Transient prehypertensive treatment in spontaneously hypertensive rats: a comparison of spironolactone and losartan regarding long-term blood pressure and target organ damage

OBJECTIVEWe previously demonstrated that when the renin–angiotensin system (RAS) is transiently blocked by an angiotensin receptor blocker (ARB) in young spontaneously hypertensive rats (SHR), this results in a prolonged blood pressure decrease and protection against target organ damage. Aldosterone...

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Veröffentlicht in:Journal of hypertension 2007-12, Vol.25 (12), p.2504-2511
Hauptverfasser: Baumann, Marcus, Hermans, JJ Rob, Janssen, Ben JA, Peutz-Kootstra, Carine, Witzke, Oliver, Heemann, Uwe, Smits, Jos FM, Boudier, Harry AJ Struijker
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container_end_page 2511
container_issue 12
container_start_page 2504
container_title Journal of hypertension
container_volume 25
creator Baumann, Marcus
Hermans, JJ Rob
Janssen, Ben JA
Peutz-Kootstra, Carine
Witzke, Oliver
Heemann, Uwe
Smits, Jos FM
Boudier, Harry AJ Struijker
description OBJECTIVEWe previously demonstrated that when the renin–angiotensin system (RAS) is transiently blocked by an angiotensin receptor blocker (ARB) in young spontaneously hypertensive rats (SHR), this results in a prolonged blood pressure decrease and protection against target organ damage. Aldosterone is an essential hormone in the RAS, and contributes to pathologic remodeling. Thus, part of the protective effects of the ARB may be due to inhibition of aldosterone-mediated effects. To test this hypothesis, in young SHR, we compared the effectiveness of transient treatment with the mineralocorticoid receptor blocker spironolactone with those obtained by the ARB losartan. METHODSSHR were transiently (i.e. between 4–8 weeks of age) treated with spironolactone (SHR-Spiro1 mg/kg per day), losartan (SHR-Los20 mg/kg per day) or saline. Rats were followed up until week 72 of age and cardiovascular parameters were repeatedly assessed by echocardiography, radiotelemetry of blood pressure and 24-h urine collection. End-point measurements included direct left ventricular contractility and relaxation, as well as cardiac and renal histomorphology. RESULTSTransient spironolactone treatment reduced blood pressure up to 36 weeks of age and cardiac and renal collagen deposition and tubular atrophy up to 72 weeks of age compared to untreated SHR. Pulse pressure was higher in SHR-Spiro compared to SHR-Los. Cardiac hypertrophy, albuminuria and glomerulosclerosis were not attenuated in SHR-Spiro compared to untreated SHR up to 72 weeks of age, whereas the effects in SHR-Los were ameliorated. CONCLUSIONSAlthough transient spironolactone treatment leads to prolonged blood pressure reduction and reduced collagen deposition, long-term organ protection only partially exists. Thus, transient spironolactone treatment is less effective than transient losartan treatment.
doi_str_mv 10.1097/HJH.0b013e3282ef84f8
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Aldosterone is an essential hormone in the RAS, and contributes to pathologic remodeling. Thus, part of the protective effects of the ARB may be due to inhibition of aldosterone-mediated effects. To test this hypothesis, in young SHR, we compared the effectiveness of transient treatment with the mineralocorticoid receptor blocker spironolactone with those obtained by the ARB losartan. METHODSSHR were transiently (i.e. between 4–8 weeks of age) treated with spironolactone (SHR-Spiro1 mg/kg per day), losartan (SHR-Los20 mg/kg per day) or saline. Rats were followed up until week 72 of age and cardiovascular parameters were repeatedly assessed by echocardiography, radiotelemetry of blood pressure and 24-h urine collection. End-point measurements included direct left ventricular contractility and relaxation, as well as cardiac and renal histomorphology. RESULTSTransient spironolactone treatment reduced blood pressure up to 36 weeks of age and cardiac and renal collagen deposition and tubular atrophy up to 72 weeks of age compared to untreated SHR. Pulse pressure was higher in SHR-Spiro compared to SHR-Los. Cardiac hypertrophy, albuminuria and glomerulosclerosis were not attenuated in SHR-Spiro compared to untreated SHR up to 72 weeks of age, whereas the effects in SHR-Los were ameliorated. CONCLUSIONSAlthough transient spironolactone treatment leads to prolonged blood pressure reduction and reduced collagen deposition, long-term organ protection only partially exists. Thus, transient spironolactone treatment is less effective than transient losartan treatment.</description><identifier>ISSN: 0263-6352</identifier><identifier>EISSN: 1473-5598</identifier><identifier>DOI: 10.1097/HJH.0b013e3282ef84f8</identifier><identifier>PMID: 17984673</identifier><language>eng</language><publisher>England: Lippincott Williams &amp; Wilkins, Inc</publisher><subject>Age Factors ; Angiotensin II Type 1 Receptor Blockers - therapeutic use ; Animals ; Base Sequence ; Blood Pressure - drug effects ; Collagen - genetics ; Collagen - metabolism ; DNA Primers - genetics ; Heart - drug effects ; Hypertension - drug therapy ; Hypertension - pathology ; Hypertension - physiopathology ; Kidney - drug effects ; Kidney - metabolism ; Kidney - pathology ; Losartan - therapeutic use ; Mineralocorticoid Receptor Antagonists - therapeutic use ; Myocardium - metabolism ; Myocardium - pathology ; Rats ; Rats, Inbred SHR ; Spironolactone - therapeutic use</subject><ispartof>Journal of hypertension, 2007-12, Vol.25 (12), p.2504-2511</ispartof><rights>2007 Lippincott Williams &amp; Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17984673$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baumann, Marcus</creatorcontrib><creatorcontrib>Hermans, JJ Rob</creatorcontrib><creatorcontrib>Janssen, Ben JA</creatorcontrib><creatorcontrib>Peutz-Kootstra, Carine</creatorcontrib><creatorcontrib>Witzke, Oliver</creatorcontrib><creatorcontrib>Heemann, Uwe</creatorcontrib><creatorcontrib>Smits, Jos FM</creatorcontrib><creatorcontrib>Boudier, Harry AJ Struijker</creatorcontrib><title>Transient prehypertensive treatment in spontaneously hypertensive rats: a comparison of spironolactone and losartan regarding long-term blood pressure and target organ damage</title><title>Journal of hypertension</title><addtitle>J Hypertens</addtitle><description>OBJECTIVEWe previously demonstrated that when the renin–angiotensin system (RAS) is transiently blocked by an angiotensin receptor blocker (ARB) in young spontaneously hypertensive rats (SHR), this results in a prolonged blood pressure decrease and protection against target organ damage. Aldosterone is an essential hormone in the RAS, and contributes to pathologic remodeling. Thus, part of the protective effects of the ARB may be due to inhibition of aldosterone-mediated effects. To test this hypothesis, in young SHR, we compared the effectiveness of transient treatment with the mineralocorticoid receptor blocker spironolactone with those obtained by the ARB losartan. METHODSSHR were transiently (i.e. between 4–8 weeks of age) treated with spironolactone (SHR-Spiro1 mg/kg per day), losartan (SHR-Los20 mg/kg per day) or saline. Rats were followed up until week 72 of age and cardiovascular parameters were repeatedly assessed by echocardiography, radiotelemetry of blood pressure and 24-h urine collection. End-point measurements included direct left ventricular contractility and relaxation, as well as cardiac and renal histomorphology. RESULTSTransient spironolactone treatment reduced blood pressure up to 36 weeks of age and cardiac and renal collagen deposition and tubular atrophy up to 72 weeks of age compared to untreated SHR. Pulse pressure was higher in SHR-Spiro compared to SHR-Los. Cardiac hypertrophy, albuminuria and glomerulosclerosis were not attenuated in SHR-Spiro compared to untreated SHR up to 72 weeks of age, whereas the effects in SHR-Los were ameliorated. CONCLUSIONSAlthough transient spironolactone treatment leads to prolonged blood pressure reduction and reduced collagen deposition, long-term organ protection only partially exists. Thus, transient spironolactone treatment is less effective than transient losartan treatment.</description><subject>Age Factors</subject><subject>Angiotensin II Type 1 Receptor Blockers - therapeutic use</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Blood Pressure - drug effects</subject><subject>Collagen - genetics</subject><subject>Collagen - metabolism</subject><subject>DNA Primers - genetics</subject><subject>Heart - drug effects</subject><subject>Hypertension - drug therapy</subject><subject>Hypertension - pathology</subject><subject>Hypertension - physiopathology</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Kidney - pathology</subject><subject>Losartan - therapeutic use</subject><subject>Mineralocorticoid Receptor Antagonists - therapeutic use</subject><subject>Myocardium - metabolism</subject><subject>Myocardium - pathology</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Spironolactone - therapeutic use</subject><issn>0263-6352</issn><issn>1473-5598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc1u1DAQxy0EokvhDRDyiVvK-COxww1VwBZV4lLO0SSeZAOJHWxvq30pnhFXWw4cZkaa-c1f88HYWwFXAlrzYf9tfwU9CEVKWkmj1aN9xnZCG1XVdWufsx3IRlWNquUFe5XSTwCwrVEv2YUwrdWNUTv25y6iTzP5zLdIh9NGMVNJ3BPPkTCvj5XZ87QFn9FTOKblxP_jIub0kSMfwrphnFPwPIylYY7BhwWHHDxx9I4vIWEsIjzShNHNfiopP1WZ4sr7JQT3OENKx3jmM8aJMg9xKj0OV5zoNXsx4pLozVO8ZD--fL673le337_eXH-6rTZhNVQIMLYSUCmlobE9DbVunB1N7RQ45YSx_QC1dUi66QX0jZS1HRspcNBaaHXJ3p91txh-Hynlbp3TQMtyPkHXWG0MSCjguyfw2K_kui3OK8ZT9-_CBdBn4CEsZdH0azk-UOwOhEs-dOUloK2RlQQwojioihXdv019lGQ</recordid><startdate>200712</startdate><enddate>200712</enddate><creator>Baumann, Marcus</creator><creator>Hermans, JJ Rob</creator><creator>Janssen, Ben JA</creator><creator>Peutz-Kootstra, Carine</creator><creator>Witzke, Oliver</creator><creator>Heemann, Uwe</creator><creator>Smits, Jos FM</creator><creator>Boudier, Harry AJ Struijker</creator><general>Lippincott Williams &amp; 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Aldosterone is an essential hormone in the RAS, and contributes to pathologic remodeling. Thus, part of the protective effects of the ARB may be due to inhibition of aldosterone-mediated effects. To test this hypothesis, in young SHR, we compared the effectiveness of transient treatment with the mineralocorticoid receptor blocker spironolactone with those obtained by the ARB losartan. METHODSSHR were transiently (i.e. between 4–8 weeks of age) treated with spironolactone (SHR-Spiro1 mg/kg per day), losartan (SHR-Los20 mg/kg per day) or saline. Rats were followed up until week 72 of age and cardiovascular parameters were repeatedly assessed by echocardiography, radiotelemetry of blood pressure and 24-h urine collection. End-point measurements included direct left ventricular contractility and relaxation, as well as cardiac and renal histomorphology. RESULTSTransient spironolactone treatment reduced blood pressure up to 36 weeks of age and cardiac and renal collagen deposition and tubular atrophy up to 72 weeks of age compared to untreated SHR. Pulse pressure was higher in SHR-Spiro compared to SHR-Los. Cardiac hypertrophy, albuminuria and glomerulosclerosis were not attenuated in SHR-Spiro compared to untreated SHR up to 72 weeks of age, whereas the effects in SHR-Los were ameliorated. CONCLUSIONSAlthough transient spironolactone treatment leads to prolonged blood pressure reduction and reduced collagen deposition, long-term organ protection only partially exists. Thus, transient spironolactone treatment is less effective than transient losartan treatment.</abstract><cop>England</cop><pub>Lippincott Williams &amp; Wilkins, Inc</pub><pmid>17984673</pmid><doi>10.1097/HJH.0b013e3282ef84f8</doi><tpages>8</tpages></addata></record>
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source MEDLINE; Journals@Ovid Complete
subjects Age Factors
Angiotensin II Type 1 Receptor Blockers - therapeutic use
Animals
Base Sequence
Blood Pressure - drug effects
Collagen - genetics
Collagen - metabolism
DNA Primers - genetics
Heart - drug effects
Hypertension - drug therapy
Hypertension - pathology
Hypertension - physiopathology
Kidney - drug effects
Kidney - metabolism
Kidney - pathology
Losartan - therapeutic use
Mineralocorticoid Receptor Antagonists - therapeutic use
Myocardium - metabolism
Myocardium - pathology
Rats
Rats, Inbred SHR
Spironolactone - therapeutic use
title Transient prehypertensive treatment in spontaneously hypertensive rats: a comparison of spironolactone and losartan regarding long-term blood pressure and target organ damage
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