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L’innovazione scientifica per la nutrizione
Giovanni SavoiniDEP. OF HEALTH, ANIMAL PRODUCTION AND FOOD SAFETY (VESPA)
UNIVERSITÀ DEGLI STUDI DI MILANO
Approccio olistico nell’ alimentazione della bovina da latte
Dietary manipulation of fatty acids (FA)composition of milk fat – CLA, omega 3 fatty acids
Omega-3 FA and rumen methanogenesis
Bioactive FA and animal health
Summary
Lodi 16 ottobre 2015 Giovanni Savoini
Ø Fat concentration : 0.1-1.0 percentage unitsØProtein concentration : 0.1-0.4 percentage unitsØ Selenium concentration : dietary selenium (organic Se) - limitation
in supplementing Se in feed (0.5 ppm)-ØTransfer of vitamin E from feed to milk is low, around 1.6% - 2.2%,
Milk is one of the most important source of healthy and functional food ingredients: can we further improve an excellent food through animal feeding ?
Baldi et al., 2011
Lodi 16 ottobre 2015 Giovanni Savoini
Dietary manipulation of fatty acids (FA)composition of milk fat – CLA, omega 3 fatty acids
Omega-3 FA and rumen methanogenesis
Bioactive FA and animal health
Summary
Lodi 16 ottobre 2015 Giovanni Savoini
CLAü Milk usually contains 0.2-0.9 % of CLA ü The major CLA isomer (cis-9, trans-11)
derives mainly from the endogenous synthesis via the action of SCD in mammary epithelial cells on vaccenic acid (trans-11 18:1)
ü CLA milk concentration can be increased by grazing, fresh grass or by feeding sources of unsaturated fatty acids (C18:2n-6,C18:3n-3), such as plant oils, oilseeds, fish oil or marine algae, CLA rumen protected
ü CLA milk concentration is affected by stage of lactation, it increases in late lactation (Wang et al., 2013, Tudisco et al., 2013, Cattaneo et al., 2006)
Linoleic acid(cis-9,cis-12 18:2)
CLA(cis-9,trans-11 CLA)
Vaccenic acid(trans-11 18:1)
Stearic acid (18:0)
Rumen biohydrogenation of FA
Lodi 16 ottobre 2015 Giovanni Savoini
Grazing CLA (%TFA)
Pasture-grazing 2.22 Coppa et al., 2011
Grass hay 0.62Pasture-alfa alfa 1.53 Abu Ghazaleh et al., 2006
Corn silage alfa alfa hay 0.84
Effect of grazing on the CLA content of milk (Shingfield et al., 2013 mod.)
Ruminal biohydrogenation can be affected by:ü Ruminant speciesü Endogenous lipolysis (LP)ü Plant secondary metabolites (PSM)ü Polyphenol oxidase (PPO)ü Role of odd branched chain fatty acids (OBCFA) (Buccioni et al., 2012)
Lodi 16 ottobre 2015 Giovanni Savoini
Effect of dietary lipids on milk CLA content
Relationship between dietary fat supplementation and milk CLA content in
sheep (Nudda et al., 2014)
CLA concentration in milk of goats fed high or low forage (HF, LF) and soybean oil (NO,O)
HF/NO HF/O LF/NO LF/O
0.61 3.79 0.8 2.67
Dietary sunflower (SF) and fish oil (FO) increase CLA concentration in dairy cows
ü Tannins can affect ruminalbiohydrogenation, increasing content of CLA when animals are fed diets rich in linoleic acid (Buccioni et al., 2015)
ü Level and type of starch influence the concentration of bioactive FA in milk (Toral et al., 2014)
Mele et al., 2008
Cruz-Hernandes et al, 2007
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CLA content increases in milk fatwhen fish oil is included in thediet because DHA reduces theconversion of vaccenic to stearicacid in rumen
Linoleic acid(cis-9,cis-12 18:2)
CLA(cis-9,trans-11 CLA)
Vaccenic acid(trans-11 18:1)
Stearic acid (18:0)
DHA (FO)
Control Soy bean +fish oil
CLA 0.57a 4.04b
Inclusion of fish oil in dairy goat diet improves milk content of CLA (% TFA) (Tsiplakou and Zervas, 2013)
16 ottobre 2015 Giovanni Savoini
Omega 3 fatty acidsü n-3 FA (α-linolenic acid -ALA-, EPA and DHA) in milk can be
increased by feedingü Fish oilü Algaeü Flax seeds
But the transfer efficiency of EPA and DHA is quite low because of the preferential incorporation of absorbed EPA and DHA into plasma PL and CE of HDL, rather than TAG of circulating VLDL and chylomicrons (Palmquist, 2009)
Apparent transfer efficiency dairy goats fed fish oil : 7.0-14.0 % EPA, 7.0-8.0 % DHA
Apparent transfer efficiency dairy cows fed fish oil : 2.6-4.73 % EPA, 2.45-7.6 % DHA
Lodi 16 ottobre 2015 Giovanni Savoini
Fish oil Dairy cows EPA-20:5n-3 (%TFA) DHA -22.6n-3(% TFA) Authors
Control 0.08 0.04 Loor et al., 2005
Fish oil (270 g/h/d)) 0.36 0.17
Algae Dairy cows
Control NR 0.09 Boeckart et al., 2008
Algae (201 g/h/d) NR 1.10
Fish oil sheep
Control 0.03 0.02 Toral et al., 2010
Fish oil (27.5 g/h/d) 0.15 0.38
Fish oil goats
Control NR NR Cattaneo et al., 2006
Fish oil (45g/h/d) 0.54 0.37
Effect of dietary fish oil and marine algae supplements on EPA and DHA content of ruminant milk (Shingfield et al., 2013 mod.)
Lodi 16 ottobre 2015 Giovanni Savoini
Plasma EPA e DHA content dairy goats (% TFA)
Plasma DHA content kids (%)Control Fish oil Stearate
DHA 1.35b 2.09a 1.62
Feeding fish oil to dairy goats increased EPA and DHA content in goats and kids plasma
Plasma EPA content kids (%)Control Fish oil Stearate
EPA 0.28b 1.38a 0.38
Ferroni et al., 2015
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Milk oxidationMilk with a high content of LCFA may benefit human health, but at the same time is more vulnerable to oxidation. In this context, increasing milk vitamin E content may represent an useful tool to protect lipids from peroxidation and to maintain milk nutritional and organoleptic quality (Baldi et al, 2011).
Item SMCFA Butterfat LCFA
SOD 5.26a 4.58ab 4.22b
GSH-Px 430.17a 395.74bc 408.13b
CAT 36.51a 33.40b 35.52a
T-AOC 1.58 1.62 1.42
MDA 1.03b 1.15a 1.14a
Zhao et al., 2013
Concentration of enzymatic radical scavenging and lipid oxidation products in milk response to
different dietary fatty acids (U/ml)
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Milk or cheese enriched in bioactive FA are useful for human health ?
Pintus et al., 2013
BASE CTRL (90g/d) ENCH (90g/d)Total cholesterol (mmol/l) 6.29a 6.62a 5.96b
LDL-C (mmol/l) 4.29a 4.41a 4.00b
Plasma total cholesterol and LDL-C levels in volunteers after an intake of 90 g/d of the control cheese (CTRL) or enriched cheese (ENCH-ALA,VA,CLA)
Plasma concentration of endocannabinoid anandamidein volunteers after an intake of 90 g/d of the control
cheese (CTRL) or enriched cheese (ENCH-ALA, VA, CLA) Trans fatty acids (TFA) mayhave adverse consequences
on human health?
Lodi 16 ottobre 2015 Giovanni Savoini
Dietary manipulation of fatty acids (FA)composition of milk fat
Omega-3 FA and rumen methanogenesis
Bioactive FA and animal health
Summary
Lodi 16 ottobre 2015 Giovanni Savoini
Omega-3 FA and rumen methanogenesisü Lipid supplementation usually decreases methane (CH4) yield
ü Increasing doses of coconut and fish oil quadratically decreased concentrations of methane in vitro (Patra and Yu, 2013)
ü Fish oil supplementation to dairy cows did not affect CH4 yield (EE 3.2 % DM), but the addition of fish oil to low starch diets lowered CH4 yield (14.5 vs 13.3 g of CH4 /kg ECM) (Pirondini et al., 2015)
ü Camelina oil decreases ruminal CH4 production, but this is related, at least in part, to lowered dry matter intake
ü Camelina oil had no effect on ruminal CH4 emission intensity (g/kg of digestible organic matter intake or milk yield)(Bayat et al., 2015).
Lodi 16 ottobre 2015 Giovanni Savoini
Dietary manipulation of fatty acids (FA)composition of milk fat
Omega-3 FA and rumen methanogenesis
Bioactive FA and animal health
Summary
Lodi 16 ottobre 2015 Giovanni Savoini
Bioactive FA and animal health
üDo bioactive FA (omega n3), used to modify fatty acids composition of milk fat, affect animal health?
Lodi 16 ottobre 2015 Giovanni Savoini
Long chain n-3 PUFA affect fertility
Fish oil
Fish oil decreases the concentration of PGF2α (Mattos
et al., 2004)
Santos et al., 2014
Lodi 16 ottobre 2015 Giovanni Savoini
Long chain n-3 FA modulate immune functions in several ways:ü By replacing arachidonic acid during the eicosanoid signaling cascade, reducing
production of inflammatory eicosanoidsü Interfering directly with cytokine gene expressionü Regulating cell surface expression of anti-inflammatory mediators (resolvins)
Long chain n-3 PUFA modulate immune response
Sordillo et al., 2009
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Agazzi et al., 2004
In transition dairy goats dietary fish oil was found to be effective
on cell-mediated immune response, with modified
mononuclear and polymorphonuclear (PMN) cells
ratio as a result
Lodi 16 ottobre 2015 Giovanni Savoini
EPA and DHA may improve the defensive performance of goat neutrophilsand monocytes against bacteria by increasing their phagocytic activity
Pisani et al., 2009
Neutrophils
Monocytes
Lecchi et al., 2012
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Gene expression of IL-6 in BAEC exposed to NEFA with differentfatty acids composition (Contreras et al., 2012)
Lodi 16 ottobre 2015 Giovanni Savoini
n-6/n-3 FA in the dietR4 3.9 ( 0.7 % fish oil)R5 4.9 (0.41 % fish oil)R6 (5.9 0.2 % fish oil)
CS of fish oil
n-6/n-3= 3.9
n-6/n-3= 3.9
LPS challenge in the mammary gland in early lactating dairy cows:
ü Haptoglobin concentration was higher 24 h after LPS challenge in the mammary gland in cows fed diet n-6/n-3 5.9
ü IL-6 concentration in plasma increased as the ratio of n-6 to n-3 FA increased
Greco et al. 2015
Lodi 16 ottobre 2015 Giovanni Savoini
Stryker et al.,2013
After a LPS challenge at 135 d of pregnancy ewes fed fish meal showed an attenuated febrile response compared to soybean meal, and the basal HP concentration was lower after a sensitization with HEWL during lactation
Lodi 16 ottobre 2015 Giovanni Savoini
Conclusion
Lodi 16 ottobre 2015 Giovanni Savoini
ü Through dairy ruminant nutrition it is possible to increase the amount of bioactive fatty acids (FA) in milk
ü Positive effects on human health from consuming milk products containing bioactive FA
ü Transfer efficiency of EPA and DHA is quite lowü Milk oxidation can increase
ü Not conclusive results on methanogenesis when ruminants are fed omega n3 FA
ü Omega 3 fatty acids can modulate immune and inflammatory response in dairy ruminants
Lodi 16 ottobre 2015 Giovanni Savoini
ü Dietary LCFA supplementation in ruminants may affect the directionand dimension of changes in lipid metabolism gene networks in keyphysiological organs such as liver, adipose tissue and mammarygland (Hosseini and Loor, 2014), temporal modulation on lipidmetabolism.
ü Some of the data available highlight differences among ruminantspecies in terms of the molecular response to dietary fatty acids,microbiome
ü Effects of feeding bioactive FA to pregnant animals and effects on progeny health status
Molecular mechanism, gene expressions, gene networks
Lodi 16 ottobre 2015 Giovanni Savoini