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1.
Tissue Cell ; 65: 101350, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32746994

ABSTRACT

This study aims to provide a histological description of different regions of the gastric and duodenal mucosa in Rhesus monkey, as well as to analyze the distribution and the relative frequency of 5-HT. The cardia region mucosa consists of simple columnar epithelium PAS + and AB + and the 5-HT cells were observed at the base of the gland (QA [5-HT cells]/mm²) = 8.72 ±â€¯4.98). The body region, has a smaller number of glands. The 5-HT cells were found predominant in the base of the gastric glands. QA= 6.96 ±â€¯3.81. When compared to body region, the stomach fundus has smaller gastric pits. The 5-HT cells are found at the base of the glands near the main cells. QA = 5.29 ±â€¯2.09. The pylorus region was found to have deep pits and well-developed gastric glands. The 5-HT cells are scarce, at the base of the pyloric gland. QA = 1.18 ±â€¯1.36. The duodenum presented goblet cells strong PAS + and AB +. 5-HT cells were found both in the lining epithelium and in the intestinal glands. QA = 8.16 ±â€¯2.59.


Subject(s)
Duodenum/metabolism , Serotonin/metabolism , Stomach/physiology , Animals , Cell Count , Duodenum/cytology , Macaca mulatta , Male , Stomach/cytology
2.
Biomed Res Int ; 2013: 474132, 2013.
Article in English | MEDLINE | ID: mdl-24171165

ABSTRACT

Allergic airway inflammation is attenuated by oral tolerization (oral exposure to allergen, followed by conventional sensitization and challenge with homologous antigen), which decreases airway allergen challenge-induced eosinophilic infiltration of the lungs and bone marrow eosinophilia. We examined its effects on bone marrow eosinophil and neutrophil production. Mice of wild type (BP-2, BALB/c, and C57BL/6) and mutant strains (lacking iNOS or CD95L) were given ovalbumin (OVA) or water (vehicle) orally and subsequently sensitized and challenged with OVA (OVA/OVA/OVA and H2O/OVA/OVA groups, resp.). Anti-OVA IgG and IgE, bone marrow eosinophil and neutrophil numbers, and eosinophil and neutrophil production ex vivo were evaluated. T lymphocytes from OVA/OVA/OVA or control H2O/OVA/OVA donors were transferred into naïve syngeneic recipients, which were subsequently sensitized/challenged with OVA. Alternatively, T lymphocytes were cocultured with bone marrow eosinophil precursors from histocompatible sensitized/challenged mice. OVA/OVA/OVA mice of the BP-2 and BALB/c strains showed, relative to H2O/OVA/OVA controls, significantly decreased bone marrow eosinophil counts and ex vivo eosinopoiesis/neutropoiesis. Full effectiveness in vivo required sequential oral/subcutaneous/intranasal exposures to the same allergen. Transfer of splenic T lymphocytes from OVA/OVA/OVA donors to naive recipients prevented bone marrow eosinophilia and eosinopoiesis in response to recipient sensitization/challenge and supressed eosinopoiesis upon coculture with syngeneic bone marrow precursors from sensitized/challenged donors.


Subject(s)
Bone Marrow Cells/immunology , Hypersensitivity/immunology , Immunity, Innate , Lung/immunology , Administration, Oral , Allergens/administration & dosage , Allergens/immunology , Animals , Eosinophils/pathology , Hematopoiesis/immunology , Humans , Hypersensitivity/pathology , Inflammation/immunology , Inflammation/pathology , Lung/pathology , Mice , Ovalbumin/administration & dosage , Ovalbumin/immunology , T-Lymphocytes/immunology
3.
Auton Neurosci ; 169(2): 102-6, 2012 Aug 16.
Article in English | MEDLINE | ID: mdl-22682704

ABSTRACT

The resting energy expenditure and the adaptation of the autonomic nervous system induced by sport activities in sedentary women and in female professional basketball players have been studied. Resting energy expenditure, body composition and the level of activity of the autonomic nervous system were measured before and after a period of six months. The physical activity induced an increase in resting energy expenditure and free fat mass without variations in body weight. Basketball players showed a significant increase in the parasympathetic activity, measured by the power spectral analysis of the heart rate variability. These findings demonstrate that resting energy expenditure is higher in the athletes than in sedentary women, despite the augmented parasympathetic activity that is usually related to lower energy expenditure.


Subject(s)
Body Composition/physiology , Energy Metabolism/physiology , Rest/physiology , Sports/physiology , Adult , Autonomic Nervous System/physiology , Body Weight/physiology , Energy Intake/physiology , Female , Heart Rate/physiology , Humans
4.
J Cell Physiol ; 227(8): 3111-5, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22015651

ABSTRACT

Long-term potentiation (LTP) and long-term depression represent important processes that modulate synaptic transmission that carries out a key role in neural mechanisms of memory. Many studies give strong evidences on a role of the reactive oxygen species in the induction of LTP in CA1 region of hippocampal slices that was inhibited by adding the scavenger enzyme superoxide dismutase (SOD1). Previous data showed that SOD1 is secreted by many cellular lines, including neuroblastoma SK-N-BE cells through microvesicles by an ATP-dependent mechanism; moreover, it has been shown that SOD1 interacts with human neuroblastoma cell membranes increasing intracellular calcium levels via a phospholipase C-protein kinase C pathway activation. The aim of this study was to investigate the effect of intracerebral injection of SOD1 or the inactive form of enzyme (ApoSOD) on the modulation of synaptic transmission in dentate gyrus of the hippocampus in urethane anesthetized rats. The results of the present research showed that intracerebral injection of SOD1 and ApoSOD in the dentate gyrus of the rat hippocampal formation inhibits LTP induced by high-frequency stimulation of the perforant path. This result cannot be only explained by the dismutation of oxygen radical induced by SOD1 since also ApoSOD, that lacks the enzymatic activity, carries out the same inhibitory effect on LTP induction.


Subject(s)
Gene Expression/drug effects , Long-Term Potentiation/drug effects , Receptor, Muscarinic M1/metabolism , Superoxide Dismutase/metabolism , Synaptic Transmission , Animals , Cell Line, Tumor , Dentate Gyrus/metabolism , Humans , Male , Neuroblastoma/metabolism , Oligodendroglia/cytology , Oligodendroglia/metabolism , Rats , Rats, Sprague-Dawley , Superoxide Dismutase/administration & dosage , Superoxide Dismutase/chemistry , Synaptic Transmission/drug effects
5.
Environ Toxicol Pharmacol ; 31(1): 198-204, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21787686

ABSTRACT

Octylphenol (OP) is an endocrine-disrupting chemical that accumulates in various organs. It has also been shown to exert noxious effects on the central nervous system. In the present study, we measured in Sprague-Dawley rats the degree of OP accumulation in different areas of the brain and investigated the effect of OP in pain modulation. Two groups of male Sprague-Dawley rats were treated for 20 days with 50mg/kg BW/day of OP (group 1) or vehicle (group 2). At the end of the treatment, the formalin test was performed to evaluate the effect of OP exposure on pain. Soon after, rats were sacrificed, and the accumulation of OP in the cerebral cortex, hippocampus, hypothalamus, cerebellum, thalamus, striatum, mesencephalus and ventral hindbrain was measured by HPLC analysis. The results showed a greater accumulation of OP in the cerebral cortex compared to all the other areas; there was also more accumulation in the cerebellum compared to the mesencephalus and thalamus. No accumulation was found in the striatum. These results suggest that there is a preferential accumulation of OP in different areas of the brain with consequences to neural behaviour. On the contrary, experiments on facial grooming did not show significant effects of OP on pain.


Subject(s)
Brain/metabolism , Endocrine Disruptors/pharmacokinetics , Environmental Pollutants/pharmacokinetics , Environmental Pollution/adverse effects , Phenols/pharmacokinetics , Animals , Chromatography, High Pressure Liquid , Grooming/drug effects , Growth/drug effects , Male , Rats , Rats, Sprague-Dawley
6.
Neuroscience ; 166(2): 416-21, 2010 Mar 17.
Article in English | MEDLINE | ID: mdl-20045451

ABSTRACT

The aim of the present study was to evaluate the production of superoxide anion (O(2)(-)) in the trigeminal complex nuclei after a functional mechanical overload of the teeth due to the preference for masticating on one side in rats. The preference for masticating on one side was induced by the discomfort due to a small abrasion of one molar; such lateralisation in mastication was confirmed by electromyography. The production of O(2)(-) was evaluated in the trigeminal nuclei by fluorescence microscopy after an injection of dihydroethidium. The results showed that there was an increased production of O(2)(-) in the subnucleus oralis of the spinal trigeminal nucleus in the same side where the mastication was preferred. This result demonstrates that an increased activity of non-painful sensory neurons can enhance the production of reactive oxygen species within the central second order sensory nuclei.


Subject(s)
Mastication/physiology , Superoxides/metabolism , Trigeminal Nuclei/metabolism , Afferent Pathways/metabolism , Analysis of Variance , Animals , Cold Temperature , Electromyography , Male , Microscopy, Fluorescence , Physical Stimulation , Rats , Rats, Sprague-Dawley , Sensory Receptor Cells/metabolism , Signal Processing, Computer-Assisted , Tooth
7.
J Muscle Res Cell Motil ; 30(3-4): 139-44, 2009.
Article in English | MEDLINE | ID: mdl-19526318

ABSTRACT

MyoD is a myogenic regulatory factor with a critical role in skeletal muscle development and regeneration. As muscle regeneration comes with an inflammatory process, it has been proposed that the inflammatory cells can play an important role in the induction of muscle fibres regeneration. The aim of the present work was to verify if a cyclooxygenase inhibitory drug (ketoprofen) would alter the normal expression of MyoD in a regenerating rat soleus muscle after an over-load lesion. Using immunohistochemical techniques, the numbers of m-cadherin-positive cells, a selective marker of satellite cells, and MyoD-positive cells were evaluated in functionally overloaded rat soleus muscles 4 days after a gastrocnemius tendon cut. The same study was conducted either with four rats injected with ketoprofen (100 mg/kg b.w./day) or with four rats injected with saline solution. The data obtained showed a very large decrease in the number of MyoD positive/m-cadherin positive cells in the ketoprofen injected group compared to the control group. Although further studies are needed to elucidate the sequence of biochemical events that induce a reduction of MyoD expression due to ketoprofen, the results demonstrate that prostaglandin synthesis is required for the induction of MyoD expression and that ketoprofen can affect this expression, with possible adverse effects on muscle regeneration.


Subject(s)
Cyclooxygenase Inhibitors/pharmacology , Ketoprofen/pharmacology , Muscle, Skeletal/drug effects , MyoD Protein/biosynthesis , Prostaglandins/biosynthesis , Regeneration/drug effects , Animals , Cadherins/metabolism , Male , Muscle, Skeletal/physiology , Rats , Rats, Sprague-Dawley
8.
Nutr Neurosci ; 12(1): 43-8, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19178791

ABSTRACT

Caffeine induces modifications of activity of the autonomic nervous system. This study analyzed the effect of a cup of espresso coffee on the heart rate variability (HRV) power spectral analysis, which is a method providing evaluation of the sympathetic and parasympathetic discharge. In young, healthy sedentary subjects (10 male, 10 female; aged 25-30 years), the HRV-power spectrum was evaluated over a period of 150 min after the administration of espresso coffee (caffeine, 75 mg) or decaffeinated coffee (caffeine, < 18 mg) in supine and seated position. Absolute values of the spectrum were summed in low (LF) and high frequencies (HF). The LF and HF spectra were used to estimate the sympathetic and parasympathetic activity, respectively. In the supine position, coffee increases HF, while decaffeinated coffee causes little modifications of HF. In the seated position, HF is not modified by coffee or decaffeinated coffee. Coffee and decaffeinated coffee do not induce any modification of LF in both positions. This experiment indicates that espresso coffee influences parasympathetic activity in the supine position.


Subject(s)
Caffeine/administration & dosage , Coffee , Heart Rate/drug effects , Parasympathetic Nervous System/drug effects , Parasympathetic Nervous System/physiology , Posture/physiology , Adult , Blood Pressure/drug effects , Female , Humans , Male , Supine Position
9.
Clin Nutr ; 27(4): 657-9, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18514973

ABSTRACT

BACKGROUND & AIMS: Few studies have investigated the age-related modification of resting energy expenditure (REE) and free fat mass (FFM) in severe obesity. This cross-sectional study analyzed REE and FFM in severely and moderately obese women and in lean subjects at different ages to find the possible differences between obese and lean subjects during aging. METHODS: Sedentary women (n=261) were divided into three groups with different body mass indexes (BMIs): 20.0-24.9; 30-34.9; >40 kg/m(2). Each group was then divided into five subgroups: 20-29; 30-39; 40-49; 50-59; 60-69 years. REE was measured with an indirect calorimetric device. The FFM was calculated by bioelectric impedance. RESULTS: The REE in severely obese women was higher than the REE in lean or moderately obese women. The FFM of severely obese women was lower than that of moderately obese or lean women. The aging induced reductions of the REE and FFM in lean and moderately obese subjects, but not in women with severe obesity. CONCLUSIONS: This experiment indicates that REE and FFM do not decline during aging in women with BMI>40, suggesting that the severe obesity induces different age-related adaptations of metabolism and body composition.


Subject(s)
Aging/physiology , Basal Metabolism/physiology , Body Composition/physiology , Muscle, Skeletal/metabolism , Obesity, Morbid/metabolism , Adult , Aged , Aging/metabolism , Body Mass Index , Cross-Sectional Studies , Electric Impedance , Female , Humans , Middle Aged , Obesity, Morbid/physiopathology , Young Adult
10.
Neuroscience ; 153(1): 182-8, 2008 Apr 22.
Article in English | MEDLINE | ID: mdl-18358626

ABSTRACT

The mechanisms of tolerance to subsequent episodes of ischemia induced by cortical spreading depression (CSD) are not clear. The effects of CSD on the expression of inducible nitric oxide synthase (iNOS), hypoxia inducible factor-1alpha (HIF-1alpha), and lactate dehydrogenase-A (LDH-A) were evaluated in the present experiment. Unilateral CSD was induced in Sprague-Dawley rats by application of KCl on the right cortex and the mRNA levels of iNOS, HIF-1alpha, and LDH-A were evaluated at 15 min, 2 h, 4 h, 6 h or 24 h after CSD. RT-PCR analysis showed: 1) an increase of iNOS mRNA at 15 min, 2 h, 4 h; 2) an increase of HIF-1alpha mRNA at 6 h; 3) an increase of LDH-A mRNA at 4 h. In situ hybridization with specific digoxigenin-labeled oligonucleotides revealed that the mRNA levels were increased at 15 min-2 h for iNOS, 2-4 h for LDH-A and 6 h for HIF-1 after CSD. Immunohistochemistry analysis revealed that levels of iNOS and HIF-1alpha were increased, respectively, at 2 h and 6 h after CSD. These data suggest that CSD promotes the expression of iNOS, HIF-1alpha, and LDH-A in nervous cells giving a neuroprotective effect.


Subject(s)
Cerebral Cortex/metabolism , Cortical Spreading Depression/physiology , Cytoprotection/genetics , Hypoxia-Inducible Factor 1, alpha Subunit/genetics , L-Lactate Dehydrogenase/genetics , Nitric Oxide Synthase Type II/genetics , Animals , Cell Survival/genetics , Cerebral Cortex/physiopathology , Gene Expression Regulation/genetics , Hypoxia-Inducible Factor 1, alpha Subunit/metabolism , Immunohistochemistry , Isoenzymes/genetics , Isoenzymes/metabolism , L-Lactate Dehydrogenase/metabolism , Lactate Dehydrogenase 5 , Male , Neurons/metabolism , Nitric Oxide/biosynthesis , Nitric Oxide Synthase Type II/metabolism , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Time Factors , Up-Regulation/genetics
11.
Physiol Res ; 57(2): 269-273, 2008.
Article in English | MEDLINE | ID: mdl-17465698

ABSTRACT

Production of superoxide anions in the incubation medium of hippocampal slices can induce long-term potentiation (LTP). Other reactive oxygen species (ROS) such as hydrogen peroxide are able to modulate LTP and are likely to be involved in aging mechanisms. The present study explored whether intracerebro-ventricular (ICV) injection of oxidant or antioxidant molecules could affect LTP in vivo. With this aim in mind, field excitatory post-synaptic potentials (fEPSPs) elicited by stimulation of the perforant pathway were recorded in the dentate gyrus of the hippocampal formation in urethane-anesthetized rats. N-acetyl-L-cysteine, hydrogen peroxide (H2O2) or hypoxanthine/xanthine-oxidase solution (a superoxide producing system) were administrated by ICV injection. The control was represented by a group injected with saline ICV. Ten minutes after the injection, LTP was induced in the granule cells of the dentate gyrus by high frequency stimulation of the perforant pathway. Neither the H(2)O(2) injection or the N-acetyl-L-cysteine injection caused any variation in the fEPSP at the 10-min post-injection time point, whereas the superoxide generating system caused a significant increase in the fEPSP. Moreover, at 60 min after tetanic stimulation, all treatments attenuated LTP compared with the control group. These results show that ICV administration of oxidant or antioxidant molecules can modulate LTP in vivo in the dentate gyrus. Particularly, a superoxide producing system can induce potentiation of the synaptic response. Interestingly, ICV injection of oxidants or antioxidants prevented a full expression of LTP compared to the saline injection.


Subject(s)
Dentate Gyrus/physiology , Excitatory Postsynaptic Potentials/physiology , Free Radical Scavengers/metabolism , Long-Term Potentiation/physiology , Perforant Pathway/physiology , Acetylcysteine/administration & dosage , Acetylcysteine/metabolism , Analysis of Variance , Anesthetics, Intravenous/pharmacology , Animals , Dentate Gyrus/drug effects , Electric Stimulation , Excitatory Postsynaptic Potentials/drug effects , Free Radical Scavengers/administration & dosage , Hydrogen Peroxide/administration & dosage , Hydrogen Peroxide/metabolism , Hypoxanthine/administration & dosage , Injections, Intraventricular , Long-Term Potentiation/drug effects , Male , Oxidants/administration & dosage , Oxidants/metabolism , Oxidation-Reduction/drug effects , Rats , Rats, Sprague-Dawley , Urethane/pharmacology , Xanthine Oxidase/administration & dosage
12.
Nutr Neurosci ; 9(3-4): 141-5, 2006.
Article in English | MEDLINE | ID: mdl-17176636

ABSTRACT

This study analyzed vegetative modulation, expressed as heart rate variability (HRV) power spectral analysis, in lean and obese women at pre-menopausal or post-menopausal age to reveal possible differences in menopause-related autonomic activity in lean and obese subjects. Sedentary women (n = 40) were divided in four groups: pre-menopausal lean and obese women, post-menopausal lean and obese subjects. The HRV-power spectrum was evaluated on a 5-min long ECG recording. The absolute values of the spectrum were summed in the following frequencies: a low-frequency (0.04-0.15 Hz; LF) and high-frequency (0.15-0.40; HF) range. LF and HF were values used to estimate the sympathetic and parasympathetic activity. LF and HF values of pre-menopausal obese women are lower than values of lean women. The menopause induced a same decrease in LF and HF values in lean and obese subjects, so that no difference was found in post-menopausal groups. This experiment indicates that modifications of autonomic modulation can be included among factors related to obesity in pre-menopausal, but not post-menopausal women.


Subject(s)
Autonomic Nervous System/physiology , Body Weight/physiology , Obesity/physiopathology , Postmenopause , Premenopause , Adult , Body Mass Index , Female , Humans , Life Style , Middle Aged , Thinness
13.
Cell Tissue Res ; 318(3): 599-608, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15578274

ABSTRACT

The balance between cell death and cell proliferation and its regulation are essential features of many physiological processes and are particularly important in fetal morphogenesis and adult tissue homeostasis. Apoptosis is a type of cell suicide that is activated in two main ways: through a receptor-mediated pathway or through a mitochondrial pathway. We have investigated the immunohistochemical distribution of proteins belonging to these two pathways in human placenta during gestation by comparing their expression levels between the first and third trimester of gestation. In the first trimester, the receptor-mediated pathway prevails over the mitochondrial pathway with a moderate/intense expression of its three components, viz., Fas ligand (FasL), Fas, and caspase-8, and weak positivity of anti-apoptotic FLIP, these proteins being mainly localized in the cytotrophoblast compartment. In the third trimester of gestation, there is an increased expression of mitochondrial pathway proteins, viz., Apaf-1 and caspase-9. We have also investigated the expression level of caspase-3, the primary effector caspase of both pathways, and have observed that it is moderately expressed during gestation, being mainly localized in the cytotrophoblast during the first trimester and in both placental compartments during the third trimester of gestation. Thus, both pathways actively function in human placenta to execute cell death. By means of immunoelectron microscopy, we have further shown that, in human placenta, the two proteins of the mitochondrial pathway together with caspase-3 are localized both in the cytoplasm and in the nucleus. In particular, Apaf-1 and caspase-9 are distributed near to the nuclear envelope suggesting an important role for these two proteins in disrupting the nuclear-cytoplasmic barrier.


Subject(s)
Apoptosis , Caspases/metabolism , Mitochondrial Proteins/metabolism , Trophoblasts/metabolism , fas Receptor/metabolism , Adult , Apoptotic Protease-Activating Factor 1 , CASP8 and FADD-Like Apoptosis Regulating Protein , Cell Nucleus/metabolism , Cytoplasm/metabolism , Fas Ligand Protein , Female , Gestational Age , Humans , Intracellular Signaling Peptides and Proteins/metabolism , Membrane Glycoproteins/metabolism , Nuclear Envelope/metabolism , Pregnancy , Proteins/metabolism , Trophoblasts/pathology
14.
Endoscopy ; 36(10): 860-3, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15452780

ABSTRACT

BACKGROUND AND STUDY AIMS: Several endoscopic techniques have been developed to prevent bleeding after the removal of large pedunculated polyps. PATIENTS AND METHODS: From January 1995 to December 2002, 488 consecutive patients with pedunculated colorectal polyps, the heads of which were larger than 10 mm in diameter, were randomly assigned to three groups. In group A (163 patients), detachable snares were placed at the base of the stalk and standard snares were then used for polypectomy. In group B (161 patients), the polyp stalk was injected with a 0.01 % epinephrine solution before conventional snare polypectomy. Group C (a control group including 164 patients) underwent conventional snare polypectomy without preventive measures. Early (< 24 h) and late (> 24 h - 30 days) bleeding complications were assessed. Each group was divided into two subgroups relative to the polyp size (polyps 1.0 - 1.9 cm and polyps > or = 2 cm). RESULTS: Overall bleeding complications occurred after 4.3 % of the polypectomies. Bleeding was successfully controlled in all patients, and no blood transfusions were required. There were three cases of bleeding in group A (1.8 %), five in group B (3.1 %), and 13 in group C (7.9 %). Early bleeding was more frequent than late bleeding (15 vs. six patients). In polyps > or = 2 cm (207 patients), postpolypectomy bleeding occurred in 14 patients (6.7 %): two (2.7 %) in the detachable snare group, two (2.9 %) in the epinephrine injection group, and 10 (15.1 %) in the control group. CONCLUSIONS: These results show that polypectomy of large pedunculated polyps is associated with a higher incidence of bleeding. Particularly in polyps larger than 2 cm, preventive measures can significantly reduce bleeding complications after polypectomy. This can be achieved with similar efficacy either by placing Endoloops or by injecting epinephrine.


Subject(s)
Colonoscopes , Colonoscopy/adverse effects , Epinephrine/administration & dosage , Intestinal Polyps/surgery , Postoperative Hemorrhage/prevention & control , Vasoconstrictor Agents/administration & dosage , Colonic Polyps/pathology , Colonic Polyps/surgery , Colonoscopy/methods , Female , Humans , Injections, Intralesional , Intestinal Polyps/pathology , Male , Middle Aged , Postoperative Hemorrhage/drug therapy , Rectal Diseases/pathology , Rectal Diseases/surgery , Treatment Outcome
15.
Acta Physiol Scand ; 182(1): 89-94, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15329061

ABSTRACT

AIM: Hypocretin 1 is an hypothalamic neuropeptide that induces an increase in food intake when administered into the cerebral lateral ventricle. As it is well known that the medial hypothalamus (MH) is involved in the feeding behaviour also through GABAergic circuits, the aim of this experiment was to investigate the effect of an hypocretin 1 intracerebroventricular (icv) injection on the extracellular levels of GABA in the MH. METHODS: GABA levels in the MH were evaluated in six rats by microdialysis and high performance liquid chromatography-electrochemical detection 30 min before and every 30 min for an over all period of 6 h after an icv injection of hypocretin 1. The same procedure was used in another group of six rats but saline was injected into the lateral ventricle as control. RESULTS: The results show that extracellular GABA increases in the MH after the injection of hypocretin 1 at 60 min and at 3 h after the injection. CONCLUSION: This finding suggests a possible mechanism by which hypocretin 1 should induce hyperphagia in the first hour after injection. As it is already known that the inhibition of the MH by injection of GABA causes an increase of food intake, it is possible that hypocretin 1 causes an increase in food intake by increasing the GABA release in the MH. The lack of an increase in the GABA level after the fourth hour is consistent with the lack of an increase in food intake at this time, as we observed in previous experiments. The finding of a biphasic increase in the GABA level, at 60 min and at 3 h, was unexpected and should be further investigated.


Subject(s)
Hypothalamus, Middle/metabolism , Intracellular Signaling Peptides and Proteins/administration & dosage , Neuropeptides/administration & dosage , gamma-Aminobutyric Acid/analysis , Adipose Tissue/drug effects , Adipose Tissue/physiology , Animals , Body Temperature/physiology , Extracellular Space/metabolism , Hypothalamus, Middle/drug effects , Injections, Intraventricular , Male , Microdialysis/methods , Neurotransmitter Agents/administration & dosage , Orexins , Rats , Rats, Sprague-Dawley
17.
In Vivo ; 15(5): 391-5, 2001.
Article in English | MEDLINE | ID: mdl-11695235

ABSTRACT

The expression of cyclin T1 in an autoptic case of AIDS-related cachexia was investigated by immunohistochemistry. When contrasted with normal human tissues, a very similar pattern of expression was found. However, a peculiar distribution of cyclin T1 was noticed in the brown fat and in lymph nodes affected by AIDS-associated lymphadenopathy.


Subject(s)
Acquired Immunodeficiency Syndrome/metabolism , Cachexia/metabolism , Cyclins/biosynthesis , Acquired Immunodeficiency Syndrome/complications , Acquired Immunodeficiency Syndrome/pathology , Adipose Tissue, Brown/metabolism , Adipose Tissue, Brown/pathology , Adult , Cachexia/etiology , Cachexia/pathology , Cell Cycle , Cyclin T , Germinal Center/metabolism , Germinal Center/pathology , Humans , Immunoenzyme Techniques , Kidney/metabolism , Kidney/pathology , Lymph Nodes/metabolism , Lymph Nodes/pathology , Male , Organ Specificity , Thymus Gland/metabolism , Thymus Gland/pathology
18.
Histol Histopathol ; 16(4): 1057-60, 2001 10.
Article in English | MEDLINE | ID: mdl-11642725

ABSTRACT

It has been proposed that tumor suppressor genes may have a role in the mechanisms of proliferation and differentiation during human placental development. The Retinoblastoma gene family is a well known family of tumor suppressor genes. Many studies have pointed out a role of this family not only in cell cycle progression, but also during development and differentiation. On the light of these observations we have investigated the immunohistochemical expression pattern of the Retinoblastoma family members, p107 and Rb2/p130 in human placenta samples in first trimester and full-term placental sections. p107 and pRb2/p130 showed the most abundant expression levels during the first trimester of gestation and progressively declined to being barely detectable in the placenta by late gestation. These results indicate that the expression of the above genes is modulated during placental development and suggest a mechanism for controlling trophoblast proliferation.


Subject(s)
Genes, Retinoblastoma/genetics , Genes, Tumor Suppressor , Nuclear Proteins/biosynthesis , Nuclear Proteins/genetics , Phosphoproteins/biosynthesis , Phosphoproteins/genetics , Placenta/metabolism , Proteins , Retinoblastoma Protein/metabolism , Adult , Decidua/metabolism , Female , Humans , Immunohistochemistry , Pregnancy , Retinoblastoma-Like Protein p107 , Retinoblastoma-Like Protein p130 , Trophoblasts/metabolism
19.
Histochem J ; 33(7): 421-5, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11858462

ABSTRACT

The placenta is the primary site of nutrient and gas exchange between mother and foetus. During human placental development, proliferation, differentiation and apoptosis occur at different stages. In order to clarify some of the molecular mechanisms underlying these events, we investigated the pattern of expression of two members of the Bcl-2 family in human placenta samples and compared them to the level of apoptosis detected by the TUNEL method. In particular, we evaluated the expression of Bcl-2 and Bax and their ratio during the first and third trimester. We found that Bcl-2 was generally expressed at low levels during the entire gestational period. On the other hand, Bax was low during the first trimester but increased towards the end of gestation. In accordance with the change of ratio of these two molecules, the increase of apoptotic cells was observable in the third trimester. These data indicate that Bcl-2 and Bax are spatio-temporally regulated during placental development and that the different expression of the above mentioned genes is at least in part responsible for the delicate balance between cell proliferation and programmed cell death in the human placenta during pregnancy.


Subject(s)
Apoptosis , Cyclin D1/metabolism , Proto-Oncogene Proteins c-bcl-2 , Proto-Oncogene Proteins/metabolism , Trophoblasts/metabolism , Adult , Cyclin D1/genetics , Female , Gene Expression Regulation, Developmental , Gestational Age , Humans , Immunohistochemistry , In Situ Nick-End Labeling , Pregnancy , Proto-Oncogene Proteins/genetics , bcl-2-Associated X Protein
20.
J Cell Biochem ; 74(3): 447-57, 1999 Sep 01.
Article in English | MEDLINE | ID: mdl-10412045

ABSTRACT

We investigate the role played by dendritic cells (DCs) in the non-obese diabetic (NOD) mouse pancreas. The early peri-islet, nondestructive infiltration phase, and intra-islet, destructive infiltration phase, which immediately precedes overt diabetes, are studied. Results show that infiltrating cells are Ia-b, ICAM-1, and, mainly, MIDC-8 immunoreactive (ir). These data from silica-treated animals and ultrastructural observations strongly support the hypothesis that DCs are both Ia-b-ir and ICAM-1-ir and that they exert a pivotal role during the period of early infiltration. This is a novel finding for NOD mice and increases the interest for this protective cell type during the rather complex islet infiltration process. Moreover, the cytokine profile demonstrates that Th2 protective cytokines are specific for peri-islet infiltrate. Disappearance of DCs from the infiltrate is concomitant with both the formation of intra-islet infiltration and the increase in proinflammatory Th1 cytokine levels. This further supports the hypothesis that DCs may exert a protective role against diabetes development.


Subject(s)
Cytokines/biosynthesis , Dendritic Cells , Islets of Langerhans/metabolism , Th2 Cells/metabolism , Age Factors , Animals , Blood Glucose/analysis , Female , Immunohistochemistry , Intercellular Adhesion Molecule-1/immunology , Male , Mice , Mice, Inbred C57BL , Mice, Inbred NOD , Microscopy, Electron , Pancreas/metabolism , Silicon Dioxide/pharmacology , Time Factors
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