Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 51
Filter
1.
Neuroscience ; 311: 430-43, 2015 Dec 17.
Article in English | MEDLINE | ID: mdl-26522789

ABSTRACT

Synapsins (Syns) are an evolutionarily conserved family of presynaptic proteins crucial for the fine-tuning of synaptic function. A large amount of experimental evidences has shown that Syns are involved in the development of epileptic phenotypes and several mutations in Syn genes have been associated with epilepsy in humans and animal models. Syn mutations induce alterations in circuitry and neurotransmitter release, differentially affecting excitatory and inhibitory synapses, thus causing an excitation/inhibition imbalance in network excitability toward hyperexcitability that may be a determinant with regard to the development of epilepsy. Another approach to investigate epileptogenic mechanisms is to understand how silencing Syn affects the cellular behavior of single neurons and is associated with the hyperexcitable phenotypes observed in epilepsy. Here, we examined the functional effects of antisense-RNA inhibition of Syn expression on individually identified and isolated serotonergic cells of the Helix land snail. We found that Helix synapsin silencing increases cell excitability characterized by a slightly depolarized resting membrane potential, decreases the rheobase, reduces the threshold for action potential (AP) firing and increases the mean and instantaneous firing rates, with respect to control cells. The observed increase of Ca(2+) and BK currents in Syn-silenced cells seems to be related to changes in the shape of the AP waveform. These currents sustain the faster spiking in Syn-deficient cells by increasing the after hyperpolarization and limiting the Na(+) and Ca(2+) channel inactivation during repetitive firing. This in turn speeds up the depolarization phase by reaching the AP threshold faster. Our results provide evidence that Syn silencing increases intrinsic cell excitability associated with increased Ca(2+) and Ca(2+)-dependent BK currents in the absence of excitatory or inhibitory inputs.


Subject(s)
Action Potentials/physiology , Calcium Channels/metabolism , Large-Conductance Calcium-Activated Potassium Channels/metabolism , Serotonergic Neurons/physiology , Synapsins/deficiency , Action Potentials/drug effects , Animals , Calcium/metabolism , Cells, Cultured , Gene Knockdown Techniques , Helix, Snails , Immunohistochemistry , Indoles/pharmacology , Large-Conductance Calcium-Activated Potassium Channels/antagonists & inhibitors , Patch-Clamp Techniques , Potassium Channel Blockers/pharmacology , Serotonergic Neurons/drug effects , Synapsins/genetics
2.
Heredity (Edinb) ; 113(5): 443-53, 2014 Nov.
Article in English | MEDLINE | ID: mdl-24781805

ABSTRACT

Although the phylogeography of European mammals has been extensively investigated since the 1990s, many studies were limited in terms of sampling distribution, the number of molecular markers used and the analytical techniques employed, frequently leading to incomplete postglacial recolonisation scenarios. The broad-scale genetic structure of the European badger (Meles meles) is of interest as it may result from historic restriction to glacial refugia and/or recent anthropogenic impact. However, previous studies were based mostly on samples from western Europe, making it difficult to draw robust conclusions about the location of refugia, patterns of postglacial expansion and recent demography. In the present study, continent-wide sampling and analyses with multiple markers provided evidence for two glacial refugia (Iberia and southeast Europe) that contributed to the genetic variation observed in badgers in Europe today. Approximate Bayesian computation provided support for a colonisation of Scandinavia from both Iberian and southeastern refugia. In the whole of Europe, we observed a decline in genetic diversity with increasing latitude, suggesting that the reduced diversity in the peripheral populations resulted from a postglacial expansion processes. Although MSVAR v.1.3 also provided evidence for recent genetic bottlenecks in some of these peripheral populations, the simulations performed to estimate the method's power to correctly infer the past demography of our empirical populations suggested that the timing and severity of bottlenecks could not be established with certainty. We urge caution against trying to relate demographic declines inferred using MSVAR with particular historic or climatological events.


Subject(s)
Evolution, Molecular , Genetic Variation , Genetics, Population , Mustelidae/genetics , Animals , Bayes Theorem , DNA, Mitochondrial/genetics , Europe , Haplotypes , Microsatellite Repeats , Models, Genetic , Phylogeography , Population Dynamics
3.
J Neurosci Res ; 87(2): 425-39, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18756517

ABSTRACT

We report on the structural and functional properties of the Helix contactin-related proteins (HCRPs), a family of closely related glycoproteins previously identified in the nervous system of the land snail Helix pomatia through antibodies against the mouse F3/contactin glycoprotein. We focus on HCRP1 and HCRP2, soluble FNIII domains-containing proteins of 90 and 45 kD bearing consensus motifs for both N- and O-glycosylation. Using the anti-HCRPs serum, we find secreted HCRPs in Helix nervous tissue isotonic extracts and in culture medium conditioned by Helix ganglia. In addition, we demonstrate expression of HCRPs on neuronal soma and on neurite extensions. Functionally, in Helix neurons, the antisense HCRP2 mRNA counteracts neurite elongation, and the recombinant HCRP2 protein exerts a strong positive effect on neurite growth when used as substrate. These data point to HCRPs as novel neurite growth-promoting molecules expressed in invertebrate nervous tissue.


Subject(s)
Cell Adhesion Molecules, Neuronal/genetics , Cell Adhesion Molecules, Neuronal/metabolism , Helix, Snails/physiology , Neurons/metabolism , Amino Acid Sequence , Animals , Base Sequence , Blotting, Western , Cells, Cultured , Contactins , Electrophoretic Mobility Shift Assay , Electrophysiology , Immunohistochemistry , Molecular Sequence Data , Protein Isoforms/genetics , Protein Isoforms/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Sequence Homology, Amino Acid , Transfection
4.
Radiol Med ; 111(3): 440-8, 2006 Apr.
Article in English, Italian | MEDLINE | ID: mdl-16683089

ABSTRACT

PURPOSE: The purpose of this study was to assess the usefulness of routine ultrasonography in women with negative mammography and dense breasts [Breast Imaging Reporting and Data System (BIRADS D3-4)]. MATERIALS AND METHODS: We applied a protocol involving routine ultrasonography in a consecutive series of subjects with negative mammography and dense breasts. After evaluation by internal and external reviewers of cancers detected by ultrasonography performed to confirm negative mammography, we determined the additional cancer detection rate of ultrasonography and the cost of the protocol. RESULTS: Out of 17,883 total mammographies, 167 cancers were diagnosed (detection rate: 0.93%). Out of 257 suspicious mammographies, 138 cancers were detected. Out of 17,626 negative mammographies, 6,449 (36.5%) were classified as "dense breast" and underwent ultrasonography: 29 cancers were detected (detection rate: 0.44%, or 17.3% of total cancers). Out of 25 cancer cases reviewed, negative mammography and asymptomatic status was confirmed in 15 (detection rate 0.23%, or 8.9% of total cancers). The cancer detection rate was 0.11%, 0.22%, 0.32% and 0.14% for age groups <40, 40-49, 50-59 and >59, respectively. The cost per additional carcinoma detected by ultrasonography alone was euro 25,847.85 whereas that per examined woman was euro 21.68. CONCLUSIONS: The study confirms the possibility that ultrasonography can detect mammographically occult breast carcinoma in dense breasts. The evidence is insufficient to recommend this policy in routine screening practice but suggests that, at least in current clinical practice, adding ultrasonography in dense breasts may be useful despite the substantial costs.


Subject(s)
Breast Neoplasms/diagnostic imaging , Breast/pathology , Carcinoma/diagnostic imaging , Mammography , Ultrasonography, Mammary , Adult , Age Factors , Aged , Aged, 80 and over , Case-Control Studies , Costs and Cost Analysis , Female , Humans , Mammography/economics , Mass Screening/economics , Middle Aged , Predictive Value of Tests , Ultrasonography, Mammary/economics
5.
Biofizika ; 50(6): 1070-8, 2005.
Article in Russian | MEDLINE | ID: mdl-16358786

ABSTRACT

The role of photosystem II in hydrogen photoproduction by Chlamydomonas reinhardtii cells was studied in mutants with modified D1-protein. In D1-R323D and D1-R323L mutants, the replacement of arginine by aspartate or leucine, respectively, resulted in the disruption of electron transport at the donor side of photosystem II. The rate of oxygen evolution in D1-R323D decreased twice as compared to the pseudo-wild type (pWT), and in D1-R323L no oxygen evolution was detected. The latter mutant was not capable of photoautotrophical growth. The dynamics of changes in oxygen content, the reduction of photosystem II active reaction centers (deltaF/F(1)m), and hydrogen production rate in pWT were found to be similar to the wild type if cultivated under sulfur deprivation in a closed bioreactor. The observed gradual decrease in the deltaF/F(1)m value turned to a sharp drop almost to zero followed by a partial recovery during which the production of hydrogen set in. The transition to the anaerobic phase in D1-R323D cultured in a sulfur-deprived medium occurred earlier than it happened in pWt under the same conditions. However, the partial recovery of photosystem II activity and hydrogen production started at a later time, and the rate of hydrogen production was low. The D1-R323L mutant incapable of oxygen evolution entered the rapidly anaerobiosis but produced no hydrogen. The kinetics of photoinduced redox transitions in P700 was similar in all investigated strains and was not affected by diuron addition. This implies that the mutants had a pool of reducers, which could donate electrons through the quinone pool or cytochrome to photosystem I. However, in D1-R323L mutant lacking the active photosystem II, this condition was not sufficient to support hydrogenase activity.


Subject(s)
Algal Proteins/metabolism , Chlamydomonas reinhardtii/metabolism , Hydrogen/metabolism , Photosystem II Protein Complex/metabolism , Point Mutation , Sulfur/metabolism , Algal Proteins/genetics , Animals , Chlamydomonas reinhardtii/genetics , Electron Transport/genetics , Photosystem II Protein Complex/genetics
6.
Neuroscience ; 134(4): 1133-51, 2005.
Article in English | MEDLINE | ID: mdl-16054762

ABSTRACT

Short-term activity-dependent synaptic plasticity has a fundamental role in short-term memory and information processing in the nervous system. Although the neuronal circuitry controlling different behaviors of land snails of the genus Helix has been characterized in some detail, little is known about the activity-dependent plasticity of synapses between identified neurons regulating specific behavioral acts. In order to study homosynaptic activity-dependent plasticity of behaviorally relevant Helix synapses independently of heterosynaptic influences, we sought to reconstruct them in cell culture. To this aim, we first investigated in culture the factors regulating synapse formation between Helix neurons, and then we studied the short-term plasticity of in vitro-reconstructed monosynaptic connections involved in the neural control of salivary secretion and whole-body withdrawal. We found that independently of extrinsic factors, cell-cell interactions are seemingly sufficient to trigger the formation of electrical and chemical synapses, although mostly inappropriate--in their type or association--with respect to the in vivo synaptic connectivity. The presence of ganglia-derived factors in the culture medium was required for the in vitro reestablishment of the appropriate in vivo-like connectivity, by reducing the occurrence of electrical connections and promoting the formation of chemical excitatory synapses, while apparently not influencing the formation of inhibitory connections. These heat-labile factors modulated electrical and chemical synaptogenesis through distinct protein tyrosine kinase signal transduction pathways. Taking advantage of in vitro-reconstructed synapses, we have found that feeding interneuron-efferent neuron synapses and mechanosensory neuron-withdrawal interneuron synapses display multiple forms of short-term enhancement-like facilitation, augmentation and posttetanic potentiation as well as homosynaptic depression. These forms of plasticity are thought to be relevant in the regulation of Helix feeding and withdrawal behaviors by inducing dramatic activity-dependent changes in the strength of input and output synapses of high-order interneurons with a crucial role in the control of Helix behavioral hierarchy.


Subject(s)
Feeding Behavior/physiology , Helix, Snails/physiology , Neuronal Plasticity/physiology , Neurons/physiology , Synapses/physiology , Animals , Cell Communication/physiology , Cells, Cultured , Excitatory Postsynaptic Potentials/physiology , Image Processing, Computer-Assisted , In Vitro Techniques , Microscopy, Electron, Transmission , Neurons/ultrastructure , Synapses/ultrastructure
7.
J Neural Eng ; 2(2): L1-7, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15928406

ABSTRACT

Multielectrode array technology constitutes a promising approach for the characterization of the activity-dependent neuronal plasticity underlying information processing in the nervous system. For this purpose, long-term monitoring and stimulation of cultured neuronal networks with one-to-one neuron-sensor interfacing is advantageous. Existing neurochips that meet these specifications have made use of custom 3D structures requiring clean-room intensive microfabrication techniques. Low-cost fabrication procedures with potential for mass production would facilitate progress in the area. To this end, we have developed a sandwich structure comprising an elastomeric film, microstructured by replica moulding and microhole punching, for neuronal patterning, and a standard planar microelectrode array (MEA), for stimulation and recording. The elastomeric film includes microwells for cell body confinement, and microchannels capable of guiding neurites for network topology specification. The device is formed by overlaying the elastomeric structures on planar arrays. The combination of replica moulding, rapid prototyping and planar MEAs results in low-cost neurochips accessible to most neurophysiology labs. Single neuron patterning and recordings of extracellular potentials are demonstrated.


Subject(s)
Action Potentials/physiology , Cell Culture Techniques/instrumentation , Helix, Snails/physiology , Microelectrodes , Microfluidic Analytical Techniques/instrumentation , Nerve Net/physiology , Neurons/physiology , Animals , Biocompatible Materials/chemistry , Cell Proliferation , Cells, Cultured , Elastomers/chemistry , Equipment Design , Equipment Failure Analysis , Extracellular Fluid/physiology , Materials Testing , Miniaturization , Surface Properties
8.
Biochem Soc Trans ; 33(Pt 1): 70-2, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15667268

ABSTRACT

The development of efficient biological systems for the direct photoproduction of H(2) gas from water faces several challenges, the more serious of which is the sensitivity of the H(2)-evolving enzymes (hydrogenases) to O(2), an obligatory by-product of photosynthesis. This high sensitivity is common to both FeFe and NiFe hydrogenases, and is caused by O(2) binding to their respective metallocatalytic sites. This overview describes approaches to (i) molecular engineering of algal FeFe-hydrogenase to prevent O(2) access to its catalytic site; (ii) transform a cyanobacterium with an O(2)-tolerant bacterial NiFe hydrogenase or (c) partially inactivate algal O(2)-evolution activity to create physiologically anaerobiosis and induce hydrogenase expression.


Subject(s)
Hydrogen/metabolism , Animals , Catalytic Domain , Chlamydomonas reinhardtii/enzymology , Hydrogenase/metabolism , Iron-Sulfur Proteins/metabolism , Oxygen/metabolism , Protein Engineering
9.
Biochem Soc Trans ; 33(Pt 1): 80-2, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15667271

ABSTRACT

The [Fe]-hydrogenase enzymes are highly efficient H(2) catalysts found in ecologically and phylogenetically diverse microorganisms, including the photosynthetic green alga, Chlamydomonas reinhardtii. Although these enzymes can occur in several forms, H(2) catalysis takes place at a unique [FeS] prosthetic group or H-cluster, located at the active site. Significant to the function of hydrogenases is how the surrounding protein structure facilitates substrate-product transfer, and protects the active site H-cluster from inactivation. To elucidate the role of protein structure in O(2) inactivation of [Fe]-hydrogenases, experimental and theoretical investigations have been performed. Molecular dynamics was used to comparatively investigate O(2) and H(2) diffusion in CpI ([Fe]-hydrogenase I from Clostridium pasteurianum). Our preliminary results suggest that H(2) diffuses more easily and freely than O(2), which is restricted to a small number of allowed pathways to and from the active site. These O(2) pathways are located in the conserved active site domain, shown experimentally to have an essential role in active site protection.


Subject(s)
Hydrogen/metabolism , Oxygen/metabolism , Catalysis , Diffusion
10.
Biochem Soc Trans ; 33(Pt 1): 102-4, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15667277

ABSTRACT

The eukaryotic green alga, Chlamydomonas reinhardtii, produces H(2) under anaerobic conditions, in a reaction catalysed by an [FeFe]-hydrogenase. To identify genes that influence H(2) production in C. reinhardtii, a library of 6000 colonies on agar plates was screened with sensitive chemochromic H(2)-sensor films for clones defective in H(2) production. Two mutants of particular interest were fully characterized. One mutant, hydEF-1, is unable to assemble an active [FeFe]-hydrogenase. This is the first reported C. reinhardtii mutant that is not capable of producing any H(2). The second mutant, sta7-10, is not able to accumulate insoluble starch and has significantly lowered H(2)-photoproduction rates in comparison with the wild-type. In hydEF-1, anaerobiosis induces transcription of the two reported C. reinhardtii hydrogenase genes, HydA1 and HydA2, indicating a normal transcriptional response to anaerobiosis. In contrast, the transcription of both hydrogenase genes in sta7-10 is significantly attenuated.


Subject(s)
Chlamydomonas reinhardtii/enzymology , Hydrogenase/genetics , Animals , Chlamydomonas reinhardtii/genetics , Genes, Bacterial , Mutagenesis
11.
Ann Ital Chir ; 74(3): 319-26, 2003.
Article in English | MEDLINE | ID: mdl-14677289

ABSTRACT

BACKGROUND AND AIMS: Improved medical therapy and bowel sparing and sphincter saving techniques have changed surgery for UC and CD. Collaboration between gastroenterologists and surgeons is necessary to uniform the indications for surgical treatment reducing emergency operations. GISMII multicentric study aimed to show indications, timing and impact of surgery, through retrospective analysis of cases observed between 1992 to 1996. METHODS: Data were obtained by 16 departments of General Surgery. RESULTS: 102 UC and 376 CD patients were analyzed. In UC patients surgery was performed for failure of medical therapy in 54%, complications in 28.4%, cancer or dysplasia in 10% of cases, 83.3% elective procedures. 30.4% ileo-anal pouch, 30.4% total procto-colectomies with definitive ileostomies, 32.4% total colectomies with ileo-rectal anastomosis, 6.8% segmental resections, were performed. In CD patients surgery was performed in 21% for medical therapy failure, in 79% for complications. 53.4% of patients were submitted to 1 operation, 84% elective procedures. Reoperations were performed in 46.6% of patients, 70.3% elective procedures. In the first operation bowel resection was performed in 79.1%, stricturoplasty in 14.3%; in the subsequent operations bowel resection 62.8%, stricturoplasty 21.7%, increasing number of temporary or definitive ileo-stomies. CONCLUSIONS: Collaboration between gastroenterologists and surgeons is necessary to obtain optimal results, reducing the incidence of emergency surgery, and complications. The short period observed between diagnosis and operation (21.4 months) is due to the increasing tendency of gastroenterologists to anticipate a surgical procedure when young patients with a chronic disease need a prolonged medical therapy.


Subject(s)
Inflammatory Bowel Diseases/surgery , Adolescent , Adult , Anastomosis, Surgical/statistics & numerical data , Colectomy/statistics & numerical data , Colonic Pouches/statistics & numerical data , Female , Hospitals, General/statistics & numerical data , Humans , Ileostomy/statistics & numerical data , Intestinal Neoplasms/surgery , Italy/epidemiology , Male , Middle Aged , Patient Care Team , Postoperative Complications/epidemiology , Reoperation/statistics & numerical data , Retrospective Studies , Surgery Department, Hospital/statistics & numerical data
12.
Biochim Biophys Acta ; 1607(2-3): 153-60, 2003 Dec 08.
Article in English | MEDLINE | ID: mdl-14670605

ABSTRACT

Chlamydomonas reinhardtii cultures, deprived of inorganic sulfur, undergo dramatic changes during adaptation to the nutrient stress [Biotechnol. Bioeng. 78 (2002) 731]. When the capacity for Photosystem II (PSII) O(2) evolution decreases below that of respiration, the culture becomes anaerobic [Plant Physiol. 122 (2000) 127]. We demonstrate that (a) the photochemical activity of PSII, monitored by in situ fluorescence, also decreases slowly during the aerobic period; (b) at the exact time of anaerobiosis, the remaining PSII activity is rapidly down regulated; and (c) electron transfer from PSII to PSI abruptly decreases at that point. Shortly thereafter, the PSII photochemical activity is partially restored, and H(2) production starts. Hydrogen production, which lasts for 3-4 days, is catalyzed by an anaerobically induced, reversible hydrogenase. While most of the reductants used directly for H(2) gas photoproduction come from water, the remaining electrons must come from endogenous substrate degradation through the NAD(P)H plastoquinone (PQ) oxido-reductase pathway. We propose that the induced hydrogenase activity provides a sink for electrons in the absence of other alternative pathways, and its operation allows the partial oxidation of intermediate photosynthetic carriers, including the PQ pool, between PSII and PSI. We conclude that the reduced state of this pool, which controls PSII photochemical activity, is one of the main factors regulating H(2) production under sulfur-deprived conditions. Residual O(2) evolved under these conditions is probably consumed mostly by the aerobic oxidation of storage products linked to mitochondrial respiratory processes involving both the cytochrome oxidase and the alternative oxidase. These functions maintain the intracellular anaerobic conditions required to keep the hydrogenase enzyme in the active, induced form.


Subject(s)
Chlamydomonas reinhardtii/metabolism , Hydrogen/metabolism , Oxygen/metabolism , Photosystem II Protein Complex/metabolism , Sulfur/metabolism , Animals , Chlorophyll/chemistry , Kinetics , Spectrometry, Fluorescence , Sulfur/deficiency
14.
Ann Ital Chir ; 74(5): 543-6, 2003.
Article in Italian | MEDLINE | ID: mdl-15139710

ABSTRACT

BACKGROUND AND AIMS: The mortality in severe episodes of ulcerative colitis (UC) has been reduced from 31-61% in the 1950 to 1-3%. Nevertheless it remains high in non specialist centers. Simple criteria are necessary to predict the outcome of severe ulcerative colitis. METHODS: 14 patients hospitalized for severe disease (Truelove and Witts criteria) from 1996 to 2000 were retrospectively analyzed. Patients were divided into two groups: 1. Group A: patients with severe disease surgically treated. 2. Group B: patients with severe disease responders to medical therapy Sex, age, length of steroids medical therapy, fever, stool frequency, CRP, ESR, haemoglobinemia, leukocytes, serum albumin values in the three days before the operation or during the hospitalization were collected. RESULTS: Total colectomy with ileostomy was necessary in 8 patients (57.1%), while 6 patients (42.90%) were responders to medical therapy. No perioperative mortality was recorded. Stool frequency, CRP, ESR, haemoglobinemia, serum albumin were significantly related to surgical operation. CONCLUSIONS: 1. No uniform criteria off severe attacks, are clearly defined in Literature. 2. The length of pre-operative medical therapy has a tendency to be too high (in our series 19 + 8.2 days). 3. Stool frequency, CRP, ESR, haemoglobinemia, serum albumin were significantly modified in operated patients.


Subject(s)
Colectomy , Colitis, Ulcerative/surgery , Adult , Colitis, Ulcerative/diagnosis , Data Interpretation, Statistical , Emergencies , Female , Humans , Ileostomy , Male , Middle Aged , Retrospective Studies
15.
Ann Ital Chir ; 74(6): 681-5, 2003.
Article in Italian | MEDLINE | ID: mdl-15206810

ABSTRACT

BACKGROUND AND AIMS: vertical banded gastroplasty (GPV) is the most frequently performed restrictive procedure for morbid obesity, but long-term follow-up is almost nonexistent. A poor outcome after GPV and a low quality of life has been reported. The aim of the study was to determine long-term outcome after 5 years follow-up. METHODS: 225 GPV were performed from 1995 to 2002. Patients were followed every month in the first three months, after 6 and 12 months, and subsequently every year. RESULTS: No mortality was observed. One gastric fistula, treated with medical therapy, was the single related complication observed. Vomiting occurred in 21.2% of patients. After 2 years 74.5% of patients had a BMI < 35, with a decrease of IEW = 50% (IEW% L 54.1%, 56.4%, and 57.1% after 12, 24 and 60 months, respectively). After 5 years, the results were unsatisfactory in 17.1% of patients; 8 patients underwent bariatric re-operation with good results. CONCLUSIONS: GPV represents a safe procedure with a low incidence of complications, with poor results in 17.1% of patients. Pre-operative identification of non responders is achievable with "BIB test". In the responders significant dietary changes are complained.


Subject(s)
Gastroplasty/methods , Adult , Algorithms , Female , Follow-Up Studies , Humans , Male , Postoperative Complications/epidemiology
16.
Pathologica ; 94(5): 234-7, 2002 Oct.
Article in Italian | MEDLINE | ID: mdl-12417970

ABSTRACT

We described the morphological, histochemical and immunohistochemical findings of a polyp detected in the left colon (splenic flexure) in which the diagnosis was atypical hyperplastic polyp. The description is focused on the capability of a hyperplastic polyp to evolve into adenomatous tissue through different modalities.


Subject(s)
Adenoma/pathology , Colon/pathology , Colonic Neoplasms/pathology , Colonic Polyps/pathology , Intestinal Mucosa/pathology , Adenoma/chemistry , Biomarkers, Tumor/analysis , Colon/metabolism , Colonic Neoplasms/chemistry , Colonic Polyps/chemistry , Disease Progression , Humans , Hyperplasia , Intermediate Filament Proteins/analysis , Intestinal Mucosa/metabolism , Keratin-20 , Ki-67 Antigen/analysis , Male , Middle Aged , Proto-Oncogene Proteins c-bcl-2/analysis , Tumor Suppressor Protein p53/analysis
17.
Ann Ital Chir ; 73(2): 155-8; discussion 158-9, 2002.
Article in Italian | MEDLINE | ID: mdl-12197289

ABSTRACT

BACKGROUND AND AIMS: Epidemiological studies have shown that ulcerative proctitis represents 25-55% of ulcerative colitis. In western countries, the incidence of ulcerative proctitis has been increased, while the incidence of more extensive colitis remained unchanged. Compared with extensive ulcerative colitis, the idiopathic proctitis seems to be a benign disease, with an extension to proximal segments in less than 30% of cases, low surgical and cancer risk. On the basis of epidemiological studies, not confirmed by endoscopic and histological features, it has been hypothesized that ulcerative colitis and proctitis could represent two different clinical entities. The aim of the study was to evaluate some clinical and demographic features related to the two different localizations, colitis and proctitis, in the attempt to clarify the above mentioned issues. METHODS: Demographic data of 156 patients observed in our institution from 1982 to 1999, were retrospectively analysed. Diagnosis, extension and severity of ulcerative procto-colitis were based on endoscopic and histological criteria. Local and systemic symptoms, extraintestinal manifestations, surgical and cancer risk, were also recorded. RESULTS AND CONCLUSIONS: Ulcerative proctitis has shown to be a benign disease, with a prevalence of local symptoms, less systemic and extraintestinal manifestations, and low endoscopic grades of activity. Furthermore no surgical intervention and cancer development were recorded. Extension to proximal segments was observed in 10.25% of cases. Young age of onset of symptoms,-smoking and appendectomy were associated to an higher risk of extension of the disease.


Subject(s)
Colitis, Ulcerative/epidemiology , Proctitis/epidemiology , Adolescent , Adult , Age Factors , Aged , Analysis of Variance , Appendectomy/adverse effects , Child , Colitis, Ulcerative/diagnosis , Diagnosis, Differential , Female , Follow-Up Studies , Humans , Incidence , Italy/epidemiology , Male , Middle Aged , Prevalence , Proctitis/diagnosis , Retrospective Studies , Risk Factors , Sex Factors , Smoking/adverse effects , Time Factors
18.
Ann Ital Chir ; 72(2): 221-5, 2001.
Article in English | MEDLINE | ID: mdl-11552478

ABSTRACT

Our previous experimental data demonstrated that a new gastrin receptor antagonist (CR2945) has a chemopreventive effect on dimethylhydrazine-induced colon cancer in mice. The aim of this study is to test the effect of CR2945 on the appearance and distribution of aberrant crypt foci (ACF), proposed as early "preneoplastic" lesions in colon carcinogenesis, in the murine model. 176 CD1 male mice were randomly divided into 4 groups: group 1, sham group received 2 daily intra-peritoneal injections of saline solution; group 2 received 1 weekly intra-peritoneal injection of DMH 20 mg/kg, for 5 weeks, and 2 daily intra-peritoneal injections of equal volume of NaCl 0.9%; group 3 and 4 received the same weekly dose of DMH and 2 daily injections of CR2945 at the respective doses of 2.5 and 7.5 mg/Kg for 5 weeks. The rodents were sacrified 15, 20, 25, and 38 weeks after receiving the first injection. The number of ACF per area (ACF frequency), their multiplicity (number of crypts per focus), ACF frequency according to each colonic site were recorded. No ACF were found in the sham group. No substantial differences were observed in ACF distribution between the remaining groups. Our hypothesis is that CR2945 does not alter the final number of ACF but might induce a regression of some dysplastic ACF.


Subject(s)
Benzodiazepines/pharmacology , Colon/pathology , Receptors, Cholecystokinin/antagonists & inhibitors , 1,2-Dimethylhydrazine , Animals , Carcinogens , Colon/drug effects , Colonic Neoplasms/pathology , Male , Mice
19.
J Neurosci Res ; 65(2): 111-20, 2001 Jul 15.
Article in English | MEDLINE | ID: mdl-11438980

ABSTRACT

The secretory capabilities of the serotonergic neuron C1 of cerebral ganglion of Helix pomatia were markedly reduced when it was cultured in contact with the wrong target neuron, C3. When the neuron B2, one of its physiological targets, was micromanipulated within the network made of intermingled neurites originating from the axonal stumps of both C1 and C3 neurons, C1 increased the amount of the evoked transmitter release, which, after 30 min, reached the level observed when cocultured with the appropriate target. The removal of the appropriate target brought C1 back to the low release condition. By imaging C1 neurites with a fluorescent dye, morphological changes involving a local increase in the number of varicosities could be observed as early as 30 min after contact with the appropriate target. Monoclonal antibody 4E8 against apCAM, a family of Aplysia adhesion molecules, recognizes apCAM-like molecules of the Helix central nervous system on immunocytochemistry and Western blot analysis. The contact with the appropriate target previously incubated in a 4E8 solution, which did not interfere with its capacity to respond to serotonin, failed to increase the transmitter release of C1 cocultured in the presence of the wrong target, C3. These results suggest that the apCAM-like antigens bound to the target membrane participate in the molecular processes responsible for the assembly of the "release machinery" present in the functional presynaptic structure.


Subject(s)
Cell Adhesion Molecules, Neuronal/metabolism , Central Nervous System/embryology , Ganglia, Invertebrate/embryology , Helix, Snails/embryology , Neurotransmitter Agents/metabolism , Presynaptic Terminals/metabolism , Synaptic Membranes/metabolism , Animals , Cell Adhesion Molecules, Neuronal/immunology , Cell Communication/physiology , Cell Differentiation/physiology , Cells, Cultured , Central Nervous System/cytology , Central Nervous System/metabolism , Ganglia, Invertebrate/cytology , Ganglia, Invertebrate/metabolism , Helix, Snails/cytology , Helix, Snails/metabolism , Membrane Potentials/physiology , Nerve Net/cytology , Nerve Net/embryology , Nerve Net/metabolism , Neural Inhibition/physiology , Neurites/metabolism , Neurites/ultrastructure , Presynaptic Terminals/ultrastructure , Serotonin/metabolism , Synaptic Membranes/ultrastructure
20.
Neuroscience ; 104(1): 271-80, 2001.
Article in English | MEDLINE | ID: mdl-11311549

ABSTRACT

The contact with the postsynaptic target induces structural and functional modifications in the serotonergic cell C1 of Helix pomatia. In previous studies we have found that the presence of a non-physiological target down-regulates the number of presynaptic varicosities formed by cultured C1 neurons and has a strong inhibitory effect on the action potential-evoked Ca(2+) influx and neurotransmitter release at C1 terminals. Since a large body of experimental evidence implicates the synapsins in the development and functional maturation of synaptic connections, we have investigated whether the injection of exogenous synapsin I into the presynaptic neuron C1 could affect the inhibitory effect of the wrong target on neurotransmitter release. C1 neurons were cultured with the wrong target neuron C3 for three to five days and then injected with either dephosphorylated or Ca(2+)/calmodulin-dependent protein kinase II-phosphorylated Cy3-labeled synapsin I. The subcellular distribution of exogenous synapsin I, followed by fluorescence videomicroscopy, revealed that only synapsin I phosphorylated by Ca(2+)/calmodulin-dependent protein kinase II diffused in the cytoplasm and reached the terminal arborizations of the axon, while the dephosphorylated form did not diffuse beyond the cell body. Evoked neurotransmitter release was measured during C1 stimulation using a freshly dissociated neuron B2 (sniffer) micromanipulated in close contact with the terminals of C1. A three-fold increase in the amplitude of the sniffer depolarization with respect to the pre-injection amplitude (190+/-29% increase, n=10, P<0.006) was found 5 min after injection of Ca(2+)/calmodulin-dependent protein kinase II-phosphorylated synapsin I that lasted for about 30 min. No significant change was observed after injection of buffer or dephosphorylated synapsin I. These data indicate that the presence of synapsin I induces a fast increase in neurotransmitter release that overcomes the inhibitory effect of the non-physiological target and suggest that the expression of synapsins may play a role in the modulation of synaptic strength and neural connectivity.


Subject(s)
Cell Communication/physiology , Ganglia, Invertebrate/growth & development , Helix, Snails/growth & development , Neural Pathways/growth & development , Neurotransmitter Agents/metabolism , Presynaptic Terminals/metabolism , Synapsins/metabolism , Actins/drug effects , Actins/metabolism , Animals , Calcium-Calmodulin-Dependent Protein Kinases/metabolism , Carbocyanines/pharmacokinetics , Cell Communication/drug effects , Cells, Cultured/cytology , Cells, Cultured/drug effects , Cells, Cultured/metabolism , Fluorescent Antibody Technique , Ganglia, Invertebrate/cytology , Ganglia, Invertebrate/metabolism , Helix, Snails/cytology , Helix, Snails/metabolism , Intracellular Fluid/drug effects , Intracellular Fluid/metabolism , Models, Animal , Neural Pathways/drug effects , Neural Pathways/metabolism , Phosphorylation/drug effects , Presynaptic Terminals/drug effects , Serotonin/metabolism , Synapsins/pharmacology , Synaptic Vesicles/drug effects , Synaptic Vesicles/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...