Substance P Mediates Estrogen Modulation Proinflammatory Cytokines Release in Intervertebral Disc
Intervertebral disc degeneration ( IDD) is a main contributor to low back pain. A close relationship exists between inflammation and pain. Estrogen can affect inflammation and may play a crucial role in IDD and pain. Substance P (SP) can also regulate the expression of pro-inflammatory cytokines in...
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Veröffentlicht in: | Inflammation 2021-04, Vol.44 (2), p.506-517 |
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description | Intervertebral disc degeneration
(
IDD) is a main contributor to low back pain. A close relationship exists between inflammation and pain. Estrogen can affect inflammation and may play a crucial role in IDD and pain. Substance P (SP) can also regulate the expression of pro-inflammatory cytokines in intervertebral disc (IVD). This study aimed to investigate the potential role of SP in estrogen regulation of IDD. Nine-week-old C57BL/6 female mice were divided into four groups as follows: sham surgery (sham), ovariectomy (OVX), ovariectomy plus estrogen replacement therapy (ERT) group (OVX+E2), and ovariectomy, ERT plus neurokinin 1 receptor (NK1R) agonist (OVX+E2+G). Serum E2, body, and uterus weight were recorded. Immunohistochemistry study and quantitative real-time PCR were used for SP, NK1R, IL-1β, IL-6, and TNF-α examination and comparison in IVD at protein and gene levels. After OVX, the gene and protein expression of TNF-α, IL-1β, IL-6, SP, and NK1R in NP cells significantly increased compared with the sham group. ERT can reverse these impacts. ERT plays anti-inflammatory and anti-hyperalgesic roles in IDD of OVX mice. The estrogen-induced changes of the pro-inflammatory cytokines, TNF-α, IL-1β, and IL-6, are significantly inhibited by NK1R agonists. SP may be a mediator of estrogen regulating pro-inflammatory factors in IDD. Estrogen may affect IVD inflammation through two ways: one is to directly affect the level of pro-inflammatory cytokines and the other is by means of modulation of SP. |
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(
IDD) is a main contributor to low back pain. A close relationship exists between inflammation and pain. Estrogen can affect inflammation and may play a crucial role in IDD and pain. Substance P (SP) can also regulate the expression of pro-inflammatory cytokines in intervertebral disc (IVD). This study aimed to investigate the potential role of SP in estrogen regulation of IDD. Nine-week-old C57BL/6 female mice were divided into four groups as follows: sham surgery (sham), ovariectomy (OVX), ovariectomy plus estrogen replacement therapy (ERT) group (OVX+E2), and ovariectomy, ERT plus neurokinin 1 receptor (NK1R) agonist (OVX+E2+G). Serum E2, body, and uterus weight were recorded. Immunohistochemistry study and quantitative real-time PCR were used for SP, NK1R, IL-1β, IL-6, and TNF-α examination and comparison in IVD at protein and gene levels. After OVX, the gene and protein expression of TNF-α, IL-1β, IL-6, SP, and NK1R in NP cells significantly increased compared with the sham group. ERT can reverse these impacts. ERT plays anti-inflammatory and anti-hyperalgesic roles in IDD of OVX mice. The estrogen-induced changes of the pro-inflammatory cytokines, TNF-α, IL-1β, and IL-6, are significantly inhibited by NK1R agonists. SP may be a mediator of estrogen regulating pro-inflammatory factors in IDD. Estrogen may affect IVD inflammation through two ways: one is to directly affect the level of pro-inflammatory cytokines and the other is by means of modulation of SP.</description><identifier>ISSN: 0360-3997</identifier><identifier>EISSN: 1573-2576</identifier><identifier>DOI: 10.1007/s10753-020-01347-1</identifier><identifier>PMID: 32965648</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Agonists ; Biomedical and Life Sciences ; Biomedicine ; Cytokines ; Degeneration ; Estrogens ; Hormone replacement therapy ; IL-1β ; Immunohistochemistry ; Immunology ; Inflammation ; Interleukin 6 ; Internal Medicine ; Low back pain ; Neurokinin ; Neurokinin NK1 receptors ; Oophorectomy ; Original Article ; Ovariectomy ; Pain ; Pathology ; Pharmacology/Toxicology ; Rheumatology ; Substance P ; Surgery ; Tumor necrosis factor-α ; Uterus</subject><ispartof>Inflammation, 2021-04, Vol.44 (2), p.506-517</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-3d73cc655b1fc2ef4bc27e0938869194239318cf509b4828c300a0578b5913883</citedby><cites>FETCH-LOGICAL-c375t-3d73cc655b1fc2ef4bc27e0938869194239318cf509b4828c300a0578b5913883</cites><orcidid>0000-0003-0095-3138</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10753-020-01347-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10753-020-01347-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32965648$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Song, Xiao-Xing</creatorcontrib><creatorcontrib>Jin, Lin-Yu</creatorcontrib><creatorcontrib>Li, Xin-Feng</creatorcontrib><creatorcontrib>Luo, Yan</creatorcontrib><creatorcontrib>Yu, Bu-Wei</creatorcontrib><title>Substance P Mediates Estrogen Modulation Proinflammatory Cytokines Release in Intervertebral Disc</title><title>Inflammation</title><addtitle>Inflammation</addtitle><addtitle>Inflammation</addtitle><description>Intervertebral disc degeneration
(
IDD) is a main contributor to low back pain. A close relationship exists between inflammation and pain. Estrogen can affect inflammation and may play a crucial role in IDD and pain. Substance P (SP) can also regulate the expression of pro-inflammatory cytokines in intervertebral disc (IVD). This study aimed to investigate the potential role of SP in estrogen regulation of IDD. Nine-week-old C57BL/6 female mice were divided into four groups as follows: sham surgery (sham), ovariectomy (OVX), ovariectomy plus estrogen replacement therapy (ERT) group (OVX+E2), and ovariectomy, ERT plus neurokinin 1 receptor (NK1R) agonist (OVX+E2+G). Serum E2, body, and uterus weight were recorded. Immunohistochemistry study and quantitative real-time PCR were used for SP, NK1R, IL-1β, IL-6, and TNF-α examination and comparison in IVD at protein and gene levels. After OVX, the gene and protein expression of TNF-α, IL-1β, IL-6, SP, and NK1R in NP cells significantly increased compared with the sham group. ERT can reverse these impacts. ERT plays anti-inflammatory and anti-hyperalgesic roles in IDD of OVX mice. The estrogen-induced changes of the pro-inflammatory cytokines, TNF-α, IL-1β, and IL-6, are significantly inhibited by NK1R agonists. SP may be a mediator of estrogen regulating pro-inflammatory factors in IDD. Estrogen may affect IVD inflammation through two ways: one is to directly affect the level of pro-inflammatory cytokines and the other is by means of modulation of SP.</description><subject>Agonists</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cytokines</subject><subject>Degeneration</subject><subject>Estrogens</subject><subject>Hormone replacement therapy</subject><subject>IL-1β</subject><subject>Immunohistochemistry</subject><subject>Immunology</subject><subject>Inflammation</subject><subject>Interleukin 6</subject><subject>Internal Medicine</subject><subject>Low back pain</subject><subject>Neurokinin</subject><subject>Neurokinin NK1 receptors</subject><subject>Oophorectomy</subject><subject>Original Article</subject><subject>Ovariectomy</subject><subject>Pain</subject><subject>Pathology</subject><subject>Pharmacology/Toxicology</subject><subject>Rheumatology</subject><subject>Substance P</subject><subject>Surgery</subject><subject>Tumor necrosis factor-α</subject><subject>Uterus</subject><issn>0360-3997</issn><issn>1573-2576</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kUtvFDEQhC0EIpuFP8ABWeLCZaD9GttHtAQSKRERj7Pl8fZEE2bsYHuQ9t9j2AASB0596K-qW1WEPGPwigHo14WBVqIDDh0wIXXHHpANU1p0XOn-IdmA6KET1uoTclrKLQAYa8RjciK47VUvzYb4T-tQqo8B6TW9wv3kKxZ6VmpONxjpVdqvs69TivQ6pymOs18WX1M-0N2hpq9TbPRHnNEXpFOkF7Fi_o654pD9TN9OJTwhj0Y_F3x6P7fky7uzz7vz7vLD-4vdm8suCK1qJ_ZahNArNbAxcBzlELhGsMKY3jIrubCCmTAqsIM03AQB4EFpMyjLGiS25OXR9y6nbyuW6pZ2HefZR0xrcVxKJbkB3Tf0xT_obVpzbN85rkAowWVLcUv4kQo5lZJxdHd5Wnw-OAbuZwHuWIBrBbhfBTjWRM_vrddhwf0fye_EGyCOQGmreIP57-3_2P4AuHKPrA</recordid><startdate>20210401</startdate><enddate>20210401</enddate><creator>Song, Xiao-Xing</creator><creator>Jin, Lin-Yu</creator><creator>Li, Xin-Feng</creator><creator>Luo, Yan</creator><creator>Yu, Bu-Wei</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0095-3138</orcidid></search><sort><creationdate>20210401</creationdate><title>Substance P Mediates Estrogen Modulation Proinflammatory Cytokines Release in Intervertebral Disc</title><author>Song, Xiao-Xing ; Jin, Lin-Yu ; Li, Xin-Feng ; Luo, Yan ; Yu, Bu-Wei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-3d73cc655b1fc2ef4bc27e0938869194239318cf509b4828c300a0578b5913883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Agonists</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cytokines</topic><topic>Degeneration</topic><topic>Estrogens</topic><topic>Hormone replacement therapy</topic><topic>IL-1β</topic><topic>Immunohistochemistry</topic><topic>Immunology</topic><topic>Inflammation</topic><topic>Interleukin 6</topic><topic>Internal Medicine</topic><topic>Low back pain</topic><topic>Neurokinin</topic><topic>Neurokinin NK1 receptors</topic><topic>Oophorectomy</topic><topic>Original Article</topic><topic>Ovariectomy</topic><topic>Pain</topic><topic>Pathology</topic><topic>Pharmacology/Toxicology</topic><topic>Rheumatology</topic><topic>Substance P</topic><topic>Surgery</topic><topic>Tumor necrosis factor-α</topic><topic>Uterus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Song, Xiao-Xing</creatorcontrib><creatorcontrib>Jin, Lin-Yu</creatorcontrib><creatorcontrib>Li, Xin-Feng</creatorcontrib><creatorcontrib>Luo, Yan</creatorcontrib><creatorcontrib>Yu, Bu-Wei</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Inflammation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Song, Xiao-Xing</au><au>Jin, Lin-Yu</au><au>Li, Xin-Feng</au><au>Luo, Yan</au><au>Yu, Bu-Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Substance P Mediates Estrogen Modulation Proinflammatory Cytokines Release in Intervertebral Disc</atitle><jtitle>Inflammation</jtitle><stitle>Inflammation</stitle><addtitle>Inflammation</addtitle><date>2021-04-01</date><risdate>2021</risdate><volume>44</volume><issue>2</issue><spage>506</spage><epage>517</epage><pages>506-517</pages><issn>0360-3997</issn><eissn>1573-2576</eissn><abstract>Intervertebral disc degeneration
(
IDD) is a main contributor to low back pain. A close relationship exists between inflammation and pain. Estrogen can affect inflammation and may play a crucial role in IDD and pain. Substance P (SP) can also regulate the expression of pro-inflammatory cytokines in intervertebral disc (IVD). This study aimed to investigate the potential role of SP in estrogen regulation of IDD. Nine-week-old C57BL/6 female mice were divided into four groups as follows: sham surgery (sham), ovariectomy (OVX), ovariectomy plus estrogen replacement therapy (ERT) group (OVX+E2), and ovariectomy, ERT plus neurokinin 1 receptor (NK1R) agonist (OVX+E2+G). Serum E2, body, and uterus weight were recorded. Immunohistochemistry study and quantitative real-time PCR were used for SP, NK1R, IL-1β, IL-6, and TNF-α examination and comparison in IVD at protein and gene levels. After OVX, the gene and protein expression of TNF-α, IL-1β, IL-6, SP, and NK1R in NP cells significantly increased compared with the sham group. ERT can reverse these impacts. ERT plays anti-inflammatory and anti-hyperalgesic roles in IDD of OVX mice. The estrogen-induced changes of the pro-inflammatory cytokines, TNF-α, IL-1β, and IL-6, are significantly inhibited by NK1R agonists. SP may be a mediator of estrogen regulating pro-inflammatory factors in IDD. Estrogen may affect IVD inflammation through two ways: one is to directly affect the level of pro-inflammatory cytokines and the other is by means of modulation of SP.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>32965648</pmid><doi>10.1007/s10753-020-01347-1</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-0095-3138</orcidid></addata></record> |
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subjects | Agonists Biomedical and Life Sciences Biomedicine Cytokines Degeneration Estrogens Hormone replacement therapy IL-1β Immunohistochemistry Immunology Inflammation Interleukin 6 Internal Medicine Low back pain Neurokinin Neurokinin NK1 receptors Oophorectomy Original Article Ovariectomy Pain Pathology Pharmacology/Toxicology Rheumatology Substance P Surgery Tumor necrosis factor-α Uterus |
title | Substance P Mediates Estrogen Modulation Proinflammatory Cytokines Release in Intervertebral Disc |
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