Brain and behavior changes in 12-month-old Tg2576 and nontransgenic mice exposed to anesthetics

Abstract Inhaled anesthetics have been shown to increase the aggregation of amyloid beta in vitro through the stabilization of intermediate toxic oligomers, which are thought to contribute to neurocognitive dysfunction in Alzheimer's disease. Inhaled anesthetics may escalate cognitive dysfuncti...

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Published in:Neurobiology of aging Vol. 29; no. 7; pp. 1002 - 1010
Main Authors: Bianchi, Shannon L, Tran, Thuy, Liu, ChuiLiang, Lin, Susan, Li, Yujuan, Keller, Jason M, Eckenhoff, Roderic G, Eckenhoff, Maryellen F
Format: Journal Article
Language:English
Published: United States Elsevier Inc 01-07-2008
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Summary:Abstract Inhaled anesthetics have been shown to increase the aggregation of amyloid beta in vitro through the stabilization of intermediate toxic oligomers, which are thought to contribute to neurocognitive dysfunction in Alzheimer's disease. Inhaled anesthetics may escalate cognitive dysfunction through enhancement of these intermediate oligomer concentrations. We intermittently exposed 12-month-old Tg2576 transgenic mice and nontransgenic littermates to isoflurane and halothane for 5 days. Cognitive function was measured before and after anesthetic exposures using the Morris Water Maze; amyloid beta plaque burden and caspase-3 mediated apoptosis were quantified by immunohistochemistry. At 12 months of age, anesthetic exposure did not further enhance cognitive decline in the transgenic mice. Immunohistochemistry, however, revealed that the halothane-exposed Tg2576 mice had more amyloidopathy than the isoflurane treated mice or the nonexposed transgenic mice. Isoflurane exposure impaired cognitive function in the nontransgenic mice, implying an alternative pathway for neurodegeneration. These findings indicate that inhaled anesthetics influence cognition and amyloidogenesis, but that the mechanistic relationship remains unclear.
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Permanent Address: Department of Anesthesia, Second Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510120, China.
Present Address: National Institute of Dental and Craniofacial Research (NIDCR), Div. PNMB, Rm 1W15, National Institutes of Health, Bethesda, MD 20892-2190.
E-mail addresses: shannon.bianchi@uphs.upenn.edu (S.L. Bianchi), roderic.eckenhoff@uphs.upenn.edu (R.G. Eckenhoff), maryellen.eckenhoff@uphs.upenn.edu (M.F. Eckenhoff).
Permanent Address: Department of Anesthesia, T.C.M Hospital of Guangdong Province, Giangzhou 510120, China.
ISSN:0197-4580
1558-1497
DOI:10.1016/j.neurobiolaging.2007.02.009