2007
DOI: 10.1016/j.jtemb.2007.09.010
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Analysis of brain regional distribution of aluminium in rats via oral and intraperitoneal administration

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Cited by 55 publications
(36 citation statements)
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References 20 publications
(18 reference statements)
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“…It can cross the blood-brain barrier and may be deposited in brain tissue [911]. It deposits in most areas of the brain (the cerebellum, ventral midbrain, cortex, hippocampus, and striatum), depending on the form of exposure: a greater and more significant increase was noted in the group of rats receiving aluminum via an intraperitoneal administration, then in rats receiving aluminum via an oral administration [9, 72, 73]. The neurodegenerative effects of the intracisternal injection of Al included the formation of intraneuronal neurofilamentous aggregates, oxidative stress, and apoptosis [74].…”
Section: Discussionmentioning
confidence: 99%
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“…It can cross the blood-brain barrier and may be deposited in brain tissue [911]. It deposits in most areas of the brain (the cerebellum, ventral midbrain, cortex, hippocampus, and striatum), depending on the form of exposure: a greater and more significant increase was noted in the group of rats receiving aluminum via an intraperitoneal administration, then in rats receiving aluminum via an oral administration [9, 72, 73]. The neurodegenerative effects of the intracisternal injection of Al included the formation of intraneuronal neurofilamentous aggregates, oxidative stress, and apoptosis [74].…”
Section: Discussionmentioning
confidence: 99%
“…This element has long been implicated in the pathogenesis of Alzheimer’s disease, but the precise mechanism of aluminum toxicity in this disease remains unknown [8]. Deposition can occur throughout the brain, as Al can cross the blood-brain barrier [911]. Disorders of steroidogenesis may arise through the deposition of Al in the hypothalamus and pituitary gland.…”
Section: Introductionmentioning
confidence: 99%
“…Unfortunately, the form by which aluminium crosses membranes and the intracellular consequences of the form remains largely speculative [18], but it is known that aluminium chemical speciation is a conditioner for its absorption and tissue distribution and accumulation [49]. Several chemical forms of aluminium such as aluminium maltol [21,23,50], aluminium chloride [13,51], aluminium hydroxide [52] and aluminium citrate [53][54][55] have been applied. In the present experiments, aluminium citrate was adopted because it is found to be next in order of abundance to the transferrin aluminium complex in the body [56,57].…”
Section: Discussionmentioning
confidence: 99%
“…Aluminium is toxic to all organisms [10]. Aluminium accumulates in all tissues of mammals such as the kidneys, liver, heart, blood, bones and brain [11][12][13]. Accumulation of aluminium in biological systems has been linked to disease conditions such as dialysis encephalopathy, renal osteodystrophy, hypochromic microcytic anemia [14][15][16].…”
Section: Introductionmentioning
confidence: 99%
“…Aluminium can cross and alter the blood-brain barrier (Yokel 2002), and differentiated distribution of aluminium in the distinct brain areas depends on the route of exposure (Sánchez-Iglesias et al 2007;Zatta et al 1993). It is known that aluminium exhibits very slow clearance from brain, but other organs also accumulate significant amounts of aluminium over time (Walker et al 1994;Yokel et al 2001).…”
mentioning
confidence: 99%