TY - JOUR
T1 - Potent suppressive effects of 3-O-methylquercetin 5,7,3′,4′-O- tetraacetate on ovalbumin-induced airway hyperresponsiveness
AU - Jiang, Jiunn Song
AU - Chien, Hui Chi
AU - Chen, Chien Ming
AU - Lin, Chun Nan
AU - Ko, Wun Chang
PY - 2007/9
Y1 - 2007/9
N2 - We investigated the suppressive effects of 3-O-methylquercetin 5,7,3′,4′-O-tetraacetate (QMTA), a more-potent phosphodiesterase (PDE)3/4 inhibitor than quercetin 3-O-methyl ether (3-MQ), which has been reported to have the potential for treating asthma, against ovalbumin (OVA)-induced airway hyperresponsiveness (AHR). The IC50 value of QMTA for PDE3 was significantly less than that for PDE4. According to the Lineweaver-Burk analysis, QMTA (1-10 μM) competitively inhibited PDE3 and PDE4 activities. The Ki values were 0.9 ± 0.3 (n = 5) and 3.9 + 0.5 (n = 5) μM, respectively, which significantly differed from each other, suggesting that QMTA has higher affinity for PDE3 than for PDE4. QMTA (3-10 μM) concentration-dependently relaxed the baseline level, and significantly inhibited cumulative OVA (10-100 μg/mL)-induced contractions in isolated sensitized guinea pig trachealis suggesting that QMTA has bronchodilator and inhibiting effects on mast cell degranulation. After the secondary challenge, the AHR was measured in unrestrained OVA-sensitized mice, with nebulized methacholine (MCh, 6.25-50 mg/ mL), by barometric plethysmography using a whole-body Plethysmograph. In the present results, QMTA (3-10 μmol/kg, i.p.) dose-dependently attenuated the enhanced pause (Penh) value induced by MCh (25-50 mg/mL). QMTA (3-10 μmol/kg, i.p.) also significantly inhibited total inflammatory cells, macrophages, neutrophils, lymphocytes, and eosinophils in BALF after determination of Penh values. It also significantly suppressed the release of interleukin (IL)-2, IL-4, IL-5, IFN-γ, and TNF-α, with the exception that 3 μmol/kg QMTA did not suppress the releases of IL-5. QMTA even at 1 μmol/kg significantly inhibited eosinophils, IL-2, and TNF-α. In conclusion, our results strongly suggest that QMTA has greater potential than 3-MQ for the treatment of asthma.
AB - We investigated the suppressive effects of 3-O-methylquercetin 5,7,3′,4′-O-tetraacetate (QMTA), a more-potent phosphodiesterase (PDE)3/4 inhibitor than quercetin 3-O-methyl ether (3-MQ), which has been reported to have the potential for treating asthma, against ovalbumin (OVA)-induced airway hyperresponsiveness (AHR). The IC50 value of QMTA for PDE3 was significantly less than that for PDE4. According to the Lineweaver-Burk analysis, QMTA (1-10 μM) competitively inhibited PDE3 and PDE4 activities. The Ki values were 0.9 ± 0.3 (n = 5) and 3.9 + 0.5 (n = 5) μM, respectively, which significantly differed from each other, suggesting that QMTA has higher affinity for PDE3 than for PDE4. QMTA (3-10 μM) concentration-dependently relaxed the baseline level, and significantly inhibited cumulative OVA (10-100 μg/mL)-induced contractions in isolated sensitized guinea pig trachealis suggesting that QMTA has bronchodilator and inhibiting effects on mast cell degranulation. After the secondary challenge, the AHR was measured in unrestrained OVA-sensitized mice, with nebulized methacholine (MCh, 6.25-50 mg/ mL), by barometric plethysmography using a whole-body Plethysmograph. In the present results, QMTA (3-10 μmol/kg, i.p.) dose-dependently attenuated the enhanced pause (Penh) value induced by MCh (25-50 mg/mL). QMTA (3-10 μmol/kg, i.p.) also significantly inhibited total inflammatory cells, macrophages, neutrophils, lymphocytes, and eosinophils in BALF after determination of Penh values. It also significantly suppressed the release of interleukin (IL)-2, IL-4, IL-5, IFN-γ, and TNF-α, with the exception that 3 μmol/kg QMTA did not suppress the releases of IL-5. QMTA even at 1 μmol/kg significantly inhibited eosinophils, IL-2, and TNF-α. In conclusion, our results strongly suggest that QMTA has greater potential than 3-MQ for the treatment of asthma.
KW - 3-o-methylquercetin 5,7,3′,4′-o-tetraacetate
KW - Asthma
KW - Cytokines
KW - Inflammatory cells
KW - Ovalbumin
KW - Phosphodiesterase inhibitor
UR - http://www.scopus.com/inward/record.url?scp=35348836037&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=35348836037&partnerID=8YFLogxK
U2 - 10.1055/s-2007-981587
DO - 10.1055/s-2007-981587
M3 - Article
C2 - 17823872
AN - SCOPUS:35348836037
VL - 73
SP - 1156
EP - 1162
JO - Planta Medica
JF - Planta Medica
SN - 0032-0943
IS - 11
ER -