Mechanisms of aluminium neurotoxicity in oxidative stress-induced ...
Mechanisms of aluminium neurotoxicity in oxidative stress-induced ... Mechanisms of aluminium neurotoxicity in oxidative stress-induced ...
ABSTRACT CHAPTER 2 In the present work, accumulation and distribution of aluminium in the rat brain following both intraperitoneal and oral administration were studied. Male Sprague- Dawley rats received a daily i.p. injection of aluminium chloride (10 mg Al 3+ /kg/day) for one week or oral and progressively increasing administration of aluminium chloride and citric acid up to 100 and 356 mg/kg/day, respectively. Electrothermal atomic absorption spectrometry was used to determine aluminium concentration in different brain areas (cerebellum, ventral midbrain, cortex, hippocampus, and striatum). The results we obtained provided us insights about the most efficiency way for aluminium administration in neurochemical studies focused to investigate the ability of this metal to induce brain oxidative stress and consequently to cause neurodegeneration. Most of the brain areas showed accumulation of aluminium, but a greater and more significant increase was noted in the group receiving aluminium via intraperitoneal administration. Aluminium distribution was also dependent on the administration route. According to the here reported results, the intraperitoneal administration of aluminium was most effective in improving aluminium accumulation in the different areas of the rat brain. Our data suggest that aluminium neurotoxicity may be mediated by its particular distribution in specific brain areas. Keywords: Aluminium, brain distribution, intraperitoneal, oral, rat. 105
- Page 77 and 78: ALUMINIUM General features INTRODUC
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- Page 85 and 86: Excretion INTRODUCTION As insoluble
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- Page 89 and 90: INTRODUCTION Oteiza 1999), non-iron
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- Page 93 and 94: INTRODUCTION mobilization of Ca 2+
- Page 95: Aluminium impairs neurotransmission
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ABSTRACT<br />
CHAPTER 2<br />
In the present work, accumulation and distribution <strong>of</strong> <strong>alum<strong>in</strong>ium</strong> <strong>in</strong> the rat bra<strong>in</strong><br />
follow<strong>in</strong>g both <strong>in</strong>traperitoneal and oral adm<strong>in</strong>istration were studied. Male Sprague-<br />
Dawley rats received a daily i.p. <strong>in</strong>jection <strong>of</strong> <strong>alum<strong>in</strong>ium</strong> chloride (10 mg Al 3+ /kg/day)<br />
for one week or oral and progressively <strong>in</strong>creas<strong>in</strong>g adm<strong>in</strong>istration <strong>of</strong> <strong>alum<strong>in</strong>ium</strong> chloride<br />
and citric acid up to 100 and 356 mg/kg/day, respectively. Electrothermal atomic<br />
absorption spectrometry was used to determ<strong>in</strong>e <strong>alum<strong>in</strong>ium</strong> concentration <strong>in</strong> different<br />
bra<strong>in</strong> areas (cerebellum, ventral midbra<strong>in</strong>, cortex, hippocampus, and striatum). The<br />
results we obta<strong>in</strong>ed provided us <strong>in</strong>sights about the most efficiency way for <strong>alum<strong>in</strong>ium</strong><br />
adm<strong>in</strong>istration <strong>in</strong> neurochemical studies focused to <strong>in</strong>vestigate the ability <strong>of</strong> this metal<br />
to <strong>in</strong>duce bra<strong>in</strong> <strong>oxidative</strong> <strong>stress</strong> and consequently to cause neurodegeneration. Most <strong>of</strong><br />
the bra<strong>in</strong> areas showed accumulation <strong>of</strong> <strong>alum<strong>in</strong>ium</strong>, but a greater and more significant<br />
<strong>in</strong>crease was noted <strong>in</strong> the group receiv<strong>in</strong>g <strong>alum<strong>in</strong>ium</strong> via <strong>in</strong>traperitoneal adm<strong>in</strong>istration.<br />
Alum<strong>in</strong>ium distribution was also dependent on the adm<strong>in</strong>istration route. Accord<strong>in</strong>g to<br />
the here reported results, the <strong>in</strong>traperitoneal adm<strong>in</strong>istration <strong>of</strong> <strong>alum<strong>in</strong>ium</strong> was most<br />
effective <strong>in</strong> improv<strong>in</strong>g <strong>alum<strong>in</strong>ium</strong> accumulation <strong>in</strong> the different areas <strong>of</strong> the rat bra<strong>in</strong>.<br />
Our data suggest that <strong>alum<strong>in</strong>ium</strong> <strong>neurotoxicity</strong> may be mediated by its particular<br />
distribution <strong>in</strong> specific bra<strong>in</strong> areas.<br />
Keywords: Alum<strong>in</strong>ium, bra<strong>in</strong> distribution, <strong>in</strong>traperitoneal, oral, rat.<br />
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