The effects of atrial natriuretic peptide and amiloride on renal haemodynamics and the renal kallikrein-kinin system
Anaesthetized rabbits were used to examine the effects of amiloride (an inhibitor of a conductive sodium channel in the distal tubule) and atrial natriuretic peptide (ANP), both singly and in combination, on renal function and the renal kallikrein-kinin system. The administration of ANP (0.05 μg/kg...
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Veröffentlicht in: | Journal of hypertension 1988-04, Vol.6 (4), p.321-327 |
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creator | Seino, Masahide Abe, Keishi Nushiro, Noboru Omata, Ken Yoshinaga, Kaoru |
description | Anaesthetized rabbits were used to examine the effects of amiloride (an inhibitor of a conductive sodium channel in the distal tubule) and atrial natriuretic peptide (ANP), both singly and in combination, on renal function and the renal kallikrein-kinin system. The administration of ANP (0.05 μg/kg per min) produced a natriuresis with increases in renal blood flow and glomerular filtration rate. The administration of ANP superimposed on amiloride infusion (5 mg/kg + 0.04 mg/kg per min) showed an additive effect on the natriuresis, although the renal haemodynamic changes were now absent. The infusion of ANP alone increased the urinary excretion of kallikrein and kinins. Prior infusion of amiloride prevented the expected increases in the urinary excretion of kallikrein and kinins after infusion of ANP was superimposed. These results suggest that the observed renal haemodynamic changes could be mediated through renal kallikrein and kinins. The additive effect on sodium excretion might be elicited by the results of alterations in the tubular handling of sodium, although distal tubular function is not modified by ANP. It seems that the renal kallikrein-kinin system is not causally involved in the increased sodium excretion by ANP. |
doi_str_mv | 10.1097/00004872-198804000-00009 |
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The administration of ANP (0.05 μg/kg per min) produced a natriuresis with increases in renal blood flow and glomerular filtration rate. The administration of ANP superimposed on amiloride infusion (5 mg/kg + 0.04 mg/kg per min) showed an additive effect on the natriuresis, although the renal haemodynamic changes were now absent. The infusion of ANP alone increased the urinary excretion of kallikrein and kinins. Prior infusion of amiloride prevented the expected increases in the urinary excretion of kallikrein and kinins after infusion of ANP was superimposed. These results suggest that the observed renal haemodynamic changes could be mediated through renal kallikrein and kinins. The additive effect on sodium excretion might be elicited by the results of alterations in the tubular handling of sodium, although distal tubular function is not modified by ANP. It seems that the renal kallikrein-kinin system is not causally involved in the increased sodium excretion by ANP.</description><identifier>ISSN: 0263-6352</identifier><identifier>EISSN: 1473-5598</identifier><identifier>DOI: 10.1097/00004872-198804000-00009</identifier><identifier>PMID: 2967862</identifier><identifier>CODEN: JOHYD3</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott-Raven Publishers</publisher><subject>Amiloride - pharmacology ; Animals ; Arterial hypertension. Arterial hypotension ; Atrial Natriuretic Factor - pharmacology ; Biological and medical sciences ; Blood and lymphatic vessels ; Cardiology. Vascular system ; Experimental diseases ; Female ; Kallikreins - physiology ; Kidney - drug effects ; Kidney - metabolism ; Kinins - physiology ; Medical sciences ; Natriuresis - drug effects ; Rabbits ; Renal Circulation - drug effects</subject><ispartof>Journal of hypertension, 1988-04, Vol.6 (4), p.321-327</ispartof><rights>Lippincott-Raven Publishers.</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2999-c7e2ec7e827d90ca2cab2314cd3ac1f7dbc4e21befca9ccd83aa83a2fb0521af3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7194241$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2967862$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seino, Masahide</creatorcontrib><creatorcontrib>Abe, Keishi</creatorcontrib><creatorcontrib>Nushiro, Noboru</creatorcontrib><creatorcontrib>Omata, Ken</creatorcontrib><creatorcontrib>Yoshinaga, Kaoru</creatorcontrib><title>The effects of atrial natriuretic peptide and amiloride on renal haemodynamics and the renal kallikrein-kinin system</title><title>Journal of hypertension</title><addtitle>J Hypertens</addtitle><description>Anaesthetized rabbits were used to examine the effects of amiloride (an inhibitor of a conductive sodium channel in the distal tubule) and atrial natriuretic peptide (ANP), both singly and in combination, on renal function and the renal kallikrein-kinin system. The administration of ANP (0.05 μg/kg per min) produced a natriuresis with increases in renal blood flow and glomerular filtration rate. The administration of ANP superimposed on amiloride infusion (5 mg/kg + 0.04 mg/kg per min) showed an additive effect on the natriuresis, although the renal haemodynamic changes were now absent. The infusion of ANP alone increased the urinary excretion of kallikrein and kinins. Prior infusion of amiloride prevented the expected increases in the urinary excretion of kallikrein and kinins after infusion of ANP was superimposed. These results suggest that the observed renal haemodynamic changes could be mediated through renal kallikrein and kinins. The additive effect on sodium excretion might be elicited by the results of alterations in the tubular handling of sodium, although distal tubular function is not modified by ANP. It seems that the renal kallikrein-kinin system is not causally involved in the increased sodium excretion by ANP.</description><subject>Amiloride - pharmacology</subject><subject>Animals</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Atrial Natriuretic Factor - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. Vascular system</subject><subject>Experimental diseases</subject><subject>Female</subject><subject>Kallikreins - physiology</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Kinins - physiology</subject><subject>Medical sciences</subject><subject>Natriuresis - drug effects</subject><subject>Rabbits</subject><subject>Renal Circulation - drug effects</subject><issn>0263-6352</issn><issn>1473-5598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kcFuGyEQhlHVKnXcPkIkDlVv2y6wXuBYRU1SKVIu6RnNsoNMzLIusIr89sWx61uRYDTzfzMj_RBCWfuNtVp-b-vplOQN00q1Xc2aY0m_IyvWSdFsNlq9J6uW96LpxYZ_JNc5v1RCaSmuyBXXvVQ9X5HyvEWKzqEtmc6OQkkeAo3HuCQs3tI97osfkUIcKUw-zOmYzZEmjBXdAk7zeIhVsvkNKnXkSdtBCH6X0Mdm56OPNB9ywekT-eAgZPx8jmvy--7n8-1D8_h0_-v2x2Njuda6sRI51kdxOerWArcwcME6OwqwzMlxsB1yNqCzoK0dlQCol7uh3XAGTqzJ19PcfZr_LJiLmXy2GAJEnJdspOJ9x6pHa6JOoE1zzgmd2Sc_QToY1pqj4eaf4eZi-FtJ19ab845lmHC8NJ4drvqXsw7ZQnAJovX5gkmmO96xinUn7HUOBVPeheUVk9kihLI1__tu8Re9lJtJ</recordid><startdate>198804</startdate><enddate>198804</enddate><creator>Seino, Masahide</creator><creator>Abe, Keishi</creator><creator>Nushiro, Noboru</creator><creator>Omata, Ken</creator><creator>Yoshinaga, Kaoru</creator><general>Lippincott-Raven Publishers</general><general>Lippincott Williams & Wilkins</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>198804</creationdate><title>The effects of atrial natriuretic peptide and amiloride on renal haemodynamics and the renal kallikrein-kinin system</title><author>Seino, Masahide ; Abe, Keishi ; Nushiro, Noboru ; Omata, Ken ; Yoshinaga, Kaoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2999-c7e2ec7e827d90ca2cab2314cd3ac1f7dbc4e21befca9ccd83aa83a2fb0521af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Amiloride - pharmacology</topic><topic>Animals</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Atrial Natriuretic Factor - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Cardiology. Vascular system</topic><topic>Experimental diseases</topic><topic>Female</topic><topic>Kallikreins - physiology</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Kinins - physiology</topic><topic>Medical sciences</topic><topic>Natriuresis - drug effects</topic><topic>Rabbits</topic><topic>Renal Circulation - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seino, Masahide</creatorcontrib><creatorcontrib>Abe, Keishi</creatorcontrib><creatorcontrib>Nushiro, Noboru</creatorcontrib><creatorcontrib>Omata, Ken</creatorcontrib><creatorcontrib>Yoshinaga, Kaoru</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>Journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seino, Masahide</au><au>Abe, Keishi</au><au>Nushiro, Noboru</au><au>Omata, Ken</au><au>Yoshinaga, Kaoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effects of atrial natriuretic peptide and amiloride on renal haemodynamics and the renal kallikrein-kinin system</atitle><jtitle>Journal of hypertension</jtitle><addtitle>J Hypertens</addtitle><date>1988-04</date><risdate>1988</risdate><volume>6</volume><issue>4</issue><spage>321</spage><epage>327</epage><pages>321-327</pages><issn>0263-6352</issn><eissn>1473-5598</eissn><coden>JOHYD3</coden><abstract>Anaesthetized rabbits were used to examine the effects of amiloride (an inhibitor of a conductive sodium channel in the distal tubule) and atrial natriuretic peptide (ANP), both singly and in combination, on renal function and the renal kallikrein-kinin system. The administration of ANP (0.05 μg/kg per min) produced a natriuresis with increases in renal blood flow and glomerular filtration rate. The administration of ANP superimposed on amiloride infusion (5 mg/kg + 0.04 mg/kg per min) showed an additive effect on the natriuresis, although the renal haemodynamic changes were now absent. The infusion of ANP alone increased the urinary excretion of kallikrein and kinins. Prior infusion of amiloride prevented the expected increases in the urinary excretion of kallikrein and kinins after infusion of ANP was superimposed. These results suggest that the observed renal haemodynamic changes could be mediated through renal kallikrein and kinins. The additive effect on sodium excretion might be elicited by the results of alterations in the tubular handling of sodium, although distal tubular function is not modified by ANP. It seems that the renal kallikrein-kinin system is not causally involved in the increased sodium excretion by ANP.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>2967862</pmid><doi>10.1097/00004872-198804000-00009</doi><tpages>7</tpages></addata></record> |
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subjects | Amiloride - pharmacology Animals Arterial hypertension. Arterial hypotension Atrial Natriuretic Factor - pharmacology Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system Experimental diseases Female Kallikreins - physiology Kidney - drug effects Kidney - metabolism Kinins - physiology Medical sciences Natriuresis - drug effects Rabbits Renal Circulation - drug effects |
title | The effects of atrial natriuretic peptide and amiloride on renal haemodynamics and the renal kallikrein-kinin system |
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