Laboratory of Ethnopharmacology, Institute of Integrated Traditional Medicine and Western Medicine, Xiangya Hospital, Central South University, Changsha 410008, China.
Phytomedicine. 2012 Sep 15;19(12):1101-7. doi: 10.1016/j.phymed.2012.05.015. Epub 2012 Jul 5.
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.
抑郁症患者从现有的抗抑郁药物中很难获得满意的疗效。为了获得更有效的治疗方法,研究了枳实(FRA)在大鼠强迫游泳试验(FST)和旷场试验(OFT)中的抗抑郁作用及其单胺能机制,以及其促动力作用。分别用 FST 和 OFT 评价 FRA 的抗抑郁作用和运动活性。观察了单胺受体拮抗剂对 FRA 诱导的大鼠抗抑郁作用的影响。评估了 FRA 对肠道转运、胃排空和离体空肠收缩活性的影响。FRA 显著降低 FST 中的不动时间(32.6±8.5、30.3±5.2 与 56.4±9.4,均 P<0.01),呈剂量依赖性增加运动活性(102±17.5、120±18.5 与 89±9.8,P<0.05 或 0.01),显著加速半液体餐的胃排空(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)。与载体相比,FRA(1 μM、10 μM)显著增加了大鼠空肠收缩的平均幅度(0.24±0.021 和 0.281±0.015),与载体(0.149±0.011)相比。FRA(10 μM)可引起空肠最大收缩幅度(0.281±0.015)。在 FST 中,FRA 的抗不动作用可被预用 p-氯苯丙氨酸甲酯、WAY100635、酮色林、氟哌啶醇、SCH233390、舒必利、育亨宾阻断,但不能被普萘洛尔阻断。FRA 可同时诱导促动力和抗抑郁作用,值得进一步研究。