Tubek Sławomir
Faculty of Physical Education and Physiotherapy, Institute of Technology-Opole, Prószkowska Street 76, 45-758 Opole, Poland.
Biol Trace Elem Res. 2007 Oct;119(1):1-9. doi: 10.1007/s12011-007-0043-7.
To accomplish its multifunctional biological roles, zinc requires precise homeostatic mechanisms. There are efficient mechanisms that regulate zinc absorption from the alimentary tract and its excretion by the kidney depending on the organism demands. The regulatory mechanisms of cellular zinc inflow, distribution, and zinc outflow are so efficient that symptoms of zinc deficiency are rare, and symptoms connected with its massive accumulation are even more rare. The efficiency of homeostatic mechanisms that prevent zinc deficiency or excessive zinc accumulation in the organism is genetically conditioned. It seems that an essential element of zinc homeostasis is the efficiency of zinc transmembrane exchange mechanisms. Intracellular free zinc concentration is higher than in extracellular space. Physiologically, the active outflow of zinc ions from the cell depends on the increase of its concentration in extracellular space. The ion pumps activity depends on the efficiency by which the cell manages energy. Considering the fact that zinc deficiency accelerates apoptosis and that excessive zinc accumulation inside cells results in a toxic effect that forces its death brings about several questions: Is intensification and acceleration of changes in zinc metabolism with age meaningful? Is there a real zinc deficiency occurring with age or in connection with the aforementioned pathological processes, or is it just a case of tissue and cell redistribution? When discussing factors that influence zinc homeostasis, can we consider zinc supplementation or regulation of zinc balance in the area of its redistribution? To clarify these aspects, an essential element will also be the clear understanding of the nomenclature used to describe changes in zinc balance. Zinc homeostasis can be different in different age groups and depends on sex, thus zinc dyshomeostasis refers to changes in its metabolism that deviate from the normal rates for a particular age group and sex. This concept is very ample and implies that zinc deficiency may result from a low-zinc diet, poor absorption, excessive loss of zinc, zinc redistribution in intra- and extracellular compartments, or a combination of these factors that is inadequate for the given age and sex group. Such factor or factors need to be considered for preventing particular homeostasis disorders (or dyshomeostasis). Regulation of zinc metabolism by influencing reversal of redistribution processes ought to be the main point of pharmacologic and nonpharmacologic actions to reestablish zinc homeostasis. Supplementation and chelation are of marginal importance and can be used to correct long-term dietary zinc deficiency or zinc poisoning or in some cases in therapeutic interventions. In view of its biological importance, the problem posed by the influence of zinc metabolism requires further investigation. To date, one cannot consider, for example, routine zinc supplementation in old age, because changes of metabolism with age are not necessarily a cause of zinc deficiency. Supplementation is warranted only in cases in which deficiency has been established unambiguously. An essential element is to prevent sudden changes in zinc metabolism, which lead to dyshomeostasis in the terms defined here. The primary prophylaxes, regular physical activity, efficient treatment of chronic diseases, are all elements of such prevention.
为实现其多功能的生物学作用,锌需要精确的稳态机制。机体存在有效的机制,可根据自身需求调节锌从消化道的吸收以及肾脏对锌的排泄。细胞锌流入、分布和流出的调节机制非常有效,以至于锌缺乏症状很少见,而与其大量蓄积相关的症状则更为罕见。预防机体锌缺乏或锌过度蓄积的稳态机制的效率是由基因决定的。锌跨膜交换机制的效率似乎是锌稳态的一个关键要素。细胞内游离锌浓度高于细胞外空间。生理上,锌离子从细胞的主动流出取决于其在细胞外空间浓度的增加。离子泵的活性取决于细胞管理能量的效率。鉴于锌缺乏会加速细胞凋亡,而细胞内锌的过度蓄积会导致毒性作用并促使细胞死亡,这引发了几个问题:随着年龄增长,锌代谢变化的加剧和加速是否有意义?随着年龄增长或与上述病理过程相关,是否真的存在锌缺乏,还是仅仅是组织和细胞的重新分布?在讨论影响锌稳态的因素时,我们能否考虑在锌重新分布方面进行锌补充或调节锌平衡?为阐明这些方面,一个关键要素还将是清楚理解用于描述锌平衡变化的术语。锌稳态在不同年龄组可能不同,并且取决于性别,因此锌稳态失调是指其代谢变化偏离特定年龄组和性别的正常速率。这个概念非常宽泛,意味着锌缺乏可能由低锌饮食、吸收不良、锌过度流失、锌在细胞内和细胞外区室的重新分布,或这些因素的组合导致,而这些因素对于给定的年龄和性别组来说是不足的。在预防特定的稳态紊乱(或稳态失调)时需要考虑这些因素。通过影响重新分布过程的逆转来调节锌代谢应该是恢复锌稳态的药理和非药理作用的重点。补充和螯合的重要性较小,可用于纠正长期的饮食锌缺乏或锌中毒,或在某些治疗干预中使用。鉴于其生物学重要性,锌代谢影响所带来的问题需要进一步研究。例如,到目前为止,不能考虑在老年人中常规补充锌,因为随着年龄增长的代谢变化不一定是锌缺乏的原因。仅在明确确定存在缺乏的情况下才需要补充。一个关键要素是防止锌代谢的突然变化,这会导致此处所定义的稳态失调。主要的预防措施,如有规律的体育活动、有效治疗慢性病,都是这种预防的要素。