Department of Pharmacology, Obafemi Awolowo University, Ile-Ife, 220005 Osun State, Nigeria.
Phytomedicine. 2013 Nov 15;20(14):1315-22. doi: 10.1016/j.phymed.2013.07.005. Epub 2013 Aug 3.
This study investigated the hypnotic, anti-convulsant and anxiolytic effects of 1-nitro-2-phenylethane (BPNE) obtained from the oil of Dennettia tripetala G. Baker (Annonaceae) and established its mechanism of action. The essential oil (EO) from the leaf, fruit and seed was obtained by hydrodistillation, followed by isolation of BPNE purified to 99.2% by accelerated gradient chromatography on silica, and identified by NMR and GC-MS. The pure BPNE and EO of the dried seed (93.6%) were comparatively evaluated for hypnotic, anticonvulsant and anxiolytic effects in mice. The acute toxicity of BPNE was determined and the LD50 was 490 mg/kg, intrapritonealy. The hypnotic activities of the EO and BPNE (50-400 mg/kg, i.p.) were assessed by loss of righting reflex, while sodium pentobarbitone (PBS) and diazepam (DZM) were used as positive controls. The anticonvulsant and anxiolytic effects of the EO and BPNE were evaluated in mice. Both BPNE and EO at doses ≥100 mg/kg induced spontaneous hypnosis with loss of righting reflex, significantly decreased sleep latency (SL) and also increased total sleeping time (TST) dose-dependently. They had comparable activity with NAP in TST. The BPNE exhibited higher hypnotic potency than EO at the same dose levels. The EO and BPNE offered comparable dose-related protections against PTZ- and strychnine-induced convulsions. Flumazenil (2 mg/kg) blocked the hypnotic and anticonvulsant (PTZ-convulsions) effects of both EO and BPNE. The essential oil at 5-20 mg/kg dose levels significantly (p<0.05) increased the percentage time spent and number of entries into the open arms. While at the same dose range BPNE significantly (p<0.05) increased the percentage time spent and the number of entries into the open arms respectively. The study concluded that 1-nitro-2-phenylethane exhibited dose dependent significant hypnotic, anticonvulsant and anxiolytic effects and it is the compound largely responsible for the neuropharmacological effects of the oil.
这项研究调查了从 Dennettia tripetala G. Baker(番荔枝科)油中获得的 1-硝基-2-苯乙烷(BPNE)的催眠、抗惊厥和抗焦虑作用,并确定了其作用机制。通过水蒸馏获得叶、果和种子的精油,然后通过硅胶加速梯度色谱分离出纯度为 99.2%的 BPNE,并通过 NMR 和 GC-MS 进行鉴定。比较评价了纯 BPNE 和干种子的精油(93.6%)在小鼠中的催眠、抗惊厥和抗焦虑作用。通过腹腔内给药测定 BPNE 的急性毒性,LD50 为 490mg/kg。通过翻正反射丧失评估精油和 BPNE(50-400mg/kg,腹腔内)的催眠活性,而戊巴比妥钠(PBS)和地西泮(DZM)用作阳性对照。评估了精油和 BPNE 在小鼠中的抗惊厥和抗焦虑作用。BPNE 和精油在≥100mg/kg 剂量下均诱导自发催眠,导致翻正反射丧失,显著降低睡眠潜伏期(SL),并呈剂量依赖性增加总睡眠时间(TST)。它们在 TST 中与 NAP 的活性相当。BPNE 在相同剂量水平下表现出比精油更高的催眠效力。精油和 BPNE 提供了可比的剂量相关保护作用,可对抗 PTZ 和士的宁引起的惊厥。氟马西尼(2mg/kg)阻断了精油和 BPNE 的催眠和抗惊厥(PTZ-惊厥)作用。在 5-20mg/kg 剂量水平下,精油显著(p<0.05)增加了进入开放臂的时间百分比和进入开放臂的次数。而在相同的剂量范围内,BPNE 分别显著(p<0.05)增加了进入开放臂的时间百分比和进入开放臂的次数。研究得出结论,1-硝基-2-苯乙烷表现出剂量依赖性的显著催眠、抗惊厥和抗焦虑作用,它是主要负责油的神经药理学作用的化合物。