REABSORPTION OF GLUCOSE IN THE RENAL SYSTEM OF VIVIPARUS

Glucose is reabsorbed from the pericardial fluid in Viviparusjaponicus, and not from the kidney or the ureter. The cpicardialcells of the ventricle are probably responsible (Received 30 October 1978;     

Ultrastructure of intestinal and gall-bladder epithelium in the teleost Gasterosteus aculeatus L., as related to their osmoregulatory function

Summary Intestinal and gall-bladder epithelial cells in sticklebacks have been examined in ultrathin sections and freeze-etch replicas. Enterocytes throughout the intestine appear to have a well-developed basal labyrinth similar to that of renal tubular cells, consisting of baso-lateral infoldings closely associated with numerous mitochondria. The lumen inside these intracellular membranes is continuous with the intercellular space via pores. Such a membrane system is also present in the epithelial cells lining the gall bladder, distinguishing them from gall-bladder cells of higher vertebrates. Morphometric analysis indicates that the basal labyrinth of enterocytes in the posterior part of the intestine increases markedly in both sexually mature males and androgen-treated females. This does not occur in the anterior part or gall bladder. In sticklebacks, androgens cause reduced urine excretion and enhanced fluid release via the anus. We conclude that the cells lining the intestine and gall bladder possess an extensive basal labyrinth that may function as a backward channel system, enabling fluid to be produced in the intestine of fish. The androgen-induced increase in the extent of the basal labyrinth in the posterior part of the intestine may be related to the enhanced rate of intestinal fluid excretion observed in sexually mature male sticklebacks.     

Tissue pressures and fluid dynamics in the kidney.

The kidney has several characteristics which make renal pressures and fluid dynamics unique when compared to other organs. Renal blood flow is roughly 100 times that of skeletal muscle. The renal circulation consists of two distinct capillary beds in series: a high pressure system in the glomerulus that favors filtration and a low pressure system in the peritubule network that favors reabsorption. The hydrostatic pressure in the glomerular capillary is 4-6 times higher than the hydrostatic pressure in the peritubule capillary so that approximately 25% of the plasma is filtered. The bulk of the filtrate is subsequently reabsorbed by the peritubule capillary network. Micropuncture techniques have been used to obtain quantitative measurements of the pressures and fluid dynamics of the peritubule microcirculation. The net force for uptake of all the fluid reabsorbed by a single proximal tubule up to the point of micropuncture is 21 mm Hg acting over a capillary bed with a permeability surface area product of 2 nl/min per mm Hg. In contrast to subcutaneous tissue and muscle, the renal interstitial fluid pressure is positive. The consequence of a positive interstitial fluid pressure is that normal lymph flow is relatively high and changes in interstitial fluid pressure have relatively little effects on lymph flow.     

Protein concentrations have little effect on reabsorption of fluid from isolated rat lungs

A study was conducted to determine whether differences in the concentrations of large molecules between the air space and perfusate solutions altered the rates at which fluid was reabsorbed from isolated fluid-filled perfused rat lungs. Four groups of experiments were conducted: 1) 5 g/dl albumin in the air spaces and perfusate, 2) 15 g/dl albumin in the air space and 5 g/dl albumin in the perfusate, 3) 5 g/dl albumin in the air space and 15 g/dl albumin in the perfusate, and 4) a mixture of 5 g/dl albumin and 7 g/dl Dextran 70 in the air spaces and 5 g/dl albumin in the perfusate. Fluid reabsorption was determined by following the concentration of albumin labeled with Evans blue (T-1824) in the air space and perfusate compartments. Because leakage of protein between the air space and perfusate compartments is very slow, increases in T-1824 concentrations in the air spaces indicated loss of fluid from this compartment, whereas decreases in these concentrations in the perfusate compartment provided evidence of fluid transport into the vasculature. Approximately 30% of the air space fluid was reabsorbed in a 2-h period, and virtually all of this fluid reached the perfusate compartment. Despite oncotic differences that ranged from -65 to 65 Torr, variations in air space or perfusate albumin concentrations did not have a significant effect on this process. A 30% decrease in fluid reabsorption was observed when dextran was in the air space solution, but this decrease did not appear to be due to the oncotic properties of this solution because albumin did not have a measurable effect on reabsorption.(ABSTRACT TRUNCATED AT 250 WORDS)     

Autoradiographic detection of indolamine and catecholamine neurons in the nervous system of Owenia fusiformis (Polychaeta,Annelida)

Summary Following immobilization stress the supraoptic nucleus exhibits an increased number of coarse, heavily immunostained fibers in the basal glia labyrinth. Ultrastructural immunocytochemistry demonstrates a labeling of the rough endoplasmic reticulum in the neurosecretory perikarya and granule-free, immunoreactive material in the axons adjacent to the basal glia labyrinth. Furthermore, a labeling of the intercellular clefts of the neuropil is demonstrable in the supraoptic nucleus. These results lead to the hypothesis that 1) vasopressin is synthesized and released in two forms, in a granule-bound form and in a granule-free, probably more soluble form, and that 2) the latter might be released already in the nuclear area into the intercellular clefts from where it may reach its target cells via the cerebrospinal fluid of the subarachnoid space.The excellent technical assistance of Mrs. Helga Prien is thankfully acknowledgedSupported by the Deutsche Forschungsgemeinschaft (Grant Nr. Kr 569/2) and the Stiftung Volkswagenwerk     

AMINO ACID TRANSPORT INTO THE CEREBROSPINAL FLUID OF THE RAT1

The concentrations of glycine and 6 other amino acids have been assayed in the CSF and plasma of the rat, and regional heterogeneity of CSF amino acid concentration has been found. Steady state flux rates into the cranial and spinal fluid compartments were determined during perfusion with amino acid free medium. The transfer of glycine from blood into both the cranial and spinal subarachnoid fluids was saturable with only several-fold elevations of plasma glycine. The results are discussed with regard to the putative neurotransmitter function of glycine in the spinal cord.     

THE DEVELOPMENT OF SURFACE SPECIALIZATION IN THE SECRETORY EPITHELIUM OF THE AVIAN SALT GLAND IN RESPONSE TO OSMOTIC STRESS

Cell surface specialization, a characteristic common to most ion-transporting epithelia, was studied in the salt (nasal) gland of the domestic duck in relation to osmotic stress. Three days after hatching, experimental ducklings were given 1% NaCl to drink for 12 hr and freshwater for the remainder of each day. Control ducklings were maintained exclusively on freshwater. The fine structure of the secretory epithelium was examined on various days of the regimen. The nasal gland epithelium of the secretory lobule is composed of several types of cells. Peripheral cells, lying at the blind ends of the branched secretory tubules, are similar in both control and experimental animals at all stages of glandular development. These generative cells contain few mitochondria and have nearly smooth cell surfaces. Partially specialized secretory cells predominate in the secretory tubules of control animals and appear as transitional cells in the tubular epithelium of salt-stressed animals. These cells contain few mitochondria and bear short folds along their lateral cell surfaces. Fully specialized cells dominate the secretory epithelium of osmotically stressed ducklings. The lateral and basal surfaces of these cells are deeply folded, forming complex intra- and extracellular compartments. This vast increase in absorptive surface area is paralleled by an increase in the number of mitochondria that pack the basal compartments. The development of this fully specialized cell is correlated with the marked increase in (Na⁺-K⁺)-ATPase activity in the glands of osmotically stressed birds.     

脑内γ—氨基丁酸（GABA）在急性失血性低血压时对血压的影响

本实验通过大鼠和家兔侧脑室注射GABA受体阻断剂荷包牡丹碱(Bicuculline)研究正常血压和急性失血性低血压时,中枢GABA对血压的调节作用。结果表明:在两种情况下,荷包牡丹碱均有明显的升压作用,但后者显著大于前者,且这种升压效应不被去肾或去肾上腺所影响。同时发现:急性失血性低血压时,兔脑脊液中GABA含量明显增加,提示在急性失血性低血压时,中枢GABA具有阻止血压回升的作用,这种作用是通过对中枢交感神经系统的抑制引起的。     

Microvascular organization of the pseudobranch and carotid labyrinth of two species of air-breathing teleostean fishes

The microvasculature of the pseudobranch in Anabas testudineus and the carotid labyrinth of Heteropneustes fossilis have been studied using scanning electronmicroscopy of Mercox-injected casts. Results confirm differences in origin and basic capillary structure. It is concluded that the pseudobranch is a glandular structure related to functioning of the eye whereas the carotid labyrinth of fishes is concerned with the regulation of fluid pressure and oxygen supply to the brain.     

THE MECHANISM OF THE WATER EXPULSION VESICLE OF THE CILIATE TETRAHYMENA PYRIFORMIS

Analysis of high-speed (150 frames/sec) cinematographs of the filling and expulsion of the water expulsion vesicle of Tetrahymena pyriformis shows that the vesicle fills as water is pumped into it by contractions of at least four ampullary sacs which are continuous with the endoplasmic reticulum. When filled, the vesicle is pressed against its two excretory pores by cyclotic movements of the cytoplasm. This pressure closes the apertures of the ampullae, preventing backflow from the vesicle into them, and also spreads the pellicle of and at the pore, thereby stretching and rupturing the pore-sealing membrane. The vesicle is then invaginated by the cytoplasmic pressure, driving fluid out of the pore. The pore-sealing membrane then reforms, apparently by constriction, and the vesicle is again filled. Electron micrographs show that crisscrossed pore-microtubules extend from the pore to the openings of the ampullae, anchoring the vesicle in place. Each pore is surrounded by a stack of at least 11 ring-microtubules, to which the anchoring pore-microtubules are attached. The pore-microtubules appear to exert tension which assists in spreading the pore, aiding cyclotic pressures in rupturing the pore-sealing membrane. A possible mechanism for the cyclotic pressure and ampullary contraction is proposed.     

THE FINE STRUCTURE OF THE TRANSITIONAL EPITHELIUM OF RAT URETER

The fine structure of the transitional epithelium of rat ureter has been studied in thin sections with the electron microscope, including some stained cytochemically to show nucleoside triphosphatase activity. The epithelium is three to four cells deep with cuboidal or columnar basal cells, intermediate cells, and superficial squamous cells. The basal cells are attached by half desmosomes, or attachment plates, on their basal membranes to a basement membrane which separates the epithelium from the lamina propria. Fine extracellular fibres, ca. 100 A in diameter, are to be found in the connective tissue layer immediately below the basement membrane of this epithelium. The plasma membranes of the basal and intermediate cells and the lateral and basal membranes of the squamous cells are deeply interdigitated, and nucleoside triphosphatase activity is associated with them. All the cells have a dense feltwork of tonofilaments which ramify throughout the cytoplasm. The existence of junctional complexes, comprising a zonula occludens, zonula adhaerens, and macula adhaerens or desmosome, between the lateral borders of the squamous cells is reported. It is suggested that this complex is the major obstacle to the free flow of water from the extracellular spaces into the hypertonic urine. The free luminal surface of the squamous cells and many cytoplasmic vesicles in these cells are bounded by an unusually thick plasma membrane. The three leaflets of this unit membrane are asymmetric, with the outer one about twice as thick as the innermost one. The vesicles and the plasma membrane maintain angular conformations which suggest the membrane to be unusually rigid. No nucleoside triphosphatase activity is associated with this membrane. Arguments are presented to support a suggestion that this thick plasma membrane is the morphological site of a passive permeability barrier to water flow across the cells, and that keratin may be included in the membrane structure. The possible origin of the thick plasma membrane in the Golgi complex is discussed. Bodies with heterogeneous contents, including characteristic hexagonally packed stacks of thick membranes, are described. It is suggested that these are "disposal units" for old or surplus thick membrane. A cell type is described, which forms only 0.1 to 0.5 per cent of the total cell population and contains bundles of tubular fibres or crystallites. Their origin and function are not known.     

Ultrastructure of the crayfish kidney--coelomosac, labyrinth, nephridial canal

Regions of the crayfish kidney were examined by electron microscopy. Coelsmosac cells are loosely bound together by desmosome-like spot junctions, and connected to the basal lamina via characteristic pedicels. The cytoplasm contains numerous vesicles and vacuoles of various sizes and is often crowded with large, lysosome-like granules or dense bodies. The morphology suggests a filtration mechanism with reabsorption of materials such as protein from the filtrate and secretion of other substances into the lumen. The labyrinth is composed of cuboidal to columnar cells which possess a brush border, long and narrow intercellular spaces, basal plasmalemmal invaginations and typical cytoplasmic components. Two sub-regions are distinguishable. The morphology of labyrinth I suggests that these cells move fluid isotonically across the epithelium. Labyrinth II, in addition to isotonic transport, appears to be more active in the endocytic uptake and intracellular digestion of large molecules such as protein. The nephridial canal consists of cells which lack a brush border, but display extensive basal invaginations associated with elongated mitochondria. A proximal and distal region are cytologically distinguishable. Proximally, the cells are small and filled with mitochondria throughout. Scattered within the cytoplasm are vesicles, vacuoles, diffuse glycogen, free ribosomes, dense bodies and some rough endoplasmic reticulum. Distally, the cells are less compact, larger, and cuboidal to columnar in shape. The cytoplasm is similar to that of the proximal cells, but the basal invaginations are even larger and more extensive. The morphology of cells in both regions of the nephridial canal is highly suggestive of active solute reabsorption, probably occurring against an osmotic gradient.     

大鼠侧位液压冲击脑损伤动物模型的病理生理学观察

目的：建立一种重复性好的大鼠分级侧位液压冲击脑损伤模型,为进一步研究外伤性脑损伤的分子机制提供物质基础。方法：雄性ＳＤ大鼠,随机分为正常对照组,手术对照组和损伤组损作组接冲击力大小分为轻（１００ｋＰａ）、中（２００ｋＰａ）、重（３００ｋＰａ）３个亚组。实验中由计算机记录冲击时脑承受的压力曲线并描记大鼠血压和心率变化。结果：脑承受的压力曲线与冲击气压呈直线正相关（ｒ＝０．９８５）,损伤组大鼠在冲击后     

THE EPIDERMAL PROLIFERATIVE UNIT: THE POSSIBLE ROLE OF THE CENTRAL BASAL CELL

A model is suggested for the organization of the epidermis based on the ordered structure of the differentiating layers, as demonstrated by published work. This ordered structure enables one to look through the epidermis at the basal cell nuclei and to see their arrangement beneath the differentiating column of cells. In dorsal skin from male DBA-2 mice there are 10.6 basal nuclei beneath a column of cells. The central nucleus of the group responds slightly earlier and more effectively than the rest to stimulation, is cycling more slowly than the majority of the basal nuclei and may spend significant periods of time out of cycle. The skin appears to contain a series of fairly independent proliferative units, each of which contain ten or eleven basal nuclei and eight to ten superficial cells of which only the youngest one or two retain their nuclei. At the centre of each group of basal nuclei is a cell that behaves differently from the rest and which is present in the skin in numbers compatible with the number of clonogenic cells. It is suggested that this represents the basic stem cell of the unit.     

Ultrastructural studies and Na+,K+-ATPase immunolocalization in the antennal urinary glands of the lobster Homarus gammarus (Crustacea, Decapoda).

Unlike in crustacean freshwater species, the structure and ultrastructure of the excretory antennal gland is poorly documented in marine species. The general organization and ultrastructure of the cells and the localization of Na(+),K(+)-ATPase were examined in the antennal gland of the adult lobster Homarus gammarus. Each gland is composed of a centrally located coelomosac surrounded ventrally by a labyrinth divided into two parts (I and II) and dorsally by a voluminous bladder. There is no differentiated nephridal tubule between them. The labyrinth and bladder cells have in common a number of ultrastructural cytological features, including basal membrane infoldings associated with mitochondria, apical microvilli, and cytoplasmic extrusions, and a cytoplasm packed with numerous vacuoles, vesicles, lysosome-like bodies, and swollen mitochondria. Each type of cell also presents distinctive characters. Na(+),K(+)-ATPase was detected through immunofluorescence in the basal part of the cells of the labyrinth and in the bladder cells with an increasing immunostaining from labyrinth I to the bladder. No immunoreactivity was detected in the coelomosac. The cells of the labyrinth and of the bladder present morphological and enzymatic features of ionocytes. The antennal glands of the lobster thus possess active ion exchanges capabilities.     

THE MECHANISM OF THE NEPHRIDIAL APPARATUS OF PARAMECIUM MUL TIMICRONUCLEATUM : I. Expulsion of Water from the Vesicle

Recent analysis of the mechanism of the nephridial apparatus of Paramecium multimicronucleatum by high-speed cinematography (300 fps at x 250) confirms the observations by electron microscopy (Schneider, 1960) that once the pore is opened, the vesicle is invaginated by adjacent cytoplasm and is emptied by collapsing under pressure from that cytoplasm, aided perhaps by pressure of the fibrils which anchor the ampullae to the excretory canal. There is no indication of active contraction of the vesicle or its membrane. There is no permanent pore to the vesicle. The vesicle is closed by a sealing of the ruptured membrane where it is in contact with the pellicular excretory canal. At onset of expulsion of vesicular fluid the membrane across the basal opening of the excretory canal is ripped along one semicircular portion of the excretory pore and is driven up against the opposite wall as a flap while the water rushes out. A constriction of the vesicular and cell membranes at the base of the excretory canal reseals the opening.     

On the transmission of external pressure fluctuations to the cerebrospinal fluid

A theory has been formulated to explain the manner in which external pressure fluctuations are transmitted to the cerebrospinal fluid (CSF). The theory is based upon a three-compartment model which consists of the cerebral ventricles, the basal cisterns and spinal subarachnoid space, and the cortical subarachnoid space. The external pressure disturbance is represented by a Fourier series summed over the frequency ω. The mathematical analysis leads to a time constant τ which depends upon the compliances of the spinal region and sources of external pressure fluctuations, the rate of CSF absorption and the rate of fluid transfer between compartments. For arterial pulsations where ωτ ? 1, the theory is in accord with the experimental observations that (i) the arterial and CSF pulse waves are nearly identical in shape, and (ii) the amplitude of the CSF pulse wave increases with intracranial pressure. Moreover, it predicts that the amplitude of the wave will be larger in the spinal region than in the ventricles. The theory also accounts for the observation of one per minute pulse waves observed in hydrocephalic patients with decreased absorption rates.     

THE COLUMNAR CELLS OCCURRING IN THE PARIETAL LAYER OF BOWMAN''S CAPSULE : Cellular Fine Structure and Protein Transport

The renal corpuscles of adult, C3H Swiss, male mice contain testosterone-sensitive, columnar cells in the parietal layer of Bowman's capsule. A study of the normal fine structure of these cells reveals several distinctive characteristics: a microvillous brush border; apical tubular invaginations and apical tubules; an elaborate infolding of the basal surface membrane forming cellular compartments, which contain numerous mitochondria; and a complex group of membrane-limited cytoplasmic inclusions. This appearance is remarkably similar to the fine structure of cells in the proximal convoluted tubule. 1 hr after an in vivo injection of horseradish peroxidase, numerous protein-absorption droplets occur in the columnar cell cytoplasm. The speed and cytomorphology of protein transport by these capsular cells closely resemble the handling of peroxidase by the proximal convoluted tubule. Origins for these testosterone-sensitive cells are discussed briefly. Morphological evidence is presented for the differentiation of squamous cells in Bowman's parietal capsule into columnar cells, which appear structurally and functionally identical with proximal convoluted tubular epithelium.