Uma A Bhosale, Rahul Khobragade, Chetana Naik, Radha Yegnanarayan, Jyoti Kale
{"title":"昂丹西琼术后药效学相互作用的研究5-HT3拮抗剂和扑热息痛在耳鼻喉科局部麻醉下的应用。","authors":"Uma A Bhosale, Rahul Khobragade, Chetana Naik, Radha Yegnanarayan, Jyoti Kale","doi":"10.4103/0976-0105.139732","DOIUrl":null,"url":null,"abstract":"Vol. 5 | Issue 3 | June-August 2014 84 Preclinical studies in incision pain models and healthy volunteers have demonstrated the central serotonergic analgesic mechanism of paracetamol.[1] This has been supported by some studies with evidence of raising serotonin concentrations in the brain following paracetamol administration.[2] Inhibition of this analgesia by ondansetron/tropisetron; the 5‐HT3 antagonists suggest that this analgesia is 5‐HT3‐mediated.[3] However, in a few studies, these 5‐HT3 antagonists themselves were found to have analgesic action.[4] These drugs are frequently co‐administered, especially in cancer and postoperative patients. Hence, in this study, we have studied the pharmacodynamic interaction between paracetamol and ondansetron with reference to following parameters:","PeriodicalId":15046,"journal":{"name":"Journal of Basic and Clinical Pharmacy","volume":"5 3","pages":"84-6"},"PeriodicalIF":0.0000,"publicationDate":"2014-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4103/0976-0105.139732","citationCount":"3","resultStr":"{\"title\":\"Postoperative pharmacodynamic interaction of ondansetron; a 5-HT3 antagonist and paracetamol in patients operated in the ENT department under local anesthesia.\",\"authors\":\"Uma A Bhosale, Rahul Khobragade, Chetana Naik, Radha Yegnanarayan, Jyoti Kale\",\"doi\":\"10.4103/0976-0105.139732\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Vol. 5 | Issue 3 | June-August 2014 84 Preclinical studies in incision pain models and healthy volunteers have demonstrated the central serotonergic analgesic mechanism of paracetamol.[1] This has been supported by some studies with evidence of raising serotonin concentrations in the brain following paracetamol administration.[2] Inhibition of this analgesia by ondansetron/tropisetron; the 5‐HT3 antagonists suggest that this analgesia is 5‐HT3‐mediated.[3] However, in a few studies, these 5‐HT3 antagonists themselves were found to have analgesic action.[4] These drugs are frequently co‐administered, especially in cancer and postoperative patients. Hence, in this study, we have studied the pharmacodynamic interaction between paracetamol and ondansetron with reference to following parameters:\",\"PeriodicalId\":15046,\"journal\":{\"name\":\"Journal of Basic and Clinical Pharmacy\",\"volume\":\"5 3\",\"pages\":\"84-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.4103/0976-0105.139732\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Basic and Clinical Pharmacy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/0976-0105.139732\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Basic and Clinical Pharmacy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/0976-0105.139732","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Postoperative pharmacodynamic interaction of ondansetron; a 5-HT3 antagonist and paracetamol in patients operated in the ENT department under local anesthesia.
Vol. 5 | Issue 3 | June-August 2014 84 Preclinical studies in incision pain models and healthy volunteers have demonstrated the central serotonergic analgesic mechanism of paracetamol.[1] This has been supported by some studies with evidence of raising serotonin concentrations in the brain following paracetamol administration.[2] Inhibition of this analgesia by ondansetron/tropisetron; the 5‐HT3 antagonists suggest that this analgesia is 5‐HT3‐mediated.[3] However, in a few studies, these 5‐HT3 antagonists themselves were found to have analgesic action.[4] These drugs are frequently co‐administered, especially in cancer and postoperative patients. Hence, in this study, we have studied the pharmacodynamic interaction between paracetamol and ondansetron with reference to following parameters: