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1.
为了探究麒麟鸡卷羽毛囊发育规律及卷羽特点,研究通过采集7~18日胚龄麒麟鸡和怀乡鸡鸡胚背部皮肤,进行石蜡切片,HE染色,在显微镜下观察毛囊形态结构,比较分析麒麟鸡和怀乡鸡胚胎期毛囊发育过程,并于出壳后观察分析麒麟鸡卷羽生长状况。结果表明:卷羽毛囊发育过程在8~16日胚龄,其中12~15日胚龄卷羽毛囊呈弯曲状态,髓质面积大于片羽毛囊,羽枝嵴小于片羽;卷羽羽轴向外弯曲、羽小枝之间不能相互钩连形成闭合羽片。  相似文献   

2.
鸡胚法氏囊的组织发育   总被引:7,自引:0,他引:7  
本试验通过对孵化至13-21日龄的鸡胚法氏囊进行组织学的连续性动态观察,较为详细地描述了早日龄鸡胚法氏囊的组织学分化发育过程。实验结果显示,直至出壳胶鸡胚法氏囊尚未形成较完整的能组织起 体液免疫促进作用的组织基础结构,其完善的形态结构需在后天环境中分化和发育。  相似文献   

3.
鸡胚免疫器官组织学发育过程观察   总被引:3,自引:0,他引:3  
通过对孵化至12-21日龄鸡胚的免疫器官胸腺、脾及腔上囊进行组织学连续性观察,较为详细地描述了鸡胚免疫器官的组织发育过程。观察结果显示,胸腺的组织结构发育和形成较早,自12日龄起胸腺就已形成原始的胸腺小叶;虽然脾在12日龄时就已初具轮廓,但脾直到18日龄才开始隐约形成形态可辨的红髓和白髓;腔上囊淋巴滤泡自鸡胚发育到17日龄时即渐趋明显,但完整的滤泡皮质和髓质结构在出壳前仍然处于分化成熟阶段。  相似文献   

4.
为了研究敖汉细毛羊毛囊的组织结构与形态发育过程,进而为解析细毛羊毛囊发育的分子调控机制奠定组织学基础,试验采用组织学和显微观测的方法,分析敖汉细毛羊胎龄为第90,120天的胎儿,及出生后1天和1个月时的羔羊体侧部皮肤的组织学特性。结果表明:在胎龄90天时,体侧的初级毛囊可见次级毛囊毛芽;胎龄120天时,部分毛囊发生角质化,初级毛囊周围可见成对的皮脂腺及之间的汗腺导管和竖毛肌;出生后1天时和出生1个月时,大部分毛囊都已形成角质化毛干,皮脂腺、汗腺、竖毛肌等进一步发育成熟。与胎龄120天时相比,出生后1个月时的毛囊纤维直径显著增大(P0.05)。出生后1个月和出生后1天时次级毛囊纤维直径差异不显著(P0.05)。  相似文献   

5.
文章对家禽羽毛的类型、发生发育过程、毛囊的基本结构与再生,以及影响羽毛发育的信号分子调控网络进行了综述,并探讨了家禽羽毛形成的遗传调控机制和生物学基础。  相似文献   

6.
鸡胚法氏囊组织发育的电镜和组织学比较观察   总被引:1,自引:0,他引:1  
本实验通过对孵化至12~21 日龄的鸡胚法氏囊进行组织学和超微结构的连续性动态观察,较为详细的描述了早日龄鸡胚法氏囊分化发育过程中显微和超显微的变化过程。实验结果显示,尽管鸡胚发育到中、后期胚体内可能已经具有一定程度的免疫效应,但直至出壳前鸡胚法氏囊尚未形成较完整的能组织起有效体液免疫组织基础结构,其完善的形态结构需在后天环境中继续分化和发育。非炎性状态下法氏囊淋巴滤泡内自始至终出现异嗜性细胞,在法氏囊的分化发育中起着重要的组织改建作用。  相似文献   

7.
营养因素对水禽羽毛发育的影响   总被引:1,自引:1,他引:0  
羽毛是水禽重要的外貌特征,其形态发生、结构组成及换羽模式等与羽毛品质高度相关。随着水禽出栏日龄的不断缩短,水禽羽毛的早期发育和及时成熟显得尤为重要。研究表明,氨基酸平衡,尤其是含硫氨基酸和支链氨基酸的平衡能够显著影响早期水禽羽毛的发育;脂类通过尾脂腺影响羽毛的光泽;粗纤维可以减少啄羽癖的发生;维生素和某些微量元素的缺乏将会引起羽毛发育异常;某些病毒、细菌和支原体可以感染毛囊进而影响羽毛的发育。  相似文献   

8.
通过对1~49日龄雏鸭胸腺组织学发育的增龄变化观察以及胸腺绝对重量、胸腺指数和外周血T淋巴细胞а-醋酸萘酯酶阳性率的测定,研究了雏鸭胸腺发育规律。结果表明:1~14日龄雏鸭胸腺生长较为缓慢;21~28日龄胸腺生长十分迅速,到28日龄时雏鸭胸腺中大部分T淋巴细胞已分化发育成熟,雏鸭胸腺已形成能有效产生细胞免疫的组织结构基础;35~49日龄胸腺发育已趋于稳定。文中对胸腺小体的形态进行了详细的描述,并对其功能进行了探讨。  相似文献   

9.
[目的]了解成年绒山羊次级毛囊组织形态的周期性变化过程,为研究绒山羊绒毛生长的分子调控机理奠定组织学基础.[方法]制作内蒙古绒山羊1年周期内每个月的皮肤组织切片,染色后显微镜下观察照相.[结果]成年绒山羊次级毛囊形态在1年中呈周期性变化,在兴盛期、退行期和休止期的形态各不相同.从4月份开始,次级毛囊外根鞘细胞向下分裂延伸,开始了毛囊的重建;8-9月毛囊完成重建,毛囊结构完整;10月毛球细胞停止分裂,毛乳头萎缩,大量细胞程序化死亡,毛根上移,毛囊进入退行期;12月毛囊根部上升到皮脂腺附近不再变化;翌年1-3月毛囊的形态基本没有变化.[结论]了解了成年绒山羊次级毛囊1年内形态的周期性变化过程,为绒山羊绒毛相关领域的研究提供一定的借鉴.  相似文献   

10.
本实验旨在探究敖汉细毛羊毛囊的组织结构与形态发生过程,为细毛羊毛囊发育的分子调控机制研究奠定组织学基础。分别采集胎龄第90、120天的胎儿及出生后1 d和30 d的羔羊体侧部(多毛区)和腹股沟部(少毛区)皮肤组织,制作纵、横切片并显微观察。结果表明:敖汉细毛羊毛囊结构包括结缔组织鞘、外根鞘、内根鞘、毛干和毛球部;在胎龄90 d时,体侧部初级毛囊可见皮脂腺原细胞及次级毛囊毛芽,在胎龄120 d时,毛囊形成角质化毛干并穿出体表,再分化次级毛囊发生;出生后1 d和30 d时,穿出体表毛干进一步增多,体侧部初级毛囊密度,在胎龄120 d时低于胎龄90 d时(P0.01),出生后1 d时低于胎龄120 d时(P0.05),次级毛囊密度,在胎龄120 d时高于胎龄90 d时(P0.01),出生后1 d时低于胎龄120 d时(P0.01),出生后1 d和30 d时差异不显著(P0.05),S/P比值,在胎龄120 d时高于胎龄90 d时(P0.01),生后30 d时高于出生后1 d时(P0.01),对腹股沟部皮肤分析显示,其毛囊密度很低。结果可为了解细毛羊毛囊形态结构变化及筛选与毛密度相关的差异基因提供参考依据。  相似文献   

11.
In vitro effects of vascular endothelial growth factor (VEGF) on heart development and total embryonic growth were investigated in 84 rat embryos (obtained from nine pregnant females) at 9.5 days of gestation that were cultured in whole rat serum (WRS), in <30 kDa + >50 kDa serum fractions [retenate (R)], and in R + VEGF. After 24-h culture, the embryos from each group were harvested and divided into two groups. One group was analysed morphologically and biochemically to obtain embryo protein content, the second group was serially sectioned and examined by light microscopy. Morphological score, embryo protein content, somite number and crown-rump length of embryos indicated that embryos cultured in R had significant embryonic retardation, whereas the addition of VEGF to R increased embryonic growth and development. The morphological scores for WRS, R and R + VEGF were 57.7 +/- 0.87, 46.6 +/- 1.90 and 52.1 +/- 0.97, somite numbers were 26.5 +/- 0.47, 20.1 +/- 0.63 and 24.4 +/- 0.46, crown-rump lengths were 3 +/- 0.07, 2.4 +/- 0.06 and 2.7 +/- 0.06 mm, and embryo protein contents were 160.5 +/- 7.41, 98.2 +/- 4.81 and 141.1 +/- 10.96 mug per embryo, respectively. The results of histological examination of heart development were similar. The hearts of embryos grown in R were unseptated and tubular. The atrioventricular endocardial cushions were incompletely developed. The addition of VEGF to R improved heart development. There were no gross morphological differences in the cardiac development between embryos grown in WRS and R + VEGF. In both groups, development of the muscular interventricular septum had begun. Development of the atrioventricular cushions was also similar in both groups and had caused narrowing of the atrioventricular canals, but the atrial septation was not observed.  相似文献   

12.
无菌采集病死红腹锦鸡肝脏、脾脏和心血,接种多种培养基分离细菌。以生化试验和小鼠攻毒试验,鉴定分离细菌及其致病性。采用PCR方法扩增分离细菌16S rRNA,测定核苷酸序列,与GenBank中大肠杆菌相应基因序列进行分析比较,绘制系统进化树。结果表明,分离细菌为大肠杆菌,可以致小鼠死亡。其16S rRNA基因序列与GenBank登录的大肠杆菌相应基因同源性超过99%。由此证明,该红腹锦鸡死于大肠杆菌病。  相似文献   

13.
试验选取健康且体重一致、12周龄的红腹锦鸡15只,随机分为5个处理,每个处理设3个重复,每个重复1只,试验期为12周,分别饲喂蛋白质水平不同的5种试验日粮(A组16.78%,B组17.76%,C组18.75%,D组19.75%,E组20.67%)。结果表明:23同龄时,在能量水平为12.14 MJ/kg、蛋白质水平为18.75%时,育成期红腹锦鸡体重最大,为511.63 g,与其他各组差异显著(P0.05)。蛋白质水平为19.75%时,育成期红腹锦鸡的体型发育最佳。  相似文献   

14.
选择成年白冠长尾雉5只,白腹锦鸡5只,白鹇3只,红腹锦鸡3只和孔雀11只,同时用L系弱毒冻干苗和新城疫油乳剂灭活疫苗进行免疫接种,通过血凝抑制试验(HI)测定其抗体滴度.结果表明,在免疫接种后26 d,白冠长尾雉抗体效价为9.8log2,白腹锦鸡为8.0log2,白鹇为8.0log2,红腹锦鸡为10.7log2;孔雀在免疫后接种0、8、15、20、25 d,抗体水平分别为3.8log2、5.0log2、6.2log2、7.5log2及8.2log2.  相似文献   

15.
1. This research focused on the embryonic development of broiler and layer embryos. 2. Egg, embryo and yolk weights were measured and partial pressure of gases in the air cell and blood were analysed at several embryonic ages. The static stiffness of the eggshell was measured before the start of incubation and at embryonic day (ED) 18 to register the change in shell strength. Times of internal pipping (IP), external pipping (EP) and hatch were recorded. Plasma corticosterone, triiodothyronine and thyroxine concentrations were determined. 3. Relative egg weight loss was higher in layer eggs. Before ED16, layer embryos showed a slower development which was reflected in lower (relative) embryo weight, lower air cell and blood pCO(2) and higher air cell O(2). From ED16 onwards, relative growth rate accelerated in the layer strain; as a consequence the difference in relative yolk-free chick weight at hatch had disappeared between strains. 4. Differences in physiological events necessary for hatching (thyroid hormones, corticosterone, air cell pCO(2)) are most probably responsible for the observed differences in timing of pipping and hatching events between layer and broilers.  相似文献   

16.
The development of methods to produce embryos in vitro in the horse has been delayed compared with other domestic species. Oocytes can be collected from excised ovaries or from the small or preovulatory follicles of live mares. Intracytoplasmic sperm injection is the only reliable method to fertilize equine oocytes in vitro. Intracytoplasmic sperm injection-produced embryos can be transferred into the oviducts of recipient mares or cultured to the morula or blastocyst stage of development for nonsurgical embryo transfers into recipients' uteri. Embryos cultured in vitro have some morphological differences compared with embryos collected from the mares' uteri. Most notably, the embryonic capsule does not form in culture, and the zona pellucida fails to expand completely. However, embryo produced in vitro can result in viable pregnancies and healthy offspring.  相似文献   

17.
The correlation between apoptosis and early bovine embryonic loss is still not fully elucidated. In the present study, the relationship between the arrest of bovine embryos at the different stages of development and apoptosis was evaluated. We used embryos 7 days after in vitro maturation and fertilization, and morphologic and biochemical apoptotic analyses were performed by using a phase contrast microscope and by the terminal transferase dUTP nick end‐labelling respectively. For the statistic, the apoptotic cell ratio (ACR) was determined as the percentage of apoptotic cells per embryo. To evaluate the relation between ACR and fragmentation pattern, embryos were divided into five groups, groups I–V. To assess the relation between ACR and cytoplasmatic fragmentation, embryos were divided into three groups, according to the fragmentation percentage (<5%; 5–15% and >15%). Of the total 139 embryos included, 65 arrested at 2–8 cells; 14 arrested at 9–16 cells; 18 compacted morula and 42 were non‐arrested blastocysts. The average number of embryonic fragmentation at different stages of the development, 2–8 cells, 9–16 cells, compacted morula and blastocyst, was 16.0 ± 1.5, 28.7 ± 4.4, 4.4 ± 2.4 and 1 ± 0.3 respectively. The embryos at the stage of arrested 9–16 cells and compacted morula had higher ACR than those at the blastocyst stage, excluding the stage of 2–8 cells (the genome is not yet active). The correlation detected between embryonic development and ACR was 0.92 (p < 0.01). It was observed that embryos possessing high fragmentation showed the higher ACR value (r = 0.98, p < 0.05). Comparing the results between fragmentation percentage and ACR, it was observed that the embryos with higher percentage of fragmentation corresponded to higher ACR (r = 0.97, p < 0.01). These results clearly demonstrated that bovine embryonic arrest at different stages of development is correlated with the apoptotic mechanisms.  相似文献   

18.
In this study, we aimed at the in vitro effects of anti-fibroblast growth factor-2 (anti-FGF-2 or anti-bFGF) on embryo culture in rats. In vitro effects of anti-bFGF on total embryonic development were investigated in 40 rat embryos (which were divided into four groups) (obtained from five pregnant females) at 9.5 days of gestation that were cultured in whole rat serum (WRS), and in WRS+ 2.5, 5, and 10 μg/ml anti-bFGF. After 48 h of culturing, the embryos from each group were harvested to be analysed morphologically according to a morphological scoring system and biochemically to obtain the embryo protein content. The morphological score, embryo protein content, somite number and crown-rump length of embryos indicated that embryos cultured in WRS+ anti-bFGF had significant embryonic retardation. Mean morphological scores for the embryos grown in WRS, in the presence of 2.5, 5 and 10 μg anti-FGF-2 were 61.4 ± 1.64, 46.3 ± 8.42, 27 ± 2.58 and13.6 ± 0.96 respectively. These results suggest that bFGF is very important for normal embryonic development and rat anti-bFGF neutralizes bFGF effect.  相似文献   

19.
本试验旨在研究胚胎期大鼠性腺生长与分化的情况。选取12.5~15.5 dpc SD大鼠胚胎为研究对象,运用PCR技术进行大鼠胚胎性别鉴定,采用H-E技术对大鼠性腺分化形态进行观察。结果表明:12.5 d的鼠胚肾管已经开始形成,生殖嵴已经建立,此时仍无明显的性别分化形态;13.5 d的鼠胚开始出现性别分化的迹象,雄性的原始性索开始形成,雌性性腺分化比雄性稍晚,此期仍不易辨别出典型的卵巢特征结构;14.5 d的鼠胚性腺形态初步成型,此期性别明显分化,雄性的原始性索开始分化为实心原始生精小管,雌性胚胎中性腺分为两层,初步形成卵巢特征;15.5 d的鼠胚,雄性胚胎性腺中已经具有明显的曲精小管的雏形,雌性胚胎卵巢特征也开始明显。大鼠胚胎性腺从13.5 d胚龄时开始分化,15.5 d胚龄性腺特征明显。  相似文献   

20.
紫花苜蓿愈伤组织及体细胞胚的细胞学观察   总被引:11,自引:1,他引:10  
以紫花苜蓿Medicago sativa的下胚轴为材料,诱导愈伤组织和体细胞胚的发生.在此过程中采用石蜡切片法观察愈伤组织和体细胞胚的内部结构,结果表明,胚性愈伤和非胚性愈伤在形态和细胞学上均有很大差别,体细胞胚的发生经历了多细胞原胚、球形胚、心形胚、子叶胚、鱼雷胚等多个阶段.观察发现,在胚性愈伤的内部和表面都有体细胞胚发生.  相似文献   

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