Dietary chia seed (Salvia hispanica L.) rich in α-linolenic acid improves adiposity and normalises hypertriacylglycerolaemia and insulin resistance in dyslipaemic rats

被引:127
作者
Chicco, Adriana G. [1 ]
D'Alessandro, Maria E. [1 ]
Hein, Gustavo J. [1 ]
Oliva, Maria E. [1 ]
Lombardo, Yolanda B. [1 ]
机构
[1] Univ Litoral, Sch Biochem, Dept Biochem, RA-3000 Santa Fe, Argentina
关键词
Dietary chia seed; Dyslipidaemia; Insulin resistance; Sucrose-rich diets; POLYUNSATURATED FATTY-ACIDS; HIGH SUCROSE DIET; LIPID-METABOLISM; FISH-OIL; OXIDATION ENZYMES; PERILLA OIL; GLUCOSE-INTOLERANCE; GENE-EXPRESSION; BLOOD-LIPIDS; SECRETION;
D O I
10.1017/S000711450899053X
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The present study investigates the benefits of the dietary intake of chia seed (Salvia hispanica L.) rich in a-linolenic acid and fibre upon dyslipidaemia and insulin resistance (IR), induced by intake of a sucrose-rich (62.5 %) diet (SRD). To achieve these goals two sets of experiments were designed: (i) to study the prevention of onset of dyslipidaemia and IR in Wistar rats fed during 3 weeks with a SRD in which chia seed was the dietary source of fat; (ii) to analyse the effectiveness of chia seed in improving or reversing the metabolic abnormalities described above. Rats were fed a SRD during 3 months; by the end of this period, stable dyslipidaemia and IR were present in the animals. From months 3-5, half the animals continued with the SRD and the other half were fed a SRD in which the source of fat was substituted by chia seed (SRD + chia). The control group received a diet in which sucrose was replaced by maize starch. The results showed that: (i) dietary chia seed prevented the onset of dyslipidaemia and IR in the rats fed the SRD for 3 weeks - glycaemia did not change; (ii) dyslipidaemia and IR in the long-term SRD-fed rats were normalised without changes in insulinaemia when chia seed provided the dietary fat during the last 2 months of the feeding period. Dietary chia seed reduced the visceral adiposity present in the SRD rats. The present study provides new data regarding the beneficial effect of chia seed upon lipid and glucose homeostasis in an experimental model of dislipidaemia and IR.
引用
收藏
页码:41 / 50
页数:10
相关论文
共 48 条
[1]  
[Anonymous], [No title captured]
[2]   Ground chia seed and chia oil effects on plasma lipids and fatty acids in the rat [J].
Ayerza, R ;
Coates, W .
NUTRITION RESEARCH, 2005, 25 (11) :995-1003
[3]   Polyunsaturated fatty acids: Biochemical, nutritional and epigenetic properties [J].
Benatti, P ;
Peluso, G ;
Nicolai, R ;
Calvani, M .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2004, 23 (04) :281-302
[4]   A high fructose diet affects the early steps of insulin action in muscle and liver of rats [J].
Bezerra, RMN ;
Ueno, M ;
Silva, MS ;
Tavares, DQ ;
Carvalho, CRO ;
Saad, MJA .
JOURNAL OF NUTRITION, 2000, 130 (06) :1531-1535
[5]   COMPARISON OF THE HEPATIC-UPTAKE AND PROCESSING OF CHOLESTEROL FROM CHYLOMICRONS OF DIFFERENT FATTY-ACID COMPOSITION IN THE RAT IN-VIVO [J].
BRAVO, E ;
ORTU, G ;
CANTAFORA, A ;
LAMBERT, MS ;
AVELLA, M ;
MAYES, PA ;
BOTHAM, KM .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1995, 1258 (03) :328-336
[6]  
BRONWYN A, 2000, AM J PHYSIOL-ENDOC M, V279, pE554
[7]   Conversion of α-linolenic acid to longer-chain polyunsaturated fatty acids in human adults [J].
Burdge, GC ;
Calder, PC .
REPRODUCTION NUTRITION DEVELOPMENT, 2005, 45 (05) :581-597
[8]   SELECTED PROPERTIES OF THE LIPID AND PROTEIN-FRACTIONS FROM CHIA SEED [J].
BUSHWAY, AA ;
WILSON, AM ;
HOUSTON, L ;
BUSHWAY, RJ .
JOURNAL OF FOOD SCIENCE, 1984, 49 (02) :555-557
[9]   Relationship to insulin resistance of the Adult Treatment Panel III diagnostic criteria for identification of the metabolic syndrome [J].
Cheal, KL ;
Abbasi, F ;
Lamendola, C ;
McLaughlin, T ;
Reaven, GM ;
Ford, ES .
DIABETES, 2004, 53 (05) :1195-1200
[10]   Troglitazone (CS-045) normalizes hypertriglyceridemia and restores the altered patterns of glucose-stimulated insulin secretion in dyslipidemic rats [J].
Chicco, A ;
Basabe, JC ;
Karabatas, L ;
Ferraris, N ;
Fortino, A ;
Lombardo, YB .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2000, 49 (10) :1346-1351