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An in vivo role of bone morphogenetic protein-6 in aldosterone production by rat adrenal gland
► Neutralization of endogenous BMP-6 by immunization reduced aldosterone production in vivo. ► Chronic Ang II treatment impaired the neutralization effect of BMP-6. ► Adrenal CYP11B2 expression and plasma aldosterone/corticosterone were reduced by blocking BMP-6. ► Endogenous BMP-6 is linked to aldo...
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Published in: | The Journal of steroid biochemistry and molecular biology 2012-10, Vol.132 (1-2), p.8-14 |
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creator | Matsumoto, Yoshinori Otsuka, Fumio Inagaki, Kenichi Tsukamoto, Naoko Takano-Narazaki, Mariko Miyoshi, Tomoko Nakamura, Eri Ogura-Ochi, Kanako Takeda, Masaya Makino, Hirofumi |
description | ► Neutralization of endogenous BMP-6 by immunization reduced aldosterone production in vivo. ► Chronic Ang II treatment impaired the neutralization effect of BMP-6. ► Adrenal CYP11B2 expression and plasma aldosterone/corticosterone were reduced by blocking BMP-6. ► Endogenous BMP-6 is linked to aldosterone synthesis in the adrenal.
Aldosterone is synthesized in the zona glomerulosa of the adrenal cortex. We previously reported the presence of a functional BMP system including BMP-6 in human adrenocortical cells. BMP-6 contributes to Ang II-induced aldosterone production by activating Smad signaling, in which endogenous BMP-6 action is negatively controlled by Ang II in vitro. In the present study, we examined the in vivo role of BMP-6 in regulation of aldosterone by neutralizing endogenous BMP-6 in rats treated with immunization against BMP-6. Three-week-old male rats were actively immunized with rat mature BMP-6 antigen conjugated with keyhole limpet hemocyanin (KLH). The immunization treatment had no effect on bilateral adrenal weight or its ratio to body weight. Urinary aldosterone excretion was time-dependently increased during the 8-week observation period in the control group. Of note, the level of urinary aldosterone excretion in BMP-6-KLH-immunized rats was significantly reduced compared to that in the control group, suggesting that endogenous BMP-6 contributes to the induction of aldosterone production in vivo. Moreover, the level of urinary aldosterone/creatinine after 8-week treatment was significantly lowered by treatment with BMP-6-KLH. In contrast, with chronic Ang II treatment, urinary aldosterone and creatinine-corrected values at 8 weeks were not significantly different between the two groups, suggesting that the effects of BMP-6-KLH were impaired under the condition of chronic treatment with Ang II. The mRNA levels of Cyp11b2, but not those of Star, P450scc and 3βhsd2, were significantly decreased in adrenal tissues isolated from BMP-6-KLH-immunized rats after 8-week treatment. Furthermore, the ratio of plasma aldosterone level to corticosterone was significantly decreased by immunization with BMP-6-KLH. Collectively, the results indicate that endogenous BMP-6 is functionally linked to aldosterone synthesis by the zona glomerulosa in the adrenal cortex in vivo. |
doi_str_mv | 10.1016/j.jsbmb.2012.04.004 |
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Aldosterone is synthesized in the zona glomerulosa of the adrenal cortex. We previously reported the presence of a functional BMP system including BMP-6 in human adrenocortical cells. BMP-6 contributes to Ang II-induced aldosterone production by activating Smad signaling, in which endogenous BMP-6 action is negatively controlled by Ang II in vitro. In the present study, we examined the in vivo role of BMP-6 in regulation of aldosterone by neutralizing endogenous BMP-6 in rats treated with immunization against BMP-6. Three-week-old male rats were actively immunized with rat mature BMP-6 antigen conjugated with keyhole limpet hemocyanin (KLH). The immunization treatment had no effect on bilateral adrenal weight or its ratio to body weight. Urinary aldosterone excretion was time-dependently increased during the 8-week observation period in the control group. Of note, the level of urinary aldosterone excretion in BMP-6-KLH-immunized rats was significantly reduced compared to that in the control group, suggesting that endogenous BMP-6 contributes to the induction of aldosterone production in vivo. Moreover, the level of urinary aldosterone/creatinine after 8-week treatment was significantly lowered by treatment with BMP-6-KLH. In contrast, with chronic Ang II treatment, urinary aldosterone and creatinine-corrected values at 8 weeks were not significantly different between the two groups, suggesting that the effects of BMP-6-KLH were impaired under the condition of chronic treatment with Ang II. The mRNA levels of Cyp11b2, but not those of Star, P450scc and 3βhsd2, were significantly decreased in adrenal tissues isolated from BMP-6-KLH-immunized rats after 8-week treatment. Furthermore, the ratio of plasma aldosterone level to corticosterone was significantly decreased by immunization with BMP-6-KLH. Collectively, the results indicate that endogenous BMP-6 is functionally linked to aldosterone synthesis by the zona glomerulosa in the adrenal cortex in vivo.</description><identifier>ISSN: 0960-0760</identifier><identifier>EISSN: 1879-1220</identifier><identifier>DOI: 10.1016/j.jsbmb.2012.04.004</identifier><identifier>PMID: 22538126</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adrenal ; Adrenal Cortex - drug effects ; Adrenal Cortex - physiology ; Aldosterone ; Aldosterone - biosynthesis ; Aldosterone - blood ; Aldosterone - urine ; Angiotensin ; Angiotensin II - pharmacology ; Animals ; Antibodies - blood ; Antigens - immunology ; Bone morphogenetic protein ; Bone Morphogenetic Protein 6 - administration & dosage ; Bone Morphogenetic Protein 6 - immunology ; Corticosterone - blood ; CYP11B2 ; Cytochrome P-450 CYP11B2 - genetics ; Hemocyanins - administration & dosage ; Hemocyanins - immunology ; Immunization ; Male ; Organ Size - drug effects ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - metabolism</subject><ispartof>The Journal of steroid biochemistry and molecular biology, 2012-10, Vol.132 (1-2), p.8-14</ispartof><rights>2012 Elsevier Ltd</rights><rights>Copyright © 2012 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-a36343011c10d84620184f0d1e4ecc66f4250b86a691dc5cc02a372c7ea08d3d3</citedby><cites>FETCH-LOGICAL-c458t-a36343011c10d84620184f0d1e4ecc66f4250b86a691dc5cc02a372c7ea08d3d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22538126$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsumoto, Yoshinori</creatorcontrib><creatorcontrib>Otsuka, Fumio</creatorcontrib><creatorcontrib>Inagaki, Kenichi</creatorcontrib><creatorcontrib>Tsukamoto, Naoko</creatorcontrib><creatorcontrib>Takano-Narazaki, Mariko</creatorcontrib><creatorcontrib>Miyoshi, Tomoko</creatorcontrib><creatorcontrib>Nakamura, Eri</creatorcontrib><creatorcontrib>Ogura-Ochi, Kanako</creatorcontrib><creatorcontrib>Takeda, Masaya</creatorcontrib><creatorcontrib>Makino, Hirofumi</creatorcontrib><title>An in vivo role of bone morphogenetic protein-6 in aldosterone production by rat adrenal gland</title><title>The Journal of steroid biochemistry and molecular biology</title><addtitle>J Steroid Biochem Mol Biol</addtitle><description>► Neutralization of endogenous BMP-6 by immunization reduced aldosterone production in vivo. ► Chronic Ang II treatment impaired the neutralization effect of BMP-6. ► Adrenal CYP11B2 expression and plasma aldosterone/corticosterone were reduced by blocking BMP-6. ► Endogenous BMP-6 is linked to aldosterone synthesis in the adrenal.
Aldosterone is synthesized in the zona glomerulosa of the adrenal cortex. We previously reported the presence of a functional BMP system including BMP-6 in human adrenocortical cells. BMP-6 contributes to Ang II-induced aldosterone production by activating Smad signaling, in which endogenous BMP-6 action is negatively controlled by Ang II in vitro. In the present study, we examined the in vivo role of BMP-6 in regulation of aldosterone by neutralizing endogenous BMP-6 in rats treated with immunization against BMP-6. Three-week-old male rats were actively immunized with rat mature BMP-6 antigen conjugated with keyhole limpet hemocyanin (KLH). The immunization treatment had no effect on bilateral adrenal weight or its ratio to body weight. Urinary aldosterone excretion was time-dependently increased during the 8-week observation period in the control group. Of note, the level of urinary aldosterone excretion in BMP-6-KLH-immunized rats was significantly reduced compared to that in the control group, suggesting that endogenous BMP-6 contributes to the induction of aldosterone production in vivo. Moreover, the level of urinary aldosterone/creatinine after 8-week treatment was significantly lowered by treatment with BMP-6-KLH. In contrast, with chronic Ang II treatment, urinary aldosterone and creatinine-corrected values at 8 weeks were not significantly different between the two groups, suggesting that the effects of BMP-6-KLH were impaired under the condition of chronic treatment with Ang II. The mRNA levels of Cyp11b2, but not those of Star, P450scc and 3βhsd2, were significantly decreased in adrenal tissues isolated from BMP-6-KLH-immunized rats after 8-week treatment. Furthermore, the ratio of plasma aldosterone level to corticosterone was significantly decreased by immunization with BMP-6-KLH. Collectively, the results indicate that endogenous BMP-6 is functionally linked to aldosterone synthesis by the zona glomerulosa in the adrenal cortex in vivo.</description><subject>Adrenal</subject><subject>Adrenal Cortex - drug effects</subject><subject>Adrenal Cortex - physiology</subject><subject>Aldosterone</subject><subject>Aldosterone - biosynthesis</subject><subject>Aldosterone - blood</subject><subject>Aldosterone - urine</subject><subject>Angiotensin</subject><subject>Angiotensin II - pharmacology</subject><subject>Animals</subject><subject>Antibodies - blood</subject><subject>Antigens - immunology</subject><subject>Bone morphogenetic protein</subject><subject>Bone Morphogenetic Protein 6 - administration & dosage</subject><subject>Bone Morphogenetic Protein 6 - immunology</subject><subject>Corticosterone - blood</subject><subject>CYP11B2</subject><subject>Cytochrome P-450 CYP11B2 - genetics</subject><subject>Hemocyanins - administration & dosage</subject><subject>Hemocyanins - immunology</subject><subject>Immunization</subject><subject>Male</subject><subject>Organ Size - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - metabolism</subject><issn>0960-0760</issn><issn>1879-1220</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkUtP3DAUha2qqAy0v6BS5WU3CdePOMmiC4R4SUjdwBbLsW-oR4k92JmR-Pf1dIBlWd3F_c59nEPIdwY1A6bO1vU6D_NQc2C8BlkDyE9kxbq2rxjn8JmsoFdQQavgmJzkvAYAIVj7hRxz3oiOcbUij-eB-kB3fhdpihPSONIhBqRzTJs_8QkDLt7STYoL-lCpPWwmF_OCaY-VhtvaxcdAhxeazEKNSxjMRJ8mE9xXcjSaKeO313pKHq4u7y9uqrvf17cX53eVlU23VEYoIQUwZhm4TqryUidHcAwlWqvUKHkDQ6eM6pmzjbXAjWi5bdFA54QTp-TnYW6553mLedGzzxancgPGbdZM9H0PjZTqYxQEiAaKjQUVB9SmmHPCUW-Sn016KZDeZ6DX-l8Gep-BBqlLBkX143XBdpjRvWveTC_ArwOAxZGdx6Sz9RgsOp_QLtpF_98FfwFWeJfR</recordid><startdate>201210</startdate><enddate>201210</enddate><creator>Matsumoto, Yoshinori</creator><creator>Otsuka, Fumio</creator><creator>Inagaki, Kenichi</creator><creator>Tsukamoto, Naoko</creator><creator>Takano-Narazaki, Mariko</creator><creator>Miyoshi, Tomoko</creator><creator>Nakamura, Eri</creator><creator>Ogura-Ochi, Kanako</creator><creator>Takeda, Masaya</creator><creator>Makino, Hirofumi</creator><general>Elsevier Ltd</general><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><scope>7QP</scope></search><sort><creationdate>201210</creationdate><title>An in vivo role of bone morphogenetic protein-6 in aldosterone production by rat adrenal gland</title><author>Matsumoto, Yoshinori ; Otsuka, Fumio ; Inagaki, Kenichi ; Tsukamoto, Naoko ; Takano-Narazaki, Mariko ; Miyoshi, Tomoko ; Nakamura, Eri ; Ogura-Ochi, Kanako ; Takeda, Masaya ; Makino, Hirofumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-a36343011c10d84620184f0d1e4ecc66f4250b86a691dc5cc02a372c7ea08d3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adrenal</topic><topic>Adrenal Cortex - drug effects</topic><topic>Adrenal Cortex - physiology</topic><topic>Aldosterone</topic><topic>Aldosterone - biosynthesis</topic><topic>Aldosterone - blood</topic><topic>Aldosterone - urine</topic><topic>Angiotensin</topic><topic>Angiotensin II - pharmacology</topic><topic>Animals</topic><topic>Antibodies - blood</topic><topic>Antigens - immunology</topic><topic>Bone morphogenetic protein</topic><topic>Bone Morphogenetic Protein 6 - administration & dosage</topic><topic>Bone Morphogenetic Protein 6 - immunology</topic><topic>Corticosterone - blood</topic><topic>CYP11B2</topic><topic>Cytochrome P-450 CYP11B2 - genetics</topic><topic>Hemocyanins - administration & dosage</topic><topic>Hemocyanins - immunology</topic><topic>Immunization</topic><topic>Male</topic><topic>Organ Size - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsumoto, Yoshinori</creatorcontrib><creatorcontrib>Otsuka, Fumio</creatorcontrib><creatorcontrib>Inagaki, Kenichi</creatorcontrib><creatorcontrib>Tsukamoto, Naoko</creatorcontrib><creatorcontrib>Takano-Narazaki, Mariko</creatorcontrib><creatorcontrib>Miyoshi, Tomoko</creatorcontrib><creatorcontrib>Nakamura, Eri</creatorcontrib><creatorcontrib>Ogura-Ochi, Kanako</creatorcontrib><creatorcontrib>Takeda, Masaya</creatorcontrib><creatorcontrib>Makino, Hirofumi</creatorcontrib><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><collection>Calcium & Calcified Tissue Abstracts</collection><jtitle>The Journal of steroid biochemistry and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsumoto, Yoshinori</au><au>Otsuka, Fumio</au><au>Inagaki, Kenichi</au><au>Tsukamoto, Naoko</au><au>Takano-Narazaki, Mariko</au><au>Miyoshi, Tomoko</au><au>Nakamura, Eri</au><au>Ogura-Ochi, Kanako</au><au>Takeda, Masaya</au><au>Makino, Hirofumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An in vivo role of bone morphogenetic protein-6 in aldosterone production by rat adrenal gland</atitle><jtitle>The Journal of steroid biochemistry and molecular biology</jtitle><addtitle>J Steroid Biochem Mol Biol</addtitle><date>2012-10</date><risdate>2012</risdate><volume>132</volume><issue>1-2</issue><spage>8</spage><epage>14</epage><pages>8-14</pages><issn>0960-0760</issn><eissn>1879-1220</eissn><abstract>► Neutralization of endogenous BMP-6 by immunization reduced aldosterone production in vivo. ► Chronic Ang II treatment impaired the neutralization effect of BMP-6. ► Adrenal CYP11B2 expression and plasma aldosterone/corticosterone were reduced by blocking BMP-6. ► Endogenous BMP-6 is linked to aldosterone synthesis in the adrenal.
Aldosterone is synthesized in the zona glomerulosa of the adrenal cortex. We previously reported the presence of a functional BMP system including BMP-6 in human adrenocortical cells. BMP-6 contributes to Ang II-induced aldosterone production by activating Smad signaling, in which endogenous BMP-6 action is negatively controlled by Ang II in vitro. In the present study, we examined the in vivo role of BMP-6 in regulation of aldosterone by neutralizing endogenous BMP-6 in rats treated with immunization against BMP-6. Three-week-old male rats were actively immunized with rat mature BMP-6 antigen conjugated with keyhole limpet hemocyanin (KLH). The immunization treatment had no effect on bilateral adrenal weight or its ratio to body weight. Urinary aldosterone excretion was time-dependently increased during the 8-week observation period in the control group. Of note, the level of urinary aldosterone excretion in BMP-6-KLH-immunized rats was significantly reduced compared to that in the control group, suggesting that endogenous BMP-6 contributes to the induction of aldosterone production in vivo. Moreover, the level of urinary aldosterone/creatinine after 8-week treatment was significantly lowered by treatment with BMP-6-KLH. In contrast, with chronic Ang II treatment, urinary aldosterone and creatinine-corrected values at 8 weeks were not significantly different between the two groups, suggesting that the effects of BMP-6-KLH were impaired under the condition of chronic treatment with Ang II. The mRNA levels of Cyp11b2, but not those of Star, P450scc and 3βhsd2, were significantly decreased in adrenal tissues isolated from BMP-6-KLH-immunized rats after 8-week treatment. Furthermore, the ratio of plasma aldosterone level to corticosterone was significantly decreased by immunization with BMP-6-KLH. Collectively, the results indicate that endogenous BMP-6 is functionally linked to aldosterone synthesis by the zona glomerulosa in the adrenal cortex in vivo.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>22538126</pmid><doi>10.1016/j.jsbmb.2012.04.004</doi><tpages>7</tpages></addata></record> |
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subjects | Adrenal Adrenal Cortex - drug effects Adrenal Cortex - physiology Aldosterone Aldosterone - biosynthesis Aldosterone - blood Aldosterone - urine Angiotensin Angiotensin II - pharmacology Animals Antibodies - blood Antigens - immunology Bone morphogenetic protein Bone Morphogenetic Protein 6 - administration & dosage Bone Morphogenetic Protein 6 - immunology Corticosterone - blood CYP11B2 Cytochrome P-450 CYP11B2 - genetics Hemocyanins - administration & dosage Hemocyanins - immunology Immunization Male Organ Size - drug effects Rats Rats, Sprague-Dawley RNA, Messenger - metabolism |
title | An in vivo role of bone morphogenetic protein-6 in aldosterone production by rat adrenal gland |
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