12 research outputs found

    Effect of lighting schedule, intensity, and colour on reproductive performance of rabbit does

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    [EN] In order to establish a lighting regime suitable for rabbit farms in East China, the effects of lighting schedule, intensity and colour on the reproductive performance of rabbit does were evaluated by three experiments, respectively. In experiment 1, does were exposed to different lighting schedules: 16L:8D-continuous, 16L:8D-18d (6 d before artificial insemination (AI) to 12 d post-AI), 16L:8D-6d (6 d before AI to the day of AI) and 12L:12D-continuous. In experiment 2, does were exposed to different light intensities: 40 lx, 60 lx, 80 lx and 120 lx. In experiment 3, does were exposed to different light colours: white, yellow, blue and red. For all experiments, conception rate, kindling rate and pre-weaning mortality were calculated; litter size at birth, litter weight at birth, litter size at weaning, litter weight at weaning and individual kit weight at weaning were recorded. Results showed that none of the reproductive parameters of does were affected by the application of 16L:8D-18d lighting schedule compared with the continuous 16L:8D group(P>0.05). Moreover, rabbits does exposed to 80 lx light performed as well as those under 120 lx light in conception rate, kindling rate, litter size (total and alive) at birth and litter weight at birth (P>0.05). Furthermore, the exposures of 60 lx and 80 lx light were beneficial for litter weight at weaning. In addition, red light had a positive effect, as it led to a larger litter size and litter weight at weaning and lower pre-weaning mortality than white light (P<0.05). In summary, a 16L:8D photoperiod with 80 lx red light from 6 d before AI to 12 d post-AI is recommended for use in breeding of rabbit does according to our results.We would like to thank the support of Earmarked Fund for Modern Agro-Industry Technology Research System (CARS-44).Wu, Y.; Zhao, A.; Qin, Y. (2021). Effect of lighting schedule, intensity, and colour on reproductive performance of rabbit does. World Rabbit Science. 29(1):59-64. https://doi.org/10.4995/wrs.2021.14623OJS5964291Abdo M., Haddad S., Emam M. 2017. Development of the New Zealand White Rabbit eye: I. pre- and postnatal development of eye tunics. Anat Histol Embryol., 46: 423-430. https://doi.org/10.1111/ahe.12284Gerencsér Zs., Matics Zs., Nagy I., Szendrő Zs. 2011. Effect of light color and reproductive rhythm on rabbit doe performance. World Rabbit Sci., 19: 161-170. https://doi.org/10.4995/wrs.2011.827Gidenne T., Fortun-Lamothe L. 2002. Feeding strategy for young rabbits around weaning: a review of digestive capacity and nutritional needs. Anim. Sci., 75: 169-184. https://doi.org/10.1017/S1357729800052942Hoy St. 2012. German regulations and guidelines on rabbit housing. In Proc.: 10th World Rabbit Congress, 3-6 September, 2012. Sharm-El Sheikh, Egypt. 1: 999-1003.Li Y., Zhang J., Xu Y., Han Y., Jiang B., Huang L., Zhu H., Xu Y., Yang W., Qin C. 2016. The histopathological investigation of red and blue light emitting diode on treating skin wounds in Japanese big-ear white rabbit. PLoS One, 11: e0157898. https://doi.org/10.1371/journal.pone.0157898.Maertens L., Luzi F. 1995. Effect of diluents and storage time of rabbit semen on the fertility of does reared under two different lighting schedules. World Rabbit Sci., 3: 57-61. https://doi.org/10.4995/wrs.1995.237Matics Zs., Gerencsér Zs., Radnai I., Kasza R., Szendrő Zs. 2016. Effect of light intensities on reproductive performance, nursing behaviour and preference of rabbit does. World Rabbit Sci., 24: 139-144. https://doi.org/10.4995/wrs.2016.4112Mattaraia V.G.M., Bianospino E., Fernandes S., Vasconcelos J.L.M., Moura A.S.A.M.T. 2005. Reproductive responses of rabbit does to a supplemental lighting program. Livest. Prod. Sci., 94: 179-184. https://doi.org/10.1016/j.livprodsci.2004.10.012Mousa-Balabel T.M., Mohamed R.A. 2011. Effect of different photoperiods and melatonin treatment on rabbit reproductive performance. Vet Q., 31: 165-171. https://doi.org/10.1080/01652176.2011.642533Nuboer J. F.W. 1985. A comparative view on color vision. Neth. J. Zool., 36: 344-380. https://doi.org/10.1163/002829686X00126Reyne Y., Prud'hon M., Angerian J. 1978. Influence d'une réduction de la durée d'éclairement du lapin en engraissement. In Proc.: 2émes Journ. Rech. Cunicole, Comm. No 7.Salehpour F., Mahmoudi J., Kamari F., Sadigh-Eteghad S., Rasta S.H., Hamblin M.R. 2018. Brain photobiomodulation therapy: a narrative review. Mol. Neurobiol., 55: 6601-6636. https://doi.org/10.1007/s12035-017-0852-4Shi H.J., Song H.B., Zhao Q.Y., Tao C.X., Liu M., Zhu Q.Q. 2018. Efficacy and safety of combined high-dose interferon and red light therapy for the treatment of human papillomavirus and associated vaginitis and cervicitis: A prospective and randomized clinical study. Medicine (Baltimore), 97: e12398. https://doi.org/10.1097/MD.0000000000012398Szendrő Zs., Gerencsér Zs., McNitt J.I., Matics Zs. 2016. Effect of lighting on rabbits and its role in rabbit production: A review. Livest. Sci., 183: 12-18. https://doi.org/10.1016/j.livsci.2015.11.012Theau-Clement M., Malpaux B., Lamothe E., Milcent N., Juin H., Bodin L. 2008. Influence of photoperiod on the sexual behaviour of non-lactating rabbit does: preliminary results. In Proc.: 9th World Rabbit Congress, 10-13 June, 2008. Verona, Italy. 1: 465-469.Uzcategui M.E., Johnston N.P. 1992. The effect of 10, 12 and 14 hour continuous and intermittent photoperiods on the reproductive performance of female rabbits. In Proc.: 5th World Rabbit Congress, 25-30 July, 1992. Corvallis, USA. 1: 553-559

    The Spatially Resolved Properties of the GW170817 Host Galaxy

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    GW170817 is the unique gravitational-wave (GW) event that is associated to the electromagnetic (EM) counterpart GRB 170817A. NGC 4993 is identified as the host galaxy of GW170817/GRB 170817A. In this paper, we particularly focus on the spatially resolved properties of NGC 4993. We present the photometric results from the comprehensive data analysis of the high spatial-resolution images in the different optical bands. The morphological analysis reveals that NGC 4993 is a typical early-type galaxy without significant remnants of major galaxy merger. The spatially resolved stellar population properties of NGC 4993 suggest that the galaxy center has passive evolution with the outskirt formed by gas accretion. We derive the merging rate of the compact object per galaxy by a co-evolution scenario of supermassive black hole and its host galaxy. If the galaxy formation is at redshift 1.0, the merging rate per galaxy is 3.2×1043.2\times 10^{-4} to 7.7×1057.7\times 10^{-5} within the merging decay time from 1.0 to 5.0 Gyr. The results provide the vital information for the ongoing GW EM counterpart detections. The HST data analysis presented in this paper can be also applied for the Chinese Space Station Telescope (CSST) research in the future.Comment: RAA accepte

    Hair follicle development and related gene and protein expression of skins in Rex rabbits during the first 8 weeks of life

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    Objective We aimed to observe hair follicle (HF) development in the dorsal skin and elucidate the expression patterns of genes and proteins related to skin and HF development in Rex rabbits from birth to 8 weeks of age. Methods Whole-skin samples were obtained from the backs of Rex rabbits at 0, 2, 4, 6, and 8 weeks of age, the morphological development of primary and secondary HFs was observed, and the gene transcript levels of insulin-like growth factor-I (IGF-I), epidermal growth factor (EGF), bone morphogenetic protein 2 (BMP2), transforming growth factor β-1, 2, and 3 (TGFβ-1, TGFβ-2, and TGFβ-3) were examined using quantitative real-time polymerase chain reaction (PCR). Additionally, Wnt family member 10b (Wnt10b) and β-Catenin gene and protein expression were examined by quantitative real-time PCR and western blot, respectively. Results The results showed significant changes in the differentiation of primary and secondary HFs in Rex rabbits during their first 8 weeks of life. The IGF-I, EGF, TGFβ-2, and TGFβ-3 transcript levels in the rabbits were significantly lower at 2 weeks of age than at birth and gradually increased thereafter, while the BMP2 and TGFβ-1 transcript levels at 2 weeks of age were significantly higher than those at birth and gradually decreased thereafter. β-Catenin gene expression was also significantly affected by age, while the Wnt10b transcript level was not. However, the Wnt10b and β-catenin protein expression levels were the lowest at 2 and 4 weeks of age. Conclusion Our data showed that a series of changes in HFs in dorsal skin occurred during the first 8 weeks. Many genes, such as IGF-I, EGF, BMP2, TGFβ-1, TGFβ-2, TGFβ-3, and β-Catenin, participated in this process, and the related proteins Wnt10b and β-Catenin in skin were also affected by age

    Natural mycotoxin contamination in dog food: A review on toxicity and detoxification methods

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    Nowadays, the companion animals (dogs or other pets) are considered as members of the family and have established strong emotional relationships with their owners. Dogs are long lived compared to food animals, so safety, adequacy, and efficacy of dog food is of great importance for their health. Cereals, cereal by-products as well as feedstuffs of plant origin are commonly employed food resources in dry food, yet are potential ingredients for mycotoxins contamination, so dogs are theoretically more vulnerable to exposure when consumed daily. Aflatoxins (AF), deoxynivalenol (DON), fumonisins (FUM), ochratoxin A (OTA), and zearalenone (ZEA) are the most frequent mycotoxins that might present in dog food and cause toxicity on the growth and metabolism of dogs. An understanding of toxicological effects and detoxification methods (physical, chemical, or biological approaches) of mycotoxins will help to improve commercial ped food quality, reduce harm and minimize exposure to dogs. Herein, we outline a description of mycotoxins detected in dog food, toxicity and clinical findings in dogs, as well as methods applied in mycotoxins detoxification. This review aims to provide a reference for future studies involved in the evaluation of the risk, preventative strategies, and clear criteria of mycotoxins for minimizing exposure, reducing harm, and preventing mycotoxicosis in dog

    Effects of chronic heat stress on the expressions of heat shock proteins 60, 70, 90, A2, and HSC70 in the rabbit testis

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    Few studies have focused on the expression of heat shock proteins (HSPs) after chronic heat stress. The objective of this study was to investigate the effect of chronic high temperature–humidity index treatment on the expressions of HSP60, HSP70, HSP90, HSPA2 and HSC70, in the Rex rabbit testis and the expressions of these proteins after recovery from the chronic heat shock. Thirty mature male rabbits of the same age were randomly divided into three groups: control, heat stress, and recovery. The western blot results showed that the expressional levels of HSP60, HSP90, and HSC70 increased significantly and HSPA2 was elevated slightly after a 9-week heat treatment. HSP70 was absent in the control testis and had a high level of expression after heat stress. All of these proteins partially reverted back to normal levels after a 9-week recovery. The immunohistochemical results indicated that the expression patterns of HSP60, HSP90, HSPA2, and HSC70 did not change
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