PACAP is expressed in sympathoexcitatory bulbospinal C1 neurons of the brain stem and increases sympathetic nerve activity in vivo
Australian School of Advanced Medicine, Macquarie University, New South Wales, Australia Submitted 17 October 2007 ; accepted in final form 11 February 2008 Pituitary adenylate cyclase-activating polypeptide (PACAP) is an excitatory neuropeptide present in the rat brain stem. The extent of its local...
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creator | Farnham, Melissa M. J Li, Qun Goodchild, Ann K Pilowsky, Paul M |
description | Australian School of Advanced Medicine, Macquarie University, New South Wales, Australia
Submitted 17 October 2007
; accepted in final form 11 February 2008
Pituitary adenylate cyclase-activating polypeptide (PACAP) is an excitatory neuropeptide present in the rat brain stem. The extent of its localization within catecholaminergic groups and bulbospinal sympathoexcitatory neurons is not established. Using immunohistochemistry and in situ hybridization, we determined the extent of any colocalization with catecholaminergic and/or bulbospinal projections from the brain stem was determined. PACAP mRNA was found in tyrosine hydroxylase-immunoreactive (TH-ir) neurons in the C1-C3 cell groups. In the rostral ventrolateral medulla (RVLM), PACAP mRNA was found in 84% of the TH-ir neurons and 82% of bulbospinal TH-ir neurons. The functional significance of these PACAP mRNA positive bulbospinal neurons was tested by intrathecal administration of PACAP-38 in anaesthetized rats. Splanchnic sympathetic nerve activity doubled (110%) and heart rate rose significantly (19%), although blood pressure was unaffected. In addition, as previously reported, PACAP was found in the A1 cell group but not in the A5 cell group or in the locus coeruleus. The RVLM is the primary site responsible for the tonic and reflex control of blood pressure through the activity of bulbospinal presympathetic neurons, the majority of which contain TH. The results indicate 1 ) that pontomedullary neurons containing both TH and PACAP that project to the intermediolateral cell column originate from C1-C3 and not A5, and 2 ) intrathecal PACAP-38 causes a prolonged, sympathoexcitatory effect.
intrathecal; barodenervation; cholera toxin B; Sprague-Dawley
Address for reprint requests and other correspondence: P. M. Pilowsky, Australian School of Advanced Medicine, Dow Corning Bldg. Level 1, 3 Innovation Rd., Macquarie Univ., New South Wales 2109, Australia (e-mail: paul.pilowsky{at}vc.mq.edu.au ) |
doi_str_mv | 10.1152/ajpregu.00753.2007 |
format | Article |
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Submitted 17 October 2007
; accepted in final form 11 February 2008
Pituitary adenylate cyclase-activating polypeptide (PACAP) is an excitatory neuropeptide present in the rat brain stem. The extent of its localization within catecholaminergic groups and bulbospinal sympathoexcitatory neurons is not established. Using immunohistochemistry and in situ hybridization, we determined the extent of any colocalization with catecholaminergic and/or bulbospinal projections from the brain stem was determined. PACAP mRNA was found in tyrosine hydroxylase-immunoreactive (TH-ir) neurons in the C1-C3 cell groups. In the rostral ventrolateral medulla (RVLM), PACAP mRNA was found in 84% of the TH-ir neurons and 82% of bulbospinal TH-ir neurons. The functional significance of these PACAP mRNA positive bulbospinal neurons was tested by intrathecal administration of PACAP-38 in anaesthetized rats. Splanchnic sympathetic nerve activity doubled (110%) and heart rate rose significantly (19%), although blood pressure was unaffected. In addition, as previously reported, PACAP was found in the A1 cell group but not in the A5 cell group or in the locus coeruleus. The RVLM is the primary site responsible for the tonic and reflex control of blood pressure through the activity of bulbospinal presympathetic neurons, the majority of which contain TH. The results indicate 1 ) that pontomedullary neurons containing both TH and PACAP that project to the intermediolateral cell column originate from C1-C3 and not A5, and 2 ) intrathecal PACAP-38 causes a prolonged, sympathoexcitatory effect.
intrathecal; barodenervation; cholera toxin B; Sprague-Dawley
Address for reprint requests and other correspondence: P. M. Pilowsky, Australian School of Advanced Medicine, Dow Corning Bldg. Level 1, 3 Innovation Rd., Macquarie Univ., New South Wales 2109, Australia (e-mail: paul.pilowsky{at}vc.mq.edu.au )</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.00753.2007</identifier><identifier>PMID: 18272663</identifier><identifier>CODEN: AJPRDO</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Baroreflex ; Blood Pressure ; Brain ; Brain Stem - enzymology ; Brain Stem - metabolism ; Cardiovascular System - innervation ; Cholera ; Denervation ; Heart Rate ; Injections, Spinal ; Locus Coeruleus - metabolism ; Male ; Nerve Fibers, Myelinated - metabolism ; Nerve Fibers, Unmyelinated - enzymology ; Nerve Fibers, Unmyelinated - metabolism ; Neural Pathways - metabolism ; Neurons ; Peptides ; Pituitary Adenylate Cyclase-Activating Polypeptide - administration & dosage ; Pituitary Adenylate Cyclase-Activating Polypeptide - genetics ; Pituitary Adenylate Cyclase-Activating Polypeptide - metabolism ; Pituitary gland ; Rats ; Rats, Sprague-Dawley ; Ribonucleic acid ; RNA ; RNA, Messenger - metabolism ; Rodents ; Spinal Nerves - enzymology ; Spinal Nerves - metabolism ; Splanchnic Nerves - metabolism ; Sympathetic Nervous System - enzymology ; Sympathetic Nervous System - metabolism ; Time Factors ; Tyrosine 3-Monooxygenase - metabolism</subject><ispartof>American journal of physiology. Regulatory, integrative and comparative physiology, 2008-04, Vol.294 (4), p.R1304-R1311</ispartof><rights>Copyright American Physiological Society Apr 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c484t-6006fde5ccb81a64806a1951c277d8461ae1908efcfb36415acaffb8323bfb0f3</citedby><cites>FETCH-LOGICAL-c484t-6006fde5ccb81a64806a1951c277d8461ae1908efcfb36415acaffb8323bfb0f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18272663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Farnham, Melissa M. J</creatorcontrib><creatorcontrib>Li, Qun</creatorcontrib><creatorcontrib>Goodchild, Ann K</creatorcontrib><creatorcontrib>Pilowsky, Paul M</creatorcontrib><title>PACAP is expressed in sympathoexcitatory bulbospinal C1 neurons of the brain stem and increases sympathetic nerve activity in vivo</title><title>American journal of physiology. Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><description>Australian School of Advanced Medicine, Macquarie University, New South Wales, Australia
Submitted 17 October 2007
; accepted in final form 11 February 2008
Pituitary adenylate cyclase-activating polypeptide (PACAP) is an excitatory neuropeptide present in the rat brain stem. The extent of its localization within catecholaminergic groups and bulbospinal sympathoexcitatory neurons is not established. Using immunohistochemistry and in situ hybridization, we determined the extent of any colocalization with catecholaminergic and/or bulbospinal projections from the brain stem was determined. PACAP mRNA was found in tyrosine hydroxylase-immunoreactive (TH-ir) neurons in the C1-C3 cell groups. In the rostral ventrolateral medulla (RVLM), PACAP mRNA was found in 84% of the TH-ir neurons and 82% of bulbospinal TH-ir neurons. The functional significance of these PACAP mRNA positive bulbospinal neurons was tested by intrathecal administration of PACAP-38 in anaesthetized rats. Splanchnic sympathetic nerve activity doubled (110%) and heart rate rose significantly (19%), although blood pressure was unaffected. In addition, as previously reported, PACAP was found in the A1 cell group but not in the A5 cell group or in the locus coeruleus. The RVLM is the primary site responsible for the tonic and reflex control of blood pressure through the activity of bulbospinal presympathetic neurons, the majority of which contain TH. The results indicate 1 ) that pontomedullary neurons containing both TH and PACAP that project to the intermediolateral cell column originate from C1-C3 and not A5, and 2 ) intrathecal PACAP-38 causes a prolonged, sympathoexcitatory effect.
intrathecal; barodenervation; cholera toxin B; Sprague-Dawley
Address for reprint requests and other correspondence: P. M. Pilowsky, Australian School of Advanced Medicine, Dow Corning Bldg. Level 1, 3 Innovation Rd., Macquarie Univ., New South Wales 2109, Australia (e-mail: paul.pilowsky{at}vc.mq.edu.au )</description><subject>Animals</subject><subject>Baroreflex</subject><subject>Blood Pressure</subject><subject>Brain</subject><subject>Brain Stem - enzymology</subject><subject>Brain Stem - metabolism</subject><subject>Cardiovascular System - innervation</subject><subject>Cholera</subject><subject>Denervation</subject><subject>Heart Rate</subject><subject>Injections, Spinal</subject><subject>Locus Coeruleus - metabolism</subject><subject>Male</subject><subject>Nerve Fibers, Myelinated - metabolism</subject><subject>Nerve Fibers, Unmyelinated - enzymology</subject><subject>Nerve Fibers, Unmyelinated - metabolism</subject><subject>Neural Pathways - metabolism</subject><subject>Neurons</subject><subject>Peptides</subject><subject>Pituitary Adenylate Cyclase-Activating Polypeptide - administration & dosage</subject><subject>Pituitary Adenylate Cyclase-Activating Polypeptide - genetics</subject><subject>Pituitary Adenylate Cyclase-Activating Polypeptide - metabolism</subject><subject>Pituitary gland</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA, Messenger - metabolism</subject><subject>Rodents</subject><subject>Spinal Nerves - enzymology</subject><subject>Spinal Nerves - metabolism</subject><subject>Splanchnic Nerves - metabolism</subject><subject>Sympathetic Nervous System - enzymology</subject><subject>Sympathetic Nervous System - metabolism</subject><subject>Time Factors</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc2O0zAURiMEYjoDL8ACWSzYpfgvTsKuqpgBaSRGaFhbjnPduEriYDudZsuTk9BWICQW1l34nM---pLkDcFrQjL6Qe0HD7txjXGesTWdx7NkNV_QlPASP09WmAmWCkLKq-Q6hD3GmDPOXiZXpKA5FYKtkp8Pm-3mAdmA4DinhQA1sj0KUzeo2Dg4ahtVdH5C1dhWLgy2Vy3aEtTD6F0fkDMoNoAqrxYtQodUv0RoDypAuCRBtHp2_AGQ0tEebJyWdw724F4lL4xqA7w-z5vk--2nx-3n9P7r3Zft5j7VvOAxFRgLU0OmdVUQJXiBhSJlRjTN87rggiggJS7AaFMxwUmmtDKmKhhllamwYTfJ-1Pu4N2PEUKUnQ0a2lb14MYgc8x5KXg2g-_-Afdu9PPeQVJa5vPBeIboCdLeheDByMHbTvlJEiyXeuS5Hvm7HrnUM0tvz8lj1UH9Rzn3MQMfT0Bjd82T9SCHZgrWtW43yduxbR_hGC_JtOSSy2-EYS6Hellw_X_58pu_JPYL5XS1DQ</recordid><startdate>20080401</startdate><enddate>20080401</enddate><creator>Farnham, Melissa M. J</creator><creator>Li, Qun</creator><creator>Goodchild, Ann K</creator><creator>Pilowsky, Paul M</creator><general>American Physiological Society</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>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20080401</creationdate><title>PACAP is expressed in sympathoexcitatory bulbospinal C1 neurons of the brain stem and increases sympathetic nerve activity in vivo</title><author>Farnham, Melissa M. J ; Li, Qun ; Goodchild, Ann K ; Pilowsky, Paul M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c484t-6006fde5ccb81a64806a1951c277d8461ae1908efcfb36415acaffb8323bfb0f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Baroreflex</topic><topic>Blood Pressure</topic><topic>Brain</topic><topic>Brain Stem - enzymology</topic><topic>Brain Stem - metabolism</topic><topic>Cardiovascular System - innervation</topic><topic>Cholera</topic><topic>Denervation</topic><topic>Heart Rate</topic><topic>Injections, Spinal</topic><topic>Locus Coeruleus - metabolism</topic><topic>Male</topic><topic>Nerve Fibers, Myelinated - metabolism</topic><topic>Nerve Fibers, Unmyelinated - enzymology</topic><topic>Nerve Fibers, Unmyelinated - metabolism</topic><topic>Neural Pathways - metabolism</topic><topic>Neurons</topic><topic>Peptides</topic><topic>Pituitary Adenylate Cyclase-Activating Polypeptide - administration & dosage</topic><topic>Pituitary Adenylate Cyclase-Activating Polypeptide - genetics</topic><topic>Pituitary Adenylate Cyclase-Activating Polypeptide - metabolism</topic><topic>Pituitary gland</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA, Messenger - metabolism</topic><topic>Rodents</topic><topic>Spinal Nerves - enzymology</topic><topic>Spinal Nerves - metabolism</topic><topic>Splanchnic Nerves - metabolism</topic><topic>Sympathetic Nervous System - enzymology</topic><topic>Sympathetic Nervous System - metabolism</topic><topic>Time Factors</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Farnham, Melissa M. J</creatorcontrib><creatorcontrib>Li, Qun</creatorcontrib><creatorcontrib>Goodchild, Ann K</creatorcontrib><creatorcontrib>Pilowsky, Paul M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Farnham, Melissa M. J</au><au>Li, Qun</au><au>Goodchild, Ann K</au><au>Pilowsky, Paul M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PACAP is expressed in sympathoexcitatory bulbospinal C1 neurons of the brain stem and increases sympathetic nerve activity in vivo</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2008-04-01</date><risdate>2008</risdate><volume>294</volume><issue>4</issue><spage>R1304</spage><epage>R1311</epage><pages>R1304-R1311</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><coden>AJPRDO</coden><abstract>Australian School of Advanced Medicine, Macquarie University, New South Wales, Australia
Submitted 17 October 2007
; accepted in final form 11 February 2008
Pituitary adenylate cyclase-activating polypeptide (PACAP) is an excitatory neuropeptide present in the rat brain stem. The extent of its localization within catecholaminergic groups and bulbospinal sympathoexcitatory neurons is not established. Using immunohistochemistry and in situ hybridization, we determined the extent of any colocalization with catecholaminergic and/or bulbospinal projections from the brain stem was determined. PACAP mRNA was found in tyrosine hydroxylase-immunoreactive (TH-ir) neurons in the C1-C3 cell groups. In the rostral ventrolateral medulla (RVLM), PACAP mRNA was found in 84% of the TH-ir neurons and 82% of bulbospinal TH-ir neurons. The functional significance of these PACAP mRNA positive bulbospinal neurons was tested by intrathecal administration of PACAP-38 in anaesthetized rats. Splanchnic sympathetic nerve activity doubled (110%) and heart rate rose significantly (19%), although blood pressure was unaffected. In addition, as previously reported, PACAP was found in the A1 cell group but not in the A5 cell group or in the locus coeruleus. The RVLM is the primary site responsible for the tonic and reflex control of blood pressure through the activity of bulbospinal presympathetic neurons, the majority of which contain TH. The results indicate 1 ) that pontomedullary neurons containing both TH and PACAP that project to the intermediolateral cell column originate from C1-C3 and not A5, and 2 ) intrathecal PACAP-38 causes a prolonged, sympathoexcitatory effect.
intrathecal; barodenervation; cholera toxin B; Sprague-Dawley
Address for reprint requests and other correspondence: P. M. Pilowsky, Australian School of Advanced Medicine, Dow Corning Bldg. Level 1, 3 Innovation Rd., Macquarie Univ., New South Wales 2109, Australia (e-mail: paul.pilowsky{at}vc.mq.edu.au )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>18272663</pmid><doi>10.1152/ajpregu.00753.2007</doi></addata></record> |
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language | eng |
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source | MEDLINE; American Physiological Society Paid; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Baroreflex Blood Pressure Brain Brain Stem - enzymology Brain Stem - metabolism Cardiovascular System - innervation Cholera Denervation Heart Rate Injections, Spinal Locus Coeruleus - metabolism Male Nerve Fibers, Myelinated - metabolism Nerve Fibers, Unmyelinated - enzymology Nerve Fibers, Unmyelinated - metabolism Neural Pathways - metabolism Neurons Peptides Pituitary Adenylate Cyclase-Activating Polypeptide - administration & dosage Pituitary Adenylate Cyclase-Activating Polypeptide - genetics Pituitary Adenylate Cyclase-Activating Polypeptide - metabolism Pituitary gland Rats Rats, Sprague-Dawley Ribonucleic acid RNA RNA, Messenger - metabolism Rodents Spinal Nerves - enzymology Spinal Nerves - metabolism Splanchnic Nerves - metabolism Sympathetic Nervous System - enzymology Sympathetic Nervous System - metabolism Time Factors Tyrosine 3-Monooxygenase - metabolism |
title | PACAP is expressed in sympathoexcitatory bulbospinal C1 neurons of the brain stem and increases sympathetic nerve activity in vivo |
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