Alavinezhad Azam, Hedayati Mahdiyeh, Boskabady Mohammad Hossein
Neurogenic Inflammation Research Center, Department of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Avicenna J Phytomed. 2017 Nov-Dec;7(6):531-541.
The preventive effect of in animal models of asthma has been reported. In the present study, its effect on wheezing, forced expiratory volume in 1 second, and plasma nitrite (NO) in asthmatic patients was studied.
In this study, forty asthmatic patients including 15 males and 25 females (aged 45.8±6.21 years) were randomly allocated in four groups including placebo group (P), and three treatment groups which received two doses of (groups Z low and Z high that received 5 and 10 mg/kg/day, respectively) and carvacrol (group C treated with 1.2 mg/kg/day). All patients were treated for two months in a double-blind manner. At three time points (before starting the treatment (pretreatment), and one and two month after treatment), wheezing during day and exercise, forced expiratory volume in 1 second and NO were measured.
Day wheeze and exercise wheeze were significantly reduced in treated groups with carvacrol and both doses of compared to pretreatment (p<0.05 to p<0.01). However, FEV% was significantly increased in treated groups with carvacrol and both doses of (p<0.05 to p<0.001). Plasma level of NO was also significantly decreased in Z high and carvacrol groups after two months of treatment (p<0.01 to p<0.001). However, most of evaluated parameters in placebo group did not show significant changes during the study.
and its constituent, carvacrol, improved FEV% while reduced wheezing and plasma level of NO in asthmatic patients. Therefore, a possible therapeutic potential for this plant and its constituent, carvacrol could be suggested to be used against asthma.
已有报道称[具体物质]在哮喘动物模型中具有预防作用。在本研究中,研究了其对哮喘患者喘息、一秒用力呼气量和血浆亚硝酸盐(NO)的影响。
在本研究中,40例哮喘患者(包括15例男性和25例女性,年龄45.8±6.21岁)被随机分为四组,包括安慰剂组(P)和三个治疗组,三个治疗组分别接受两剂[具体物质](低剂量Z组和高剂量Z组,分别接受5和10mg/kg/天)以及香芹酚(C组,接受1.2mg/kg/天治疗)。所有患者均以双盲方式治疗两个月。在三个时间点(治疗开始前(预处理)、治疗后1个月和2个月),测量白天和运动时的喘息、一秒用力呼气量和NO。
与预处理相比,香芹酚治疗组以及两种剂量[具体物质]治疗组的白天喘息和运动性喘息均显著降低(p<0.05至p<0.01)。然而,香芹酚治疗组以及两种剂量[具体物质]治疗组的FEV%显著升高(p<0.05至p<0.001)。治疗两个月后,高剂量Z组和香芹酚组的血浆NO水平也显著降低(p<0.01至p<0.001)。然而,安慰剂组的大多数评估参数在研究期间未显示出显著变化。
[具体物质]及其成分香芹酚可改善哮喘患者的FEV%,同时减少喘息和血浆NO水平。因此,可认为该植物及其成分香芹酚具有对抗哮喘的潜在治疗作用。