Influence of differing classes of antihypertensive agents on mesangial kinetics following partial renal ablation in rats

Mesangial kinetics were studied in six groups of rats. Rats were either sham operated or were subjected to 1 1/3 nephrectomy (4/6 Nx). Each group was either untreated or was treated with enalapril (EN) or the drug regimen of hydralazine, hydrochlorothiazide, and reserpine (HHR). Four weeks after sur...

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Veröffentlicht in:Nephrology, dialysis, transplantation dialysis, transplantation, 1994, Vol.9 (2), p.131-137
Hauptverfasser: ODUM, J, PURKISS, J, NAISH, P. F
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NAISH, P. F
description Mesangial kinetics were studied in six groups of rats. Rats were either sham operated or were subjected to 1 1/3 nephrectomy (4/6 Nx). Each group was either untreated or was treated with enalapril (EN) or the drug regimen of hydralazine, hydrochlorothiazide, and reserpine (HHR). Four weeks after surgery rats were injected with iodinated aggregated bovine serum albumin (I-aggBSA) and mesangial localization quantified 2, 4, or 8 h later. Mesangial kinetics in untreated 4/6 Nx rats were characterized by accumulation of I-aggBSA to 4 h after injection with rapid clearance over the 4-8-h period; i.e. mesangial trafficking was increased following 4/6 Nx. Mesangial trafficking in 4/6 Nx rats treated with EN was reduced by virtue of lesser uptake of I-aggBSA at 4 h and retarded clearance over 4-8 h when compared with untreated 4/6 Nx animals. Treatment of 4/6 Nx rats with HHR maintained the increased trafficking observed in untreated 4/6 Nx rats. At 30 weeks untreated 4/6 Nx rats had severe albuminuria and glomerulosclerosis. Both indices of renal damage were significantly less in 4/6 Nx rats treated with enalapril. Treatment with HHR did not prevent albuminuria and had only limited effectiveness in preventing glomerulosclerosis. The different effects of EN and HHR on mesangial trafficking and glomerulosclerosis provide further evidence for a relationship between mesangial trafficking following partial renal ablation and subsequent development of glomerulosclerosis.
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F</creator><creatorcontrib>ODUM, J ; PURKISS, J ; NAISH, P. F</creatorcontrib><description>Mesangial kinetics were studied in six groups of rats. Rats were either sham operated or were subjected to 1 1/3 nephrectomy (4/6 Nx). Each group was either untreated or was treated with enalapril (EN) or the drug regimen of hydralazine, hydrochlorothiazide, and reserpine (HHR). Four weeks after surgery rats were injected with iodinated aggregated bovine serum albumin (I-aggBSA) and mesangial localization quantified 2, 4, or 8 h later. Mesangial kinetics in untreated 4/6 Nx rats were characterized by accumulation of I-aggBSA to 4 h after injection with rapid clearance over the 4-8-h period; i.e. mesangial trafficking was increased following 4/6 Nx. Mesangial trafficking in 4/6 Nx rats treated with EN was reduced by virtue of lesser uptake of I-aggBSA at 4 h and retarded clearance over 4-8 h when compared with untreated 4/6 Nx animals. Treatment of 4/6 Nx rats with HHR maintained the increased trafficking observed in untreated 4/6 Nx rats. At 30 weeks untreated 4/6 Nx rats had severe albuminuria and glomerulosclerosis. Both indices of renal damage were significantly less in 4/6 Nx rats treated with enalapril. Treatment with HHR did not prevent albuminuria and had only limited effectiveness in preventing glomerulosclerosis. 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Drug treatments ; Rats ; Rats, Wistar ; Reserpine - pharmacology ; Serum Albumin, Bovine - pharmacokinetics ; Tissue Distribution</subject><ispartof>Nephrology, dialysis, transplantation, 1994, Vol.9 (2), p.131-137</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,4024,4050,4051,23930,23931,25140,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3985960$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8190327$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ODUM, J</creatorcontrib><creatorcontrib>PURKISS, J</creatorcontrib><creatorcontrib>NAISH, P. F</creatorcontrib><title>Influence of differing classes of antihypertensive agents on mesangial kinetics following partial renal ablation in rats</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol Dial Transplant</addtitle><description>Mesangial kinetics were studied in six groups of rats. Rats were either sham operated or were subjected to 1 1/3 nephrectomy (4/6 Nx). Each group was either untreated or was treated with enalapril (EN) or the drug regimen of hydralazine, hydrochlorothiazide, and reserpine (HHR). Four weeks after surgery rats were injected with iodinated aggregated bovine serum albumin (I-aggBSA) and mesangial localization quantified 2, 4, or 8 h later. Mesangial kinetics in untreated 4/6 Nx rats were characterized by accumulation of I-aggBSA to 4 h after injection with rapid clearance over the 4-8-h period; i.e. mesangial trafficking was increased following 4/6 Nx. Mesangial trafficking in 4/6 Nx rats treated with EN was reduced by virtue of lesser uptake of I-aggBSA at 4 h and retarded clearance over 4-8 h when compared with untreated 4/6 Nx animals. Treatment of 4/6 Nx rats with HHR maintained the increased trafficking observed in untreated 4/6 Nx rats. At 30 weeks untreated 4/6 Nx rats had severe albuminuria and glomerulosclerosis. Both indices of renal damage were significantly less in 4/6 Nx rats treated with enalapril. Treatment with HHR did not prevent albuminuria and had only limited effectiveness in preventing glomerulosclerosis. The different effects of EN and HHR on mesangial trafficking and glomerulosclerosis provide further evidence for a relationship between mesangial trafficking following partial renal ablation and subsequent development of glomerulosclerosis.</description><subject>Albuminuria - etiology</subject><subject>Albuminuria - prevention &amp; control</subject><subject>Animals</subject><subject>Antihypertensive agents</subject><subject>Antihypertensive Agents - classification</subject><subject>Antihypertensive Agents - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Biological Transport, Active</subject><subject>Cardiovascular system</subject><subject>Enalapril - pharmacology</subject><subject>Glomerular Mesangium - drug effects</subject><subject>Glomerular Mesangium - metabolism</subject><subject>Hydralazine - pharmacology</subject><subject>Hydrochlorothiazide - pharmacology</subject><subject>Hypertrophy</subject><subject>Kidney Glomerulus - pathology</subject><subject>Kinetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nephrectomy - adverse effects</subject><subject>Pharmacology. Drug treatments</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reserpine - pharmacology</subject><subject>Serum Albumin, Bovine - pharmacokinetics</subject><subject>Tissue Distribution</subject><issn>0931-0509</issn><issn>1460-2385</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1rGzEQhkVpSJ20p5wLeyi5lLWl_ZSOJSRNINBLchaz0shRK2tdjdzE_74yMb7MwDzPvIeXsSvBl4KrdhVtXqllsxSt-MAWoht43bSy_8gWhYqa91x9YhdEvznnqhnHc3YuheJtMy7Y20N0YYfRYDW7ynrnMPm4rkwAIqTDEWL2L_stpoyR_D-sYI0xFxSrDRLEtYdQ_fERszdUuTmE-fUQsYWUDyhhLBOmANmXHx-rBJk-szMHgfDLcV-y57vbp5v7-vHXz4ebH4-1aUaRa-C8U846lAC2R2usElwKEAPYbmikMA7Hru_EYEBNTuI02RaF6rHrimzbS3b9nrtN898dUtYbTwZDgIjzjvQ4dEpIqYr4_V00aSZK6PQ2-Q2kvRZcH3rWpWetdKNLz8X-eozdTRu0J_dYbOHfjhzIQHAJovF00lolezXw9j_p5om6</recordid><startdate>1994</startdate><enddate>1994</enddate><creator>ODUM, J</creator><creator>PURKISS, J</creator><creator>NAISH, P. F</creator><general>Oxford University Press</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>1994</creationdate><title>Influence of differing classes of antihypertensive agents on mesangial kinetics following partial renal ablation in rats</title><author>ODUM, J ; PURKISS, J ; NAISH, P. F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c271t-a0049fdfe8aad5edcd91081a16ad46281cfe745416ca9bf8ebbd3e195e44dcdd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Albuminuria - etiology</topic><topic>Albuminuria - prevention &amp; control</topic><topic>Animals</topic><topic>Antihypertensive agents</topic><topic>Antihypertensive Agents - classification</topic><topic>Antihypertensive Agents - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Biological Transport, Active</topic><topic>Cardiovascular system</topic><topic>Enalapril - pharmacology</topic><topic>Glomerular Mesangium - drug effects</topic><topic>Glomerular Mesangium - metabolism</topic><topic>Hydralazine - pharmacology</topic><topic>Hydrochlorothiazide - pharmacology</topic><topic>Hypertrophy</topic><topic>Kidney Glomerulus - pathology</topic><topic>Kinetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nephrectomy - adverse effects</topic><topic>Pharmacology. Drug treatments</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reserpine - pharmacology</topic><topic>Serum Albumin, Bovine - pharmacokinetics</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ODUM, J</creatorcontrib><creatorcontrib>PURKISS, J</creatorcontrib><creatorcontrib>NAISH, P. F</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>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ODUM, J</au><au>PURKISS, J</au><au>NAISH, P. F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of differing classes of antihypertensive agents on mesangial kinetics following partial renal ablation in rats</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>1994</date><risdate>1994</risdate><volume>9</volume><issue>2</issue><spage>131</spage><epage>137</epage><pages>131-137</pages><issn>0931-0509</issn><issn>1460-2385</issn><eissn>1460-2385</eissn><coden>NDTREA</coden><abstract>Mesangial kinetics were studied in six groups of rats. Rats were either sham operated or were subjected to 1 1/3 nephrectomy (4/6 Nx). Each group was either untreated or was treated with enalapril (EN) or the drug regimen of hydralazine, hydrochlorothiazide, and reserpine (HHR). Four weeks after surgery rats were injected with iodinated aggregated bovine serum albumin (I-aggBSA) and mesangial localization quantified 2, 4, or 8 h later. Mesangial kinetics in untreated 4/6 Nx rats were characterized by accumulation of I-aggBSA to 4 h after injection with rapid clearance over the 4-8-h period; i.e. mesangial trafficking was increased following 4/6 Nx. Mesangial trafficking in 4/6 Nx rats treated with EN was reduced by virtue of lesser uptake of I-aggBSA at 4 h and retarded clearance over 4-8 h when compared with untreated 4/6 Nx animals. Treatment of 4/6 Nx rats with HHR maintained the increased trafficking observed in untreated 4/6 Nx rats. At 30 weeks untreated 4/6 Nx rats had severe albuminuria and glomerulosclerosis. Both indices of renal damage were significantly less in 4/6 Nx rats treated with enalapril. Treatment with HHR did not prevent albuminuria and had only limited effectiveness in preventing glomerulosclerosis. The different effects of EN and HHR on mesangial trafficking and glomerulosclerosis provide further evidence for a relationship between mesangial trafficking following partial renal ablation and subsequent development of glomerulosclerosis.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>8190327</pmid><doi>10.1093/ndt/9.2.131</doi><tpages>7</tpages></addata></record>
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subjects Albuminuria - etiology
Albuminuria - prevention & control
Animals
Antihypertensive agents
Antihypertensive Agents - classification
Antihypertensive Agents - pharmacology
Biological and medical sciences
Biological Transport, Active
Cardiovascular system
Enalapril - pharmacology
Glomerular Mesangium - drug effects
Glomerular Mesangium - metabolism
Hydralazine - pharmacology
Hydrochlorothiazide - pharmacology
Hypertrophy
Kidney Glomerulus - pathology
Kinetics
Male
Medical sciences
Nephrectomy - adverse effects
Pharmacology. Drug treatments
Rats
Rats, Wistar
Reserpine - pharmacology
Serum Albumin, Bovine - pharmacokinetics
Tissue Distribution
title Influence of differing classes of antihypertensive agents on mesangial kinetics following partial renal ablation in rats
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