Development of neuropeptide Y-containing neurons in sympathetic ganglia of rats

Abstract Expression of neuropeptide Y (NPY) in the sympathetic ganglia was investigated by immunohistochemistry and tract tracing. The distribution of NPY immunoreactivity (IR) was studied in the superior cervical ganglion (SCG), stellate ganglion (SG) and celiac ganglion (CG) from rats of different...

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Veröffentlicht in:Neuropeptides (Edinburgh) 2012-12, Vol.46 (6), p.345-352
Hauptverfasser: Masliukov, Petr M, Konovalov, Vladimir V, Emanuilov, Andrey I, Nozdrachev, Alexandr D
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container_end_page 352
container_issue 6
container_start_page 345
container_title Neuropeptides (Edinburgh)
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creator Masliukov, Petr M
Konovalov, Vladimir V
Emanuilov, Andrey I
Nozdrachev, Alexandr D
description Abstract Expression of neuropeptide Y (NPY) in the sympathetic ganglia was investigated by immunohistochemistry and tract tracing. The distribution of NPY immunoreactivity (IR) was studied in the superior cervical ganglion (SCG), stellate ganglion (SG) and celiac ganglion (CG) from rats of different ages (newborn, 10-day-old, 20-day-old, 30-day-old, 2-month-old, 6-month-old, 24-month-old). We observed that the percentage of NPY-IR neuronal profiles increased during early postnatal development. In the SCG and SG, the percentage of NPY-IR profiles enlarged in the first month of life from 43 ± 3.6% (SCG) and 46 ± 3.8% (SG) until 64 ± 4.1% (SCG) and 58 ± 3.5% (SG). The percentage of NPY-IR profiles in the CG increased during the period between 20 days (65 ± 3.8%) and 30 days (82 ± 5.1%) of animals’ life and did not change in further development. In newborn and 10-day-old rats, a large portion of NPY-IR neurons was also calbindin D28K (CB)-IR in all sympathetic ganglia. The proportion of CB-IR substantially decreased during next 10 days in the SCG, SG and CG. NPY-IR was approximately present in a half of the postganglionic neurons innervating muscle vessels of the neck and forearm, and the percentage of labeled NPY-IR profiles did not change during the development. Only single Ki67-IR neurons were also NPY-IR in the SCG, SG and CG in newborns and not in older animals. No NPY+/caspase 3 + IR neurons were observed. Finally, the process of morphological changes in the size and percentages of NPY-IR profiles is complete in rats by the first month of life.
doi_str_mv 10.1016/j.npep.2012.08.003
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The distribution of NPY immunoreactivity (IR) was studied in the superior cervical ganglion (SCG), stellate ganglion (SG) and celiac ganglion (CG) from rats of different ages (newborn, 10-day-old, 20-day-old, 30-day-old, 2-month-old, 6-month-old, 24-month-old). We observed that the percentage of NPY-IR neuronal profiles increased during early postnatal development. In the SCG and SG, the percentage of NPY-IR profiles enlarged in the first month of life from 43 ± 3.6% (SCG) and 46 ± 3.8% (SG) until 64 ± 4.1% (SCG) and 58 ± 3.5% (SG). The percentage of NPY-IR profiles in the CG increased during the period between 20 days (65 ± 3.8%) and 30 days (82 ± 5.1%) of animals’ life and did not change in further development. In newborn and 10-day-old rats, a large portion of NPY-IR neurons was also calbindin D28K (CB)-IR in all sympathetic ganglia. The proportion of CB-IR substantially decreased during next 10 days in the SCG, SG and CG. NPY-IR was approximately present in a half of the postganglionic neurons innervating muscle vessels of the neck and forearm, and the percentage of labeled NPY-IR profiles did not change during the development. Only single Ki67-IR neurons were also NPY-IR in the SCG, SG and CG in newborns and not in older animals. No NPY+/caspase 3 + IR neurons were observed. 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NPY-IR was approximately present in a half of the postganglionic neurons innervating muscle vessels of the neck and forearm, and the percentage of labeled NPY-IR profiles did not change during the development. Only single Ki67-IR neurons were also NPY-IR in the SCG, SG and CG in newborns and not in older animals. No NPY+/caspase 3 + IR neurons were observed. 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development</subject><subject>Stellate Ganglion - metabolism</subject><subject>superior cervical ganglion</subject><subject>Superior Cervical Ganglion - cytology</subject><subject>Superior Cervical Ganglion - growth &amp; development</subject><subject>Superior Cervical Ganglion - metabolism</subject><subject>Sympathetic ganglia</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><issn>0143-4179</issn><issn>1532-2785</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU2P1SAYhYnRONfRP-DCdOmmFV5ooYkxMTN-JZPMQl24Ilz69sq1hQp0kvvvpbmjCxfGFQvOcwLPIeQ5ow2jrHt1bPyCSwOUQUNVQyl_QHas5VCDVO1DsqNM8Fow2V-QJykdKaUClHpMLgD6TvCO78jtNd7hFJYZfa7CWHlcYyit2Q1Yfatt8Nk47_zhfONT5XyVTvNi8nfMzlYH4w-TMxsbTU5PyaPRTAmf3Z-X5Ov7d1-uPtY3tx8-Xb29qa0QItfQwtAPXPZCGdNx00K3V3LcY2dEedqgbMsYw5EpDlKCkXKUrGctUGg7LhS_JC_PvUsMP1dMWc8uWZwm4zGsSTOQIDktLf8RBco7KaUoUThHbQwpRRz1Et1s4kkzqjfn-qg353pzrqnSxXmBXtz3r_sZhz_Ib8kl8PocwCLkzmHUyTr0FgcX0WY9BPfv_jd_4XYqk1gz_cATpmNYoy-qNdOpMPrztvo2OoMyePkW_wWwAKXZ</recordid><startdate>20121201</startdate><enddate>20121201</enddate><creator>Masliukov, Petr M</creator><creator>Konovalov, Vladimir V</creator><creator>Emanuilov, Andrey I</creator><creator>Nozdrachev, Alexandr D</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>7TK</scope></search><sort><creationdate>20121201</creationdate><title>Development of neuropeptide Y-containing neurons in sympathetic ganglia of rats</title><author>Masliukov, Petr M ; Konovalov, Vladimir V ; Emanuilov, Andrey I ; Nozdrachev, Alexandr D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-252d9d37948aa63a526b87fbe6a4964d8c5111ef1832772a77f71915202563483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Advanced Basic Science</topic><topic>Age</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Autonomic nervous system</topic><topic>Calbindin-D28K</topic><topic>Caspase 3 - metabolism</topic><topic>Caspase-3</topic><topic>celiac ganglion</topic><topic>Choline O-Acetyltransferase - metabolism</topic><topic>Endocrinology &amp; Metabolism</topic><topic>Forearm</topic><topic>Ganglia, Sympathetic - cytology</topic><topic>Ganglia, Sympathetic - growth &amp; development</topic><topic>Ganglia, Sympathetic - metabolism</topic><topic>Immunohistochemistry</topic><topic>Ki-67 Antigen - metabolism</topic><topic>Muscles</topic><topic>Neck</topic><topic>Neonates</topic><topic>Neurons</topic><topic>Neurons - cytology</topic><topic>Neurons - physiology</topic><topic>Neuropeptide Y</topic><topic>Neuropeptide Y - metabolism</topic><topic>Neuropeptide Y - physiology</topic><topic>Nitric Oxide Synthase - metabolism</topic><topic>Postnatal ontogenesis</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Somatostatin - metabolism</topic><topic>stellate ganglion</topic><topic>Stellate Ganglion - cytology</topic><topic>Stellate Ganglion - growth &amp; development</topic><topic>Stellate Ganglion - metabolism</topic><topic>superior cervical ganglion</topic><topic>Superior Cervical Ganglion - cytology</topic><topic>Superior Cervical Ganglion - growth &amp; development</topic><topic>Superior Cervical Ganglion - metabolism</topic><topic>Sympathetic ganglia</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Masliukov, Petr M</creatorcontrib><creatorcontrib>Konovalov, Vladimir V</creatorcontrib><creatorcontrib>Emanuilov, Andrey I</creatorcontrib><creatorcontrib>Nozdrachev, Alexandr D</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>Neurosciences Abstracts</collection><jtitle>Neuropeptides (Edinburgh)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Masliukov, Petr M</au><au>Konovalov, Vladimir V</au><au>Emanuilov, Andrey I</au><au>Nozdrachev, Alexandr D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of neuropeptide Y-containing neurons in sympathetic ganglia of rats</atitle><jtitle>Neuropeptides (Edinburgh)</jtitle><addtitle>Neuropeptides</addtitle><date>2012-12-01</date><risdate>2012</risdate><volume>46</volume><issue>6</issue><spage>345</spage><epage>352</epage><pages>345-352</pages><issn>0143-4179</issn><eissn>1532-2785</eissn><abstract>Abstract Expression of neuropeptide Y (NPY) in the sympathetic ganglia was investigated by immunohistochemistry and tract tracing. The distribution of NPY immunoreactivity (IR) was studied in the superior cervical ganglion (SCG), stellate ganglion (SG) and celiac ganglion (CG) from rats of different ages (newborn, 10-day-old, 20-day-old, 30-day-old, 2-month-old, 6-month-old, 24-month-old). We observed that the percentage of NPY-IR neuronal profiles increased during early postnatal development. In the SCG and SG, the percentage of NPY-IR profiles enlarged in the first month of life from 43 ± 3.6% (SCG) and 46 ± 3.8% (SG) until 64 ± 4.1% (SCG) and 58 ± 3.5% (SG). The percentage of NPY-IR profiles in the CG increased during the period between 20 days (65 ± 3.8%) and 30 days (82 ± 5.1%) of animals’ life and did not change in further development. In newborn and 10-day-old rats, a large portion of NPY-IR neurons was also calbindin D28K (CB)-IR in all sympathetic ganglia. The proportion of CB-IR substantially decreased during next 10 days in the SCG, SG and CG. NPY-IR was approximately present in a half of the postganglionic neurons innervating muscle vessels of the neck and forearm, and the percentage of labeled NPY-IR profiles did not change during the development. Only single Ki67-IR neurons were also NPY-IR in the SCG, SG and CG in newborns and not in older animals. No NPY+/caspase 3 + IR neurons were observed. Finally, the process of morphological changes in the size and percentages of NPY-IR profiles is complete in rats by the first month of life.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>22964363</pmid><doi>10.1016/j.npep.2012.08.003</doi><tpages>8</tpages></addata></record>
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subjects Advanced Basic Science
Age
Animals
Animals, Newborn
Autonomic nervous system
Calbindin-D28K
Caspase 3 - metabolism
Caspase-3
celiac ganglion
Choline O-Acetyltransferase - metabolism
Endocrinology & Metabolism
Forearm
Ganglia, Sympathetic - cytology
Ganglia, Sympathetic - growth & development
Ganglia, Sympathetic - metabolism
Immunohistochemistry
Ki-67 Antigen - metabolism
Muscles
Neck
Neonates
Neurons
Neurons - cytology
Neurons - physiology
Neuropeptide Y
Neuropeptide Y - metabolism
Neuropeptide Y - physiology
Nitric Oxide Synthase - metabolism
Postnatal ontogenesis
Rats
Rats, Wistar
Somatostatin - metabolism
stellate ganglion
Stellate Ganglion - cytology
Stellate Ganglion - growth & development
Stellate Ganglion - metabolism
superior cervical ganglion
Superior Cervical Ganglion - cytology
Superior Cervical Ganglion - growth & development
Superior Cervical Ganglion - metabolism
Sympathetic ganglia
Tyrosine 3-Monooxygenase - metabolism
title Development of neuropeptide Y-containing neurons in sympathetic ganglia of rats
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