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In the same model of asthma, a chimeric peptide constructed from modified NT and endomorphin-2 pharmacophores also reduced airway hyperresponsiveness, inflammatory cells influx in BALF, concentration of mouse mast cell protease, malondialdehyde, NF-B expression and secretory phospholipase 2 activity in lung tissue, as well as production of pro-inflammatory cytokines in BALF and lung [26]

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