首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Structure-specific adipogenic capacity of novel, well-defined ternary Zn(II)-Schiff base materials. Biomolecular correlations in zinc-induced differentiation of 3T3-L1 pre-adipocytes to adipocytes
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Structure-specific adipogenic capacity of novel, well-defined ternary Zn(II)-Schiff base materials. Biomolecular correlations in zinc-induced differentiation of 3T3-L1 pre-adipocytes to adipocytes

机译:新型,定义明确的三元Zn(II)-Schiff基础材料的结构特异性成脂能力。锌诱导的3T3-L1前脂肪细胞分化为脂肪细胞的生物分子相关性

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Among the various roles of zinc discovered to date, its exogenous activity as an insulin mimetic agent stands as a contemporary challenge currently under investigation and a goal to pursue in the form of a metallodrug against type 2 Diabetes Mellitus. Poised to investigate the adipogenic potential of Zn(II) and appropriately configure its coordination sphere into well-defined anti-diabetic forms, (a) a series of new well-defined ternary dinuclear Zn(II)-L (L = Schiff base ligands with a variable number of alcoholic moieties) compounds were synthesized and physicochemically characterized, (b) their cytotoxicity and migration effect(s) in both pre- and mature adipocytes were assessed, (c) their ability to effectively induce cell differentiation of 3T3-L1 pre-adipocytes into mature adipocytes was established, and (d) closely linked molecular targets involving or influenced by the specific Zn(II) forms were perused through molecular biological techniques, cumulatively delineating factors involved in Zn(II)-induced adipogenesis. Collectively, the results (a) reveal the significance of key structural features of Schiff ligands coordinated to Zn(II), thereby influencing its (a)toxicity behavior and insulin-like activity, (b) project molecular targets influenced by the specific forms of Zn(II) formulating its adipogenic potential, and (c) exemplify the interwoven relationship between Zn(II)-L structural speciation and insulin mimetic biological activity, thereby suggesting ways of fine tuning structure-specific zinc-induced adipogenicity in future efficient antidiabetic drugs. (C) 2015 Elsevier Inc. All rights reserved.
机译:在迄今为止发现的锌的各种作用中,其作为胰岛素模拟剂的外源活性是当前正在研究中的当代挑战,并且是以金属药物的形式追求针对2型糖尿病的目标。准备研究Zn(II)的成脂潜力并适当地将其配位域配置为明确的抗糖尿病形式,(a)一系列新的明确的三元双核Zn(II)-L(L = Schiff碱配体(具有可变数量的醇部分)合成化合物并进行物理化学表征,(b)评估其在前脂肪细胞和成熟脂肪细胞中的细胞毒性和迁移效果,(c)有效诱导3T3-L1细胞分化的能力建立将前脂肪细胞转变为成熟脂肪细胞的方法,并(d)通过分子生物学技术研究涉及特定Zn(II)形式或受其影响的紧密联系的分子靶标,以累积描述Zn(II)诱导的脂肪形成的因子。总的来说,结果(a)揭示了与Zn(II)配位的席夫(Schiff)配体的关键结构特征的重要性,从而影响了(a)毒性行为和类胰岛素活性,(b)受特定形式的Zn影响的分子靶标Zn(II)发挥其成脂潜力,并且(c)举例说明Zn(II)-L结构形态与胰岛素模拟生物活性之间的交织关系,从而提出了微调结构特异性锌诱导的成脂性的方法,这些都是未来有效的抗糖尿病药物。 (C)2015 Elsevier Inc.保留所有权利。

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