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Constant light in early life induces fear-related behavior in chickens with suppressed melatonin secretion and disrupted hippocampal expression of clock- and BDNF-associated genes

Abstract

Background

Light management plays an important role in the growth and behavior of broiler chickens. Constant light in early post hatch stage has been a common practice in broiler industry for improving growth performance, while whether and how constant light in early life affects the behavior of broiler chickens is rarely reported.

Results

In this study, newly hatched chicks were kept in either constant (24 L:0 D, LL) or (12 L:12 D, LD) photoperiod for 7 d and then maintained in 12 L:12 D thereafter until 21 days of age. Constant light increased the average daily feed intake but not the body weight, which led to higher feed conversion ratio. Chickens in LL group exhibited fear-related behaviors, which was associated with higher corticosterone, lower melatonin and 5-HT levels. Concurrently, constant light exposure increased the mRNA expression of clock-related genes and suppressed the expression of antioxidative genes in the hippocampus. Moreover, brain derived neurotrophic factor/extracellular signal-regulated kinase (BDNF/ERK) pathway was suppressed in the hippocampus of chickens exposed to constant light in the first week post hatching.

Conclusions

These findings indicate that constant light exposure in early life suppress melatonin secretion and disrupts hippocampal expression of genes involved in circadian clock and BDNF/ERK pathway, thereby contributing to fear-related behaviors in the chicken.

Introduction

Light is an important factor affecting the growth and development, behavior and welfare, as well as stress and immune responses [1, 2]. Photoperiod, light wavelength and intensity are three major variables in light management that affect growth and behavior of broiler chickens [3, 4]. Broiler chickens are usually maintained under lighting regimes (hours in light = L, dark = D) with constant (24 L:0 D) or near-constant photoperiod (23 L:1 D) in modern industrialized farms, especially during the early post hatch period, because it was demonstrated that constant lighting regimen stimulates feed intake and promote growth [5]. However, there are some controversial reports questioning the long photoperiods application in broiler industry. It was reported [6] that 12 L:12 D photoperiod improves meat quality attributes in Ross 308 broilers chickens, compared with long photoperiod (20 L: 4 D). Also, near-constant photoperiod (23 L:1 D) increases stress and fear levels in Ross 308 broilers chickens [7], disrupts circadian clock gene expression and cecal microbiome diversity in Hy-Line Brown Layer chickens [8]. Nevertheless, the mechanisms underlying constant or near-constant light-induced malfunctions in the chicken remain largely unknown.

In mammals, constant light has been reported to induce circadian disruption, fatigue, irritability, depression and anxiety [9, 10]. In searching for the underlying mechanisms, many studies focus on melatonin, a hormone secreted by the pineal gland in response to the external light cues [11]. Constant light disrupts circadian rhythm through inhibiting melatonin secretion from the pineal gland. Previously, we found that mice exposed to constant light exhibited fear-related behavior with lower melatonin and higher corticosterone (CORT) levels in the blood [12]. Higher plasma CORT levels are linked with depression-like behavior in weanling mice [13] and adult rats [14] exposed to dim light at night. CORT is commonly used as an important indicator of stress in both rodents and chickens [15]. Conversely, melatonin and its precursor 5-hydroxytryptamine (5-HT) are related to improved behavior and wellbeing in both mammalian [16] and avian [17] species. Melatonin is reported to play important roles in regulating circadian clock, alleviating depression and anxiety, and mitigating oxidation-induced injuries [18, 19].

Hippocampus is the key brain structure governing many important functions including learning and memory, as well as depressive and anxiety-like behaviors [20]. Brain derived neurotrophic factor (BDNF) is critical for the hippocampal neurogenesis and synaptic plasticity [21, 22]. BDNF acts through binding to its receptor tropomyosin receptor kinase B (TrκB), thereby triggering the activation of phosphatidylinositol 3-kinase (PI3K) and/or extracellular signal-regulated kinase (ERK) pathways [23]. Previously, we reported that mice exposed to constant light for 3 weeks show reduced hippocampal neurogenesis and impaired cognitive behaviors, which is associated with suppressed BDNF/TrκB/ERK pathway in hippocampus [24]. In birds, hippocampus performs the same functions as in mammals, including spatial memory [25] and fear-related behaviors [4]. Chronic CORT exposure disrupted hippocampal expression of clock genes in the chicken [26]. Moreover, light exposure has been reported to influence the expression of clock genes in the pineal gland, hypothalamus and retina of chicks [27, 28]. However, no data is available regarding the effects of constant light exposure on hippocampal expression of BDNF/TrκB/ERK and clock genes in the chicken.

Therefore, in this study we exposed the chicks to either constant (24 L:0 D) or 12 L:12 D photoperiods for 1 week after hatching, to elaborate the effects of constant light in early life on fear-related behaviors, serum 5-HT, melatonin and CORT levels, and the hippocampal expression of genes involved in BDNF/ERK pathway and circadian clocks in the chicken.

Materials and methods

Ethics statement

The experimental protocol was approved by the Animal Ethics Committee of Nanjing Agricultural University. The project number is 31972638. The sampling procedures according to the “Guidelines on Ethical Treatment of Experimental Animals” (2006) No.398 set by the Ministry of Science and Technology, China.

Animals and experimental design

The chicken model employed in this study is a locally bred chicken line used for meat production in China. Eighty 1-day-old male Yellow-footed chickens were purchased from Changzhou Lihua Livestock and Poultry Co., Ltd., and randomly divided into normal (LD) and constant (LL) photoperiods for the 1st week after hatching. Light regime in LD group was 12 h light: 12 h dark, with light on at 07:00 h and off at 19:00 h; light regime in LL group was 24 h light:0 h dark. The light intensity was about 200 lx for both groups in the first week, due to the illumination from the heat lamps. From 8 d to 21 d, chickens from both groups were maintained under the same light regime (12 L:12 D) until the end of the experiment (21 d). The light intensity was about 80 lx for both groups from the second week when the heat lamps were removed. The birds in LD and LL groups were housed in 2 adjacent rooms with the same condition except the lighting regime set for each group. Birds in each room were housed in 2 individual cages with 20 birds per cage for the 1st week, and then distributed into 4 cages with 10 birds per cage thereafter till the end of the experiment. Feed and water were provided ad libitum. The room temperature was set according to the standard established by the breeding company. In detail, the temperature was 35 °C for the first 2 d, 32–34 °C from 3 to 7 d, 30–32 °C from 8 to 14 d, and 27–30 °C from 15 to 21 d. The feed consumption per cage was recorded daily, and body weight was recorded every week. By the end of the experiment, chickens were anesthetized with sodium pentobarbital and the brain was quickly separated from the skull. The brain was separated in the middle and both hemispheres of the rostral and caudal hippocampus were dissected as described in a previous publication [29] according to the chicken brain atlas [30]. Both hemispheres were combined and frozen immediately in liquid nitrogen and stored at − 80 °C until use. The tissue was homogenized, and part of the homogenate was used for mRNA or protein extraction. All chickens were killed by rapid decapitation that is considered acceptable for euthanasia of birds according to American Veterinary Medical Association (AVMA) Guidelines for the Euthanasia of Animals: 2013 Edition.

Behavior tests

On 7 days of age, chickens from both groups were captured from their home pen and carried individually to the adjacent room where the behavior tests were performed. Open field test, balance beam test, and the tonic immobility test were carried out to explore the effects of constant light on fear-related behaviors in chickens.

Open field test

The chicken to be tested was placed in the center of a 58 cm × 58 cm open field box with sides 70 cm high. This box was made of white wood and the floor was marked off into 25 squares of 12 cm × 12 cm each, illuminated by a 100 W overhead bulb [31]. After the test for each chicken, the floor of the box was cleaned with towels wetted with 70% ethanol. The behavioral performances were filmed with the observer standing out of the view of the tested chicken. The recorded videos were then analyzed by a fellow student who was not aware of the experimental design. The time of the first step, the counts of grid crossed, defecation, steps, escape attempts and vocalizations with 10 min of observation were recorded for statistical analysis.

Balance beam test

The test was conducted using an elevated narrow balance beam (6 cm wide and 35 cm long). The balance beam was 22 cm high, so that chicks could jump down onto soft bedding without injuring themselves. The balance beam was used to assess fear-related behaviors, similar to the test in rodents [32]. The test was performed as follows. Each chick was placed on the starting line at one end of the balance beam and then allowed to walk. We recorded the following parameters: (i) the time of the chick stayed on the beam and (ii) the distance the chick walked on the beam. If a chick stayed on the starting line or was afraid of walking on the beam, it received a score of 0 and scored as 120 s.

Tonic immobility test

Chicks were placed on their backs in a metal cradle and restrained for 10 s to induce tonic immobility (TI) by the experimenter placing one hand on the bird’s chest and another over its head with the head hanging down. Chickens that did not remain still for 10 s were allowed maximum 5 times to induce TI. TI was successfully induced for all the chickens used in this study in less than 5 times, and the exact duration of the successful TI was recorded. When the chicken remained still for over 6 min, the TI test was terminated and the TI score for this chicken was 6 min.

Measurement of corticosterone, melatonin and 5-hydroxytryptamine

On 7 and 21 days of age, chickens were randomly selected from each group for sampling. Chickens were sacrificed and blood samples were collected. Serum corticosterone (CORT) concentration was determined by Enzyme Immunoassay (EIA) kit (No. ADI-900-097, Enzo, Farmingdale, NY, USA) following the manufacturer’s instructions. Serum melatonin levels were measured using Chicken Melatonin (MT) ELISA Kit (MM-34278O1, ImmunoWay Biotechnology, USA) following the manufacturer’s instructions. Serum 5-hydroxytryptamine (5-HT) levels were measured using Chicken 5-HT ELISA Kit (E-EL-0033c, Elabscience, USA) following the manufacturer’s instructions.

RNA isolation and real-time PCR

High quality total RNA was isolated from 30 mg hippocampal tissue using 600 μL Trizol reagents (Invitrogen, Carlsbad, California, USA). One microgram RNA was reverse-transcribed according to the manufacturer’s protocol (Vazyme Biotech, Nanjing, Jiangsu, China). Four microliter cDNA was diluted (1:25) and then used for real-time PCR in a QuantStudioTM 6 Flex Real-Time PCR System (Applied Biosystems, Foster City, California, USA). Peptidylprolyl isomerase A (PPIA) was used as an internal control to normalize the technical variations. Data were analyzed using the method of 2-ΔΔCT and presented relative to the CON group. All primers (Table 1) were synthesized by Suzhou GENEWIZ Biological Technology Co., Ltd. (Suzhou, Jiangsu, China).

Table 1 The primers sequences for RT-PCR

Total protein extraction and Western blotting

Total protein was extracted from about 50 mg frozen hippocampus samples. Protein concentrations were measured using BCA Protein Assay kit (NO.23227, Thermos Scientific, Rockford, Illinois, USA) according to the manufacturer’s instructions. Protein (50 μg/lane) was loaded for electrophoresis on a 6–14% SDS-PAGE gel and transferred onto a nitrocellulose membrane. After transfer, the membranes were blocked with 4% milk and then incubated with primary and secondary antibodies. Western blot analysis for NRF2 (16396–1-AP, proteintech, USA, diluted 1:1000), BDNF (ab108319, Abcam, USA, diluted 1:500), TrκB (bs-0288R, Bioss, USA, diluted 1:1000), Doublecortin (DCX; 4604, Cell Signaling Technology, USA, diluted 1:1000), ERK (4695, Cell Signaling Technology, USA, diluted 1:1000), phospho-ERK (4370, Cell Signaling Technology, USA, diluted 1:1000) was performed, using tubulin α (BS1699, Bioworld, diluted 1:10,000) as loading control. Images were captured by VersaDoc 4000MP system (Bio-Rad, USA) and the band density was analyzed with Quantity One software (Bio-Rad, USA).

Statistical analysis

All data are presented as means ± SEM. The behavior data were analyzed using U-Test, and the hormones and gene expression data were analyzed by T-Test for independent samples with SPSS 20.0. The differences were considered statistically significant when P < 0.05.

Results

Effect of constant light in early life on feed conversion ratio, serum CORT, melatonin and 5-HT concentration

Constant light did not affect (P > 0.05) the body weight (Fig. 1A), but increased the average daily feed intake in 2nd week (P = 0.08) and 3rd week (P < 0.05) (Fig. 1B), which led to significantly higher feed conversion ratio (P < 0.05) in 3rd week (Fig. 1C). Meanwhile, serum CORT levels (Fig. 1D) were significantly higher (P < 0.05), while serum melatonin (Fig. 1E) levels were significantly lower (P < 0.05) in LL group at both 7 and 21 days of age. Chickens from LL group exhibited significantly lower (P < 0.05) serum 5-HT concentration (Fig. 1F) at 7 days of age, with a trend of decrease (P = 0.06) detected at 21 days of age, as compared with their counterparts from LD group.

Fig. 1
figure 1

Effect of constant light exposure on growth performance and serum hormone concentration. A Body weight (1 d, 7 d, n = 39 (LD), n = 40 (LL); 14 d, 21 d, n = 20); B Average daily feed intake (1st week, n = 2; 2nd and 3rd week, n = 4); (C) Feed conversion ratio (1st week, n = 2; 2nd and 3rd week, n = 4); D Serum corticosterone content (n = 10); E Serum melatonin content (n = 10); F Serum 5-HT content (n = 10). Values are mean ± SEM, *P < 0.05, **P < 0.01, compared with LD

Effect of constant light in early life on the fear-related behaviors in chickens

Chickens from LL group spent significantly longer (P < 0.01) time before taking the first step in the open filed test (Fig. 2A). Moreover, the counts of the grid crossed (Fig. 2B) and the counts of steps (Fig. 2C), defecation (Fig. 2D), escape (Fig. 2E) and vocalizations (Fig. 2F) were all significantly decreased (P < 0.01) in LL group. Also, the time stayed on the balance beam (Fig. 2G) was significantly increased (P < 0.01), and the distance moved along the beam (Fig. 2H) was significantly decreased (P < 0.01) in LL group. In tonic immobility test, chickens from LL group showed significantly longer (P < 0.01) immobility time, compared to their LD counterparts (Fig. 2I). See Table 2 for detailed behavioral data. Raw data of behavioral test were showed in Supplementary Table 1. These behavior results indicate that constant light in early life significantly increased fear-related behaviors in chickens.

Fig. 2
figure 2

Effect of constant light exposure on anxiety and fear-related behavior. To elaborate the effect of constant light exposure on locomotor activity and fear-related activity, the open-field test, balance beam test and tonic immobility test were performed. A The times of first step; B-F The counts of grid number, defecation, steps, escape and vocalizations in the open field test; G Times stayed in balance beam test; H The distance moved in balance beam test; I The immobility time in tonic immobility test. Values are mean ± SEM (LD, n = 39, LL, n = 40); **P < 0.01, compared with LD. The data were analyzed using U-Test with SPSS 20.0

Table 2 Effect of lighting time on the behavior of Yellow-footed chickens

Effect of constant light in early life on hippocampal 5-HT receptors and clock genes mRNA expression in chickens

Hippocampal expression of 5-HT receptors 5-hta and 5-htb mRNA was significantly decreased (P < 0.05) in LL chickens at 7 days of age (Fig. 3A). At 21 days of age, chickens from LL group showed a significant down-regulation (P < 0.05) of hippocampal expression of 5-htb and maob, the key enzymes for 5-HT degradation (Fig. 3B), with a tendency of down-regulation (P = 0.07) for 5-hta mRNA. In addition, hippocampal mRNA expression of clock-related genes, cry1, cry2, per3, rorα and rev-erbα, was significantly increased (P < 0.05) in LL group at 7 days of age (Fig. 3C). At 21 days of age, cry1, cry2, per3 and rev-erbα mRNA expression was significantly increased (P < 0.05), while per2 mRNA expression tended (P = 0.07) to increase (Fig. 3D) in the hippocampus of LL chickens.

Fig. 3
figure 3

Effect of constant light exposure on 5-HT receptor and clock related gene mRNA expression in chicken’s hippocampus. A-B The mRNA expression of 5-hta, 5-htb, maoa and maob in 7 d and 21 d chickens; C-D The circadian clock genes mRNA expression in 7 d and 21 d chickens. Values are mean ± SEM (n = 12); *P < 0.05, compared with LD

Effect of constant light in early life on oxidative stress related genes mRNA and protein expression chicken hippocampus

Hippocampal expression of oxidative stress-related genes was modified by constant light exposure. The expression of NF-E2-related factor 2 (nrf2), Kelch-like ECH-associated protein 1 (keap1) and superoxide dismutase 2 (sod2) were significantly decreased (P < 0.05), while that of nqo1 and gpx1 was significantly increased (P < 0.01) in LL group at 7 days of age (Fig. 4A). Accordantly, NRF2 protein content in hippocampus was significantly decreased (P < 0.05) in 7-day-old LL chickens (Fig. 4B). Similar changes in the pattern of oxidative stress-related genes were detected at 21 d, with decreased nrf2, keap, sod1 and nqo1 (P < 0.05) and increased (P < 0.05) gpx1 and gpx2 mRNA expression (Fig. 4C) in the hippocampus of LL chickens. NRF2 protein content tended to decrease (P = 0.07) in the hippocampus of LL chickens at 21 days of age (Fig. 4D).

Fig. 4
figure 4

Effect of constant light exposure on oxidative stress related gene mRNA and. Protein expression in chicken’s hippocampus. A Oxidative stress related gene mRNA expression in 7 d chickens (n = 12); B Nrf2 protein expression in 7 d chickens (n = 6); C Oxidative stress related gene mRNA expression in 7 d chickens (n = 12); D Nrf2 protein expression in 7 d chickens (n = 6). Values are mean ± SEM; *P < 0.05, compared with LD

Effect of constant light in early life on BDNF/TrκB/ERK mRNA and protein expression in chicken hippocampus

Constant light exposure significantly decreased (P < 0.05) hippocampal expression of bdnf, trκb and dcx mRNA (Fig. 5A). Accordantly, TrκB and p-ERK protein content was significantly decreased (P < 0.05), while BDNF protein tended to decrease (P = 0.05), in the hippocampus of LL chickens at 7 days of age (Fig. 5B and C). Similar alterations occur at 21 d, with significantly decreased (P < 0.05) bdnf and trκb mRNA (Fig. 5D) and BDNF and p-ERK protein (Fig. 5E and F) determined in the hippocampus of LL chickens.

Fig. 5
figure 5

Effect of constant light exposure on BDNF/TrκB/ERK pathway mRNA and protein expression in chicken’s hippocampus. A The mRNA expression of bdnf, trκb and dcx in 7 d chickens (n = 12); B BDNF, TrκB and DCX protein expression in 7 d chickens (n = 6); C ERK and p-ERK protein expression in 7 d chickens (n = 6); D The mRNA expression of bdnf, trκb and dcx in 21 d chickens (n = 12); E BDNF, TrκB and DCX protein expression in 21 d chickens (n = 6); F ERK and p-ERK protein expression in 21 d chickens (n = 6). Values are mean ± SEM; *P < 0.05, **P < 0.01, compared with LD

Discussion

In this study, the light intensity (200 lx in the 1st week and about 80 lx thereafter) was much brighter than the commercial conditions (less than 30 lx). A study performed under commercial light intensity (29 ± 2.3 lx) reported that 24 h constant light increased food intake but not body weight in 21 d males Cobb 500 and Ross 308 broiler chickens [5]. Despite the difference in light intensity and the chicken lines, we also found that constant light regime increased feed intake but did not increase the body weight gain, which led to higher FCR value. Therefore, the constant light regime does not provide benefits either to chickens or farmers.

In the present study, chickens show unique behaver patterns in the open field test. Most of the chickens from LL group did not move within 6 min, so the number of grids crossed and attempts of escape were basically zero. In addition, the number of defecation and vocalizations was also significantly reduced in LL group. This finding agrees with a previous publication that increased defecation latency and decreased defecation frequency were associated with anxiety-like behavior in neonatal broiler chicks [33]. Also, chicks with higher plasma corticosterone levels show longer vocalization latency [34]. Defection and vocalization are normal physiological responses for a chicken when separated from the group in the open field test. Decreased frequency of defection and vocalization in LL group indicates fear-related condition. Similar fear-related responses were observed in the balance beam test, chickens from LL group showing longer latency, shorter walking distance and longer immobility time. Our findings in chickens are in line with a previous report that near-constant light (23 L:1 D) exposure increased stress and fear-related behaviors in Ross 308 broilers chickens [7].

Melatonin is a potent antioxidant by scavenging reactive oxygen species [35]. Constant light-induced depressive-like behavior in rodents is usually associated with low melatonin and high oxidative stress levels [36, 37]. Indeed, we detected lower plasma melatonin and 5-HT levels in LL chickens, which was associated with suppressed hippocampal mRNA expression of 5-HT receptors at both 7 and 21 days of age. Similar results have been reported that 23 L:1 D photoperiod significantly reduced plasma melatonin in 7-week-old broiler chickens, as compared with 12 L:12 D photoperiod [38]. In addition, we found that constant light exposure increased the plasma CORT levels in the chicken at both 7 and 21 days of age. CORT levels are associated to depression-like behavior in rodents [21]. The same is true for chicken that increased fear-related behavior is related to lower serum levels of melatonin and 5-HT, and higher serum levels of CORT.

Nrf2 and its endogenous inhibitor, Keap1, play critical roles in counteracting oxidative stress [39]. In this study, constant light exposure reduced nrf2/keap1 and sod mRNA expression, as well as Nrf2 protein content in chicken hippocampus at both 7 and 21 days of age. In agreement with our findings, constant light was reported to induce oxidative stress in rat hippocampus, cortex and cerebellum [40] and melatonin was reported to rescue the suppressed Nrf2 expression in the thymus of rats exposed to constant light [41].

A number of studies indicate that constant light exposure influences the mRNA expression of clock-related genes, including clock, bmal1, cry, and per [42, 43]. Disrupted expression of clock-related genes is associated with impaired hippocampal neurogenesis and depressive-like behavior in mice [44, 45]. Similarly, we also found that constant light exposure significantly increased the mRNA expression of clock-related genes, including cry1, cry2 and rev-erbα, in the hippocampus of chickens at both 7 and 21 days of age.

BDNF/ERK pathway, which is critical for hippocampal neurogenesis [21], plays an important role in regulating depressive-like behavior [20]. In the present study, we found that constant light exposure significantly suppressed BDNF/ERK pathway in the hippocampus of chickens at both 7 and 21 days of age. These results are consistent with our previous findings in mice that constant light suppressed BDNF/ERK pathway in hippocampus [24]. Melatonin was able to rescue chronic restraint stress-induced depressive-like behavior in mice via activating the hippocampal BDNF/TrκB signaling pathway [46]. The role of hippocampal BDNF in the chicken is less understood, yet in a chick anxiety-depression model, hippocampal BDNF response was linked to stress resilience [47].

Conclusion

In conclusion, our study shows that constant light exposure in early life induces fear-related behaviors in the chicken, which is accompanied by higher CORT and lower melatonin/5-HT levels in the blood. Constant light exposure in early life disrupted expression pattern of genes involved in circadian clock, oxidation stress, and BDNF/TrκB/ERK pathway in chicken hippocampus. These findings extend our understanding on hormonal and hippocampal responses to constant light exposure in the chicken, and provide implications for the light management in broiler industry in favor of production efficiency as well as chicken behavior and welfare.

Availability of data and materials

Not applicable.

Abbreviations

5-HT:

5-hydroxytryptamine

ADFI:

Average daily feed intake

BDNF:

Brain derived neurotrophic factor

CORT:

Corticosterone

EIA:

Enzyme Immunoassay

ERK:

Extracellular signal-regulated kinase

FCR:

Feed conversion ratio

Keap1:

Kelch-like ECH-associated protein 1

LD:

Natural photoperiod

LL:

Constant light

MT:

Melatonin

Nrf2:

NF-E2-related factor 2

PPIA:

Peptidylprolyl isomerase A

PI3K:

Phosphatidylinositol 3-kinase

SOD:

Superoxide dismutase

TrκB:

Tropomyosin receptor kinase B

References

  1. Zheng L, Ma YE, Gu LY, Yuan D, Shi ML, Guo XY, et al. Growth performance, antioxidant status, and nonspecific immunity in broilers under different lighting regimens. J Appl Poult Res. 2013;22(4):798–807. https://doi.org/10.3382/japr.2012-00713.

    Article  CAS  Google Scholar 

  2. Olanrewaju HA, Purswell JL, Collier SD, Branton SL. Interactive effects of photoperiod and light intensity on blood physiological and biochemical reactions of broilers grown to heavy weights. Poult Sci. 2013;92(4):1029–39. https://doi.org/10.3382/ps.2012-02792.

    Article  CAS  PubMed  Google Scholar 

  3. Lewis PD. A review of lighting for broiler breeders. Br Poult Sci. 2006;47(4):393–404. https://doi.org/10.1080/00071660600829092.

    Article  CAS  PubMed  Google Scholar 

  4. Armstrong EA, Rufener C, Toscano MJ, Eastham JE, Guy JH, Sandilands V, et al. Keel bone fractures induce a depressive-like state in laying hens. Sci Rep. 2020;10(1):3007. https://doi.org/10.1038/s41598-020-59940-1.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Lewis PD, Danisman R, Gous RM. Photoperiodic responses of broilers. I. Growth, feeding behaviour, breast meat yield, and testicular growth. Br Poult Sci. 2009;50(6):657–66. https://doi.org/10.1080/00071660903338452.

    Article  CAS  PubMed  Google Scholar 

  6. Tuell JR, Park JY, Wang W, Cheng HW, Kim YHB. Functional/physicochemical properties and oxidative stability of ground meat from broilers reared under different photoperiods. Poult Sci. 2020;99(7):3761–88. https://doi.org/10.1016/j.psj.2020.04.021.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Wang B, Rathgeber BM, Astatkie T, MacIsaac JL. The stress and fear levels of microwave toe-treated broiler chickens grown with two photoperiod programs. Poult Sci. 2008;87(7):1248–52. https://doi.org/10.3382/ps.2006-00440.

    Article  CAS  PubMed  Google Scholar 

  8. Hieke AC, Hubert SM, Athrey G. Circadian disruption and divergent microbiota acquisition under extended photoperiod regimens in chicken. PeerJ. 2019;7:e6592. https://doi.org/10.7717/peerj.6592.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Germain A, Kupfer DJ. Circadian rhythm dist urbances in depression. Hum Psychopharm. 2008;23(7):571–85. https://doi.org/10.1002/hup.964.

    Article  Google Scholar 

  10. Tapia-Osorio A, Salgado-Delgado R, Angeles-Castellanos M, Escobar C. Disruption of circadian rhythms due to chronic constant light leads to depressive and anxiety-like behaviors in the rat. Behav Brain Res. 2013;252:1–9. https://doi.org/10.1016/j.bbr.2013.05.028.

    Article  PubMed  Google Scholar 

  11. Bernard M, Guerlotte J, Greve P, Grechez-Cassiau A, Iuvone MP, Zatz M, et al. Melatonin synthesis pathway: circadian regulation of the genes encoding the key enzymes in the chicken pineal gland and retina. Reprod Nutr Dev. 1999;39(3):325–34. https://doi.org/10.1051/rnd:19990305.

    Article  CAS  PubMed  Google Scholar 

  12. Yang Y, Jiang W, Feng Y, Liu J, Chen H, Wang D, et al. Melatonin alleviates hippocampal GR inhibition and depression-like behavior induced by constant light exposure in mice. Ecotox and Environ Safe. 2021;228:112979. https://doi.org/10.1016/j.ecoenv.2021.112979.

    Article  CAS  Google Scholar 

  13. Cisse YM, Peng J, Nelson RJ. Dim light at night prior to adolescence increases adult anxiety-like behaviors. Chronobiol Int. 2016;33(10):1473–80. https://doi.org/10.1080/07420528.2016.1221418.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Dauchy RT, Dauchy EM, Tirrell RP, Hill CR, Davidson LK, Greene MW, et al. Dark-phase light contamination disrupts circadian rhythms in plasma measures of endocrine physiology and metabolism in rats. Comparative Med. 2010;60(5):348–56.

    CAS  Google Scholar 

  15. Lee DY, Kim E, Choi MH. Technical and clinical aspects of cortisol as a biochemical marker of chronic stress. BMB Rep. 2015;48(4):209–16. https://doi.org/10.5483/BMBRep.2015.48.4.275.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Cardinali DP, Srinivasan V, Brzezinski A, Brown GM. Melatonin and its analogs in insomnia and depression. J Pineal Res. 2012;52(4):365–75. https://doi.org/10.1111/j.1600-079X.2011.00962.x.

    Article  CAS  PubMed  Google Scholar 

  17. Iuvone PM, Bernard M, Alonso-Gomez A, Greve P, Cassone VM, Klein DC. Cellular and molecular regulation of serotonin N-acetyltransferase activity in chicken retinal photoreceptors. Biol Signals. 1997;6(4–6):217–24. https://doi.org/10.1159/000109131.

    Article  CAS  PubMed  Google Scholar 

  18. Won E, Na KS, Kim YK. Associations between melatonin, Neuroinflammation, and brain alterations in depression. Int J Mol Sci. 2021;23(1):305. https://doi.org/10.3390/ijms23010305.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Stiedl O, Pappa E, Konradsson-Geuken A, Ogren SO. The role of the serotonin receptor subtypes 5-HT1A and 5-HT7 and its interaction in emotional learning and memory. Front Pharmacol. 2015;6:162. https://doi.org/10.3389/fphar.2015.00162.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Anacker C, Hen R. Adult hippocampal neurogenesis and cognitive flexibility - linking memory and mood. Nat Rev Neurosci. 2017;18(6):335–46. https://doi.org/10.1038/nrn.2017.45.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Karpova NN. Role of BDNF epigenetics in activity-dependent neuronal plasticity. Neuropharmacology. 2014;76 Pt C:709–18.

    Article  Google Scholar 

  22. Leal G, Afonso PM, Salazar IL, Duarte CB. Regulation of hippocampal synaptic plasticity by BDNF. Brain Res. 2015;1621:82–101. https://doi.org/10.1016/j.brainres.2014.10.019.

    Article  CAS  PubMed  Google Scholar 

  23. Huang EJ, Reichardt LF. Trk receptors: roles in neuronal signal transduction. Annu Rev Biochem. 2003;72(1):609–42. https://doi.org/10.1146/annurev.biochem.72.121801.161629.

    Article  CAS  PubMed  Google Scholar 

  24. Yang Y, Feng Y, Hu Y, Liu J, Shi H, Zhao R. Exposure to constant light impairs cognition with FTO inhibition and m (6) A-dependent TrkappaB repression in mouse hippocampus. Environ Pollut. 2021;283:117037. https://doi.org/10.1016/j.envpol.2021.117037.

    Article  CAS  PubMed  Google Scholar 

  25. Payne HL, Lynch GF, Aronov D. Neural representations of space in the hippocampus of a food-caching bird. Science. 2021;373(6552):343–8. https://doi.org/10.1126/science.abg2009.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Yang Y, Han W, Zhang A, Zhao M, Cong W, Jia Y, et al. Chronic corticosterone disrupts the circadian rhythm of CRH expression and m (6) a RNA methylation in the chicken hypothalamus. J Anim Sci Biotechnol. 2022;13(1):29. https://doi.org/10.1186/s40104-022-00677-4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Jin E, Jia L, Li J, Yang G, Wang Z, Cao J, et al. Effect of monochromatic light on melatonin secretion and arylalkylamine N-acetyltransferase mRNA expression in the retina and pineal gland of broilers. Anat Rec. 2011;294(7):1233–41. https://doi.org/10.1002/ar.21408.

    Article  CAS  Google Scholar 

  28. Jiang N, Wang Z, Cao J, Dong Y, Chen Y. Effect of monochromatic light on circadian rhythmic expression of clock genes in the hypothalamus of chick. J Photochem Photobiol B. 2017;173:476–84. https://doi.org/10.1016/j.jphotobiol.2017.06.027.

    Article  CAS  PubMed  Google Scholar 

  29. Kadhim HJ, Kang SW, Kuenzel WJ. Differential and temporal expression of corticotropin releasing hormone and its receptors in the nucleus of the hippocampal commissure and paraventricular nucleus during the stress response in chickens (Gallus gallus). Brain Res. 2019;1714:1–7. https://doi.org/10.1016/j.brainres.2019.02.018.

    Article  CAS  PubMed  Google Scholar 

  30. Kuenzel WJ, Masson M. A stereotaxic atlas of the brain of the chick (Gallus domesticus). Poultry Science Faculty Publications and Presentations; 1988. Retrieved from: https://scholarworks.uark.edu/poscpub/1.

  31. Smith SM, Flentke GR, Kragtorp KA, Tessmer L. Ethanol exposure during the early first trimester equivalent impairs reflexive motor activity and heightens fearfulness in an avian model. Alcohol. 2011;45(1):57–63. https://doi.org/10.1016/j.alcohol.2010.06.001.

    Article  CAS  PubMed  Google Scholar 

  32. Pellow S, Chopin P, File SE, Briley M. Validation of open:closed arm entries in an elevated plus-maze as a measure of anxiety in the rat. J Neurosci Methods. 1985;14(3):149–67. https://doi.org/10.1016/0165-0270(85)90031-7.

    Article  CAS  PubMed  Google Scholar 

  33. Gaston MS, Schioth HB, De Barioglio SR, Salvatierra NA. Gabaergic control of anxiety-like behavior, but not food intake, induced by ghrelin in the intermediate medial mesopallium of the neonatal chick. Horm Behav. 2015;67:66–72. https://doi.org/10.1016/j.yhbeh.2014.11.015.

    Article  CAS  PubMed  Google Scholar 

  34. de Haas EN, Kops MS, Bolhuis JE, Groothuis TG, Ellen ED, Rodenburg TB. The relation between fearfulness in young and stress-response in adult laying hens, on individual and group level. Physiol Behav. 2012;107(3):433–9. https://doi.org/10.1016/j.physbeh.2012.08.002.

    Article  CAS  PubMed  Google Scholar 

  35. Galano A, Tan DX, Reiter RJ. Melatonin as a natural ally against oxidative stress: a physicochemical examination. J Pineal Res. 2011;51(1):1–16. https://doi.org/10.1111/j.1600-079X.2011.00916.x.

    Article  CAS  PubMed  Google Scholar 

  36. Tchekalarova J, Stoynova T, Ilieva K, Mitreva R, Atanasova M. Agomelatine treatment corrects symptoms of depression and anxiety by restoring the disrupted melatonin circadian rhythms of rats exposed to chronic constant light. Pharmacol Biochem Behav. 2018;171:1–9. https://doi.org/10.1016/j.pbb.2018.05.016.

    Article  CAS  PubMed  Google Scholar 

  37. Wideman CH, Murphy HM. Constant light induces alterations in melatonin levels, food intake, feed efficiency, visceral adiposity, and circadian rhythms in rats. Nutr Neurosci. 2009;12(5):233–40. https://doi.org/10.1179/147683009X423436.

    Article  CAS  PubMed  Google Scholar 

  38. Lauber JK, Oishi T, Vriend J. Plasma melatonin rhythm lost in preglaucomatous chicks. J Ocul Pharmacol. 1986;2(3):205–13. https://doi.org/10.1089/jop.1986.2.205.

    Article  CAS  PubMed  Google Scholar 

  39. Bellezza I, Giambanco I, Minelli A, Donato R. Nrf2-Keap1 signaling in oxidative and reductive stress. Biochim Biophys Acta, Mol Cell Res. 2018;1865(5):721–33. https://doi.org/10.1016/j.bbamcr.2018.02.010.

    Article  CAS  Google Scholar 

  40. Baydas G, Reiter RJ, Nedzvetskii VS, Nerush PA, Kirichenko SV. Altered glial fibrillary acidic protein content and its degradation in the hippocampus, cortex and cerebellum of rats exposed to constant light: reversal by melatonin. J Pineal Res. 2002;33(3):134–9. https://doi.org/10.1034/j.1600-079X.2002.02110.x.

    Article  CAS  PubMed  Google Scholar 

  41. El-Bakry HA, Ismail IA, Soliman SS. Immunosenescence-like state is accelerated by constant light exposure and counteracted by melatonin or turmeric administration through DJ-1/Nrf2 and P53/Bax pathways. J Photochem Photobiol B. 2018;186:69–80. https://doi.org/10.1016/j.jphotobiol.2018.07.003.

    Article  CAS  PubMed  Google Scholar 

  42. Novakova M, Polidarova L, Sladek M, Sumova A. Restricted feeding regime affects clock gene expression profiles in the suprachiasmatic nucleus of rats exposed to constant light. Neuroscience. 2011;197:65–71. https://doi.org/10.1016/j.neuroscience.2011.09.028.

    Article  CAS  PubMed  Google Scholar 

  43. Grone BP, Chang D, Bourgin P, Cao V, Fernald RD, Heller HC, et al. Acute light exposure suppresses circadian rhythms in clock gene expression. J Biol Rhythm. 2011;26(1):78–81. https://doi.org/10.1177/0748730410388404.

    Article  Google Scholar 

  44. Fujioka A, Fujioka T, Tsuruta R, Izumi T, Kasaoka S, Maekawa T. Effects of a constant light environment on hippocampal neurogenesis and memory in mice. Neurosci Iett. 2011;488(1):41–4. https://doi.org/10.1016/j.neulet.2010.11.001.

    Article  CAS  Google Scholar 

  45. Ma WP, Cao J, Tian M, Cui MH, Han HL, Yang YX, et al. Exposure to chronic constant light impairs spatial memory and influences long-term depression in rats. Neurosci Res. 2007;59(2):224–30. https://doi.org/10.1016/j.neures.2007.06.1474.

    Article  PubMed  Google Scholar 

  46. Li K, Shen S, Ji YT, Li XY, Zhang LS, Wang XD. Melatonin augments the effects of fluoxetine on depression-like behavior and hippocampal BDNF-TrkB signaling. Neurosci Bull. 2018;34(2):303–11. https://doi.org/10.1007/s12264-017-0189-z.

    Article  CAS  PubMed  Google Scholar 

  47. Loria MJ, White SW, Robbins SA, Salmeto AL, Hymel KA, Murthy SN, et al. Brain-derived neurotrophic factor response in vulnerable and resilient genetic lines in the chick anxiety-depression model. Behav Brain Res. 2013;245:29–33. https://doi.org/10.1016/j.bbr.2013.01.045.

    Article  CAS  PubMed  Google Scholar 

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Funding

This work was supported by the National Natural Science Foundation of China (31972638), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Postgraduate Research & Practice Innovation Program of Jiangsu Province (KYCX18_0716), and Jiangsu Collaborative Innovation Center of Meat Production and Processing, Quality, and Safety Control. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Authors

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YY, WC, PX contributed to behavior tests, data analysis, and drafting of the manuscript. YY, JL and MZ were responsible for animal care, breeding and sampling. MZ and WH provided technical support. RZ and YY contributed to conception, experimental design, and data interpretation. RZ and DW contributed to critical revision of the manuscript. Tha authors read and approved the final manuscript.

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Correspondence to Ruqian Zhao.

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Ethics approval and consent to participate

The experimental protocol was approved by the Animal Ethics Committee of Nanjing Agricultural University. The project number is 31972638. The sampling procedures according to the “Guidelines on Ethical Treatment of Experimental Animals” (2006) No.398 set by the Ministry of Science and Technology, China.

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All the authors have read and approved the final submitted manuscript.

Competing interests

The authors declare no competing financial interest.

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Yang, Y., Cong, W., Liu, J. et al. Constant light in early life induces fear-related behavior in chickens with suppressed melatonin secretion and disrupted hippocampal expression of clock- and BDNF-associated genes. J Animal Sci Biotechnol 13, 67 (2022). https://doi.org/10.1186/s40104-022-00720-4

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