts of rats with experimentally induced diabetes (single dose of streptozotocin, 45 mg/kg i.V., 6 U/kg insulin daily) develop considerable resistance against calcium overload (induced by means of Ca-paradox). On the day 63 after the beginning of experiment, when the diabetic cardiomyopathy became fully developed but the hearts were still not failing, their calcium resistance was increased to 83.33 %. Our results provide evidence that, when applied in a special regimen, resorcylidene aminoguanidine (RAG, 4 mg/kg) prevented both, the formation of fructosamine (a source of ROS generation), and also that of the advanced Maillard products, in the heart sarcolemma of diabetic rats. The effect of RAG was accompanied by a decrease in calcium resistance in the group of rats with chronic diabetes (63 days) from 83.3 to 46.7 %. It is concluded that NEGP and ROS formation are inevitably needed for development of calcium resistance in the diabetic hearts.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>10576454</pmid><doi>10.1016/S0024-3205(99)00464-6</doi><tpages>3</tpages></addata></record> |
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subjects | Animals Antioxidants - pharmacology Calcium - metabolism calcium resistance Diabetes Mellitus, Experimental - metabolism diabetic heart Free Radicals - metabolism fructosamine Glycoproteins - metabolism Guanidines - pharmacology Male Myocardium - metabolism non-enzymatic protein glycation Rats Rats, Wistar reactive oxygen species Reactive Oxygen Species - metabolism resorcylidene aminoguanidine Sarcolemma - drug effects Sarcolemma - metabolism |
title | Prevention of processes coupled with free radical formation prevents also the development of calcium-resistance in the diabetic heart |
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