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某些4,2和5,2双噻唑衍生物对急性实验性炎症中硝基氧化应激和吞噬作用的影响。

The effect of some 4,2 and 5,2 bisthiazole derivatives on nitro-oxidative stress and phagocytosis in acute experimental inflammation.

作者信息

Araniciu Cătălin, Pârvu Alina Elena, Palage Mariana Doina, Oniga Smaranda Dafina, Benedec Daniela, Oniga Ilioara, Oniga Ovidiu

机构信息

Department of Therapeutic Chemistry, Faculty of Pharmacy, "Iuliu Haţieganu" University of Medicine and Pharmacy, 12 Ion Creanga Street, 400010 Cluj-Napoca, Romania.

Department of Physiopathology, Faculty of Medicine, "Iuliu Haţieganu" University of Medicine and Pharmacy, 2-4 Victor Babes Street, 400010 Cluj-Napoca, Romania.

出版信息

Molecules. 2014 Jul 2;19(7):9240-56. doi: 10.3390/molecules19079240.

Abstract

Nineteen bisthiazoles were tested in order to assess their anti-inflammatory and antioxidant properties. First, we evaluated the in vitro direct antioxidant capacity of the bisthiazoles using the DPPH radical scavenging method. Then, the anti-inflammatory effect was tested in acute rat experimental inflammation by measuring the acute phase bone marrow response, the phagocytic capacity and the serum nitro-oxidative stress status. Although none of the substances showed significant direct antioxidant potential in the DPPH assay, most of them improved serum oxidative status, when administered to rats with inflammation. Four of the bisthiazoles proved to have good anti-inflammatory properties, similar or superior to that of equal doses meloxicam.

摘要

为评估其抗炎和抗氧化特性,对19种双噻唑进行了测试。首先,我们使用DPPH自由基清除法评估了双噻唑的体外直接抗氧化能力。然后,通过测量急性期骨髓反应、吞噬能力和血清硝基氧化应激状态,在急性大鼠实验性炎症中测试了其抗炎作用。尽管在DPPH试验中没有一种物质显示出显著的直接抗氧化潜力,但当给炎症大鼠给药时,它们中的大多数改善了血清氧化状态。其中四种双噻唑被证明具有良好的抗炎特性,与等剂量美洛昔康相似或更优。

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