酚类牙科药物对大鼠牙髓和人血小板脂氧合酶的抑制作用。

Dentistry in Japan Pub Date : 1990-01-01
T Dohi, S Anamura, H Okamoto, A Tsujimoto
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引用次数: 0

摘要

研究了酚类牙科药物对大鼠牙髓和人血小板脂氧合酶活性的影响。[14C]花生四烯酸经大鼠牙髓匀浆得到的主要产物是12-HETE (15-HETE)。丁香酚和对氯酚的剂量依赖性抑制HETEs的形成。丁香酚和对氯酚的IC50值分别为0.62和0.34 mM。这些抑制脂加氧酶的化合物浓度与抑制环加氧酶所需的浓度相似。这些化合物也以相似的浓度范围抑制人血小板的12-脂氧合酶。结果表明,酚类牙科药物对牙髓和血小板脂氧合酶有抑制作用。因此,酚类牙科药物通过脂氧合酶途径抑制花生四烯酸代谢可能参与了这些药物在牙髓治疗中的镇痛和抗炎作用。
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Inhibition of lipoxygenase of rat dental pulp and human platelets by phenolic dental medicaments.

The effects of phenolic dental medicaments on lipoxygenase activities of rat dental pulp and human platelets were studied. The major product derived from [14C] arachidonic acid by the homogenate of rat dental pulp was 12-HETE (15-HETE). Eugenol and p-chlorophenol dose-dependently inhibited HETEs formation. The IC50 values of eugenol and p-chlorophenol were 0.62 and 0.34 mM respectively. The concentrations of these compounds that inhibit lipoxygenase were similar to those required to inhibit cyclooxygenase. These compounds also inhibited 12-lipoxygenase of human platelets with a similar range of concentrations. The results show that phenolic dental medicaments inhibit pulpal and platelet lipoxygenase. Thus, inhibition of arachidonic acid metabolism by phenolic dental medicaments via the lipoxygenase pathway may be involved in the analgesic and anti-inflammatory effects of the medicaments in endodontic therapy.

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