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. 2013 May 27;2013:172537. doi: 10.1155/2013/172537

Table 4.

Effects of obesity, P. balsamifera, and salicortin treatments on tissue components involved in glucose and lipid homeostasis.

DIO P. balsamifera 125 mg/kg P. balsamifera 250 mg/kg DIO Salicortin 12.5 mg/kg
Muscle
 Glut4 150 ± 63 321 ± 174 151 ± 52 70 ± 33 59 ± 7
 pAkt/Akt 214 ± 59 195 ± 47 267 ± 82 96 ± 23 120 ± 29
 phospho p44/42 Mapk/44/42Mapk 178 ± 83 99 ± 15 273 ± 84 47 ± 11 146 ± 34§  
 pAMPk/AMPk 138 ± 43 79 ± 10 97 ± 22 108 ± 16 108 ± 22
 pACC/ACC 122 ± 28 171 ± 56 157 ± 38 106 ± 22 89 ± 26
 PPARα/β-actine 97 ± 23 229 ± 50§ 143 ± 44 195 ± 90 162 ± 69
 FAS/β-actine 118 ± 30 100 ± 39 77 ± 18 114 ± 16 143 ± 29

Liver
 pAkt/Akt 66 ± 14 139 ± 18* 124 ± 17* 106 ± 28 129 ± 37
 phospho p44/42 Mapk/44/42Mapk 68 ± 21 48 ± 21 66 ± 14 109 ± 35 96 ± 44
 pACC/ACC 105 ± 41 117 ± 74 114 ± 62 71 ± 26 77 ± 31
 PPARα/β-actine 63 ± 6 88 ± 20 75 ± 13 107 ± 26 147 ± 26
 UCP-2/β-actine 94 ± 19 107 ± 29 88 ± 26 151 ± 32 149 ± 27
 CPT-l/β-actine 84 ± 12 100 ± 8 86 ± 9 86 ± 6 83 ± 9
 FAS/β-actine 69 ± 17 69 ± 22 59 ± 25 86 ± 27 74 ± 15
 SREBPl-c/β-actine 88 ± 16 112 ± 27 121 ± 37 109 ± 14 109 ± 17
 CD36/β-actine 63 ± 7 93 ± 19 64 ± 3 69 ± 8 67 ± 6
 pIKKαβ/β-actine 108 ± 23 62 ± 31 75 ± 12 114 ± 21 129 ± 21

Adipose tissue
 pAkt/Akt 112 ± 13 186 ± 37
(P = 0.068)
110 ± 15 138 ± 18 109 ± 14
 phospho p44/42 Mapk/44/42Mapk 133 ± 31 103 ± 12 79 ± 10 156 ± 23 128 ± 21
 PPARγ/β-actine 73 ± 17 74 ± 15 102 ± 30 85 ± 12 116 ± 15
 pACC/ACC 139 ± 46 119 ± 66 157 ± 70 95 ± 30 86 ± 20
 CPT-l/β-actine 81 ± 9 86 ± 10 119 ± 19
(P = 0.079)
89 ± 11 99 ± 14
 FABP4/β-actine 85 ± 11 131 ± 11§ 136 ± 19§ 71 ± 6 83 ± 10
 FAS/β-actine 40 ± 5 33 ± 8 56 ± 11 49 ± 7 45 ± 7
 SREBP-1 c/β-actine 77 ± 6 88 ± 9 96 ± 19 86 ± 7 87 ± 11

Samples of muscle, liver, and WAT were obtained after 16 weeks of treatment with either standard diet (Chow), HFD (DIO), and for the last 8 of the 16 weeks with HFD in combination with P. balsamifera at 125 or 250 mg/kg, or with the active salicortin at 12.5 mg/kg. The samples were homogenized and analyzed by immunoblotting. Blots were quantified by densitometry. All values are expressed as percentage of respective Chow (reference set at 100%) and represent the mean ± SEM. The number of animals for each group for the P. balsamifera protocol was: CHOW (n = 12); DIO (n = 8); P. balsamifera 125 (n = 5); P. balsamifera 250 (n = 7); and for the salicortin protocol: CHOW (n = 12); DIO (n = 7); salicortin (n = 9). denotes DIO significantly different as compared to Chow (unpaired Student's t test; P < 0.05). *denotes significantly different as compared to respective DIO (one way ANOVA, Bonferroni post hoc test; P < 0.05).§denotes significantly different as compared to respective DIO (unpaired Student's t test; P < 0.05).