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The effects of sildenafil citrate on urinary podocin and nephrin mRNA expression in an l-NAME model of pre-eclampsia
We investigated the effects of sildenafil citrate (SC) on podocyturia in N ω -nitro- l -arginine methyl ester hydrochloride ( l -NAME) model of pre-eclampsia (PE). One hundred and twenty Sprague–Dawley rats (SDR) were divided into five groups like pregnant control (PC), early-onset PE (EOPE), late-o...
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Published in: | Molecular and cellular biochemistry 2017-03, Vol.427 (1-2), p.59-67 |
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container_title | Molecular and cellular biochemistry |
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creator | Baijnath, Sooraj Murugesan, Saravanakumar Mackraj, Irene Gathiram, Prem Moodley, Jagidesa |
description | We investigated the effects of sildenafil citrate (SC) on podocyturia in
N
ω
-nitro-
l
-arginine methyl ester hydrochloride (
l
-NAME) model of pre-eclampsia (PE). One hundred and twenty Sprague–Dawley rats (SDR) were divided into five groups like pregnant control (PC), early-onset PE (EOPE), late-onset PE(LOPE), early and late-onset PE with SC-treated groups [EOPE (SC); LOPE (SC)]. PE was induced in SDR by oral administration of
l
-NAME in drinking water for 4–8 days for EOPE and 8–14 day for LOPE. The blood pressure, urine volume and total urine protein were increased in EOPE and LOPE groups when compared to PC, and all the above parameters decreased in EOPE (SC) and LOPE (SC) groups when compared to EOPE and LOPE groups, respectively. The EOPE and LOPE groups showed an increase in urinary nephrin mRNA and podocin mRNA levels compared to PC group. Increases in serum and renal soluble fms-like tyrosine kinase-1 (sFlt-1) expression levels and decreases in renal vascular endothelial growth factor (VEGF) expression and serum placenta growth factor (PlGF) levels were observed in EOPE and LOPE groups when compared to PC group. In addition, decreases in serum and renal sFlt-1 expression levels and increases in renal VEGF expression and serum PlGF levels were observed in EOPE (SC) and LOPE (SC) groups when compared to EOPE and LOPE groups, respectively. The light microscopy showed that the renal tissue of
l
-NAME-treated rats had extensive glomerular damage, tubular damage and infiltration by mononuclear cells when compared to PC group. Therefore, SC ameliorated podocyturia through its effects on the antiangiogenic/angiogenic status in this animal model. |
doi_str_mv | 10.1007/s11010-016-2897-5 |
format | article |
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N
ω
-nitro-
l
-arginine methyl ester hydrochloride (
l
-NAME) model of pre-eclampsia (PE). One hundred and twenty Sprague–Dawley rats (SDR) were divided into five groups like pregnant control (PC), early-onset PE (EOPE), late-onset PE(LOPE), early and late-onset PE with SC-treated groups [EOPE (SC); LOPE (SC)]. PE was induced in SDR by oral administration of
l
-NAME in drinking water for 4–8 days for EOPE and 8–14 day for LOPE. The blood pressure, urine volume and total urine protein were increased in EOPE and LOPE groups when compared to PC, and all the above parameters decreased in EOPE (SC) and LOPE (SC) groups when compared to EOPE and LOPE groups, respectively. The EOPE and LOPE groups showed an increase in urinary nephrin mRNA and podocin mRNA levels compared to PC group. Increases in serum and renal soluble fms-like tyrosine kinase-1 (sFlt-1) expression levels and decreases in renal vascular endothelial growth factor (VEGF) expression and serum placenta growth factor (PlGF) levels were observed in EOPE and LOPE groups when compared to PC group. In addition, decreases in serum and renal sFlt-1 expression levels and increases in renal VEGF expression and serum PlGF levels were observed in EOPE (SC) and LOPE (SC) groups when compared to EOPE and LOPE groups, respectively. The light microscopy showed that the renal tissue of
l
-NAME-treated rats had extensive glomerular damage, tubular damage and infiltration by mononuclear cells when compared to PC group. Therefore, SC ameliorated podocyturia through its effects on the antiangiogenic/angiogenic status in this animal model.</description><identifier>ISSN: 0300-8177</identifier><identifier>EISSN: 1573-4919</identifier><identifier>DOI: 10.1007/s11010-016-2897-5</identifier><identifier>PMID: 27995418</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Animal models ; Animals ; Biochemistry ; Biomedical and Life Sciences ; Blood pressure ; Cardiology ; Clinical outcomes ; Comparative analysis ; Disease Models, Animal ; Drinking water ; Drug therapy ; Female ; Gene Expression Regulation - drug effects ; Humans ; Intracellular Signaling Peptides and Proteins - urine ; Kidney - metabolism ; Kidney - pathology ; Life Sciences ; Light microscopy ; Medical Biochemistry ; Membrane Proteins - urine ; NG-Nitroarginine Methyl Ester - adverse effects ; NG-Nitroarginine Methyl Ester - pharmacology ; Oncology ; Pre-Eclampsia - chemically induced ; Pre-Eclampsia - drug therapy ; Pre-Eclampsia - pathology ; Pre-Eclampsia - urine ; Preeclampsia ; Pregnancy ; Prescription drugs ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - biosynthesis ; Sildenafil Citrate - pharmacology ; Vascular endothelial growth factor</subject><ispartof>Molecular and cellular biochemistry, 2017-03, Vol.427 (1-2), p.59-67</ispartof><rights>Springer Science+Business Media New York 2016</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Molecular and Cellular Biochemistry is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c538t-360b953bb74b21ea828015fb309af7987ca29b18297888f4ed07c444141af2993</citedby><cites>FETCH-LOGICAL-c538t-360b953bb74b21ea828015fb309af7987ca29b18297888f4ed07c444141af2993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27995418$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baijnath, Sooraj</creatorcontrib><creatorcontrib>Murugesan, Saravanakumar</creatorcontrib><creatorcontrib>Mackraj, Irene</creatorcontrib><creatorcontrib>Gathiram, Prem</creatorcontrib><creatorcontrib>Moodley, Jagidesa</creatorcontrib><title>The effects of sildenafil citrate on urinary podocin and nephrin mRNA expression in an l-NAME model of pre-eclampsia</title><title>Molecular and cellular biochemistry</title><addtitle>Mol Cell Biochem</addtitle><addtitle>Mol Cell Biochem</addtitle><description>We investigated the effects of sildenafil citrate (SC) on podocyturia in
N
ω
-nitro-
l
-arginine methyl ester hydrochloride (
l
-NAME) model of pre-eclampsia (PE). One hundred and twenty Sprague–Dawley rats (SDR) were divided into five groups like pregnant control (PC), early-onset PE (EOPE), late-onset PE(LOPE), early and late-onset PE with SC-treated groups [EOPE (SC); LOPE (SC)]. PE was induced in SDR by oral administration of
l
-NAME in drinking water for 4–8 days for EOPE and 8–14 day for LOPE. The blood pressure, urine volume and total urine protein were increased in EOPE and LOPE groups when compared to PC, and all the above parameters decreased in EOPE (SC) and LOPE (SC) groups when compared to EOPE and LOPE groups, respectively. The EOPE and LOPE groups showed an increase in urinary nephrin mRNA and podocin mRNA levels compared to PC group. Increases in serum and renal soluble fms-like tyrosine kinase-1 (sFlt-1) expression levels and decreases in renal vascular endothelial growth factor (VEGF) expression and serum placenta growth factor (PlGF) levels were observed in EOPE and LOPE groups when compared to PC group. In addition, decreases in serum and renal sFlt-1 expression levels and increases in renal VEGF expression and serum PlGF levels were observed in EOPE (SC) and LOPE (SC) groups when compared to EOPE and LOPE groups, respectively. The light microscopy showed that the renal tissue of
l
-NAME-treated rats had extensive glomerular damage, tubular damage and infiltration by mononuclear cells when compared to PC group. Therefore, SC ameliorated podocyturia through its effects on the antiangiogenic/angiogenic status in this animal model.</description><subject>Animal models</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Blood pressure</subject><subject>Cardiology</subject><subject>Clinical outcomes</subject><subject>Comparative analysis</subject><subject>Disease Models, Animal</subject><subject>Drinking water</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Humans</subject><subject>Intracellular Signaling Peptides and Proteins - urine</subject><subject>Kidney - metabolism</subject><subject>Kidney - pathology</subject><subject>Life Sciences</subject><subject>Light microscopy</subject><subject>Medical Biochemistry</subject><subject>Membrane Proteins - urine</subject><subject>NG-Nitroarginine Methyl Ester - adverse effects</subject><subject>NG-Nitroarginine Methyl Ester - pharmacology</subject><subject>Oncology</subject><subject>Pre-Eclampsia - chemically induced</subject><subject>Pre-Eclampsia - drug therapy</subject><subject>Pre-Eclampsia - pathology</subject><subject>Pre-Eclampsia - urine</subject><subject>Preeclampsia</subject><subject>Pregnancy</subject><subject>Prescription drugs</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Sildenafil Citrate - pharmacology</subject><subject>Vascular endothelial growth factor</subject><issn>0300-8177</issn><issn>1573-4919</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kUFrFTEUhYMo9ln9AW4k4MZNam5m5iVZPkqtQq0gdR0ymZs2ZSYZk3lQ_72ZvlpUlCwCud89nJxDyGvgJ8C5fF8AOHDGYcuE0pJ1T8gGOtmwVoN-Sja84ZwpkPKIvCjllleYAzwnR0Jq3bWgNmS5ukGK3qNbCk2eljAOGK0PI3VhyXZBmiLd5xBt_kHnNCQXIrVxoBHnm_pMp6-XO4p3c8ZSQmXvx3Rkl7vPZ3RKA46rbh0zdKOd5hLsS_LM27Hgq4f7mHz7cHZ1-pFdfDn_dLq7YK5r1MKaLe911_S9bHsBaJVQHDrfN1xbL7WSzgrdgxJaKqV8iwOXrm1baMF6oXVzTN4ddOecvu-xLGYKxeE42ohpXwyoraoRackr-vYv9Dbtc6zuVkrqRvBq5ZG6tiOaEH2qEblV1Oy6DrjQnV61Tv5B1TPgFFyKWNPFPxfgsOByKiWjN3MOUw3cADdr0-bQtKlNm7Vps1p582B43084PG78qrYC4gCUOorXmH_70X9VfwILPrAb</recordid><startdate>20170301</startdate><enddate>20170301</enddate><creator>Baijnath, Sooraj</creator><creator>Murugesan, Saravanakumar</creator><creator>Mackraj, Irene</creator><creator>Gathiram, Prem</creator><creator>Moodley, Jagidesa</creator><general>Springer 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effects of sildenafil citrate on urinary podocin and nephrin mRNA expression in an l-NAME model of pre-eclampsia</title><author>Baijnath, Sooraj ; Murugesan, Saravanakumar ; Mackraj, Irene ; Gathiram, Prem ; Moodley, Jagidesa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c538t-360b953bb74b21ea828015fb309af7987ca29b18297888f4ed07c444141af2993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Blood pressure</topic><topic>Cardiology</topic><topic>Clinical outcomes</topic><topic>Comparative analysis</topic><topic>Disease Models, Animal</topic><topic>Drinking water</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Humans</topic><topic>Intracellular Signaling Peptides and Proteins - urine</topic><topic>Kidney - metabolism</topic><topic>Kidney - pathology</topic><topic>Life Sciences</topic><topic>Light microscopy</topic><topic>Medical Biochemistry</topic><topic>Membrane Proteins - urine</topic><topic>NG-Nitroarginine Methyl Ester - adverse effects</topic><topic>NG-Nitroarginine Methyl Ester - pharmacology</topic><topic>Oncology</topic><topic>Pre-Eclampsia - chemically induced</topic><topic>Pre-Eclampsia - drug therapy</topic><topic>Pre-Eclampsia - pathology</topic><topic>Pre-Eclampsia - urine</topic><topic>Preeclampsia</topic><topic>Pregnancy</topic><topic>Prescription drugs</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Sildenafil Citrate - pharmacology</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baijnath, Sooraj</creatorcontrib><creatorcontrib>Murugesan, 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Biochem</addtitle><date>2017-03-01</date><risdate>2017</risdate><volume>427</volume><issue>1-2</issue><spage>59</spage><epage>67</epage><pages>59-67</pages><issn>0300-8177</issn><eissn>1573-4919</eissn><abstract>We investigated the effects of sildenafil citrate (SC) on podocyturia in
N
ω
-nitro-
l
-arginine methyl ester hydrochloride (
l
-NAME) model of pre-eclampsia (PE). One hundred and twenty Sprague–Dawley rats (SDR) were divided into five groups like pregnant control (PC), early-onset PE (EOPE), late-onset PE(LOPE), early and late-onset PE with SC-treated groups [EOPE (SC); LOPE (SC)]. PE was induced in SDR by oral administration of
l
-NAME in drinking water for 4–8 days for EOPE and 8–14 day for LOPE. The blood pressure, urine volume and total urine protein were increased in EOPE and LOPE groups when compared to PC, and all the above parameters decreased in EOPE (SC) and LOPE (SC) groups when compared to EOPE and LOPE groups, respectively. The EOPE and LOPE groups showed an increase in urinary nephrin mRNA and podocin mRNA levels compared to PC group. Increases in serum and renal soluble fms-like tyrosine kinase-1 (sFlt-1) expression levels and decreases in renal vascular endothelial growth factor (VEGF) expression and serum placenta growth factor (PlGF) levels were observed in EOPE and LOPE groups when compared to PC group. In addition, decreases in serum and renal sFlt-1 expression levels and increases in renal VEGF expression and serum PlGF levels were observed in EOPE (SC) and LOPE (SC) groups when compared to EOPE and LOPE groups, respectively. The light microscopy showed that the renal tissue of
l
-NAME-treated rats had extensive glomerular damage, tubular damage and infiltration by mononuclear cells when compared to PC group. Therefore, SC ameliorated podocyturia through its effects on the antiangiogenic/angiogenic status in this animal model.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>27995418</pmid><doi>10.1007/s11010-016-2897-5</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
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source | Springer Nature |
subjects | Animal models Animals Biochemistry Biomedical and Life Sciences Blood pressure Cardiology Clinical outcomes Comparative analysis Disease Models, Animal Drinking water Drug therapy Female Gene Expression Regulation - drug effects Humans Intracellular Signaling Peptides and Proteins - urine Kidney - metabolism Kidney - pathology Life Sciences Light microscopy Medical Biochemistry Membrane Proteins - urine NG-Nitroarginine Methyl Ester - adverse effects NG-Nitroarginine Methyl Ester - pharmacology Oncology Pre-Eclampsia - chemically induced Pre-Eclampsia - drug therapy Pre-Eclampsia - pathology Pre-Eclampsia - urine Preeclampsia Pregnancy Prescription drugs Rats Rats, Sprague-Dawley RNA, Messenger - biosynthesis Sildenafil Citrate - pharmacology Vascular endothelial growth factor |
title | The effects of sildenafil citrate on urinary podocin and nephrin mRNA expression in an l-NAME model of pre-eclampsia |
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