Adrenocorticosteroid excretion in salt-sensitive and salt-resistant spontaneously hypertensive rats

Two strains of spontaneously hypertensive rats (SHRs) differ in their susceptibility to the hypertensive effects of dietary NaCl. One strain exhibits a significant elevation of blood pressure after dietary NaCl loading (SHR-S), whereas the other does not (SHR-R). Since differences in adrenocortical...

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Veröffentlicht in:Steroids 1992-02, Vol.57 (2), p.90-94
Hauptverfasser: Griffing, George T., Melby, James C., Holbrook, Monica, Wilson, Thomas C., Wyss, Michael J.
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container_issue 2
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creator Griffing, George T.
Melby, James C.
Holbrook, Monica
Wilson, Thomas C.
Wyss, Michael J.
description Two strains of spontaneously hypertensive rats (SHRs) differ in their susceptibility to the hypertensive effects of dietary NaCl. One strain exhibits a significant elevation of blood pressure after dietary NaCl loading (SHR-S), whereas the other does not (SHR-R). Since differences in adrenocortical steroid production may contribute to NaCl sensitivity, we compared 19-nordeoxycorticosterone (DOC), 18-OH-DOC, aldosterone, and corticosterone excretion in 6-week-old male rats from the SHR-S (n = 24) and SHR-R (n = 24) strains. The rats were housed in metabolic cages (two rats per cage) and given either basal (1%) or high (8%) NaCl diet. Urinary steroids were analyzed using thin-layer chromatography and radioimmunoassay methods. The high NaCl diet elevated the urinary excretion of the four corticosteroids in both rat strains. 19-nor-DOC decreased with time in both the SHR-S and SHR-R strains, and was not different between strains on either diet. Aldosterone was increased in the SHR-S strain compared with the SHR-R strain on the low NaCl diet, but aldosterone was not different between the two strains on the high NaCl diet. Corticosterone and 18-OH-DOC did not differ between strains. These data confirm that 19-nor-DOC is higher in young prehypertensive SHRs and decreases with age. Aldosterone excretion is higher in the SHR-S strain compared with the SHR-R strain on the low NaCl diet. Aldosterone levels are not different in the SHR-S strain compared with the SHR-R strain on the high NaCl diet, but these levels may be inappropriately high in the SHR-S strain, which has excess blood pressure elevation. The failure of aldosterone to suppress appropriately in the SHR-S strain may contribute to the susceptibility of these rats to the hypertensive effects of dietary NaCl.
doi_str_mv 10.1016/0039-128X(92)90036-9
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One strain exhibits a significant elevation of blood pressure after dietary NaCl loading (SHR-S), whereas the other does not (SHR-R). Since differences in adrenocortical steroid production may contribute to NaCl sensitivity, we compared 19-nordeoxycorticosterone (DOC), 18-OH-DOC, aldosterone, and corticosterone excretion in 6-week-old male rats from the SHR-S (n = 24) and SHR-R (n = 24) strains. The rats were housed in metabolic cages (two rats per cage) and given either basal (1%) or high (8%) NaCl diet. Urinary steroids were analyzed using thin-layer chromatography and radioimmunoassay methods. The high NaCl diet elevated the urinary excretion of the four corticosteroids in both rat strains. 19-nor-DOC decreased with time in both the SHR-S and SHR-R strains, and was not different between strains on either diet. Aldosterone was increased in the SHR-S strain compared with the SHR-R strain on the low NaCl diet, but aldosterone was not different between the two strains on the high NaCl diet. Corticosterone and 18-OH-DOC did not differ between strains. These data confirm that 19-nor-DOC is higher in young prehypertensive SHRs and decreases with age. Aldosterone excretion is higher in the SHR-S strain compared with the SHR-R strain on the low NaCl diet. Aldosterone levels are not different in the SHR-S strain compared with the SHR-R strain on the high NaCl diet, but these levels may be inappropriately high in the SHR-S strain, which has excess blood pressure elevation. 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One strain exhibits a significant elevation of blood pressure after dietary NaCl loading (SHR-S), whereas the other does not (SHR-R). Since differences in adrenocortical steroid production may contribute to NaCl sensitivity, we compared 19-nordeoxycorticosterone (DOC), 18-OH-DOC, aldosterone, and corticosterone excretion in 6-week-old male rats from the SHR-S (n = 24) and SHR-R (n = 24) strains. The rats were housed in metabolic cages (two rats per cage) and given either basal (1%) or high (8%) NaCl diet. Urinary steroids were analyzed using thin-layer chromatography and radioimmunoassay methods. The high NaCl diet elevated the urinary excretion of the four corticosteroids in both rat strains. 19-nor-DOC decreased with time in both the SHR-S and SHR-R strains, and was not different between strains on either diet. Aldosterone was increased in the SHR-S strain compared with the SHR-R strain on the low NaCl diet, but aldosterone was not different between the two strains on the high NaCl diet. Corticosterone and 18-OH-DOC did not differ between strains. These data confirm that 19-nor-DOC is higher in young prehypertensive SHRs and decreases with age. Aldosterone excretion is higher in the SHR-S strain compared with the SHR-R strain on the low NaCl diet. Aldosterone levels are not different in the SHR-S strain compared with the SHR-R strain on the high NaCl diet, but these levels may be inappropriately high in the SHR-S strain, which has excess blood pressure elevation. The failure of aldosterone to suppress appropriately in the SHR-S strain may contribute to the susceptibility of these rats to the hypertensive effects of dietary NaCl.</description><subject>18-hydroxydeoxycorticosterone</subject><subject>19-nordeoxycorticosterone</subject><subject>aldosterone</subject><subject>Aldosterone - urine</subject><subject>Animals</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Pressure - drug effects</subject><subject>Cardiology. Vascular system</subject><subject>Chromatography, Thin Layer</subject><subject>Corticosterone - urine</subject><subject>corticosterone in hypertensive rats</subject><subject>Desoxycorticosterone - analogs &amp; derivatives</subject><subject>Desoxycorticosterone - urine</subject><subject>Experimental diseases</subject><subject>Hydroxycorticosteroids - urine</subject><subject>Hypertension - urine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Radioimmunoassay</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>salt-sensitive, salt-resistant rats</subject><subject>Sodium, Dietary - administration &amp; dosage</subject><subject>Sodium, Dietary - pharmacology</subject><subject>spontaneously hypertensive rats</subject><subject>steroids</subject><issn>0039-128X</issn><issn>1878-5867</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE2LFDEQhoO4rOPqP1Dog4geWvPRnUxdFpZF3YWFvSh4C-mkBiM9yZjKLM6_N2MP681TpVJPFS8PY68E_yC40B85V9ALuf7-DuR7aJ3u4QlbibVZ9-Nam6ds9Yg8Y8-JfnLOtQJ5zs6FlkJqtWL-KhRM2edSo89UseQYOvztC9aYUxdTR26uPWGiWOMDdi6F5asgRaou1Y52ObUH5j3Nh-7HYYelHvlGF1fpBTvbuJnw5alesG-fP329vunv7r_cXl_d9X4YZe2d96ND59Qg9DAGmEAb9AG8FzLAxowCYOB8clKAHLmWAIEbM3Hg2oCe1AV7u9zdlfxrj1TtNpLHeV6iWaO4EmoYGjgsoC-ZqODG7krcunKwgtujW3sUZ4_iLEj7162Ftvb6dH8_bTH8W1pktvmb09yRd_OmuOQjPWItvzJaNOxywbC5eIhYLPmIyWOIBX21Icf_5_gDUbWXyA</recordid><startdate>19920201</startdate><enddate>19920201</enddate><creator>Griffing, George T.</creator><creator>Melby, James C.</creator><creator>Holbrook, Monica</creator><creator>Wilson, Thomas C.</creator><creator>Wyss, Michael J.</creator><general>Elsevier Inc</general><general>Elsevier Science</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>19920201</creationdate><title>Adrenocorticosteroid excretion in salt-sensitive and salt-resistant spontaneously hypertensive rats</title><author>Griffing, George T. ; Melby, James C. ; Holbrook, Monica ; Wilson, Thomas C. ; Wyss, Michael J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-acc5aeaa341645d9b967ecd9cc12d9f75199400ba2192506299d077b0906796b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>18-hydroxydeoxycorticosterone</topic><topic>19-nordeoxycorticosterone</topic><topic>aldosterone</topic><topic>Aldosterone - urine</topic><topic>Animals</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Pressure - drug effects</topic><topic>Cardiology. Vascular system</topic><topic>Chromatography, Thin Layer</topic><topic>Corticosterone - urine</topic><topic>corticosterone in hypertensive rats</topic><topic>Desoxycorticosterone - analogs &amp; derivatives</topic><topic>Desoxycorticosterone - urine</topic><topic>Experimental diseases</topic><topic>Hydroxycorticosteroids - urine</topic><topic>Hypertension - urine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Radioimmunoassay</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>salt-sensitive, salt-resistant rats</topic><topic>Sodium, Dietary - administration &amp; dosage</topic><topic>Sodium, Dietary - pharmacology</topic><topic>spontaneously hypertensive rats</topic><topic>steroids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Griffing, George T.</creatorcontrib><creatorcontrib>Melby, James C.</creatorcontrib><creatorcontrib>Holbrook, Monica</creatorcontrib><creatorcontrib>Wilson, Thomas C.</creatorcontrib><creatorcontrib>Wyss, Michael J.</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>Steroids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Griffing, George T.</au><au>Melby, James C.</au><au>Holbrook, Monica</au><au>Wilson, Thomas C.</au><au>Wyss, Michael J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adrenocorticosteroid excretion in salt-sensitive and salt-resistant spontaneously hypertensive rats</atitle><jtitle>Steroids</jtitle><addtitle>Steroids</addtitle><date>1992-02-01</date><risdate>1992</risdate><volume>57</volume><issue>2</issue><spage>90</spage><epage>94</epage><pages>90-94</pages><issn>0039-128X</issn><eissn>1878-5867</eissn><coden>STEDAM</coden><abstract>Two strains of spontaneously hypertensive rats (SHRs) differ in their susceptibility to the hypertensive effects of dietary NaCl. One strain exhibits a significant elevation of blood pressure after dietary NaCl loading (SHR-S), whereas the other does not (SHR-R). Since differences in adrenocortical steroid production may contribute to NaCl sensitivity, we compared 19-nordeoxycorticosterone (DOC), 18-OH-DOC, aldosterone, and corticosterone excretion in 6-week-old male rats from the SHR-S (n = 24) and SHR-R (n = 24) strains. The rats were housed in metabolic cages (two rats per cage) and given either basal (1%) or high (8%) NaCl diet. Urinary steroids were analyzed using thin-layer chromatography and radioimmunoassay methods. The high NaCl diet elevated the urinary excretion of the four corticosteroids in both rat strains. 19-nor-DOC decreased with time in both the SHR-S and SHR-R strains, and was not different between strains on either diet. Aldosterone was increased in the SHR-S strain compared with the SHR-R strain on the low NaCl diet, but aldosterone was not different between the two strains on the high NaCl diet. Corticosterone and 18-OH-DOC did not differ between strains. These data confirm that 19-nor-DOC is higher in young prehypertensive SHRs and decreases with age. Aldosterone excretion is higher in the SHR-S strain compared with the SHR-R strain on the low NaCl diet. Aldosterone levels are not different in the SHR-S strain compared with the SHR-R strain on the high NaCl diet, but these levels may be inappropriately high in the SHR-S strain, which has excess blood pressure elevation. The failure of aldosterone to suppress appropriately in the SHR-S strain may contribute to the susceptibility of these rats to the hypertensive effects of dietary NaCl.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>1621263</pmid><doi>10.1016/0039-128X(92)90036-9</doi><tpages>5</tpages></addata></record>
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identifier ISSN: 0039-128X
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language eng
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subjects 18-hydroxydeoxycorticosterone
19-nordeoxycorticosterone
aldosterone
Aldosterone - urine
Animals
Arterial hypertension. Arterial hypotension
Biological and medical sciences
Blood and lymphatic vessels
Blood Pressure - drug effects
Cardiology. Vascular system
Chromatography, Thin Layer
Corticosterone - urine
corticosterone in hypertensive rats
Desoxycorticosterone - analogs & derivatives
Desoxycorticosterone - urine
Experimental diseases
Hydroxycorticosteroids - urine
Hypertension - urine
Male
Medical sciences
Radioimmunoassay
Rats
Rats, Inbred SHR
salt-sensitive, salt-resistant rats
Sodium, Dietary - administration & dosage
Sodium, Dietary - pharmacology
spontaneously hypertensive rats
steroids
title Adrenocorticosteroid excretion in salt-sensitive and salt-resistant spontaneously hypertensive rats
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