Itthipanichpong Chandhanee, Ruangrungsi Nijsiri, Pattanaautsahakit Chararin
Department of Pharmacology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
J Med Assoc Thai. 2002 Jun;85 Suppl 1:S344-54.
Examination of chemical compositions of essential oil distilled from the fruit of Zanthoxylum limonella Alston (Rutaceae) revealed the presence of 33 chemical components. Evaluation of the oil composition was achieved by GC/MS analysis. Limonene (31.09%), terpin-4-ol (13.94%) and sabinene (9.13%) were found to be the major components. Effects of essential oil have been performed in isolated guinea pig ileum, rat thoracic aorta and conscious mice. The essential oil at the concentration of 7.68 x 10(-5)-1.92 x 10(-3) microl/25 ml, produced dose-dependent contraction of the isolated rat thoracic aorta. These contractions were significantly reduced by pretreatment with prazosin (1 x 10(-7) M) and verapamil (1 x 10(-7) M). Its contraction was abolished in calcium free Krebs solution. Contractile response to the volatile oil (2 x 10(-6)-5.12 x 10(-4) microl/25 ml) was examined in isolated guinea pig ileum, it evoked ileal contraction in concentration-dependent manner and the contractions were suppressed after exposure to chlorpheniramine (1 x 10(-7) M) cypoheptadine (1 x 10(-7) M) atropine (1 x 10(-7) M) and verapamil (1 x 10(-7) M). Therefore, it could be concluded that the essential oil from the fruit of Zanthoxylum limonella possessed stimulation effect on different smooth muscle preparations by non-specific mechanisms. It involved the non receptor and receptor-mediated mechanism. Gastrointestinal stimulant effect of the essential oil was confirmed in intact mice since the oil significantly increased black ink movement from the stomach to ileo-caecal junction after oral feeding.
对山鸡椒(芸香科)果实中蒸馏得到的挥发油化学成分进行分析,结果显示其中含有33种化学成分。通过气相色谱/质谱联用(GC/MS)分析对该挥发油的成分进行了评估。发现柠檬烯(31.09%)、萜品-4-醇(13.94%)和桧烯(9.13%)为主要成分。对该挥发油的作用进行了离体豚鼠回肠、大鼠胸主动脉和清醒小鼠实验。该挥发油在浓度为7.68×10⁻⁵ - 1.92×10⁻³微升/25毫升时,可使离体大鼠胸主动脉产生剂量依赖性收缩。预先用哌唑嗪(1×10⁻⁷摩尔/升)和维拉帕米(1×10⁻⁷摩尔/升)处理可显著减弱这些收缩。在无钙的克雷布斯溶液中,其收缩作用消失。在离体豚鼠回肠中检测了该挥发油(2×10⁻⁶ - 5.12×10⁻⁴微升/25毫升)的收缩反应,它以浓度依赖性方式引起回肠收缩,且在暴露于氯苯那敏(1×10⁻⁷摩尔/升)、赛庚啶(1×10⁻⁷摩尔/升)、阿托品(1×10⁻⁷摩尔/升)和维拉帕米(1×10⁻⁷摩尔/升)后收缩受到抑制。因此,可以得出结论,山鸡椒果实挥发油通过非特异性机制对不同平滑肌制剂具有刺激作用。它涉及非受体和受体介导的机制。由于该挥发油在口服给药后能显著增加墨汁从胃向回盲部的移动,因此在完整小鼠中证实了其对胃肠道的刺激作用。