Molecular Nutrition

Effects of Glucocorticoid and Dietary Fat Level on Lipid Metabolism of Broilers

Expand
  • Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, College of Animal Science, Shandong Agricultural University, Tai'an 271018, China

Received date: 2018-02-12

  Online published: 2018-09-20

Abstract

This study aimed to research the effects of glucocorticoid[dexamethasone (DEX)] and dietary fat level on lipid metabolism of broilers. A total of 200 Arbor Acre broilers with similar body weight were exposed to diets with high (HFD) or low fat level (LFD) from 22 days of age, each treatment had 100 broilers. The diets were fed from 22 to 38 days of age. At 35 to 38 days of age, broilers in each dietary treatment were divided into two sub-treatments, and broilers in which were subcutaneous injected DEX (2 mg/kg BW) and saline with equal volume. Each sub-treatment had 50 broilers. The results showed as follows:1) under the conditions of LFD and HFD, glucocorticoid both significantly decreased body weight and thigh muscle weight (P<0.05), and significantly raised liver proportion and blood concentration of triglyceride (TG) (P<0.05). 2) Under the condition of LFD, glucocorticoid significantly increased abdominal fat proportion and TG content in muscle (P<0.05). 3) Under the condition of HFD, glucocorticoid significantly increased carnitine palmitoyl transferase 1 (CPT1) content in abdominal fat and thigh muscle (P<0.05), while significantly decreased CPT1 content in liver and breast muscle (P<0.05). 4) There were overall up-regulated trends of expression levels of glucocorticoids receptor (GR), peroxisome proliferator-activated receptor α (PPARα) and fatty acid transport protein (FATP1) mRNAs in breast and abdominal fat after the treatment of glucocorticoid, while they were contrary for thigh muscle and liver. The results indicate that glucocorticoid may affect lipid metabolism through regulating GR, PPARα and FATP1, and facilitate the fat ectopic deposit in liver and muscle. High fat diet may activate CPT1 and lipid oxidation in abdominal fat and thigh muscle, thereby alleviate glucocorticoids' effect on fat deposition.

Cite this article

WANG Minghui, LIU Zhimei, WANG Haoqi, GUAN Jiajia, HU Qingmei, WANG Xiaojuan . Effects of Glucocorticoid and Dietary Fat Level on Lipid Metabolism of Broilers[J]. Chinese Journal of Animal Nutrition, 2018 , 30(9) : 3772 -3780 . DOI: 10.3969/j.issn.1006-267x.2018.09.049

References

[1] MUTRYN M F,BRANNICK E M,FU W X,et al.Characterization of a novel chicken muscle disorder through differential gene expression and pathway analysis using RNA-sequencing[J].BMC Genomics,2015,16(1):399.

[2] YAO L L,DU Q,YAO H D,et al.Roles of oxidative stress and endoplasmic reticulum stress in selenium deficiency-induced apoptosis in chicken liver[J].Biometals,2015,28(2):255-265.  

[3] HUANG C,JIAO H,SONG Z,et al.Heat stress impairs mitochondria functions and induces oxidative injury in broiler chickens[J].Journal of Animal Science,2015,93(5):2144-2153.  

[4] FALLAHSHAROUDI A,DE KOCK N,JOHNSSON M,et al.Genetic and targeted eQTL mapping reveals strong candidate genes modulating the stress response during chicken domestication[J].Genes,Genomes,Genetics,2017,7(2):497-504.

[5] BAZIZ H A,GERAERT P A,PADILHA J C F,et al.Chronic heat exposure enhances fat deposition and modifies muscle and fat partition in broiler carcasses[J].Poultry Science,1996,75(4):505-513.  

[6] BONNARD C,DURAND A,PEYROL S,et al.Mitochondrial dysfunction results from oxidative stress in the skeletal muscle of diet-induced insulin-resistant mice[J].Journal of Clinical Investigation,2008,118(2):789-800.

[7] ZHAO L Y,COZZO A J,JOHNSON A R,et al.Lack of myeloid Fatp1 increases atherosclerotic lesion size in Ldlr-/- mice[J].Atherosclerosis,2017,266:182-189.

[8] OKAMOTO S,SHIUCHI T,SUZUKI A,et al.Activation of AMP-kinase in the paraventricular hypothalamus increases the preference for high carbohydrate diet in mice[J].Diabetes,2007,56:402.

[9] LV Z P,PENG Y Z,ZHANG B B,et al.Glucose and lipid metabolism disorders in the chickens with dexamethasone-induced oxidative stress[J].Journal of Animal Physiology & Animal Nutrition,2018,102(2):e706-e717.

[10] GRIFFIN H D,WHITEHEAD C C.Plasma lipoprotein concentration as an indicator of fatness in broilers:development and use of a simple assay for plasma very low density lipoproteins[J].British Poultry Science,1982,23(4):307-313.  

[11] ZSCHUCKE E,RENNEBERG B,DIMEO F,et al.The stress-buffering effect of acute exercise:evidence for HPA axis negative feedback[J].Psychoneuroendocrinology,2015,51:414-425.

[12] JOSEPH D N,WHIRLEDGE S.Stress and the HPA axis:balancing homeostasis and fertility[J].International Journal of Molecular Sciences,2017,18(10):2224-2239.  

[13] LEFAI E,BLANC S,MOMKEN I,et al.Exercise training improves fat metabolism independent of total energy expenditure in sedentary overweight men,but does not restore lean metabolic phenotype[J].International Journal of Obesity,2017,41(12):1728-1736.  

[14] WANG X J,SONG Z G,JIAO H C,et al.Dexamethasone facilitates lipid accumulation in chicken skeletal muscle[J].Stress,2012,15(4):443-456.  

[15] WANG X J,LIN H,SONG Z G,et al.Dexamethasone facilitates lipid accumulation and mild feed restriction improves fatty acids oxidation in skeletal muscle of broiler chicks (Gallus gallus domesticus)[J].Comparative Biochemistry and Physiology Part C:Toxicology & Pharmacology,2010,151(4):447-454.  

[16] 李艳.糖皮质激素和热应激对蛋鸡肝脏脂肪代谢影响[D].硕士学位论文.泰安:山东农业大学,2011:45-48.

[17] MAPLES J M,BRAULT J J,WITCZAK C A,et al.Differential epigenetic and transcriptional response of the skeletal muscle carnitine palmitoyltransferase 1B (CPT1B) gene to lipid exposure with obesity[J].American Journal of Physiology Endocrinology & Metabolism,2015,309(4):E345-E356.

[18] STAHL A.A current review of fatty acid transport proteins (SLC27)[J].Pflügers Archiv,2004,447(5):722-727.  

[19] HARASIM E,KALINOWSKA A,CHABOWSKI A,et al.The role of fatty-acid transport proteins (FAT/CD36,FABPpm,FATP) in lipid metabolism in skeletal muscles[J].Postepy Higieny Ⅰ:Medycyny Doswiadczalnej,2008,62:433-441.

[20] OCHIAI Y,UCHIDA Y,OHTSUKI S,et al.The blood-brain barrier fatty acid transport protein 1(FATP1/SLC27A1) supplies docosahexaenoic acid to the brain,and insulin facilitates transport[J].Journal of Neurochemistry,2017,141(3):400-412.  

[21] ANDERSON C M,STAHL A.SLC27 fatty acid transport proteins[J].Molecular Aspects of Medicine,2013,34(2/3):516-528.

[22] WU Q W,ORTEGON A M,TSANG B,et al.FATP1 is an insulin-sensitive fatty acid transporter involved in diet-induced obesity[J].Molecular and Cellular Biology,2006,26(9):3455-3467.  

[23] KAZANTZIS M,STAHL A.Fatty acid transport proteins,implications in physiology and disease[J].Biochimica et Biophysica Acta:Molecular and Cell Biology of Lipids,2012,1821(5):852-857.  

[24] SONG Z G,ZHANG X H,ZHU L X,et al.Dexamethasone alters the expression of genes related to the growth of skeletal muscle in chickens (Gallus gallus domesticus)[J].Journal of Molecular Endocrinology,2011,46(3):217-225.  

[25] 解相林,王栋,王慧.PPAR基因多态性与肉鸡脂肪性状的相关性研究[J].畜牧兽医学报,2005,36(12):1261-1264.

[26] MENG H,ZHAO J G,LI Z H,et al.Single nucleotide polymorphisms on peroxisome proliferator-activated receptor genes associated with fatness traits in chicken[J].Asian-Australasian Journal of Animal Sciences,2005,18(9):1221-1225.  

[27] CUI H X,LIU R R,ZHAO G P,et al.Identification of differentially expressed genes and pathways for intramuscular fat deposition in Pectoralis major tissues of fast-and slow-growing chickens[J].BMC Genomics,2012,13:213.
Outlines

/