To investigate the effect of HDL on GW3965-induced neurorestoration, ABCA1−B/−B stroke mice were randomly assigned to two groups (total 18 mice, n=9/group) and intraventricularly-infused with artificial cerebrospinal-fluid (CSF, Tocris Bioscience) 100μl as vehicle control, or human-plasma HDL3 (hHDL3, Cell Biolabs Inc.) 25μg in 100μl artificial-CSF by transplanting a micro-osmotic pump (D1002, Alzet) into the right lateral-ventricle initiated at 24h after dMCAo for 14 days. All mice were sacrificed 14 days after dMCAo.
Investigating ABCA1/ApoE in GW3965-induced neurorestoration after stroke
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Corresponding Organization :
Other organizations : Oakland University, Henry Ford Health System
Protocol cited in 1 other protocol
Variable analysis
- Treatment with saline as vehicle control or GW3965 10mg/kg daily for 14 days
- Infusion of artificial cerebrospinal-fluid (CSF) or human-plasma HDL3 (hHDL3) 25μg in 100μl artificial-CSF for 14 days
- Protein expression (Western blot) and gene expression (RT-PCR)
- Behavioral testing
- Blood biochemistry
- Lesion volume and immunostaining measurements
- ABCA1^fl/fl and ABCA1^-B/-B stroke mice
- Randomization of mice into groups by a non-team member
- Not explicitly mentioned
- Saline as vehicle control for GW3965 treatment
- Artificial CSF as vehicle control for HDL3 infusion
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