L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis

L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis. We examined the effect of 1% L-arginine in the drinking water on the infiltration of the kidney by macrophages in rats with puromycin aminonucleoside-induced nephrosis (PAN)...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Kidney international 1994-05, Vol.45 (5), p.1346-1354
Hauptverfasser: Reyes, Alvaro A., Porras, Beatriz H., Chasalow, Fred I., Klahr, Saulo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1354
container_issue 5
container_start_page 1346
container_title Kidney international
container_volume 45
creator Reyes, Alvaro A.
Porras, Beatriz H.
Chasalow, Fred I.
Klahr, Saulo
description L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis. We examined the effect of 1% L-arginine in the drinking water on the infiltration of the kidney by macrophages in rats with puromycin aminonucleoside-induced nephrosis (PAN) and in rats with bilateral ureteral obstruction (BUO) of 24 hours duration. Rats given L-arginine in the drinking water for three days before BUO or PAN was initiated had a greater glomerular filtration rate after release of BUO or induction of PAN than similar rats not given L-arginine (P < 0.0001). Administration of L-arginine decreased the renal infiltration by macrophages in rats with PAN (P < 0.0001) or BUO (P < 0.0001) compared to rats with PAN or BUO given tap water alone. Chemotaxis studies suggested that macrophages were activated during obstruction as evidenced by the greater random migration of peritoneal macrophages obtained from rats with 24-hour urethral obstruction than from sham-operated rats (SOR; P < 0.0001). In vitro, maximal chemotaxis induced by 7% zymosan-activated serum (ZAS) in peritoneal macrophages from SOR was enhanced by low (10−6 to 10−5M) and decreased by high concentrations (10−3 to 10−2M) of L-arginine in the incubation medium. Migration of macrophages from rats with urethral obstruction was increased by 7% ZAS but the increase diminished with high concentrations of L-arginine (10−3 to 10−2M). Random migration of peritoneal macrophages obtained from rats with urethral obstruction given L-arginine prior to obstruction was significantly lower than that of peritoneal macrophages obtained from similar rats given tap water alone prior to obstruction. Plasma levels of corticosterone were greater (P < 0.002) in rats with BUO given L-arginine than in rats with BUO given tap water alone. Thus, administration of L-arginine improves renal function of rats with PAN or BUO. This may be due, at least in part, to decreased renal macrophage infiltration. L-arginine may cause this decrease in macrophage infiltration by directly inhibiting macrophage chemotaxis and by increasing the levels of circulating corticosterone.
doi_str_mv 10.1038/ki.1994.176
format Article
fullrecord <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1038_ki_1994_176</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0085253815584573</els_id><sourcerecordid>S0085253815584573</sourcerecordid><originalsourceid>FETCH-LOGICAL-c462t-d02e2b9f36810a6880a2ed04ac54ce43d7cf0b6cc6792417799ba8d2f9764d083</originalsourceid><addsrcrecordid>eNptkDtPwzAURi0EKuUxMSN5YEMptuPEzogQL6kSC8yRY9-0l7ZOZKdIGfjvuLRiYrKuv6P7OIRccTbjLNd3K5zxqpIzrsojMuWFyDOuiuKYTBnTRSaKXJ-Ssxg_WaqrnE3IRDMlhFRT8j3PTFigRw_UgQ1gIkQ6LIGib3E9BDNg52nX_v6t0HkYaTPSjbGh65dmkWhMeROHsLUDfgH10C9TZoblSI13tN-GbjNa9Bl6t7XgDkTEeEFOWrOOcHl4z8nH0-P7w0s2f3t-fbifZ1aWYsgcEyCaqs1LzZkptWZGgGPS2EJakLlTtmVNaW2pKiG5UlXVGO1EW6lSOqbzc3K775uWjjFAW_cBNyaMNWf1zmG9wnrnsE4OE329p_ttswH3xx6kpfzmkJtozboNxluMf5jkvGRyN7TYY5Au-0IIdbQIPgnAAHaoXYf_jv8BfTKOSw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><source>EZB Electronic Journals Library</source><creator>Reyes, Alvaro A. ; Porras, Beatriz H. ; Chasalow, Fred I. ; Klahr, Saulo</creator><creatorcontrib>Reyes, Alvaro A. ; Porras, Beatriz H. ; Chasalow, Fred I. ; Klahr, Saulo</creatorcontrib><description>L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis. We examined the effect of 1% L-arginine in the drinking water on the infiltration of the kidney by macrophages in rats with puromycin aminonucleoside-induced nephrosis (PAN) and in rats with bilateral ureteral obstruction (BUO) of 24 hours duration. Rats given L-arginine in the drinking water for three days before BUO or PAN was initiated had a greater glomerular filtration rate after release of BUO or induction of PAN than similar rats not given L-arginine (P &lt; 0.0001). Administration of L-arginine decreased the renal infiltration by macrophages in rats with PAN (P &lt; 0.0001) or BUO (P &lt; 0.0001) compared to rats with PAN or BUO given tap water alone. Chemotaxis studies suggested that macrophages were activated during obstruction as evidenced by the greater random migration of peritoneal macrophages obtained from rats with 24-hour urethral obstruction than from sham-operated rats (SOR; P &lt; 0.0001). In vitro, maximal chemotaxis induced by 7% zymosan-activated serum (ZAS) in peritoneal macrophages from SOR was enhanced by low (10−6 to 10−5M) and decreased by high concentrations (10−3 to 10−2M) of L-arginine in the incubation medium. Migration of macrophages from rats with urethral obstruction was increased by 7% ZAS but the increase diminished with high concentrations of L-arginine (10−3 to 10−2M). Random migration of peritoneal macrophages obtained from rats with urethral obstruction given L-arginine prior to obstruction was significantly lower than that of peritoneal macrophages obtained from similar rats given tap water alone prior to obstruction. Plasma levels of corticosterone were greater (P &lt; 0.002) in rats with BUO given L-arginine than in rats with BUO given tap water alone. Thus, administration of L-arginine improves renal function of rats with PAN or BUO. This may be due, at least in part, to decreased renal macrophage infiltration. L-arginine may cause this decrease in macrophage infiltration by directly inhibiting macrophage chemotaxis and by increasing the levels of circulating corticosterone.</description><identifier>ISSN: 0085-2538</identifier><identifier>EISSN: 1523-1755</identifier><identifier>DOI: 10.1038/ki.1994.176</identifier><identifier>PMID: 8072247</identifier><identifier>CODEN: KDYIA5</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Administration, Oral ; Animals ; Arginine - administration &amp; dosage ; Arginine - pharmacology ; Biological and medical sciences ; Cell Count ; Cell Movement ; Chemotaxis - drug effects ; Corticosterone - blood ; Female ; Glomerular Filtration Rate ; Glomerulonephritis ; Kidney - metabolism ; Macrophages, Peritoneal - metabolism ; Medical sciences ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Nephrosis - chemically induced ; Nephrosis - metabolism ; Puromycin ; Rats ; Rats, Sprague-Dawley ; Ureteral Obstruction - metabolism</subject><ispartof>Kidney international, 1994-05, Vol.45 (5), p.1346-1354</ispartof><rights>1994 International Society of Nephrology</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-d02e2b9f36810a6880a2ed04ac54ce43d7cf0b6cc6792417799ba8d2f9764d083</citedby><cites>FETCH-LOGICAL-c462t-d02e2b9f36810a6880a2ed04ac54ce43d7cf0b6cc6792417799ba8d2f9764d083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4116048$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8072247$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Reyes, Alvaro A.</creatorcontrib><creatorcontrib>Porras, Beatriz H.</creatorcontrib><creatorcontrib>Chasalow, Fred I.</creatorcontrib><creatorcontrib>Klahr, Saulo</creatorcontrib><title>L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis</title><title>Kidney international</title><addtitle>Kidney Int</addtitle><description>L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis. We examined the effect of 1% L-arginine in the drinking water on the infiltration of the kidney by macrophages in rats with puromycin aminonucleoside-induced nephrosis (PAN) and in rats with bilateral ureteral obstruction (BUO) of 24 hours duration. Rats given L-arginine in the drinking water for three days before BUO or PAN was initiated had a greater glomerular filtration rate after release of BUO or induction of PAN than similar rats not given L-arginine (P &lt; 0.0001). Administration of L-arginine decreased the renal infiltration by macrophages in rats with PAN (P &lt; 0.0001) or BUO (P &lt; 0.0001) compared to rats with PAN or BUO given tap water alone. Chemotaxis studies suggested that macrophages were activated during obstruction as evidenced by the greater random migration of peritoneal macrophages obtained from rats with 24-hour urethral obstruction than from sham-operated rats (SOR; P &lt; 0.0001). In vitro, maximal chemotaxis induced by 7% zymosan-activated serum (ZAS) in peritoneal macrophages from SOR was enhanced by low (10−6 to 10−5M) and decreased by high concentrations (10−3 to 10−2M) of L-arginine in the incubation medium. Migration of macrophages from rats with urethral obstruction was increased by 7% ZAS but the increase diminished with high concentrations of L-arginine (10−3 to 10−2M). Random migration of peritoneal macrophages obtained from rats with urethral obstruction given L-arginine prior to obstruction was significantly lower than that of peritoneal macrophages obtained from similar rats given tap water alone prior to obstruction. Plasma levels of corticosterone were greater (P &lt; 0.002) in rats with BUO given L-arginine than in rats with BUO given tap water alone. Thus, administration of L-arginine improves renal function of rats with PAN or BUO. This may be due, at least in part, to decreased renal macrophage infiltration. L-arginine may cause this decrease in macrophage infiltration by directly inhibiting macrophage chemotaxis and by increasing the levels of circulating corticosterone.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Arginine - administration &amp; dosage</subject><subject>Arginine - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cell Count</subject><subject>Cell Movement</subject><subject>Chemotaxis - drug effects</subject><subject>Corticosterone - blood</subject><subject>Female</subject><subject>Glomerular Filtration Rate</subject><subject>Glomerulonephritis</subject><subject>Kidney - metabolism</subject><subject>Macrophages, Peritoneal - metabolism</subject><subject>Medical sciences</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Nephrosis - chemically induced</subject><subject>Nephrosis - metabolism</subject><subject>Puromycin</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Ureteral Obstruction - metabolism</subject><issn>0085-2538</issn><issn>1523-1755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkDtPwzAURi0EKuUxMSN5YEMptuPEzogQL6kSC8yRY9-0l7ZOZKdIGfjvuLRiYrKuv6P7OIRccTbjLNd3K5zxqpIzrsojMuWFyDOuiuKYTBnTRSaKXJ-Ssxg_WaqrnE3IRDMlhFRT8j3PTFigRw_UgQ1gIkQ6LIGib3E9BDNg52nX_v6t0HkYaTPSjbGh65dmkWhMeROHsLUDfgH10C9TZoblSI13tN-GbjNa9Bl6t7XgDkTEeEFOWrOOcHl4z8nH0-P7w0s2f3t-fbifZ1aWYsgcEyCaqs1LzZkptWZGgGPS2EJakLlTtmVNaW2pKiG5UlXVGO1EW6lSOqbzc3K775uWjjFAW_cBNyaMNWf1zmG9wnrnsE4OE329p_ttswH3xx6kpfzmkJtozboNxluMf5jkvGRyN7TYY5Au-0IIdbQIPgnAAHaoXYf_jv8BfTKOSw</recordid><startdate>19940501</startdate><enddate>19940501</enddate><creator>Reyes, Alvaro A.</creator><creator>Porras, Beatriz H.</creator><creator>Chasalow, Fred I.</creator><creator>Klahr, Saulo</creator><general>Elsevier Inc</general><general>Nature Publishing</general><scope>6I.</scope><scope>AAFTH</scope><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></search><sort><creationdate>19940501</creationdate><title>L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis</title><author>Reyes, Alvaro A. ; Porras, Beatriz H. ; Chasalow, Fred I. ; Klahr, Saulo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-d02e2b9f36810a6880a2ed04ac54ce43d7cf0b6cc6792417799ba8d2f9764d083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Arginine - administration &amp; dosage</topic><topic>Arginine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cell Count</topic><topic>Cell Movement</topic><topic>Chemotaxis - drug effects</topic><topic>Corticosterone - blood</topic><topic>Female</topic><topic>Glomerular Filtration Rate</topic><topic>Glomerulonephritis</topic><topic>Kidney - metabolism</topic><topic>Macrophages, Peritoneal - metabolism</topic><topic>Medical sciences</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Nephrosis - chemically induced</topic><topic>Nephrosis - metabolism</topic><topic>Puromycin</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Ureteral Obstruction - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reyes, Alvaro A.</creatorcontrib><creatorcontrib>Porras, Beatriz H.</creatorcontrib><creatorcontrib>Chasalow, Fred I.</creatorcontrib><creatorcontrib>Klahr, Saulo</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><jtitle>Kidney international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reyes, Alvaro A.</au><au>Porras, Beatriz H.</au><au>Chasalow, Fred I.</au><au>Klahr, Saulo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis</atitle><jtitle>Kidney international</jtitle><addtitle>Kidney Int</addtitle><date>1994-05-01</date><risdate>1994</risdate><volume>45</volume><issue>5</issue><spage>1346</spage><epage>1354</epage><pages>1346-1354</pages><issn>0085-2538</issn><eissn>1523-1755</eissn><coden>KDYIA5</coden><abstract>L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis. We examined the effect of 1% L-arginine in the drinking water on the infiltration of the kidney by macrophages in rats with puromycin aminonucleoside-induced nephrosis (PAN) and in rats with bilateral ureteral obstruction (BUO) of 24 hours duration. Rats given L-arginine in the drinking water for three days before BUO or PAN was initiated had a greater glomerular filtration rate after release of BUO or induction of PAN than similar rats not given L-arginine (P &lt; 0.0001). Administration of L-arginine decreased the renal infiltration by macrophages in rats with PAN (P &lt; 0.0001) or BUO (P &lt; 0.0001) compared to rats with PAN or BUO given tap water alone. Chemotaxis studies suggested that macrophages were activated during obstruction as evidenced by the greater random migration of peritoneal macrophages obtained from rats with 24-hour urethral obstruction than from sham-operated rats (SOR; P &lt; 0.0001). In vitro, maximal chemotaxis induced by 7% zymosan-activated serum (ZAS) in peritoneal macrophages from SOR was enhanced by low (10−6 to 10−5M) and decreased by high concentrations (10−3 to 10−2M) of L-arginine in the incubation medium. Migration of macrophages from rats with urethral obstruction was increased by 7% ZAS but the increase diminished with high concentrations of L-arginine (10−3 to 10−2M). Random migration of peritoneal macrophages obtained from rats with urethral obstruction given L-arginine prior to obstruction was significantly lower than that of peritoneal macrophages obtained from similar rats given tap water alone prior to obstruction. Plasma levels of corticosterone were greater (P &lt; 0.002) in rats with BUO given L-arginine than in rats with BUO given tap water alone. Thus, administration of L-arginine improves renal function of rats with PAN or BUO. This may be due, at least in part, to decreased renal macrophage infiltration. L-arginine may cause this decrease in macrophage infiltration by directly inhibiting macrophage chemotaxis and by increasing the levels of circulating corticosterone.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>8072247</pmid><doi>10.1038/ki.1994.176</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0085-2538
ispartof Kidney international, 1994-05, Vol.45 (5), p.1346-1354
issn 0085-2538
1523-1755
language eng
recordid cdi_crossref_primary_10_1038_ki_1994_176
source MEDLINE; Alma/SFX Local Collection; EZB Electronic Journals Library
subjects Administration, Oral
Animals
Arginine - administration & dosage
Arginine - pharmacology
Biological and medical sciences
Cell Count
Cell Movement
Chemotaxis - drug effects
Corticosterone - blood
Female
Glomerular Filtration Rate
Glomerulonephritis
Kidney - metabolism
Macrophages, Peritoneal - metabolism
Medical sciences
Nephrology. Urinary tract diseases
Nephropathies. Renovascular diseases. Renal failure
Nephrosis - chemically induced
Nephrosis - metabolism
Puromycin
Rats
Rats, Sprague-Dawley
Ureteral Obstruction - metabolism
title L-arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T18%3A23%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=L-arginine%20decreases%20the%20infiltration%20of%20the%20kidney%20by%20macrophages%20in%20obstructive%20nephropathy%20and%20puromycin-induced%20nephrosis&rft.jtitle=Kidney%20international&rft.au=Reyes,%20Alvaro%20A.&rft.date=1994-05-01&rft.volume=45&rft.issue=5&rft.spage=1346&rft.epage=1354&rft.pages=1346-1354&rft.issn=0085-2538&rft.eissn=1523-1755&rft.coden=KDYIA5&rft_id=info:doi/10.1038/ki.1994.176&rft_dat=%3Celsevier_cross%3ES0085253815584573%3C/elsevier_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/8072247&rft_els_id=S0085253815584573&rfr_iscdi=true