金雕肾脏的组织学观察

利用生物显微技术观察了金雕Aquila chrysaetos肾脏的组织结构.结果表明,金雕肾实质由许多肾小叶构成,每个肾小叶可分为皮质和髓质两部分.肾单位由一个肾小体和一条与其相连的肾小管构成.肾小体由肾小囊和肾小球组成.肾小管分为近曲小管、髓袢、远曲小管和连接小管.集合管分为小叶周集合小管和髓质集合管两部分.具有发达的极周细胞.     

棕熊肾脏的解剖学及光电镜观察

本文观察了棕熊肾脏的大体解剖和光、电镜下的组织结构。棕熊的肾脏为分叶肾,每个肾叶为多面锥体形。光镜下H—E染色切片标本可见肾实质有皮质和髓质两部分。皮质可见清晰的皮质迷路和髓放线结构。肾小体可分出血管极和尿极。血管球由毛细血管缠绕形成,外包有肾小囊。近曲小管管腔面可见刷状缘。在透射电镜下可见到摅过屏障由有孔内皮、基膜及足细胞的次级突起构成。电镜下还可看到近曲小管游离面紧密排列的微绒毛和基底面的质膜内褶结构。     

肾小球旁器组织结构及其生理作用

肾单位包括肾小体和肾小管两部分,肾小体的功能为超滤过作用,肾小管主要是再吸收作用。肾小管又分为近曲小管、髓袢及远曲小管几部分。由若干肾单位的远曲小管汇合成为集合管,再开口于锥体乳头处。集合管不属于肾单位,它和肾单位的胚胎发育来源不同。肾小体、近曲小管、远曲小管以及集合管的一部分位于肾皮质内、髓袢、直集合管和直血管位于髓质锥体之内,因此在断面上可见皮质呈现颗粒状,髓质为纹状。肾小球旁器也称球旁复合体或近血管球复合体,由入球小动脉的球旁细胞、远曲小管的致密斑和球外系膜细胞组成。三者在肾小体血管极处排列成三角形,入球小动脉和     

小熊猫肾脏和输尿管的组织学研究

小熊猫的肾脏呈蚕豆形,表面光滑不分叶,只有1个肾锥体和1个肾盏,无肾盂。肾脏皮质内可见皮质迷路和髓放线。皮质迷路内有近曲小管、远曲小管和肾小体等结构。髓放线内有近端小管直部和远端小管直部。髓质可分为外髓和内髓两个区域。外髓有较多的集合管断面,少量的远端小管直部和细段,较多的直小血管束。内髓部位有大量的细段和乳头管。各种泌尿小管之间有少量的疏松结缔组织构成的间质,间质内有丰富的毛细血管。输尿管横切面呈圆形或卵圆形,管腔呈不规则的裂隙状。管壁由粘膜、肌肉层和外膜组成。并与大熊猫肾脏和输尿管的组织结构作了比较研究。     

金钱豹肾的组织学和微血管铸型的观察

为探讨金钱豹(Panthera pardus)肾的组织结构和微血管构筑特点,利用生物显微技术与微血管铸型技术及扫描电镜对金钱豹肾的组织结构和肾小球微血管构筑进行了观察。结果显示,金钱豹的肾皮质与髓质厚度比为1∶(1.5~3),肾近端小管上皮为单层立方细胞,胞体较大,细胞排列紧密,分界不清楚,其腔面有刷状缘,胞质嗜酸性;远端小管无明显的刷状缘,胞质弱嗜酸性,胞核多位于中央;集合管细胞排列紧密,管腔较大,上皮细胞呈矮柱状,胞质弱嗜酸性。金钱豹的肾小球多呈球形或卵圆形,直径为99~142μm,入球小动脉管径13~15μm,出球小动脉管径9.5~11.5μm。     

甘肃鼢鼠肾结构特征

甘肃鼢鼠(Myospalax cansus)在缺水的黄土高原营严格地下生活,主要从食物中摄取水分.为研究甘肃鼢鼠的调水机制,用组织解剖学方法对其肾的形态结构进行观察.结果显示,甘肃鼢鼠肾为单乳头肾,呈蚕豆形,表面光滑,不分叶;皮质与髓质的厚度比为0.71:1;皮质中髓旁肾单位相对分布密度小于浅表肾单位的相对分布密度;髓旁肾单位中的血管球直径大于浅表肾单位中的血管球直径;近曲小管与远曲小管的截面数量比为2.25:1.结果表明,甘肃鼢鼠肾的重吸收能力较小,其组织形态学结构有显著的生态适应意义.     

中华鳖肾脏的组织化学特性研究

利用光镜组织化学反应对中华鳖肾单位的结构和组织化学特性进行了详细的观察和分析。结果表明,中华鳖肾脏为分叶形的实质器官,肾小叶由被膜和实质组成,实质无髓质和皮质之分,但可以区分为外侧区和内侧区。外侧区嗜酸性,主要分布有近端小管和集合管。内侧区呈弱嗜酸性,肾小体、颈段、中间段和远端小管主要分布在内侧区。肾小球PAS反应呈阳性,但其琥珀酸脱氢酶(SDH)弱阳性,碱性磷酸酶(ALPase)、Na+/K+-ATPase和阿利新兰(AB)反应为阴性。足细胞酸性磷酸酶(ACPase)反应呈阳性。近端小管刷状缘嗜伊红,PAS反应以及ALPase、ACPase和Na+/K+-ATPase酶反应呈阳性,而SDH弱阳性。中间段、远端小管、集合管弱嗜酸性,SDH阳性。中间段Na+/K+-ATPase弱阳性。远端小管细胞侧面呈PAS阳性,腔面显示AB阳性。集合管胞质含有许多ACPase阳性颗粒,腔面呈PAS强阳性,AB阳性。甲苯胺兰(TB)染色可见集合管腔面有阳性颗粒,肾小管上皮含有亮、暗两种细胞。上述组化反应和分布结果表明,鳖的肾小管细胞类型较多,近端小管在原尿的重吸收中起主要作用,远端小管和集合管具有分泌黏液作用。中华鳖肾单位的结构与组化特性不仅与哺乳类和鸟类有一定差异,也与其他爬行动物不完全相同。       

版纳鱼螈泌尿系统解剖学及组织学观察

采用常规解剖学和组织学方法对版纳鱼螈Ichthyophis bannanica的泌尿系统进行研究.结果表明,版纳鱼螈泌尿系统包括中肾、输尿管、膀胱.版纳鱼螈的中肾由肾小体和肾小管组成,无皮质、髓质之分,肾小体主要分布在肾脏背外侧缘,肾小管由颈段、第1近曲小管、第2近曲小管、间段、第1远曲小管、第2远曲小管和集合管组成;输尿管位于两肾外侧缘,其上皮由前端的单层立方上皮过渡到后端的假复层上皮;膀胱为泄殖腔膀胱,内壁具有发达的绒毛,绒毛上皮为变移上皮.     

肾小管的功能分段

近年来,随着超微结构和肾单位微穿刺灌注研究的发展,特别是发展了游离肾小管段体外灌注和质膜囊泡等新技术,对肾小管各段结构和功能的差异性有了更深入的认识。现在一般认为,肾小管按其形态和功能特征,可依次分为下列11个标准段:(1)近曲小管(PCT);(2)近直小管(PST)或称直部(PR);(3)髓袢降支细段(DTLH);(4)髓袢升支细段(ATLH);(5)髓袢升支髓质粗段(MTALH);(6)髓袢升支皮质粗段(CTALH),     

不同盐度下人工选育卵形鲳鲹(Trachinotus ovatus)子代鳃线粒体丰富细胞结构变化

该文采用光学显微镜和透射电镜技术观察不同盐度下(5、20、30)人工选育卵形鲳鲹(Trachinotus ovatus)鳃线粒体丰富细胞的分布和超微结构变化。结果表明,线粒体丰富细胞主要分布于鳃丝和鳃小片基部,且随盐度升高而体积增大,数量增多;三个盐度组均存在由线粒体丰富细胞、扁平细胞和附细胞构成的顶端小窝,盐度5组线粒体丰富细胞顶膜面积较大,微脊发达,顶端小窝内凹,盐度20和30组线粒体丰富细胞顶膜面积相对较小,微脊不发达,顶端小窝明显内陷;盐度5和30组线粒体丰富细胞胞质内存在发达的微细小管系统,线粒体内脊丰富,盐度20组胞质内微细小管系统分布不均匀,结构松散,部分收缩成珠泡状结构,与粗面内质网相混杂。线粒体丰富细胞的结构变化与其所处的渗透压环境相适应。     

Ultrastructure of the Malpighian Tubule Cells in the Mosquito Larvae, Anopheles sinesis

Ultrastructure of epithelial cells constituting the Malpighian tubule of Anopheles sinesis last instar larvae was observed with electron microscope. Malpighian tubule consists of four long and narrow tubule structures with principal cells in typical absorptive cells and regenerative cells forming the simple epithelium. Apical plasma membrane of the principal cell is differentiated into microvilli with one mitochondrion in each microvilli. Basal plasma membrane had extreme infolding to form a canaliculi and a well developed mitochondria was attached in the infoldings. And, rER, ribosomes, and vacuoles were well developed inside the cells. However, there were two main cell types depending on the differentiation of cell organelles. Type 1 cell was cubic, forming the distal portion of Malpighian tubule. The length of microvilli was approximately 4 μm and the basal infoldings were introjected to the depth of 2 μm inside the cell. On the other hand, Type II cell that formed the main proxinal portion was a low squamous type cells with shorter 2 μm of microvilli and the basal infoldings were introjected to the depths of 4 μm inside the cell. As for vacuoles scattered inside the cells, they were regularly observed in both Type I and II and the Type II cells had better developed cellular organelles. Although regenerative cells were extremely small, their cellular organelles were developed and their overall electron density was high that they appeared darker than the principal cells.     

Na-K]ATPase activity in proximal and distal tubules of the rat kidney: modification and application of a quantitative cytochemical technique

A modified cytochemical assay for [Na-K]ATPase in cryostat sections of kidney was further characterized and used to quantify activity in seven functionally distinct sites along the rat nephron. The activity of [Na-K]ATPase was defined as the difference in ATPase activity in specifically identified tubules contained in serial sections incubated with and without ouabain. Preincubation of sections with ouabain was required for maximal inhibition of [Na-K]ATPase activity in several distal sites. The concentration of ouabain necessary for maximal inhibition of activity was 3.0 mM and half-maximal inhibition was obtained in all regions with 30-100 microM ouabain. In distal sites, [Na-K]ATPase formed a higher proportion of total ATPase activity (60-80 per cent) than in proximal sites (20-40 per cent). Enzyme activity was quantified using two different methods. The first measured activity over the basal region of tubules and gave an index of the concentration of [Na-K]ATPase over the basal lateral infoldings of cells composing the tubule. The second read activity over the entire cross section of tubules and provided an estimate of [Na-K]ATPase per length of tubule. The highest activities over the basal basal region were obtained from tubules of the distal nephron including the inner (MALin) and outer (MALout) medullary ascending limb, distal convoluted tubule (DCT) and connecting segment (CS). Lower activities were obtained in proximal convoluted (PCT) tubules, proximal straight (PS) tubules and the papillary collecting duct (PD). Distal convoluted tubules contained the highest activity per length of tubule. Other sites contained lower levels of activity in the following order: MALin greater than MALout greater than PCT greater than PD greater than PS. The modifications introduced increase the sensitivity and precision of this assay and permit the application of this technique to studies of [Na-K]ATPase activity in the major functional regions of the rat nephron.     

Fine structure of larval malpighian tubules and rectal sac in the tick Ornithodoros (Pavlovskyella) erraticus (Ixodoidea: Argasidae)

The fine structure of the Malpighian tubules (Mts) and rectal sac (rs) is described in the larval tick Ornithodoros (Pavlovskyella) erraticus before and after feeding up to molting. Mts consist of structurally different pyramidal and cuboidal cells along the entire length of the tubule. In unfed ticks, the two types of cell are characterized by apical microvilli and a few basal membrane infoldings. The abundant pyramidal cells contain glycogen particles, lipid droplets, lysosomelike structures, and rickettsialike microorganisms. After feeding but before molting, pyramidal cells loose glycogen particles and become very dense and dramatically reduced in size. These cells are possibly involved in the formation of guanine crystalloids as an excretory product. In contrast, cuboidal cells, filled with glycogen particles, free ribosomes, and mitochondria in unfed larvae, grow steadily after feeding; their cytoplasm becomes rich in lipid droplets in addition to showing an increase in glycogen particles. Lipid and glycogen could be the source of energy required for water and ion reabsorption in which cuboidal cells are probably involved. The paired-lobe rs consists of one type of cuboidal cells with basal membrane infoldings and a brush-border microvilli covered by a fuzzy coat of glycocalyx. These cells grow rapidly after feeding; they have functional features indicating extensive, selective reabsorption of essential components from excretory products.     

Dissociation of parathyroid hormone and cyclic-3', 5'AMP effects on Na-Pi uptake by cells isolated from proximal straight tubules of rat kidney.

Studies in respiratory alkalotic or short-term phosphate deprived rats raised the possibility that in straight portion of proximal tubules (PST) cAMP might be not a mediator of PTH in inhibition of phosphate reabsorption. The present experiments directly compared the sensitivity of Na-dependent phosphate [32P] (Na-Pi) uptake to PTH or cAMP by PCT or PST cells freshly prepared from outer cortex and outer stripe of outer medulla of rat kidney. The purity of the cells was examined by activity of enzymes specific for PST i.e. glutamine synthetase, gamma-glutamyl transpeptidase and creatine kinase, a marker enzyme for medullary thick ascending limb (MTAL) and distal convoluted tubule. Similar inhibition of Na-Pi uptake by 1-34 bPTH by PST and PCT cells was observed: -33.0 and -30.0% (ns), respectively. In contrast, dibutyryl cAMP decreased Na-Pi uptake only by PCT but not by PST cells: -31.0 and -3.6% (p<0.02), respectively. The 3-isobutyl-1-methylxanthine (IBMX), a phosphodiesterase inhibitor, resulted in slight stimulation of Na-Pi uptake by PST but strong inhibition by PCT cells: 7.8 vs -26.0% (p<0.001). In contrast to PCT in PST cells cAMP seems to play a minor role as a mediator of inhibition of Na-Pi uptake by PTH.     

Differential expression of the Kv1 voltage-gated potassium channel family in the rat nephron

Several potassium (K⁺) channels contribute to maintaining the resting membrane potential of renal epithelial cells. Apart from buffering the cell membrane potential and cell volume, K⁺ channels allow sodium reabsorption in the proximal tubule (PT), K⁺ recycling and K⁺ reabsorption in the thick ascending limb (TAL) and K⁺ secretion and K⁺ reabsorption in the distal convoluted tubule (DCT), connecting tubule (CNT) and collecting duct. Previously, we identified Kv.1.1, Kv1.3 and Kv1.6 channels in collecting ducts of the rat inner medulla. We also detected intracellular Kv1.3 channel in the acid secretory intercalated cells, which is trafficked to the apical membrane in response to dietary K⁺ to function as a secretory K⁺ channel. In this work we sought to characterize the expression of all members of the Kv1 family in the rat nephron. mRNA and protein expression were detected for all Kv1 channels. Immunoblots identified differential expression of each Kv1 in the cortex, outer and inner medulla. Immunofluorescence labeling detected Kv1.5 in Bowman´s capsule and endothelial cells and Kv1.7 in podocytes, endothelial cells and macula densa in glomeruli; Kv1.4, Kv1.5 and Kv1.7 in PT; Kv1.2, Kv1.4 and Kv1.6 in TAL; Kv1.1, Kv1.4 and Kv1.6 in DCT and CNT and Kv1.3 in DCT, and all the Kv1 family in the cortical and medullary collecting ducts. Recently, some hereditary renal syndromes have been attributed to mutations in K⁺ channels. Our results expand the repertoire of K⁺ channels that contribute to K⁺ homeostasis to include the Kv1 family.     

Carbonic anhydrase in the monkey kidney

The distribution of carbonic anhydrase in the kidney of the cynomolgus monkey was studied by the histochemical method of Hansson. Glomeruli and Bowman's capsule were inactive. Convoluted proximal tubules showed high enzyme activity at the brush border and the basolateral membranes and the cytoplasm. Straight proximal tubules were less intensely stained. In nephrons with long loops of Henle, the descending thin limb contained weak enzyme activity, whereas the ascending thin limb was inactive. The thick limb of Henle's loop displayed most enzyme activity at the luminal cell border. In distal convoluted tubules enzyme activity was restricted to the basal part of the cells. In the late distal tubule, intercalated cells appeared among the "ordinary" distal cells and contained abundant cytoplasmic enzyme. Many intensely stained intercalated cells were also found in the cortical and outer medullary segments of the collecting duct, intermingled with more weakly stained chief cells. In the inner medullary segment of the collecting duct, enzyme activity gradually disappeared. Many capillaries were clearly stained for enzyme activity. The capillary staining apparently varied with that of the kidney tubules; virtually all capillaries in the cortex, but very few in the inner medulla, were stained. The distribution of carbonic anhydrase in the kidney tubules of the monkey is very similar to that in man and in the rat, but the primate kidney differs from the rat kidney by the presence of capillary enzyme activity. The functional importance of this difference is not clear at present.     

Gross,histological and ultrastructural morphology of the aglomerular kidney in the lined seahorse Hippocampus erectus

Histologic evaluation of the renal system in the lined seahorse Hippocampus erectus reveals a cranial kidney with low to moderate cellularity, composed of a central dorsal aorta, endothelial lined capillary sinusoids, haematopoietic tissue, fine fibrovascular stroma, ganglia and no nephrons. In comparison, the caudal kidney is moderately to highly cellular with numerous highly convoluted epithelial lined tubules separated by interlacing haematopoietic tissue, no glomeruli, fine fibrovascular stroma, numerous capillary sinusoids, corpuscles of Stannius and clusters of endocrine cells adjacent to large calibre vessels. Ultrastructural evaluation of the renal tubules reveals minimal variability of the tubule epithelium throughout the length of the nephron and the majority of tubules are characterized by epithelial cells with few apical microvilli, elaborate basal membrane infolding, rare electron dense granules and abundant supporting collagenous matrix.     

Innervation of the renal proximal convoluted tubule of the rat

Experimental data suggest the proximal tubule as a major site of neurogenic influence on tubular function. The functional and anatomical axial heterogeneity of the proximal tubule prompted this study of the distribution of innervation sites along the early, mid, and late proximal convoluted tubule (PCT) of the rat. Serial section autoradiograms, with tritiated norepinephrine serving as a marker for monoaminergic nerves, were used in this study. Freehand clay models and graphic reconstructions of proximal tubules permitted a rough estimation of the location of the innervation sites along the PCT. In the subcapsular nephrons, the early PCT (first third) was devoid of innervation sites with most of the innervation occurring in the mid (middle third) and in the late (last third) PCT. Innervation sites were found in the early PCT in nephrons located deeper in the cortex. In juxtamedullary nephrons, innervation sites could be observed on the PCT as it left the glomerulus. This gradient of PCT innervation can be explained by the different tubulovascular relationships of nephrons at different levels of the cortex. The absence of innervation sites in the early PCT of subcapsular nephrons suggests that any influence of the renal nerves on the early PCT might be due to an effect of neurotransmitter released from renal nerves reaching the early PCT via the interstitium and/or capillaries.     

A structural basis for fluid secretion by malpighian tubules

The Malpighian tubules of Calliphora are described, emphasizing the possible role of surface specializations in solute-linked water transport. The tubules are composed of two cell types, primary and stellate, intermingling along the tubule length. The primary cells have long narrow basal infoldings and a microvillate luminal border, both intimately associated with mitochondria. The stellate cells have shorter and wider basal infoldings and their apical microvilli do not contain mitochondria. Application of the standing gradient hypothesis to this sytem provides a model for urine formation in which the local gradients for osmotic water flow occur within the long narrow channels of the basal infolds and microvilli of the primary cells. Stellate cells may modify the initial secretion by reabsorbing sodium.     

(Na-K)ATPase activity along the nephrons in normal and adrenalectomized rats measured by quantitative cytochemistry

A cytochemical method was used to measure total, ouabain insensitive and specific (Na-K)ATPase activities along the rat nephron. Enzyme activity was expressed as per cent of mean integrated extinction with reference to a calibrated filter. The lowest mean values of total, ouabain-insensitive, and (Na-K)ATPase activities were found in the proximal convoluted tubule (PCT). In the distal convoluted tubule (DCT), total and ouabain-insensitive activities (77.8 per cent and 45.8 per cent, respectively) were significantly higher than in the medullary thick ascending limb (MAL) (66.0 per cent and 24.6 per cent, respectively). Mean values of (Na-K)ATPase activity were significantly lower in DCT than in MAL (32.0 per cent and 41.3 per cent, respectively). Using Lineweaver-Burk plots, the KM ATP value for total ATPase activity was found to be 2.33, 1.79, and 3.63 mM in DCT, MAL, and PCT respectively. Maximal velocity was lower in PCT than in MAL and DCT. For (Na-K)ATPase, the smallest KM value was found in MAL (0.95 mM) and was 2.73 and 5.71 mM in DCT and PCT respectively. Maximal velocity was the highest in MAL (49.3 per cent), lower in DCT (36.1 per cent) and least in PCT (22.5 per cent). ATPase was measured in the MAL and DCT from rats fed a normal (N-Na+) or a high (Hi-Na+) sodium diet, and from Hi-Na+ rats one week after adrenalectomy (ADX). In the MAL, (Na-K)ATPase tended to be higher in Hi-Na+ than in rats, but was significantly lower in ADX than in Hi-Na+.(ABSTRACT TRUNCATED AT 250 WORDS)