Kuan-Ting Chen, O. Hu, S. Ho, Yu-Wen Chen, Jhi-Joung Wang
{"title":"纳布啡及其长效前药哌酸纳布啡对大鼠的镇痛作用。","authors":"Kuan-Ting Chen, O. Hu, S. Ho, Yu-Wen Chen, Jhi-Joung Wang","doi":"10.6955/AAS.200212.0191","DOIUrl":null,"url":null,"abstract":"BACKGROUND\nNalbuphine is an opioid-analgesic with agonist-antagonist properties. Recently, we have synthesized a nalbuphine prodrug, nalbuphine pivalate. The aim of the present study was to evaluate the analgesic effect and the analgesic duration of this prodrug.\n\n\nMETHODS\nForty-eight male Sprague-Dawley rats (4 groups, n = 12 in each group) were used. Rats in group 1 received nalbuphine HCl 25 mumol/kg (in saline) intramuscular injection; rats in group 2 received nalbuphine pivalate 25 mumol/kg (in sesame oil) intramuscular injection, whereas those in groups 3 and 4 received saline and sesame oil respectively. The analgesic effects of testing agents were evaluated using the cold ethanol tail-flick test (-30 degrees C).\n\n\nRESULTS\nBoth nalbuphine HCl and nalbuphine pivalate demonstrated significant analgesic effects. The analgesic duration of nalbuphine HCl was 2 h while that of nalbuphine pivalate was 30 h.\n\n\nCONCLUSIONS\nNalbuphine pivalate has a very long duration of analgesic action. This fascinating finding is worth further evaluation.","PeriodicalId":79312,"journal":{"name":"Acta anaesthesiologica Sinica","volume":"40 4 1","pages":"191-5"},"PeriodicalIF":0.0000,"publicationDate":"2002-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"The analgesic effect of nalbuphine and its long-acting prodrug, nalbuphine pivalate, in rats.\",\"authors\":\"Kuan-Ting Chen, O. Hu, S. Ho, Yu-Wen Chen, Jhi-Joung Wang\",\"doi\":\"10.6955/AAS.200212.0191\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUND\\nNalbuphine is an opioid-analgesic with agonist-antagonist properties. Recently, we have synthesized a nalbuphine prodrug, nalbuphine pivalate. The aim of the present study was to evaluate the analgesic effect and the analgesic duration of this prodrug.\\n\\n\\nMETHODS\\nForty-eight male Sprague-Dawley rats (4 groups, n = 12 in each group) were used. Rats in group 1 received nalbuphine HCl 25 mumol/kg (in saline) intramuscular injection; rats in group 2 received nalbuphine pivalate 25 mumol/kg (in sesame oil) intramuscular injection, whereas those in groups 3 and 4 received saline and sesame oil respectively. The analgesic effects of testing agents were evaluated using the cold ethanol tail-flick test (-30 degrees C).\\n\\n\\nRESULTS\\nBoth nalbuphine HCl and nalbuphine pivalate demonstrated significant analgesic effects. The analgesic duration of nalbuphine HCl was 2 h while that of nalbuphine pivalate was 30 h.\\n\\n\\nCONCLUSIONS\\nNalbuphine pivalate has a very long duration of analgesic action. This fascinating finding is worth further evaluation.\",\"PeriodicalId\":79312,\"journal\":{\"name\":\"Acta anaesthesiologica Sinica\",\"volume\":\"40 4 1\",\"pages\":\"191-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta anaesthesiologica Sinica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.6955/AAS.200212.0191\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta anaesthesiologica Sinica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.6955/AAS.200212.0191","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The analgesic effect of nalbuphine and its long-acting prodrug, nalbuphine pivalate, in rats.
BACKGROUND
Nalbuphine is an opioid-analgesic with agonist-antagonist properties. Recently, we have synthesized a nalbuphine prodrug, nalbuphine pivalate. The aim of the present study was to evaluate the analgesic effect and the analgesic duration of this prodrug.
METHODS
Forty-eight male Sprague-Dawley rats (4 groups, n = 12 in each group) were used. Rats in group 1 received nalbuphine HCl 25 mumol/kg (in saline) intramuscular injection; rats in group 2 received nalbuphine pivalate 25 mumol/kg (in sesame oil) intramuscular injection, whereas those in groups 3 and 4 received saline and sesame oil respectively. The analgesic effects of testing agents were evaluated using the cold ethanol tail-flick test (-30 degrees C).
RESULTS
Both nalbuphine HCl and nalbuphine pivalate demonstrated significant analgesic effects. The analgesic duration of nalbuphine HCl was 2 h while that of nalbuphine pivalate was 30 h.
CONCLUSIONS
Nalbuphine pivalate has a very long duration of analgesic action. This fascinating finding is worth further evaluation.