Henrik Thyge Corfitsen, Katrine Bilde, Trine Rerup, Agnete Larsen
{"title":"伏替西汀对暴露于高脂饮食的小鼠粪便微生物群的影响--与体重保护有关。","authors":"Henrik Thyge Corfitsen, Katrine Bilde, Trine Rerup, Agnete Larsen","doi":"10.1111/bcpt.14058","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objective</h3>\n \n <p>Weight gain is a common side effect of antidepressive treatment, causing distress among patients and caretakers as it can lead to treatment discontinuation and complications such as diabetes type II and cardiovascular disease. Vortioxetine is one of the newer antidepressants and the pharmacodynamics differ from the selective serotonin reuptake inhibitors. It is marketed as being weight neutral; however, there is little evidence as to why. In recent years, there has been an increased focus on the faecal microbiota and its impact on body weight and mental and physical health. In the current work, we examine the effect of vortioxetine on weight gain and faecal microbiota composition.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Forty male C57BL/6NTac mice were primed for 8 weeks with a high-fat diet (Hfd) or control diet (Cd), followed by a 4-week period on the same diet and additional +/− vortioxetine 10 mg/kg/daily.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Vortioxetine reduced Hfd-induced weight gain (Hfd + V: 8.2%, Hfd − V: 12.7%; <i>p</i> = 0.0374) but did not affect weight gain of the control group (Cd + V: 7.54%, Cd − V: 7.56%; <i>p</i> = 0.4944). Significant differences in faecal microbiota were observed in mice who received vortioxetine.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Vortioxetine caused significant changes to the faecal microbiota composition and appeared to limit Hfd-induced weight gain.</p>\n </section>\n </div>","PeriodicalId":8733,"journal":{"name":"Basic & Clinical Pharmacology & Toxicology","volume":"135 4","pages":"417-428"},"PeriodicalIF":2.7000,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The effect of vortioxetine on faecal microbiota in high-fat diet-exposed mice—A link to weight protection\",\"authors\":\"Henrik Thyge Corfitsen, Katrine Bilde, Trine Rerup, Agnete Larsen\",\"doi\":\"10.1111/bcpt.14058\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Objective</h3>\\n \\n <p>Weight gain is a common side effect of antidepressive treatment, causing distress among patients and caretakers as it can lead to treatment discontinuation and complications such as diabetes type II and cardiovascular disease. Vortioxetine is one of the newer antidepressants and the pharmacodynamics differ from the selective serotonin reuptake inhibitors. It is marketed as being weight neutral; however, there is little evidence as to why. In recent years, there has been an increased focus on the faecal microbiota and its impact on body weight and mental and physical health. In the current work, we examine the effect of vortioxetine on weight gain and faecal microbiota composition.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Forty male C57BL/6NTac mice were primed for 8 weeks with a high-fat diet (Hfd) or control diet (Cd), followed by a 4-week period on the same diet and additional +/− vortioxetine 10 mg/kg/daily.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Vortioxetine reduced Hfd-induced weight gain (Hfd + V: 8.2%, Hfd − V: 12.7%; <i>p</i> = 0.0374) but did not affect weight gain of the control group (Cd + V: 7.54%, Cd − V: 7.56%; <i>p</i> = 0.4944). Significant differences in faecal microbiota were observed in mice who received vortioxetine.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>Vortioxetine caused significant changes to the faecal microbiota composition and appeared to limit Hfd-induced weight gain.</p>\\n </section>\\n </div>\",\"PeriodicalId\":8733,\"journal\":{\"name\":\"Basic & Clinical Pharmacology & Toxicology\",\"volume\":\"135 4\",\"pages\":\"417-428\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Basic & Clinical Pharmacology & Toxicology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/bcpt.14058\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Basic & Clinical Pharmacology & Toxicology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/bcpt.14058","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
The effect of vortioxetine on faecal microbiota in high-fat diet-exposed mice—A link to weight protection
Objective
Weight gain is a common side effect of antidepressive treatment, causing distress among patients and caretakers as it can lead to treatment discontinuation and complications such as diabetes type II and cardiovascular disease. Vortioxetine is one of the newer antidepressants and the pharmacodynamics differ from the selective serotonin reuptake inhibitors. It is marketed as being weight neutral; however, there is little evidence as to why. In recent years, there has been an increased focus on the faecal microbiota and its impact on body weight and mental and physical health. In the current work, we examine the effect of vortioxetine on weight gain and faecal microbiota composition.
Methods
Forty male C57BL/6NTac mice were primed for 8 weeks with a high-fat diet (Hfd) or control diet (Cd), followed by a 4-week period on the same diet and additional +/− vortioxetine 10 mg/kg/daily.
Results
Vortioxetine reduced Hfd-induced weight gain (Hfd + V: 8.2%, Hfd − V: 12.7%; p = 0.0374) but did not affect weight gain of the control group (Cd + V: 7.54%, Cd − V: 7.56%; p = 0.4944). Significant differences in faecal microbiota were observed in mice who received vortioxetine.
Conclusion
Vortioxetine caused significant changes to the faecal microbiota composition and appeared to limit Hfd-induced weight gain.
期刊介绍:
Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.