Serena Carolina, Calvo Enrique, Clares Mari Paz, Diaz María Luisa, Chicote Javier U, Beltrán-Debon Raúl, Fontova Ramón, Rodriguez Alejandro, García-España Enrique, García-España Antonio
Research Unit, Hospital Joan XXIII, Institut d'Investigació Sanitaria Pere Virgili (IISPV), Universitat Rovira i Virgili, Tarragona, Spain.
Instituto de Ciencia Molecular, Departamento de Química Inorgánica, Universidad de Valencia, Valencia, Spain.
PLoS One. 2015 Mar 5;10(3):e0119102. doi: 10.1371/journal.pone.0119102. eCollection 2015.
The clinical use of purified SOD enzymes has strong limitations due to their large molecular size, high production cost and immunogenicity. These limitations could be compensated by using instead synthetic SOD mimetic compounds of low molecular weight.
BACKGROUND/METHODOLOGY: We have recently reported that two SOD mimetic compounds, the Mn(II) complexes of the polyamines Pytren2Q and Pytren4Q, displayed high antioxidant activity in bacteria and yeast. Since frequently molecules with antioxidant properties or free-radical scavengers also have anti-inflammatory properties we have assessed the anti-inflammatory potential of Pytren2Q and Pytren4Q Mn(II) complexes, in cultured macrophages and in a murine model of inflammation, by measuring the degree of protection they could provide against the cellular injury produced by lipopolisacharide, a bacterial endotoxin.
In this report we show that the Mn(II) complex of Pytren4Q but not that of Pytren2Q effectively protected human cultured THP-1 macrophages and whole mice from the inflammatory effects produced by LPS. These results obtained with two molecules that are isomers highlight the importance of gathering experimental data from animal models of disease in assessing the potential of candidate molecules.
CONCLUSION/SIGNIFICANCE: The effective anti-inflammatory activity of the Mn(II) complex of Pytren4Q in addition to its low toxicity, water solubility and ease of production would suggest it is worth taking into consideration for future pharmacological studies.
纯化的超氧化物歧化酶(SOD)酶在临床应用中存在很大局限性,因其分子量大、生产成本高且具有免疫原性。使用低分子量的合成SOD模拟化合物可弥补这些局限性。
背景/方法:我们最近报道,两种SOD模拟化合物,即多胺Pytren2Q和Pytren4Q的锰(II)配合物,在细菌和酵母中显示出高抗氧化活性。由于具有抗氧化特性的分子或自由基清除剂通常也具有抗炎特性,我们通过测量它们对脂多糖(一种细菌内毒素)所产生的细胞损伤的保护程度,评估了Pytren2Q和Pytren4Q锰(II)配合物在培养的巨噬细胞和小鼠炎症模型中的抗炎潜力。
在本报告中,我们表明Pytren4Q的锰(II)配合物而非Pytren2Q的锰(II)配合物能有效保护人类培养的THP - 1巨噬细胞和整个小鼠免受脂多糖产生的炎症影响。这两个同分异构体分子所获得的结果凸显了在评估候选分子潜力时从疾病动物模型收集实验数据的重要性。
结论/意义:Pytren4Q的锰(II)配合物具有有效的抗炎活性,此外还具有低毒性、水溶性和易于生产的特点,这表明它值得在未来的药理学研究中加以考虑。