Effects of Pharmacological Amounts of Nicotinic Acid on Lipolysis and Feed Intake in Cattle
The objective of the study was to determine if pharmacological supplies of nicotinic acid could reduce lipolysis in cattle. Six ruminally cannulated steers (225 kg) were used. In an initial study, steers received abomasal infusion of nicotinic acid at 0, 8, or 16 g day-1 then were challenged with a pulse dose of isoproterenol. Nicotinic acid at 16 g day-1 inhibited isoproterenol-stimulated increases in plasma free fatty acid concentrations, whereas 8 g day-1 did not. All 6 steers were then fed 60 mg day-1 zilpaterol-HCl and 3 were continuously abomasally infused with water and 3 with 16 g day-1 nicotinic acid. Steers receiving 16 g day-1 nicotinic acid demonstrated reductions in feed intake and nicotinic acid infusions were terminated after 3.2 days. Plasma glucose and insulin were elevated in response to the nicotinic acid infusion but glucagon was largely unaffected. Elevations in plasma free fatty acids in response to nicotinic acid were observed when feed intake was reduced, suggesting that 16 g day-1 nicotinic acid did not completely block mobilization of fatty acids. Temporal patterns for free fatty acids and insulin did not suggest that elevated free fatty acids were causatively related to insulin resistance during nicotinic acid treatment. Reductions in feed intake of cattle given pharmacological amounts of nicotinic acid indicate there may be risks associated with over-consumption of nicotinic acid.
February 25, 2011; Accepted: May 05, 2011;
Published: June 03, 2011
At pharmacological doses, Nicotinic Acid (NA) has been shown to inhibit lipolysis
in cattle (Pires and Grummer, 2007; Pires
et al., 2007), presumably by acting on the niacin receptor GPR109A,
a Gi-coupled receptor (Gille et al., 2008). Activation
of GPR109A by NA leads to inhibition of adenylyl cyclase activity and, subsequently,
a decrease in cAMP concentrations within the cell. Decreases in cAMP in adipocytes
lead to sequelae (inactivation of protein kinase A and decreased phosphorylation
of hormone sensitive lipase) that reduce lipolysis (Gille
et al., 2008). The NA receptor GPR109A is predominantly localized
in adipose tissue and immune cells in humans (Wise et
al., 2003) and mice (Tunaru et al., 2003)
but present study has indicated a much wider tissue distribution pattern for
GPR109A in cattle with the concentrations of GRP109A protein being as great
in liver as in adipose tissue (Bradford et al., 2009).
In addition, we observed GPR109A mRNA in multiple regions of the bovine brain
(our unpublished observations) which was not overly surprising because it has
also been found in human brain (Miller and Dulay, 2008).
The United State Food and Drug Administration has approved several β-agonists,
including ractopamine and zilpaterol, as growth promotants for cattle. These
β-agonists act through β1- and β2-receptors,
which are Gs-coupled receptors that increase intracellular concentrations of
cAMP (Moody et al., 2000). The β1-
and β2-receptors are found in various tissues including muscle
and adipose (Sillence and Matthews, 1994). Responses
to β-agonists are increases in muscle deposition with reductions in adipose
accumulation (Moody et al., 2000).
A large proportion of variation in back fat and intramuscular fat in cattle
is dependent on management and environment (Mirzaei et
al., 2009), so an improved ability to control fat deposition might help
to improve carcass quality. Within adipocytes which contain GPR109A and β-adrenergic
receptors, NA and β-agonists have opposing actions. The objectives of the
current research were to determine 1) if NA could reduce lipolysis induced by
β-agonists, 2) the amount of NA supplementation required to induce this
effect and 3) the impact of NA supplementation in cattle fed zilpaterol, a β-adrenergic
MATERIALS AND METHODS
Animals and management: Experimental procedures were approved by the
Kansas State University Institutional Animal Care and Use Committee in 2008.
The same 6 ruminally cannulated Holstein steers (initial BW 225±22 kg)
were used in these experiments. Steers were fed a grain-based diet (Table
1) near ad libitum intake at 12-h intervals and were housed in metabolism
crates throughout the experiments. Infusion lines were placed through the ruminal
cannulae and the omasum and into the abomasum, where they were anchored with
a 10 cm diameter rubber flange. The infusion lines were designed to allow for
continuous post-ruminal infusion of NA. The NA was infused abomasally to prevent
ruminal microbial degradation of NA which can be substantial (Santschi
et al., 2005).
Dose-response trial: Six steers were used to determine what amount of
NA supplementation might reduce lipolysis stimulated by β-agonists. Nicotinic
acid (≥99.5%, Fluka Biochemika, Buchs, Switzerland) was continuously infused
into the abomasum at 0, 8, or 16 g day-1 in a replicated 3x3 Latin
square with 1-day periods.
|| Ingredient and nutrient composition of the diet (g kg-1
|*Provided (per kg diet DM): Mn: 55 mg, Zn: 55 mg, Cu: 9 mg,
I: 0.5 mg, Se: 0.25 mg, Retinyl acetate: 0.76 mg, Cholecalciferol: 6.75
μg, All-rac-α-tocopherol: 27 mg
Pires and Grummer (2007) showed almost complete inhibition
of lipolysis induced by feed-restriction in non-lactating cows given 6 mg NA/kg
BW hourly but lower doses were not tested. Present greatest dose provided NA
at about one-half of their rate.
After 1 day of adaptation to the NA treatment, steers were challenged at 3
h after feeding with a pulse dose of isoproterenol-HCl (0.5 μg kg-1
BW; 0.1125 mg in 5 mL saline) into a jugular vein and contralateral jugular
blood samples were collected just before isoproterenol dosing as well as 8 min
after the isoproterenol challenge. Isoproterenol is a β-agonist that quickly
stimulates lipolysis from bovine adipocytes, leading to a peak in plasma Free
Fatty Acid (FFA) concentrations 5 to 10 min after dosing (Chilliard
and Ottou, 1995). Blood samples (10 mL) were collected in Vacutainer tubes
(Becton Dickinson, Franklin Lakes, NJ, USA) containing EDTA as an anticoagulant
and immediately placed in ice. Plasma was isolated by centrifugation at 1,000xg
for 15 min and immediately analyzed for FFA (Shimizu et
al., 1980; NEFA HR kit, Wako Chemicals USA, Richmond, VA, USA).
Zilpaterol feeding and responsiveness to NA: This trial was initiated 3 days after completion of the dose-response trial. Cattle were maintained without any β-agonist in the diet and without NA supplementation for the initial 4 days of this trial. Next, zilpaterol feeding (60 mg day-1) was initiated for all steers and continued without NA treatment for 4 days. Then, NA treatments were initiated; 3 steers received continuous abomasal infusions of 16 g NA in 2 L of water daily and 3 steers received continuous abomasal infusions of water only. All steers continued to receive zilpaterol during the NA treatment period. The initial plan was to maintain steers on their NA treatment for 7 days. However, cattle receiving 16 g day-1 of NA demonstrated progressive reductions in voluntary feed intake, so NA infusions were terminated after 3.2 days of treatment. Steers were maintained on their diets through the initially planned trial (4 days after NA withdrawal) and then euthanized with 187 mg of sodium pentobarbital kg-1 BW followed by exsanguination.
Blood samples were collected 4 h after feeding on day 1 (no treatments applied),
day 5 (after 1 day of zilpaterol feeding to all steers), day 8 (4 h after initiation
of NA treatments), day 9 (28 h after initiation of NA treatments), day 10 (52
h after initiation of NA treatments), day 12 (1 day after termination of NA
treatments) and day 14 (3 days after termination of NA treatments). Jugular
blood (10 mL) was collected in Vacutainer tubes containing EDTA, immediately
placed in ice and centrifuged at 1,000xg for 15 min to separate plasma. Plasma
was frozen and later analyzed for FFA (Shimizu et al.,
1980; NEFA HR kit, Wako Chemicals USA), glucose (Raabo
and Terkildsen, 1960; Autokit Glucose, Wako Chemicals USA), insulin (Park
et al., 2010) and glucagon (RIA kit GL-32K, Linco Research Inc.,
St. Charles, MO, USA).
Statistical analyses: Data from the dose-titration trial were analyzed as a Latin square with steer included as a random effect and data from the NA responsiveness trial were analyzed as a completely randomized design using the mixed procedure of SAS (SAS Inst. Inc., Cary, NC, USA). Data with repeated observations over time (e.g., feed intake, blood metabolites) were analyzed as repeated measures using the mixed procedure of SAS, with steer as the subject for repeated measures. Means over time were compared using pairwise t-tests.
RESULTS AND DISCUSSION
Isoproterenol challenge: Feed refusals during this trial were small.
After the isoproterenol challenge, plasma FFA concentrations were 696 μmol
L-1 for control steers, 651 μmol L-1 for steers receiving
8 g day-1 NA and 363 μmol/l for steers receiving 16 g day-1
NA (p<0.01; SEM 166).
||Dry matter intake (SEM = 1.1) of cattle receiving 0 or 16
g day-1 of Nicotinic Acid (NA) abomasally. Cattle received no
treatment for the initial 4 days and then received dietary zilpaterol (60
mg day-1) continuously from that point forward. The 16 g day-1
NA treatment was provided continuously from the beginning of day 9 for a
total of 3.2 days and then discontinued. Intake never differed from day-1
amounts for steers receiving no NA but for steers receiving 16 g day-1
NA, dry matter intakes were less (p = 0.02) than day-1 amounts on day 11
Thus, 16 g day-1 NA was effective in limiting isoproterenol stimulation
of FFA release but 8 g day-1 NA was not effective in inhibiting lipolysis.
Pre-challenge FFA concentrations were not different among treatments (p = 0.76,
Mean = 87 μmol L-1), so they did not affect conclusions.
Feed intake responses to NA: Before NA administration, control cattle consumed less feed than cattle that were to be infused with NA (Fig. 1). The 16 g day-1 dose of NA decreased intake (Fig. 1) and this effect led to feed intakes on the third day of NA infusion (2.2 kg dry matter) being less (p=0.02) than those on day 1 (6.0 kg dry matter). Because feed intakes were decreasing at a rapid rate, NA infusions were terminated after 3.2 days of treatment. Feed intake progressively increased over the next 4 days after termination of NA treatment (Fig. 1).
Depression of feed intake by supplementation with pharmacological amounts of
NA has not been previously demonstrated in cattle, likely due to the methodologies
that have been employed. In some previous work, pharmacological doses of NA
were administered to cows that were feed-restricted for 48 h as a means of inducing
lipolysis (Pires and Grummer, 2007; Pires
et al., 2007) and thus feed intake responses could not be measured.
Piresa et al. (2009) did not observe changes in
feed intake when they infused pharmacological doses of NA for 3 days to cows
that were fed only 33% of ad libitum intake; however, their research model was
unlikely to demonstrate depressions in feed intake due to the experimentally
restricted intake as well as the moderately short length of NA infusion. Modest
doses of NA (6 g day-1 for 632 kg cows) have been provided post-ruminally
to cows for a longer period of time (3 wk) without depressing feed intake (Ottou
et al., 1995) but the ineffectiveness of NA in reducing isoproterenol-stimulated
lipolysis in that study (Chilliard and Ottou, 1995)
suggested that the NA supply was not a pharmacological dose. Other studies have
fed relatively large doses of NA to cattle without large effects on feed intake.
However, because only a small portion of dietary niacin reaches the small intestine
(Santschi et al., 2005), feeding unprotected NA
is an ineffective in providing pharmacological amounts of NA to cattle.
||Effects of abomasal supplementation of growing steers with
0 or 16 g day-1 of Nicotinic Acid (NA) on plasma concentrations
of (a) glucose; SEM = 0.34; for 16 g day-1 NA, glucose increased
(p<0.10) above day-1 concentrations on day 10 and 12 (b) insulin; SEM
= 0.49; for 16 g day-1 NA, insulin increased (p=0.04) above day-1
concentrations on day 12 (c) glucagon; SEM = 15 and (d) FFA; SEM = 114;
for 16 g day-1 NA, FFA increased (p = 0.07) above day-1 concentrations
on day 10. Cattle received no treatment for the initial 4 days and then
received dietary zilpaterol (60 mg day-1) continuously from that
point forward. The 16 g day-1 NA treatment was provided continuously
from the beginning of day 9 for a total of 3.2 days and then discontinued
We are unaware of any reports from the many human and rodent studies that pharmacological
amounts of NA depress intake.
A significant proportion of dairy cattle develop ketosis during the initial
2 months of lactation (Haghighat-Jahromi and Nahid, 2011)
and these cows exhibit elevated serum concentrations of β-hydroxybutyrate
(Nazifi et al., 2008). Because β-hydroxybutyrate
is the endogenous ligand for GPR109A (Gille et al.,
2008), it is possible that reductions in feed intake associated with ketosis
could be related to stimulation of GPR109A in cattle. This is a particularly
intriguing hypothesis because GPR109A is much more widely distributed in cattle
than in other species (Bradford et al., 2009).
Blood metabolite responses to NA: Plasma glucose concentration (Fig.
2a) was somewhat elevated (p<0.10) in response to the NA infusion on
days 10 and 12 (6.5 mmol L-1 on day 10 and 12 vs. 5.6 mmol L-1
on day 1). This is notable because it occurred in the face of reductions in
feed intake. The elevation in blood glucose persisted for at least 1 day after
termination of NA treatment but was not different from day-1 values 3 days after
termination of NA treatment (5.9 mmol L-1). Ghorbani
et al. (2008) demonstrated that 6 or 12 g or niacin fed orally as
a solute in water to lactating dairy cows led to increases in plasma glucose.
The NA treatment also elevated plasma insulin concentration (Fig. 2b). There seemed to be a progressive increase in insulin during the initial 2 days that steers received 16 g day-1 NA. Plasma insulin on day 12 (1 day after termination of NA treatment; 2.55 ng mL-1) was greater (p<0.05) than on day 1 (1.0 ng mL-1). The increase in insulin in steers receiving 16 g day-1 NA appeared in the face of reduced feed intake. It is difficult to know if increases in plasma glucose led to the elevation in insulin or if insulin resistance led to the elevations in glucose.
Previous studies with cattle have shown various responses in plasma insulin
in response to NA. Feed-restricted cows that received pharmacologic doses of
NA infused for 8 h had increased plasma insulin concentrations during the rebound
phase, around 4 to 8 h after NA provision was terminated (Pires
and Grummer, 2007). Similar short-term treatment of feed-restricted cows
with NA transiently (1 to 4 h) reduced plasma insulin and improved glucose clearance
at 8 h after NA initiation (Pires et al., 2007).
This response was attributed to reductions in plasma FFA concentrations. However,
NA treatment of feed-restricted lactating cows for 48 or 72 h but not for 24
h, increased plasma insulin and reduced glucose clearance at 72 h, demonstrating
insulin resistance in response to longer-term treatment of cattle with pharmacological
doses of NA (Piresa et al., 2009). In goats, Thornton
and Schultz (1980) observed increases in blood glucose 2 days after providing
an oral pulse-dose of NA (0.8 g kg-0.75 BW); goats also demonstrated
impaired glucose tolerance during this time period. In a single cow dosed orally
with 160 g of NA, insulin increased more in response to a glucose challenge
at 1 or 2 days after the NA dose than before the NA dose (Thornton
and Schultz, 1980). Because Thornton and Schultz (1980)
used large oral doses of NA, it is difficult to know when and how much of the
NA the animals were absorbing. Thus, it is unknown what time periods would lead
to direct effects or rebound effects after dissipation of NA supply.
Plasma glucagon was largely unaffected by treatment (Fig. 2c), suggesting that it played a minor role, if any, in the NA effects on blood glucose. However, it is possible that the relatively unchanged plasma glucagon concentrations reflect parallel changes in glucagon secretion and uptake.
Baseline concentrations of FFA (Fig. 2d) were low, at least for steers that later received 16 g day-1 NA; the greater FFA concentrations for the control steers can be attributed to a single steer that demonstrate delevated plasma FFA (over this study, FFA averaged 468, 54 and 75 μmol L-1 for each of the 3 control steers). The elevations in plasma FFA in response to NA on day 10 (360 μmol L-1 vs. 53 μmol L-1 on day 1) could be related to reductions in feed intake; however, the elevation in FFA, which presumably reflects increases in lipolysis, suggests that 16 g day-1 NA did not completely block the steers ability to mobilize fatty acids.
Presumably during an NA rebound response, Thornton and
Schultz (1980) observed in goats that elevations in plasma insulin occurred
before increases in glucose were present which suggests the NA rebound was leading
to insulin resistance. Pires and Grummer (2007) suggested
that elevations in insulin and glucose during an NA rebound could be induced
by the extremely high concentrations of plasma FFA. The temporal patterns that
we observed for FFA and insulin do not suggest that elevated FFA concentrations
were causatively related to insulin resistance during continuous NA provision.
The reductions in feed intake of cattle provided with continuous NA supplementation indicates there may be risks associated with over-consumption of NA. The unusual distribution of GPR109A in comparison to other species is likely related to the impact of NA on feed intake and insulin. It is also possible that NA acts directly on the brain because GPR109A mRNA was also observed in bovine brain, including the hypothalamus (our unpublished observations).
Financial support for this project was provided by Lonza. This study is contribution no. 11-208-J from the Kansas Agricultural Experiment Station, Manhattan.
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