铁代谢异常与β细胞功能改变和糖尿病发生损害的关联:一项系统综述

Kulvinder Kochar Kaur
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引用次数: 0

摘要

铁是一种与许多生理功能有关的基本元素。在胰腺β细胞中,它们是铁-S簇蛋白的组成部分,而铁-S簇蛋白是胰岛素生成和加工的必要条件。就线粒体而言,作为呼吸链的一个组成部分,它有助于ATP和活性氧(ROS)的产生,从而诱导β细胞去极化,从而导致钙基胰岛素释放的增强。重要的是,在铁细胞数量方面建立了一个明显的微调,以保证正常的铁供应,同时避免铁过载。实际上,考虑到与氧的巨大反应以及自由基的产生,铁超载可能导致细胞氧化损伤,鉴于ROS发育的正常升级以及抗氧化酶作用的可用性较低,对这种情况具有易感性的细胞。因此,我们利用常用的搜索引擎利用MeSH进行了系统的综述;铁代谢;糖尿病;haemochromatosis;thallasemia;阿尔茨海默病,帕金森病;弗里德里希的共济失调;铁稳态;铁结合蛋白;转铁结合铁(TBI);非TBINTBI);二价金属转运体I(DMT1);;运铁素胰岛淀粉样多肽;锌输送器zip14;伴侣蛋白-聚CR结合蛋白(PCBPs);mitoferrin (Mfrn);Fe-S簇-酶CDKAL1;hepcidin;hephaestin;frataxin;不稳定铁池;ABCT7;PDX1; MafA;博士学位;播出;Miner 1;妊娠DM;ferroptosis;;运铁素铁超载及治疗;脑毒性;GIT;从1980年到2022年至今。我们共找到4500篇文章,从中选择了135篇文章纳入本综述。未进行meta分析。本综述的主要目的是更好地了解β细胞中的铁稳态模式,以及在这种情况下它们的损伤模式的变化。异常的铁储存/伴侣蛋白如何导致糖尿病。
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Association of Iron Metabolism Abnormalities as Etiopathogenetic Factor in Alteration of Beta Cell Function and Impairment in Generation of Diabetes Mellitus: A Systematic Review
Iron constitutes an essential element that is implicated innumerous physiological functions. In the context of the pancreatic β cells, they act as components of the Fe –S cluster proteins, which are a must for the appropriate insulin generation and processing. As far as mitochondria are concerned , in the form of a constituent of the respiratory chain it aids in the generation of ATP along with Reactive oxygen species(ROS),that result in induction of β cells depolarization that causes potentiation of insulin liberation that is calcium based .It is of great importance that a marked fiine tuning gets established with regards to the iron cellular amounts to guarantee normal provision of Iron along with avoidance of iron overload. Actually, in view of the great reaction with oxygen in addition to the generation of free radicals , iron overload might result in Oxidative injury of cells that possess susceptibility to this situations in view of the normal escalation of ROS development besides lesser availability of antioxidant enzymes action .Thus here we conducted a systematic review utilizing usual search engine utilizing the MeSH; iron metabolism; DM; haemochromatosis; thallasemia; Alzheimer’s ;Parkinson’s disease ; Friedrich’s ataxia; Iron homeostasis; Iron binding protein; transferrin bound iron(TBI); non TBINTBI); Divalentmetal transporter I(DMT1); ferroportin; islet amyloid polypeptide; zinc transporter ZIP 14; Chaperone proteins- poly CR binding proteins(PCBPs); mitoferrin(Mfrn); Fe-S clusters - enzyme CDKAL1; hepcidin; hephaestin; frataxin ; labile iron pool (LIP); ABCT7; PDX1;MafA; PHD; MAMs; Miner 1;gestational DM; ferroptosis; ferroportin; iron overload &treatment ;toxicity in brain, GIT; from 1980 till 2022 till date. We found a total of 4500 articles out of which we selected 135 articles for this review. No meta-analysis was done. Main aim of this review was to get a better insight in mode of iron homeostasis in β cells, with mode of changed in this event in their damage. How abnormal iron storage/chaperon proteins might cause diabetes.
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