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Toxicology And Industrial Health • January 1998<br />

Neurobehavioral alteration in rodents<br />

following developmental exposure to aluminum<br />

Author information<br />

Alleva E1, Rankin J, Santucci D.<br />

Behavioural Pathophysiology Section<br />

Istituto Superiore di Sanità, Roma, Italy<br />

alleva@iss.it<br />

Abstract<br />

Aluminum (Al) is one of the most abundant metals in the earth’s crust, and humans can be<br />

exposed to it from several sources. It is present in food, water, pharmaceutical compounds,<br />

and in the environment, e.g., as a result of acid rain leaching it from the soil. Exposure to<br />

Al has recently been implicated in a number of human pathologies, but it has not yet been<br />

definitely proved that it plays a major causal role in any of them. In this paper we review the<br />

effects of developmental exposure of laboratory animals to Al salts as a model for human<br />

pathological conditions. The data presented show behavioral and neurochemical changes<br />

in the offspring of AL-exposed mouse dams during gestation, which include alterations in<br />

the pattern of ultrasonic vocalizations and a marked reduction in central nervous system<br />

(CNS) choline acetyltransferase activity. Prenatal Al also affects CNS cholinergic functions<br />

under Nerve Growth Factor (NGF) control, as shown by increased central NGF levels and<br />

impaired performances in a maze learning task in young-adult mice. The need for more<br />

detailed studies to evaluate the risks for humans associated with developmental exposure<br />

to Al, as well as the importance of using more than one strain of laboratory animal in the<br />

experimental design, is emphasized.<br />

http://www.ncbi.nlm.nih.gov/pubmed/9460176<br />

“The data presented show<br />

behavioral and neurochemical changes<br />

in the offspring of Aluminum-exposed mouse dams<br />

during gestation, which include alterations in the pattern<br />

of ultrasonic vocalizations and a marked reduction<br />

in central nervous system choline acetyltransferase<br />

activity. Prenatal Al also affects central nervous system<br />

cholinergic functions under Nerve Growth Factor (NGF)<br />

control, as shown by increased central NGF levels<br />

and impaired performances in a maze learning<br />

task in young-adult mice.”

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