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Increased Expression of the Mineralocorticoid Receptor in the Brain of Spontaneously Hypertensive Rats
The mineralocorticoid receptor (MR) has been considered as both neuroprotective and damaging to the function of the central nervous system. MR may be also involved in central regulation of blood pressure. In the present study, we compared the expression of MR and the glucocorticoid receptor (GR) in...
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Published in: | Journal of neuroendocrinology 2012-09, Vol.24 (9), p.1249-1258 |
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description | The mineralocorticoid receptor (MR) has been considered as both neuroprotective and damaging to the function of the central nervous system. MR may be also involved in central regulation of blood pressure. In the present study, we compared the expression of MR and the glucocorticoid receptor (GR) in the hippocampus and hypothalamus of 16‐week‐old spontaneously hypertensive rats (SHR) and normotensive control Wistar Kyoto (WKY) rats. In the hippocampus, MR expression was studied by in situ hybridization (ISH), quantitative polymerase chain reaction (PCR) and immunohistochemistry, whereas GR expression was analysed using the latter two procedures. Hypertensive animals showed an increased expression of MR mRNA in the whole hippocampus according to qPCR data and also in CA3 by ISH. Immunocytochemical staining for MR of the dorsal hippocampus, however, did not reveal differences between SHR and WKY rats. SHR showed elevated hypothalamic MR mRNA by qPCR, as well as an increased number of MR immunopositive cells in the magnocellular paraventricular region, compared to WKY rats. By contrast, expression levels of GR mRNA or protein in the hippocampus and hypothalamus of SHR were similar to those of WKY rats. Furthermore, we investigated the role of MR in the hypertensive rats by i.c.v. injection of the MR antagonist RU‐2831. This compound produced a significant drop in blood pressure for SHR. In conclusion, MR expression is increased in the hippocampus and hypothalamus of SHR. We suggest that pathological MR overdrive may take responsibility for up‐regulation of blood pressure and the encephalopathy of hypertension. |
doi_str_mv | 10.1111/j.1365-2826.2012.02332.x |
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E. ; Cymeryng, C. ; Gomez-Sanchez, E. ; Gomez-Sanchez, C. E. ; Roig, P. ; Lima, A. ; De Nicola, A. F.</creator><creatorcontrib>Pietranera, L. ; Brocca, M. E. ; Cymeryng, C. ; Gomez-Sanchez, E. ; Gomez-Sanchez, C. E. ; Roig, P. ; Lima, A. ; De Nicola, A. F.</creatorcontrib><description>The mineralocorticoid receptor (MR) has been considered as both neuroprotective and damaging to the function of the central nervous system. MR may be also involved in central regulation of blood pressure. In the present study, we compared the expression of MR and the glucocorticoid receptor (GR) in the hippocampus and hypothalamus of 16‐week‐old spontaneously hypertensive rats (SHR) and normotensive control Wistar Kyoto (WKY) rats. In the hippocampus, MR expression was studied by in situ hybridization (ISH), quantitative polymerase chain reaction (PCR) and immunohistochemistry, whereas GR expression was analysed using the latter two procedures. Hypertensive animals showed an increased expression of MR mRNA in the whole hippocampus according to qPCR data and also in CA3 by ISH. Immunocytochemical staining for MR of the dorsal hippocampus, however, did not reveal differences between SHR and WKY rats. SHR showed elevated hypothalamic MR mRNA by qPCR, as well as an increased number of MR immunopositive cells in the magnocellular paraventricular region, compared to WKY rats. By contrast, expression levels of GR mRNA or protein in the hippocampus and hypothalamus of SHR were similar to those of WKY rats. Furthermore, we investigated the role of MR in the hypertensive rats by i.c.v. injection of the MR antagonist RU‐2831. This compound produced a significant drop in blood pressure for SHR. In conclusion, MR expression is increased in the hippocampus and hypothalamus of SHR. We suggest that pathological MR overdrive may take responsibility for up‐regulation of blood pressure and the encephalopathy of hypertension.</description><identifier>ISSN: 0953-8194</identifier><identifier>EISSN: 1365-2826</identifier><identifier>DOI: 10.1111/j.1365-2826.2012.02332.x</identifier><identifier>PMID: 22564091</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>aldosterone ; Animals ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood pressure ; Blood Pressure - drug effects ; Brain ; Cardiology. Vascular system ; Central nervous system ; cortisol/corticosterone ; Data processing ; Encephalopathy ; Experimental diseases ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Glucocorticoid receptors ; glucocorticoids ; Hippocampus ; Hippocampus - metabolism ; Hypertension ; Hypothalamus ; Hypothalamus - metabolism ; Immunohistochemistry ; Medical sciences ; membrane/nuclear ; Mineralocorticoid Receptor Antagonists - pharmacology ; Mineralocorticoid receptors ; mineralocorticoids ; mRNA ; neuroactive steroids ; Neuroprotection ; Polymerase chain reaction ; Rats ; Rats, Inbred SHR - metabolism ; Rats, Inbred WKY ; receptors ; Receptors, Glucocorticoid - biosynthesis ; Receptors, Mineralocorticoid - biosynthesis ; Spironolactone - analogs & derivatives ; Spironolactone - pharmacology ; steroids ; Vertebrates: endocrinology</subject><ispartof>Journal of neuroendocrinology, 2012-09, Vol.24 (9), p.1249-1258</ispartof><rights>2012 The Authors. Journal of Neuroendocrinology © 2012 British Society for Neuroendocrinology</rights><rights>2015 INIST-CNRS</rights><rights>2012 The Authors. Journal of Neuroendocrinology © 2012 British Society for Neuroendocrinology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4982-8a83391fc7a395c37b8d4ab30f2461cddc4f35bba85db8cca91e8154bb6366293</citedby><cites>FETCH-LOGICAL-c4982-8a83391fc7a395c37b8d4ab30f2461cddc4f35bba85db8cca91e8154bb6366293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26250338$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22564091$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pietranera, L.</creatorcontrib><creatorcontrib>Brocca, M. E.</creatorcontrib><creatorcontrib>Cymeryng, C.</creatorcontrib><creatorcontrib>Gomez-Sanchez, E.</creatorcontrib><creatorcontrib>Gomez-Sanchez, C. E.</creatorcontrib><creatorcontrib>Roig, P.</creatorcontrib><creatorcontrib>Lima, A.</creatorcontrib><creatorcontrib>De Nicola, A. F.</creatorcontrib><title>Increased Expression of the Mineralocorticoid Receptor in the Brain of Spontaneously Hypertensive Rats</title><title>Journal of neuroendocrinology</title><addtitle>J Neuroendocrinol</addtitle><description>The mineralocorticoid receptor (MR) has been considered as both neuroprotective and damaging to the function of the central nervous system. MR may be also involved in central regulation of blood pressure. In the present study, we compared the expression of MR and the glucocorticoid receptor (GR) in the hippocampus and hypothalamus of 16‐week‐old spontaneously hypertensive rats (SHR) and normotensive control Wistar Kyoto (WKY) rats. In the hippocampus, MR expression was studied by in situ hybridization (ISH), quantitative polymerase chain reaction (PCR) and immunohistochemistry, whereas GR expression was analysed using the latter two procedures. Hypertensive animals showed an increased expression of MR mRNA in the whole hippocampus according to qPCR data and also in CA3 by ISH. Immunocytochemical staining for MR of the dorsal hippocampus, however, did not reveal differences between SHR and WKY rats. SHR showed elevated hypothalamic MR mRNA by qPCR, as well as an increased number of MR immunopositive cells in the magnocellular paraventricular region, compared to WKY rats. By contrast, expression levels of GR mRNA or protein in the hippocampus and hypothalamus of SHR were similar to those of WKY rats. Furthermore, we investigated the role of MR in the hypertensive rats by i.c.v. injection of the MR antagonist RU‐2831. This compound produced a significant drop in blood pressure for SHR. In conclusion, MR expression is increased in the hippocampus and hypothalamus of SHR. We suggest that pathological MR overdrive may take responsibility for up‐regulation of blood pressure and the encephalopathy of hypertension.</description><subject>aldosterone</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</subject><subject>Blood Pressure - drug effects</subject><subject>Brain</subject><subject>Cardiology. Vascular system</subject><subject>Central nervous system</subject><subject>cortisol/corticosterone</subject><subject>Data processing</subject><subject>Encephalopathy</subject><subject>Experimental diseases</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Glucocorticoid receptors</subject><subject>glucocorticoids</subject><subject>Hippocampus</subject><subject>Hippocampus - metabolism</subject><subject>Hypertension</subject><subject>Hypothalamus</subject><subject>Hypothalamus - metabolism</subject><subject>Immunohistochemistry</subject><subject>Medical sciences</subject><subject>membrane/nuclear</subject><subject>Mineralocorticoid Receptor Antagonists - pharmacology</subject><subject>Mineralocorticoid receptors</subject><subject>mineralocorticoids</subject><subject>mRNA</subject><subject>neuroactive steroids</subject><subject>Neuroprotection</subject><subject>Polymerase chain reaction</subject><subject>Rats</subject><subject>Rats, Inbred SHR - metabolism</subject><subject>Rats, Inbred WKY</subject><subject>receptors</subject><subject>Receptors, Glucocorticoid - biosynthesis</subject><subject>Receptors, Mineralocorticoid - biosynthesis</subject><subject>Spironolactone - analogs & derivatives</subject><subject>Spironolactone - pharmacology</subject><subject>steroids</subject><subject>Vertebrates: endocrinology</subject><issn>0953-8194</issn><issn>1365-2826</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkU9v0zAYhy0EYt3GV0CREBKXBNtv7DgHDmwr3dDYpPFn0i6W4zjCJY2DnUL77XGaUiRO88WW_Pxe_6wHoYTgjMT1dpkR4CylgvKMYkIzTAFotnmCZoeLp2iGSwapIGV-hI5DWGJMCgb4OTqilPEcl2SGmqtOe6OCqZP5pvcmBOu6xDXJ8N0kn2xnvGqddn6w2tk6uTPa9IPzie12xJlXdod_7l03qM64dWi3yeW2N34wXbC_THKnhnCKnjWqDebFfj9BXz_Mv5xfpte3i6vz99epzktBU6EEQEkaXSgomYaiEnWuKsANzTnRda3zBlhVKcHqSmitSmIEYXlVceCclnCC3kxze-9-rk0Y5MoGbdp2qiYJBsEJgRIeg-YklmIkoq_-Q5du7bv4EUlyoIALICxSYqK0dyF408je25Xy2zhKjtrkUo525GhHjtrkTpvcxOjL_QPramXqQ_Cvpwi83gMqaNU2XnXahn8cpwwDiMi9m7jftjXbRxeQH2_m4ynm0ylvw2A2h7zyPyQvoGDy_mYhF4uz-28XD4V8gD82bMHe</recordid><startdate>201209</startdate><enddate>201209</enddate><creator>Pietranera, L.</creator><creator>Brocca, M. 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Psychology</topic><topic>Gene expression</topic><topic>Glucocorticoid receptors</topic><topic>glucocorticoids</topic><topic>Hippocampus</topic><topic>Hippocampus - metabolism</topic><topic>Hypertension</topic><topic>Hypothalamus</topic><topic>Hypothalamus - metabolism</topic><topic>Immunohistochemistry</topic><topic>Medical sciences</topic><topic>membrane/nuclear</topic><topic>Mineralocorticoid Receptor Antagonists - pharmacology</topic><topic>Mineralocorticoid receptors</topic><topic>mineralocorticoids</topic><topic>mRNA</topic><topic>neuroactive steroids</topic><topic>Neuroprotection</topic><topic>Polymerase chain reaction</topic><topic>Rats</topic><topic>Rats, Inbred SHR - metabolism</topic><topic>Rats, Inbred WKY</topic><topic>receptors</topic><topic>Receptors, Glucocorticoid - biosynthesis</topic><topic>Receptors, Mineralocorticoid - biosynthesis</topic><topic>Spironolactone - analogs & derivatives</topic><topic>Spironolactone - pharmacology</topic><topic>steroids</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pietranera, L.</creatorcontrib><creatorcontrib>Brocca, M. 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E.</au><au>Cymeryng, C.</au><au>Gomez-Sanchez, E.</au><au>Gomez-Sanchez, C. E.</au><au>Roig, P.</au><au>Lima, A.</au><au>De Nicola, A. F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased Expression of the Mineralocorticoid Receptor in the Brain of Spontaneously Hypertensive Rats</atitle><jtitle>Journal of neuroendocrinology</jtitle><addtitle>J Neuroendocrinol</addtitle><date>2012-09</date><risdate>2012</risdate><volume>24</volume><issue>9</issue><spage>1249</spage><epage>1258</epage><pages>1249-1258</pages><issn>0953-8194</issn><eissn>1365-2826</eissn><abstract>The mineralocorticoid receptor (MR) has been considered as both neuroprotective and damaging to the function of the central nervous system. MR may be also involved in central regulation of blood pressure. In the present study, we compared the expression of MR and the glucocorticoid receptor (GR) in the hippocampus and hypothalamus of 16‐week‐old spontaneously hypertensive rats (SHR) and normotensive control Wistar Kyoto (WKY) rats. In the hippocampus, MR expression was studied by in situ hybridization (ISH), quantitative polymerase chain reaction (PCR) and immunohistochemistry, whereas GR expression was analysed using the latter two procedures. Hypertensive animals showed an increased expression of MR mRNA in the whole hippocampus according to qPCR data and also in CA3 by ISH. Immunocytochemical staining for MR of the dorsal hippocampus, however, did not reveal differences between SHR and WKY rats. SHR showed elevated hypothalamic MR mRNA by qPCR, as well as an increased number of MR immunopositive cells in the magnocellular paraventricular region, compared to WKY rats. By contrast, expression levels of GR mRNA or protein in the hippocampus and hypothalamus of SHR were similar to those of WKY rats. Furthermore, we investigated the role of MR in the hypertensive rats by i.c.v. injection of the MR antagonist RU‐2831. This compound produced a significant drop in blood pressure for SHR. In conclusion, MR expression is increased in the hippocampus and hypothalamus of SHR. We suggest that pathological MR overdrive may take responsibility for up‐regulation of blood pressure and the encephalopathy of hypertension.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22564091</pmid><doi>10.1111/j.1365-2826.2012.02332.x</doi><tpages>10</tpages></addata></record> |
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subjects | aldosterone Animals Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels Blood pressure Blood Pressure - drug effects Brain Cardiology. Vascular system Central nervous system cortisol/corticosterone Data processing Encephalopathy Experimental diseases Fundamental and applied biological sciences. Psychology Gene expression Glucocorticoid receptors glucocorticoids Hippocampus Hippocampus - metabolism Hypertension Hypothalamus Hypothalamus - metabolism Immunohistochemistry Medical sciences membrane/nuclear Mineralocorticoid Receptor Antagonists - pharmacology Mineralocorticoid receptors mineralocorticoids mRNA neuroactive steroids Neuroprotection Polymerase chain reaction Rats Rats, Inbred SHR - metabolism Rats, Inbred WKY receptors Receptors, Glucocorticoid - biosynthesis Receptors, Mineralocorticoid - biosynthesis Spironolactone - analogs & derivatives Spironolactone - pharmacology steroids Vertebrates: endocrinology |
title | Increased Expression of the Mineralocorticoid Receptor in the Brain of Spontaneously Hypertensive Rats |
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