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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
Main Authors: Baijnath, Sooraj, Murugesan, Saravanakumar, Mackraj, Irene, Gathiram, Prem, Moodley, Jagidesa
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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
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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. 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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>
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identifier ISSN: 0300-8177
ispartof Molecular and cellular biochemistry, 2017-03, Vol.427 (1-2), p.59-67
issn 0300-8177
1573-4919
language eng
recordid cdi_proquest_miscellaneous_1868300970
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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