Jabri Mohamed-Amine, Sani Mamane, Rtibi Kais, Marzouki Lamjed, El-Benna Jamel, Sakly Mohsen, Sebai Hichem
Laboratoire de Physiologie Intégrée, Faculté des Sciences de Bizerte, 7021, Zarzouna, Tunisia.
Laboratoire de Physiologie Fonctionnelle et Valorisation des Bio-Ressources - Institut, Supérieur de Biotechnologie de Béja, Université de Jendouba, Avenue Habib Bourguiba, B.P. 382-9000, Béja, Tunisia.
Lipids Health Dis. 2016 Mar 31;15:65. doi: 10.1186/s12944-016-0233-4.
The aim of this study was to evaluate the protective effects of subacute pre-treatment with chamomile (Matricaria recutita L.) decoction extract (CDE) against stimulated neutrophils ROS production as well as ethanol (EtOH)-induced haematological changes and erythrocytes oxidative stress in rat.
Neutrophils were isolated and ROS generation was measured by luminol-amplified chemiluminescence. Superoxide anion generation was detected by the cytochrome c reduction assay. Adult male wistar rats were used and divided into six groups of ten each: control, EtOH, EtOH + various doses of CDE (25, 50, and 100 mg/kg, b.w.), and EtOH+ ascorbic acid (AA). Animals were pre-treated with CDE extract during 10 days.
We found that CDE inhibited (P ≤ 0.0003) luminol-amplified chemiluminescence of resting neutrophils and N-formyl methionylleucyl-phenylalanine (fMLF) or phorbolmyristate acetate (PMA) stimulated neutrophils, in a dose-dependent manner. CDE had no effect on superoxide anion, but it inhibited (P ≤ 0.0004) H2O2 production in cell free system. In vivo, CDE counteracted (P ≤ 0.0034) the effect of single EtOH administration which induced (P < 0.0001) an increase of white blood cells (WBC) and platelets (PLT) counts. Our results also demonstrated that alcohol administration significantly (P < 0.0001) induced erythrocytes lipoperoxidation increase and depletion of sulfhydryl groups (-SH) content as well as antioxidant enzyme activities as superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx). More importantly, we found that acute alcohol administration increased (P < 0.0001) erythrocytes and plasma hydrogen peroxide (H2O2), free iron, and calcium levels while the CDE pre-treatment reversed increased (P ≤ 0.0051) all these intracellular disturbances.
These findings suggest that CDE inhibits neutrophil ROS production and protects against EtOH-induced haematologiacal parameters changes and erythrocytes oxidative stress. The haematoprotection offered by chamomile might involve in part its antioxidant properties as well as its opposite effect on some intracellular mediators such as H2O2, free iron, and calcium.
本研究旨在评估用洋甘菊(母菊)水煎剂提取物(CDE)进行亚急性预处理对刺激的中性粒细胞活性氧生成的保护作用,以及对大鼠乙醇(EtOH)诱导的血液学变化和红细胞氧化应激的保护作用。
分离中性粒细胞,通过鲁米诺增强化学发光法测量活性氧生成。通过细胞色素c还原试验检测超氧阴离子生成。使用成年雄性Wistar大鼠,将其分为六组,每组十只:对照组、乙醇组、乙醇 + 不同剂量的CDE(25、50和100毫克/千克,体重)组,以及乙醇 + 抗坏血酸(AA)组。动物用CDE提取物预处理10天。
我们发现CDE以剂量依赖的方式抑制(P≤0.0003)静息中性粒细胞以及N - 甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLF)或佛波酯(PMA)刺激的中性粒细胞的鲁米诺增强化学发光。CDE对超氧阴离子没有影响,但它抑制(P≤0.0004)无细胞体系中过氧化氢的产生。在体内,CDE抵消(P≤0.0034)了单次给予乙醇诱导(P<0.0001)的白细胞(WBC)和血小板(PLT)计数增加的作用。我们的结果还表明,给予乙醇显著(P<0.0001)诱导红细胞脂质过氧化增加、巯基(-SH)含量减少以及超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPx)等抗氧化酶活性降低。更重要的是,我们发现急性给予乙醇会增加(P<0.0001)红细胞和血浆中的过氧化氢(H2O2)、游离铁和钙水平,而CDE预处理可逆转所有这些细胞内紊乱(P≤0.0051)。
这些发现表明CDE抑制中性粒细胞活性氧生成,并保护大鼠免受乙醇诱导的血液学参数变化和红细胞氧化应激的影响。洋甘菊提供血液保护作用可能部分涉及其抗氧化特性以及对某些细胞内介质如过氧化氢、游离铁和钙的相反作用。