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 |
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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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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 & 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 & 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 & Wilkins, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200712</creationdate><title>Transient prehypertensive treatment in spontaneously hypertensive rats: a comparison of spironolactone and losartan regarding long-term blood pressure and target organ damage</title><author>Baumann, Marcus ; Hermans, JJ Rob ; Janssen, Ben JA ; Peutz-Kootstra, Carine ; Witzke, Oliver ; Heemann, Uwe ; Smits, Jos FM ; Boudier, Harry AJ Struijker</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p1840-a00f920a3334068bec546d8f75d30d3d178bc058dae46b10b62258f621ac44143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Age Factors</topic><topic>Angiotensin II Type 1 Receptor Blockers - therapeutic use</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Blood Pressure - drug effects</topic><topic>Collagen - genetics</topic><topic>Collagen - metabolism</topic><topic>DNA Primers - genetics</topic><topic>Heart - drug effects</topic><topic>Hypertension - drug therapy</topic><topic>Hypertension - pathology</topic><topic>Hypertension - physiopathology</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Kidney - pathology</topic><topic>Losartan - therapeutic use</topic><topic>Mineralocorticoid Receptor Antagonists - therapeutic use</topic><topic>Myocardium - metabolism</topic><topic>Myocardium - pathology</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Spironolactone - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baumann, Marcus</au><au>Hermans, JJ Rob</au><au>Janssen, Ben JA</au><au>Peutz-Kootstra, Carine</au><au>Witzke, Oliver</au><au>Heemann, Uwe</au><au>Smits, Jos FM</au><au>Boudier, Harry AJ Struijker</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transient prehypertensive treatment in spontaneously hypertensive rats: a comparison of spironolactone and losartan regarding long-term blood pressure and target organ damage</atitle><jtitle>Journal of hypertension</jtitle><addtitle>J Hypertens</addtitle><date>2007-12</date><risdate>2007</risdate><volume>25</volume><issue>12</issue><spage>2504</spage><epage>2511</epage><pages>2504-2511</pages><issn>0263-6352</issn><eissn>1473-5598</eissn><abstract>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.</abstract><cop>England</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>17984673</pmid><doi>10.1097/HJH.0b013e3282ef84f8</doi><tpages>8</tpages></addata></record> |
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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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