Rabelo M, Souza E P, Soares P M G, Miranda A V, Matos F J A, Criddle D N
Laborat rio de Farmacologia dos Canais Iônicos, Departamento de Ciências Fisiológicas, Universidade Estadual do Ceará, Fortaleza, CE, Brasil.
Braz J Med Biol Res. 2003 Apr;36(4):521-4. doi: 10.1590/s0100-879x2003000400016. Epub 2003 Apr 8.
We have investigated the antinociceptive effects of the essential oil of Ocimum gratissimum L. (Labiatae) (EOOG) in two classical models of pain in male Swiss mice (25-35 g), the writhing test and the formalin test. At doses of 30, 100 and 300 mg/kg (po), EOOG produced a dose-dependent inhibition (from 58.3 4.4 to 40.7 6.3, 36.4 3.6 and 24.6 3.6, respectively; N = 8-10, P<0.05) of acetic acid-induced writhing, causing up to a ~60% inhibition at the highest dose used, comparable to that obtained with indomethacin (10 mg/kg, po). At the same doses, EOOG predominantly inhibited the late (inflammatory) phase of the formalin-induced pain response (from 59.3 8.3 to 40.4 4.8, 23.2 2.8 and 25.3 5.5, respectively; N = 6, P<0.05), with a maximal reduction of ~60% of the control, although a significant reduction of the initial (neurogenic) phase was also observed at 300 mg/kg (from 62.5 6.07 to 37 5.9; P<0.05). On the basis of these data, we conclude that EOOG possesses interesting antinociceptive properties in the writhing and formalin tests. Due to the relatively low toxicity of EOOG, further detailed examination is strongly indicated for a better characterization of its pharmacological properties and its potential therapeutic value.
我们研究了唇形科植物丁香罗勒(Ocimum gratissimum L.)精油(EOOG)对雄性瑞士小鼠(25 - 35克)两种经典疼痛模型——扭体试验和福尔马林试验的镇痛作用。在30、100和300毫克/千克(口服)剂量下,EOOG对醋酸诱导的扭体反应产生剂量依赖性抑制(分别从58.3±4.4降至40.7±6.3、36.4±3.6和24.6±3.6;N = 8 - 10,P<0.05),在最高使用剂量下抑制率高达约60%,与吲哚美辛(10毫克/千克,口服)相当。在相同剂量下,EOOG主要抑制福尔马林诱导的疼痛反应的晚期(炎症)阶段(分别从59.3±8.3降至40.4±4.8、23.2±2.8和25.3±5.5;N = 6,P<0.05),最大降低幅度约为对照组的60%,尽管在300毫克/千克剂量下也观察到初始(神经源性)阶段有显著降低(从62.5±6.07降至37±5.9;P<0.05)。基于这些数据,我们得出结论,在扭体试验和福尔马林试验中,EOOG具有显著的镇痛特性。由于EOOG毒性相对较低,强烈建议进一步详细研究以更好地表征其药理特性及其潜在治疗价值。