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Fructus Aurantii induced antidepressant effect via its monoaminergic mechanism and prokinetic action in rat

机译:Au仁通过其单胺能机制和促运动作用诱导抗抑郁作用

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Depression could hardly get a satisfactory effect from the currently available antidepressants. To get a more effective treatment, antidepressant effect and monoaminergic mechanism of Fructus Aurantii (FRA) in the rat forced swimming test (FST) and open field test (OFT), and its prokinetics were examined. FST and OFT were respectively used to evaluate the antidepressant effect and locomotor activity of FRA. We observed the effects of monoamine receptor antagonists on FRA-induced antidepressant effect in rat. The effects of FRA on intestinal transit, gastric emptying and in vitro jejunum contractile activity were assessed. FRA decreased significantly the immobility time (32.6 ± 8.5, 30.3 ± 5.2 vs 56.4 ± 9.4, all p < 0.01) in FST, dose-dependent increased the locomotor activity (102 ± 17.5, 120 ± 18.5 vs 89 ± 9.8, p < 0.05 or 0.01), significantly accelerated gastric emptying (GE: 48.1 ± 6.3, 39.5 ± 5.7 vs 19.5 ± 3.8, p < 0.01) and intestinal transit (IT: 67.3 ± 9.1, 64.2 ± 6.3 vs 49.1 ± 8.2, p < 0.01) of the semi-liquid meal, compared with vehicle. And FRA (1 μM, 10 μM) significantly increased the mean amplitude (0.24 ± 0.021 and 0.281 ± 0.015) of contraction in jejunum of rat compared with vehicle (0.149 ± 0.011) in vitro. FRA (10 μM) could induce a largest amplitude (0.281 ± 0.015) of contraction in jejunum. The anti-immobility effect of FRA in FST was prevented by pre-treatment of rat with p-chlorophenylalanine methyl ester, WAY100635, ketanserin, haloperidol, SCH233390, sulpiride, yohimbine, but not prazosin. FRA could simultaneously induce prokinetics and antidepressant effect, deserves further to investigate.
机译:从目前可用的抗抑郁药中很难获得令人满意的效果。为了获得更有效的治疗方法,研究了野果(FRA)在大鼠强迫游泳试验(FST)和野外试验(OFT)中的抗抑郁作用和单胺能机制,并研究了其动力学。 FST和OFT分别用于评估FRA的抗抑郁作用和运动活性。我们观察到单胺受体拮抗剂对FRA诱导的大鼠抗抑郁作用的影响。评估了FRA对肠运输,胃排空和体外空肠收缩活性的影响。 FRA显着降低FST的固定时间(32.6±8.5,30.3±5.2 vs 56.4±9.4,所有p <0.01),剂量依赖性增加了运动活动(102±17.5,120±18.5 vs 89±9.8,p <0.05或0.01),显着加速的胃排空(GE:48.1±6.3、39.5±5.7与19.5±3.8,p <0.01)和肠转运(IT:67.3±9.1,64.2±6.3与49.1±8.2,p <0.01)与车辆相比,半流质餐。 FRA(1μM,10μM)显着增加了大鼠空肠收缩的平均幅度(0.24±0.021和0.281±0.015),而在载体中则为(0.149±0.011)。 FRA(10μM)可能导致空肠收缩的最大幅度(0.281±0.015)。通过用对氯苯丙氨酸甲酯,WAY100635,酮色林,氟哌啶醇,SCH233390,舒必利,育亨宾而不是哌唑嗪预处理可预防FRA在FST中的抗固定作用。 FRA可以同时诱导运动和抗抑郁作用,值得进一步研究。

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