Melatonin implantation improved the egg-laying rate and quality in hens past their peak egg-laying age

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作者
Yaxiong Jia
Minghui Yang
Kuanfeng Zhu
Liang Wang
Yukun Song
Jing Wang
Wenxiang Qin
Zhiyuan Xu
Yu Chen
Guoshi Liu
机构
[1] Beijing Animal Husbandry Station,
[2] National Engineering Laboratory for Animal Breeding,undefined
[3] Key Laboratory of Animal Genetics and Breeding of the Ministry of Agriculture,undefined
[4] Beijing Key Laboratory for Animal Genetic Improvement,undefined
[5] College of Animal Science and Technology,undefined
[6] China Agricultural University,undefined
[7] College of Animal Science and Technology,undefined
[8] Jilin Agricultural University,undefined
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摘要
The egg-laying rates of hens approximately 470 days of age exhibited a positive correlation to blood melatonin levels. The hens with an egg-laying rate <30%, 30~90% and ≥90% had blood melatonin levels of 5.8 ± 2.6, 74.0 ± 32.9 and 445.9 ± 115.3 ng/ml, respectively. When 10 mg of melatonin was implanted into the hens at 300, 360, 470 and 550 days of age, the egg-laying rates increased 4.63 ± 0.46%, 8.38 ± 1.45%, 4.93 ± 0.85% and 7.93 ± 0.91%, respectively, compared to that of the controls. Melatonin implantation in hens at 300–470 days of age was observed to enhance egg production and reduce the rate of appearance of sharpei eggs. Melatonin (10 mg) implanted in hens 360 days of age did not influence the blood levels of progesterone (P4) or the gene expression levels of ovarian follicle stimulating hormone receptor (FSHR), luteinizing hormone receptor (LHR), oestradiol receptor alpha (ERα), superoxide dismutase 2 (SOD2) or melatonin receptor 1 (MT1). In contrast, melatonin significantly elevated the serum oestradiol-17β (E2) content, down-regulated the gene expression of gonadotropin-inhibitory hormone receptor (GnIHR), and enhanced the expression of melatonin receptor 2 (MT2). This result indicates that the improved egg-laying rate by melatonin was the result of increased serum oestradiol and decreased ovarian GnIHR. These alterations may be mediated by MT2 activation.
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