The bio-distribution of [3H]PF-7191 in rat brain was determined through an ex vivo binding study.
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 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.
The rat brain was preconditioned with 1 U thrombin by direct infusion into the left caudate nucleus.
Fos expression in the rat brain was detected by means of the immunohistochemical technique with a rabbit polyclonal antiserum directed against Fos protein (residues 4 17 of human Fos).
In addition, [14C]phenylacetate uptake in the rat brain was compared by autoradiography with that of [14C]acetate following the injection of fluorocitrate, a selective glial toxin, into the brain.
We investigated the effect of the anaesthetic isoflurane on the uptake of FDG in the rat brain, and a clear and significant impact of the isoflurane on the regional distribution of FDG uptake in the rat brain was observed.
