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. 2017 Jul 25;7:6413. doi: 10.1038/s41598-017-06844-2

Table 1.

The effect of hyperoside pre-treatment on proteinuria, glucose and lipid metabolism, blood pressure, serum RAS and ROS in DN mice (n = 15).

Index Control DN LHPS HHPS
UmAlb/Cr (mg/g) 16.5 ± 3.8 115.4 ± 14.2a 98.5 ± 10.5a 68.6 ± 7.3a,b
FBG (mmol/L) 5.7 ± 0.8 15.8 ± 2.8a 15.7 ± 2.4a 15.4 ± 3.3a
HbA1c (%) 5.6 ± 0.8 10.5 ± 1.5a 10.2 ± 1.4a 10.3 ± 1.2a
MAP (mmHg) 80.2 ± 5.8 82.6 ± 6.6 82.6 ± 5.4 82.3 ± 5.8
TC (mmol/L) 4.2 ± 0.5 4.9 ± 0.6 4.5 ± 0.7 4.6 ± 0.6
LDL (mmol/L) 2.3 ± 0.5 3.1 ± 0.6a 2.9 ± 0.5a 3.0 ± 0.5a
Ang II (pg/ml) 52.8 ± 7.3 68.3 ± 11.2a 66.4 ± 10.4a 62.7 ± 9.8a
Aldosterone (pg/ml) 108.4 ± 11.6 128.5 ± 10.4a 125.2 ± 11.6a 124.6 ± 13.5a
MDA (µmol/L) 3.2 ± 0.4 9.7 ± 1.5a 6.4 ± 0.8a,b 5.2 ± 0.7a,b
SOD (mU/L) 48.3 ± 6.5 22.3 ± 4.1a 34.5 ± 6.2a,b 40.6 ± 5.7a,b

Control: Normal mice; DN: DM mice were treated with vehicle solution; LHPS and HHPS: DM mice were treated with 10 or 30 mg/kg/d hyperoside for four weeks from two weeks after DM establishment respectively. Data are presented as mean ± SD. P < 0.05 is statistically significant. aIndicates significant vs. Control, bindicates significant vs. DN.