{"title":"[Ultrastructural Pathology of the human prostatic gland. Cyto- and histormophogenesis of atrophy, hyperplasia, metaplasia, dysplasia and carcinoma (author's transl)].","authors":"H Kastendieck","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":" 106","pages":"1-163"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11292988","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[Pathomorphologic studies of the endocrine cells in the gastrointestinal mucosa. Physiology, cytochemistry and ultrastructure (author's transl].","authors":"H Mitschke","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>With combined immunofluorescent, cytochemical and electron microscopic investigations the enterochromaffin cell system has been differentiated into 5 distinct endocrine cell types in the human stomach and into 8 cell types in the intestine. These endocrine cells are probably of neuroectodermal origin and belong to the APUD (amine precursor uptake and decarboxylation)-system. Maximal gastrointestinal hormone concentrations as determined by tissue extracts correlate fairly well to the location of each endocrine cell type in various segments of the gastrointestinal tract. In certain gastroenteropathies the pathophysiological disturbances can be explained by pathomorphological alterations of the disseminated endocrine cells. 1. The gastrin-producing G-cell is the predominating endocrine cell in the gastric antrum. Besides immunocytochemistry the G-cell can be demonstrated with argyrophilic reaction (Grimelius, 1968), masked metachromasia and leadhematoxylin. The ultrastructural features are variable, depending on functional activity. The secretory granules are usually only slightly osmiophilic, measuring 200 till 250 nm in diameter. By some working groups a positive immunofluorescence with gastrin-antisera has been demonstrated in A1- or D-cells of the pancreatic islets. However, numerous negative results have been reported, too. Considering physiological conditions, a gastrin-secretion of the human pancreatic islets has not been secured without doubt. 2. The EC-cell produces serotonin and in the intestine motilin, too. Besides the formaldehyde-induced fluorescence, these cells can be demonstrated with diazonium and argentaffin reactions, less specific with argyrophilic methods. Ultrastructurally the EC-granules are easily differeniated from the other endocrine cells by their pronounced osmiophilia and pleomorphism. In experimental conditions the EC-cells demonstrate species- and site-specific alterations. With reserpine no ultrastructural changes were demonstrable in EC-cells of the rat. However, marked ultrastructural alterations with an increase of the hormone-producing organelle system were noticed after administration of parachlorophenylalanine (PCPA) which interferes with serotonine synthesis; 5. The gastric D-cells are characterized by large secretory granules similar to pancreatic D-cells. They secrete the HCl-inhibitory peptide somatostatin. 4. The D1-cell is a cell type with unknown function. The cytoplasm contains small granules with variable electron density. According to most authors, they represent a distinct cell type and not just a variant of the G-cells. It may be very difficult, however, to separate certain forms of D1-cells from functionally altered G-cells. 5. The A-cell can be found in the gastric mucosa of certain animal species, where it has been demonstrated by immunocytochemistry with antisera to gut-glucagon. This cell type does not occur in the human gastric mucosa. 6...</p>","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":"104 ","pages":"1-203"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11407146","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[Functional pathomorphology of the pancreatic B cell system. Ultrastructural and calcium-cytochemical studies on insulin biosynthesis and secretion (author's transl)].","authors":"G Klöppel","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":" 108","pages":"1-108"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11548582","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[Age dependent morphokinetics of the thyroid gland. Histochemical, morphometric, light-microscopical and functional investigations (author's transl)].","authors":"H Stötzer","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The aim of the animal experiments was to investigate the question of the age dependence of the morphokinetic reactions of the thyroid gland under standardised conditions. Through the administration of pharmaceutical substances, it was possible to produce defined functional states of the thyroid in the various age groups. Materials and Methods 700 Albino rats of the Chbb: Thom (SPF) strain, age 0 days (newborn) to 110 weeks, were used in the investigations. The animals were divided into 4 groups each with 12 subgroups according to age. One group received 300 mug/kg/day triiodothyronine (T3) for 10 days for the suppression of thyroid gland function, one group received methylthiouracil (MTU) for 10 days to block hormone synthesis, and one group received 10 IU/kg/day thyrotrophic hormone (TSH) for 5 days to stimulate the gland. The control group received distilled water. Investigations carried out: Protein-bound iodine (PBI) and total thyroxine (T4) in the serum; enzyme histochemical demonstration in the thyroid of alkaline phosphatase (a. Ph.), acid phsophatase (s. Ph.), cytochrome oxidase (Cyt. ox.), succinic dehydrogenase (SDH), iso-citric acid dehydrogenase (ICDH), ATP-ase and nonspecific esterase. The height of the follicular epithelium and the nuclear diameters of the follicular epithelial cells were estimated in embedded material. Light-microscopical investigations were performed using Paraplast and Epon embedded material. Staining methods: H. and E., Azan, PAS-alcian blue, Elastica-van Gieson, Perl's method for iron, Gomori's reticulin stain and von Kossa's calcium method (in aged animals). Staining of semithin sections with toluidine blue, Movat's stain and Morgenroth's stain. Biometric analysis of results: Simple and two factor analysis of variance, Scheffé test, graphic demonstration after polynomial fitting of third to fifth degree. Results a. Histochemical findings In the thyroid gland, all the above mentioned enzyme histochemical reactions studied show a mostly distinct age dependent relationship in the intensity of enzyme activity. Age dependent changes in the histo-topochemical behaviour of individual reactions are also demonstrable on light-microscopical examination. In control animals at the time of birth, alkaline phosphatase and cytochrome oxidase react moderately, the others weakly. With hydrolases the activity of alkaline phosphatassr remains at a moderate level throughout the life span, while acid phosphatase and ATP-ase show a marked increase up to puberty, and the reaction is still mnd I.C.D.H. an increase during the growth period, a marked response in middle life, and a lessening of activity in ageing animals can be demonstrated. Cytochrome oxidase increases up to the seventeenth week of life, and then decreases in older animals. The activity of nonspecific esterase increases up to the eleventh week, remains at a high level up to the forty fourth week and then lessen after one year of life...</p>","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":" 101","pages":"1-76"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11283391","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[Posttraumatic pyogenic and granulomatous encephalitis. An animal experimental contribution on inflammation (author's transl)].","authors":"W Schachenmayr","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The present studies were performed to elucidate the factors responsible for the relative resistance of the brain to bacterial infections. As a model, group A streptococci were used to produce an experimental brain infection in mice. Attention was focussed on the activity of brain macrophages, the function of which to date is poorly understood. The primary purpose of the experiments was to compare the types of inflammation elicited in the brain by the injection of either killed or living group A streptococci. As a result, two fundamentally different types of encephalitis were observed histologically. A granulomatous inflammation was induced by killed streptococci; when deposited in the brain by intracerebral injection, these were phagocytosed by invading mononuclear macrophages and polymorphonuclear granulocytes during the first day p.i. There was no necrosis of brain tissue excepting the stab wound at the site of injection. The number of granulocytes in the inflammatory infiltrates decreased during the first week p.i. whereas, during the same period, the number of macrophages forming granuloma-like cell accummulations increased. At the beginning of the third week a fading of the granulomatous encephalitis was observed. In contrast, living streptococci produced a pyogenic inflammation of the meninges as well as of the grey and white matter in the region of the stab wound combined with extended tissue necrosis surrounding deposits of bacteria. This pyogenic infection progressed until the end of the first week, forming a brain abscess. A phlegmonous spreading of the pyogenic inflammation predominantly in the white matter and pyocephalus internus was also observed. In contrast to the increase of mononuclear macrophages in the border zone of the abscesses, the granulocytic inflammation decreased. During the second and third weeks p.i. granulation tissue consisting of proliferating connective tissue cells, macrophages and lymphocytes replaced pyogenic necrosis. A secondary purpose was to determine the fate of living and killed streptococci within the pyogenic and granulomatous encephalitis. In these studies immunohistologic, electron microscopic, bacteriologic and serologic methods were employed in addition to the techniques already mentioned. In the majority of the experimental animals streptococci were killed by granulocytes within the first week after injection of the living bacteria. At this time, most of the streptococci were contained within granulocytes and macrophages located to the periphery of the brain abscesses. Corresponding to the granulomatous encephalitis produced by injection of killed streptococci it was possible to detect persistent cell wall material in macrophages by immunohistology. By electronmicroscopy streptococci and their cell walls were found within the phagocytic vacuoles of macrophages. During the course of degradation the group-specific cell wall carbohydrate was enzymatically converted into the group A-variant spec","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":"100 ","pages":"1-87"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11978016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[On the pathogenesis of the glomerulosclerosis ultrastructural and autoradiographic investigations on the rat kidney (author's transl)].","authors":"W Romen","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The light- and electron microscopic changes in the glomeruli of the rat's kidney have been investigated in the course of ageing and after subtotal nephrectomy, constriction of the renal vein, and intoxication by N-nitrosomorpholine. In spite of the fact that four different experimental models have been used, identical changes were always found in the glomeruli. Morphologically they consisted of a diffuse thickening of the glomerular basement membrane and of an increase in the mesangial matrix without a proliferation of the glomerular cells. Despite this thickening of the glomerular basement membrane, functionally an increased permeability of the glomerular capillaries for macroproteins could be observed, shown by a moderate proteinuria. For these morphological changes the term \"glomerulosclerosis\" is suggested; they are interpreted as a non-specific, non-inflammatory reaction of the glomerulus to an impairment caused by a number of varied influences. From the study of the formal pathogenesis of the glomerulosclerosis presented here one can conclude that in the individual experimental models the same result has been achieved in different ways. One possibility in the development of glomerulosclerosis is an increased production of the components of the basement membrane and of the mesangial matrix. This is the pathway which appears to be followed after nephrectomy. Another possibility is a slowing down of the breakdown of both the matrix and the membrane. This seems to be the case in the glomerulosclerosis occuring in the course of ageing, and after hypoxic and toxic changes. It could be accounted for by a functional disturbance of, presumably, the mesangial cells responsible for the breakdown of the basement membrane and of the matrix. On the other hand, one may have to consider a primary alteration of the macromolecules of these structures, as is already known from studies of the, chemically closely related, collagen. The light- and electron microscopic studies of the normal and of the altered glomeruli have led to certain conclusions concerning the origin and the fomation of the glomerular basement membrane and the mesangial matrix. In order to widen the scope of the studies, additional autoradiographic investigations with 3H-proline and 3H-leucine have been performed in ultrathin and semithin sections of the rat's glomeruli. The results of the studies presented here suggest that of the three cell types of the glomerulus the visceral epithelial cells (podocytes, \"Deckzellen\") may participate on the formation of the glomerular basement membrane, whereas the mesangial cells appear to be responsible for the synthesis of the mesangial matrix.</p>","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":" 102","pages":"1-101"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11980257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[Sialadenosis of the parotid gland. Ultrastructural, clinical and experimental findings in disturbances of secretion (author's transl)].","authors":"K Donath","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Among the secretory disturbances (\"Dyschylien\") of salivary glands the sialadenosis of the parotid gland is a clinic and a morphologic definited entity. The typical clinical symptom is a bilateral, often recurrent, and painless swelling of the parotid gland. The characteristic pathological findings consist in an acinar cell hypertrophy without any inflammatory signs. According to this definition, sialadenosis has to be separated from those diseases of salivary glands, which are primarily altered by inflammation of the salivary tissue with secondary secretory disturbances. From flinical point of view it is possible to distinguish the following kinds of sialadenosis according to the syntropy with various diseases: Endocrine sialadenosis (in diabetes mellitus, dysfunction of gonads, pituitary gland, thyroid gland etc.); dystrophic-metabolic sialadenosis (malnutrition, avitaminosis, alcohilsm, chronic liver diseases etc.), and neurogenic sialadenosis (dysfunction of the vegetative nervous system, drug damages e.g. antihypertensive agents). The question arises, whether all forms of sialadenosis have a common etiology and a coincidental pathogenic factor. The following studies were carried out with the aim to find further details concerning the etiology and pathogenesis of sialadenosis. The study is based on the following material: a) 126 Biopsies of parotid glands from patients with sialadenosis (Register of salivary gland diseases at the Institute of Pathology, University of Hamburg, supported by Deutsche Forschungsgemeinschaft). This material was collected from 1965 to 1973. b) 80 Biopsies of parotid glands from patients with other diseases (parotitis [4]; acinic cell carcinoma [4]; other parotid and oral tumors [72]; for comparison. c) Experimental studies on the parotid salivary glands of Wistar-rats. The biopsies of the parotid glands were studied histologically, morphometrically, and ultrastructurally. The investigations centered on the ultrastruct of sialadenosis. Before interpreting the ultrastructural findings in view of etiology and pathogenesis of sialadenosis, it was primarily necessary to study the normal ultrastructure of the human parotid gland including the vegetative nervous system. Furthermore it was necessary to elucidate details of a functional morphology of the secretory cycle and to integrade the findings into a concept of general pathology of secretory disturbances. The following results were achieved by our investigations: 1. Normal ultrastructure of human parotid gland: The architecture of the acinar cells is identical with these of other animal species (cytoplasm with a basal standing nucleus, rough endoplasmatic reticulum, Golgi-apparatus, secretory granules etc.). Further identical elements are intercalated and striated ducts, myoepithelial cells, and the vegetative nervous system (postganglionic sympathetic and parasympathetic neurites, however no ganglionic cells in the parotid gland)...</p>","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":" 103","pages":"1-122"},"PeriodicalIF":0.0,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12188230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[Endocrine bone diseases morphology, histomorphometry and differential diagnosis (author's transl)].","authors":"G Delling","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":" 98","pages":"1-111"},"PeriodicalIF":0.0,"publicationDate":"1975-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11977050","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[T and B lymphocytes in chronic lymphocytic leukemia and Hodgkin's disease. Electron microscopic and immunologic studies].","authors":"G Cohnen","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The number of lymphocytes forming spontaneous rosettes with sheep erythrocytes, a property of thymus-dependent (T) cells, and the number of lymphocytes bearing surface immunoglobulins, a characteristic feature of bone marrow-dependent (B) cells, were determined in the peripheral blood of normals and of patients with chronic lymphocytic leukemia (CLL) and Hodgkin's disease. As compared with normal individuals CLL patients had an increased percentage of lymphocytes with membrane-bound immunoglobulins, whereas the proportion of rosette-forming lymphocytes was reduced. In Hodgkin's disease either normal, diminished, or increased B cell values were obtained; the percentage of T cells was decreased or within the lower range of normals. Lymphocyte transformation by various mitogenic agents in vitro may be regarded as a model of lymphocyte reactivity during immunologic processes in vivo. In order to study the functional capacity of lymphocytes in CLL and Hodgkin's disease in comparison with normal cells, purified peripheral blood lymphocytes from normals and patients with these diseases were incubated in vitro with phytohemagglutinin (PHA) and pokeweed mitogen (PWM) over 7 to 11 days. DNA synthesis was determined by incorporation of 3-H-thymidine. The cyto-architectural features of the cells before and during incubation with these phytomitogens were studied by electron microscopy. Planimetric measurements were performed on micrographs of comparable cell sections (through nucleus and Golgi zone) for the determiniation of cell, nuclear, cytoplasmic, and mitochondrial area. Furthermore, the number of mitochondria and of membrane-bounded acid phosphatase-positive lysosome-like organelles was determined in comparable sections of unstimulated and mitogen transformed lymphocytes.</p>","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":" 0","pages":"1-99"},"PeriodicalIF":0.0,"publicationDate":"1975-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11272328","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[The regulation of cell proliferation by chalones experimental investigations on epidermal hyperplasia (author's transl)].","authors":"R Rohrbach","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The pattern of epidermal cell proliferation, following a single application of a hyperplasia inducing agent, can well be interpreted in cybernetic terms. This concept implies that the local concentration of a possible growth inhibiting signal substance should exhibit variations compatible with the changes seen in the cell kinetics of the epidermis. This signal substance has been called the epidermal chalone, first preliminary characterized by Bullough et al. (1964c). Meanwhile a considerable number of other chalone systems have been identified in different organs. From the experimental results a chalone was considered an anti-mitotic substance, which is synthesized within the same tissue on which it specifically acts. It was found not to be species-specific; it reveals a rapid and reversible inhibition by diffusion and passes throughout the tissue and into the blood. Later investigations have exhibited that the epidermal chalone probably consists of at least two separate compounds (proteins), one acting on cells in the postsynthetic, pre-mitotic G 2-phase, the other one on cells in late G 1 (Marks, 1971; Elgjo et al., 1971, 1972). The proliferative behavior of epidermal cells following an application of different irritants was the main subject of the present investigations. All experiments were performed in vivo with hairless mouse epidermis, which was treated with 20-methylcholanthrene (MCA) as carcinogen and crotonoil as cocarcinogen, both dissolved in acetone, and with repeated Scotch tape stripping. Different methods were employed in order to determine epidermal proliferation parameters such as: a. the cytophotometrically measured amount of nucleic deoxyribonucleic acid (DNA) of Feulgen-stained epidermal basal cells, b. the total DNA content of whole epidermis, c. the number of Colcemid(R) arrested metaphases (mitotic rate) in the basal cell layer, d. the incorporation of H3-thymidine into DNA of epidermal basal cells. The number of epidermal basal cells revealing an increased DNA content is significantly lowered for more than 24 hours after MCA and for 12 hours after Crotonoil administration. This effect was not observed after Scotch tape stripping. In all the treated groups this period was followed by a proliferation wave exhibiting more cells with an increased DNA-content during the first 6-10 days after irritation. Only after MCA treatment this higher cell number appeared with a lag phase of 3 to 4 days and coincided with a decrease of the total amount of epidermal DNA. All irritants produced a marked epidermal hyperplasia during the first two weeks after application.</p>","PeriodicalId":76795,"journal":{"name":"Veroffentlichungen aus der Pathologie","volume":" 99","pages":"1-67"},"PeriodicalIF":0.0,"publicationDate":"1975-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11352152","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}