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Switching from morphine to fentanyl attenuates the decline of μ-opioid receptor expression in periaqueductal gray of rats with morphine tolerance
Background Opioid switching is a therapeutic maneuver to improve analgesic response and/or reduce adverse side effects although the underlying mechanisms remain unknown.The μ-opioid receptor (MOR) has an important role in mediating the actions of morphine and other analgesic agents.This study is aim...
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Published in: | Chinese medical journal 2013, Vol.126 (19), p.3712-3716 |
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description | Background Opioid switching is a therapeutic maneuver to improve analgesic response and/or reduce adverse side effects although the underlying mechanisms remain unknown.The μ-opioid receptor (MOR) has an important role in mediating the actions of morphine and other analgesic agents.This study is aimed at exploring the changes of MOR in the periaqueductal gray (PAG) in rats when morphine is substituted for equianalgesic fentanyl.Methods Forty rats were randomly assigned to five treatment groups:7 days normal saline group (N group),7 days fentanyl group (F group),7 days morphine group (M group),7 days morphine and 7 days fentanyl-switching group (MF group),and 14 days morphine group (MM group).Rats repeatedly received subcutaneous injections of morphine sulfate (10 mg/kg) or equianalgesic fentanyl sulfate (0.1 mg/kg) twice daily.Rats' antinociceptive response to thermal pain was evaluated by the tail flick latency assay.MOR mRNA and protein expression in the PAG were measured using RT-PCR and Western blotting analyses respectively.Results This study showed that after morphine was substituted with fentanyl on day 8,the tail flick latency (TFL) increased from (3.9±0.4) seconds to (11.4±0.4) seconds.The results also demonstrated that both MOR mRNA and protein expression in the PAG of rats in the MF group were less than that in the M group (P〈0.05) but more than that in MM group (P〈0.05).Conclusions Equianalgesic fentanyl was still antinociceptive effective in rats with morphine tolerance,which may be due to the switching from morphine to fentanyl attenuating the decline of MOR expression in the PAG of rats. |
doi_str_mv | 10.3760/cma.j.issn.0366-6999.20122848 |
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Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3521-6df2640cf6b335ab7120c04663d6e57d09f8c2f01d1ae4ea623983c0dc080043</citedby><cites>FETCH-LOGICAL-c3521-6df2640cf6b335ab7120c04663d6e57d09f8c2f01d1ae4ea623983c0dc080043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85656X/85656X.jpg</thumbnail><link.rule.ids>314,780,784,4022,27921,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24112169$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dong, Yan-peng</creatorcontrib><creatorcontrib>Sun, Li</creatorcontrib><creatorcontrib>Liu, Xiao-yan</creatorcontrib><creatorcontrib>Liu, Ruo-shan</creatorcontrib><title>Switching from morphine to fentanyl attenuates the decline of μ-opioid receptor expression in periaqueductal gray of rats with morphine tolerance</title><title>Chinese medical journal</title><addtitle>Chinese Medical Journal</addtitle><description>Background Opioid switching is a therapeutic maneuver to improve analgesic response and/or reduce adverse side effects although the underlying mechanisms remain unknown.The μ-opioid receptor (MOR) has an important role in mediating the actions of morphine and other analgesic agents.This study is aimed at exploring the changes of MOR in the periaqueductal gray (PAG) in rats when morphine is substituted for equianalgesic fentanyl.Methods Forty rats were randomly assigned to five treatment groups:7 days normal saline group (N group),7 days fentanyl group (F group),7 days morphine group (M group),7 days morphine and 7 days fentanyl-switching group (MF group),and 14 days morphine group (MM group).Rats repeatedly received subcutaneous injections of morphine sulfate (10 mg/kg) or equianalgesic fentanyl sulfate (0.1 mg/kg) twice daily.Rats' antinociceptive response to thermal pain was evaluated by the tail flick latency assay.MOR mRNA and protein expression in the PAG were measured using RT-PCR and Western blotting analyses respectively.Results This study showed that after morphine was substituted with fentanyl on day 8,the tail flick latency (TFL) increased from (3.9±0.4) seconds to (11.4±0.4) seconds.The results also demonstrated that both MOR mRNA and protein expression in the PAG of rats in the MF group were less than that in the M group (P〈0.05) but more than that in MM group (P〈0.05).Conclusions Equianalgesic fentanyl was still antinociceptive effective in rats with morphine tolerance,which may be due to the switching from morphine to fentanyl attenuating the decline of MOR expression in the PAG of rats.</description><subject>Analgesics, Opioid - pharmacology</subject><subject>Animals</subject><subject>Drug Tolerance</subject><subject>Fentanyl - pharmacology</subject><subject>Male</subject><subject>Morphine - pharmacology</subject><subject>Periaqueductal Gray - chemistry</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Opioid, mu - analysis</subject><subject>Receptors, Opioid, mu - genetics</subject><subject>RNA, Messenger - analysis</subject><subject>Western印迹</subject><subject>中脑导水管周围灰质</subject><subject>切换</subject><subject>受体表达</subject><subject>吗啡耐受</subject><subject>大鼠</subject><subject>芬太尼</subject><subject>衰减</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpNkctu1DAUhi0EokPhFZBZULHJ4FucZMECVdykSizo3vI4JxNHiZ3ajtrhMfo8PAPPhKOZjlgdWfr-8-v4Q-g9JVteSfLRTHo7bG2Mbku4lIVsmmbLCGWsFvUztGGlYEUpBX2ONmfgAr2KcSCElWUlX6ILJihlVDYb9Pjr3ibTW7fHXfATnnyY8wtw8rgDl7Q7jFinBG7RCSJOPeAWzLgivsN__xR-tt62OICBOfmA4WEOEKP1DluHZwhW3y3QLibpEe-DPqy5oFPEubn_v3CEoJ2B1-hFp8cIb07zEt1-_XJ7_b24-fntx_Xnm8LwktFCth2TgphO7jgv9a6ijBgipOSthLJqSdPVhnWEtlSDAC0Zb2puSGtITYjgl-jquPZeu067vRr8ElwuVL97Mw35SzltCKMZ_HAE5-DzJTGpyUYD46gd-CUqKgQXhJa0zuinI2qCjzFAp-ZgJx0OihK16lNZnxrUqk-tdtRqRz3py_m3p6plN0F7Tj_5ysC7U0Hv3f4uazszohJltS75B88pqEY</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>Dong, Yan-peng</creator><creator>Sun, Li</creator><creator>Liu, Xiao-yan</creator><creator>Liu, Ruo-shan</creator><general>Department of Anesthesiology, Cancer Hospital and Institute, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100021, China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</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><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>2013</creationdate><title>Switching from morphine to fentanyl attenuates the decline of μ-opioid receptor expression in periaqueductal gray of rats with morphine tolerance</title><author>Dong, Yan-peng ; Sun, Li ; Liu, Xiao-yan ; Liu, Ruo-shan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3521-6df2640cf6b335ab7120c04663d6e57d09f8c2f01d1ae4ea623983c0dc080043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Analgesics, Opioid - pharmacology</topic><topic>Animals</topic><topic>Drug Tolerance</topic><topic>Fentanyl - pharmacology</topic><topic>Male</topic><topic>Morphine - pharmacology</topic><topic>Periaqueductal Gray - chemistry</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Opioid, mu - analysis</topic><topic>Receptors, Opioid, mu - genetics</topic><topic>RNA, Messenger - analysis</topic><topic>Western印迹</topic><topic>中脑导水管周围灰质</topic><topic>切换</topic><topic>受体表达</topic><topic>吗啡耐受</topic><topic>大鼠</topic><topic>芬太尼</topic><topic>衰减</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dong, Yan-peng</creatorcontrib><creatorcontrib>Sun, Li</creatorcontrib><creatorcontrib>Liu, Xiao-yan</creatorcontrib><creatorcontrib>Liu, Ruo-shan</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>维普中文期刊数据库</collection><collection>维普中文医药期刊数据库</collection><collection>中文科技期刊数据库- 镜像站点</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><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dong, Yan-peng</au><au>Sun, Li</au><au>Liu, Xiao-yan</au><au>Liu, Ruo-shan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Switching from morphine to fentanyl attenuates the decline of μ-opioid receptor expression in periaqueductal gray of rats with morphine tolerance</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chinese Medical Journal</addtitle><date>2013</date><risdate>2013</risdate><volume>126</volume><issue>19</issue><spage>3712</spage><epage>3716</epage><pages>3712-3716</pages><issn>0366-6999</issn><eissn>2542-5641</eissn><abstract>Background Opioid switching is a therapeutic maneuver to improve analgesic response and/or reduce adverse side effects although the underlying mechanisms remain unknown.The μ-opioid receptor (MOR) has an important role in mediating the actions of morphine and other analgesic agents.This study is aimed at exploring the changes of MOR in the periaqueductal gray (PAG) in rats when morphine is substituted for equianalgesic fentanyl.Methods Forty rats were randomly assigned to five treatment groups:7 days normal saline group (N group),7 days fentanyl group (F group),7 days morphine group (M group),7 days morphine and 7 days fentanyl-switching group (MF group),and 14 days morphine group (MM group).Rats repeatedly received subcutaneous injections of morphine sulfate (10 mg/kg) or equianalgesic fentanyl sulfate (0.1 mg/kg) twice daily.Rats' antinociceptive response to thermal pain was evaluated by the tail flick latency assay.MOR mRNA and protein expression in the PAG were measured using RT-PCR and Western blotting analyses respectively.Results This study showed that after morphine was substituted with fentanyl on day 8,the tail flick latency (TFL) increased from (3.9±0.4) seconds to (11.4±0.4) seconds.The results also demonstrated that both MOR mRNA and protein expression in the PAG of rats in the MF group were less than that in the M group (P〈0.05) but more than that in MM group (P〈0.05).Conclusions Equianalgesic fentanyl was still antinociceptive effective in rats with morphine tolerance,which may be due to the switching from morphine to fentanyl attenuating the decline of MOR expression in the PAG of rats.</abstract><cop>China</cop><pub>Department of Anesthesiology, Cancer Hospital and Institute, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100021, China</pub><pmid>24112169</pmid><doi>10.3760/cma.j.issn.0366-6999.20122848</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analgesics, Opioid - pharmacology Animals Drug Tolerance Fentanyl - pharmacology Male Morphine - pharmacology Periaqueductal Gray - chemistry Rats Rats, Wistar Receptors, Opioid, mu - analysis Receptors, Opioid, mu - genetics RNA, Messenger - analysis Western印迹 中脑导水管周围灰质 切换 受体表达 吗啡耐受 大鼠 芬太尼 衰减 |
title | Switching from morphine to fentanyl attenuates the decline of μ-opioid receptor expression in periaqueductal gray of rats with morphine tolerance |
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