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Comparative Study 2006; 27(5): 595-599 PubMed PMID: 17159816 Citation  Keywords:  Animals, Antioxidants:pharmacology, Antithyroid Agents:pharmacology, Diet, Dose-Response Relationship, Drug, Kidney:chemistry, Liver:chemistry, Lung:chemistry, Male, Oxidative Stress:drug effects, Potassium Iodide:administration & dosage, Propylthiouracil.   

OBJECTIVES: Iodide administration to animals, living in iodine-deficient areas, can induce oxidative processes in the thyroid gland and increase concentration of lipid peroxidation (LPO). Propylthiouracil (PTU)--a well-known antithyroid drug--may also act as an antioxidant. There are some reports, which consider the protective ability of this drug against LPO. The goal of the study was to evaluate oxidative processes and the protective role of PTU in three rat organs during treatment with pharmacological doses of iodide.

MATERIAL AND METHODS: Schiff's bases (SB) concentrations (a parameter of oxidative stress) were measured in liver, lung and kidney homogenates of male Wistar rats. For 2 weeks the animals received iodides in their diet in the following concentrations: Group 1--Controls (standard diet, approx. 0.7 mg of potassium iodide per kg; KI/kg); Group 2--diet containing 0.25 mg KI/kg; Group 3--diet with 4.0 mg KI/kg; Group 4--diet with 8.0 mg KI/kg. Group 5--standard diet with 0.1% of PTU in drinking water for two weeks. Subsequent tree groups (6-8) received KI in their diet in doses as above, respectively, together with PTU.

RESULTS: We noted increased SB levels in the lungs and in the liver, compared to those observed in the control group. We also found decreased SB concentrations in liver and lung homogenates after the administration of PTU but, unexpectedly, the level of SB increased in kidney homogenates of all the groups.

CONCLUSIONS: The results of this study indicate that iodine is involved in oxidative processes in different organs and PTU protects against iodine-induced oxidative stress....

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Journal Article 2006; 27(4): 517-522 PubMed PMID: 16892003 Citation  Keywords:  Adenocarcinoma:metabolism, Aged, Aged, 80 and over, Antibody Specificity, Cell Nucleus:metabolism, Cytoplasm:metabolism, Humans, Immunohistochemistry, Male, Middle Aged, Prognosis, Prostate:metabolism, Prostatic Hyperplasia:metabolism, Prostatic Neoplasms.   

BACKGROUND: Ubiquitin is a low molecular weight protein which has been detected in a variety of normal and cancerous tissues. It is involved in many regulatory processes including protein proteolysis. It has been implicated in tumor pathogenesis. The role of ubiquitin in human prostate gland is investigated in this study.

METHODS: In this study, we utilized immunohistochemistry technique to localize ubiquitin in human prostate gland and correlate it with different pathological conditions of the prostate.

RESULTS: Ubiquitin was localized in normal, benign prostatic hyperplasia (BPH) and prostatic adenocarcinoma with variations in the distribution and intensity. In BPH, ubiquitin immunoreactivity was localized mainly in the nuclei while in the adenocarcinoma was localized mainly in the cytoplasm.

CONCLUSION: The presence of ubiquitin mainly in the nuclei and in the cytoplasm of BPH and prostatic adenocarcinoma, respectively, may suggest a role of ubiquitin in the development of the above mentioned conditions. Ubiquitin could be used as a potential marker for the diagnosis and prognosis of pathological conditions of the prostate....

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Journal Article 2006; 27(4): 415-423 PubMed PMID: 16891999 Citation  Keywords:  Adult, Apolipoprotein E2:genetics, Chronic Disease, Dental Amalgam:adverse effects, Dental Restoration, Permanent, Depression:chemically induced, Fatigue:chemically induced, Female, Genetic Predisposition to Disease, Genotype, Humans, Male, Memory Disorde.   

: In a group of 465 patients diagnosed as having chronic mercury toxicity (CMT), 32.3% had severe fatigue, 88.8% had memory loss, and 27.5% had depression. A significant correlation was found between CMT and the Apo-lipoprotein E4 genotype (p=0.001). An investigation into an additional 864 consecutively seen general practice patients, resulted in 30.3% having evidence consistent with CMT, and once again a significant correlation was found with the APO-E4 genotype (p=0.001). Removal of amalgam mercury fillings when combined with appropriate treatment resulted in a significant symptom reduction (p<0.001) to levels reported by healthy subjects....

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Journal Article 2006; 27(4): 539-546 PubMed PMID: 16891988 Citation  Keywords:  Animals, Astrocytes:physiology, Brain Injuries:pathology, Capillaries:metabolism, Cell Differentiation:physiology, Cerebral Cortex:blood supply, Endoplasmic Reticulum:metabolism, Endothelium, Vascular:cytology, Immunohistochemistry, Male, Microscopy, Elec.   

OBJECTIVES: We investigated neovasculatization in the cerebral cortex of the adult rat after surgical brain injury by ultrastructural, immunocytochemical and immunochemical means. Previously we described endothelial-like cell that participates in new vessel formation on plasma proteins that served as a provisional matrix in the region immediately adjacent to the traumatic injury. In the present study we describe new vessel formation in the multistep process with the alterations in endothelial-like cell immunophenotype.

METHOD: The observations were conducted from 2 to 7 days after induction of cortical trauma. Traumatic injury was induced in the frontotemporal region of cerebral cortex.

RESULTS: We show that endothelial-like cell could not successfully terminate its development without the presence of pericyte and astrocyte. New formed blood vessels were accompanied by fibroblast and lipofibroblast cells differentiated probably from common progenitor.

MAIN FINDINGS: Our result suggests that endothelial-like cell is committed endothelial cell between progenitor endothelial cell and terminally differentiated endothelium stage. Therefore, we propose that our of endothelial stem cells present in blood at different stages of morphogenetic differentiation and specifically arrested in "check points" of development trauma mobilize the group of the most differentiated progenitors. These may contribute to new vessel formation.

CONCLUSION: Our model should be useful for the characterization of endothelial commitment and endothelial cell differentiation after brain injury....

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Journal Article 2006; 27(4): 401-413 PubMed PMID: 16807526 Citation  Keywords:  Child, Preschool, Developmental Disabilities:chemically induced, Diphtheria-Tetanus-Pertussis Vaccine:adverse effects, Haemophilus Vaccines:adverse effects, Humans, Nervous System Diseases:chemically induced, Thimerosal:adverse effects, United States:epid.   

BACKGROUND: Thimerosal is an ethylmercury-containing compound (49.6% mercury by weight) used as at the preservative level in vaccines (0.005% to 0.01%).

METHODS: Statistical modeling in a meta-analysis epidemiological assessment of the Vaccine Adverse Event Reporting System (VAERS) for neurodevelopment disorders (NDs) reported following Diphtheria-Tetanus-whole-cell-Pertussis (DTP) vaccines in comparison to Diphtheria-Tetanus-whole-cell-Pertussis-Haemophilus Influenzae Type b (DTPH) vaccines (administered: 1994-1997) and following Thimerosal-containing Diphtheria-Tetanus-acellular-Pertussis (DTaP), vaccines in comparison to Thimerosal-free DTaP vaccines (administered: 1997-2000), was undertaken.

RESULTS: Significantly increased adjusted (sex, age, vaccine type, vaccine manufacturer) risks of autism, speech disorders, mental retardation, personality disorders, thinking abnormalities, ataxia, and NDs in general, with minimal systematic error or confounding, were associated with TCV exposure.

CONCLUSION: It is clear from the results of the present epidemiological study and other recently published data associating mercury exposure with childhood NDs, additional ND research should be undertaken in the context of evaluating mercury-associated exposures, especially from Thimerosal-containing vaccines....

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Journal Article 2006; 27(3): 345-349 PubMed PMID: 16816835 Citation  Keywords:  Aged, Aged, 80 and over, Female, Humans, Immunohistochemistry, Male, Middle Aged, RNA, Messenger:analysis, Receptor, Endothelin A:genetics, Receptor, Endothelin B:genetics, Reference Values, Reverse Transcriptase Polymerase Chain Reaction, Tissue Distribu.   

OBJECTIVES: Endothelin is a potent peptide mediator that is synthesized by a number of cells. Previous studies have revealed the occurrence of endothelin in nerve cell bodies of some peripheral ganglia. Endothelin mediates its effects via two distinct receptor subtypes ETA and ETB. The present study was designed to investigate the presence of these two receptors in the human trigeminal ganglion.

METHODS: Reverse transcriptase-polymerase chain reaction (RT-PCR) was used to show the presence of mRNA encoding ETA and ETB receptors in the human trigeminal ganglion. To localize the protein immunocytochemistry with antibodies against the endothelin receptors was used.

RESULTS: Reverse transcriptase-polymerase chain reaction (RT-PCR) analysis revealed mRNA for both receptor subtypes in the human trigeminal ganglion. Immunocytochemistry revealed numerous cell bodies containing the ETA and the ETB receptor proteins.

CONCLUSIONS: The expression of ETA and ETB receptors in the human trigeminal ganglion suggests a role for endothelin in autonomic and sensory neural transmission....

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Comparative Study 2006; 27(3): 351-354 PubMed PMID: 16816834 Citation  Keywords:  Adenocarcinoma:drug therapy, Animals, Antimetabolites, Antineoplastic:pharmacology, Antineoplastic Agents, Hormonal:pharmacology, Antineoplastic Combined Chemotherapy Protocols:pharmacology, Breast Neoplasms:drug therapy, Cell Line, Tumor, Cell Proliferat.   

OBJECTIVES: Melatonin may influence directly tumor cells through the specific binding sites. The best known melatonin binding sites are membrane receptors. Recently, the participation of nuclear signalling via estrogen as well as RZR/ROR receptors in oncostatic action of melatonin on the breast cancer has been widely discussed. The aim of present study was to investigate effects of melatonin, the selective ligand for nuclear RZR/ROR receptors - CGP 52608, and methotrexate on growth of murine 16/C breast cancer cells.

MATERIAL AND METHODS: The experiment was performed in vitro. The breast cancer cells were incubated for 2 days in the presence of melatonin, CGP 52608 (at concentrations of 10(-5)M, 10(-7)M, 10(-9)M, 10-(11)M ) and methotrexate (at concentrations of 0.25 and 0.125 microg/ml). The growth of cells was measured using the modified Mossman method.

RESULTS: All examined compounds significantly inhibited the growth of cancer cells. The effects of MLT and CGP 52 608 were comparable with suppression caused by methotrexate. The significant differences of efficacy between two examined concentrations of methotrexate were not observed.

CONCLUSION: The obtained data together with our previous results indicate that nuclear receptors RZR/ROR play an important, although not sufficiently recognized role in the oncostatic action of melatonin....

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Journal Article 2006; 27(3): 297-305 PubMed PMID: 16807525 Citation  Keywords:  Alzheimer Disease:cerebrospinal fluid, Amyloid beta-Peptides:cerebrospinal fluid, Biomarkers:cerebrospinal fluid, Brain:metabolism, Cerebrospinal Fluid:chemistry, Depressive Disorder, Major:cerebrospinal fluid, Female, Humans, Male, Neurotransmitter Agent.   

: Cerebrospinal fluid (CSF) is a clear and colourless fluid that surrounds the brain and spine. Due to the close proximity of CSF to the brain, pathological brain-processes are likely to be reflected in CSF. CSF can be obtained through lumbar puncture and is frequently performed in the differential diagnosis of neuropsychiatric disorders. Beyond clinical applications, CSF has been studied as part of different research-protocols. In this review, we will focus on CSF-analysis in Alzheimer Disease, major depression and schizophrenia. We will review both clinical applications as well as research applications in all three disorders. We will also assess new technological advances that have made it possible to study large numbers of proteins in CSF and how these advances may change CSF-analysis in the years to come....

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