Dhingra Dinesh, Valecha Rekha
Department of Pharmaceutical Sciences, Guru Jambheshwar University of Science and Technology , Hisar, Haryana , India.
Pharm Biol. 2014 Jun;52(6):767-74. doi: 10.3109/13880209.2013.870583. Epub 2014 Feb 21.
Boerhaavia diffusa Linn. (Nyctaginaceae) roots possess potent antioxidant, antistress, and anticonvulsant activities. It is used as a medicinal plant in Ayurvedic and natural herbal medicines.
To evaluate the effect of Boerhaavia diffusa root ethanol extract and its active constituent, punarnavine, on depression in Swiss albino mice.
Ethanol extract (50, 100, and 200 mg/kg, p.o.) and punarnavine (20 and 40 mg/kg, p.o.) were separately administered to 22 and 17 groups of mice, respectively, for 14 successive days followed by testing in the tail suspension and forced swim tests (FST). About 2% w/v gum acacia and double distilled water were used as controls for the extract and punarnavine, respectively.
Antidepressant-like effect of the lowest dose (50 mg/kg) of the extract and lower dose (20 mg/kg) of punarnavine were found to be comparable to fluoxetine. The ED50 value of the ethanol extract was 26.30 mg/kg (FST) and 33.11 mg/kg (tail suspension test); and of punarnavine was 15.14 mg/kg (FST) and 17.38 mg/kg (tail suspension test). The drugs did not show any significant effect on locomotor activities of mice. Prazosin (α1-adrenoceptor antagonist), sulpiride (selective D2-receptor antagonist), para-chlorophenylalanine) (p-CPA) (tryptophan hydroxylase inhibitor), and baclofen (GABAB agonist) significantly attenuated the extract and punarnavine induced-antidepressant-like effect in the tail suspension test. The extract and punarnavine also significantly reduced mouse brain monoamine oxidase (MAO)-A levels, but there was no significant effect on plasma corticosterone levels.
Ethanol extract of Boerhaavia diffusa and punarnavine produced an antidepressant-like effect in mice probably through interaction with monoaminergic and GABAergic systems.
胀果甘草(紫茉莉科)根具有强大的抗氧化、抗应激和抗惊厥活性。它在阿育吠陀医学和天然草药中用作药用植物。
评估胀果甘草根乙醇提取物及其活性成分胀果草碱对瑞士白化小鼠抑郁的影响。
分别给22组和17组小鼠连续14天口服乙醇提取物(50、100和200mg/kg)和胀果草碱(20和40mg/kg),随后进行悬尾试验和强迫游泳试验(FST)。分别用约2%w/v阿拉伯胶和双蒸水作为提取物和胀果草碱的对照。
提取物最低剂量(50mg/kg)和胀果草碱较低剂量(20mg/kg)的抗抑郁样作用与氟西汀相当。乙醇提取物的半数有效剂量(ED50)在强迫游泳试验中为26.30mg/kg,在悬尾试验中为33.11mg/kg;胀果草碱在强迫游泳试验中为15.14mg/kg,在悬尾试验中为17.38mg/kg。这些药物对小鼠的运动活动没有显著影响。哌唑嗪(α1肾上腺素能受体拮抗剂)、舒必利(选择性D2受体拮抗剂)、对氯苯丙氨酸(p-CPA)(色氨酸羟化酶抑制剂)和巴氯芬(GABAB激动剂)在悬尾试验中显著减弱了提取物和胀果草碱诱导的抗抑郁样作用。提取物和胀果草碱还显著降低了小鼠脑单胺氧化酶(MAO)-A水平,但对血浆皮质酮水平没有显著影响。
胀果甘草乙醇提取物和胀果草碱可能通过与单胺能和GABA能系统相互作用在小鼠中产生抗抑郁样作用。