{"title":"Effect of morphine on rectal temperature after acute and chronic treatment in the rat","authors":"Robert Numan , Harbans Lal","doi":"10.1016/0364-7722(81)90087-4","DOIUrl":null,"url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. In naive male rats morphine sulfate administered intraperitoneally in doses less than 25 mg/kg produced hyperthermia, while higher doses produced hypothermia.</p></span></li><li><span>2.</span><span><p>2. In morphine tolerant rats, morphine produced only hyperthermia at all doses with a markedly reduced time of onset.</p></span></li><li><span>3.</span><span><p>3. When morphine was acutely administered intravenously, all doses tested (2,5,10 and 20 mg/kg) led to an initial hypothermia; hyperthermia subsequently occurred at doses 2,5 and 10 mg/kg, but not at 20 mg/kg.</p></span></li><li><span>4.</span><span><p>4. Naltrexone (5 mg/kg) antagonized both the hyperthermic and hypothermic response to intraperitoneally administered morphine, and when the hypothermic response was antagonized, hyperthermia occurred.</p></span></li><li><span>5.</span><span><p>5. Adrenalectomy retarded the hyperthermic effects of intraperitoneally administered morphine in both naive and tolerant subjects.</p></span></li><li><span>6.</span><span><p>6. It is suggested that hypothermia is a primary action of morphine on central thermoreceptors, and that certain components of the hyperthermic response are induced indirectly, perhaps through hormones of the adrenal glands.</p></span></li></ul></div>","PeriodicalId":20801,"journal":{"name":"Progress in neuro-psychopharmacology","volume":"5 4","pages":"Pages 363-371"},"PeriodicalIF":0.0000,"publicationDate":"1981-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0364-7722(81)90087-4","citationCount":"22","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in neuro-psychopharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0364772281900874","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 22
Abstract
1.
1. In naive male rats morphine sulfate administered intraperitoneally in doses less than 25 mg/kg produced hyperthermia, while higher doses produced hypothermia.
2.
2. In morphine tolerant rats, morphine produced only hyperthermia at all doses with a markedly reduced time of onset.
3.
3. When morphine was acutely administered intravenously, all doses tested (2,5,10 and 20 mg/kg) led to an initial hypothermia; hyperthermia subsequently occurred at doses 2,5 and 10 mg/kg, but not at 20 mg/kg.
4.
4. Naltrexone (5 mg/kg) antagonized both the hyperthermic and hypothermic response to intraperitoneally administered morphine, and when the hypothermic response was antagonized, hyperthermia occurred.
5.
5. Adrenalectomy retarded the hyperthermic effects of intraperitoneally administered morphine in both naive and tolerant subjects.
6.
6. It is suggested that hypothermia is a primary action of morphine on central thermoreceptors, and that certain components of the hyperthermic response are induced indirectly, perhaps through hormones of the adrenal glands.