可口革囊星虫消化道的形态结构特征

采用解剖及组织学显微技术观察研究了可口革囊星虫消化道的形态及组织学结构特征。消化道始于口,经咽、食道、游离肠、螺旋肠(上行肠及下行肠)、直肠,止于肛门,各段从内向外均由粘膜层、粘膜下层、肌层及外膜组成。粘膜层表面具微绒毛及纤毛,微绒毛增加了消化道的表面积,纤毛的摆动有利于消化道内食物或消化后残渣的运送;螺旋肠及直肠的粘膜层中均有杯状细胞,在下行肠前段与中段及上行肠前段与直肠中尤其多,杯状细胞能够分泌粘液,保护粘膜上皮,润滑食物及残渣。粘膜下层为结缔组织,肌层为环肌,外膜为浆膜。肠沿纺锤肌盘绕的特点延长了食物的滞留、消化和吸收时间,弥补了缺乏消化腺的不足。肠各段除直肠肌层较厚外,其余各段肌层薄或不明显。     

宽体金线蛭消化道的组织学观察

运用解剖学和组织学方法对宽体金线蛭消化道的结构进行了组织学研究。结果表明,宽体金线蛭的嗉囊向两侧伸出11对侧盲囊,第6对侧盲囊狭长并延伸到直肠两侧;咽主要由黏膜层、肌层和外膜构成,外膜几乎不可见;食道、嗉囊、肠和直肠管壁由黏膜层、黏膜下层、肌层和浆膜构成;咽和直肠的上皮具纹状缘。除肠外,其他消化道的上皮细胞均无发达的纤毛,且黏膜上皮皆为单层柱状上皮;除肠和直肠外,腺体及导管较少;直肠的黏膜肌层为内环外纵两层,其他各部均为纵行肌一层;消化道各部黏膜下层较发达;外膜为浆膜,与黏膜下层分界不明显。     

中华绒螯蟹肠道内间质样细胞的显微和超微结构观察

目的探究中华绒螯蟹(Eriocher sinens is)肠道中是否存在间质样细胞。方法通过对中华绒螯蟹中肠和后肠进行全层铺片和肠cajal间质细胞(interstitial cells of cajal,ICC)特殊染色法碘化锌-锇酸(zinc iodide-osmium,ZIO)染色,并结合后肠透射电镜观察中华绒螯蟹后肠ICC样细胞分布及形态。结果光镜检查结果显示:中华绒螯蟹间质样细胞常分布在中肠和后肠的黏膜下层。这些细胞形态相似,多为圆形或卵圆形,胞体直径约为10μm左右,呈灰黑色,常成群呈块状或片状分布,在后肠中的分布更为密集。电镜检测结果显示:这些细胞分布于黏膜下层、肌层与肌层之间和肌肉束边缘。后肠中间质样细胞多为梭形及纺锤形,也有不规则型,常有两个或两个以上突起,与邻近的细胞连接方式多为缝隙连接。此外,本研究还在后肠肠道固有膜层、肌层间和黏膜下层发现了大量颗粒细胞的分布。结论本研究通过传统的特异性ZIO染色和超微形态的观察初步发现中华绒螯蟹肠道内有ICC样细胞的分布。     

版纳鱼螈消化道解剖学和组织学观察

对我国特有珍稀濒危两栖动物版纳鱼螈(Ichthyophis bannanicus)的消化道进行解剖和组织学观察.结果表明,版纳鱼螈消化道呈直管状,无盘曲;胃、肠分化明显,肠可分为十二指肠、空肠、大肠和直肠;黏膜上皮食管为复层柱状纤毛上皮,胃后段为单层柱状上皮,直肠为复层扁平上皮,其余均为复层柱状上皮;口咽腔黏膜含大量巨型杯状细胞,有单泡状颌间腺;食道中下段有团泡状食道腺;胃体部含大量单管状胃腺;十二指肠和空肠有单泡状肠腺,绒毛发达;口咽腔的黏膜下层不明显,食道和直肠的黏膜下层为疏松结缔组织,其余均为细密的结缔组织;肌层除口咽腔为骨骼肌外,其余均为内环外纵两层平滑肌,其中,在十二指肠和空肠的两肌层间有细密的结缔组织连接.     

可口革囊星虫消化道的形态及组织学结构

对可口革囊星虫(Phascolosoma esculenta)消化道各部分结构进行了形态学和组织学观察,表明可口革囊星虫消化道由翻吻、咽、食道、肠、直肠和肛门组成。翻吻收缩性很强;肠道极长,沿纺锤肌螺旋缠绕成肠索。消化道管壁由内向外分为粘膜层、粘膜下层、肌层和外膜。粘膜上皮主要由柱状细胞组成。除肠外,消化道上皮细胞均有发达的纤毛,肠上皮细胞主要具发达的微绒毛;粘膜下层及肌层的发达程度因消化道的部位不同而异。     

银鲳消化道形态与组织学结构特征及其消化酶活性

为了解银鲳(Pampus argenteus)消化道结构特点与其功能及食性的相关性, 采用解剖、石蜡切片、AB-PAS染色及酶活性检测技术对银鲳消化道的形态、组织结构、黏液细胞分布及消化酶活性进行研究。结果显示, 银鲳的消化道由口咽腔(舌)、食道侧囊、食道、胃及肠构成, 胃肠交界处有很多幽门盲囊。食道侧囊呈椭球形, 食道粗短, 胃呈U型, 肠有多个盘曲, 肠指数为2.03。舌上皮内有少量味蕾及较多黏液细胞。食道侧囊、食道、胃及肠均由黏膜层、黏膜下层、肌层及浆膜组成。食道侧囊内皱襞较发达, 被覆复层扁平上皮, 内含较多黏液细胞, 且以Ⅳ型为主, 皱襞顶端及侧面有内含角质刺的次级突起; 黏膜下层及肌层中有固定皱襞的骨质脚根; 侧囊内胃蛋白酶活性较高。食道内皱襞较高, 被覆复层扁平上皮, 内含较多黏液细胞, 且以Ⅳ型为主。胃内皱襞发达, 被覆单层柱状上皮, 未见黏液细胞分布; 胃腺发达, 胃内蛋白酶活性较高。肠道内褶襞多, 高度呈先下降后上升趋势, 黏液细胞密度前、中肠较高, 后肠较低, 且均以Ⅰ型为主; 肠道内胰蛋白酶、脂肪酶、淀粉酶及碱性磷酸酶活性较高。幽门盲囊组织结构与肠相似。银鲳的消化道结构特点、黏液细胞分布及消化酶活性与其功能及偏肉食的杂食性相适应。     

圆尾鲎消化道组织结构与黏液细胞分布

利用石蜡切片、苏木素-伊红(H.E)和阿利新兰-高碘酸雪夫试剂(AB-PAS,AB,pH 2.5)组化染色技术研究圆尾鲎(Carcinoscorpius rotundicauda)消化道组织结构及其黏液细胞的分布特征。圆尾鲎消化道外形为一直管状,中肠部位有分支。H.E染色结果显示,食道、胃、幽门、中肠与后肠的管壁一般结构由外至内分为外膜、肌肉层、黏膜下层、黏膜层。食道是一段短管状结构,肌肉层较胃壁的薄但几丁质层极厚。胃则为一膨大的砂囊结构,内含一定数量的纵行黏膜皱褶,肌肉纤维排列整齐,几丁质层较薄。幽门与中肠套叠,幽门壁肌肉层很薄,几丁质层清晰可见。中肠和后肠结构差异不大,具有一定数量的黏膜皱褶,上皮细胞间分布比较多的黏液细胞,均无几丁质层。AB-PAS组化染色结果显示,消化道有Ⅰ和Ⅱ型两种黏液细胞,不同部位分布数量差别很大。食道和幽门未见黏液细胞。胃黏膜下层有少量Ⅱ型黏液细胞。中肠和后肠黏液细胞数量比较多,尤其是与幽门套叠的中肠前端区域,均以Ⅱ型黏液细胞为主,主要分布在黏膜下层和黏膜上皮。在后肠黏膜下层有Ⅰ型黏液细胞分布,而黏膜上皮则分布密集的Ⅱ型黏液细胞。圆尾鲎消化道组织结构及黏液细胞分布特征反映其不同部位功能的差别,体现食性与消化机能相协调的特点。     

中华绒螯蟹肠道肥大细胞的组织化学研究

目的应用2种染色方法对中华绒螯蟹肠道肥大细胞进行组织化学定位。方法甲苯胺蓝(TB)和阿尔新兰-藏红染色(AB/SO)对中肠,后肠和之间的肠球进行了染色。结果 TB和AB/SO两种染色均能不同程度的显示中华绒螯蟹肠道肥大细胞,且TB更为适合。肠道粘膜上皮肥大细胞的形态主要为椭圆形或者圆形。中肠的前段和中段的肥大细胞主要分布在粘膜层的上皮细胞、基膜及外膜的结缔组织中;后肠的肥大细胞主要分布在粘膜下层的结缔组织颗粒和肠腺中;肠球中肥大细胞主要分布在肠球边缘少数存在的嗜酸性颗粒和嗜碱性颗粒中。结论中华绒螯蟹肠道肥大细胞具有与其他动物有相似之处,但是也存在自身的特异性。     

文县疣螈消化道和肝脏的形态学及组织学观察

利用生物显微技术对文县疣螈的消化道和肝脏进行了观察.结果 表明:文县疣螈的消化道管壁由粘膜层、粘膜下层、肌层和外膜组成.食管粘膜为复层扁平柱状上皮,胃、小肠和直肠上皮为单层柱状上皮.各段皱褶丰富.胃有发达的腺体,肠的各段无多细胞腺体分布.杯状细胞丰富,其中十二指肠最少,直肠部最多,胃的各部无杯状细胞.肝小叶分界不清,肝...     

鳜鱼消化道黏液细胞和6种酶的组织化学定位

采用阿利新蓝-过碘酸雪夫氏(AB-PAS)染色和酶组织化学方法对鳜鱼消化道各部位黏液细胞和6种酶的分布与定位进行了研究。结果显示,黏液细胞可为分为4种类型,食道黏液细胞多数为Ⅲ型和Ⅳ型,未见Ⅰ型和Ⅱ型;胃贲门和胃幽门黏膜上皮仅有Ⅰ型黏液细胞;胃体黏膜上皮则以Ⅲ型细胞为主;幽门盲囊中主要为Ⅱ型细胞;前肠和中肠中Ⅳ型黏液细胞最多,Ⅰ型最少;后肠黏液细胞则以Ⅳ型和Ⅱ型为主。酸性磷酸酶(ACP)主要分布于幽门盲囊和前肠的黏膜上皮;碱性磷酸酶(ALP)主要分布于食道、幽门盲囊和整个肠道黏膜上皮;非特异性酯酶(NSE)主要分布于胃幽门、中肠和后肠黏膜上皮;过氧化物酶(POX)在胃幽门黏膜上皮中活性较高;琥珀酸脱氢酶(SDH)主要分布于胃腺中;腺苷三磷酸酶(ATPase)在消化道各部位均有较多分布。鳜鱼消化道黏液细胞和酶的分布型与其它动物有相似之处,也有其一定的特异性,与消化道不同部位的消化吸收机能相适应。     

The larval alimentary canal of the Antarctic insect, Belgica antarctica

On the Antarctica continent the wingless midge, Belgica antarctica (Diptera, Chironomidae) occurs further south than any other insect. The digestive tract of the larval stage of Belgica that inhabits this extreme environment and feeds in detritus of penguin rookeries has been described for the first time. Ingested food passes through a foregut lumen and into a stomodeal valve representing an intussusception of the foregut into the midgut. A sharp discontinuity in microvillar length occurs at an interface separating relatively long microvilli of the stomodeal midgut region, the site where peritrophic membrane originates, from the midgut epithelium lying posterior to this stomodeal region. Although shapes of cells along the length of this non-stomodeal midgut epithelium are similar, the lengths of their microvilli increase over two orders of magnitude from anterior midgut to posterior midgut. Infoldings of the basal membranes also account for a greatly expanded interface between midgut cells and the hemocoel. The epithelial cells of the hindgut seem to be specialized for exchange of water with their environment, with the anterior two-thirds of the hindgut showing highly convoluted luminal membranes and the posterior third having a highly convoluted basal surface. The lumen of the middle third of the hindgut has a dense population of resident bacteria. Regenerative cells are scattered throughout the larval midgut epithelium. These presumably represent stem cells for the adult midgut, while a ring of cells, marked by a discontinuity in nuclear size at the midgut-hindgut interface, presumably represents stem cells for the adult hindgut.     

光唇鱼消化道的形态结构特征

采用解剖及石蜡切片显微技术,观察研究了光唇鱼消化道的形态结构特征。消化道由口咽腔、食道、肠构成。口下位、马蹄形,无颌齿,具咽齿,齿式为4/4。舌较小,前端游离,舌粘膜表层为复层鳞状上皮,有较多的杯状细胞和味蕾。食道及肠均由粘膜层、粘膜下层、肌层及外膜构成。食道内皱襞发达,粘膜层有大量杯状细胞。肠道盘曲,由前、中、后肠组成,肠长/体长为1.84±0.24;前肠管腔较大,中、后肠管腔渐变小;前、中肠皱襞及纹状缘比后肠发达;前肠及后肠杯状细胞较少,中肠杯状细胞较多。光唇鱼消化道的形态结构特征与其食性相适应。     

Morphology and ultrastructure of the alimentary canal of the cicada Platypleura kaempferi (Hemiptera: Cicadidae)

The alimentary canal of cicada Platypleura kaempferi is described. It comprises the oesophagus, filter chamber, external midgut section and hindgut. The elongate oesophagus expands posteriorly, with its posterior end constricting to become a bulb. The filter chamber consists of two parts: a very thin sheath and a filter organ. The filter organ is composed of the anterior and posterior ends of the midgut (internal midgut section), and the internal proximal ends of the Malpighian tubules. The external midgut section differentiates into a collapsed sac and a midgut loop. The latter is divided into three distinct segments. The hindgut contains a dilated rectum and a long narrow ileum. The distal portions of the four Malpighian tubules are enclosed in a peritoneal sheath together with the distal ileum before reaching to the rectum. Ultrastructurally, the oesophagus and the hindgut are lined with a cuticle. The filter chamber sheath consists of cells with large irregular nuclei. Filamentous substances coat the microvilli of the cells of the internal midgut section. The posterior end of the midgut comprises two types of cells, with the first type of cells containing many vesicles and scattered elements of rough endoplasmic reticulum. The anterior and posterior segments of the midgut loop cells have ferritin‐like granules. The ileum cells have well‐developed apical leaflets associated with mitochondria. Accumulations of virus‐like particles enclosed in the membrane are observed in the esophagus, conical segment, mid‐ and posterior segments of the midgut loop.     

The anatomy and histology of the midgut and hindgut of Charybdis (Goniohellenus) truncata (Fabricius, 1798) (Decapoda: Brachyura)

The midgut of C. (G.) truncata accounts for half of the postgastric intestinal tract. The paired anterior midgut caeca arise just behind the pyloric stomach, on either side of the midgut. The unpaired posterior midgut caecum arises dorsally at the rear end of the midgut, where this joins the hindgut. The midgut and its caeca help in the digestive absorption of food. The hindgut is of ectodermal origin and is lined with chitin of a collagenous nature. The connective tissue of the anterior part of the hindgut is packed with tegumental glands whose secretion contains both sulphated and weakly acidic mucosubstances, which facilitate the passage of faecal matter and help to bind food particles. The digestive gland - the hepatopancreas - opens into the anterior part of the midgut, below the anterior midgut caeca. Histologically, its tubules contain three different types of cells - "F", "R" and "B" cells.     

Ciliated epithelium in the developing digestive tract of the larva of the Atlantic halibut, and comparison with that of the cod

Two regions of ciliated epithelium are described in the digestive tract of the halibut larva. The anterior region, present by 5 days post-hatch and still present at 25 days post-hatch, probably moves water through the branchial openings into the oesophagus and on to the midgut until the mouth forms at about 29 days post-hatch. A ciliated region was present also in the occluded posterior hindgut, which joins the excretory duct to form a common duct to the exterior. This posterior ciliated region may help to circulate water in the mid- and hindgut until the anus opens directly to the exterior, at about 25 days post-hatch.     

仿刺参消化系统的组织学和组织化学研究

用组织学和组织化学方法研究了仿刺参的消化系统。消化道管壁由粘膜层、粘膜下层、肌层和外膜组成。粘膜层为假复层或单层的柱状细胞或立方细胞与粘液细胞。粘液细胞分布于前肠的前段和排泄腔。前肠和中肠上皮具蛋白酶、脂酶和非特异性酯酶活性。中肠上皮细胞游离端有密集微绒毛,游离端质膜呈碱性磷酸酶活性,上皮下有丰富的血窦,表明具吸收作用。     

西藏高原鳅、细尾高原鳅和异尾高原鳅消化道结构的比较

运用解剖学、组织学方法比较研究西藏高原鳅(Triplophysa tibetana)、细尾高原鳅(Triplophysa stenura)和异尾高原鳅(Triplophysastewarti) 3种高原鳅的消化道结构。结果表明: (1)3种高原鳅的消化道均由口咽腔、食道、胃、肠组成。胃“U”型, 无幽门盲囊, 肠道短, 可分为前、中、后三个部分。异尾高原鳅胃长与消化道长比值最大, 比肠长最短, 为0.51±0.07, 与西藏高原鳅比肠长0.64±0.08和细尾高原鳅比肠长0.70±0.06, 差异显著。(2)异尾高原鳅胃黏膜层相对高度大于西藏高原鳅和细尾高原鳅, 肌肉层相对厚度也比其他2种鱼厚。前肠黏膜层为异尾高原鳅相对高度最大, 肌肉层为西藏高原鳅相对最厚。中肠与后肠黏膜层相对厚度由大到小为异尾高原鳅>细尾高原鳅>西藏高原鳅。综上所述, 3种高原鳅的消化道结构均符合肉食性鱼类特征, 推测异尾高原鳅的结构特征适于消化更多的动物性饵料。     

Ultrastructure of the midgut and hindgut of Derocheilocaris remanei (Crustacea, Mystacocarida)

Ultrastructural features and structure of the midgut and hindgut of Derocheilocaris remanei were studied. The large endodermal midgut is differentiated into an anterior midgut and a posterior midgut separated by a conspicuous constriction. Both circular and longitudinal striated muscle bands surround the midgut, while the hindgut only presents longitudinal muscles. The limit between the midgut and the cuticle-lined hindgut is marked by a rectal valve. In cross-section, the short hindgut is triradiate and has a distinct Y-shaped lumen. The hindgut cuticular lining appears interrupted at the tip of every branch of the Y. Three different cell types are found in the midgut epithelium: basally located undifferentiated cells that give rise to the other two specialized cell types; secretory zymogen-like cells responsible for extracellular digestion and located mainly in the anterior midgut; and vacuolated cells, distributed all along the midgut and appearing to have several functions, including absorption, intracellular digestion, and nutrient transport. A single basic cell type forms the hindgut epithelium. The suggested function for the hindgut is the transport and ejection of waste products.     

Fine Structure of the Midgut and Hindgut in Lepidocampa weberi (Insecta,Diplura)

The fine structure of the alimentary canal, especially the midgut and hindgut of Lepidocampa weberi (Diplura: Campodeidae) is described. The general organization of the canal is similar to that of Campodea. The midgut epithelium is composed of columnar apical microvillated cells. Each nucleus contains a single intranuclear crystal. Close to the pyloric region, the posterior midgut cells are devoid of microvilli and intranuclear crystals. There is no special pyloric chamber as in Protura or pyloric cuticular ring as in Collembola but a morphological transformation from midgut to hindgut cells. Eight globular Malpighian papillae, consisting of distal microvillated cells and flat proximal cells, open into the gut lumen via ducts formed by hindgut cells. The structure of the hindgut is complicated and can be divided into three segments. The anterior hindgut cells have an irregular shape and compact cytoplasm. A striking interdigitation between the large bottle-shaped epithelial cells and longitudinal muscle cells occurs in the middle segment of the hindgut. The thick cuticle gives rise to long spikes projecting into the gut lumen. The posterior hindgut cells possess the morphological features for water reabsorption. Some hypotheses are advanced about the function of the different regions of the gut.