Adrenal adrenaline- and noradrenaline-containing cells and celiac sympathetic ganglia are differentially controlled by centrally administered corticotropin-releasing factor and arginine–vasopressin in rats

The adrenal glands and sympathetic celiac ganglia are innervated mainly by the greater splanchnic nerves, which contain preganglionic sympathetic nerves that originated from the thoracic spinal cord. The adrenal medulla has two separate populations of chromaffin cells, adrenaline-containing cells (A...

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Veröffentlicht in:European journal of pharmacology 2007-06, Vol.564 (1-3), p.94-102
Hauptverfasser: Yamaguchi-Shima, Naoko, Okada, Shoshiro, Shimizu, Takahiro, Usui, Daisuke, Nakamura, Kumiko, Lu, Lianyi, Yokotani, Kunihiko
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container_end_page 102
container_issue 1-3
container_start_page 94
container_title European journal of pharmacology
container_volume 564
creator Yamaguchi-Shima, Naoko
Okada, Shoshiro
Shimizu, Takahiro
Usui, Daisuke
Nakamura, Kumiko
Lu, Lianyi
Yokotani, Kunihiko
description The adrenal glands and sympathetic celiac ganglia are innervated mainly by the greater splanchnic nerves, which contain preganglionic sympathetic nerves that originated from the thoracic spinal cord. The adrenal medulla has two separate populations of chromaffin cells, adrenaline-containing cells (A-cells) and noradrenaline-containing cells (NA-cells), which have been shown to be differentially innervated by separate groups of the preganglionic sympathetic neurons. The present study was designed to characterize the centrally activating mechanisms of the adrenal A-cells, NA-cells and celiac sympathetic ganglia with expression of cFos (a marker for neural excitation), in regard to the brain prostanoids, in anesthetized rats. Intracerebroventricularly (i.c.v.) administered corticotropin-releasing factor (CRF) induced cFos expression in the adrenal A-cells, but not NA-cells, and celiac ganglia. On the other hand, i.c.v. administered arginine–vasopressin (AVP) resulted in cFos induction in both A-cells and NA-cells in the adrenal medulla, but not in the celiac ganglia. Intracerebroventricular pretreatment with indomethacin (an inhibitor of cyclooxygenase) abolished the CRF- and AVP-induced cFos expression in all regions described above. On the other hand, intracerebroventricular pretreatment with furegrelate (an inhibitor of thromboxane A2 synthase) abolished the CRF-induced cFos expression in the adrenal A-cells, but not in the celiac ganglia, and also abolished the AVP-induced cFos expression in both A-cells and NA-cells in the adrenal medulla. These results suggest that centrally administered CRF activates adrenal A-cells and celiac sympathetic ganglia by brain thromboxane A2-mediated and other prostanoid than thromboxane A2 (probably prostaglandin E2)-mediated mechanisms, respectively. On the other hand, centrally administered AVP activates adrenal A-cells and NA-cells by brain thromboxane A2-mediated mechanisms in rats.
doi_str_mv 10.1016/j.ejphar.2007.02.021
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The adrenal medulla has two separate populations of chromaffin cells, adrenaline-containing cells (A-cells) and noradrenaline-containing cells (NA-cells), which have been shown to be differentially innervated by separate groups of the preganglionic sympathetic neurons. The present study was designed to characterize the centrally activating mechanisms of the adrenal A-cells, NA-cells and celiac sympathetic ganglia with expression of cFos (a marker for neural excitation), in regard to the brain prostanoids, in anesthetized rats. Intracerebroventricularly (i.c.v.) administered corticotropin-releasing factor (CRF) induced cFos expression in the adrenal A-cells, but not NA-cells, and celiac ganglia. On the other hand, i.c.v. administered arginine–vasopressin (AVP) resulted in cFos induction in both A-cells and NA-cells in the adrenal medulla, but not in the celiac ganglia. Intracerebroventricular pretreatment with indomethacin (an inhibitor of cyclooxygenase) abolished the CRF- and AVP-induced cFos expression in all regions described above. On the other hand, intracerebroventricular pretreatment with furegrelate (an inhibitor of thromboxane A2 synthase) abolished the CRF-induced cFos expression in the adrenal A-cells, but not in the celiac ganglia, and also abolished the AVP-induced cFos expression in both A-cells and NA-cells in the adrenal medulla. These results suggest that centrally administered CRF activates adrenal A-cells and celiac sympathetic ganglia by brain thromboxane A2-mediated and other prostanoid than thromboxane A2 (probably prostaglandin E2)-mediated mechanisms, respectively. 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The adrenal medulla has two separate populations of chromaffin cells, adrenaline-containing cells (A-cells) and noradrenaline-containing cells (NA-cells), which have been shown to be differentially innervated by separate groups of the preganglionic sympathetic neurons. The present study was designed to characterize the centrally activating mechanisms of the adrenal A-cells, NA-cells and celiac sympathetic ganglia with expression of cFos (a marker for neural excitation), in regard to the brain prostanoids, in anesthetized rats. Intracerebroventricularly (i.c.v.) administered corticotropin-releasing factor (CRF) induced cFos expression in the adrenal A-cells, but not NA-cells, and celiac ganglia. On the other hand, i.c.v. administered arginine–vasopressin (AVP) resulted in cFos induction in both A-cells and NA-cells in the adrenal medulla, but not in the celiac ganglia. Intracerebroventricular pretreatment with indomethacin (an inhibitor of cyclooxygenase) abolished the CRF- and AVP-induced cFos expression in all regions described above. On the other hand, intracerebroventricular pretreatment with furegrelate (an inhibitor of thromboxane A2 synthase) abolished the CRF-induced cFos expression in the adrenal A-cells, but not in the celiac ganglia, and also abolished the AVP-induced cFos expression in both A-cells and NA-cells in the adrenal medulla. These results suggest that centrally administered CRF activates adrenal A-cells and celiac sympathetic ganglia by brain thromboxane A2-mediated and other prostanoid than thromboxane A2 (probably prostaglandin E2)-mediated mechanisms, respectively. 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Drug treatments</subject><subject>Photomicrography</subject><subject>Prostaglandins - metabolism</subject><subject>Prostaglandins - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Thromboxane A2 - metabolism</subject><subject>Thromboxane A2 - physiology</subject><issn>0014-2999</issn><issn>1879-0712</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc-KFDEQxhtR3HH1DURy0VuPlfTfXIRlcVdhwYueQ3W6ejZDOmmTnoW57Tv4YL6DT2J6emA9CQWVfPzqq6Iqy95y2HLg9cf9lvbTPYatAGi2IFLwZ9mGt43MoeHiebYB4GUupJQX2asY9wBQSVG9zC54U1RQ82qT_b7qAzm0DNdsHOUMXc-cD_9I2rsZjTNuxzRZG09IehnULB7HCed7mo1mO3S7JDIMxHozDJQcZoPWHtliEby11LMu_ZIeTjr2YzKOc0KTpQ_JxidwMi4PZAnj0nRAPftw6ophtwxCfx5_PWD0U6CYEJYi4BxfZy8GtJHenPNl9uPm8_frL_ndt9uv11d3ua7Kes4JZMe7oSTeFT0RaCkrWYqKF1xwKXooQeoK9CBbuaytqLuW16Uoy2GAAkRxmX1Yfafgfx4ozmo0cVkNOvKHqBqooOInsFxBHXyMgQY1BTNiOCoOajmk2qv1kGo5pAKRgqeyd2f_QzdS_1R0vlwC3p8BjBrtENBpE5-4tinboi4S92nlKG3jwVBQURtymnoTSM-q9-b_k_wFCSzEmw</recordid><startdate>20070614</startdate><enddate>20070614</enddate><creator>Yamaguchi-Shima, Naoko</creator><creator>Okada, Shoshiro</creator><creator>Shimizu, Takahiro</creator><creator>Usui, Daisuke</creator><creator>Nakamura, Kumiko</creator><creator>Lu, Lianyi</creator><creator>Yokotani, Kunihiko</creator><general>Elsevier B.V</general><general>Elsevier</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>20070614</creationdate><title>Adrenal adrenaline- and noradrenaline-containing cells and celiac sympathetic ganglia are differentially controlled by centrally administered corticotropin-releasing factor and arginine–vasopressin in rats</title><author>Yamaguchi-Shima, Naoko ; Okada, Shoshiro ; Shimizu, Takahiro ; Usui, Daisuke ; Nakamura, Kumiko ; Lu, Lianyi ; Yokotani, Kunihiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c546t-e09b1bf4e1b3dee0c99594251312192d0409c50cf989000536b8164244ff03023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adrenal Medulla - drug effects</topic><topic>Adrenal Medulla - innervation</topic><topic>Adrenal Medulla - metabolism</topic><topic>Animals</topic><topic>Arachidonic Acid - metabolism</topic><topic>Arachidonic Acid - physiology</topic><topic>Arginine Vasopressin - pharmacology</topic><topic>Benzofurans - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Brain - cytology</topic><topic>Brain - metabolism</topic><topic>Brain arachidonic acid cascade</topic><topic>Brain thromboxane A2</topic><topic>Central sympatho-adrenomedullary outflow</topic><topic>cFos expression</topic><topic>Corticotropin-Releasing Hormone - pharmacology</topic><topic>Epinephrine - metabolism</topic><topic>Ganglia, Sympathetic - drug effects</topic><topic>Ganglia, Sympathetic - metabolism</topic><topic>Gene Expression</topic><topic>Genes, fos - drug effects</topic><topic>Indomethacin - pharmacology</topic><topic>Injections, Intraventricular</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Norepinephrine - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>Photomicrography</topic><topic>Prostaglandins - metabolism</topic><topic>Prostaglandins - physiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Thromboxane A2 - metabolism</topic><topic>Thromboxane A2 - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamaguchi-Shima, Naoko</creatorcontrib><creatorcontrib>Okada, Shoshiro</creatorcontrib><creatorcontrib>Shimizu, Takahiro</creatorcontrib><creatorcontrib>Usui, Daisuke</creatorcontrib><creatorcontrib>Nakamura, Kumiko</creatorcontrib><creatorcontrib>Lu, Lianyi</creatorcontrib><creatorcontrib>Yokotani, Kunihiko</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>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamaguchi-Shima, Naoko</au><au>Okada, Shoshiro</au><au>Shimizu, Takahiro</au><au>Usui, Daisuke</au><au>Nakamura, Kumiko</au><au>Lu, Lianyi</au><au>Yokotani, Kunihiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adrenal adrenaline- and noradrenaline-containing cells and celiac sympathetic ganglia are differentially controlled by centrally administered corticotropin-releasing factor and arginine–vasopressin in rats</atitle><jtitle>European journal of pharmacology</jtitle><addtitle>Eur J Pharmacol</addtitle><date>2007-06-14</date><risdate>2007</risdate><volume>564</volume><issue>1-3</issue><spage>94</spage><epage>102</epage><pages>94-102</pages><issn>0014-2999</issn><eissn>1879-0712</eissn><coden>EJPHAZ</coden><abstract>The adrenal glands and sympathetic celiac ganglia are innervated mainly by the greater splanchnic nerves, which contain preganglionic sympathetic nerves that originated from the thoracic spinal cord. The adrenal medulla has two separate populations of chromaffin cells, adrenaline-containing cells (A-cells) and noradrenaline-containing cells (NA-cells), which have been shown to be differentially innervated by separate groups of the preganglionic sympathetic neurons. The present study was designed to characterize the centrally activating mechanisms of the adrenal A-cells, NA-cells and celiac sympathetic ganglia with expression of cFos (a marker for neural excitation), in regard to the brain prostanoids, in anesthetized rats. Intracerebroventricularly (i.c.v.) administered corticotropin-releasing factor (CRF) induced cFos expression in the adrenal A-cells, but not NA-cells, and celiac ganglia. On the other hand, i.c.v. administered arginine–vasopressin (AVP) resulted in cFos induction in both A-cells and NA-cells in the adrenal medulla, but not in the celiac ganglia. Intracerebroventricular pretreatment with indomethacin (an inhibitor of cyclooxygenase) abolished the CRF- and AVP-induced cFos expression in all regions described above. On the other hand, intracerebroventricular pretreatment with furegrelate (an inhibitor of thromboxane A2 synthase) abolished the CRF-induced cFos expression in the adrenal A-cells, but not in the celiac ganglia, and also abolished the AVP-induced cFos expression in both A-cells and NA-cells in the adrenal medulla. These results suggest that centrally administered CRF activates adrenal A-cells and celiac sympathetic ganglia by brain thromboxane A2-mediated and other prostanoid than thromboxane A2 (probably prostaglandin E2)-mediated mechanisms, respectively. On the other hand, centrally administered AVP activates adrenal A-cells and NA-cells by brain thromboxane A2-mediated mechanisms in rats.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>17350615</pmid><doi>10.1016/j.ejphar.2007.02.021</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adrenal Medulla - drug effects
Adrenal Medulla - innervation
Adrenal Medulla - metabolism
Animals
Arachidonic Acid - metabolism
Arachidonic Acid - physiology
Arginine Vasopressin - pharmacology
Benzofurans - pharmacology
Biological and medical sciences
Brain - cytology
Brain - metabolism
Brain arachidonic acid cascade
Brain thromboxane A2
Central sympatho-adrenomedullary outflow
cFos expression
Corticotropin-Releasing Hormone - pharmacology
Epinephrine - metabolism
Ganglia, Sympathetic - drug effects
Ganglia, Sympathetic - metabolism
Gene Expression
Genes, fos - drug effects
Indomethacin - pharmacology
Injections, Intraventricular
Male
Medical sciences
Norepinephrine - metabolism
Pharmacology. Drug treatments
Photomicrography
Prostaglandins - metabolism
Prostaglandins - physiology
Rats
Rats, Wistar
Thromboxane A2 - metabolism
Thromboxane A2 - physiology
title Adrenal adrenaline- and noradrenaline-containing cells and celiac sympathetic ganglia are differentially controlled by centrally administered corticotropin-releasing factor and arginine–vasopressin in rats
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