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Under normal circumstances, there is a dynamic balance between fatty acid synthesis and oxidation, preventing intracellular lipid accumulation
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Western Blot Western blotting was carried out as described previously [21,22], and brain homogenates were lysed on ice for 30 min in 100 mL of lysis buffer (120 mM NaCl, 40 mM Tris (pH 8), and 0.1% NP40) and centrifuged at 12,000 rpm for 30 min
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