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Effect of opioid receptor ligands injected into the rostral lateral hypothalamus on c-fos and feeding behavior.

The lateral hypothalamic area (LHa) is an important brain site for the regulation of food intake. Central injection of opioids increases food intake, and the LHa contains mu and kappa opioid receptors, both of which are involved in feeding behavior. It is unclear whether opioids impact feeding when injected directly into the rostral portion of the LHa (rLHa) in rats. We performed a series of studies in which free-feeding rLHa-cannulated rats were injected with opioid agonists (DAMGO, morphine, dynorphin, U-50488H) followed by the measurement of food intake at 1, 2, and 4 h postinjection. To determine whether opioid receptor ligands administered into the rLHa affect neuronal activation in this brain site, we studied cFos immunoreactivity (cFos IR) in response to rLHa stimulation with naltrexone. We found that the only compound that stimulated feeding behavior was morphine. The other agonists had no effect on food consumption. Naltrexone injection into the rLHa increased neural activation in the LHa, indicating the presence of functional opioid receptors in this region. These data suggest that although neuronal activity is affected by opioid agents acting in the rLHa, administration of selective mu and kappa opioid ligands in this subdivision of the LHa does not have a reliable effect on feeding behavior.

3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cycloh↗

The ontogeny of aquatic feeding behavior in Salamandra salamandra: stereotypy and isometry in feeding kinematics

To examine the extent to which aquatic prey-capture behavior in salamanders is stereotyped and how feeding kinematics scales with size, the ontogenetic variability of aquatic feeding behavior was examined in eight Salamandra salamandra. Feeding kinematics (seven duration and angular displacement variables), kinematic variance and capture performance were quantified and compared in the first several feedings after birth with a series of feedings 8 weeks later, just prior to metamorphosis. Analysis of variance revealed no statistically significant ontogenetic differences in the kinematic variables, and individual differences were found in only two variables (maximum gape angle and gape cycle time). A comparison of the relative kinematic variance within individuals revealed no significant differences in variance during ontogeny. In addition, capture success rate did not change. The strike is significantly faster than that of other salamanders. These results indicate that the initial prey-capture behavior remains unchanged throughout larval ontogeny. Thus, aquatic strike behavior in S. salamandra is developmentally fixed (innate) and does not appear to be influenced by learning or improvement in 'skill', supporting the hypothesis that aquatic salamander feeding is a highly stereotyped, unmodulated behavior. In addition, the lack of kinematic change through ontogeny indicates that feeding kinematics do not scale with body size, contrary to predictions that movements should be slower in larger animals.

Journal Article↗

Influence of 5-HT1A agonist on the feeding behavior of Coturnix japonica (Galliformes: Aves).

In this study, we investigate the effect of serotonin receptor 5-HT1A stimulation on the feeding behavior of quails (Coturnix japonica). The administration of 5-HT1A agonist, 8-OH-DPAT (0.05 to 5.0 mg/Kg) dose-dependently inhibited the food intake in normally fed quails. Greater inhibition was attained with 5.0 mg/kg (0.93 +/- 0.21 g vs. 5.83 +/- 0.25 g, P < 0.05, 2 h after food offer). A comparable response was obtained from previously fasted quails. At end of 2 h, a higher dose of 8-OH-DPAT induced more intense hypophagy (1.59 +/- 0.41 g vs. 6.85 +/- 1.04 g, P < 0.0001). Previous treatment with the antagonist 5-HT1A/beta-adrenergic, propranolol, failed to block the inhibitory action of 8-OH-DPAT, but instead, intensified it (controls, 5.22 +/- 1.09 g; 8-OH-DPAT, 1.41 +/- 0.19 g; propranolol + 8-OH-DPAT, 0.44 +/- 0.25 g, P < 0.01, for all comparisons). The administration of an isolated higher dose of propranolol induced a hypophagic action (controls, 4.5 +/- 0.8 g vs. propranolol, 2.0 +/- 0.2 g, P < 0.01). Current outcomes suggest a possible role of 5-HT1A receptor on the feeding behavior of quails, as opposed to mammals. On the other hand, the intensified hypophagy induced by previous administration of propranolol raises the hypothesis of a beta-adrenergic excitatory mechanism that controls the feeding behavior of quails.

8-Hydroxy-2-(di-n-propylamino)tetralin↗

Characterization of the impaired feeding behavior in rats given haloperidol or dopamine-depleting brain lesions.

Systemic administration of 0.2 mg/kg of the dopamine antagonist haloperidol reduced the rate of feeding in food-deprived rats, whereas a dose of 0.4 mg/kg suppressed both the rate of feeding and time spent feeding. Pre-feeding a group of rats decreased the time spent feeding but had minimal effects on the rate of feeding. Regression analysis showed that food intake, time spent feeding, and rate of feeding were related to each other in different ways in haloperidol-treated and pre-fed rats. Near-total depletion of brain dopamine by injection of the neurotoxin 6-hydroxydopamine into the medial forebrain bundle initially decreased both time spent feeding and feeding rate. When rats that were initially aphagic after dopamine depletion recovered feeding behavior, their rate of feeding did not return to control values, and they spent more time feeding than control rats. Similarly, 6-hydroxydopamine-treated rats with smaller dopamine depletions, which were not initially aphagic after the lesions, nevertheless had a prolonged reduction in the rate of feeding. Although control rats typically held the food pellets in both forepaws while feeding, dopamine-depleted rats often fed with one or no paws holding the pellet. The suppression of food intake and rate of feeding in 6-hydroxydopamine-treated rats was correlated with the depletion of dopamine in the lateral striatum, but not the medial striatum. These results indicate that dopamine in the striatum is involved in aspects of motor control that are necessary for efficient feeding behavior in rats.

Animals↗

Effects of feeding systems on social and feeding behavior and performance of finishing pigs.

Two experiments were conducted to study the effects of feeding systems on feeding behavior, aggression, social ranks and average daily gain (ADG) of pigs. In Exp. 1, feed was delivered during the day from 1100 to 1400 and at night from 2300 to 0200. One pen containing 10 barrows and 10 gilts was used. Correlation coefficients were calculated between pairs of traits. In Exp. 2, four feeding systems were tested using similar group composition as in Exp. 1. Two feeding systems were ad libitum, offering either dry or wet feed; the other two used time-restricted feeding from 0900 to 1100 and from 1600 to 1800, but with water supplied either ad libitum or time-restricted. Analyses of variance were used to test feeding system effects; correlation coefficients were calculated for pairs of traits. Results of Exp. 1 indicated that pigs displayed predominantly daytime activities. Frequency of aggressive acts were correlated significantly with feeding frequency (r = .48), time to first feeding (r = -.50) and ADG (r = .56). In Exp. 2, pigs on time-restricted feeding with ad libitum water had significantly depressed ADG and reduced feed intake. A possible association between time-restricted feeding and water intake is postulated. Feeding behavior, aggression and social rank were associated with ADG in time-restricted systems but not in ad libitum systems. There was a tendency in time-restricted-fed pigs for the more aggressive pigs to perform more feeding activities, to rank higher in the social order, and to gain faster.

Aggression↗

Feed stalls affect the social and feeding behavior of lactating dairy cows.

The first objective of this study was to study the effects of increased bunk space on the frequency of aggressive behavior at the feed bunk and on feed access. The second objective was to determine whether the addition of partitions (feed stalls) between adjacent cows would provide additional protection while feeding, particularly for subordinate cows. Twenty-four lactating Holstein cows were subjected to each of 3 treatments in 3 successive 10-d treatment periods using a 3 x 3 Latin square design. The treatments tested were: 1) 0.64 m of feed bunk space/cow, 2) 0.92 m of feed bunk space/cow, and 3) feed stalls (0.87 m of feed bunk space/cow with feed stall partitions separating adjacent cows). Time-lapse video was used to quantify the feeding and standing behavior, as well as the aggressive behavior (displacements) displayed by the cows at the feed bunk. To meet our first and second objectives, we compared data from the 0.64 m/cow treatment with that from the 0.92 m/cow treatment, and data from the 0.92 m/cow treatment with that from the feed-stall treatment, respectively. Total daily feeding time increased when feed bunk space was increased from 0.64 to 0.92 m/cow. Further, the time spent standing in the feeding area while not feeding and the frequency of aggressive interactions at the feed bunk decreased when more bunk space was provided. The addition of feed stalls resulted in more pronounced effects compared with when cows had 0.92 m/cow of bunk space. The feed stalls also forced cows to change the strategy by which they displaced others from the feed bunk, forcing them to also initiate contact at the rear of the animal they were displacing rather than only from the front and side, as in the other 2 treatments. Further, when the cows were provided with additional feeding space, particularly when combined with feed stalls, those cows with lower social status at the feed bunk experienced the greatest decreases in the number of times they were displaced per day. The results indicated that providing increased feed bunk space, particularly when combined with feed stalls, will improve access to the feed and reduce competition at the feed bunk, particularly for subordinate cows.

Aggression↗

Neuronal elements that mediate escape swimming and suppress feeding behavior in the predatory sea slug Pleurobranchaea.

1. The white, bilaterally paired A1 interneurons of the cerebropleural ganglion of Pleurobranchaea californica fire rhythmic bursts of action potentials during escape swimming behavior. We studied the role of the A1s in swimming behavior and pattern generation in whole animal and isolated CNS preparations. 2. The escape swim is a cyclic sequence of dorsal and ventral flexions of the body. During the swim, A1 bursts precede and accompany the dorsal flexion phase of the cycle. Hyperpolarization of A1 to prevent spike activity interrupts swimming behavior in the whole animal and fictive swimming in the isolated CNS. Stimulated A1 activity was not observed to cause swimming in whole animals, and was only occasionally sufficient to trigger fictive swimming activity in the isolated CNS. 3. In quiescent whole animal preparations, stimulation of a single A1 normally causes a single dorsal flexion followed by body flexion to the side contralateral to the stimulated cell; characteristically, A1 spike activity stimulates feedback inhibition coinciding with the end of dorsal flexion and the onset of contralateral flexion. 4. A1 spike activity suppresses feeding behavior and causes proboscis retraction in whole animal preparations induced to feed. A1 activity also suppresses fictive feeding driven by stimulation of the critical phasic paracerebral neurons (PCps) of the motor network of feeding in the isolated CNS. Concomitantly, A1 spikes cause potent inhibition of the PCp interneurons. 5. The A1s are specifically excited by noxious mechanical and chemical stimuli, but are not affected by feeding stimuli or the occurrence of feeding behavior. 6. We conclude that the A1 neurons are elements of an escape swimming pattern generator, and that they are probably homologous to the similar C2 neurons of the nudibranch Tritonia diomedea. One of their functions outside of generating the swim pattern may be the suppression of feeding behavior in response to noxious stimulation. These observations provide a neural mechanism for the original observations of the dominance of escape swimming behavior over feeding.

Action Potentials↗

Feeding behavior in primiparous lactating sows: impact of a high-fiber diet during pregnancy.

Voluntary feed intake of hyperprolific sows can be insufficient to cover the requirements for milk production and maintenance of body condition. A bulky diet fed during pregnancy is known to prepare sows for an ad libitum feed supply after parturition as shown by the increased feed intake during lactation. The aim of this study was to investigate the feeding behavior of young sows during their first lactation to evaluate the further impact of the feeding experience acquired during pregnancy, through the addition of dietary fiber in the diet. Analysis of the feeding pattern and the profile of feed intake tested the hypothesis that lactating sows would exhibit different feeding strategies depending on the diet during pregnancy. During pregnancy, 24 primiparous sows (Large White x Landrace) were offered either 2.4 kg of a control diet/d containing 3.16% crude fiber or 2.8 kg of a high-fiber diet/d containing 12.42% crude fiber. All sows received 33 MJ of DE/d. From the first day postpartum until weaning, all sows were offered the same lactation diet ad libitum. The feeding pattern during lactation was recorded as ADFI, meal frequency, and meal size. In lactation, the ADFI did not differ according to the treatment. Compared with control sows, high-fiber sows consumed their diet in more (P < 0.05) but smaller meals (P < 0.05). In both treatments, ADFI and the number of daily meals increased over weeks of lactation (P < 0.001). All sows presented a strong diurnal and bimodal feeding activity evolving toward 2 distinct feeding periods occurring from 0500 to 0900 and from 1400 to 1800 and accounting for 0.64 of the total daily feed intake during the third week of lactation. The provision of a fibrous diet during pregnancy pointed out the role of an early feeding experience on the development of feeding behavior during the first reproductive cycle.

Animal Feed↗

Changes in the feeding behavior of rats elicited by histamine infusion.

In this study, we examined the effect of a putative neurotransmitter or a neuromodulator histamine (HA) on the feeding behavior to elucidate its physiological function in the central nervous system. Rats were implanted with a cannula into the suprachiasmatic nucleus through which HA was continuously infused for 200 hours with an Alzet osmotic minipump. The food intake was recorded automatically. This infusion resulted in decrease in food intake during the dark period and increase in it during the light period which contributed to the decrease in total food intake and increase in the percentage of food intake during the light period. Percentage of food intake during the light period is a good index of the amplitude of the circadian rhythm. Presumably, HA is concerned not only in the meal size, but also in the chronological aspect of the feeding behavior. The administration of H1-antagonist, pyrilamine, antagonized the HA induced increase in food intake during the light period. These findings suggest that continuous infusion of HA affected the feeding behavior which is possibly mediated through the H1-receptors in rat brain.

Animals↗

Interaction between estradiol replacement and chronic stress on feeding behavior and on serum leptin.

Exposure to stress may cause either an increase or a decrease in food intake. Behavioral and physiological responses to stress, including alterations in feeding behavior, are sexually dimorphic. This study aimed to evaluate the interaction between estradiol levels and chronic variate stress on the intake of sweet food and on serum levels of leptin, a hormone secreted by the adipose cells with a role in the regulation of body weight. Adult female Wistar rats were used. After ovariectomy, the animals received estradiol replacement (or oil) subcutaneously. Rats were then divided in controls and stressed (submitted to 30 days of variate stress). Consumption of sweet food and of serum leptin was measured. Although animals receiving estradiol replacement presented smaller weight gain, they showed an increased consumption of sweet food. Chronic variate stress decreased sweet food intake at 30, but not at 20, days of treatment. Estradiol replacement in the stressed group prevented both the reduction observed in sweet food intake and the increase in leptin levels. These results suggest that there is an interaction between chronic stress and estradiol replacement in feeding behavior concerning sweet food consumption, and this interaction may be related to altered leptin levels.

Animals↗

[Distorted control of feeding behavior induced by abnormally regulated peripheral energy metabolism].

To regulate feeding behavior and energy metabolism, a variety of neuronal and hormonal messages are integrated by glucose sensing system located in peripheral organ and central nervous system. Among them, a hepatoportal glucose sensor plays a major role in perception of peripheral humoral information such as brain-gut peptides and cytokines. These signals are transmitted to the hypothalamus through the hepatic afferent vagus nerve and the nucleus of the solitary tract. Recent molecular approaches using knock out or transgenic mice have indicated important effects of peripheral energy metabolism on feeding control. Particularly, fatty acid metabolism in the liver and functions of uncoupling protein family in the brown adipose tissue and the muscle play an essential role as detector for energy storage, and in turn may be contributable to regulation of feeding behavior.

Adipose Tissue, Brown↗

The role of norepinephrine in feeding behavior.

When dopamine-beta-hydroxylase is inhibited with FLA-63 (10 mg/kg) free feeding behavior is disrupted in satiated rats. While the average number of meals taken was not different from vehicle injected controls, meal size was decreased 58% in the first 9 hr after treatment with FLA-63. In starved animals, FLA-63, when given alone, produced little effect on feeding behavior, even though norepinephrine depletion was in excess of 40%. When given in combination with RO4-1284 (5 mg/kg), a vesicular reuptake inhibitor, feeding was reduced to 16% of control intake and norepinephrine was specifically depleted 99%. Feeding was reliably reinstated in animals which received FLA-63 plus RO4-1284 with either dl-threo-DOPs, a metabolic precursor to NE, or direct intrahypothalamic injections of NE. These findings suggest that the feeding inhibition observed after treatment with FLA-63 plus RO4-1284 is due to disruption of transmission in brain NE systems. A non-anorectic dosage of L110-140 (3.73 mg/kg), a specific FLA-63. Taken collectively, these findings suggest that the primary role of NE in feeding is maintenance of the consummatory response and that these effects are expressed in relation to activity in other neurochemical systems.

2H-Benzo(a)quinolizin-2-ol, 2-Ethyl-1,3,4,6,7,11b-↗

The rise, fall, and resurrection of the ventromedial hypothalamus in the regulation of feeding behavior and body weight.

Early researchers found that lesions of the ventromedial hypothalamus (VMH) resulted in hyperphagia and obesity in a variety of species including humans, which led them to designate the VMH as the brain's "satiety center." Many researchers later dismissed a role for the VMH in feeding behavior when Gold claimed that lesions restricted to the VMH did not result in overeating and that obesity was observed only with lesions or knife cuts that extended beyond the borders of the VMH and damaged or severed the ventral noradrenergic bundle (VNAB) or paraventricular nucleus (PVN). However, anatomical studies done both before and after Gold's study did not replicate his results with lesions, and in nearly every published direct comparison of VMH lesions vs. PVN or VNAB lesions, the group with VMH lesions ate substantially more food and gained twice as much weight. Several other important differences have also been found between VMH and both PVN and VNAB lesion-induced obesity. Concerns regarding (a) motivation to work for food and (b) the effects of nonirritative lesions have also been addressed and answered in many studies. Lesion studies with weanling rats and adult pair-tube-fed rats, as well as recent studies of knockout mice deficient in the orphan nuclear receptor steroidogenic factor 1, indicate that VMH lesion-induced obesity is in large part a metabolic obesity (due to autonomic nervous system disorders) independent of hyperphagia. However, there is ample evidence that the VMH also plays a primary role in feeding behavior. Neuroimaging studies in humans have shown a marked increase in activity in the area of the VMH during feeding. The VMH has a large population of glucoresponsive neurons that dynamically respond to blood glucose levels and numerous histamine, dopamine, serotonin, and GABA neurons that respond to feeding-related stimuli. Recent studies have implicated melanocortins in the VMH regulation of feeding behavior: food intake decreases when arcuate nucleus pro-opiomelanocortin (POMC) neurons activate VMH brain-derived neurotrophic factor (BDNF) neurons. Moderate hyperphagia and obesity have also been observed in female rats with damage to the efferent projections from the posterodorsal amygdala to the VMH. Hypothalamic obesity can result from damage to either the POMC or BDNF neurons. The concept of hypothalamic feeding and satiety centers is outdated and unnecessary, and progress in understanding hypothalamic mechanisms of feeding behavior will be achieved only by appreciating the different types of neural and blood-borne information received by the various nuclei, and then attempting to determine how this information is integrated to obtain a balance between energy intake and energy output.

Animals↗

The relationship of enzyme activity to feeding behavior in rats: lipoprotein lipase as the metabolic gatekeeper.

A model for peripheral modulation of feeding behavior is discussed. This model proposes that under certain genetic, hormonal or dietary conditions adipose tissue lipoprotein lipase (AT-LPL) acts as a gatekeeper directing triglyceride derived fuels to adipose tissue and away from other tissues. It is proposed that shifts in the activity of the gatekeeper enzyme LPL result in changed feeding behaviors in rodents and possibly in man. In the fafa rat, the alterations in LPL activity may play the role of a developmental trigger or initiator. In other cases, the changes in AT-LPL may be adaptive rather than initiatory and may be permissive of behaviors rather than necessary antecedents.

Animals↗

Neuropeptide Y (NPY)-induced feeding behavior in female rats: comparison with human NPY ([Met17]NPY), NPY analog ([norLeu4]NPY) and peptide YY.

Porcine neuropeptide Y (pNPY) administered into the third ventricle of the brain is known to elicit a powerful feeding response in steroid-treated ovariectomized and intact male rats. The present study compared the effects of pNPY and 3 structurally related peptides, human NPY (hNPY), an analog of NPY (NPY-A, [norLeu4]NPY) and peptide YY (PYY) on feeding behavior in intact female rats. Intraventricular administration of pNPY, hNPY, NPY-A and PYY over a dose range of 0.5 to 10 micrograms evoked feeding behavior to a varying extent. Cumulative food intake during 60 and 120 min was increased in a dose-related fashion at 0.5 and 2.0 microgram for the 4 peptides. Whereas the 10-micrograms dose of pNPY evoked a feeding response smaller than that seen after 2 micrograms, the responses to either 10 micrograms hNPY or 10 micrograms PYY were similar to that seen after 2 micrograms. The effects of these peptides on the time spent eating were quite different: while pNPY increased the time spent eating, this effect was not dose-related, whereas hNPY, NPY-A and PYY produced dose-related increments in the time spent eating. The most dramatic increment in local eating rate was observed after 2.0 micrograms pNPY, with lesser increments seen after 2.0 microgram hNPY and NPY-A. This increased local eating was apparently responsible for the highest cumulative food intake observed. These results demonstrate that (a) 2 micrograms pNPY is equally effective in stimulating feeding behavior in intact female rats as it is in steroid-primed ovariectomized female and intact male rats.(ABSTRACT TRUNCATED AT 250 WORDS)

Amino Acid Sequence↗

Multimodal integration in the feeding behaviors of predatory teleost fishes.

The search for useful model systems to study sensory processing in vertebrate nervous systems has resulted in many neuroethological studies investigating the roles played by a single sensory modality in a given behavior. However, animals behaving in a complex, three-dimensional environment receive a large amount of information from external and internal receptor arrays. Clearly, the integration of sensory afference arising from different modalities into a coherent 'gestalt' of the world is essential to the behaviors of most animals. Over the past several years researchers in my laboratory have examined the roles played by the visual and lateral line sensory systems in organizing the feeding behavior of two species of predatory teleost fishes, the largemouth bass, Micropterus salmoides and the muskellunge, Esox masquinongy. The free-field feeding behaviors of these fishes was studied quantitatively in intact animals and compared to animals in which the lateral line and visual systems had been selectively suppressed. The data show that both bass and muskie employ similar approach and strike behaviors. Vision is crucial to the initial detection of, and orientation to, prey. Lateral line and vision together determine the optimum distance and angular deviation for the initiation of a rapid strike toward the prey. Blinded animals are able to strike accurately at prey at very close ranges and small angular deviations, indicating that this modality presents sufficient information to direct the behavior during the final phases of the strike. The results demonstrate that there is a hierarchy of senses involved in feeding behavior, with different modalities playing critical roles in succeeding phases.

Animals↗

The role of the melanocortin system and the melanocortin-4 receptor in ring dove (Streptopelia risoria) feeding behavior.

The melanocortin-4 receptor (MC4-R) is an important mediator of the effects of two melanocortin system ligands, alpha melanocyte stimulating hormone (alpha-MSH) and agouti-related peptide (AGRP), on feeding behavior and energy balance in mammals. Although an avian homologue of the mammalian MC4-R has recently been identified, there is little information on the role of this receptor and the melanocortin system in avian feeding and body weight regulation. In these studies, we measured changes in feeding behavior in ring doves (Streptopelia risoria) following intracerebroventricular (i.c.v.) injection of various melanocortin receptor agonists and antagonists. The selective MC4-R antagonist HS014 elevated food intake within 4 h at all three doses tested (0.02, 0.2, and 2 nmol). A 1 nmol dose of the endogenous antagonist AGRP also stimulated feeding but only after a post-injection interval of 10 h. Surprisingly, the MC3-R and MC4-R antagonist SHU9119 not only failed to stimulate food intake at the same doses as HS014, but actually inhibited food intake at 8 h after injection. Whether this was due to toxicity effects or differences in the pharmacology of avian and mammalian melanocortin receptors remains to be determined. Food-deprived doves showed a fourfold increase in the number of AGRP-immunoreactive cells in the tuberal region of the hypothalamus and 5 ng of the MC3-R and MC4-R agonist MTII significantly attenuated the amount of food consumed by food-deprived birds that were allowed to re-feed. These data support a role for the melanocortin system and the melanocortin-4 receptor in the ring dove feeding behavior.

Agouti-Related Protein↗

Genome-wide association studies for feed efficiency, production and feeding behavior traits in Canadian purebred Duroc pigs.

This study aimed to identify potential genetic variants and candidate genes associated with feed efficiency (FE), production, and feeding behavior traits in Canadian purebred Duroc pigs. Genome-wide association studies (GWAS) were conducted using 8,861 individuals and an imputed Affymetrix PigGen Canada 50K panel v2.0 using a linear mixed model (LMM) and a Bayesian B model. This analysis used an adjusted P-value threshold (ranging from 6.6&#x202f;&#xd7;&#x202f;10-5 to 1.3&#x202f;&#xd7;&#x202f;10-4) using a false-discovery rate to determine significance. The number of significant SNPs identified for each trait was as follows: average daily gain (ADG, 48), daily feed intake (DFI, 85), feed conversion ratio (FCR, 101), residual feed intake (RFI, 37), residual gain (RG, 64), residual intake and gain (RIG, 55), backfat thickness (BF, 100), loin depth (LD, 6), Kleiber's ratio (KR, 0), total time spent eating per day (TPD, 7), and number of visits to the feeder per day (NVD, 6). Several traits (BF, DFI, FCR, RFI, RG, and RIG) showed strong overlapping signals on chromosomes 7 and 10 with 24 shared significant SNPs, indicating potential shared genetic mechanisms. These traits also had 71 overlapping candidate genes, such as PACSIN1, PTCH1, ADIPOR1, and ITPR3, associated with glucose, lipid, and cholesterol metabolism. Well-known candidate genes in literature associated with growth and fatness such as MC4R and CDH20 were also identified to be associated with ADG, BF, FCR, and DFI in this study. Gene ontology enrichment analysis revealed that a set of the candidate genes were involved in the gonadotropin-releasing hormone (GnRH) and the platelet-derived growth factor (PDGF) signaling pathways. Overall, this study contributed to understanding the genetic architecture and provided a biological foundation for improving FE, production, and feeding behavior traits in Canadian Duroc pigs, facilitating the selection of more efficient pigs.

Sus scrofa↗