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首页> 外文期刊>Journal of medicinal food >Anti-Inflammatory and Anti-Nociceptive Activities of Native and Modified Hen Egg White Lysozyme
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Anti-Inflammatory and Anti-Nociceptive Activities of Native and Modified Hen Egg White Lysozyme

机译:天然和修饰的鸡蛋清溶菌酶的抗炎和抗伤害活性

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Persistent inflammatory conditions can have severe pathological consequences. Although the use of nonsteroidal anti-inflammatory drugs (NSAIDs) is effective, it has side effects, particularly at the gastrointestinal level. There is then a high interest to identify natural anti-inflammatory compounds with no side effects. The anti-inflammatory and anti-nociceptive activities of hen egg lysozyme (LZ), both in its native form and modified by heat treatment, chemically or by enzymatic digestion have been tested in this study. The carrageenan-induced model in mice using native LZ or modified LZ has been applied. It was observed that LZ denatured by heat treatment at pH 6.0 presented 39.47% of inhibition of paw edema when administered at 30mg/kg. LZ denatured with DL-dithiothreitol (DTT) presented a significant result of 42.10% inhibition of paw edema when administered at 30mg/kg of animal weight. Modified LZ showed anti-inflammatory capacity comparable with the activity of the positive control dexamethasone. A classical model of acetic acid-induced abdominal writhing tests in mice was used to assess anti-nociceptive activity of native LZ and denatured heat treatment LZ and denatured chemical agent LZ. Finally, hydrolyzed native LZ presented 48% of inhibition of abdominal writhing in mice. Modified LZ with heat, chemical, and hydrolysis presented anti-inflammatory and anti-nociceptive activities independently of their natural enzymatic activity. These novel data point out the potential use of denatured and digested LZ as therapeutic agents and offer alternatives to the use of NSAIDs. LZ can be a natural source of anti-inflammatory and anti-nociceptive agents.
机译:持续的炎症会导致严重的病理后果。尽管使用非甾体类抗炎药(NSAIDs)是有效的,但它具有副作用,尤其是在胃肠道方面。因此,非常需要鉴定没有副作用的天然抗炎化合物。鸡蛋溶菌酶(LZ)的天然形式和通过热处理,化学或酶消化改性后的抗炎和抗伤害感受活性均已在本研究中进行了测试。已经应用了使用天然LZ或修饰的LZ在小鼠中由角叉菜胶诱导的模型。观察到当以30mg / kg施用时,通过在pH 6.0下热处理而变性的LZ表现出39.47%的抑制爪水肿。用DL-二硫苏糖醇(DTT)变性的LZ在以30mg / kg的动物体重施用时显示了42.10%的爪水肿抑制作用。修饰的LZ显示出与阳性对照地塞米松的活性相当的抗炎能力。使用小鼠乙酸诱发的腹部扭体试验的经典模型来评估天然LZ,变性热处理LZ和变性化学试剂LZ的抗伤害感受活性。最后,水解的天然LZ对小鼠腹部扭动具有48%的抑制作用。具有热,化学和水解作用的改性LZ呈现出抗炎和抗伤害感受活性,而与它们的天然酶活性无关。这些新颖的数据指出了变性和消化的LZ作为治疗剂的潜在用途,并为NSAID的使用提供了替代方法。 LZ可以是抗炎和抗伤害药的天然来源。

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