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    <title>Digitum Colección:</title>
    <link>http://hdl.handle.net/10201/17721</link>
    <description />
    <pubDate>Wed, 19 Jun 2013 10:10:24 GMT</pubDate>
    <dc:date>2013-06-19T10:10:24Z</dc:date>
    <item>
      <title>A comparison of cyclosporine A and cyclosporine 
G in a rabbit heterotopic cardiac transplant model: 
graft outcome and histological findings</title>
      <link>http://hdl.handle.net/10201/18850</link>
      <description>Título: A comparison of cyclosporine A and cyclosporine 
G in a rabbit heterotopic cardiac transplant model: 
graft outcome and histological findings
Autor/es principal/es: Fryer, J.P.; Pascoe, E.A.; Yatscoff, R.W.; Thliveris, J.A.
Resumen: Cervical heterotopic heart transplants 
were performed on 20 male New Zealand white 
rabbits comprising 4 treatment groups. Animals in each 
group were injected daily via the marginal ear vein 
and received one of the following regimes: Cyclosporine 
A, 10 mglkglday; Cyclosporine G, 15 mglkglday; 
cremophor-El, 3mllday; or normal saline. Measurement 
of 24 hour trough blood concentrations revealed 
no significant differences between the average 
concentrations of Cyclosporine A and Cyclosporine 
G. Animals were examined daily and the cervical 
allografts assessed by palpation for viabilitylrejection. 
The duration of the study ended for each animal 
when the graft stopped beating at which time the animals 
was euthanized and the transplanted heart and 
native kidneys harvested and processed for light 
microscopy evaluation of rejection and drug toxicity, 
respectively. 
Graft survival in the Cyclosporine A group 
significantly surpassed that seen in the Cyclosporine G 
group as well as the control groups, whereas in animals 
treated with Cyclosporine G, graft survival was not 
different from controls. In the native kidney, there were 
no differences in glomerular tuft area or volume density 
amongst drug-treated or control animals. In contrast, 
tubule atrophy and interstitial fibrosis were markedly 
greater in Cyclosporine A-treated vs Cyclosporine Gtreated 
animals. 
The results of this study indicate that, whereas 
Cyclosporine G is less nephrotoxic than Cyclosporine A, 
given equivalent blood concentrations Cyclosporine A 
delays rejection of a cardiac allograft significantly 
longer than Cyclosporine G in this animal species.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:38 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18850</guid>
      <dc:date>2011-02-22T10:32:38Z</dc:date>
    </item>
    <item>
      <title>Odontogenic jaw cysts: light and 
electron microscopical investigations</title>
      <link>http://hdl.handle.net/10201/18849</link>
      <description>Título: Odontogenic jaw cysts: light and 
electron microscopical investigations
Autor/es principal/es: Domenici Lombardo, L.; Amunni, F.; Bergamini, M.; Romagnoli, P.
Resumen: Light and electron microscopy were used to 
analyze the epithelial lining of odontogenic cysts excised 
from edentulous regions of the jaws. Clinically, three 
cases were identified as keratocysts, and 21 cases as 
cysts other than keratocysts («non-keratocysts~)T. he 
epithelium of the former was found to achieve 
keratinization over most of the surface and to never 
contain mucus secreting cells. The epithelium of the 
latter appeared to be in part stratified squamous, with 
cells loosely connected to each other, and in part 
stratified columnar, with superficial cells connected to 
each other by tight junctions and secreting mucus. The 
results suggest that cysts arising from edentulous regions 
of the jaws may be either keratocysts or cysts with 
heterogeneous, non-keratinizing epithelium; the content 
of keratocysts can be formed mainly by shedding of 
comified epithelial layers, and that of non-keratocysts by 
mucus secretion from columnar epithelium associated to 
fluid filtration through non-keratinizing squamous 
epithelium.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:37 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18849</guid>
      <dc:date>2011-02-22T10:32:37Z</dc:date>
    </item>
    <item>
      <title>Retinal pigment epithelial fine structure in 
the Australian Galah (Eolophus roseicapillus) (Aves)</title>
      <link>http://hdl.handle.net/10201/18848</link>
      <description>Título: Retinal pigment epithelial fine structure in 
the Australian Galah (Eolophus roseicapillus) (Aves)
Autor/es principal/es: Braekevelt, C. R.; Richardson, K.C.
Resumen: As part of a comparative morphological 
study, the fine structure of the retinal epithelium (RPE), 
choriocapillaris and Bruch's membrane (complexus 
basalis) has been investigated by light and electron 
microscopy in the galah (Eolophus I-oseicapillus), an 
Australian cockatoo. The RPE consists of a single layer 
of low cuboidal cells joined basally by a series of 
zonulae occludentes. Basally (sclerally) the retinal 
epithelial cells display numerous deep infoldings while 
apically (vitreally) microvillar processes interdigitate 
with photoreceptor outer segments. Internally the RPE 
cells show a large vesicular nucleus, plentiful smooth 
endoplasmic reticulum (SER) and numerous polysomes 
but very little rough endoplasmic reticulum (RER). 
Numerous mitochondria are located basally. In the lightadapted 
specimens studied, the melanosomes of the RPE 
are almost exclusively located within the apical 
processes indicating that retinomotor movement of this 
pigment probably occurs. Phagosomes and lysosomelike 
bodies are present as are myeloid bodies which may 
show ribosomes on their outer surface. The choriocapillaris 
endothelium is thin but only minimally fenestrated 
facing Bruch's membrane. Most fenestrations of the 
choriocapillaris display a single-layered diaphragm 
while the remainder have a double-layered diaphragm. 
Bruch's membrane (complexus basalis) is typical of 
avian species in that it is pentalaminate with the central 
lamina densa displaced towards the choriocapillaris.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:36 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18848</guid>
      <dc:date>2011-02-22T10:32:36Z</dc:date>
    </item>
    <item>
      <title>lnitiation and post-initiation chemopreventive 
effects of O-carotene in toad liver carcinogenesis</title>
      <link>http://hdl.handle.net/10201/18846</link>
      <description>Título: lnitiation and post-initiation chemopreventive 
effects of O-carotene in toad liver carcinogenesis
Autor/es principal/es: Sadek, I.A.; Hayat, L.G.
Resumen: Hepatocellular carcinoma were recognized in 
the toad, Blfo iliridis, in 14 cases out of 50 by injection 
of 1 mg 7,12 dimethylbenz(a)anthracene (DMBA)/toad 
twicelweek for 12 weeks. In contrast, toads treated with 
DMB at the same dose level and B-carotene (BC), 0.05 
mg (3 hr prior to the carcinogen)/toad, twicelweek for 12 
weeks showed no tumor incidence. However, BC at the 
same dose level was less effective when administered 
3 hr. after the carcinogen (DMBA). In 8 cases out of 50 
cases neither tumor growth nor neoplastic changes were 
observed in toads treated with BC alone or olive oil. It is 
concluded that BC completely blocked hepatocarcinogenesis 
in toads when given 3 hr. before 
initiation.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:35 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18846</guid>
      <dc:date>2011-02-22T10:32:35Z</dc:date>
    </item>
    <item>
      <title>Seasonality and freezability vs 
routine parameters in stallion semen</title>
      <link>http://hdl.handle.net/10201/18847</link>
      <description>Título: Seasonality and freezability vs 
routine parameters in stallion semen
Autor/es principal/es: Rodríguez, H.; Bustos-Obregón, E.
Resumen: The fertilizing ability of stallion semen was 
analyzed using fresh and frozen samples, obtained 
before (June-July) or during (October-November) the 
breeding season. Thirty ejaculates obtained from 4 
stallions, were used. The analysis comprises routine 
seminogram; ATP concentration (Comhaire et al., 1983); 
subjective and objective motility and sperm velocity 
(Makler, 1980). Freezing was done following the 
technique of Martin et al. (1979). Sperm velocity, ATP 
content and objective motility in ejaculates of subjective 
motility &gt;50% show values of 14.010.84 ym S-l; 
4.8f 2 . 7 1~O - ~ Man d 54.0I7.4%, respectively. For 
ejaculates with subjective motility ~ 5 0 %the~se values 
are 8.412.4; 0.74f 0 . 3 6 1~ 0 - 7 a~n d 27.0+0.8%. No 
significant changes in these characteristics were elicited 
by freezing, though ATP content dropped to 50% after 
thawing. These characteristics are highly associated 
between them (pc0.05) and with some conventional 
parameters of the routine seminogram such as sperm 
motility, count, total spermatozoal number and 
morphology. Additionally, sperm chromatin packing was 
analyzed by decondensing sperm nuclei using a thiol 
reducing agent. This parameter was not modified by 
freezing and it may depend on prolonged epididymal 
sperm storage during the non-breeding season. 
Epididymal maturation then results in an excessive 
disulphur bridging in sperm basic proteins, so that 
hypermaturation with faultly male pronuclear formation 
can follow.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:35 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18847</guid>
      <dc:date>2011-02-22T10:32:35Z</dc:date>
    </item>
    <item>
      <title>A change in the localization of the region trapping 
immune complexes in rat popliteal lymph nodes 
during development of germinal centers, with regard 
to the distribution of follicular dendritic cells</title>
      <link>http://hdl.handle.net/10201/18845</link>
      <description>Título: A change in the localization of the region trapping 
immune complexes in rat popliteal lymph nodes 
during development of germinal centers, with regard 
to the distribution of follicular dendritic cells
Autor/es principal/es: Sato, H.; Dobashi, Michio; Maeda, K.
Resumen: A study was conducted to clarify changes in 
the relationship between the region of irnrnune complex 
(IC) trapping by follicular dendritic cells (FDCs) and the 
distribution of FDC during reaction of germinal centers 
(GCs), and to examine the relationship between the 
tridiniensional shape of the IC-trapping regions and their 
two-dimensional shape. Five-week-old rats were given 
footpad injections of sheep red blood cells, and then 
their popliteal lymph nodes were excised between days O 
and 42, 24 h after injection of peroxidase-antiperoxidase 
complex (PAP) as an IC. The specimens were 
immunostained for PAP trapping on serial paraffin 
sections, and for S-100 protein as a marker of FDCs. It 
was found that during the GC reaction, PAP trapping 
became weak and then disappeared on the basal side of 
developing GCs where S-100 protein-positive FDCs 
were still present. Al1 of the 1933 lymph follicles 
examined were found to trap PAP. Whereas the 
tridiniensional shapes of the trapping regions showed 
similar pattems according to the development of lymph 
follicles, their two-dimensional shapes varied. We 
suggest that FDCs in primary follicles may differentiate 
into FDCs in the light zone and FDCs in the dark zone in 
secondary follicles. To evaluate each of the 
compartments of a lymph follicle more accurately, 
investigators should pay attention to the tridimensional 
shape of the compartment.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:34 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18845</guid>
      <dc:date>2011-02-22T10:32:34Z</dc:date>
    </item>
    <item>
      <title>Use of lectin-probes for correlative 
histochemical and biochemical assessments 
of the glycosylation patterns of secretory proteins, 
including kallikreins, in salivary glands and saliva</title>
      <link>http://hdl.handle.net/10201/18844</link>
      <description>Título: Use of lectin-probes for correlative 
histochemical and biochemical assessments 
of the glycosylation patterns of secretory proteins, 
including kallikreins, in salivary glands and saliva
Autor/es principal/es: Garrett, J.R.; Proctor, G.B.; Zhang, X.S.; Shori, D.K.; Schulte, B.A.
Resumen: Labelled lectins were used as probes to study 
the glycosylation and secretion of submandibular 
glycoproteins not only in sections of fixed glands but 
also in glandular extracts and in nerve-induced saliva, 
after electrophoretic separations and immobilization in 
nitrocellulose membranes. 
In cats the glycoproteins in sympathetic saliva 
differed considerably from those in parasympathetic 
saliva. In sympathetic saliva they were found to 
originate mainly from striated ducts, to some extent from 
demilunar cells and to a small extent from acinar cells, 
whereas in parasympathetic saliva they arose mainly 
from acinar-cells añd demilunes and only to a small 
extent from striated ducts. 
In rat submandibular glands sympathetic stimulation 
caused extensive depletion of lectin stainable granules 
from granular tubules. Corresponding strong binding 
occurred with the same lectins to constituents in saliva 
that ran between 25 and 35 kD on SDS gel electrophoresis 
and were shown to contain tissue kallikreins. 
Their binding patterns suggested that individual 
kallikreins from the same gland may be glycosylated in 
different ways. This possibility was tested on five 
different kallikreins after separation from submandibular 
extracts by isoelectric focussing. Lectin bindings on slot 
blot preparations of these kallikreins were tested before 
and after N-glycosidase F, sialidase or endo-a-Nacetylgalactosaminidase 
digestions. Results showed that, 
despite their close genetic and structural similarities, the 
kallikreins are in fact differently sialylated and 
fucosylated and the novel finding that some contain Oglycosidically 
linked side chains as well as the 
anticipated N-glycosidically linked side chains was 
revealed. 
Thus, correlative histochemical and biochemical 
Offprint requests to: Professor J.R. Garrett, Secretory and Soft Tissue 
Research Unit, Department of Oral Pathology, The Rayne Institute, 
KCSMD, 123 Coldharbour Lane, London, SE5 9NU, England 
assessments of bindings with lectin probes has provided 
important new information about differences in the 
glycosylation pattems of individual glycoproteins stored 
within the same secretory granules.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:33 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18844</guid>
      <dc:date>2011-02-22T10:32:33Z</dc:date>
    </item>
    <item>
      <title>Alterations in the alveolar epithelium 
after injury leading to pulmonary fibrosis</title>
      <link>http://hdl.handle.net/10201/18843</link>
      <description>Título: Alterations in the alveolar epithelium 
after injury leading to pulmonary fibrosis
Autor/es principal/es: Kasper, M.; Haroske, G.
Resumen: This review discusses current knowledge of 
the involvement of the alveolar epithelium in tissue 
remodelling during fibrogenesis. The purpose of the 
present paper is to give an overview, including the 
authors' own results, of knowledge of ultrastructural 
alterations, proliferation kinetics and phenotypic changes 
of pneumocytes in experimental and clinical pathology 
of pulmonary fibrosis. After lung injury, the alveolar 
epithelial cells show ultrastructural alterations, 
hypertrophy and hyperplasia, and a modulation of a 
series of structural and membrane proteins such as 
cytoskeletal changes, loss or de novo expression of 
epithelial adhesion molecules, and altered lectin binding. 
Furthermore, enhanced secretion of proteases, of 
cytokines and other soluble factors can be observed in 
the alveolar epithelium. These findings suggest the 
contribution of the epithelium in the remodelling process 
to be greater than expected. Estimations of the cell 
kinetics show that type 11 pneumocytes have the 
proliferative capacity to restore high proportions of 
damaged type 1 cells within few hours. In fibrosis this 
capacity also seems to be affected seriously, resulting in 
transitional phenotypes between type 11 and type 1 cells. 
Additionally, in the light of the detection of CD44 type 
of adhesion molecules at the foot processes of type 11 
pneumocytes, some aspects of epithelial-fibroblast 
interaction are described.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:32 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18843</guid>
      <dc:date>2011-02-22T10:32:32Z</dc:date>
    </item>
    <item>
      <title>Morphological changes of autoclaved 
autogenic bone implantation and autoclaved 
autogenic bone supplernented with allogenic 
demineralized bone matrix in rat parietal bone</title>
      <link>http://hdl.handle.net/10201/18842</link>
      <description>Título: Morphological changes of autoclaved 
autogenic bone implantation and autoclaved 
autogenic bone supplernented with allogenic 
demineralized bone matrix in rat parietal bone
Autor/es principal/es: Young, T.Q.; Matsuda, Mikio; Takekawa, M.; Ohtsubo, S.; Tsuyama, K.; Kita, S.
Resumen: The healing process of resected, autoclaved 
(121 7,20 minutes) and re-implanted bone in the rat 
parietal bone was compared with that of autoclaved bone 
that was supplemented with allogenic bone matrix 
(AAA-bone), using a scanning electron microscope and 
a light microscope. 
In the implant without AAA-bone, bone union and 
replacement of the autoclaved bone was seen at 2 weeks 
after implantation. There was no evidence of any 
inflammatory reaction around the autoclaved bone. The 
implant was gradually replaced by the new bone. In the 
implant with AAA-bone, the new bone formation around 
the implanted bone was more abundant than that of the 
implant without AAA-bone. An inflammatory reaction 
was also observed after 1 week. The replacement of the 
implant with AAA-bone was inferior to the nonsupplemented 
group. The reason for the poor 
replacement was the disturbance of the blood supply in 
the implant by abundant new bone formation. 
In these results, the autoclaved bone re-implantation 
was an excellent bone substitute with osteoconductive 
ability and biocompatibility. The implantation with 
AAA-bone was good for the new bone formation, but 
the position and the technique of supplement with AAAbone 
have to be more deeply investigated.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:31 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18842</guid>
      <dc:date>2011-02-22T10:32:31Z</dc:date>
    </item>
    <item>
      <title>Tenascin and type IV collagen expression in 
liver cell dysplasia and in hepatocellular carcinoma</title>
      <link>http://hdl.handle.net/10201/18841</link>
      <description>Título: Tenascin and type IV collagen expression in 
liver cell dysplasia and in hepatocellular carcinoma
Autor/es principal/es: Zhao, M.; Laissue, J.A.; Zimmermann, Astrid
Resumen: The extracellular matrix (ECM) located in 
and around tumors is different from normal organ 
stroma, and there is evidence that it is critically involved 
in carcinogenesis and malignant growth. Whereas an 
abnormal composition of ECM in hepatocellular 
carcinomas (HCC's) has previously been demonstrated, 
not much is known so far with respect to putative HCC 
precursor lesions. We have, therefore, systematically 
analyzed the immunohistochemical reactivity for two 
major ECM components, tenascin and type IV collagen, 
in three types of liver cell dysplasia (LCD), and 
compared the findings with patterns observed in HCC's 
of different types and grades. Tenascin reactivity was 
generally stronger in HCC's than in cirrhosis. In 
cirrhotic nodules harboring areas of LCD, tenascin 
expression was significantly lower in small cell LCD 
than in large cell LCD. Type IV collagen reactivity in 
and around HCC's decreased as a function of a lower 
differentiation grade. In both groups of cirrhosis, ¡.e. 
with or without HCC, cirrhotic nodules occupied by the 
small cell variant of LCD exhibited a significantly lower 
type IV collagen reactivity than those with large cell 
LCD or simple regenerative cells. Taken together these 
findings suggest that, similar to adenomatous 
hyperplasia, small cell LCD is characterized by an 
abnormal tenascin and type IV collagen expression, thus 
reflecting the defective ECM pattern observed in HCC's.</description>
      <pubDate>Tue, 22 Feb 2011 10:32:30 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/10201/18841</guid>
      <dc:date>2011-02-22T10:32:30Z</dc:date>
    </item>
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