Exley C, Birchall J D
Institute of Aquaculture, University of Stirling, Scotland, U.K.
J Theor Biol. 1992 Nov 7;159(1):83-98. doi: 10.1016/s0022-5193(05)80769-6.
Aluminium is a serious environmental toxicant and is inimical to biota. Omnipresent, it is linked with a number of disorders in man including Alzheimer's disease, Parkinson's dementia and osteomalacia. Evidence supporting aluminium as an aetiological agent in such disorders is not conclusive and suffers principally from a lack of consensus with respect to aluminium's toxic mode of action. Obligatory to the elucidation of toxic mechanisms is an understanding of the biological availability of aluminium. This describes the fate of and response to aluminium in any biological system and is thus an important influence of the toxicity of aluminium. A general theme in much aluminium toxicity is an accelerated cell death. Herein mechanisms are described to account for cell death from both acute and chronic aluminium challenges. Aluminium associations with both extracellular surfaces and intracellular ligands are implicated. The cellular response to aluminium is found to be biphasic having both stimulatory and inhibitory components. In either case the disruption of second messenger systems is observed and GTPase cycles are potential target sites. Specific ligands for aluminium at these sites are unknown though are likely to be proteins upon which oxygen-based functional groups are orientated to give exceptionally strong binding with the free aluminium ion.
铝是一种严重的环境毒物,对生物群有害。它无处不在,与人类的多种疾病有关,包括阿尔茨海默病、帕金森痴呆症和骨软化症。支持铝作为这些疾病病因的证据并不确凿,主要问题在于对于铝的毒性作用方式缺乏共识。阐明毒性机制的关键在于了解铝的生物可利用性。这描述了铝在任何生物系统中的归宿和反应,因此是铝毒性的重要影响因素。铝毒性的一个普遍主题是细胞死亡加速。本文描述了急性和慢性铝挑战导致细胞死亡的机制。铝与细胞外表面和细胞内配体的结合都有涉及。发现细胞对铝的反应是双相的,具有刺激和抑制成分。在这两种情况下,都观察到第二信使系统的破坏,GTP酶循环是潜在的靶点。这些位点上铝的特异性配体尚不清楚,但可能是那些带有氧基官能团、能与游离铝离子形成异常强结合的蛋白质。