Charles Kwaku Benneh , Wonder Kofi Mensah Abotsi , Robert Peter Biney , Priscilla Kolibea Mante , Mustapha Kobina Abeka , Augustine Tandoh , Eric Woode
{"title":"木犀草酸与特定抗抑郁药合用的协同抗抑郁作用","authors":"Charles Kwaku Benneh , Wonder Kofi Mensah Abotsi , Robert Peter Biney , Priscilla Kolibea Mante , Mustapha Kobina Abeka , Augustine Tandoh , Eric Woode","doi":"10.1016/j.ibneur.2024.01.011","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Xylopic acid (XA), a kaurene diterpene from the dried fruits of <em>Xylopia aethiopica,</em> has anxiolytic- and antidepressant-like activity in mice and zebrafish. We aimed to assess the potential synergistic antidepressant-like effects of XA when combined with selected antidepressants in the mouse forced-swim test.</p></div><div><h3>Materials and methods</h3><p>The antidepressant-like effect of xylopic acid (XA) (10, 30, 100 mgkg<sup>−1</sup>), fluoxetine (Flx) (3, 10, 30 mgkg<sup>−1</sup>), sertraline (Sert) (3, 10, 30 mgkg<sup>−1</sup>), imipramine (Imi) (10, 30, 100 mgkg-1) and ketamine (Ket) (0.1, 0.3, 1.0 mgkg<sup>−1</sup>), was evaluated in forced swim test. The dose (ED<sub>50</sub>) that achieved a 50% reduction in immobility time was determined from the respective log-dose response curves. XA and the selected antidepressants were co-administered in fixed-dose ratio combinations (1/2:1/2, 1/4:1/4, 1/8:1/8) of the ED<sub>50</sub> to identify the experimental ED<sub>50</sub> (ED<sub>50mix</sub>). The theoretical ED<sub>50</sub>(ED<sub>50add</sub>), of all combinations was determined using isobolograms and compared with the ED<sub>50mix</sub> to identify the nature of the interaction. The effect of dose combinations on general locomotor activity was assessed in the open-field test.</p></div><div><h3>Results</h3><p>The interaction index (γ) for the following XA combinations, XA/Flx, XA/Sert, XA/Imi and XA/Ket were 0.42, 0.41, 0.31 and 0.34. An independent sample <em>t-</em>test revealed that the experimental ED<sub>50</sub> (ED<sub>50mix</sub>) was significantly lower than the theoretical ED<sub>50</sub> (ED<sub>50add</sub>) in all combinations of XA, indicative of a synergistic antidepressant-like effect. However, combinations of XA with ketamine significantly reduced general locomotor activity at all dose combinations.</p></div><div><h3>Conclusion</h3><p>The co-administration of xylopic acid and fluoxetine, imipramine, sertraline and ketamine produces a synergistic antidepressant-like effect in mice.</p></div>","PeriodicalId":13195,"journal":{"name":"IBRO Neuroscience Reports","volume":null,"pages":null},"PeriodicalIF":2.0000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667242124000083/pdfft?md5=04929d699d5628705a370862a5f5ca7b&pid=1-s2.0-S2667242124000083-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Synergistic antidepressant-like effect of xylopic acid co-administered with selected antidepressants\",\"authors\":\"Charles Kwaku Benneh , Wonder Kofi Mensah Abotsi , Robert Peter Biney , Priscilla Kolibea Mante , Mustapha Kobina Abeka , Augustine Tandoh , Eric Woode\",\"doi\":\"10.1016/j.ibneur.2024.01.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Xylopic acid (XA), a kaurene diterpene from the dried fruits of <em>Xylopia aethiopica,</em> has anxiolytic- and antidepressant-like activity in mice and zebrafish. We aimed to assess the potential synergistic antidepressant-like effects of XA when combined with selected antidepressants in the mouse forced-swim test.</p></div><div><h3>Materials and methods</h3><p>The antidepressant-like effect of xylopic acid (XA) (10, 30, 100 mgkg<sup>−1</sup>), fluoxetine (Flx) (3, 10, 30 mgkg<sup>−1</sup>), sertraline (Sert) (3, 10, 30 mgkg<sup>−1</sup>), imipramine (Imi) (10, 30, 100 mgkg-1) and ketamine (Ket) (0.1, 0.3, 1.0 mgkg<sup>−1</sup>), was evaluated in forced swim test. The dose (ED<sub>50</sub>) that achieved a 50% reduction in immobility time was determined from the respective log-dose response curves. XA and the selected antidepressants were co-administered in fixed-dose ratio combinations (1/2:1/2, 1/4:1/4, 1/8:1/8) of the ED<sub>50</sub> to identify the experimental ED<sub>50</sub> (ED<sub>50mix</sub>). The theoretical ED<sub>50</sub>(ED<sub>50add</sub>), of all combinations was determined using isobolograms and compared with the ED<sub>50mix</sub> to identify the nature of the interaction. The effect of dose combinations on general locomotor activity was assessed in the open-field test.</p></div><div><h3>Results</h3><p>The interaction index (γ) for the following XA combinations, XA/Flx, XA/Sert, XA/Imi and XA/Ket were 0.42, 0.41, 0.31 and 0.34. An independent sample <em>t-</em>test revealed that the experimental ED<sub>50</sub> (ED<sub>50mix</sub>) was significantly lower than the theoretical ED<sub>50</sub> (ED<sub>50add</sub>) in all combinations of XA, indicative of a synergistic antidepressant-like effect. However, combinations of XA with ketamine significantly reduced general locomotor activity at all dose combinations.</p></div><div><h3>Conclusion</h3><p>The co-administration of xylopic acid and fluoxetine, imipramine, sertraline and ketamine produces a synergistic antidepressant-like effect in mice.</p></div>\",\"PeriodicalId\":13195,\"journal\":{\"name\":\"IBRO Neuroscience Reports\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2024-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2667242124000083/pdfft?md5=04929d699d5628705a370862a5f5ca7b&pid=1-s2.0-S2667242124000083-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IBRO Neuroscience Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667242124000083\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IBRO Neuroscience Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667242124000083","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
背景木犀草酸(XA)是从木犀草(Xylopia aethiopica)干果中提取的一种高烯烃二萜,在小鼠和斑马鱼中具有抗焦虑和抗抑郁类似活性。我们的目的是在小鼠强迫游泳试验中评估 XA 与某些抗抑郁药联合使用时可能产生的协同抗抑郁样作用。材料和方法在强迫游泳试验中评估了木犀草酸(XA)(10、30、100 毫克/千克-1)、氟西汀(Flx)(3、10、30 毫克/千克-1)、舍曲林(Sert)(3、10、30 毫克/千克-1)、丙咪嗪(Imi)(10、30、100 毫克/千克-1)和氯胺酮(Ket)(0.1、0.3、1.0 毫克/千克-1)的抗抑郁样作用。根据各自的对数剂量反应曲线确定了能使不动时间减少 50%的剂量(ED50)。以 ED50 的固定剂量比组合(1/2:1/2、1/4:1/4、1/8:1/8)联合给药 XA 和选定的抗抑郁药,以确定实验 ED50(ED50mix)。使用等全息图确定所有组合的理论 ED50(ED50add),并与 ED50mix 进行比较,以确定相互作用的性质。结果 下列 XA 组合(XA/Flx、XA/Sert、XA/Imi 和 XA/Ket)的交互作用指数(γ)分别为 0.42、0.41、0.31 和 0.34。独立样本 t 检验显示,所有 XA 组合的实验 ED50(ED50mix)均显著低于理论 ED50(ED50add),这表明存在类似抗抑郁剂的协同效应。结论:在小鼠体内同时服用木犀草酸和氟西汀、丙咪嗪、舍曲林和氯胺酮会产生类似抗抑郁的协同作用。
Synergistic antidepressant-like effect of xylopic acid co-administered with selected antidepressants
Background
Xylopic acid (XA), a kaurene diterpene from the dried fruits of Xylopia aethiopica, has anxiolytic- and antidepressant-like activity in mice and zebrafish. We aimed to assess the potential synergistic antidepressant-like effects of XA when combined with selected antidepressants in the mouse forced-swim test.
Materials and methods
The antidepressant-like effect of xylopic acid (XA) (10, 30, 100 mgkg−1), fluoxetine (Flx) (3, 10, 30 mgkg−1), sertraline (Sert) (3, 10, 30 mgkg−1), imipramine (Imi) (10, 30, 100 mgkg-1) and ketamine (Ket) (0.1, 0.3, 1.0 mgkg−1), was evaluated in forced swim test. The dose (ED50) that achieved a 50% reduction in immobility time was determined from the respective log-dose response curves. XA and the selected antidepressants were co-administered in fixed-dose ratio combinations (1/2:1/2, 1/4:1/4, 1/8:1/8) of the ED50 to identify the experimental ED50 (ED50mix). The theoretical ED50(ED50add), of all combinations was determined using isobolograms and compared with the ED50mix to identify the nature of the interaction. The effect of dose combinations on general locomotor activity was assessed in the open-field test.
Results
The interaction index (γ) for the following XA combinations, XA/Flx, XA/Sert, XA/Imi and XA/Ket were 0.42, 0.41, 0.31 and 0.34. An independent sample t-test revealed that the experimental ED50 (ED50mix) was significantly lower than the theoretical ED50 (ED50add) in all combinations of XA, indicative of a synergistic antidepressant-like effect. However, combinations of XA with ketamine significantly reduced general locomotor activity at all dose combinations.
Conclusion
The co-administration of xylopic acid and fluoxetine, imipramine, sertraline and ketamine produces a synergistic antidepressant-like effect in mice.