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25 μg cefazolin/g and 0.1 μg buprenorphine/g mouse were administrated, and after surgery, one mouse per cage was housed.
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route, each mouse was administrated with 100 μL of recombinant AAV-GFP (5 × 10 vg/mL in PBS) into nostrils.
For oral route, each mouse was administrated with 100 μL of recombinant AAV-GFP (5 × 10 vg/mL in PBS) via gastric duodenal levin tube.
C13 Mab (0.5 mg per mouse) was administrated intraperitoneally on day 6, then followed by 0.25 mg C13 twice a week for 3 weeks.
NASH mice were administrated with or without DIM at different concentrations for 8 weeks.
Microarray was also applied in this study [70], and pregnant ICR mice were administrated with anatase TiO2 NPs.
6 h after injection, mice were administrated i.p. with drug cocktails (Combination and dosage of each compound was same as the above treatment) or saline.
When CP mice were administrated with IOP, the proportion of Bacteroidetes was increased with the increasing dose of IOP, but Firrmicutes was decreased.
In depressive behavior tests, the immobility time of forced swimming test (FST) and tail suspension test (TST) was increased when mice were administrated a single dose of LPS (0.83 mg/kg, i.p ., whereas these alterations were reversed by proanthocyanidin treatment (80 mg/kg, p.o).
For control groups, mice were administrated with 1X PBS.
Following weaning the mice were administrated IFG in drinking water under various specified regimens.
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