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Those in the model group received intraperitoneal injections of physiological saline vehicle solution instead.
Mice in model group received the 697 cells only by intravenous injection.
The treatment group received daily intraperitoneal injections of astragalus (0.03 ml/10 g.d), while the model group received injections of an equivalent volume of saline.
The treatment group received daily intraperitoneal injections of astragalus (0.03 ml/10 g.d), while the model group received an injection of an equivalent volume of saline.
The s.c. tumour model mice were treated via tail vein injection and the mice in the i.p. tumour model group received treatment by intraperitoneal injection.
The drug was infused to stomach of mice every morning, whereas the control group (wild type Kunming mice, n = 6) and the model group received no addition.
The sham-operated group and the model group received the same volume of water, and the Aspirin group was given the same volume of Aspirin solution (53.3 mg/kg) via oral gavage.
The mice in the infection model group received two intraperitoneal injections of 150 mg/kg cyclophosphamide (Jiangsu Hengrui Medicine Co., Ltd, Jiangsu, China) in sterile saline 2 days before and 1 day after fungal inoculation.
Rats in normal, shamed, and model group received 10 mL/kg of distilled water per day by oral administration, as well as 120 mg/kg berberine, 600 mg/kg CRAE, 270 mg/kg BB or 20 mg/kg TUDCA, respectively.
Control and model groups received an equivalent amount of normal saline.
Rabbits in the normal and AIA model groups received the same volume of normal saline.
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