An aqueous pomegranate peel extract inhibits neutrophil myeloperoxidase in vitro and attenuates lung inflammation in mice

被引:83
作者
Bachoual, Rafik [1 ]
Talmoudi, Wifak [1 ]
Boussetta, Tarek [2 ,3 ]
Braut, Francoise [2 ,3 ]
El-Benna, Jamel [2 ,3 ]
机构
[1] Univ Gabes, Fac Sci Gabes, Gabes 6072, Tunisia
[2] Univ Paris 07, INSERM, U773, F-75018 Paris, France
[3] Univ Paris 07, Fac Med, F-75018 Paris, France
关键词
Punica granatum; Pomegranate; Inflammation; Neutrophils; ROS; MPO; OBSTRUCTIVE PULMONARY-DISEASE; AIRWAY INFLAMMATION; ANTIOXIDANT ACTIVITIES; OXIDATIVE STRESS; JUICE; ASTHMA; FRUIT; MACROPHAGES; PHAGOCYTES; CHALLENGES;
D O I
10.1016/j.fct.2011.02.024
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Punica granatum peel aqueous extract (PGE) is widely used to treat disorders such as inflammation, ulcers and infections, but its pharmacological target is not known. In this study we investigated the effect of PGE on human neutrophil reactive oxygen species (ROS) production in vitro and on LPS-induced lung inflammation in vivo in mice. Neutrophils were isolated and ROS generation was measured by luminol-amplified chemiluminescence. Superoxide anion generation was detected by the cytochrome c reduction assay. H(2)O(2) was detected by DCFH fluorescence assay. Myeloperoxidase (MPO) activity was measured by the tetramethyl benzidine oxidation method. Lung inflammation was induced in mice by LPS instillation. PGE inhibited luminol-amplified chemiluminescence of resting neutrophils and N-formyl-methionyl-leucyl-phenylalanine (fMLF)- or phorbol myristate acetate (PMA)-stimulated neutrophils, in a concentration-dependent manner. PGE had no effect on superoxide anion generation, suggesting that it does not directly inhibit NADPH oxidase activity or activation pathways, or scavenge superoxide anions. PGE did not scavenge H(2)O(2) but directly inhibited myeloperoxidase activity in vitro. In vivo studies showed that PGE also attenuated LPS-induced lung inflammation in mice. So this study reveals that PGE inhibits neutrophil MPO activity and attenuates LPS-induced lung inflammation in mice. Inhibition of MPO activity by PGE could explain its anti-inflammatory action. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1224 / 1228
页数:5
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