Institute of Pharmaceutical Engineering, College of Chemical Engineering, Huaqiao University, Xiamen 361021, Fujian province, PR China.
Physiol Behav. 2011 Jan 10;102(1):1-6. doi: 10.1016/j.physbeh.2010.10.008. Epub 2010 Oct 15.
Nobiletin isolated from citrus peels up-regulates synaptic transmission and improves memory impairment in rodents. This study investigated the antidepressant-like effect of nobiletin in the forced swimming test (FST) and tail suspension test (TST) in mice. Additionally, the monoaminergic mechanisms involved in the antidepressant-like effect of nobiletin in mice were also assessed. Nobiletin (25, 50 and 100mg/kg, p.o.) decreased the immobility time in both the FST and TST without locomotor alterations in the open-field test (OFT). The anti-immobility effect of nobiletin (50mg/kg, p.o.) was completely prevented by the pretreatment of mice with WAY 100635 (0.1mg/kg, s.c., a serotonin 5-HT(1A) receptor antagonist), cyproheptadine (3mg/kg, i.p., a serotonin 5-HT(2) receptor antagonist), prazosin (62.5μg/kg, i.p., an α(1)-adrenoceptor antagonist), SCH23390 (0.05mg/kg, s.c., a dopamine D(1) receptor antagonist) or sulpiride (50mg/kg, i.p., a dopamine D(2) receptor antagonist). On the other hand, the pretreatment of mice with yohimbine (1mg/kg, i.p., an α(2)-adrenoceptor antagonist) or propranolol (5mg/kg, i.p., a β-adrenoceptor antagonist) did not block the antidepressant-like effect of nobiletin in the TST. Taken together, the data demonstrated that nobiletin produced an antidepressant-like effect that seems to be dependent on its interaction with the serotonergic, noradrenergic and dopaminergic systems. Thus, the present study suggests the therapeutic potential of this dietary flavonoid for the treatment of depression.
从柑橘皮中分离得到的诺必灵能上调突触传递,并改善啮齿动物的记忆障碍。本研究在小鼠的强迫游泳试验(FST)和悬尾试验(TST)中,考察了诺必灵的抗抑郁样作用。此外,还评估了诺必灵在小鼠中抗抑郁样作用的单胺能机制。诺必灵(25、50 和 100mg/kg,po)可降低 FST 和 TST 中的不动时间,而对开放场试验(OFT)中的运动能力没有影响。诺必灵(50mg/kg,po)的抗不动作用可被 WAY 100635(0.1mg/kg,sc,5-HT1A 受体拮抗剂)、赛庚啶(3mg/kg,ip,5-HT2 受体拮抗剂)、哌唑嗪(62.5μg/kg,ip,α1-肾上腺素受体拮抗剂)、SCH23390(0.05mg/kg,sc,多巴胺 D1 受体拮抗剂)或舒必利(50mg/kg,ip,多巴胺 D2 受体拮抗剂)预处理的小鼠完全阻断。另一方面,预先给予育亨宾(1mg/kg,ip,α2-肾上腺素受体拮抗剂)或普萘洛尔(5mg/kg,ip,β-肾上腺素受体拮抗剂)并不阻断诺必灵在 TST 中的抗抑郁样作用。综上所述,数据表明,诺必灵产生了一种抗抑郁样作用,这似乎依赖于其与 5-羟色胺能、去甲肾上腺素能和多巴胺能系统的相互作用。因此,本研究表明,这种饮食类黄酮具有治疗抑郁症的潜力。