Rat renal epinephrine synthesis
Rats that underwent adrenal demedullation had a 93% decrease in plasma epinephrine (E) levels, but did not decrease their renal E. Even further treatment with 6-hydroxydopamine and reserpine failed to lower renal E levels. Similarly, urine E levels failed to decrease after adrenal demedullation and...
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Veröffentlicht in: | The Journal of clinical investigation 1989-10, Vol.84 (4), p.1130-1133 |
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description | Rats that underwent adrenal demedullation had a 93% decrease in plasma epinephrine (E) levels, but did not decrease their renal E. Even further treatment with 6-hydroxydopamine and reserpine failed to lower renal E levels. Similarly, urine E levels failed to decrease after adrenal demedullation and renal denervation. There is a renal E-synthesizing enzyme that differs from adrenal phenylethanolamine-N-methyltransferase (PNMT) in that it is only weakly inhibited by SKF 29661 and can synthesize epinine from dopamine, while adrenal PNMT does so poorly. When an adrenalectomized rat received intravenous [3H]methionine, its urine contained radioactivity that appeared to be [3H]E, with small amounts of [3H]epinine. However, after [3H]methionine was infused in the renal artery, the major product in urine appeared to be [3H]epinine, with a small amount of [3H]E. Adrenal demedullation induced renal E synthesis, but denervation returned the rate of renal E synthesis to control values. The combination of adrenal demedullation, 6-hydroxydopamine, and reserpine treatments increased renal E-forming activity to 350% of control. We conclude that appreciable portions of renal and urinary E are synthesized in the kidney by an enzyme distinct from PNMT. The enzyme is induced by some treatments that lower E and NE levels. |
doi_str_mv | 10.1172/JCI114276 |
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G ; KENNEDY, B ; ELAYAN, H</creator><creatorcontrib>ZIEGLER, M. G ; KENNEDY, B ; ELAYAN, H</creatorcontrib><description>Rats that underwent adrenal demedullation had a 93% decrease in plasma epinephrine (E) levels, but did not decrease their renal E. Even further treatment with 6-hydroxydopamine and reserpine failed to lower renal E levels. Similarly, urine E levels failed to decrease after adrenal demedullation and renal denervation. There is a renal E-synthesizing enzyme that differs from adrenal phenylethanolamine-N-methyltransferase (PNMT) in that it is only weakly inhibited by SKF 29661 and can synthesize epinine from dopamine, while adrenal PNMT does so poorly. When an adrenalectomized rat received intravenous [3H]methionine, its urine contained radioactivity that appeared to be [3H]E, with small amounts of [3H]epinine. However, after [3H]methionine was infused in the renal artery, the major product in urine appeared to be [3H]epinine, with a small amount of [3H]E. Adrenal demedullation induced renal E synthesis, but denervation returned the rate of renal E synthesis to control values. The combination of adrenal demedullation, 6-hydroxydopamine, and reserpine treatments increased renal E-forming activity to 350% of control. We conclude that appreciable portions of renal and urinary E are synthesized in the kidney by an enzyme distinct from PNMT. The enzyme is induced by some treatments that lower E and NE levels.</description><identifier>ISSN: 0021-9738</identifier><identifier>EISSN: 1558-8238</identifier><identifier>DOI: 10.1172/JCI114276</identifier><identifier>PMID: 2794049</identifier><identifier>CODEN: JCINAO</identifier><language>eng</language><publisher>Ann Arbor, MI: American Society for Clinical Investigation</publisher><subject>Adrenal Glands - enzymology ; Animals ; Biological and medical sciences ; Catecholamines - blood ; Catecholamines - urine ; Denervation ; epinephrine ; Epinephrine - biosynthesis ; Epinephrine - blood ; Epinephrine - urine ; Fundamental and applied biological sciences. Psychology ; Kidney - innervation ; Kidney - metabolism ; Male ; Methyltransferases - metabolism ; Phenylethanolamine N-Methyltransferase - antagonists & inhibitors ; Phenylethanolamine N-Methyltransferase - metabolism ; Rats ; Rats, Inbred Strains ; Vertebrates: urinary system</subject><ispartof>The Journal of clinical investigation, 1989-10, Vol.84 (4), p.1130-1133</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c429t-bd3f1823756c7096e318bbd9006e0eff74a0114ef0165f1ef384e91ca3986b543</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC329769/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC329769/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6877662$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2794049$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ZIEGLER, M. G</creatorcontrib><creatorcontrib>KENNEDY, B</creatorcontrib><creatorcontrib>ELAYAN, H</creatorcontrib><title>Rat renal epinephrine synthesis</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>Rats that underwent adrenal demedullation had a 93% decrease in plasma epinephrine (E) levels, but did not decrease their renal E. Even further treatment with 6-hydroxydopamine and reserpine failed to lower renal E levels. Similarly, urine E levels failed to decrease after adrenal demedullation and renal denervation. There is a renal E-synthesizing enzyme that differs from adrenal phenylethanolamine-N-methyltransferase (PNMT) in that it is only weakly inhibited by SKF 29661 and can synthesize epinine from dopamine, while adrenal PNMT does so poorly. When an adrenalectomized rat received intravenous [3H]methionine, its urine contained radioactivity that appeared to be [3H]E, with small amounts of [3H]epinine. However, after [3H]methionine was infused in the renal artery, the major product in urine appeared to be [3H]epinine, with a small amount of [3H]E. Adrenal demedullation induced renal E synthesis, but denervation returned the rate of renal E synthesis to control values. The combination of adrenal demedullation, 6-hydroxydopamine, and reserpine treatments increased renal E-forming activity to 350% of control. We conclude that appreciable portions of renal and urinary E are synthesized in the kidney by an enzyme distinct from PNMT. The enzyme is induced by some treatments that lower E and NE levels.</description><subject>Adrenal Glands - enzymology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Catecholamines - blood</subject><subject>Catecholamines - urine</subject><subject>Denervation</subject><subject>epinephrine</subject><subject>Epinephrine - biosynthesis</subject><subject>Epinephrine - blood</subject><subject>Epinephrine - urine</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Kidney - innervation</subject><subject>Kidney - metabolism</subject><subject>Male</subject><subject>Methyltransferases - metabolism</subject><subject>Phenylethanolamine N-Methyltransferase - antagonists & inhibitors</subject><subject>Phenylethanolamine N-Methyltransferase - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Vertebrates: urinary system</subject><issn>0021-9738</issn><issn>1558-8238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLw0AUhQdRan0s_AFiFyK4iM77sXAhxUelIIiuh8n0jo2kSZxJhf57Iw1BV27uXZzv3Hs4CJ0QfEWIotdP0xkhnCq5g8ZECJ1pyvQuGmNMSWYU0_voIKUPjAnngo_QiCrDMTdjdPbi2kmEypUTaIoKmmXs5iRtqnYJqUhHaC-4MsFxvw_R2_3d6_Qxmz8_zKa388xzatosX7BAuqdKSK-wkcCIzvOFwVgChhAUd7hLCAETKQKBwDQHQ7xjRstccHaIbrZ3m3W-goWHqo2utE0sVi5ubO0K-1epiqV9r78so0ZJ0_kven-sP9eQWrsqkoeydBXU62SVoYwbyv8FieBKUCI78HIL-linFCEMYQi2P63bofWOPf2dfiD7mjv9vNdd8q4M0VW-SAMmtVJSUvYNIqKIVQ</recordid><startdate>19891001</startdate><enddate>19891001</enddate><creator>ZIEGLER, M. G</creator><creator>KENNEDY, B</creator><creator>ELAYAN, H</creator><general>American Society for Clinical Investigation</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>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19891001</creationdate><title>Rat renal epinephrine synthesis</title><author>ZIEGLER, M. G ; KENNEDY, B ; ELAYAN, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c429t-bd3f1823756c7096e318bbd9006e0eff74a0114ef0165f1ef384e91ca3986b543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adrenal Glands - enzymology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Catecholamines - blood</topic><topic>Catecholamines - urine</topic><topic>Denervation</topic><topic>epinephrine</topic><topic>Epinephrine - biosynthesis</topic><topic>Epinephrine - blood</topic><topic>Epinephrine - urine</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Kidney - innervation</topic><topic>Kidney - metabolism</topic><topic>Male</topic><topic>Methyltransferases - metabolism</topic><topic>Phenylethanolamine N-Methyltransferase - antagonists & inhibitors</topic><topic>Phenylethanolamine N-Methyltransferase - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Vertebrates: urinary system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ZIEGLER, M. G</creatorcontrib><creatorcontrib>KENNEDY, B</creatorcontrib><creatorcontrib>ELAYAN, H</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ZIEGLER, M. G</au><au>KENNEDY, B</au><au>ELAYAN, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rat renal epinephrine synthesis</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>1989-10-01</date><risdate>1989</risdate><volume>84</volume><issue>4</issue><spage>1130</spage><epage>1133</epage><pages>1130-1133</pages><issn>0021-9738</issn><eissn>1558-8238</eissn><coden>JCINAO</coden><abstract>Rats that underwent adrenal demedullation had a 93% decrease in plasma epinephrine (E) levels, but did not decrease their renal E. Even further treatment with 6-hydroxydopamine and reserpine failed to lower renal E levels. Similarly, urine E levels failed to decrease after adrenal demedullation and renal denervation. There is a renal E-synthesizing enzyme that differs from adrenal phenylethanolamine-N-methyltransferase (PNMT) in that it is only weakly inhibited by SKF 29661 and can synthesize epinine from dopamine, while adrenal PNMT does so poorly. When an adrenalectomized rat received intravenous [3H]methionine, its urine contained radioactivity that appeared to be [3H]E, with small amounts of [3H]epinine. However, after [3H]methionine was infused in the renal artery, the major product in urine appeared to be [3H]epinine, with a small amount of [3H]E. Adrenal demedullation induced renal E synthesis, but denervation returned the rate of renal E synthesis to control values. The combination of adrenal demedullation, 6-hydroxydopamine, and reserpine treatments increased renal E-forming activity to 350% of control. We conclude that appreciable portions of renal and urinary E are synthesized in the kidney by an enzyme distinct from PNMT. The enzyme is induced by some treatments that lower E and NE levels.</abstract><cop>Ann Arbor, MI</cop><pub>American Society for Clinical Investigation</pub><pmid>2794049</pmid><doi>10.1172/JCI114276</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adrenal Glands - enzymology Animals Biological and medical sciences Catecholamines - blood Catecholamines - urine Denervation epinephrine Epinephrine - biosynthesis Epinephrine - blood Epinephrine - urine Fundamental and applied biological sciences. Psychology Kidney - innervation Kidney - metabolism Male Methyltransferases - metabolism Phenylethanolamine N-Methyltransferase - antagonists & inhibitors Phenylethanolamine N-Methyltransferase - metabolism Rats Rats, Inbred Strains Vertebrates: urinary system |
title | Rat renal epinephrine synthesis |
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