The Role of Apolipoprotein E and Ethanol Exposure in Age-Related Changes in Choline Acetyltransferase and Brain-Derived Neurotrophic Factor Expression in the Mouse Hippocampus

• Published in: Journal of molecular neuroscience Vol. 65; no. 1; pp. 84 - 92
• Main Authors: Jamal, Mostofa, Ito, Asuka, Tanaka, Naoko, Miki, Takanori, Takakura, Ayaka, Suzuki, Shingo, Ameno, Kiyoshi, Kinoshita, Hiroshi
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.05.2018; Springer Nature B.V
• Subjects: Acetyltransferase; Age; Alcohols; Apolipoprotein E; Apolipoproteins; Biomedical and Life Sciences; Biomedicine; Brain; Brain-derived neurotrophic factor; Cell Biology; Choline; Choline O-acetyltransferase; Cognition; Cognitive ability; Ethanol; Exposure; Gene expression; Geriatrics; Hippocampus; Memory; Mice; mRNA; Neurochemistry; Neurodegeneration; Neurology; Neurosciences; Older people; Proteomics; Rodents; Western blotting; Aging; KO mice; Choline acetyltransferase; Brain-derived neurotrophic factor; Ethanol; ApoE-KO mice
• ISSN: 0895-8696; 1559-1166
• DOI: 10.1007/s12031-018-1074-6

Disruption of apolipoprotein E (APOE) is responsible for age-dependent neurodegeneration and cognitive impairment. Elderly individuals are more sensitive than young individuals to the effects of ethanol (EtOH), particularly those affecting cognition. We investigated the role of APOE deficiency and EtOH exposure on age-dependent alterations in choline acetyltransferase (ChAT) and brain-derived neurotrophic factor (BDNF) mRNA and protein expression in the mouse hippocampus. Three-month-old (young) and 12-month-old (aged) ApoE -knockout ( ApoE -KO) and wild-type (WT) mice were treated with saline or 2 g/kg EtOH, and the bilateral hippocampus was collected after 60 min for real-time PCR and western blotting analyses. ChAT ( P < 0.01) and BDNF ( P < 0.01) expression were significantly decreased in both young and aged saline- and EtOH-treated ApoE -KO mice versus young and aged saline- and EtOH-treated WT mice. Aged saline- and EtOH-treated ApoE -KO mice exhibited greater differences in ChAT and BDNF expression ( P < 0.01) than young saline- and EtOH-treated ApoE -KO mice. Aged EtOH-treated WT mice also exhibited larger decreases in BDNF expression ( P < 0.01)—but not in ChAT expression—than young EtOH-treated WT mice. EtOH decreased ChAT and BDNF expression in both young ( P < 0.01) and aged ( P < 0.01) ApoE -KO mice versus EtOH-free ApoE -KO mice of the same age. EtOH also decreased BDNF expression in aged ( P < 0.01) WT mice versus EtOH-free aged WT mice. In summary, these results suggest that APOE deficiency and EtOH exposure cause age-dependent decreases in ChAT and BDNF in the hippocampus. Importantly, the decreases in ChAT and BDNF were greater in aged EtOH-treated mice, particularly those lacking APOE, raising the possibility that APOE-deficient individuals who consume alcohol may be at greater risk of memory deficit.