Abundance of solute carrier family 27 member 6 (SLC27A6) in the bovine mammary gland alters fatty acid metabolism

2021 ◽  
Author(s):  
Huimin Zhang ◽  
Ziliang Shen ◽  
Zhendong Yang ◽  
Hui Jiang ◽  
Shuangfeng Chu ◽  
...  
Keyword(s):  
Mammary Gland ◽  
Fatty Acid ◽  
Fatty Acid Metabolism ◽  
Acid Metabolism ◽  
Mammary Tissue ◽  
Mammary Cells ◽  
Solute Carrier Family ◽  
Bovine Mammary Gland ◽  
Solute Carrier

The Milk FA and transcriptome of bovine mammary tissue indicated that LCFA transport into mammary cells during late lactation. In vitro test underscored how FA transport via SLC27A6 could dictate the utilization of FA for TG synthesis versus oxidation.

scholarly journals Lipid and glucose metabolism in hepatocyte cell lines and primary mouse hepatocytes: a comprehensive resource for in vitro studies of hepatic metabolism

2019 ◽  
Vol 316 (4) ◽  
pp. E578-E589 ◽  
Author(s):  
Shilpa R. Nagarajan ◽  
Moumita Paul-Heng ◽  
James R. Krycer ◽  
Daniel J. Fazakerley ◽  
Alexandra F. Sharland ◽  
...  
Keyword(s):  
Fatty Acid ◽  
Glucose Metabolism ◽  
Cell Lines ◽  
Fatty Acid Metabolism ◽  
Acid Metabolism ◽  
Primary Hepatocytes ◽  
Primary Mouse Hepatocytes ◽  
Primary Mouse ◽  
Mouse Hepatocytes

The liver is a critical tissue for maintaining glucose, fatty acid, and cholesterol homeostasis. Primary hepatocytes represent the gold standard for studying the mechanisms controlling hepatic glucose, lipid, and cholesterol metabolism in vitro. However, access to primary hepatocytes can be limiting, and therefore, other immortalized hepatocyte models are commonly used. Here, we describe substrate metabolism of cultured AML12, IHH, and PH5CH8 cells, hepatocellular carcinoma-derived HepG2s, and primary mouse hepatocytes (PMH) to identify which of these cell lines most accurately phenocopy PMH basal and insulin-stimulated metabolism. Insulin-stimulated glucose metabolism in PH5CH8 cells, and to a lesser extent AML12 cells, responded most similarly to PMH. Notably, glucose incorporation in HepG2 cells were 14-fold greater than PMH. The differences in glucose metabolic activity were not explained by differential protein expression of key regulators of these pathways, for example glycogen synthase and glycogen content. In contrast, fatty acid metabolism in IHH cells was the closest to PMHs, yet insulin-responsive fatty acid metabolism in AML12 and HepG2 cells was most similar to PMH. Finally, incorporation of acetate into intracellular-free cholesterol was comparable for all cells to PMH; however, insulin-stimulated glucose conversion into lipids and the incorporation of acetate into intracellular cholesterol esters were strikingly different between PMHs and all tested cell lines. In general, AML12 cells most closely phenocopied PMH in vitro energy metabolism. However, the cell line most representative of PMHs differed depending on the mode of metabolism being investigated, and so careful consideration is needed in model selection.

scholarly journals Atypical antipsychotics alter cholesterol and fatty acid metabolism in vitro

2012 ◽  
Vol 54 (2) ◽  
pp. 310-324 ◽  
Author(s):  
Alberto Canfrán-Duque ◽  
María E. Casado ◽  
Óscar Pastor ◽  
Jana Sánchez-Wandelmer ◽  
Gema de la Peña ◽  
...  
Keyword(s):  
Fatty Acid ◽  
Fatty Acid Metabolism ◽  
Atypical Antipsychotics ◽  
Acid Metabolism

Free fatty acid metabolism and obesity in man: In vivo in vitro comparisons

Metabolism ◽  
1986 ◽  
Vol 35 (6) ◽  
pp. 505-514 ◽  
Author(s):  
S. Lillioja ◽  
J. Foley ◽  
C. Bogardus ◽  
D. Mott ◽  
B.V. Howard
Keyword(s):  
Fatty Acid ◽  
Free Fatty Acid ◽  
Fatty Acid Metabolism ◽  
Acid Metabolism ◽  
Free Fatty Acid Metabolism

In Vitro Studies of Fatty Acid Metabolism in Vitamin B6 Deficient Rats

1979 ◽  
Vol 109 (1) ◽  
pp. 138-141 ◽  
Author(s):  
Pierre E. Dussault ◽  
Marius Lepage
Keyword(s):  
Fatty Acid ◽  
Fatty Acid Metabolism ◽  
Vitamin B6 ◽  
Acid Metabolism ◽  
In Vitro Studies

scholarly journals In vitro Silencing of Acetyl-CoA Carboxylase beta (ACACB) Gene Reduces Cholesterol Synthesis in Knockdown Chicken Myoblast Cells

2021 ◽  
Author(s):  
G. Sushma ◽  
P. Jaya Laxmi ◽  
S.T. Viroji Rao ◽  
R.M.V. Prasad ◽  
M. Kanakachari ◽  
...  
Keyword(s):  
Cell Culture ◽  
Fatty Acid ◽  
Fatty Acid Metabolism ◽  
Culture System ◽  
Acid Metabolism ◽  
Cell Culture System ◽  
Acetyl Coa Carboxylase ◽  
Significant Difference ◽  
Myoblast Cells

Abstract The poultry industry provides cost-effective, healthy, and protein-enriched food for the growing population and achieving the nutritional security to the country. Excessive abdominal and subcutaneous fat deposition is one of the major setbacks to the poultry industry that reduces carcass yield and feed efficiency. In chicken abdominal fat constitutes 20% of total body fat which make up 2–3% of live weight of the bird. In fatty acid metabolism, acetyl-CoA Carboxylase (ACC) is one of the key enzymes with two isoforms i.e. ACACA and ACACB each of which plays a different role. In chicken, ACACB is involved in the β-oxidation of fatty acids and thereby potentially regulating the quality of meat and egg. The RNAi strategy is widely used for silencing the target gene expression. In this study, we designed five shRNA constructs and identified the most efficient shRNA molecule for silencing the ACACB gene under in vitro chicken embryo myoblast (CEM) primary cell culture system. After knocking down the ACACB gene, for understanding how fatty acid metabolism is regulated, we tracked the expression of key fatty acid metabolism genes like ACACA, FASN, SCD, ELOVL2, and CPT1. Also, checked the expression of immune response genes like IFNA, IFNB, and BLB1 in control as well as ACACB knockdown myoblast cells and observed no significant difference. We observed the down-regulation of key fatty acid metabolism genes along with ACACB, which may leads to the less fat accumulation in CEM cells. We also estimated the cholesterol and triglycerides in control and ACACB knockdown myoblast cells and found a significant difference between control and the knockdown cells. In vitro knockdown of the ACACB gene in a cell culture system by a short hairpin RNA (shRNA) expressing construct would help to produce a knockdown chicken with reduced fat deposition.

Fatty acid metabolism in segments of rat intestine

1965 ◽  
Vol 208 (4) ◽  
pp. 607-614 ◽  
Author(s):  
Daniel Porte ◽  
Cecil Entenman
Keyword(s):  
Small Intestine ◽  
Fatty Acid ◽  
Palmitic Acid ◽  
Fatty Acid Metabolism ◽  
Acid Metabolism ◽  
Sodium Taurocholate ◽  
Tissue Uptake ◽  
Rat Intestine ◽  
A Minor

The in vitro metabolism of albumin-bound palmitic acid-1-C14 by segments of small intestine was studied. Tissue uptake, esterification, and oxidation of the fatty acid were measured separately and found to respond independently to altered incubation conditions. Uptake was reversible, and did not require glucose or oxygen. It was not inhibited by fluoride or arsenate. Esterification required both glucose and oxygen, but was unaffected by insulin. It was depressed by succinate and almost completely inhibited by fluoride and arsenate. Oxidation was a minor fate for fatty acid. It was independent of glucose but inhibited by succinate, fluoride, and arsenate. Sodium taurocholate stimulated uptake, but not esterification, as has been previously reported. The possible significance of the reversible tissue uptake reaction is discussed.

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