Faculty of Medical Sciences, Poznan University of Medical Sciences, 60-812 Poznan, Poland.
Department of Bromatology, Poznan University of Medical Sciences, 60-354 Poznan, Poland.
Nutrients. 2021 Jun 11;13(6):2023. doi: 10.3390/nu13062023.
Numerous studies indicate that zinc and the new zinc-related adipokine, zinc-α2-glycoprotein (ZAG), are involved in lipid metabolism. Excess body fat lowers blood concentrations of Zn and ZAG, leading not only to the development of obesity but also to other components of the metabolic syndrome. Zinc homeostasis disorders in the body negatively affect the lipid profile and cytokine secretion. Zinc appears to be a very important ZAG homeostasis regulator. The physiological effects of ZAG are related to lipid metabolism, but studies show that ZAG also affects glucose metabolism and is linked to insulin resistance. ZAG has a zinc binding site in its structure, which may indicate that ZAG mediates the effect of zinc on lipid metabolism. The review aimed to verify the available studies on the effects of zinc and ZAG on lipid metabolism. A literature review within the scope of this research area was conducted using articles available in PubMed (including MEDLINE), Web of Science and Cochrane Library databases. An analysis of available studies has shown that zinc improves hepatic lipid metabolism and has an impact on the lipid profile. Numerous studies have found that zinc supplementation in overweight individuals significantly reduced blood levels of total cholesterol, LDL (Low-density lipoprotein)cholesterol and triglycerides, potentially reducing cardiovascular morbidity and mortality. Some results also indicate that it increases HDL-C (High-density lipoprotein) cholesterol levels. ZAG has been shown to play a significant role in reducing obesity and improving insulin sensitivity, both in experimental animal model studies and in human studies. Furthermore, ZAG at physiologically relevant concentrations increases the release of adiponectin from human adipocytes. In addition, ZAG has been shown to inhibit in vitro leptin production. Further studies are needed to provide more data on the role of zinc and zinc-α2-glycoprotein.
大量研究表明,锌和新的锌相关脂肪因子,锌-α2-糖蛋白(ZAG),参与脂质代谢。体脂过多会降低血液中的锌和 ZAG 浓度,不仅导致肥胖的发展,还导致代谢综合征的其他成分。体内锌平衡紊乱会对脂质谱和细胞因子分泌产生负面影响。锌似乎是 ZAG 平衡的非常重要的调节剂。ZAG 的生理作用与脂质代谢有关,但研究表明 ZAG 还影响葡萄糖代谢,并与胰岛素抵抗有关。ZAG 在其结构中具有锌结合位点,这可能表明 ZAG 介导了锌对脂质代谢的影响。本综述旨在验证有关锌和 ZAG 对脂质代谢影响的现有研究。在 PubMed(包括 MEDLINE)、Web of Science 和 Cochrane Library 数据库中检索了本研究领域内的文献,进行了文献综述。对现有研究的分析表明,锌可改善肝脏脂质代谢,并对脂质谱产生影响。许多研究发现,超重人群补充锌可显著降低总胆固醇、LDL(低密度脂蛋白)胆固醇和甘油三酯的血液水平,从而降低心血管发病率和死亡率。一些结果还表明,它可以增加 HDL-C(高密度脂蛋白)胆固醇水平。ZAG 在减少肥胖和改善胰岛素敏感性方面,无论是在实验动物模型研究还是在人类研究中,都发挥了重要作用。此外,在生理相关浓度下,ZAG 可增加人脂肪细胞中脂联素的释放。此外,ZAG 已被证明可抑制体外瘦素的产生。需要进一步的研究来提供更多关于锌和锌-α2-糖蛋白作用的数据。