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1.
Soc Psychiatry Psychiatr Epidemiol ; 59(8): 1437-1448, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38112803

ABSTRACT

BACKGROUND: The COVID-19 pandemic and related measures have negatively impacted mental health worldwide. The main objective of the present longitudinal study was to investigate mental health in people living in Tyrol (Austria) and South Tyrol (Italy) during the COVID-19 pandemic and to report the prevalence of psychological distress among individuals with versus those without pre-existing mental health disorders (MHD) in the long-term (summer 2020-winter 2022). Here, we specifically focus on the relevance of spirituality and perceived social support in this regard. METHODS: 161 individuals who had been diagnosed with MHD and 446 reference subjects participated in this online survey. Electronic data capture was conducted using the Computer-based Health Evaluation System and included both sociodemographic and clinical aspects as well as standardized questionnaires on psychological distress, spirituality, and the perception of social support. RESULTS: The prevalence of psychological distress was significantly higher in individuals with MHD (36.6% vs. 12.3%) and remained unchanged among both groups over time. At baseline, the perception of social support was significantly higher in healthy control subjects, whereas the two groups were comparable in regards of the subjective relevance of faith. Reference subjects indicated significantly higher spiritual well-being in terms of the sense of meaning in life and peacefulness, which mediated in large part the between-group difference of psychological distress at follow-up. Notably, both faith and the perception of social support did not prove to be relevant in this context. CONCLUSIONS: These findings point to a consistently high prevalence of psychological distress among people suffering from MHD and underscore the prominent role of meaning in life and peacefulness as a protective factor in times of crisis. Therapeutic strategies that specifically target spirituality may have a beneficial impact on mental health.


Subject(s)
COVID-19 , Mental Disorders , Mental Health , Social Support , Spirituality , Humans , COVID-19/psychology , COVID-19/epidemiology , Male , Female , Longitudinal Studies , Middle Aged , Adult , Mental Disorders/epidemiology , Mental Disorders/psychology , Italy/epidemiology , Psychological Distress , SARS-CoV-2 , Surveys and Questionnaires , Aged , Prevalence
2.
Int J Mol Sci ; 23(6)2022 Mar 10.
Article in English | MEDLINE | ID: mdl-35328403

ABSTRACT

The therapeutic activities of natural plant extracts have been well known for centuries. Many of them, in addition to antiviral and antibiotic effects, turned out to have anti-tumor activities by targeting different signaling pathways. The canonical Wnt pathway represents a major tumorigenic pathway deregulated in numerous tumor entities, including colon cancer. Here, we investigated the acylphloroglucinols hyperforin (HF) from St. John's wort (Hypericum perforatum L.) and myrtucommulone A (MC A) from myrtle (Myrtus communis) and semi-synthetic derivatives thereof (HM 177, HM 297, HM298) for their effects on Wnt/ß-catenin signaling. None of these substances revealed major cytotoxicity on STF293 embryonic kidney and HCT116 colon carcinoma cells at concentrations up to 10 µM. At this concentration, HF and HM 177 showed the strongest effect on cell proliferation, whereas MC A and HM 177 most prominently inhibited anchorage-independent growth of HCT116 cells. Western blot analyses of active ß-catenin and ß-catenin/TCF reporter gene assays in STF293 cells revealed inhibitory activities of HF, MC A and HM 177. In line with this, the expression of endogenous Wnt target genes, Axin and Sp5, in HCT116 cells was significantly reduced. Our data suggest that the acylphloroglucinols hyperforin, myrtucommulone A and its derivative HM 177 represent potential new therapeutic agents to inhibit Wnt/ß-catenin signaling in colon cancer.


Subject(s)
Colonic Neoplasms , Hypericum , Colonic Neoplasms/drug therapy , HCT116 Cells , Humans , Phloroglucinol/analogs & derivatives , Terpenes , Wnt Signaling Pathway , beta Catenin/metabolism
3.
Article in English | MEDLINE | ID: mdl-32078575

ABSTRACT

Background Gabapentinoids are known to reduce neuropathic pain. The aim of this experimental study was to investigate whether gabapentinoids exert anti-inflammatory and/or anti-nociceptive effects at the cellular level using primary cultures of rat dorsal root ganglia (DRG). Methods Cells from rat DRG were cultured in the presence of gabapentin or pregabalin, and we tested the effects of subsequent stimulation with lipopolysaccharide (LPS) on the expression of genes (real-time polymerase chain reaction) and production of tumor necrosis factor-α (TNFα) and interleukin-6 (IL-6) by specific bioassays. Using Ca2+ imaging, we further investigated in neurons the effects of gabapentinoids upon stimulation with the TRPV-1 agonist capsaicin. Results There is a small influence of gabapentinoids on the inflammatory response to LPS stimulation, namely, a significantly reduced expression of IL-6. Pregabalin and gabapentin further seem to exert a moderate inhibitory influence on capsaicin-induced Ca2+ signals in DRG neurons. Conclusions Although the single inhibitory effects of gabapentinoids on inflammatory and nociceptive responses are moderate, a combination of both effects might provide an explanation for the proposed function of these substances as an adjuvant for the reduction of neuropathic pain.


Subject(s)
Gabapentin/pharmacology , Ganglia, Spinal/drug effects , Inflammation/physiopathology , Lipopolysaccharides/toxicity , Neuralgia/drug therapy , Somatosensory Cortex/physiopathology , Analgesics/pharmacology , Animals , Capsaicin/pharmacology , Female , Ganglia, Spinal/immunology , Ganglia, Spinal/metabolism , Inflammation/chemically induced , Male , Neuralgia/metabolism , Neurons/drug effects , Pregabalin/pharmacology , Primary Cell Culture , Rats , Rats, Wistar , Sensory System Agents/pharmacology , Somatosensory Cortex/drug effects
4.
Plant J ; 90(6): 1156-1175, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28257158

ABSTRACT

The methylation of cytosines shapes the epigenetic landscape of plant genomes, coordinates transgenerational epigenetic inheritance, represses the activity of transposable elements (TEs), affects gene expression and, hence, can influence the phenotype. Sugar beet (Beta vulgaris ssp. vulgaris), an important crop that accounts for 30% of worldwide sugar needs, has a relatively small genome size (758 Mbp) consisting of approximately 485 Mbp repetitive DNA (64%), in particular satellite DNA, retrotransposons and DNA transposons. Genome-wide cytosine methylation in the sugar beet genome was studied in leaves and leaf-derived callus with a focus on repetitive sequences, including retrotransposons and DNA transposons, the major groups of repetitive DNA sequences, and compared with gene methylation. Genes showed a specific methylation pattern for CG, CHG (H = A, C, and T) and CHH sites, whereas the TE pattern differed, depending on the TE class (class 1, retrotransposons and class 2, DNA transposons). Along genes and TEs, CG and CHG methylation was higher than that of adjacent genomic regions. In contrast to the relatively low CHH methylation in retrotransposons and genes, the level of CHH methylation in DNA transposons was strongly increased, pointing to a functional role of asymmetric methylation in DNA transposon silencing. Comparison of genome-wide DNA methylation between sugar beet leaves and callus revealed a differential methylation upon tissue culture. Potential epialleles were hypomethylated (lower methylation) at CG and CHG sites in retrotransposons and genes and hypermethylated (higher methylation) at CHH sites in DNA transposons of callus when compared with leaves.


Subject(s)
Beta vulgaris/genetics , DNA Methylation/physiology , DNA Transposable Elements/genetics , Retroelements/genetics , Retroelements/physiology , DNA Methylation/genetics , DNA Transposable Elements/physiology , Gene Expression Regulation, Plant/genetics , Gene Expression Regulation, Plant/physiology , Genome, Plant/genetics , Plant Proteins/genetics , Plant Proteins/metabolism
5.
J Avian Med Surg ; 29(3): 216-23, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26378668

ABSTRACT

A 6-week-old, parent-reared peregrine falcon ( Falco peregrinus ) was presented with spastic hypertonus of its hind limbs of unknown origin and duration. Radiologic examination revealed smooth periosteal reactions ventrally at thoracic vertebrae 5 to 7. Contrast-enhanced computed tomography identified the swelling as inflammation; antibiotic, antimycotic, anti-inflammatory, and analgesic treatments were initiated, and vitamins and minerals were supplemented. Because the bird's condition did not improve after 10 days, it was euthanatized and submitted for postmortem examination. On histopathologic examination, chronic, active osteomyelitis was diagnosed in thoracic vertebrae 5 to 7, and chronic, active arthritis was present in both the right shoulder and left elbow joints. Staphylococcus hyicus was isolated from these 3 locations, as well as from lungs and liver, indicating a chronic septic staphylococcosis. Although infections with Staphylococcus species are occasional causes of vertebral osteomyelitis in juvenile poultry with active growth plates, it is only sporadically reported in raptors and companion birds. This case report is the first description of the clinical features and diagnostic and pathologic findings in a juvenile peregrine falcon with hematogenous osteomyelitis and arthritis associated with septicemia caused by S hyicus.


Subject(s)
Arthritis, Infectious/veterinary , Bird Diseases/microbiology , Falconiformes , Osteomyelitis/veterinary , Spine/pathology , Staphylococcal Infections/veterinary , Staphylococcus hyicus/isolation & purification , Animals , Anti-Bacterial Agents/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Arthritis, Infectious/drug therapy , Arthritis, Infectious/microbiology , Arthritis, Infectious/pathology , Bird Diseases/pathology , Fluoroquinolones/therapeutic use , Male , Meloxicam , Osteomyelitis/drug therapy , Osteomyelitis/microbiology , Osteomyelitis/pathology , Staphylococcal Infections/drug therapy , Staphylococcal Infections/microbiology , Staphylococcal Infections/pathology , Thiazines/therapeutic use , Thiazoles/therapeutic use
6.
Cytogenet Genome Res ; 143(1-3): 157-67, 2014.
Article in English | MEDLINE | ID: mdl-24994030

ABSTRACT

DNA methylation is an essential epigenetic feature for the regulation and maintenance of heterochromatin. Satellite DNA is a repetitive sequence component that often occurs in large arrays in heterochromatin of subtelomeric, intercalary and centromeric regions. Knowledge about the methylation status of satellite DNA is important for understanding the role of repetitive DNA in heterochromatization. In this study, we investigated the cytosine methylation of the ancient satellite family pEV in the wild beet Beta procumbens. The pEV satellite is widespread in species-specific pEV subfamilies in the genus Beta and most likely originated before the radiation of the Betoideae and Chenopodioideae. In B. procumbens, the pEV subfamily occurs abundantly and spans intercalary and centromeric regions. To uncover its cytosine methylation, we performed chromosome-wide immunostaining and bisulfite sequencing of pEV satellite repeats. We found that CG and CHG sites are highly methylated while CHH sites show only low levels of methylation. As a consequence of the low frequency of CG and CHG sites and the preferential occurrence of most cytosines in the CHH motif in pEV monomers, this satellite family displays only low levels of total cytosine methylation.


Subject(s)
Beta vulgaris/genetics , Beta vulgaris/metabolism , Cytosine/metabolism , DNA Methylation/genetics , DNA, Satellite/genetics , Base Sequence , Centromere/genetics , Chromosomes, Plant/genetics , CpG Islands/genetics , Molecular Sequence Data
9.
Forensic Sci Int ; 206(1-3): 92-7, 2011 Mar 20.
Article in English | MEDLINE | ID: mdl-20650576

ABSTRACT

BACKGROUND: A vast array of substances are marketed as "legal highs" in the UK. These products are mainly marketed online and are packaged and produced to mimic illicit drugs. Little is known about the full range of products available at present and no studies have evaluated the product information provided to consumers. AIMS & HYPOTHESIS: To describe the available legal high products marketed by UK-based Internet retailers and evaluate the product information provided to consumers. METHODS: Websites were identified using the terms "buy legal highs+UK" and two search engines. The first 100 hits and a random sample of 5% of the remaining results were screened. Websites based in the UK were included and all products were entered on a database. Information on product name, list price, claimed effects, side effects, contraindications and interactions was extracted. A descriptive analysis was conducted using SPSS v14. RESULTS: 115 Websites met the inclusion criteria but due to duplicate listings this was reduced to 39 unique Websites. 1308 products were found and evaluated. The average product price was 9.69 British pounds. Products took the form of pills (46.6%), smoking material (29.7%) and single plant material/extract (18.1%). Most products claimed to be stimulants (41.7%), sedatives (32.3%), or hallucinogens (12.9%). 40.1% of products failed to list ingredients, 91.9% failed to list side effects, 81.9% failed to list contraindications and 86.3% failed to list drug interactions. Top 5 products (with active ingredients in brackets) by frequency were Salvia divinorum (Salivinorin A), Kratom (Mitragynine), Hawaiian Baby Woodrose Seeds (Lysergic Acid Amide), Fly Agaric (Ibotenic Acid, Muscimol) and Genie (JWH018, CP47497). CONCLUSIONS: Products marketed as "legal highs" are easily available from UK-based Internet retailers and are reasonably affordable. Safety information provided to consumers is poor. Uninformed users risk serious adverse effects.


Subject(s)
Central Nervous System Agents , Commerce , Internet , Consumer Health Information , Consumer Product Safety , Designer Drugs , Dosage Forms , Drug Labeling , Humans , Marketing , Plant Extracts , Search Engine , United Kingdom
10.
Ann Rheum Dis ; 69(10): 1853-60, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20498218

ABSTRACT

BACKGROUND: The proinflammatory and anti-inflammatory role of the sympathetic nervous system in early and late inflammation is an unresolved paradox. A drastic loss of sympathetic nerve fibres in the synovial tissue of patients with rheumatoid arthritis (RA) has previously been demonstrated. The presence of tyrosine hydroxylase (TH)-positive cells in RA and osteoarthritis (OA) has been determined, but the role of these cells in inflammation is still unclear. OBJECTIVE: To characterise TH-positive cells in inflamed RA and OA synovial tissue and to study their role in inflammation. METHODS: Synovial samples were obtained from 32 patients with OA and 19 patients with RA and from 10 control patients. Synovial tissue samples were used for immunofluorescence staining. Synovial cells were isolated by tissue digestion and immediately used for cell culture. For in vivo experiments, collagen type-II arthritis in DBA/1J mice was induced. RESULTS: TH+ cells were present only in inflamed tissue and not in controls. Catecholamine-storing vesicles and vesicular monoamine transporter 2 (VMAT2) were identified in the synovial tissue. Experimental increase of cytoplasmic catecholamines by VMAT2 blockade strongly reduced tumour necrosis factor (TNF) independently of canonical extracellular ß-adrenergic signalling. In addition, VMAT2 blockade increased cyclic AMP (cAMP) and cAMP responsive element binding protein, responsible for TNF inhibition. In vivo, appearance of VMAT2 positive cells was confirmed. VMAT2 blockade ameliorated inflammation also in vivo. CONCLUSIONS: This study demonstrates that local catecholamine-producing cells start to replace sympathetic nerve fibres around the onset of disease, and modulation of locally produced catecholamines has strong anti-inflammatory effects in vivo and in vitro.


Subject(s)
Arthritis, Rheumatoid/metabolism , Catecholamines/biosynthesis , Neurotransmitter Agents/metabolism , Osteoarthritis, Knee/metabolism , Synovial Membrane/metabolism , Adrenergic Fibers/metabolism , Adrenergic Fibers/pathology , Adult , Animals , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Arthritis, Experimental/drug therapy , Arthritis, Experimental/metabolism , Arthritis, Experimental/pathology , Arthritis, Rheumatoid/pathology , Cells, Cultured , Cytoplasm/metabolism , Drug Evaluation, Preclinical/methods , Humans , Mice , Mice, Inbred DBA , Middle Aged , Osteoarthritis, Knee/pathology , Reserpine/pharmacology , Reserpine/therapeutic use , Synovial Membrane/innervation , Synovial Membrane/pathology , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Tumor Necrosis Factor-alpha/metabolism , Tyrosine 3-Monooxygenase/metabolism , U937 Cells
11.
J Cardiovasc Electrophysiol ; 21(11): 1202-7, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20487119

ABSTRACT

UNLABELLED: Intracardiac Echocardiography Guided Cryoballoon Ablation. BACKGROUND: Cryoballoon ablation is increasingly used for pulmonary vein isolation (PVI) in patients with atrial fibrillation (AF). This new technique aims to perform PVI safer and faster. However, procedure and fluoroscopy times were similar to conventional RF approaches. We compared ICE plus fluoroscopy versus fluoroscopy alone for anatomical guidance of PVI. METHODS: Forty-three consecutive patients with paroxysmal AF were randomly assigned to ICE plus fluoroscopy (n = 22) versus fluoroscopy alone (n = 21) for guidance of cryoballoon PVI. A "single big balloon" procedure using a 28 mm cryoballoon was performed. The optimal ICE-guided position of the cryoballoon was assessed by full ostial occlusion and loss of Doppler coded reflow to the left atrium (LA). Any further freezes were ICE-guided only without use of fluoroscopy or contrast media injection. RESULTS: A total of 171 pulmonary veins could be visualized with ICE. 80% of ICE-guided freezes were performed with excellent ICE quality. Acute procedural success and AF recurrence rate at 6 months were similar in both groups (AF recurrence: ICE-guided = 27% vs Fluoroscopy = 33%; P = ns). Patients without ICE guidance had significantly longer procedure (143 ± 27 minutes vs 130 ± 19 minutes; P = 0.05) and fluoroscopy times (42 ± 13 minutes vs 26 ± 10, P = 0.01). The total amount of contrast used during the procedure was significantly lower in patients with ICE guidance (88 ± 31 mL vs 169 ± 38 mL, P < 0.001). CONCLUSION: Additional ICE guidance appears to be associated with lower fluoroscopy, contrast, and procedure times, with similar efficacy rates. Specifically, ICE allows for better identification of the PV LA junction and more precise anatomically guided cryoballoon ablations.


Subject(s)
Atrial Fibrillation/diagnostic imaging , Atrial Fibrillation/surgery , Catheterization/methods , Cryosurgery/methods , Echocardiography/methods , Surgery, Computer-Assisted/methods , Electrophysiologic Techniques, Cardiac/methods , Female , Humans , Male , Middle Aged , Pilot Projects , Radiography , Treatment Outcome
12.
Pain ; 148(1): 26-35, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19879047

ABSTRACT

Both cyclooxygenase-1 and -2 are expressed in the spinal cord, and the spinal COX product prostaglandin E(2) (PGE(2)) contributes to the generation of central sensitization upon peripheral inflammation. Vice versa spinal COX inhibition is considered an important mechanism of antihyperalgesic pain treatment. Recently, however, COX-2 was shown to be also involved in the metabolism of endocannabinoids. Because endocannabinoids can have analgesic actions it is conceivable that inhibition of spinal COX produces analgesia not only by inhibition of PG synthesis but also by inhibition of endocannabinoid breakdown. In the present study, we recorded from spinal cord neurons with input from the inflamed knee joint and we measured the spinal release of PGE(2) and the endocannabinoid 2-arachidonoyl glycerol (2-AG) in vivo, using the same stimulation procedures. COX inhibitors were applied spinally. Selective COX-1, selective COX-2 and non-selective COX inhibitors attenuated the generation of spinal hyperexcitability when applied before and during development of inflammation but, when inflammation and spinal hyperexcitability were established, only selective COX-2 inhibitors reversed spinal hyperexcitability. During established inflammation all COX inhibitors reduced release of spinal PGE(2) almost equally but only the COX-2 inhibitor prevented breakdown of 2-AG. The reversal of spinal hyperexcitability by COX-2 inhibitors was prevented or partially reversed by AM-251, an antagonist at the cannabinoid-1 receptor. We conclude that inhibition of spinal COX-2 not only reduces PG production but also endocannabinoid breakdown and provide evidence that reversal of inflammation-evoked spinal hyperexcitability by COX-2 inhibitors is more related to endocannabinoidergic mechanisms than to inhibition of spinal PG synthesis.


Subject(s)
Arachidonic Acids/metabolism , Arthritis, Experimental/enzymology , Dinoprostone/metabolism , Glycerides/metabolism , Prostaglandin-Endoperoxide Synthases/metabolism , Spinal Cord/enzymology , Action Potentials/drug effects , Animals , Arthritis, Experimental/chemically induced , Arthritis, Experimental/drug therapy , Arthritis, Experimental/pathology , Disease Models, Animal , Drug Administration Routes , Endocannabinoids , Enzyme Inhibitors/pharmacology , Enzyme Inhibitors/therapeutic use , Indans/pharmacology , Indans/therapeutic use , Injections, Spinal/methods , Knee Joint/pathology , Male , Neurons/drug effects , Neurons/physiology , Pain Measurement , Physical Stimulation/methods , Piperidines/pharmacology , Piperidines/therapeutic use , Pyrazoles/pharmacology , Pyrazoles/therapeutic use , Rats , Rats, Wistar , Spinal Cord/drug effects , Spinal Cord/pathology , Statistics, Nonparametric
13.
Psychosom Med ; 72(2): 156-62, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19995883

ABSTRACT

OBJECTIVE: To examine prospectively whether early parental child-rearing behavior is a predictor of cardiometabolic outcome in young adulthood when other potential risk factors are controlled. Metabolic factors associated with increased risk for cardiovascular disease have been found to vary, depending on lifestyle as well as genetic predisposition. Moreover, there is evidence suggesting that environmental conditions, such as stress in pre- and postnatal life, may have a sustained impact on an individual's metabolic risk profile. METHODS: Participants were drawn from a prospective, epidemiological, cohort study followed up from birth into young adulthood. Parent interviews and behavioral observations at the age of 3 months were conducted to assess child-rearing practices and mother-infant interaction in the home setting and in the laboratory. In 279 participants, anthropometric characteristics, low-density lipoprotein and high-density lipoprotein cholesterol, apolipoproteins, and triglycerides were recorded at age 19 years. In addition, structured interviews were administered to the young adults to assess indicators of current lifestyle and education. RESULTS: Adverse early-life interaction experiences were significantly associated with lower levels of high-density lipoprotein cholesterol and apolipoprotein A1 in young adulthood. Current lifestyle variables and level of education did not account for this effect, although habitual smoking and alcohol consumption also contributed significantly to cardiometabolic outcomes. CONCLUSIONS: These findings suggest that early parental child-rearing behavior may predict health outcome in later life through its impact on metabolic parameters in adulthood.


Subject(s)
Cardiovascular Diseases/epidemiology , Child Rearing/psychology , Maternal Behavior , Mother-Child Relations , Adolescent , Anthropometry , Breast Feeding/psychology , Cardiovascular Diseases/etiology , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Infant , Longitudinal Studies , Male , Plant Extracts/blood , Prospective Studies , Risk Factors , Triglycerides/blood , Young Adult
14.
Future Cardiol ; 6(1): 113-27, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20014991

ABSTRACT

Cardiac imaging, both noninvasive and invasive, has become a crucial part of evaluating patients during the electrophysiology procedure experience. These anatomical data allow electrophysiologists to not only assess who is an appropriate candidate for each procedure, but also to determine the rate of success from these procedures. This article incorporates a review of the various cardiac imaging techniques available today, with a focus on atrial arrhythmias, ventricular arrhythmias and device therapy.


Subject(s)
Electrophysiologic Techniques, Cardiac/trends , Heart Diseases/diagnosis , Heart Diseases/therapy , Arrhythmias, Cardiac/diagnosis , Atrial Fibrillation/diagnosis , Atrial Fibrillation/diagnostic imaging , Atrial Fibrillation/therapy , Cardiac Pacing, Artificial , Catheter Ablation , Echocardiography , Heart Atria/diagnostic imaging , Humans , Magnetic Resonance Imaging , Pulmonary Veins/anatomy & histology , Pulmonary Veins/diagnostic imaging , Tomography, X-Ray Computed
15.
Int J Microbiol ; 2010: 930465, 2010.
Article in English | MEDLINE | ID: mdl-21234349

ABSTRACT

Boric acid (BA) has broad antimicrobial activity that makes it a popular treatment for yeast vaginitis in complementary and alternative medicine. In the model yeast S. cerevisiae, BA disturbs the cytoskeleton at the bud neck and impairs the assembly of the septation apparatus. BA treatment causes cells to form irregular septa and leads to the synthesis of irregular cell wall protuberances that extend far into the cytoplasm. The thick, chitin-rich septa that are formed during BA exposure prevent separation of cells after abscission and cause the formation of cell chains and clumps. As a response to the BA insult, cells signal cell wall stress through the Slt2p pathway and increase chitin synthesis, presumably to repair cell wall damage.

16.
J Antimicrob Chemother ; 63(2): 325-36, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19059942

ABSTRACT

BACKGROUND: Boric acid is a commonly cited treatment for recurrent and resistant yeast vaginitis, but data about the extent and mechanism of its antifungal activity are lacking. OBJECTIVES: The aim of this study was to use in vitro methods to understand the spectrum and mechanism of boric acid as a potential treatment for vaginal infection. METHODS: Yeast and bacterial isolates were tested by agar dilution to determine the intrinsic antimicrobial activity of boric acid. Established microbial physiology methods illuminated the mechanism of the action of boric acid against Candida albicans. RESULTS: C. albicans strains (including fluconazole-resistant strains) were inhibited at concentrations attainable intravaginally; as were bacteria. Broth dilution MICs were between 1563 and 6250 mg/L and boric acid proved fungistatic (also reflected by a decrease in CO(2) generation); prolonged culture at 50,000 mg/L was fungicidal. Several organic acids in yeast nitrogen broth yielded a lower pH than equimolar boric acid and sodium borate but were less inhibitory. Cold or anaerobic incubation protected yeast at high boric acid concentrations. Cells maintained integrity for 6 h in boric acid at 37 degrees C, but after 24 h modest intrusion of propidium iodide occurred; loss of plate count viability preceded uptake of vital stain. Growth at sub-MIC concentrations of boric acid decreased cellular ergosterol. The drug efflux pump CDR1 did not protect Candida as CDR1 expression was abrogated by boric acid. Boric acid interfered with the development of biofilm and hyphal transformation. CONCLUSIONS: Boric acid is fungistatic to fungicidal depending on concentration and temperature. Inhibition of oxidative metabolism appears to be a key antifungal mechanism, but inhibition of virulence probably contributes to therapeutic efficacy in vivo.


Subject(s)
Antifungal Agents/pharmacology , Boric Acids/pharmacology , Candida albicans/drug effects , Bacteria/drug effects , Candida albicans/chemistry , Candidiasis, Vulvovaginal/drug therapy , Colony Count, Microbial , Ergosterol/analysis , Female , Humans , Microbial Sensitivity Tests , Microbial Viability
17.
Wien Med Wochenschr ; 156(3-4): 102-10, 2006 Feb.
Article in German | MEDLINE | ID: mdl-16699941

ABSTRACT

Modern services for persons with disorders resulting from psychoactive drug abuse must conform to the complexity of their needs. Low threshold access, standards for the prescription of opiates, out-patient, in-patient and day-hospital detoxification, rehabilitation and abstinence oriented strategies are fundamental prerequisites. The quality of services for drug dependent patients is defined by the percentage finding access to the service, the percentage of those continuing in the service, the easy and rapid transition between the different elements of the service, the degree of abstinence, decriminalization, physical comorbidity and mortality. Finally the cost of treated and untreated drug dependence should be considered.


Subject(s)
Day Care, Medical/standards , Delivery of Health Care, Integrated/standards , Health Services Accessibility/standards , Psychotropic Drugs , Quality Assurance, Health Care/standards , Regional Medical Programs/standards , Substance Abuse Treatment Centers/standards , Substance-Related Disorders/rehabilitation , Austria , Comorbidity , Cooperative Behavior , Cross-Sectional Studies , Day Care, Medical/organization & administration , Delivery of Health Care, Integrated/organization & administration , Health Services Accessibility/organization & administration , Health Services Needs and Demand/organization & administration , Health Services Needs and Demand/standards , Humans , Patient Care Team/organization & administration , Patient Care Team/standards , Quality Assurance, Health Care/organization & administration , Regional Medical Programs/organization & administration , Substance Abuse Treatment Centers/organization & administration , Substance-Related Disorders/epidemiology
18.
Schizophr Res ; 77(1): 11-24, 2005 Sep 01.
Article in English | MEDLINE | ID: mdl-16005381

ABSTRACT

BACKGROUND: We studied descriptive and causal associations between schizophrenia, depressive symptoms and episodes of depression. METHODS: Untreated psychotic, depressive and negative symptoms were assessed retrospectively from onset until first admission using the IRAOS in a population-based sample of 232 first episodes of schizophrenia. A representative subsample of 130 patients, studied retrospectively until onset and followed up prospectively over 6 months after first admission, were compared with 130 age- and sex-matched healthy population controls and with 130 equally matched first admissions for unipolar depressive episodes. RESULTS: The lifetime prevalence of depressive mood (>or=2 weeks) at first admission for schizophrenia was 83%. The most frequent initial symptom of schizophrenia was depressive mood, appearing more than 4 years before first admission and followed by negative symptoms and functional impairment. Showing considerable overlap in symptoms and functional impairment at their initial stages, schizophrenia and unipolar depression became clearly distinguishable with the emergence of psychotic symptoms. In the first psychotic episode 71% presented clinically relevant depressive symptoms, 23% fulfilled the ICD-10 criteria for a depressive episode. With remitting psychosis the prevalence of depression, too, decreased. The high frequency of depressive symptoms at the prepsychotic prodromal stage and their increase and decrease with the psychotic episode suggests that depression in schizophrenia might be expression of an early, mild stage of the same neurobiological process that causes psychosis. CONCLUSIONS: The high prevalence of depression in the population and the diversity of its causes prompted us to speculate about a hierarchical model of preformed dimensional patterns of psychopathology.


Subject(s)
Depression/epidemiology , Depression/physiopathology , Schizophrenia/epidemiology , Schizophrenia/physiopathology , Schizophrenic Psychology , Adolescent , Adult , Age of Onset , Case-Control Studies , Child , Demography , Depression/diagnosis , Diagnosis, Differential , Female , Follow-Up Studies , Humans , Male , Middle Aged , Models, Psychological , Psychiatric Status Rating Scales/statistics & numerical data , Schizophrenia/diagnosis
19.
Arthritis Rheum ; 52(6): 1721-9, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15934093

ABSTRACT

OBJECTIVE: Use of anti-tumor necrosis factor (anti-TNF) antibody therapy in rheumatoid arthritis (RA) has expanded our understanding of possible mechanisms by which this treatment reduces inflammation. Beyond its effects on local immune responses, anti-TNF treatment may also modulate the local hormone supply. Because androgens are thought to inhibit immune responses, their presence in inflamed tissue is an additional important antiinflammatory factor. METHODS: We investigated conversion of the ubiquitous dehydroepiandrosterone sulfate (DHEAS), the biologically inactive precursor of DHEA, to the androgen DHEA in mixed synovial cells from patients with RA and patients with osteoarthritis (OA), making use of thin-layer chromatography and phosphorimaging. Using immunohistochemical analysis, we detected the key enzyme, steroid sulfatase. RESULTS: DHEAS-to-DHEA conversion in synovial cells from patients with RA was significantly lower than that in synovial cells from patients with OA (mean +/- SEM 3.3 +/- 0.5% versus 6.0 +/- 0.9% of applied (3)H-DHEAS per 10(6) synovial cells; P = 0.042). In RA, but not in OA, the level of converted (3)H-DHEA was inversely correlated with the density of synovial macrophages (for RA, R(rank) = -0.725, P = 0.005; for OA, R(rank) = 0.069, P not significant [NS]) and T cells (for RA, R(rank) = -0.621, P = 0.024; for OA, R(rank) = 0.247, P NS). Double immunohistochemistry analysis revealed that steroid sulfatase was located mainly in synovial macrophages but was also observed in fibroblasts. Neutralization of TNF largely up-regulated the conversion of DHEAS to DHEA in RA, but not in OA. A similar neutralizing effect was observed with polyclonal human immunoglobulins; this effect is most probably mediated via TNF neutralization at low TNF concentrations. CONCLUSION: These data indicate that TNF inhibits the conversion of DHEAS to DHEA in RA synovial cells. Because androgens are antiinflammatory mediators, TNF-induced inhibition of the local androgen supply is a supplementary proinflammatory factor. Consequently, anti-TNF strategies may also exert their positive effects by increasing tissue androgens.


Subject(s)
Arthritis, Rheumatoid/immunology , Dehydroepiandrosterone Sulfate/metabolism , Dehydroepiandrosterone/metabolism , Tumor Necrosis Factor-alpha/immunology , Aged , Female , Humans , Male , Middle Aged , Osteoarthritis/immunology , Synovial Membrane/immunology
20.
J Biomol Screen ; 10(1): 46-55, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15695343

ABSTRACT

Although fluorescence imaging plate reader (FLIPR)-based assays have been widely used in high-throughput screening, improved efficiencies in throughput and fidelity continue to be investigated. This study presents an offline compound addition protocol coupled with a testing strategy using mixtures of compounds in a 384-well format to identify antagonists of the neurokinin-1 receptor expressed in the human astrocytoma cell line (U373 MG). Substance P evoked a concentration-dependent increase in intracellular cellular Ca(2+) with an EC(50) value of 0.30 +/- 0.17 nM, which was inhibited by neurokinin-1 (NK1) antagonists L-733,060 and L-703,606. Test compounds, as mixtures of 10 compounds/well, were added to the cells offline using an automated dispensing unit and incubated prior to performing the assay in the FLIPR. Using the offline protocol, a higher through put of ~200,000 compounds was achieved in an 8-h working day, and several novel structural classes of compounds were identified as antagonists for the NK1 receptor. These studies demonstrate that the offline compound addition format using a mixture of compounds in a 384-well FLIPR assay provides an efficient platform for screening and identifying modulators for G-protein-coupled receptors.


Subject(s)
Drug Evaluation, Preclinical/instrumentation , Drug Evaluation, Preclinical/methods , Receptors, G-Protein-Coupled/metabolism , Cell Line, Tumor , Fluorescent Dyes/chemistry , Fluorescent Dyes/pharmacology , Humans , Inhibitory Concentration 50 , Kinetics , Receptors, G-Protein-Coupled/antagonists & inhibitors , Receptors, Neurokinin-1/metabolism
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