Abbasi-Maleki Saeid, Mousavi Zahra
Department of Pharmacology & Toxicology, Faculty of Veterinary Medicine, Urmia Branch, Islamic Azad University, Urmia, Iran.
Department of Pharmacology & Toxicology, Faculty of Pharmacy, Pharmaceutical Science Branch, Islamic Azad University, Tehran, Iran.
Iran J Basic Med Sci. 2017 Sep;20(9):1063-1073. doi: 10.22038/IJBMS.2017.9277.
Studies indicate that major deficiency in the levels of monoaminergic transmitters is a reason for severe depression. On the other hand, it is shown that L. (CT) may improve neuropsychological injuries by regulation of the monoamine transporter action. Hence, the present study was undertaken to evaluate the involvement of monoaminergic systems in antidepressant-like effect of CT extract in the tail suspension test (TST) in mice.
The mice were intraperitoneally (IP) treated with CT extract (100-400 mg/kg) 1 hr before the TST. To investigate the involvement of monoaminergic systems in antidepressant-like effect, the mice were treated with receptor antagonists 15 min before CT extract treatment (400 mg/kg, IP) and 1 hr before the TST.
Findings showed that CT extract (100-400 mg/kg, IP), dose-dependently induced antidepressant-like effect (<0.001), but it was not accompanied by alterations in spontaneous locomotor activity in the open-field test. Pretreatment of mice with SCH23390, sulpiride, haloperidol, WAY100135, cyproheptadine, ketanserin and p-chlorophenylalanine (PCPA) inhibited the antidepressant-like effect of CT extract (400 mg/kg, IP), but not with prazosin and yohimbine. Co-administration of CT extract (100 mg/kg, IP) with sub-effective doses of fluoxetine (5 mg/kg, IP) or imipramine (5 mg/kg, IP) increased their antidepressant-like response.
Our findings firstly showed that components (especially N-Hexadecanoic acid) of CT extract induce antidepressant-like effects by interaction with dopaminergic (D1 and D2) and serotonergic (5HT1A, 5-HT2A receptors) systems. These findings validate the folk use of CT extract for the management of depression.
研究表明单胺能递质水平的严重缺乏是重度抑郁症的一个原因。另一方面,已表明L.(CT)可通过调节单胺转运体的作用来改善神经心理损伤。因此,本研究旨在评估单胺能系统在CT提取物对小鼠悬尾试验(TST)的抗抑郁样作用中的参与情况。
在TST前1小时,给小鼠腹腔注射(IP)CT提取物(100 - 400 mg/kg)。为研究单胺能系统在抗抑郁样作用中的参与情况,在CT提取物处理(400 mg/kg,IP)前15分钟以及TST前1小时,给小鼠注射受体拮抗剂。
研究结果表明,CT提取物(100 - 400 mg/kg,IP)剂量依赖性地诱导抗抑郁样作用(<0.001),但在旷场试验中未伴有自发运动活动的改变。用SCH23390、舒必利、氟哌啶醇、WAY100135、赛庚啶、酮色林和对氯苯丙氨酸(PCPA)预处理小鼠可抑制CT提取物(400 mg/kg,IP)的抗抑郁样作用,但哌唑嗪和育亨宾则无此作用。CT提取物(100 mg/kg,IP)与亚有效剂量的氟西汀(5 mg/kg,IP)或丙咪嗪(5 mg/kg,IP)联合给药可增强它们的抗抑郁样反应。
我们的研究结果首次表明,CT提取物的成分(尤其是十六烷酸)通过与多巴胺能(D1和D2)和5-羟色胺能(5HT1A、5-HT2A受体)系统相互作用诱导抗抑郁样作用。这些研究结果证实了民间使用CT提取物治疗抑郁症的做法。