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Anim Biosci > Volume 29(9); 2016 > Article
Liu, Xu, Wang, Jiao, and Lin: Peripheral Insulin Doesn’t Alter Appetite of Broiler Chicks


An experiment was conducted to investigate the effect of peripheral insulin treatment on appetite in chicks. Six-d-age chicks with ad libitum feeding or fasting for 3 h before injection received a subcutaneous injection of 0, 1, 3, 5, 10, or 20 IU of insulin or vehicle (saline). The results showed peripheral insulin treatment (1 to 20 IU) did not alter significantly the feed intake in chicks under either ad libitum feeding or fasting conditions within 4 h (p>0.05). Compared with the control, plasma glucose concentration was significantly decreased after insulin treatment of 3, 5, 10, and 20 IU for 4 h in chicks with ad libitum feeding (p<0.05). In fasted chicks, 10 and 20 IU insulin treatments significantly decreased the plasma glucose level for 4 h (p<0.05). Peripheral insulin treatment of 10 IU for 2 or 4 h did not significantly affect the hypothalamic genes expression of neuropeptide Y, proopiomelanocortin, corticotropin-releasing factor and insulin receptors (p>0.05). All results suggest peripheral administration of insulin has no effect on appetite in chicks.


The hypothalamus plays a pivotal role in integrating external environmental cues and generates the appropriate responses to influence feed intake in mammals, as well as in birds (Schwartz et al., 2000). As in mammals, a population of neurons that influence appetite exist in the hypothalamus of avian species: Orexigenic neurons (e.g., neuropeptide Y [NPY]) (Schwartz et al., 2000) and anorexigenic neurons (e.g., proopiomelanocortin [POMC], corticotropin-releasing factor) (Richards, 2003; Boswell, 2005). Peripheral signal reflecting energy balance can be integrated at the hypothalamic arcuate nucleus in mammals and infundibular nucleus in avian species.
Insulin has multiple functions in insulin receptor (INSR)-expressing tissues (hypothalamus, fat, muscle, liver) (Saltiel and Kahn, 2001; Shiraishi, et al., 2011a). The INSRs are also widely distributed in the central nervous system, and regulate vital physiological processes in mammals (Pagotto, 2009). Intracerebroventricularly (ICV) injection of insulin can decrease feed consumption in layer chicks when compared with control (Shiraishi et al., 2011b). Honda et al. (2007) demonstrated that central insulin was as an appetite-suppressive peptide in chicken central nervous system, and this anorexigenic action was mediated by POMC and corticotropin-releasing hormone (CRH). But the regulation of peripheral insulin on appetite in chickens remains unknown. In the present study, we examined the changes in feed intake and appetite-related peptides in the hypothalamus of broiler chicks after subcutaneous insulin injection and determined the relationship between peripheral insulin and appetite.



Male broiler (Arbor Acres) chicks were obtained from a local hatchery at 1 day of age and reared in an environmentally controlled room. Temperature and lighting was maintained according to commercial conditions. All chicks received a starter diet containing 21.5% crude protein and 12.33 MJ/kg of metabolizable energy. All birds had free access to feed and water. This study was approved by the Shandong Agricultural University and carried out in accordance with the “Guidelines for Experimental Animals” of the Ministry of Science and Technology (Beijing, China).

Experimental protocol and sample collection

Experiment 1. Effects of insulin on feed intake in chicks under feeding condition

A total of 72, 6-d-old chicks of similar body weight were divided into 6 groups, 6 replicates per group, and 4 chicks per replicate. The chicks with ad libitum feeding received a subcutaneous injection of 0, 1, 3, 5, 10, or 20 IU of insulin or vehicle (saline). Food intake was recorded in 0.5, 1, 2, 3, and 4 h after injection. A blood sample was drawn from a wing vein using a heparinised syringe for 30 s and collected in iced tubes 4 h after injection. Plasma was obtained following centrifugation at 400 g for 10 min at 4°C and stored at −20°C for subsequent analysis of glucose and insulin.

Experiment 2. Effects of insulin on feed intake in chicks under fasting condition

A total of 72, 6-d-old chicks of similar body weight were divided into 6 groups, 6 replicates per group, and 2 chicks per replicate. The chicks, after fasting for 3 h, received a subcutaneous injection of 0, 1, 3, 5, 10, or 20 IU of insulin or vehicle (saline). Feed intake was recorded 0.5, 1, 2, 3, and 4 h after injection. A blood sample was collected 4 h after injection. The treatment of control and 10 IU insulin were repeated twice. During the second experiment, the chicks were continuously fasted for 2 or 4 h after peripheral insulin administration, and the hypothalamus samples were collected according to Yuan et al. (2009). After being flash-frozen in liquid nitrogen, the samples were stored at −80°C for subsequent RNA extraction.

Measurement of plasma glucose and insulin levels

Plasma glucose concentration was measured spectrophotometrically with commercial diagnostic kits (Hitachi High-Technologies Corp.; Jiancheng Bioengineering Institute, Nanjing, China) that have been successfully applied in poultry research (Wang et al., 2012).
Plasma insulin was measured by radioimmunoassay with a guinea pig anti-porcine insulin serum (3V Bio-engineering group Co., Weifang, China). In this procedure, 125I-labelled porcine insulin competes with chicken insulin for sites on anti-porcine insulin antibodies that are immobilised on the wall of a polypropylene tube. Significant cross-reactivity has been observed between chicken insulin and guinea pig anti-porcine sera (Simon et al., 1974). The insulin in this study is referred to as immunoreactive insulin. The sensitivity of the assay was 1 μIU/mL, and all samples were included in the same assay to avoid interassay variability. The intraassay coefficient of variation was 2.88%.

RNA isolation and analysis

Total RNA extraction and quantitative real-time polymerase chain reaction (PCR) were performed as described previously (Liu et al., 2014). Sequences of primers are shown in Table 1. The PCR data were analyzed with the 2−ΔΔCT method (Livak and Schmittgen, 2001). The mRNA levels of target genes were normalized to 18S and β-actin (ΔCT). On the basis of the Ct values, 18S and glyceraldehydes-3-phosphate dehydrogenase (GAPDH) mRNA expression were stable across the treatments in this study (p>0.1).

Statistical analysis

The data are presented as means±standard error of the mean. Homogeneity of variances among the treatments was confirmed using Bartlett’s test. All data were subjected to one-way analysis of variance analysis to test the main effect of the treatment (n = 8). When the main effect of the treatment was significant, the differences between means were assessed by Duncan’s multiple range analysis. Less than 0.05 p value was considered statistically significant.


Peripheral insulin treatment (1 to 20 IU) did not significantly alter the feed intake of chicks either under ad libitum feeding or fasting conditions in 0.5, 1, 2, 3, and 4 h (p>0.05). Compared with the control, plasma glucose concentration was significantly decreased 4 h after insulin treatment of 3, 5, 10, and 20 IU in chicks under ad libitum feeding (p<0.05). But the increased plasma insulin concentration was only observed in the doses of 10 and 20 IU in chicks under ad libitum feeding (p<0.05). In fasted chicks, 4 h after 10 and 20 IU insulin treatment the plasma glucose concentration was significantly decreased (p<0.05), but not following the dose of 1, 3, and 5 IU (p>0.05). Peripheral insulin treatment (1 to 20 IU) induced a dose-dependent increase in insulin concentration of plasma in fasted chicks (p<0.05). Two or 4 h after peripheral insulin treatment of 10 IU there was no significant effects on the hypothalamic genes expression of NPY, POMC, CRH, and INSR.


In the present study, we investigated the effect of peripheral insulin treatment on appetite of chicks. Our data demonstrated that i) Peripheral insulin injection dose not significantly affect the feed intake of chicks; ii) Peripheral insulin treatment dose not significantly alter the hypothalamic INSR and appetite-related genes expression of NPY, POMC, and CRH. The results suggest that peripheral insulin injection does not alter appetite of chicks.
In mammals, changes in the circulating level of insulin signal the hypothalamus to effect long-term changes in energy balance by activating and/or inhibiting specific anabolic and catabolic pathways (Schwartz et al., 2000; Woods et al., 2006). Obici et al. (2002) found that insulin could decrease appetite via INSRs in mammals. Although INSRs have been identified in the chicken brain (Simon and Leroith, 1986), the effect of peripheral administration of insulin on appetite in birds is not clear. Because plasma insulin levels rise and fall with increases and decreases in energy state in chickens such as during fasting and refeeding, it is possible that peripheral insulin could serve as peripheral signal of energy state in birds as they have been postulated to do in mammals (Niswender et al., 2004; Woods et al., 2006). But the feed intake was not changed by peripheral insulin treatment in fasted and fed chicks, which is consistent with the previous observation of ICV injection of insulin-induced no change in the feed consumption in boiler chicks under fasting and ad libitum conditions (Shiraishi et al., 2011b). But the result is inconsistent with the study in layer chicks and sheep. Thirty min following an ICV insulin injection the feed consumption in layer chicks was significantly inhibited under both fasting and ad libitum conditions (Shiraishi et al., 2011b). And 1 h after the intrajugular administration of insulin the feed intake of sheep was significantly depressed (Deetz and Wangsness, 1980). These conflicting results suggest that insulin resistance exists of broiler chicks, possibly due to persistent hyperinsulinemia, which results in a down-regulation of central nervous system INSR expression (Shiraishi et al., 2011b).
Chickens have a blood glucose level that is twice as high as that of most mammals, and can survive massive doses of insulin that would be lethal in mammals (Gibson et al., 1980). So chickens are regarded as an insulin resistant animal. In our experiment, the high dose insulin changed plasma glucose level, but not low doses. Therefore, large doses of insulin are required for stimulation of glucose uptake in insulin responsive tissues in chickens (Gomez-Capilla and Langslow, 1977). The regulation of blood glucose in chickens is unorthodox and not well understood, yet glucose is an important signal of energy or nutritional status that is integrated into the regulation of feed intake and energy metabolism in mammals. Transient change in plasma glucose level caused by insulin did not alter feed intake in chicks, which is consistent with the previous study in chickens (Simon et al., 2000), but not in mammals (Branton et al., 2014). Therefore, the role of insulin, as an afferent signal for energy stores in broiler chickens remains to be determined.
Blood insulin is thought to cross the blood-brain barrier to act within the brain to help control appetite via blinding INSR. In neonatal chicks, immunostaining revealed hypothalamic neuron expressing INSRs in the infundibular nucleus (the avian equivalent of the mammalian arcuate nucleus), paraventricular nucleus, ventromedial hypothalamus and lateral hypothalamus (Shiraishi et al., 2011a). However, INSR levels were not affected by feeding condition in broiler chicks, but were affected in layer chicks (Shiraishi et al., 2011b). In our experiment, peripheral insulin did not significantly affect hypothalamic INSR levels. The results imply that hypothalamic INSR are not sensitive to the insulin in fat-line chickens, and it may be an explanation why insulin resistance or typrII diabetes easily occurs in obese animals.
NPY has been shown to be a potent orexigenic agent in chickens when administered centrally (Kuenzel and McMurtry, 1988). ICV NPY injection can elevate the plasma insulin level in broiler chicks (Kuenzel and McMurtry, 1988). In addition, hypothalamus-damaged cockerels appeared hypertrophy of pancreatic B cells, hyperactivity of insulin secretion and hyperphagia (Sonoda, 1983). But we did not detect any change of hypothalamic NPY mRNA levels, which is inconsistent with ICV insulin injection in chicks (Shiraishi et al., 2011a) and with ICV insulin injection in rats (Schwartz et al., 1992). The results suggest regulation of insulin on hypothalamic NPY is subject to species diversity. In addition, the effect of central NPY on peripheral insulin is non-reversible in chicks.
Different from NPY, hypothalamic POMC neurons play an important role in transducing the afferent input, i.e., hormonal and metabolic signals, into a neuronal anorexigenic response in both chickens and mammals. Hypothalamic POMC mRNA levels are increased by peripheral insulin and decreased by fasting in mammals (Benoit et al., 2002). Although central insulin administration could up-regulate POMC mRNA level in chicks (Honda et al., 2007), fasting for 48 h (Song et al., 2012) or peripheral leptin (Dridi et al., 2005), insulin administration has no significant effect on hypothalamic POMC mRNA levels (Song et al., 2012). The results suggest that hypothalamic POMC of chick is insensitive to peripheral metabolic signals.
ICV CRH injection significantly decreased feed intake in both feeding and overnight-fasting broiler chickens and laying hens (Denbow et al., 1999). Chan et al. (2005) has reported that peripheral insulin administration increases CRH mRNA level in rat hypothalamus. Hypothalamic CRH mRNA level in chicks hypothalamus is significantly increased by central insulin administration (Honda et al., 2007), but not by peripheral insulin injection. All results imply that the effect of insulin is not only associated with species, but also with treatment method (e.g., central and peripheral administration).


Peripheral insulin (1 to 20 IU) administration didn’t alter the feed intake in chicks under ad libitum and fasting conditions. And hypothalamic INSR, POMC, CRH, and NPY genes were also not changed by peripheral insulin administration. All results suggest peripheral insulin administration has no effect on appetite in chicks.



We certify that there is no conflict of interest with any financial organization regarding the material discussed in the manuscript.


This work was supported by grants from the National Natural Science Foundation of China (31072045, 31301993, 31472114, 31172226, 31472115) and the Natural Science Foundation of Shandong Province (ZR2014CP028).

Figure 1
Effect of insulin on feed intake in chicks. (A) chicks under ad libitum condition; (B) chicks under fasting condition.
Figure 2
Effect of insulin on plasma glucose and insulin levels in chicks. (A) and (B) chicks under ad libitum condition; (C) and (D) chicks under fasting condition.
Figure 3
Effect of insulin on mRNA levels of hypothalamic neuropeptide Y (NPY), proopiomelanocortin (POMC), corticotropin-releasing hormone (CRH), and insulin receptor (INSR) in chicks. (A) chicks under ad libitum condition; (B) chicks under fasting condition.
Table 1
Gene-specific primers used for the analysis of chick gene expression
Gene GenBank accession no. Primer sequences (5′-3′) Product size (bp)

NPY, neuropeptide Y; CRH, corticotropin-releasing hormone; INSR, insulin receptor; POMC, proopiomelanocortin.


Benoit SC, Air EL, Coolen LM, Strauss R, Jackman A, Clegg DJ, Seeley RJ, Woods SC. 2002. The catabolic action of insulin in the brain is mediated by melanocortins. J Neurosci 22:9048–9052.
crossref pmid pmc
Boswell T. 2005. Regulation of energy balance in birds by the neuroendocrine hypothalamus. J Poult Sci 42:161–181.
Branton A, Akhavan T, Gladanac B, Pollard D, Welch J, Rossiter M, Bellissimo N. 2014. Pre-meal video game playing and a glucose preload suppress food intake in normal weight boys. Appetite 83:256–262.
crossref pmid
Chan O, Inouye K, Akirav E, Park E, Riddell MC, Vranic M, Matthews SG. 2005. Insulin alone increases hypothalamo–pituitary–adrenal activity, and diabetes lowers peak stress responses. Endocrinology 146:1382–1390.
crossref pmid
Denbow DM, Snapir N, Furuse M. 1999. Inhibition of food intake by CRF in chickens. Physiol Behav 66:645–649.
crossref pmid
Deetz LE, Wangsness PJ. 1980. Effect of intrajugular administration of insulin on feed intake, plasma glucose and plasma insulin of sheep. J Nutr 110:1976–1982.
crossref pmid
Dridi S, Swennen Q, Decuypere E, Buyse J. 2005. Mode of leptin action in chicken hypothalamus. Brain Res 1047:214–223.
crossref pmid
Gibson WR, Bourne AR, Sernia C. 1980. D-xylose transport in isolated skeletal muscle of chickens: Effects of insulin and tolbutamide. Comp Biochem Physiol C Comp Pharmacol 67:41–47.
Gomez-Capilla JA, Langslow DR. 1977. Insulin action on glucose utilization in chicken adipocytes. Int J Biochem 8:417–420.
Honda K, Kamisoyama H, Saneyasu T, Sugahara K, Hasegawa S. 2007. Central administration of insulin suppresses food intake in chicks. Neurosci Lett 423:153–157.
crossref pmid
Kuenzel WJ, McMurtry J. 1988. Neuropeptide Y: brain localization and central effects on plasma insulin levels in chicks. Physiol Behav 44:669–678.
crossref pmid
Livak KJ, Schmittgen TD. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2 (Delta Delta C(T)) method. Methods 25:402–408.
crossref pmid
Niswender KD, Baskin DG, Schwartz MW. 2004. Insulin and its evolving partnership with leptin in the hypothalamic control of energy homeostasis. Trends Endocrinol Metab 15:362–369.
crossref pmid
Obici S, Feng Z, Karkanias G, Baskin DG, Rossetti L. 2002. Decreasing hypothalamic insulin receptors causes hyperphagia and insulin resistance in rats. Nat Neurosci 5:566–572.
crossref pmid
Pagotto U. 2009. Where does insulin resistance start? Diabetes Care 32:S174–S177.
crossref pmid pmc
Richards MP. 2003. Genetic regulation of feed intake and energy balance in poultry. Poult Sci 82:907–916.
crossref pmid
Saltiel AR, Kahn CR. 2001. Insulin signalling and the regulation of glucose and lipid metabolism. Nature 414:799–806.
crossref pmid
Schwartz MW, Sipols AJ, Marks JL, Sanacora G, White JD, Scheurink A, Kahn SE, Baskin DG, Woods SC, Figlewicz DP. 1992. Inhibition of hypothalamic neuropeptide Y gene expression by insulin. Endocrinology 130:3608–3616.
crossref pmid
Schwartz MW, Woods SC, Porte D, Seeley RJ, Baskin DG. 2000. Central nervous system control of food intake. Nature 404:661–671.
crossref pmid
Shiraishi J, Tanizawa H, Fujita M, Kawakami S, Bungo T. 2011a. Localization of hypothalamic insulin receptor in neonatal chicks: Evidence for insulinergic system control of feeding behavior. Neurosci Lett 491:177–180.
crossref pmid
Shiraishi J, Yanagita K, Fukumori R, Sugino T, Fujita M, Kawakami S, McMurtry JP, Bungo T. 2011b. Comparisons of insulin related parameters in commercial-type chicks: Evidence for insulin resistance in broiler chicks. Physiol Behav 103:233–239.
crossref pmid
Simon J, Derouet M, Gespach C. 2000. An anti-insulin serum, but not a glucagon antagonist, alters glycemia in fed chickens. Horm Metab Res 32:139–141.
crossref pmid
Simon J, Freychet P, Rosselin G. 1974. Chicken insulin: radioimmunological characterization and enhanced activity in rat fat cells and liver plasma membranes. Endocrinology 95:1439–1449.
crossref pmid
Simon J, Leroith D. 1986. Insulin receptors of chicken liver and brain. Characterization of alpha and beta subunit properties. Eur J Biochem 158:125–132.
crossref pmid
Song Z, Liu L, Yue Y, Jiao H, Lin H, Sheikhahmadi A, Everaert N, Decuypere E, Buyse J. 2012. Fasting alters protein expression of AMP-activated protein kinase in the hypothalamus of broiler chicks (Gallus gallus domesticus). Gen Comp Endocrinol 178:546–555.
crossref pmid
Sonoda T. 1983. Hyperinsulinemia and its role in maintaining the hypothalamic hyperphagia in chickens. Physiol Behav 30:325–329.
crossref pmid
Wang XJ, Wei DL, Song ZG, Jiao HC, Lin H. 2012. Effects of fatty acid treatments on the dexamethasone-induced intramuscular lipid accumulation in chickens. PLoS ONE 7:e36663
crossref pmid pmc
Woods SC, Benoit SC, Clegg DJ. 2006. The brain-gut-islet connection. Diabetes 55:S114–S121.
Yuan L, Ni Y, Barth S, Wang Y, Grossmann R, Zhao R. 2009. Layer and broiler chicks exhibit similar hypothalamic expression of orexigenic neuropeptides but distinct expression of genes related to energy homeostasis and obesity. Brain Res 1273:18–28.
crossref pmid

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