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. 2019 Jan 7;9:1520. doi: 10.3389/fphar.2018.01520

Table 1.

Details of animal experiments investigating the effects of rapamycin (RAPA) in atherosclerosis (AS).

Author and year Animal model Diet Duration Concentration Administration Lipid level
Decrease in AS lesion Elloso et al., 2003 ApoE KO C57 HF 12 weeks 1, 2, 4, and 8 mg/kg Oral Increase in LDLc and HDLc
Gadioli et al., 2009 ApoE KO C57 NC 12 weeks 5 mg/kg Oral Increase in TC
Castro et al., 2004 ApoE KO C57 HF 6 weeks 1 and 4 mg/kg Oral NS
Zhao et al., 2009 LDLR-deficient C57 HF 8 or 16 weeks 0.1, 0.3, and 1 mg/kg Oral NS
Liu et al., 2016 ApoE KO C57 HF 8 weeks Not noted Intra-peritoneal Not noted
Basso et al., 2003 ApoE KO C57 HF 12 weeks 4 mg/kg Oral Not noted
Enhance AS stability Chen et al., 2009 Rabbit HC 20 weeks 0.5 mg/kg Oral NS
Ma et al., 2017 ApoE KO C57 HF 8 weeks 0.5 mg/kg Oral Decrease in lipid levels
Decrease in AS lesion and enhance AS stability Luo Z. et al., 2017 ApoE KO C57 HF and HC 16 weeks 50 and 100 mg/kg Oral Not noted
Dou et al., 2016 ApoE KO C57 HF 12 weeks 1 and 3 mg/Kg Subcutaneously Increase in LDLc
Decrease eNOS expression Cheng et al., 2008 ApoE KO C57 HC 3–4 weeks 3 μg/kg, 3 mg/kg Oral Not noted

HF, high fat diet; NC, normal chow diet; HC, high cholesterol diet; LDLc, LDL-cholesterol; HDLc, HDL-cholesterol; TC, total cholesterol; NS, non-significant; AS, atherosclerosis.