Daily administration of Sake Lees (Sake Kasu) reduced psychophysical stress-induced hyperalgesia and Fos responses in the lumbar spinal dorsal horn evoked by noxious stimulation to the hindpaw in the rats
We tested whether Sake Lees (SL) had inhibitory effects on hyperalgesia in the hindpaw under psychophysical stress conditions. Male rats were subjected to repeated forced swim stress treatments (FST) from Day −3 to Day −1. Intraperiotoneal administration of SL which contained low concentration of et...
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description | We tested whether Sake Lees (SL) had inhibitory effects on hyperalgesia in the hindpaw under psychophysical stress conditions. Male rats were subjected to repeated forced swim stress treatments (FST) from Day −3 to Day −1. Intraperiotoneal administration of SL which contained low concentration of ethanol (SLX) was conducted after each FST. On Day 0, formalin-evoked licking behaviors and Fos responses in the lumbar spinal cord (DH) and several areas within the rostral ventromedial medulla (RVM) were quantified as nociceptive responses. FST-induced hyperalgesia in the hindpaw was prevented by repeated SL and SLX treatments. Fos expression was significantly increased in DH and some areas within the RVM under FST, which was prevented by repeated SL or SLX. These findings indicated that daily administration of SL had the potential to alleviate stress-induced hyperalgesia.
Modulatory roles of Sake Lees on stress-induced hyperalgesia. |
doi_str_mv | 10.1080/09168451.2019.1662278 |
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Modulatory roles of Sake Lees on stress-induced hyperalgesia.</description><identifier>ISSN: 0916-8451</identifier><identifier>EISSN: 1347-6947</identifier><identifier>DOI: 10.1080/09168451.2019.1662278</identifier><identifier>PMID: 31483212</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Animals ; Behavior, Animal - drug effects ; Ethanol - chemistry ; Fermentation ; forced swim stress ; Formaldehyde - administration & dosage ; Formaldehyde - pharmacology ; Hindlimb - metabolism ; Hyperalgesia - drug therapy ; Hyperalgesia - etiology ; Immunohistochemistry ; Male ; Oryza - chemistry ; pain ; Pain Management ; Pain Measurement ; Plant Extracts - administration & dosage ; Plant Extracts - pharmacology ; Proto-Oncogene Proteins c-fos - immunology ; Proto-Oncogene Proteins c-fos - metabolism ; rat ; Rats ; Rats, Sprague-Dawley ; Serotonergic Neurons - drug effects ; Serotonergic Neurons - metabolism ; Serotonin - immunology ; Serotonin - metabolism ; spinal cord ; Spinal Cord Dorsal Horn - metabolism ; Stress ; Stress, Physiological - physiology ; Swimming - physiology ; Tissue Distribution</subject><ispartof>Bioscience, biotechnology, and biochemistry, 2020-01, Vol.84 (1), p.159-170</ispartof><rights>2019 Japan Society for Bioscience, Biotechnology, and Agrochemistry 2019</rights><rights>2020 Japan Society for Bioscience, Biotechnology, and Agrochemistry 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c497t-6ecd6d9a29a8c6bdcde7c251ddae783135fa4f748955024fd1bee9335fc8bc613</citedby><cites>FETCH-LOGICAL-c497t-6ecd6d9a29a8c6bdcde7c251ddae783135fa4f748955024fd1bee9335fc8bc613</cites><orcidid>0000-0002-3519-9561</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31483212$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shimizu, Shiho</creatorcontrib><creatorcontrib>Nakatani, Yosuke</creatorcontrib><creatorcontrib>Kakihara, Yoshito</creatorcontrib><creatorcontrib>Taiyoji, Mayumi</creatorcontrib><creatorcontrib>Saeki, Makio</creatorcontrib><creatorcontrib>Takagi, Ritsuo</creatorcontrib><creatorcontrib>Yamamura, Kensuke</creatorcontrib><creatorcontrib>Okamoto, Keiichiro</creatorcontrib><title>Daily administration of Sake Lees (Sake Kasu) reduced psychophysical stress-induced hyperalgesia and Fos responses in the lumbar spinal dorsal horn evoked by noxious stimulation to the hindpaw in the rats</title><title>Bioscience, biotechnology, and biochemistry</title><addtitle>Biosci Biotechnol Biochem</addtitle><description>We tested whether Sake Lees (SL) had inhibitory effects on hyperalgesia in the hindpaw under psychophysical stress conditions. Male rats were subjected to repeated forced swim stress treatments (FST) from Day −3 to Day −1. Intraperiotoneal administration of SL which contained low concentration of ethanol (SLX) was conducted after each FST. On Day 0, formalin-evoked licking behaviors and Fos responses in the lumbar spinal cord (DH) and several areas within the rostral ventromedial medulla (RVM) were quantified as nociceptive responses. FST-induced hyperalgesia in the hindpaw was prevented by repeated SL and SLX treatments. Fos expression was significantly increased in DH and some areas within the RVM under FST, which was prevented by repeated SL or SLX. These findings indicated that daily administration of SL had the potential to alleviate stress-induced hyperalgesia.
Modulatory roles of Sake Lees on stress-induced hyperalgesia.</description><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Ethanol - chemistry</subject><subject>Fermentation</subject><subject>forced swim stress</subject><subject>Formaldehyde - administration & dosage</subject><subject>Formaldehyde - pharmacology</subject><subject>Hindlimb - metabolism</subject><subject>Hyperalgesia - drug therapy</subject><subject>Hyperalgesia - etiology</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Oryza - chemistry</subject><subject>pain</subject><subject>Pain Management</subject><subject>Pain Measurement</subject><subject>Plant Extracts - administration & dosage</subject><subject>Plant Extracts - pharmacology</subject><subject>Proto-Oncogene Proteins c-fos - immunology</subject><subject>Proto-Oncogene Proteins c-fos - metabolism</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Serotonergic Neurons - drug effects</subject><subject>Serotonergic Neurons - metabolism</subject><subject>Serotonin - immunology</subject><subject>Serotonin - metabolism</subject><subject>spinal cord</subject><subject>Spinal Cord Dorsal Horn - metabolism</subject><subject>Stress</subject><subject>Stress, Physiological - physiology</subject><subject>Swimming - physiology</subject><subject>Tissue Distribution</subject><issn>0916-8451</issn><issn>1347-6947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1TAQhS0EopfCI4C8LItcbOd_ByoUEJVYAOtoYk-IaWIHT9KSd-Sh8G3uZYlYjTVzzjcjH8aeS7GXohKvRC2LKsvlXglZ72VRKFVWD9hOplmZFHVWPmS7gyY5iM7YE6IfQsRGLh-zs1RmVaqk2rHfb8EOKwczWmdpDjBb77jv-Be4QX6NSPzi_vkJaHnJA5pFo-ETrbr3U7-S1TDwaESixLpt2q8TBhi-I1ng4Ay_8hStNHlHEWgdn3vkwzK2EDhN1kWE8YFi6X1wHG_9TcS0K3f-l_ULxQV2XIbtuNnf2_u4bYK7Ey1eTk_Zow4GwmfHes6-Xb37evkhuf78_uPlm-tEZ3U5JwVqU5gaVA2VLlqjDZZa5dIYwLJKZZp3kHVlVtV5LlTWGdki1mls66rVhUzP2cXGnYL_uSDNzWhJ4zCAw3hto1T89EJUdR2l-SbVwRMF7Jop2BHC2kjRHIJsTkE2hyCbY5DR9-K4YmlHNH9dp-SiQGwCv0z_zXy9WazrfBjhzofBNDOsgw9dAKctRf4_EX8ATJPAeQ</recordid><startdate>20200102</startdate><enddate>20200102</enddate><creator>Shimizu, Shiho</creator><creator>Nakatani, Yosuke</creator><creator>Kakihara, Yoshito</creator><creator>Taiyoji, Mayumi</creator><creator>Saeki, Makio</creator><creator>Takagi, Ritsuo</creator><creator>Yamamura, Kensuke</creator><creator>Okamoto, Keiichiro</creator><general>Taylor & Francis</general><general>Oxford University Press</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><orcidid>https://orcid.org/0000-0002-3519-9561</orcidid></search><sort><creationdate>20200102</creationdate><title>Daily administration of Sake Lees (Sake Kasu) reduced psychophysical stress-induced hyperalgesia and Fos responses in the lumbar spinal dorsal horn evoked by noxious stimulation to the hindpaw in the rats</title><author>Shimizu, Shiho ; Nakatani, Yosuke ; Kakihara, Yoshito ; Taiyoji, Mayumi ; Saeki, Makio ; Takagi, Ritsuo ; Yamamura, Kensuke ; Okamoto, Keiichiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c497t-6ecd6d9a29a8c6bdcde7c251ddae783135fa4f748955024fd1bee9335fc8bc613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Ethanol - chemistry</topic><topic>Fermentation</topic><topic>forced swim stress</topic><topic>Formaldehyde - administration & dosage</topic><topic>Formaldehyde - pharmacology</topic><topic>Hindlimb - metabolism</topic><topic>Hyperalgesia - drug therapy</topic><topic>Hyperalgesia - etiology</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Oryza - chemistry</topic><topic>pain</topic><topic>Pain Management</topic><topic>Pain Measurement</topic><topic>Plant Extracts - administration & dosage</topic><topic>Plant Extracts - pharmacology</topic><topic>Proto-Oncogene Proteins c-fos - immunology</topic><topic>Proto-Oncogene Proteins c-fos - metabolism</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Serotonergic Neurons - drug effects</topic><topic>Serotonergic Neurons - metabolism</topic><topic>Serotonin - immunology</topic><topic>Serotonin - metabolism</topic><topic>spinal cord</topic><topic>Spinal Cord Dorsal Horn - metabolism</topic><topic>Stress</topic><topic>Stress, Physiological - physiology</topic><topic>Swimming - physiology</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shimizu, Shiho</creatorcontrib><creatorcontrib>Nakatani, Yosuke</creatorcontrib><creatorcontrib>Kakihara, Yoshito</creatorcontrib><creatorcontrib>Taiyoji, Mayumi</creatorcontrib><creatorcontrib>Saeki, Makio</creatorcontrib><creatorcontrib>Takagi, Ritsuo</creatorcontrib><creatorcontrib>Yamamura, Kensuke</creatorcontrib><creatorcontrib>Okamoto, Keiichiro</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><jtitle>Bioscience, biotechnology, and biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shimizu, Shiho</au><au>Nakatani, Yosuke</au><au>Kakihara, Yoshito</au><au>Taiyoji, Mayumi</au><au>Saeki, Makio</au><au>Takagi, Ritsuo</au><au>Yamamura, Kensuke</au><au>Okamoto, Keiichiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Daily administration of Sake Lees (Sake Kasu) reduced psychophysical stress-induced hyperalgesia and Fos responses in the lumbar spinal dorsal horn evoked by noxious stimulation to the hindpaw in the rats</atitle><jtitle>Bioscience, biotechnology, and biochemistry</jtitle><addtitle>Biosci Biotechnol Biochem</addtitle><date>2020-01-02</date><risdate>2020</risdate><volume>84</volume><issue>1</issue><spage>159</spage><epage>170</epage><pages>159-170</pages><issn>0916-8451</issn><eissn>1347-6947</eissn><abstract>We tested whether Sake Lees (SL) had inhibitory effects on hyperalgesia in the hindpaw under psychophysical stress conditions. Male rats were subjected to repeated forced swim stress treatments (FST) from Day −3 to Day −1. Intraperiotoneal administration of SL which contained low concentration of ethanol (SLX) was conducted after each FST. On Day 0, formalin-evoked licking behaviors and Fos responses in the lumbar spinal cord (DH) and several areas within the rostral ventromedial medulla (RVM) were quantified as nociceptive responses. FST-induced hyperalgesia in the hindpaw was prevented by repeated SL and SLX treatments. Fos expression was significantly increased in DH and some areas within the RVM under FST, which was prevented by repeated SL or SLX. These findings indicated that daily administration of SL had the potential to alleviate stress-induced hyperalgesia.
Modulatory roles of Sake Lees on stress-induced hyperalgesia.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>31483212</pmid><doi>10.1080/09168451.2019.1662278</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-3519-9561</orcidid></addata></record> |
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subjects | Animals Behavior, Animal - drug effects Ethanol - chemistry Fermentation forced swim stress Formaldehyde - administration & dosage Formaldehyde - pharmacology Hindlimb - metabolism Hyperalgesia - drug therapy Hyperalgesia - etiology Immunohistochemistry Male Oryza - chemistry pain Pain Management Pain Measurement Plant Extracts - administration & dosage Plant Extracts - pharmacology Proto-Oncogene Proteins c-fos - immunology Proto-Oncogene Proteins c-fos - metabolism rat Rats Rats, Sprague-Dawley Serotonergic Neurons - drug effects Serotonergic Neurons - metabolism Serotonin - immunology Serotonin - metabolism spinal cord Spinal Cord Dorsal Horn - metabolism Stress Stress, Physiological - physiology Swimming - physiology Tissue Distribution |
title | Daily administration of Sake Lees (Sake Kasu) reduced psychophysical stress-induced hyperalgesia and Fos responses in the lumbar spinal dorsal horn evoked by noxious stimulation to the hindpaw in the rats |
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