Effects of abomasal lipid infusion on liver triglyceride accumulation and adipose lipolysis during fatty liver induction in dairy cows

The objective was to determine the effects of abomasal infusion of linseed oil on liver triglyceride (TG) accumulation and adipose tissue lipolysis during an experimental protocol for induction of fatty liver. Eight nonpregnant, nonlactating Holstein cows were randomly assigned to treatments in a re...

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Veröffentlicht in:Journal of dairy science 2009-10, Vol.92 (10), p.4954-4961
Hauptverfasser: Brickner, A.E., Pires, J.A.A., Gressley, T.F., Grummer, R.R.
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creator Brickner, A.E.
Pires, J.A.A.
Gressley, T.F.
Grummer, R.R.
description The objective was to determine the effects of abomasal infusion of linseed oil on liver triglyceride (TG) accumulation and adipose tissue lipolysis during an experimental protocol for induction of fatty liver. Eight nonpregnant, nonlactating Holstein cows were randomly assigned to treatments in a replicated 4×4 Latin square design. Treatments were abomasal infusion of water (W), tallow (T), linseed oil (LO), or half linseed oil and half tallow (LOT) at a rate of 0.56g/kg of body weight per day. Each experimental period consisted of a 4-d fast concurrent with administration of treatments into the abomasum in 6 equal doses per day (every 4h). Cows were fed ad libitum for 24 d between periods of fasting and lipid infusion. Infusion of linseed oil (LO and LOT) increased α-linolenic acid (C18:3n-3) content in serum (12.2, 10.4, 4.2, and 4.6g/100g of fatty acids for LO, LOT, T, and W, respectively), but not in the nonesterified fatty acid (NEFA) fraction of plasma. Treatments had no effect on plasma NEFA concentrations. Abomasal infusion of lipid increased in vitro stimulated lipolysis in subcutaneous adipose tissue, compared with W (4,294, 3,809, 4,231, and 3,293 nmol of glycerol released×g−1 tissue×2h−1 for LO, LOT, T, and W, respectively), but there was no difference between fat sources. Hepatic TG accumulation over 4-d fast was 2.52, 2.60, 2.64, and 2.09±0.75μg of TG/μg of DNA for W, LO, LOT, and T, respectively, which did not differ. Abomasal infusion of LO did not reduce liver TG accumulation, plasma NEFA concentration, or alter in vitro adipose tissue lipolysis when compared with T. These results contrast with a previous study involving i.v. infusion of lipid emulsion derived from LO. Discrepancies might be explained by the use of different administration routes and a relatively modest induction of liver TG accumulation in the current experiment.
doi_str_mv 10.3168/jds.2009-2147
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Eight nonpregnant, nonlactating Holstein cows were randomly assigned to treatments in a replicated 4×4 Latin square design. Treatments were abomasal infusion of water (W), tallow (T), linseed oil (LO), or half linseed oil and half tallow (LOT) at a rate of 0.56g/kg of body weight per day. Each experimental period consisted of a 4-d fast concurrent with administration of treatments into the abomasum in 6 equal doses per day (every 4h). Cows were fed ad libitum for 24 d between periods of fasting and lipid infusion. Infusion of linseed oil (LO and LOT) increased α-linolenic acid (C18:3n-3) content in serum (12.2, 10.4, 4.2, and 4.6g/100g of fatty acids for LO, LOT, T, and W, respectively), but not in the nonesterified fatty acid (NEFA) fraction of plasma. Treatments had no effect on plasma NEFA concentrations. Abomasal infusion of lipid increased in vitro stimulated lipolysis in subcutaneous adipose tissue, compared with W (4,294, 3,809, 4,231, and 3,293 nmol of glycerol released×g−1 tissue×2h−1 for LO, LOT, T, and W, respectively), but there was no difference between fat sources. Hepatic TG accumulation over 4-d fast was 2.52, 2.60, 2.64, and 2.09±0.75μg of TG/μg of DNA for W, LO, LOT, and T, respectively, which did not differ. Abomasal infusion of LO did not reduce liver TG accumulation, plasma NEFA concentration, or alter in vitro adipose tissue lipolysis when compared with T. These results contrast with a previous study involving i.v. infusion of lipid emulsion derived from LO. 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Psychology ; In Vitro Techniques ; Life Sciences ; linseed oil ; Linseed Oil - administration &amp; dosage ; Linseed Oil - chemistry ; lipids ; lipolysis ; Lipolysis - drug effects ; liver ; Liver - chemistry ; Liver - drug effects ; Liver - metabolism ; liver triglyceride ; Milk and cheese industries. 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Eight nonpregnant, nonlactating Holstein cows were randomly assigned to treatments in a replicated 4×4 Latin square design. Treatments were abomasal infusion of water (W), tallow (T), linseed oil (LO), or half linseed oil and half tallow (LOT) at a rate of 0.56g/kg of body weight per day. Each experimental period consisted of a 4-d fast concurrent with administration of treatments into the abomasum in 6 equal doses per day (every 4h). Cows were fed ad libitum for 24 d between periods of fasting and lipid infusion. Infusion of linseed oil (LO and LOT) increased α-linolenic acid (C18:3n-3) content in serum (12.2, 10.4, 4.2, and 4.6g/100g of fatty acids for LO, LOT, T, and W, respectively), but not in the nonesterified fatty acid (NEFA) fraction of plasma. Treatments had no effect on plasma NEFA concentrations. 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Discrepancies might be explained by the use of different administration routes and a relatively modest induction of liver TG accumulation in the current experiment.</description><subject>abomasal lipid infusion</subject><subject>abomasum</subject><subject>Abomasum - drug effects</subject><subject>adipose tissue</subject><subject>Adipose Tissue - metabolism</subject><subject>Agricultural sciences</subject><subject>alpha-Linolenic Acid - analysis</subject><subject>alpha-Linolenic Acid - blood</subject><subject>Animal productions</subject><subject>Animals</subject><subject>application methods</subject><subject>Biological and medical sciences</subject><subject>bovine</subject><subject>Cattle</subject><subject>cattle diseases</subject><subject>dairy cows</subject><subject>Fats - administration &amp; dosage</subject><subject>Fats - chemistry</subject><subject>Fatty Acids - analysis</subject><subject>Fatty Acids - blood</subject><subject>Fatty Acids, Nonesterified - blood</subject><subject>fatty liver</subject><subject>Fatty Liver - chemically induced</subject><subject>Fatty Liver - veterinary</subject><subject>Female</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>In Vitro Techniques</subject><subject>Life Sciences</subject><subject>linseed oil</subject><subject>Linseed Oil - administration &amp; dosage</subject><subject>Linseed Oil - chemistry</subject><subject>lipids</subject><subject>lipolysis</subject><subject>Lipolysis - drug effects</subject><subject>liver</subject><subject>Liver - chemistry</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>liver triglyceride</subject><subject>Milk and cheese industries. 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Eight nonpregnant, nonlactating Holstein cows were randomly assigned to treatments in a replicated 4×4 Latin square design. Treatments were abomasal infusion of water (W), tallow (T), linseed oil (LO), or half linseed oil and half tallow (LOT) at a rate of 0.56g/kg of body weight per day. Each experimental period consisted of a 4-d fast concurrent with administration of treatments into the abomasum in 6 equal doses per day (every 4h). Cows were fed ad libitum for 24 d between periods of fasting and lipid infusion. Infusion of linseed oil (LO and LOT) increased α-linolenic acid (C18:3n-3) content in serum (12.2, 10.4, 4.2, and 4.6g/100g of fatty acids for LO, LOT, T, and W, respectively), but not in the nonesterified fatty acid (NEFA) fraction of plasma. Treatments had no effect on plasma NEFA concentrations. Abomasal infusion of lipid increased in vitro stimulated lipolysis in subcutaneous adipose tissue, compared with W (4,294, 3,809, 4,231, and 3,293 nmol of glycerol released×g−1 tissue×2h−1 for LO, LOT, T, and W, respectively), but there was no difference between fat sources. Hepatic TG accumulation over 4-d fast was 2.52, 2.60, 2.64, and 2.09±0.75μg of TG/μg of DNA for W, LO, LOT, and T, respectively, which did not differ. Abomasal infusion of LO did not reduce liver TG accumulation, plasma NEFA concentration, or alter in vitro adipose tissue lipolysis when compared with T. These results contrast with a previous study involving i.v. infusion of lipid emulsion derived from LO. Discrepancies might be explained by the use of different administration routes and a relatively modest induction of liver TG accumulation in the current experiment.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>19762812</pmid><doi>10.3168/jds.2009-2147</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-3773-9293</orcidid><oa>free_for_read</oa></addata></record>
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subjects abomasal lipid infusion
abomasum
Abomasum - drug effects
adipose tissue
Adipose Tissue - metabolism
Agricultural sciences
alpha-Linolenic Acid - analysis
alpha-Linolenic Acid - blood
Animal productions
Animals
application methods
Biological and medical sciences
bovine
Cattle
cattle diseases
dairy cows
Fats - administration & dosage
Fats - chemistry
Fatty Acids - analysis
Fatty Acids - blood
Fatty Acids, Nonesterified - blood
fatty liver
Fatty Liver - chemically induced
Fatty Liver - veterinary
Female
Food industries
Fundamental and applied biological sciences. Psychology
In Vitro Techniques
Life Sciences
linseed oil
Linseed Oil - administration & dosage
Linseed Oil - chemistry
lipids
lipolysis
Lipolysis - drug effects
liver
Liver - chemistry
Liver - drug effects
Liver - metabolism
liver triglyceride
Milk and cheese industries. Ice creams
Subcutaneous Fat - metabolism
Terrestrial animal productions
therapeutics
triacylglycerols
Triglycerides - analysis
Triglycerides - metabolism
Vertebrates
title Effects of abomasal lipid infusion on liver triglyceride accumulation and adipose lipolysis during fatty liver induction in dairy cows
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