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Arch Pharm Res ; 42(12): 1063-1070, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31802426

ABSTRACT

Hesperetin, a major bioflavonoid in sweet oranges and lemons, exerts an anti-inflammatory effect in pulmonary diseases; however, its effect on lipopolysaccharide (LPS)-induced acute lung injury is unclear. This study investigated the effect of hesperetin on LPS-induced lung inflammatory response. Mice were intratracheally instilled with 5 mg/kg body weight LPS, and then were given hesperetin orally (10, 20, and 30 mg/kg body weight) 1 h later. Hesperetin dramatically suppressed the levels of interleukin-6 and tumor necrosis factor-α, as well as the number of inflammatory cells in bronchoalveolar lavage fluid. Besides, it reduced lung injury, wet weight/dry weight ratio, and myeloperoxidase and lactate dehydrogenase activities, and enhanced superoxide dismutase activity. In addition, hesperetin significantly downregulated the Toll-like receptor 4 (TLR4) and myeloid differentiation factor 88 (MyD88) protein expression and suppressed nuclear factor-kappa B (NF-κB) activation in lung tissue. Together, these results indicated that the anti-inflammatory effect of hesperetin is associated with the TLR4-MyD88-NF-κB pathway, and that hesperetin shows therapeutic potential for LPS-induced acute lung injury.


Subject(s)
Acute Lung Injury/drug therapy , Hesperidin/pharmacology , Lipopolysaccharides/antagonists & inhibitors , Myeloid Differentiation Factor 88/antagonists & inhibitors , Toll-Like Receptor 4/antagonists & inhibitors , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Acute Lung Injury/chemically induced , Acute Lung Injury/pathology , Animals , Dose-Response Relationship, Drug , Hesperidin/administration & dosage , Inflammation/chemically induced , Inflammation/drug therapy , Inflammation/pathology , Male , Mice , Mice, Inbred C57BL , Myeloid Differentiation Factor 88/metabolism , Signal Transduction/drug effects , Toll-Like Receptor 4/metabolism , Tumor Necrosis Factor-alpha/metabolism
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