Yaoxing Chen

Morphologic analysis and classification of ganglion cells of the chick retina by intracellular injection of Lucifer Yellow and retrograde labeling with DiI.

Retinal ganglion cells (RGCs) of chicks were labeled by using the techniques of intracellular filling with Lucifer Yellow and retrograde axonal labeling with carbocyanine dye (DiI). Labeled RGCs were morphologically analyzed and classified into four major groups: Group I cells (57.1%) with a small somal area (77.5 μm2 on average) and narrow dendritic field (17,160 μm2 on average), Group II cells (28%) with a middle‐sized somal area (186 μm2) and middle‐sized dendritic field (48,800 μm2), Group III cells (9.9%) with a middle‐sized somal area (203 μm2) and wide dendritic field (114,000 μm2), and Group IV cells (5%) with a large somal area (399 μm2) and wide dendritic field (117,000 μm2). Of the four groups, Groups I and II were further subdivided into two types, simple and complex, on the basis of dendritic arborization: Groups Is, Ic, and Groups IIs, IIc. However, Group III and IV showed either a simple or complex type, Group IIIs and Group IVc, respectively. The density of branching points of dendrites was approximately 10 times higher in the complex types (18,350, 6,190, and 3,520 points/mm2 in Group Ic, IIc, and IVc, respectively) than in the simple types (1,890, 640, and 480 points/mm2 in Group Is, IIs, and IIIs). The branching density of Group I cells was extremely high in the central zone. The chick inner plexiform layer was divided into eight sublayers by dendritic strata of RGCs and 26 stratification patterns were discriminated. The central and peripheral retinal zones were characterized by branching density of dendrites and composition of RGC groups, respectively. J. Comp. Neurol. 469:360–376, 2004.

Effects of Monochromatic Light on Proliferation Response of Splencyte in Broilers

To investigate the effects of various monochromatic lights on splenocyte proliferation responses, a total of 260 Arbor Acre male broilers on P1 (post‐hatching day 1) were exposed to blue light (BL), green light (GL), red light (RL) and white light treatments by light emitting diode system for 7 weeks, respectively. All light sources were equalized on the intensity of 15 lx and light period of 23 h daily. Morphological change of spleen and response of splenocyte proliferation were assessed by using histochemistry staining and colorimetric test in cultures of purified splenic cells. The results were as follows: (1) At P21, GL increased significantly the spleen weight by 163.6% and spleen index by 118.8% compared with RL (P < 0.05). Until P49, BL enhanced significantly the spleen weights by 42.2% compared with RL (P < 0.05), but no significant difference was found in the spleen index among four light‐treated groups (P > 0.05). (2) Compared with RL, GL increased significantly the diameter of splenic nodule and area of periarterial lymphatic sheath at P21 by 87.2 and 58.1%, respectively (P < 0.05); BL increased significantly the diameter of splenic nodule and area of periarterial lymphatic sheath at P49 by 64.4 and 50.5%, respectively (P < 0.05). (3) At P21, GL enhanced spleen lymphocytes proliferation in response to concanavalin A compared with RL by 50.0% (P < 0.05). Until P49, the mitogenic response in BL was significantly higher (29.4%) than that of RL (P < 0.05). (4) The interleukin‐2 (IL‐2) bioactivity was significantly increased to 34.3% in GL than in RL at P21 (P < 0.05). Until P49, the IL‐2 bioactivity in BL was significantly higher (62.2%) than that of RL (P < 0.05). (5) There was no significant difference in the nitric oxide (NO) concentration of splenocyte among RL, GL and BL groups at P21 (P > 0.05), but the concentration in RL group at P49 was significantly increased, 59.0 and 63.7% compared to that of GL and BL groups, respectively (P < 0.05). These results suggested that the monochromatic light affected splenocyte proliferation mainly because of alterations in IL‐2 bioactivity and NO production in splenocyte of broiler. In early stage of broiler growth, the action of GL was obvious, while the response of BL was stronger in later stage.

Effect of a combination of green and blue monochromatic light on broiler immune response

Our previous study suggested that green light or blue light would enhance the broiler immune response; this study was conducted to evaluate whether a combination of green and blue monochromatic light would result in improved immune response. A total of 192 Arbor Acre male broilers were exposed to white light, red light, green light, and blue light from 0 to 26 days. From 27 to 49 days, half of the broilers in green light and blue light were switched to blue light (G-B) and green light (B-G), respectively. The levels of anti-Newcastle disease virus (NDV) and anti-bovine serum albumin (BSA) IgG in G-B group were elevated by 11.9-40.3% and 17.4-48.7%, respectively, compared to single monochromatic lights (P<0.05). Moreover, the proliferation of peripheral blood T and B lymphocytes and the IL-2 concentration in the G-B groups increased by 10.4-36.2%, 10.0-50.0% and 24.7-60.3% (P<0.05), respectively, compared with the single monochromatic light groups. However, the serum TNF-α concentration in the G-B group was reduced by 3.64-40.5% compared to other groups, and no significant difference was found between the G-B and B-G groups in any type of detection index at the end of the experiment. These results suggested that the combination of G-B and B-G monochromatic light could effectively enhance the antibody titer, the proliferation index of lymphocytes and alleviate the stress response in broilers. Therefore, the combination of green and blue monochromatic light can improve the immune function of broilers.

Effect of Oestradiol on Mast Cell Number and Histamine Level in the Mammary Glands of Rat

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Melatonin plays a critical role in inducing B lymphocyte proliferation of the bursa of Fabricius in broilers via monochromatic lights

To study the role of melatonin in the monochromatic light-induced B lymphocyte proliferation of bursa, a total of 360 newly hatched broilers, including intact, sham-operated, and pinealectomized groups, were exposed to blue light (BL), green light (GL), red light (RL) and white light (WL) from a light-emitting diode system for 14d. Both in vivo and in vitro studies showed that the percentage of proliferating cell nuclear antigen (PCNA)-immunoreactive lymphocytes and the lymphocyte proliferation in response to lipopolysaccharide in the bursa of broilers in the GL intact group was the highest values among the different intact groups with altered plasma melatonin levels. Additionally, the superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities and total antioxidant capability (T-AOC) were the highest, whereas malondialdehyde (MDA) content and inducible nitric oxide synthase (iNOS) expression were significantly decreased in the GL intact group. After pinealectomy, the levels of SOD, GSH-Px and T-AOC decreased remarkably in the various light-treatment groups, whereas the MDA content and iNOS expression significantly increased. The administration of exogenous melatonin (250pg/mL) in vitro also significantly enhanced the bursal B lymphocyte proliferation. These findings suggest that GL illumination effectively elevates the antioxidative capacity to promote B lymphocyte proliferation of bursa in young broilers, which might depend on enhanced melatonin secretion.

Morphological properties of chick retinal ganglion cells in relation to their central projections

Morphological properties of chick retinal ganglion cells (RGCs) were studied in relation to their central projections in 23 chicks. A total of 217 RGCs were retrogradely labeled by applying a carbocyanine dye (DiI) to the thalamus and optic tectum. The labeled RGCs were classified into six groups on the basis of their somal areas, dendritic fields, and branching patterns. The dendrites of these RGCs extended horizontally in the inner plexiform layer (IPL) forming eight dendritic strata. The RGCs in each group showed certain specificities in their central projections. Group Ic predominantly projected to the tectum. Groups IIs and IIIs showed a high thalamic dominance. Groups Is and IIc were nonspecific with regard to their tectal and thalamic projections. Group IVc showed tectal‐specific projections. Occurrence rates of the dendritic strata increased progressively toward the inner part of the IPL, i.e., DSs (dendritic strata) 1–4 were scantily distributed, DSs 5 and 6 were moderately distributed, and DSs 7 and 8 were the most frequently distributed. A total of 42 dendritic stratification patterns were identified, and of these, 18 patterns were common to the tectal RGCs (tec‐RGCs) and thalamic RGCs (tha‐RGCs). The common patterns were detected very frequently in the tec‐ and tha‐RGCs (≈85%), and the dendritic strata were largely distributed in the inner part of the IPL (DSs 5–8). In contrast, the remaining 24 noncommon stratification patterns showed low occurrence rates (≈15%); however, these dendritic strata were widely distributed in both the outer (DSs 1–4) and inner (DSs 5–8) IPL. J. Comp. Neurol. 514:117–130, 2009.

Restraint stress alters immune parameters and induces oxidative stress in the mouse uterus during embryo implantation

Abstract The influence of stress on embryo implantation is not well understood. Prior studies have focused on later gestational stages and the long-term impact of stress on immune function. The objective of this study is to investigate the effects of restraint stress on the immune parameters and the oxidative states of the uterus during implantation. In this study, pregnant CD1 mice were subjected to restraint stress (4 h/d) on embryonic day 1 (E1) and sacrificed on E3, E5, and E7. Maternal plasma corticosterone (CORT) secretion and implantation sites in the uterus were examined. The uterine (excluding embryos) homogenate and uterine lymphocytes were collected to examine oxidative stress states and associated immune parameters. The results demonstrated that restraint stress increased maternal plasma CORT secretion and reduced the number of implantation sites by 15.3% on E5 and by 26.1% on E7. Moreover, restraint stress decreased the density of uterine natural killer (uNK) cells in the endometrium by 22.1–47.9% and increased the density of mast cells in the myometrium by 55.6–76.9%. Restraint stress remarkably decreased the CD3+CD4+ T/CD3+CD8+ T cell ratio (by 26.2–28.9%) and attenuated uterine lymphocyte proliferation and secretion of cytokines. In addition, restraint stress threatened the intracellular equilibrium between oxidants and antioxidants, resulting in decreased glutathione peroxidase (GSH-PX) (32.2% and 45.7%), superoxide dismutase (SOD) (15.5% and 26.1%), and total antioxidant capacity (T-AOC) (18.4% and 18.2%) activities and increased malondialdehyde (MDA) (34.4% and 43.0%) contents on E5 and E7. In conclusion, these findings demonstrate that restraint stress causes abnormal implantation and negatively impacts immune parameters in association with oxidative stress in mice.

Afferent and Efferent Connections of the Nucleus Rotundus Demonstrated by WGA‐HRP in the Chick

Organization of the fibre connections in the chick nucleus rotundus (Rt) was investigated by an axonal tracing method using wheat germ agglutinin conjugated to horseradish peroxidase (WGA‐HRP). After an injection of WGA‐HRP into the Rt, labelled neurones were observed in the striatum griseum centrale (SGC) in both sides of the tectum (TO) and in the ipsilateral nucleus subpretectalis/nucleus interstito‐pretecto‐subpretectalis (SP/IPS). Labelled fibres and terminals were also found in the ipsilateral ectostriatum (Ect). These fibre connections were topographically organized rostrocaudally. In the TO‐Rt projection, the rostral and the dorsocaudal parts of the Rt received afferents from the superficial part of the SGC, the middle part of the Rt received afferents from the intermediate part of the SGC, and the ventrocaudal part of the Rt received mainly fibres from the deep part of the SGC. These topographic projections were accompanied by a considerable number of diffuse projections to the thalamic regions surrounding the Rt. In addition, the rostral and middle caudal parts of the Rt received afferents from the lateral and medial parts of the SP/IPS, respectively, and respective parts of the Rt sent efferents to the lateral and medial parts of the Ect.

Monochromatic light affects the development of chick embryo liver via an anti-oxidation pathway involving melatonin and the melatonin receptor Mel1c

Wang, T., Wang, Z., Cao, J., Dong, Y. and Chen, Y. 2014. Monochromatic light affects the development of chick embryo liver via an anti-oxidation pathway involving melatonin and the melatonin receptor Mel1c. Can. J. Anim. Sci. 94: 391-400. Monochromatic light can influence muscle development during incubation and post-hatching. This process is related to IGF-1, which is primarily secreted by the liver. However, the effect of monochromatic light on liver development of chick embryo is unclear. In this study, 600 Arbor Acres fertile broiler eggs were randomly assigned to four incubators and exposed to continuous red light (R-group), green light (G-group), blue light (B-group), or a dark environment (D-group, control). The liver index of the G-group was higher than that of other groups (6.47-15.46%) at E21, accompanied by a higher percentage of proliferating cell nuclear antigen (PCNA). The superoxide dismutase (T-SOD), glutathione peroxidase (GSH-PX), and total antioxidant capability (T-AOC) contents were the highest in the G-group, and this trend was positively correlated with plasma melatonin (Mel) levels and the Mel receptor Mel1c expression of liver, while the malondialdehyde (MDA) content appeared to follow an opposite trend. In vitro, the administration of exogenous melatonin (250 pg mL-1) increased the proliferative activity and the antioxidant status of hepatocytes. However, this effect was significantly inhibited by Prazosin, a Mel1c inhibitor. These results suggest that green light improves the antioxidant status of the liver, which is mediated by melatonin and mel1c, and finally accelerates liver development.

Afferent and Efferent Connections of the Nucleus Geniculatus Lateralis Ventralis Demonstrated by WGA-HRP in the Chick

Fibre connections of the chick nucleus geniculatus lateralis ventralis (GLv) were investigated using the axonal tracing method with wheat germ agglutinin conjugated to horseradish peroxidase (WGA‐HRP). After an injection of WGA‐HRP into the GLv, many labelled neurons were observed in layer i of the stratum griseum et fibrosum superficiale (SGFS) in the ipsilateral tectum opticum (TO) and in the nucleus lentiformis mesencephali (LM). In the TO‐GLv projection, cells of origin were located in the deeper part of layer i of the TO and were topographically distributed along the direction from the rostrodorsal part to the caudoventral part of the TO relating to a rostrocaudal axis of the GLv. In the LM‐GLv connection, the dorsal and ventral parts of the LM connected reciprocally with the rostral and caudal halves of the GLv, respectively. In contrast, in the GLv efferent connection, labelled axon terminals spread widely in the ipsilateral area pretectalis without any clear topographical arrangement.