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Decreased ADP-Ribosyl Cyclase Activity in Peripheral Blood Mononuclear Cells from Diabetic Patients with Nephropathy
Aims/hypothesis. ADP-ribosyl-cyclase activity (ADPRCA) of CD38 and other ectoenzymes mainly generate cyclic adenosine 5'diphosphate-(ADP-) ribose (cADPR) as a second messenger in various mammalian cells, including pancreatic beta cells and peripheral blood mononuclear cells (PBMCs). Since PBMCs...
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Published in: | Experimental diabetes research 2008-01, Vol.2008 (2008), p.1-8 |
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creator | Yagi, Kunimasa Ohtsuji, Michio Shintaku-Kubota, Miyuki Kojima-Koba, Yukiko Ito, Naoko Sugihara, Masako Yamaaki, Naoto Chujo, Daisuke Nohara, Atsushi Takeda, Yoshiyu Kobayashi, Junji Yamagishi, Masakazu Higashida, Haruhiro |
description | Aims/hypothesis. ADP-ribosyl-cyclase activity (ADPRCA) of CD38 and other ectoenzymes mainly generate cyclic adenosine 5'diphosphate-(ADP-) ribose (cADPR) as a second messenger in various mammalian cells, including pancreatic beta cells and peripheral blood mononuclear cells (PBMCs). Since PBMCs contribute to the pathogenesis of diabetic nephropathy, ADPRCA of PBMCs could serve as a clinical prognostic marker for diabetic nephropathy. This study aimed to investigate the connection between ADPRCA in PBMCs and diabetic complications. Methods. PBMCs from 60 diabetic patients (10 for type 1 and 50 for type 2) and 15 nondiabetic controls were fluorometrically measured for ADPRCA based on the conversion of nicotinamide guanine dinucleotide (NGD+) into cyclic GDP-ribose. Results. ADPRCA negatively correlated with the level of HbA1c (P=.040, R2=.073), although ADPRCA showed no significant correlation with gender, age, BMI, blood pressure, level of fasting plasma glucose and lipid levels, as well as type, duration, or medication of diabetes. Interestingly, patients with nephropathy, but not other complications, presented significantly lower ADPRCA than those without nephropathy (P=.0198) and diabetes (P=.0332). ANCOVA analysis adjusted for HbA1c showed no significant correlation between ADPRCA and nephropathy. However, logistic regression analyses revealed that determinants for nephropathy were systolic blood pressure and ADPRCA, not HbA1c. Conclusion/interpretation. Decreased ADPRCA significantly correlated with diabetic nephropathy. ADPRCA in PBMCs would be an important marker associated with diabetic nephropathy. |
doi_str_mv | 10.1155/2008/897508 |
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ADP-ribosyl-cyclase activity (ADPRCA) of CD38 and other ectoenzymes mainly generate cyclic adenosine 5'diphosphate-(ADP-) ribose (cADPR) as a second messenger in various mammalian cells, including pancreatic beta cells and peripheral blood mononuclear cells (PBMCs). Since PBMCs contribute to the pathogenesis of diabetic nephropathy, ADPRCA of PBMCs could serve as a clinical prognostic marker for diabetic nephropathy. This study aimed to investigate the connection between ADPRCA in PBMCs and diabetic complications. Methods. PBMCs from 60 diabetic patients (10 for type 1 and 50 for type 2) and 15 nondiabetic controls were fluorometrically measured for ADPRCA based on the conversion of nicotinamide guanine dinucleotide (NGD+) into cyclic GDP-ribose. Results. ADPRCA negatively correlated with the level of HbA1c (P=.040, R2=.073), although ADPRCA showed no significant correlation with gender, age, BMI, blood pressure, level of fasting plasma glucose and lipid levels, as well as type, duration, or medication of diabetes. Interestingly, patients with nephropathy, but not other complications, presented significantly lower ADPRCA than those without nephropathy (P=.0198) and diabetes (P=.0332). ANCOVA analysis adjusted for HbA1c showed no significant correlation between ADPRCA and nephropathy. However, logistic regression analyses revealed that determinants for nephropathy were systolic blood pressure and ADPRCA, not HbA1c. Conclusion/interpretation. Decreased ADPRCA significantly correlated with diabetic nephropathy. ADPRCA in PBMCs would be an important marker associated with diabetic nephropathy.</description><identifier>ISSN: 1687-5214</identifier><identifier>ISSN: 2314-6745</identifier><identifier>EISSN: 1687-5303</identifier><identifier>EISSN: 2314-6753</identifier><identifier>DOI: 10.1155/2008/897508</identifier><identifier>PMID: 19300526</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Puplishing Corporation</publisher><subject>ADP-ribosyl Cyclase - blood ; ADP-ribosyl Cyclase 1 - physiology ; Diabetic Nephropathies - enzymology ; Female ; Glycated Hemoglobin A - analysis ; Humans ; Leukocytes, Mononuclear - enzymology ; Male ; Membrane Glycoproteins - physiology</subject><ispartof>Experimental diabetes research, 2008-01, Vol.2008 (2008), p.1-8</ispartof><rights>Copyright © 2008</rights><rights>Copyright © 2008 Michio Ohtsuji et al. 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-5f4c7ffde625ed5a8f6e6bd006c84dede25b6b0ad514eb552f2115d01a7a246a3</citedby><cites>FETCH-LOGICAL-c480t-5f4c7ffde625ed5a8f6e6bd006c84dede25b6b0ad514eb552f2115d01a7a246a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656910/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656910/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19300526$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Pfützner, Andreas</contributor><creatorcontrib>Yagi, Kunimasa</creatorcontrib><creatorcontrib>Ohtsuji, Michio</creatorcontrib><creatorcontrib>Shintaku-Kubota, Miyuki</creatorcontrib><creatorcontrib>Kojima-Koba, Yukiko</creatorcontrib><creatorcontrib>Ito, Naoko</creatorcontrib><creatorcontrib>Sugihara, Masako</creatorcontrib><creatorcontrib>Yamaaki, Naoto</creatorcontrib><creatorcontrib>Chujo, Daisuke</creatorcontrib><creatorcontrib>Nohara, Atsushi</creatorcontrib><creatorcontrib>Takeda, Yoshiyu</creatorcontrib><creatorcontrib>Kobayashi, Junji</creatorcontrib><creatorcontrib>Yamagishi, Masakazu</creatorcontrib><creatorcontrib>Higashida, Haruhiro</creatorcontrib><title>Decreased ADP-Ribosyl Cyclase Activity in Peripheral Blood Mononuclear Cells from Diabetic Patients with Nephropathy</title><title>Experimental diabetes research</title><addtitle>Exp Diabetes Res</addtitle><description>Aims/hypothesis. ADP-ribosyl-cyclase activity (ADPRCA) of CD38 and other ectoenzymes mainly generate cyclic adenosine 5'diphosphate-(ADP-) ribose (cADPR) as a second messenger in various mammalian cells, including pancreatic beta cells and peripheral blood mononuclear cells (PBMCs). Since PBMCs contribute to the pathogenesis of diabetic nephropathy, ADPRCA of PBMCs could serve as a clinical prognostic marker for diabetic nephropathy. This study aimed to investigate the connection between ADPRCA in PBMCs and diabetic complications. Methods. PBMCs from 60 diabetic patients (10 for type 1 and 50 for type 2) and 15 nondiabetic controls were fluorometrically measured for ADPRCA based on the conversion of nicotinamide guanine dinucleotide (NGD+) into cyclic GDP-ribose. Results. ADPRCA negatively correlated with the level of HbA1c (P=.040, R2=.073), although ADPRCA showed no significant correlation with gender, age, BMI, blood pressure, level of fasting plasma glucose and lipid levels, as well as type, duration, or medication of diabetes. Interestingly, patients with nephropathy, but not other complications, presented significantly lower ADPRCA than those without nephropathy (P=.0198) and diabetes (P=.0332). ANCOVA analysis adjusted for HbA1c showed no significant correlation between ADPRCA and nephropathy. However, logistic regression analyses revealed that determinants for nephropathy were systolic blood pressure and ADPRCA, not HbA1c. Conclusion/interpretation. Decreased ADPRCA significantly correlated with diabetic nephropathy. ADPRCA in PBMCs would be an important marker associated with diabetic nephropathy.</description><subject>ADP-ribosyl Cyclase - blood</subject><subject>ADP-ribosyl Cyclase 1 - physiology</subject><subject>Diabetic Nephropathies - enzymology</subject><subject>Female</subject><subject>Glycated Hemoglobin A - analysis</subject><subject>Humans</subject><subject>Leukocytes, Mononuclear - enzymology</subject><subject>Male</subject><subject>Membrane Glycoproteins - physiology</subject><issn>1687-5214</issn><issn>2314-6745</issn><issn>1687-5303</issn><issn>2314-6753</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkc1v1DAQxS0EoqVw4gzyiQNVqO3YTvaCtOyWD6nACsHZcuwxMcrGwfa2yn-PqywFTpw88vz05s08hJ5S8opSIS4YIe1Fu2oEae-hUyrbphI1qe__rhnlJ-hRSj8I4VKI9iE6oauaEMHkKcpbMBF0AovX2131xXchzQPezGYon3htsr_2ecZ-xDuIfuoh6gG_GUKw-GMYw3gwA-iINzAMCbsY9njrdQfZG7zT2cOYE77xucefYOpjmHTu58fogdNDgifH9wx9e3v5dfO-uvr87sNmfVUZ3pJcCcdN45wFyQRYoVsnQXaWEGlabsECE53siLaCcuiEYI6Vg1hCdaMZl7o-Q68X3enQ7cGaYqa4V1P0ex1nFbRX_3ZG36vv4VoxKeSKkiLw4igQw88DpKz2Ppmyqh4hHJKSsiG8obyA5wtoYkgpgrsbQom6TUndpqSWlAr9_G9ff9hjLAV4uQC9H62-8f9Re7bAUBBw-g4WRNaruv4FUiamfg</recordid><startdate>20080101</startdate><enddate>20080101</enddate><creator>Yagi, Kunimasa</creator><creator>Ohtsuji, Michio</creator><creator>Shintaku-Kubota, Miyuki</creator><creator>Kojima-Koba, Yukiko</creator><creator>Ito, Naoko</creator><creator>Sugihara, Masako</creator><creator>Yamaaki, Naoto</creator><creator>Chujo, Daisuke</creator><creator>Nohara, Atsushi</creator><creator>Takeda, Yoshiyu</creator><creator>Kobayashi, Junji</creator><creator>Yamagishi, Masakazu</creator><creator>Higashida, Haruhiro</creator><general>Hindawi Puplishing Corporation</general><general>Hindawi Publishing Corporation</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</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><scope>5PM</scope></search><sort><creationdate>20080101</creationdate><title>Decreased ADP-Ribosyl Cyclase Activity in Peripheral Blood Mononuclear Cells from Diabetic Patients with Nephropathy</title><author>Yagi, Kunimasa ; Ohtsuji, Michio ; Shintaku-Kubota, Miyuki ; Kojima-Koba, Yukiko ; Ito, Naoko ; Sugihara, Masako ; Yamaaki, Naoto ; Chujo, Daisuke ; Nohara, Atsushi ; Takeda, Yoshiyu ; Kobayashi, Junji ; Yamagishi, Masakazu ; Higashida, Haruhiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c480t-5f4c7ffde625ed5a8f6e6bd006c84dede25b6b0ad514eb552f2115d01a7a246a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>ADP-ribosyl Cyclase - blood</topic><topic>ADP-ribosyl Cyclase 1 - physiology</topic><topic>Diabetic Nephropathies - enzymology</topic><topic>Female</topic><topic>Glycated Hemoglobin A - analysis</topic><topic>Humans</topic><topic>Leukocytes, Mononuclear - enzymology</topic><topic>Male</topic><topic>Membrane Glycoproteins - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yagi, Kunimasa</creatorcontrib><creatorcontrib>Ohtsuji, Michio</creatorcontrib><creatorcontrib>Shintaku-Kubota, Miyuki</creatorcontrib><creatorcontrib>Kojima-Koba, Yukiko</creatorcontrib><creatorcontrib>Ito, Naoko</creatorcontrib><creatorcontrib>Sugihara, Masako</creatorcontrib><creatorcontrib>Yamaaki, Naoto</creatorcontrib><creatorcontrib>Chujo, Daisuke</creatorcontrib><creatorcontrib>Nohara, Atsushi</creatorcontrib><creatorcontrib>Takeda, Yoshiyu</creatorcontrib><creatorcontrib>Kobayashi, Junji</creatorcontrib><creatorcontrib>Yamagishi, Masakazu</creatorcontrib><creatorcontrib>Higashida, Haruhiro</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental diabetes research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yagi, Kunimasa</au><au>Ohtsuji, Michio</au><au>Shintaku-Kubota, Miyuki</au><au>Kojima-Koba, Yukiko</au><au>Ito, Naoko</au><au>Sugihara, Masako</au><au>Yamaaki, Naoto</au><au>Chujo, Daisuke</au><au>Nohara, Atsushi</au><au>Takeda, Yoshiyu</au><au>Kobayashi, Junji</au><au>Yamagishi, Masakazu</au><au>Higashida, Haruhiro</au><au>Pfützner, Andreas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased ADP-Ribosyl Cyclase Activity in Peripheral Blood Mononuclear Cells from Diabetic Patients with Nephropathy</atitle><jtitle>Experimental diabetes research</jtitle><addtitle>Exp Diabetes Res</addtitle><date>2008-01-01</date><risdate>2008</risdate><volume>2008</volume><issue>2008</issue><spage>1</spage><epage>8</epage><pages>1-8</pages><issn>1687-5214</issn><issn>2314-6745</issn><eissn>1687-5303</eissn><eissn>2314-6753</eissn><abstract>Aims/hypothesis. ADP-ribosyl-cyclase activity (ADPRCA) of CD38 and other ectoenzymes mainly generate cyclic adenosine 5'diphosphate-(ADP-) ribose (cADPR) as a second messenger in various mammalian cells, including pancreatic beta cells and peripheral blood mononuclear cells (PBMCs). Since PBMCs contribute to the pathogenesis of diabetic nephropathy, ADPRCA of PBMCs could serve as a clinical prognostic marker for diabetic nephropathy. This study aimed to investigate the connection between ADPRCA in PBMCs and diabetic complications. Methods. PBMCs from 60 diabetic patients (10 for type 1 and 50 for type 2) and 15 nondiabetic controls were fluorometrically measured for ADPRCA based on the conversion of nicotinamide guanine dinucleotide (NGD+) into cyclic GDP-ribose. Results. ADPRCA negatively correlated with the level of HbA1c (P=.040, R2=.073), although ADPRCA showed no significant correlation with gender, age, BMI, blood pressure, level of fasting plasma glucose and lipid levels, as well as type, duration, or medication of diabetes. Interestingly, patients with nephropathy, but not other complications, presented significantly lower ADPRCA than those without nephropathy (P=.0198) and diabetes (P=.0332). ANCOVA analysis adjusted for HbA1c showed no significant correlation between ADPRCA and nephropathy. However, logistic regression analyses revealed that determinants for nephropathy were systolic blood pressure and ADPRCA, not HbA1c. Conclusion/interpretation. Decreased ADPRCA significantly correlated with diabetic nephropathy. ADPRCA in PBMCs would be an important marker associated with diabetic nephropathy.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Puplishing Corporation</pub><pmid>19300526</pmid><doi>10.1155/2008/897508</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ADP-ribosyl Cyclase - blood ADP-ribosyl Cyclase 1 - physiology Diabetic Nephropathies - enzymology Female Glycated Hemoglobin A - analysis Humans Leukocytes, Mononuclear - enzymology Male Membrane Glycoproteins - physiology |
title | Decreased ADP-Ribosyl Cyclase Activity in Peripheral Blood Mononuclear Cells from Diabetic Patients with Nephropathy |
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