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1.
Allergy ; 70(8): 1013-9, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25913298

ABSTRACT

BACKGROUND: An increasing number of patients show immediate selective hypersensitivity reactions to clavulanic acid (CLV) and amoxicillin (AX), probably due to their increased prescription. The maintenance of this response should be established. OBJECTIVE: To assess that the immediate hypersensitivity selective response to AX or to CLV is maintained after repeated administration of penicillin G (PG)/penicillin V (PV) and AX. METHODS: Patients with proven immediate hypersensitivity to AX (Group A) or CLV (Group B) were included. Diagnosis was performed using skin tests with major and minor determinants of PG (PPL/MDM), AX and CLV and by drug provocation test (DPT) if required. Selectivity was established by confirming tolerance to PG/PV (Group A) and to PG/PV and AX (Group B). The maintenance of the selective response was verified by repeating DPT, 15 days after the initial investigation, with the same procedure. RESULTS: Of 51 patients, 78% belonged to Group A and 22% to Group B. Most had anaphylaxis. In Group A, 72% were skin test positive; 28% required DPT. In Group B, 63% were skin test positive; 37% required DPT. Only two AX-selective cases developed positive responses after re-provocation with PG/PV. No cases selective for CLV developed a positive response to PG, PV or AX. DISCUSSION: The selective response to AX appears consistent, and a response to penicillin determinants only develops in a minority of cases. For the case of CLV, the selective response appears not to be modified by exposure to penicillin determinants, meaning that patients with CLV allergy can take penicillin derivatives safely.


Subject(s)
Amoxicillin/adverse effects , Clavulanic Acid/adverse effects , Drug Hypersensitivity/etiology , Hypersensitivity, Immediate/epidemiology , Penicillin G/immunology , Adolescent , Adult , Age Distribution , Aged , Amoxicillin/immunology , Chi-Square Distribution , Clavulanic Acid/immunology , Cohort Studies , Drug Hypersensitivity/diagnosis , Drug Hypersensitivity/epidemiology , Female , Humans , Hypersensitivity, Immediate/diagnosis , Hypersensitivity, Immediate/etiology , Incidence , Male , Middle Aged , Prospective Studies , Risk Assessment , Sex Distribution , Skin Tests , Young Adult
2.
Minerva Endocrinol ; 37(4): 315-27, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23235188

ABSTRACT

Thyroid hormone (TH) is a pleiotropic agent that has widespread biological functions, i.e., it controls cellular growth, tissue development and homeostasis and neoplastic transformation. Suitable TH levels are critical for the development of various types of tissues and are essential for the regulation of metabolic processes throughout life. The serum concentrations of TH affect its biological activity. Moreover, at tissue level, TH action is regulated by the expression and activity of deiodinases, i.e., the enzymes that mediate the metabolic pathways by activating and/or inactivating TH. The type I and II deiodinases (D1 and D2) initiate TH action by converting thyroxine (T4) into the active TH form (T3), whereas type III deiodinase (D3) mediates the local attenuation of TH by converting T4 and T3 into the inactive metabolites rT3 and T2, respectively. The deiodinase system is a potent mechanism of pre-receptoral control of TH action; it is often altered in such pathological conditions as cancer. D3 is widely expressed in embryonic tissues and in placenta, where it blocks excessive maternal-to-fetal transfer of TH. In contrast, during late neonatal and adult life, D3 is expressed mainly in the central nervous system and skin. Interestingly, D3 expression is re-activated in various types of human cancers. Here we review recent evidence that D3 expression plays a crucial role in human carcinogenesis, and speculate as to its complex role in the regulation of cell proliferation in several neoplastic contexts. It is conceivable that the local modulation of TH action via deiodinases is a powerful molecular tool to manipulate the intracellular TH status, thus influencing the growth and maintenance of selected hormone-dependent cancers.


Subject(s)
Iodide Peroxidase/physiology , Neoplasm Proteins/physiology , Neoplasms/enzymology , Cell Division/physiology , Cell Transformation, Neoplastic , Enzyme Activation , Enzyme Induction , Gene Expression Regulation, Neoplastic , Humans , Hypothyroidism/etiology , Hypothyroidism/physiopathology , Iodide Peroxidase/genetics , Molecular Targeted Therapy , Neoplasms/complications , Neoplasms/drug therapy , Neoplasms/pathology , Neoplasms, Hormone-Dependent/enzymology , Neoplasms, Hormone-Dependent/pathology , Organ Specificity , Subcellular Fractions/enzymology , Thyroxine/metabolism , Triiodothyronine/metabolism , Triiodothyronine, Reverse/biosynthesis
4.
G Chir ; 28(3): 73-81, 2007 Mar.
Article in Italian | MEDLINE | ID: mdl-17419903

ABSTRACT

Primary adenocarcinoma of the appendix is a rare malignancy that constitutes less than 0.5% of all gastrointestinal neoplasms. Usually the diagnosis is made only after histological examination of surgically removed inflamed appendix. Alternatively represent an unexpected finding, confirmed by frozen section, during surgery performed for acute appendicitis or other non appendiceal pathologies. Natural history is strongly influenced by anatomic peculiarities of the appendix that predispose to early spread and perforation. Frequently is associated with synchronous and metachronous colorectal or extraintestinal cancers. The correct management is the right hemicolectomy as a primary procedure in the case of preoperatively or intraoperatively diagnosis or as secondary procedure, after two-three weeks from appendectomy, when the microscopic examination of specimen reveals the presence of adenocarcinoma. Right hemicolectomy is the best treatment for all histologic types (colonic, mucinous, adenocarcinoid), in presence of perforation and even in Dukes A tumors. A careful intraoperative search for synchronous lesions and a life-long program of surveillance for the detection of early stage metachronous carcinomas are recommended. The Authors report a case of primary adenocarcinoma of the appendix occurred in a 78 year-old female patient, diagnosed incidentally during surgery performed for ileus from suspected cecal neoplasm.


Subject(s)
Appendiceal Neoplasms , Carcinoma, Signet Ring Cell , Aged , Appendiceal Neoplasms/diagnostic imaging , Appendiceal Neoplasms/surgery , Carcinoma, Signet Ring Cell/diagnostic imaging , Carcinoma, Signet Ring Cell/surgery , Female , Humans , Radiography
5.
G Chir ; 27(1-2): 15-20, 2006.
Article in Italian | MEDLINE | ID: mdl-16608627

ABSTRACT

Colovesical fistulas represent a possible less frequent complication of diverticular disease of colon. They represent a complex condition because of the possible and unexpected evolution into a septic shock with a high risk of death. The Authors report three cases of colovesical fistula as a complication of diverticular disease. They underline the importance of early diagnosis, specific antibiotic therapy and appropriate surgical therapy realized in one or two stages according to general and local conditions of each patient.


Subject(s)
Diverticulitis, Colonic/complications , Intestinal Fistula/etiology , Aged , Colon, Sigmoid/surgery , Diverticulitis, Colonic/diagnosis , Diverticulitis, Colonic/surgery , Humans , Intestinal Fistula/diagnosis , Intestinal Fistula/surgery , Laparoscopy , Male , Middle Aged , Treatment Outcome
6.
Diabetes ; 50(3): 667-74, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11246889

ABSTRACT

Impaired wound healing is a well-documented phenomenon in experimental and clinical diabetes. Experimental evidence suggests that a defect in vascular endothelial growth factor (VEGF) regulation might be associated with wound-healing disorders. We studied the involvement of lipid peroxidation in the pathogenesis of altered VEGF expression in diabetes-related healing deficit by using an incisional skin-wound model produced on the back of female diabetic C57BL/KsJ db+/ db+ mice and their normal (db+/+m) littermates. Animals were then randomized to the following treatment: raxofelast (15 mg.kg(-1).day(-1) i.p.), an inhibitor of lipid peroxidation, or its vehicle (DMSO/NaCl 0.9%, 1:1 vol: vol). The animals were killed on different days (3, 6, and 12 days after skin injury), and the wounded skin tissues were used for histological evaluation, for analysis of conjugated dienes (CDs), as an index of lipid peroxidation and wound breaking strength. Furthermore, we studied the time course of VEGF mRNA expression throughout the skin-repair process (3, 6, and 12 days after skin injury), by means of reverse transcriptase-polymerase chain reaction, as well as the mature protein in the wounds. Diabetic mice showed impaired wound healing with delayed angiogenesis, low breaking strength, and increased wound CD content when compared with their normal littermates. In healthy control mice, a strong induction of VEGF mRNA was found between day 3 and day 6 after injury, while no significant VEGF mRNA expression was observed at day 12 after injury. In contrast, VEGF mRNA levels, after an initial increase (day 3), were significantly lower in diabetic mice than in normal littermates, and light induction of VEGF mRNA expression was also present at day 12 after injury. Similarly, the wound content of the angiogenic factor was markedly changed in diabetic mice. Administration of raxofelast did not modify the process of wound repair in normal mice, but significantly improved the impaired wound healing in diabetic mice through the stimulation of angiogenesis, re-epithelization, and synthesis and maturation of extracellular matrix. Moreover, raxofelast treatment significantly reduced wound CD levels and increased the breaking strength of the wound. Lastly, the inhibition of lipid peroxidation restored the defect in VEGF expression during the process of skin repair in diabetic mice and normalized the VEGF wound content. The current study provides evidence that lipid peroxidation inhibition restores wound healing to nearly normal levels in experimental diabetes-impaired wounds and normalizes the defect in VEGF regulation associated with diabetes-induced skin-repair disorders.


Subject(s)
Benzofurans/pharmacology , Diabetes Mellitus/physiopathology , Endothelial Growth Factors/metabolism , Lipid Peroxides/antagonists & inhibitors , Lymphokines/metabolism , Neovascularization, Physiologic/physiology , Vitamin E/analogs & derivatives , Vitamin E/pharmacology , Wound Healing/physiology , Animals , Diabetes Mellitus/genetics , Female , Mice , Mice, Inbred C57BL , Skin/injuries , Tensile Strength , Vascular Endothelial Growth Factor A , Vascular Endothelial Growth Factors , Wounds and Injuries/pathology , Wounds and Injuries/physiopathology
7.
J Gen Physiol ; 114(3): 377-92, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10469728

ABSTRACT

In voltage- and cyclic nucleotide-gated ion channels, the amino-acid loop that connects the S5 and S6 transmembrane domains, is a major component of the channel pore. It determines ion selectivity and participates in gating. In the alpha subunit of cyclic nucleotide-gated channels from bovine rod, the pore loop is formed by the residues R345-S371, here called R1-S27. These 24 residues were mutated one by one into a cysteine. Mutant channels were expressed in Xenopus laevis oocytes and currents were recorded from excised membrane patches. The accessibility of the substituted cysteines from both sides of the plasma membrane was tested with the thiol-specific reagents 2-aminoethyl methanethiosulfonate (MTSEA) and [2-(trimethylammonium)ethyl]methanethiosulfonate (MTSET). Residues V4C, T20C, and P22C were accessible to MTSET only from the external side of the plasma membrane, and to MTSEA from both sides of the plasma membrane. The effect of MTSEA applied to the inner side of T20C and P22C was prevented by adding 10 mM cysteine to the external side of the plasma membrane. W9C was accessible to MTSET from the internal side only. L7C residue was accessible to internal MTSET, but the inhibition was partial, approximately 50% when the MTS compound was applied in the absence of cGMP and 25% when it was applied in the presence of cGMP, suggesting that this residue is not located inside the pore lumen and that it changes its position during gating. Currents from T15C and T16C mutants were rapidly potentiated by intracellular MTSET. In T16C, a slower partial inhibition took place after the initial potentiation. Current from I17C progressively decayed in inside-out patches. The rundown was accelerated by inwardly applied MTSET. The accessibility results of MTSET indicate a well-defined topology of the channel pore in which residues between L7 and I17 are inwardly accessible, residue G18 and E19 form the narrowest section of the pore, and T20, P21, P22 and V4 are outwardly accessible.


Subject(s)
Cysteine/genetics , Cysteine/physiology , Genes, Reporter/physiology , Ion Channel Gating/physiology , Ion Channels/physiology , Nucleotides, Cyclic/physiology , Amino Acid Sequence , Animals , Cell Membrane/drug effects , Cell Membrane/metabolism , Ethyl Methanesulfonate/analogs & derivatives , Ethyl Methanesulfonate/pharmacology , Genes, Reporter/genetics , Ion Channel Gating/genetics , Ion Channels/genetics , Membrane Potentials/physiology , Mesylates/pharmacology , Molecular Sequence Data , Mutagenesis/genetics , Mutagenesis/physiology , Oocytes/metabolism , Patch-Clamp Techniques , Xenopus laevis
8.
FEBS Lett ; 477(1-2): 37-42, 2000 Jul 14.
Article in English | MEDLINE | ID: mdl-10899307

ABSTRACT

Molecular dynamics simulations and electrostatic modeling are used to investigate structural and dynamical properties of the potassium ions and of water molecules inside the KcsA channel immersed in a membrane-mimetic environment. Two potassium ions, initially located in the selectivity filter binding sites, maintain their position during 2 ns of dynamics. A third potassium ion is very mobile in the water-filled cavity. The protein appears engineered so as to polarize water molecules inside the channel cavity. The resulting water induced dipole and the positively charged potassium ion within the cavity are the key ingredients for stabilizing the two K(+) ions in the binding sites. These two ions experience single file movements upon removal of the potassium in the cavity, confirming the role of the latter in ion transport through the channel.


Subject(s)
Potassium Channels/chemistry , Potassium Channels/metabolism , Potassium/metabolism , Streptomyces/chemistry , Water/metabolism , Bacterial Proteins/chemistry , Bacterial Proteins/metabolism , Binding Sites , Cations, Monovalent/metabolism , Computer Simulation , Models, Molecular , Motion , Protein Conformation , Static Electricity , Thermodynamics
9.
Rev Neurosci ; 10(3-4): 279-90, 1999.
Article in English | MEDLINE | ID: mdl-10526892

ABSTRACT

Properties of neural computation were studied in two types of neuronal networks: isolated leech ganglia and neuronal cultures of dissociated cortical neurons from neonatal rats. With appropriate experimental set-ups it was possible to obtain a precise description of the spread of excitation induced by specific inputs. The evoked spatio-temporal electrical activity was characterized by large variability and the electrical activity of neurons activated by the same stimulation was found to be statistically independent to a high degree. The variability presumably originates from basic properties of synaptic transmission, which is stochastic in nature. As a consequence, the large variability of the evoked spatio-temporal electrical activity appears to be a general property of neural computation and a typical feature of neuronal assemblies. It is shown, however, that the observed statistical independence of co-activated neurons may be used to reduce the effects of variability by appropriately averaging or pooling the electrical activity.


Subject(s)
Evoked Potentials/physiology , Nerve Net/physiology , Neurons/physiology , Synapses/physiology , Animals , Computational Biology , Rats , Time Factors
10.
Neuroscience ; 115(3): 723-9, 2002.
Article in English | MEDLINE | ID: mdl-12435411

ABSTRACT

In neuronal cells, excessive activation of glutamate receptors causes excitotoxic damage culminating in apoptotic and necrotic cell death. The molecular mechanism of excitotoxicity has been associated with excessive Ca(2+) influx and overload, triggering biochemical events that lead to cell death and tissue degeneration. Following mild insults via NMDA-receptor activation, central neurons undergo several biochemical modifications recognizable as early events in apoptotic machinery.Tissue transglutaminase, the most ubiquitous among cell transglutaminases, catalyzes the Ca(2+)-dependent protein cross-linking probably associated with morphological changes in several neurodegenerative disorders. The possible involvement of this enzyme in excitotoxicity-mediated events was investigated in primary cultures of cerebellar granule cells exposed for 30 min to NMDA (100 microM) in Locke's buffer. Under these conditions time-dependent increases in transglutaminase activity were observed. Tissue transglutaminase expression reached the highest levels within 3-4 h of NMDA exposure. Similarly, high levels of incorporation of fluorescent substrates were observed in living cells. Confocal laser microscopy analysis showed that fluorescein-labelled structures were distributed within the cytoplasm and close to the membranes of NMDA-exposed cells. These effects were dependent on the Ca(2+) influx triggered by the excitotoxic stimulus. Morphological changes in NMDA-treated cells gave evidence of significant cell damage which appeared within 5-6 h of NMDA exposure. These results suggest that increases in tissue transglutaminase may be associated to the effects of NMDA-induced excitotoxicity. Therefore, it is reasonable to hypothesize that if tissue transglutaminase levels and activity are up-regulated under such conditions, the protein cross-linking could be likely involved in excitotoxic response.


Subject(s)
Cerebellar Cortex/enzymology , Glutamic Acid/metabolism , Neurodegenerative Diseases/enzymology , Neurons/enzymology , Receptors, N-Methyl-D-Aspartate/metabolism , Transglutaminases/metabolism , Up-Regulation/physiology , Animals , Animals, Newborn , Calcium Signaling/drug effects , Calcium Signaling/physiology , Cells, Cultured , Cerebellar Cortex/drug effects , Cerebellar Cortex/physiopathology , Excitatory Amino Acid Antagonists/pharmacology , Membrane Potentials/drug effects , Membrane Potentials/physiology , N-Methylaspartate/pharmacology , Neurodegenerative Diseases/physiopathology , Neurons/drug effects , Neurotoxins/pharmacology , Rats , Rats, Wistar , Receptors, N-Methyl-D-Aspartate/agonists , Synaptic Transmission/drug effects , Synaptic Transmission/physiology , Transglutaminases/drug effects , Up-Regulation/drug effects
11.
Proc Biol Sci ; 250(1329): 209-15, 1992 Dec 22.
Article in English | MEDLINE | ID: mdl-1283637

ABSTRACT

We report that two types of cGMP-activated channel coexist in the photoreceptor plasma membrane, with the most commonly encountered class appearing broadly similar to the channel reported in previous patch-pipette experiments. However, we find that flickering of this channel between the open and closed states is so rapid that a discrete single-channel conductance cannot unequivocally be resolved; the occurrence of flickering is largely independent of membrane voltage and of the presence of cytoplasmic Ca2+ or Mg2+. In recordings from the inner segment we occasionally find a second class of cGMP-gated channel, with activity resembling that reported for cloned channels. This channel does not flicker, but instead exhibits distinct open-close transitions. Our results suggest that the predominant form of channel in vivo differs significantly from cloned channels, and that its gating properties are not as simple as reported previously.


Subject(s)
Cyclic GMP/pharmacology , Ion Channels/physiology , Photoreceptor Cells/physiology , Rod Cell Outer Segment/physiology , Ambystoma , Animals , Calcium/pharmacology , Cell Membrane/physiology , Ion Channel Gating/drug effects , Magnesium/pharmacology , Membrane Potentials/drug effects , Rod Cell Outer Segment/drug effects
12.
Proc Biol Sci ; 254(1339): 69-74, 1993 Oct 22.
Article in English | MEDLINE | ID: mdl-7505453

ABSTRACT

Single-channel properties of a cloned channel activated by cyclic GMP have been analysed. The mRNA encoding for the channel was injected into oocytes of Xenopus laevis and the current flowing through a single ionic channel activated by cGMP was studied in excised patches under voltage-clamp conditions. The ionic channel activated by cGMP had a single-channel conductance of 32 +/- 2 pS at +120 mV and 25 +/- 4 pS at -120 mV, and its conductance was not significantly affected by increasing the cGMP concentration from 20 microM to 200 microM. The single-channel currents in the presence of NH+4, Na+, K+, Li+ and Rb+ in the medium bathing the cytoplasmic side of the membrane at +140 mV were 5.3, 4.7, 3.8, 1.3 and 0.8 pA, respectively. The single-channel current in the presence of Cs+ was less than 0.5 pA. Ca2+ and Mg2+ (both 0.5 mM) in the presence of 100 microM cGMP did not appreciably affect the channel activity at membrane potentials more negative than -80 mV, whereas at +100 mV they reduced the single-channel conductance by about threefold. The ionic selectivity and the blockage by divalent cations of the native channel found in amphibian rods and in the cloned channel from bovine rods are quite similar. However, the cloned channel has well-resolved openings, especially at positive membrane voltages, whereas the native channel is characterized by a continuous flickering between the open and closed state.


Subject(s)
Cyclic GMP/pharmacology , Ion Channels/physiology , Oocytes/physiology , Retinal Rod Photoreceptor Cells/metabolism , Animals , Cations, Monovalent/pharmacology , Cattle , Chorionic Gonadotropin/pharmacology , Cyclic GMP/metabolism , Female , Humans , Ion Channel Gating/drug effects , Ion Channels/biosynthesis , Membrane Potentials/drug effects , Microinjections , Oocytes/drug effects , Probability , RNA, Messenger/administration & dosage , RNA, Messenger/metabolism , Xenopus laevis
13.
Surgery ; 129(4): 467-77, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11283539

ABSTRACT

BACKGROUND: Impaired wound healing is a well-documented phenomenon in experimental and clinical diabetes. Emerging evidence favors the involvement of free radicals in the pathogenesis of diabetes-related healing deficit. This study assessed the effect of systemic administration of raxofelast, a protective membrane antioxidant agent, on wound healing by using healing-impaired (db/db) mice. METHODS: The wound healing effect of raxofelast was investigated by using an incisional skin-wound model produced on the back of female diabetic C57BL/KsJ db+/db+ mice and their healthy littermates (db+/+m). Animals were then randomized to the following treatment: raxofelast (15 mg/kg/d intraperitoneally) or its vehicle (dimethyl sulfoxide/sodium chloride 0.9%, 1:1, vol/vol). The animals were killed on different days, and the wounded skin tissues were used for histologic evaluation and for analysis of malondialdehyde (MDA) level and myeloperoxidase (MPO) activity, wound breaking strength, and collagen content. RESULTS: Diabetic mice showed delayed wound healing together with low collagen content, breaking strength, and increased MDA levels and MPO activity when compared with their healthy littermates. The administration of raxofelast did not modify the process of wound repair in healthy (db/+) mice, but significantly improved impaired wound healing in diabetic mice through the stimulation of angiogenesis, reepithelialization, synthesis, and maturation of extracellular matrix. Furthermore, raxofelast treatment significantly reduced MDA levels, MPO activity, and increased the breaking strength and collagen content of the wound. CONCLUSIONS: The current study provides evidence that raxofelast restores wound healing to nearly normal levels in experimental diabetes-impaired wounds and suggests that an increased lipid peroxidation in diabetic mice may have a role in determining a defect of wound repair.


Subject(s)
Antioxidants/pharmacology , Benzofurans/pharmacology , Vitamin E/pharmacology , Wound Healing/drug effects , Animals , Diabetes Mellitus, Experimental/genetics , Diabetes Mellitus, Experimental/metabolism , Diabetes Mellitus, Experimental/physiopathology , Female , Hydroxyproline/metabolism , Malondialdehyde/metabolism , Mice , Mice, Inbred C57BL , Mice, Mutant Strains , Peroxidase/metabolism , Skin/drug effects , Skin/injuries , Skin/metabolism , Vitamin E/analogs & derivatives , Wound Healing/physiology
14.
J Neurosci Methods ; 110(1-2): 65-80, 2001 Sep 30.
Article in English | MEDLINE | ID: mdl-11564526

ABSTRACT

Muscle contraction is usually measured and characterized with force and displacement transducers. The contraction of muscle fibers, however, evokes in the tissue a two and even three-dimensional displacement field, which is not properly quantified by these transducers because they provide just a single scalar quantity. This problem can be circumvented by using optical measurements and standard tools of computer vision, developed for the analysis of time varying image sequences. By computing the so called optical flow, i.e. the apparent motion of points in a time varying image sequence, it is possible to recover a two-dimensional motion field, describing rather precisely the displacement caused by muscle contraction in a flattened piece of skin. The obtained two-dimensional optical flow can be further analyzed by computing its elementary deformation components, providing a novel and accurate characterization of the contraction induced by different motoneurons. This technique is demonstrated analyzing the displacement caused by muscle contraction in the skin of the leech, Hirudo medicinalis. The proposed technique can be applied to monitor and characterize all contractions in almost flat tissues with enough visual texture.


Subject(s)
Electronic Data Processing/methods , Image Processing, Computer-Assisted/methods , Microscopy, Video , Muscle Contraction/physiology , Neurophysiology/methods , Action Potentials/physiology , Algorithms , Animals , Biomechanical Phenomena , Electronic Data Processing/instrumentation , Image Processing, Computer-Assisted/instrumentation , Leeches/cytology , Leeches/physiology , Mechanoreceptors/cytology , Mechanoreceptors/physiology , Microscopy, Video/instrumentation , Microscopy, Video/methods , Models, Neurological , Motor Neurons/cytology , Motor Neurons/physiology , Nervous System/cytology , Nervous System/metabolism , Neurons, Afferent/cytology , Neurons, Afferent/physiology , Neurophysiology/instrumentation
15.
Am J Ophthalmol ; 115(6): 800-5, 1993 Jun 15.
Article in English | MEDLINE | ID: mdl-8506916

ABSTRACT

We assessed the usefulness of silver staining of nucleolar organizer regions in the diagnosis of pigmented conjunctival tumors. Fifty-one biopsy specimens were silver stained to identify the nucleolar organizer regions. Nineteen nevi without atypia, three nevi with atypia, eight primary acquired melanosis lesions, and 14 melanomas were studied. In each specimen, silver staining of the nucleolar organizer regions was counted in 100 cells to yield an average of the silver staining of the nucleolar organizer region count. The mean silver staining of the nucleolar organizer region counts per cell was correlated with the degree of malignancy of pigmented conjunctival lesions as follows: nevi, 3.0; primary acquired melanosis, 3.2; nevi with atypia, 3.9; primary acquired melanosis with atypia, 5.0; and melanoma, 5.7 (Spearman correlation [rS] = .83, P = .0001; analysis of variance [ANOVA] F test = 20.9, P = .0001). A cutoff value of 4.0 (mean silver staining of nucleolar organizer regions per cell) will differentiate melanoma and primary acquired melanosis with atypia from other lesions (sensitivity, 100%; specificity, 96%). The silver staining of nucleolar organizer regions is a useful adjunct in determining the malignancy of pigmented conjunctival tumors.


Subject(s)
Conjunctival Neoplasms/diagnosis , Nucleolus Organizer Region , Adolescent , Adult , Aged , Aged, 80 and over , Biopsy , Conjunctival Neoplasms/ultrastructure , Evaluation Studies as Topic , Female , Humans , Male , Melanoma/diagnosis , Melanoma/ultrastructure , Melanosis/diagnosis , Middle Aged , Nevus, Pigmented/diagnosis , Nevus, Pigmented/ultrastructure , Observer Variation , Predictive Value of Tests , Silver Staining
16.
Pathol Res Pract ; 197(6): 449-52, 2001.
Article in English | MEDLINE | ID: mdl-11432673

ABSTRACT

Primary adenocarcinoma of the larynx is a rare neoplasm that tends to spread to both regional lymph nodes and distant sites. A case of primary adenocarcinoma of the arytenoid in a 74-year-old man is presented. The tumor was evaluated by light and electron microscopy. A high percentage of intranuclear pseudoinclusions (more than 20% of the neoplastic cells) was a peculiar characteristic of the tumor. To the best of our knowledge, such a feature has not been reported previously and should be considered a hallmark of more aggressive behavior.


Subject(s)
Adenocarcinoma/ultrastructure , Arytenoid Cartilage/ultrastructure , Laryngeal Neoplasms/ultrastructure , Adenocarcinoma/radiotherapy , Aged , Cell Nucleus/ultrastructure , Humans , Inclusion Bodies/ultrastructure , Laryngeal Neoplasms/radiotherapy , Laryngoscopy , Magnetic Resonance Imaging , Male , Palliative Care
17.
Biosystems ; 48(1-3): 171-8, 1998.
Article in English | MEDLINE | ID: mdl-9886645

ABSTRACT

An important question in the analysis of the electrical activity of a large population of neurons is the detection of families of neurons having a similar pattern of electrical activity, so that the original neuronal network can be decomposed into distinct clusters. This paper describes how it is possible to segment the activity of a neuronal network into clusters of sites with similar patterns of activity. Such a segmentation gives insight on how the network is organized, on how it functions and on its behavior as a dynamical system. Simulation and experiments on real data suggest that the correct approach to solve these problems must use multiresolution analysis. The method has been applied to both synthetic data and real data coming from a network of dissociated cortical neurons from neonatal rat brain.


Subject(s)
Nerve Net , Action Potentials , Animals , Neurons/physiology , Rats
18.
IEEE Trans Pattern Anal Mach Intell ; 8(2): 147-63, 1986 Feb.
Article in English | MEDLINE | ID: mdl-21869334

ABSTRACT

Edge detection is the process that attempts to characterize the intensity changes in the image in terms of the physical processes that have originated them. A critical, intermediate goal of edge detection is the detection and characterization of significant intensity changes. This paper discusses this part of the edge detection problem. To characterize the types of intensity changes derivatives of different types, and possibly different scales, are needed. Thus, we consider this part of edge detection as a problem in numerical differentiation. We show that numerical differentiation of images is an ill-posed problem in the sense of Hadamard. Differentiation needs to be regularized by a regularizing filtering operation before differentiation. This shows that this part of edge detection consists of two steps, a filtering step and a differentiation step. Following this perspective, the paper discusses in detail the following theoretical aspects of edge detection. 1) The properties of different types of filters-with minimal uncertainty, with a bandpass spectrum, and with limited support-are derived. Minimal uncertainty filters optimize a tradeoff between computational efficiency and regularizing properties. 2) Relationships among several 2-D differential operators are established. In particular, we characterize the relation between the Laplacian and the second directional derivative along the gradient. Zero crossings of the Laplacian are not the only features computed in early vision. 3) Geometrical and topological properties of the zero crossings of differential operators are studied in terms of transversality and Morse theory.

19.
Acta Otorhinolaryngol Ital ; 20(1): 40-6, 2000 Feb.
Article in Italian | MEDLINE | ID: mdl-10885154

ABSTRACT

This study examined 71 pediatric tonsillectomy patients through accurate case history and clinical examination, placing particular emphasis on pathologies concomitant to tonsillopathy. In an attempt to find anatomo-clinical correlations, these data were processed together with the results of a histomorphological study of thetonsil epithelium, performed on all tonsillectomy samples. The majority of these patients were females and none more than 13 years of age. Numerous pathologies were found associated with the tonsillopathy and in varying combinations, first and foremost of which was adenoid hypertrophy. Only approximately one fifth of the patients did not show any concomitant pathology of note. All patients presented a history of recurrent pharyngotonsillitis (at least 4 episodes a year) with symptoms arising from 1 to 10 years prior to surgery. The concomitant pathologies included: respiratory, cutaneous and food allergies, asthma, obstructive sleep apnea, rheumatic diseases, etc. From the histomorphological point of view, particular modifications were found in the follicle epithelium and interstitial cells of the palatine tonsil. An exasperated fibrotic interstitial reaction and chronic duration of the disease appeared to prevent tonsil filter function, facilitating chronicization of the tonsillopathy or onset of recurrent infections and concomitant allergies. In the allergic patients the tonsil epithelium was thickened and compact and showed various degrees of chorion edema, in agreement with what is found in the literature. On the contrary, few morphostructural palatine tonsil mutations were found in those subjects which did not present any concomitant pathology or were affected by tonsillopathy of brief duration. All the histomorphological modifications encountered appear related to the individual patient history, confirming the hypothesis that tonsil epithelium can not only condition the evolution of tonsillopathy--reflecting the effect of various factors--but, above all, it directs the immune response, thus playing a role in the development of various concomitant pathologies.


Subject(s)
Palatine Tonsil/pathology , Tonsillitis/pathology , Adolescent , Child , Child, Preschool , Female , Humans , Male , Tonsillectomy/methods , Tonsillitis/surgery
20.
Acta Otorhinolaryngol Ital ; 20(5): 347-53, 2000 Oct.
Article in Italian | MEDLINE | ID: mdl-11284263

ABSTRACT

For poorly differentiated rhinopharyngeal carcinomas, the clinical presentation (association with the Epstein-Barr virus, paraneoplastic syndromes, onset of lymphoma) and the histopathological features can be polymorphous and they can confound or delay diagnosis and preparation of an adequate treatment plan (radio-chemotherapy). Often these neoplasms arise as clinically primitive laterocervical metastases, masked by clinical findings and a history that can lead to the mistaken diagnosis of systemic lymphoproliferative processes such as Hodgkin's disease. Here an observation of this type is presented in a young patient (19 years old) who came under observation for a laterocervical tumefaction recurrent from a previous exeresis performed at another hospital and symptoms of serotine febricula, dysphagia and serology positive for the Epstein-Barr virus (EBV). The patient underwent surgery and then radiotherapy and has been under close post-operative follow-up for two years. To date the patient's condition--both local and general--is good. The particular histology of the neoformation lies in the abundant infiltration of plasma cell and lymphocyte eosinophils, at times in blastic form. Moreover, elements with a large clear nucleus and evident nucleolus (Hodgkin-like) and scattered multinucleate Langhans-type giant cells can be seen. Immunohistologically the tumor cells markedly express for cytokeratin and the latent membrane protein (LMP1) of the Epstein-Barr virus (EBV) and show a high growth fraction. Under the electron microscope, the plurinucleate giant cells present large nuclei with morphology similar to that of tumor cells. The clear cytokeratin-positivity of the tumor elements and the histological and ultrastructural features mentioned led to the diagnosis of a massive metastasis from lymphoepithelial carcinoma, the Schmincke variant, plus EBV infection of the neoplastic cells. The authors conclude assuming that the particular granulomatous reaction is due to the host's reaction to the tumor cells, but also to the reaction to the viral antigens. In the former case we find an attempt to limit the carcinomatous process; in the latter it is a response caused by the EBV and is not, apparently, aimed at protecting against the neoplasm rather it facilitates the neoplastic process.


Subject(s)
Carcinoma, Squamous Cell/virology , Epstein-Barr Virus Infections/complications , Nasopharyngeal Neoplasms/virology , Adult , Carcinoma, Squamous Cell/diagnosis , Female , Humans , Nasopharyngeal Neoplasms/diagnosis
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