The intake of β-sitosterol partially counteracts metformin beneficial effects in diet-induced obese rats

被引:0
|
作者
Reynes, Barbara [1 ,2 ,4 ]
Palou, Mariona [1 ,2 ,3 ,4 ]
Palou, Andreu [1 ,2 ,3 ]
Serra, Francisca [1 ,2 ,3 ,4 ]
机构
[1] Univ Balearic Isl, Lab Mol Biol Nutr & Biotechnol Nutrigen, Biomarkers & Risk Evaluat Grp, Palma De Mallorca 07122, Spain
[2] Balearic Isl IdISBa, Hlth Res Inst, Palma De Mallorca 07010, Spain
[3] Inst Salud Carlos III, CIBER Fisiopatol Obesidad & Nutr, Madrid 28029, Spain
[4] Univ Balearic Isl, Aliment SL, Spin Off 1, Palma De Mallorca 07121, Spain
关键词
Metformin; Sitosterol; Bioactive compounds; Insulin; HOMA-IR; Food intake; Hypothalamus; NEUROPEPTIDE-Y; GENE-EXPRESSION; LIPID-METABOLISM; LEPTIN RECEPTOR; FOOD-INTAKE; GLUCOSE; SUPPLEMENTATION; SENSITIVITY; MECHANISMS; LACTATION;
D O I
10.1016/j.jff.2022.105223
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Despite the high coexistence of hyperlipidaemia and the prediabetes state, little is known about the effects of the beta-sitosterol and metformin (MET) combination. This study aimed to evaluate the effects of low doses of MET (75 or 150 mg/kg bw; M75 or M150) on western-diet induced obese (WDIO) rats, in combination or not with beta-sitosterol (176 mg/kg bw; SIT and N-SIT, respectively). The gains of body weight and body fat mass, calorie food intake and plasma leptin were reduced in M150 animals, both SIT and N-SIT groups. Only N-SIT animals showed that insulin levels and HOMA-IR were reduced in the M150 group. M150 group showed a tendency towards lower mRNA levels of Npy and increased Lepr mRNA levels in hypothalamus, but only in N-SIT animals. In conclusion, these results show that the co-administration of MET with beta-sitosterol seems to neutralise part of the beneficial effects of MET in WDIO rats.
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收藏
页数:9
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