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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Characterization of the antinociceptive and anti-inflammatory activities of riboflavin in different experimental models.
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Characterization of the antinociceptive and anti-inflammatory activities of riboflavin in different experimental models.

机译:核黄素在不同实验模型中的镇痛和抗炎活性的表征。

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摘要

Riboflavin, similar to other vitamins of the B complex, presents anti-inflammatory activity but its full characterization has not yet been carried out. Therefore, we aimed to investigate the effect of this vitamin in different models of nociception, edema, fever and formation of fibrovascular tissue. Riboflavin (25, 50 or 100 mg/kg, i.p.) did not alter the motor activity of mice in the rota-rod or the open field models. The second phase of the nociceptive response induced by formalin in mice was inhibited by riboflavin (50 or 100 mg/kg). The first phase of this response and the nociceptive behavior in the hot-plate model were inhibited only by the highest dose of this vitamin. Riboflavin (25, 50 or 100 mg/kg, i.p.), administered immediately and 2 h after the injection of carrageenan, induced antiedema and antinociceptive effects. The antinociceptive effect was not inhibited by the pretreatment with cadmium sulfate (1 mg/kg), an inhibitor of flavokinase. Riboflavin (50 or 100 mg/kg, i.p., 0 and 2 h) also inhibited the fever induced by lipopolysaccharide (LPS) in rats. Moreover, the formation of fibrovascular tissue induced by s.c. implant of a cotton pellet was inhibited by riboflavin (50 or 100 mg/kg, i.p., twice a day for one week). Riboflavin (10 or 25 mg/kg, i.p.) also exacerbated the effect of morphine (2, 4 or 8 mg/kg, i.p.) in the mouse formalin test. In conclusion, the study demonstrates the antinociceptive and anti-inflammatory activities of riboflavin in different experimental models. These results, associated with the fact that riboflavin is a safe drug, is approved for clinical use and exacerbates the antinociceptive effect of morphine, may warrant clinical trials to assess its potential in the treatment of different painful or inflammatory conditions.
机译:核黄素与B复合物中的其他维生素类似,具有抗炎活性,但尚未完全表征。因此,我们旨在研究这种维生素在不同模型的伤害感受,水肿,发烧和纤维血管组织形成中的作用。核黄素(25、50或100 mg / kg,腹腔注射)在旋转棒或旷场模型中不会改变小鼠的运动活性。核黄素(50或100 mg / kg)抑制福尔马林在小鼠中引起的伤害感受反应的第二阶段。该反应的第一阶段和热板模型中的伤害感受行为仅受到最高剂量的这种维生素的抑制。角叉菜胶注射后立即和2小时服用核黄素(25、50或100 mg / kg,腹膜内),可引起抗水肿和抗伤害感受。用黄酮激酶抑制剂硫酸镉(1 mg / kg)进行预处理不会抑制其抗伤害作用。核黄素(50或100 mg / kg,i.p.,0和2 h)也抑制大鼠脂多糖(LPS)诱发的发烧。此外,皮下注射引起的血管组织的形成。核黄素(50或100 mg / kg,腹腔注射,每天两次,抑制一周)可抑制棉粒的植入。核黄素(10或25 mg / kg,腹膜内)在小鼠福尔马林试验中也加剧了吗啡(2、4或8 mg / kg,腹膜内)的作用。总之,该研究证明了核黄素在不同实验模型中的抗伤害性和抗炎活性。这些结果与核黄素是一种安全药物的事实有关,已被批准用于临床并加重吗啡的抗伤害感受作用,可能需要进行临床试验,以评估其在不同疼痛或炎性病症中的潜力。

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