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Each rat brain was cut into six sections and mouse brain into five sections.
The fluorescent visualisation of the whole rat brain was achieved using a simple low power handheld UV lamp [58].
These results indicated that mitochondria-mediated apoptosis in the rat brain was induced by TiO2 NPs [63].
The bio-distribution of [3H]PF-7191 in rat brain was determined through an ex vivo binding study.
The gold NP content in the rat brain was enhanced 24 h after the intravenous injection [31].
Besides, a decrease in mitochondrial DNA copy number and mitochondrial content in both regions of rat brain was observed.
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Alterations of H1R expression in the post-mortem rat brain were detected by [3H]-pyrilamine binding autoradiography.
Then, the pharmacokinetics of these candidate compounds in the rat brain were compared by ex vivo LC-MS/MS assays.
A set of in vivo 1H and 23Na axial images to cover the whole rat brain were obtained.
α4β2 nnAChRs from rat brain were expressed in Xenopus oocytes and studied using the two-electrode voltage-clamp technique.
For this, 400 µL of homogenized rat brain were mixed with 50 µL of extracts (500 1000 µg/mL) and incubated for 30 min at 37 °C.
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