Kielmeyera coriacea Mart. (Clusiaceae), known as "Pau Santo", is used to treat several tropical diseases. The hydroethanolic extract (HE) of Kielmeyera coriacea stems and its semi-pure dichloromethane constituent (DCM) produced an anti-immobility effect in rats submitted to the forced swimming test (FST), suggesting a antidepressant-like profile. This study evaluated the effect of intra-median raphe nucleus (MRN) microinjection of 1,3,7-trihydroxy-2-(3-methylbut-2-enyl)-xanthone, present in large quantity in the HE from Kielmeyera coriacea stems, on immobility behaviour in the FST in rats. The effects of xanthone were compared with intra-MRN microinjections of Way100635 (5-HT1A antagonist) or (+) 8-OH-DPAT (5-HT1A agonist). Locomotor activity in the open-field test (OFT) was evaluated as a complementary measure. Xanthone (0.3ng) or Way100635 (2.5microg) reduced, whereas (+) 8-OH-DPAT (5.0microg) increased immobility time in the FST. Way100635 (2.5 or 5.0microg) completely reversed the effects of (+) 8-OHDPAT (5.0microg), and potentiated the anti-immobility effect of the ineffective dose of xanthone (0.2ng) in the FST. The association of effective doses of (+) 8-OH-DPAT (5.0microg) and xanthone (0.3ng) annulled the effect of each compound on immobility time. These results suggest that xanthone acts as an antagonist at 5-HT1A autoreceptors in MRN and increases serotonin (5-HT) availability in projection regions, proving to be a prototype drug that may be useful in mood isorders such as depression, or indeed be a beneficial adjunctive treatment improving the efficacy and/or accelerating the effects of antidepressant drugs in patients with major depression.

译文

:基尔米耶拉(Kielmeyera)coriacea Mart。 (Clusiaceae),被称为“ Pau Santo”,用于治疗几种热带疾病。菊苣茎杆的氢乙醇提取物(HE)及其半纯二氯甲烷成分(DCM)在接受强迫游泳试验(FST)的大鼠中产生了抗固定作用,表明其具有类似抗抑郁药的特性。这项研究评估了Kielmeyera coriacea茎中大量存在于HE中的1,3,7-三羟基-2-(3-甲基丁-2-烯基)-蒽酮对中缝内核(MRN)显微注射的影响,在大鼠FST中的不动行为将x吨酮的作用与Way100635(5-HT1A拮抗剂)或()8-OH-DPAT(5-HT1A激动剂)的MRN显微注射进行了比较。开放场测试(OFT)中的运动活动被评估为一项补充措施。黄酮(0.3ng)或Way100635(2.5microg)减少,而()8-OH-DPAT(5.0microg)增加了FST中的固定时间。 Way100635(2.5或5.0microg)完全逆转了()8-OHDPAT(5.0microg)的作用,并增强了FST中无效剂量的蒽酮(0.2ng)的抗固定作用。有效剂量的()8-OH-DPAT(5.0microg)和x吨酮(0.3ng)的结合消除了每种化合物对固定时间的影响。这些结果表明,an吨酮可作为MRN中5-HT1A自身受体的拮抗剂,并增加投射区域的5-羟色胺(5-HT)利用率,被证明是一种原型药物,可用于情绪障碍(例如抑郁症),或者确实是一种抑郁症。有益的辅助治疗可改善重度抑郁症患者的抗抑郁药的疗效和/或加速其作用。

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