ABSTRACT
BACKGROUND: Empirical studies on migration and mental health of migrants are still rare. In Germany they are often characterised by low sample sizes and are limited to certain diseases and geographical areas (old federal states). The comparability of their results is limited. Nonetheless, the assessment of migrants' health is necessary for adequate medical and psychosocial care for this target group. AIM: To provide data on mental health of migrants from Poland and from Vietnam in Germany. METHODS: We have assessed a random sample of migrants from Poland (n=140) and from Vietnam (n=88) using the Giessen Subjective Complaints List - 24 (GSCL-24) and the Hospital Anxiety and Depression Scale (HADS). Additionally we asked migrants about their knowledge of health care institutions in case of psychosocial problems, their demands and the existing barriers to health care utilisation. RESULTS: Migrants from Poland and Vietnam have a higher general score of complaints of physical ill-health and higher anxiety and depression values than Germans. Psychosocial and medical institutions are visited less. CONCLUSION: Further analytical studies are needed to clarify health differences between these groups. Migrants are a heterogeneous group and only group-specific investigations will clarify associations between countries of origin, health status and use of health care institutions.
Subject(s)
Emigrants and Immigrants/psychology , Mental Disorders/ethnology , Adult , Female , Germany/epidemiology , Humans , Male , Mental Disorders/psychology , Mental Disorders/therapy , Mental Health , Mental Health Services/statistics & numerical data , Poland/ethnology , Psychology , Vietnam/ethnologyABSTRACT
The article provides an overview of the contemporary literature on the social and psychological factors which are associated with migration. Derived from the operationalisation of "migration" and an examination of the methodological peculiarities of migration research, a (transactional) stress model of migration is proposed incorporating potentially stress-eliciting influences of migration including occupational pressures, social isolation and/or family-related problems and their impact on psychological and physical health. There are inconsistencies in the findings regarding psychological health, which can in part be explained through the phenomena of the "healthy migrant effect", duration of stay in the host culture or the culture-specificity. Moreover, a discussion is provided of the extent that disorders associated with differentially stressed migrants will be manifested in the health care system. Finally, concluding remarks are offered together with a short discussion of the implication of these findings for future research and social and health policy decision-making.
Subject(s)
Mental Disorders/epidemiology , Stress, Psychological , Transients and Migrants/psychology , Acculturation , Adult , Alcoholism/epidemiology , Child , Cultural Diversity , Delivery of Health Care , Ethnicity , Europe , Germany , Health Policy , Humans , Mental Health , Public Policy , Research , Risk Factors , Social Isolation , Social Support , Socioeconomic Factors , Substance-Related Disorders/epidemiology , Time FactorsABSTRACT
OBJECTIVES: The aim of the study is the description of subjective morbidity, health care system utilisation and complaints of ethnic German migrants from the former Soviet Union at the beginning of migration. At present no data are available concerning aspects of health behaviour among this largest immigrant population in Germany. METHODS: 300 ethnic German migrants and their families (mean age 37.2 and 51% female) were interrogated shortly after migration to Germany. They answered questions about prevalence of diseases, health care system utilization, actual health status and completed the Giessen Subjective Complaints List (GSCL-24). German standards exist for all questionnaires. RESULTS: 237 ethnic German migrants report to have suffered from at least one disease during the course of the last year. They see the gynaecologist and dentist as often as the German population, pay fewer visits to practitioners and specialists but seek more medical advice from the medical lay system. The majority of subjects are satisfied with their health. Migrants describe their health status as lower than the German population compared to which they also report more complaints (Overall distress in GSCL-24 : 17.2 for migrants and 14.0 for Germans) and different complaints (headaches, fatigue). CONCLUSIONS: The different medical care system and differences in the treatment of patients could account for the less frequent use of medical services by ethnic German migrants. Actual stressors like language differences and acculturation problems are discussed as possible reasons for the increased rate of complaints among ethnic German migrants. Although they suffer from more complaints the German migrants do not seem to modify their help-seeking behaviour.
Subject(s)
Emigration and Immigration/statistics & numerical data , Ethnicity/statistics & numerical data , Health Resources/statistics & numerical data , Health Status Indicators , National Health Programs/statistics & numerical data , Acculturation , Adolescent , Adult , Aged , Attitude to Health , Female , Germany , Humans , Male , Middle Aged , Morbidity , Patient Acceptance of Health Care/ethnology , Patient Acceptance of Health Care/statistics & numerical data , USSR/ethnology , Utilization Review/statistics & numerical dataABSTRACT
Enormous amounts of data result from genome sequencing projects and new experimental methods. Within this tremendous amount of genomic data 30-40 per cent of the genes being identified in an organism remain unknown in terms of their biological function. As a consequence of this lack of information the overall schema of all the biological functions occurring in a specific organism cannot be properly represented. To understand the functional properties of the genomic data more experimental data must be collected. A pathway database is an effort to handle the current knowledge of biochemical pathways and in addition can be used for interpretation of sequence data. Some of the existing pathway databases can be interpreted as detailed functional annotations of genomes because they are tightly integrated with genomic information. However, experimental data are often lacking in these databases. This paper summarises a list of pathway databases and some of their corresponding biological databases, and also focuses on information about the content and the structure of these databases, the organisation of the data and the reliability of stored information from a biological point of view. Moreover, information about the representation of the pathway data and tools to work with the data are given. Advantages and disadvantages of the analysed databases are pointed out, and an overview to biological scientists on how to use these pathway databases is given.
Subject(s)
Databases, Factual , Metabolism , Animals , Computational Biology , Genome , Humans , Internet , User-Computer InterfaceABSTRACT
The correct functioning of Ras proteins requires post-translational modification of the GTP hydrolases (GTPases). These modifications provide hydrophobic moieties that lead to the attachment of Ras to the inner side of the plasma membrane. In this study we investigated the role of Ras processing in the interaction with various putative Ras-effector proteins. We describe a specific, GTP-independent interaction between post-translationally modified Ha- and Ki-Ras4B and the G-protein responsive phosphoinositide 3-kinase p110gamma. Our data demonstrate that post-translational processing increases markedly the binding of Ras to p110gamma in vitro and in Sf9 cells, whereas the interaction with p110alpha is unaffected under the same conditions. Using in vitro farnesylated Ras, we show that farnesylation of Ras is sufficient to produce this effect. The complex of p110gamma and farnesylated RasGTP exhibits a reduced dissociation rate leading to the efficient shielding of the GTPase from GTPase activating protein (GAP) action. Moreover, Ras processing affects the dissociation rate of the RasGTP complex with the Ras binding domain (RBD) of Raf-1, indicating that processing induces alterations in the conformation of RasGTP. The results suggest a direct interaction between a moiety present only on fully processed or farnesylated Ras and the putative target protein p110gamma.
Subject(s)
GTP Phosphohydrolases/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Protein Processing, Post-Translational , ras Proteins/metabolism , Animals , GTPase-Activating Proteins/metabolism , Nucleopolyhedroviruses/genetics , Protein Binding , Protein Prenylation , Proto-Oncogene Proteins c-raf/metabolism , Proto-Oncogene Proteins p21(ras)/metabolism , Recombinant Fusion Proteins/metabolism , SpodopteraABSTRACT
An institute in Mainz, Germany (Mainzer Institut für Prüfungsfragen, IMPP), regularly publishes statistics comparing the results of the written examinations for medical students in the first stage of their course at different universities. These figures apply to those students who sit the examination in the normal course of their studies and lead to a ranking of the various Medical Schools in Germany according to exam results. Those with a low failure rate and above average exam marks range at the top of the list and are generally considered to provide a better quality medical training than those lower down on the list. For the first time these figures are set in relation to the number of students admitted to the course in the first place, thus including those students who do not sit the exams after the normal period of time. This reveals a very different picture. Taking into account the current political and economic discussion criticising university courses for being too long or too costly a department would then achieve a higher ranking if it can prove that more students sit and pass their first-stage medical exam after the standard period of four semesters, even if this involves lower average exam results and higher failure rates.
Subject(s)
Educational Measurement/statistics & numerical data , Quality Assurance, Health Care/statistics & numerical data , Schools, Medical/statistics & numerical data , Students, Medical/statistics & numerical data , Germany , HumansABSTRACT
The aim of this study was to determine effects of prostaglandin E2 (PGE2) on amount and composition of high molecular weight glycoproteins (HMG), released by human gastric mucous cells in primary culture. PGE2 stimulated the release of HMG, as evidenced by measurement of total carbohydrate and protein content, in a concentration-dependent manner. At the maximally tested concentration of 10(-5) mol/l, the increase amounted to 53% and 85%, over controls, for carbohydrate and protein, respectively. The stimulated release was accompanied by alterations of HMG glycosylation. As detected by lectin-ELISA, there was a relative decrease in N-acetyl glucosamine and an increase in mannose and galactose content. The sialic acid content increased in parallel to the total carbohydrate content. These results suggest that PGE2 plays a regulatory role in the synthesis and secretion of HMG by human gastric mucous cells.
Subject(s)
Dinoprostone/pharmacology , Gastric Mucosa/drug effects , Glycoproteins/metabolism , 16,16-Dimethylprostaglandin E2/pharmacology , Carbohydrates/analysis , Cells, Cultured , Enzyme-Linked Immunosorbent Assay , Gastric Mucosa/metabolism , Glycoproteins/chemistry , Glycosylation/drug effects , Humans , Lectins , Mannose/analysis , Molecular Weight , Protein BindingABSTRACT
During microbial colonization, mucin-releasing goblet cells of germ-free (GF) rats proliferate and upregulate their mucin synthesis, thus improving the intestinal mucus barrier. The present study determined the significance of bacterial membrane constituents for this development. A single dose of lipopolysaccharide (LPS) (35 micrograms/100 g body weight) and lipid A (3.5 micrograms/100 g body weight, respectively), was perorally administered to GF AS/Ztm rats. One, 3 and 5 days later, sections of the proximal and distal colon served for characterization of mucin-secreting goblet cells, released mucins were isolated in parallel. Maximal goblet cell diameters were evidenced at day 3. LPS generated a maximal goblet cell hyperplasia one day after challenge, lipid A stimulated the goblet cell proliferation continuously up to day 5. Three days after challenge with one of the stimuli, either, intracellular mucins had shifted significantly to neutral constituents. In addition, mucins, adherent to the colon mucosa and submerged to the luminal content, respectively, then were augmented. At day 5, adherent mucins were similar to the controls, while luminal, soluble constituents had further increased. Histometrical and biochemical methods evidenced a transient, inflammatory response of mucin-secreting cells, followed by an upregulated release of immature mucins.
Subject(s)
Colon/drug effects , Germ-Free Life/drug effects , Intestinal Mucosa/drug effects , Lipopolysaccharides/pharmacology , Mucins/biosynthesis , Administration, Oral , Amino Sugars/analysis , Animals , Carbohydrates/chemistry , Colon/anatomy & histology , Intestinal Mucosa/anatomy & histology , Lipid A/pharmacology , Monosaccharides/analysis , Mucins/chemistry , N-Acetylneuraminic Acid/analysis , Rats , Rats, Inbred StrainsABSTRACT
BACKGROUND: The intestinal epithelium, with the potential to restrict luminal noxae from the host, secretes a mucous layer with various protective functions. Microbial colonization of germfree (GF) rats stimulates this mucin-secreting tissue. The present study determined the effect of bacterial lipopolysaccharides (LPS) on this process. METHODS: One, 3, and 5 days after peroral application of 35 micrograms LPS/100 g body weight (from Escherichia coli O55:B5), LPS concentrations were monitored in ingesta, intestinal tissue, and liver. Mucin high molecular weight glycoproteins (HMG), released in response to LPS, were isolated and separated into mucins, i) attached to the colonic epithelium (EM) and ii) mixed to the luminal content (LM), respectively. Subsequently, the binding capacity of both mucin fractions for various lectins and for type-1 pili expressing E. coli was determined. RESULTS: Ingesta and tissue had maximal LPS concentrations on days 3 (jejunum) and 5 (colon). Maximal EM secretion was found on day 3, release of LM further increased to day 5. Both mucin fractions had altered glycosylation patterns: augmentation of beta-galactose, alpha-N-acetyl galactosamine, and mannose coincided with a decrease in alpha-fucose. Compared with the controls, attachment of E. coli to EM increased slightly on day 1 only; the binding capacity of LM increased continuously up to day 5. CONCLUSION: Results suggest that mucins, released in response to LPS, in addition to the epithelial protection, support the gut microbial clearance system.
Subject(s)
Colon/metabolism , Intestinal Mucosa/metabolism , Lipopolysaccharides/administration & dosage , Mucins/metabolism , Administration, Oral , Animals , Bacterial Adhesion , Escherichia coli , Germ-Free Life , Glycoproteins/metabolism , Lectins/metabolism , Male , Rats , Rats, Inbred StrainsABSTRACT
Secreting lubricating mucins, colonic crypt goblet cells, contribute to the intestinal protection against mechanical challenge. After feeding germ-free (GF) and specific pathogen-free (SPF) AS/Ztm rats for 6 weeks, the proliferative response of colonic goblet to a commercial bulky diet (37.1% fiber) was compared to that of a standard diet. (4.4% fiber). An increased uptake of the high fiber diet by GF rats significantly augmented the capacity for mucin secretion as indicated by the amount and length of crypts, crypt cells and mature goblet cells. The response of SPF rats was limited to a crypt elongation, generated by more crypt cells. In both study groups, the goblet cell replication activity was similar to their controls. The increase in the mucin-secreting capacity, induced by a constant mechanical challenge, highly suggests an improved intestinal protection.
Subject(s)
Colon/cytology , Dietary Fiber/pharmacology , Intestinal Mucosa/cytology , Animals , Cell Division , Dietary Fiber/administration & dosage , Intestinal Mucosa/metabolism , Male , Mucins/metabolism , Rats , Weight GainABSTRACT
We studied the expression of arachidonate 5-lipoxygenase (5-LO) in a cell line of human keratinocytes (HaCaT) and in normal human skin keratinocytes in tissue culture. In undifferentiated keratinocytes 5-LO gene expression was low or undetectable as determined by 5-LO mRNA, protein, cell-free enzyme activity, and leukotriene production in intact cells. However, after shift to culture conditions that promote conversion of prokeratinocytes into a more differentiated phenotype, 5-LO gene expression was markedly induced in HaCaT cells and, to a lesser extent, in normal keratinocytes. These results show that 5-LO gene expression is an intrinsic property of human skin keratinocytes.
Subject(s)
Arachidonate 5-Lipoxygenase/biosynthesis , Gene Expression Regulation, Enzymologic , Keratinocytes/metabolism , Skin/metabolism , Arachidonate 5-Lipoxygenase/genetics , Cell Differentiation , Cell Line , Cells, Cultured , Enzyme Induction , Humans , Hydroxyeicosatetraenoic Acids/analysis , Leukotriene B4/biosynthesis , Leukotriene C4/biosynthesis , Male , Penis/cytology , RNA, Messenger/analysis , Skin/cytologyABSTRACT
The gastric mucus layer consists of high molecular weight glycoproteins (HMG). E-Type prostaglandins (PGs) stimulate total HMG release from isolated gastric mucous cells. We determined the effects of PGE2 on HMG glycosylation. Pig gastric mucous cells were cultured for 20 h with 1 mumol/l PGE2. Released HMG were isolated by gel chromatography and periodic acid-Schiff (PAS)-positive sugars and protein-bound [14C]GlcNAc were determined. Monosaccharides terminally linked to HMG oligosaccharide chains were monitored by lectin enzyme linked immunosorbent assay (ELISA): N-acetylglucosamine (GlcNAc) with Datura stramonium agglutinin, N-acetylgalactosamine (GalNAc) with soy bean agglutinin, fucose (Fuc) with Ulex europaeus I agglutinin and sialic acids (Sial) with Sambucus nigra agglutinin. PGE2 stimulated total HMG release, indicated by an increase of PAS-positive sugars to 170% and [14C]GlcNAc to 220% of controls. Terminal GlcNAc increased to 128%, GalNAc to 133%, Fuc to 165% and Sial to 182%. In addition to stimulation of total HMG release, PGE2 caused alterations of HMG glycosylation, which may modulate HMG viscosity and microbiological barrier function.
Subject(s)
Dinoprostone/pharmacology , Gastric Mucosa/metabolism , Glycoproteins/metabolism , Acetylglucosamine/metabolism , Animals , Cells, Cultured , Chromatography, Gel , Enzyme-Linked Immunosorbent Assay , Glycosylation , Lectins , Molecular Weight , Oligosaccharides/metabolism , Periodic Acid-Schiff Reaction , SwineABSTRACT
An assay for the quantitative determination of the hydroxylation profile of long-chain fatty acids is described for gas chromatography negative-ion chemical ionization mass spectrometry and stable isotope dilution using [carboxyl-18O2]-labeled internal standards. The assay has been applied to the study of fatty acids isolated from body fluids, tissue, and cultured cells. Examples for the analyses of biological systems expressing 5-, 8-, 12-, or 15-lipoxygenase activity are given and the most important sources of analytical errors are addressed. Increased specificity compared to analysis by negative-ion chemical ionization, at the cost of sensitivity, can be achieved by the use of positive-ion electron impact ionization for the investigation of hydrogenated pentafluorobenzylester/trimethylsilylether derivatives. The method described provides complete, specific, and quantitative profiles of hydroxylated fatty acids originally present in biological samples or generated in vitro by incubation with polyunsaturated fatty acid substrates such as linoleic or arachidonic acid.
Subject(s)
Linoleic Acids, Conjugated , Lipoxygenase/metabolism , Animals , Cell Line , Female , Gas Chromatography-Mass Spectrometry , Humans , Hydroxyeicosatetraenoic Acids/analysis , Linoleic Acids/analysis , MiceABSTRACT
The effect of intraluminal challenge on rat colonic mucin producing cells and the amount and composition of released mucins was investigated. Germfree rats (GF) were maintained on a commercial high fiber (HF) diet (37% of undigestable fiber, Altromin 1640 p), in order to increase volume, dry weight and abrasive effect of the ingesta. GF control rats were fed a standard (ST) laboratory diet with 4.5% fiber (Altromin 1314 f). In the HF diet group, histological sections of the proximal and distal colon revealed a significantly increased number of mucin secreting goblet cells and an elevated goblet cell replication activity, as determined by 5'-bromo-deoxyuridine incorporation. The total amount of colonic mucins, isolated by gel filtration, was increased versus the control group. According to the results of ion exchange chromatography, carbohydrate and amino acid analysis, mucins from rats, given the HF diet, had an elevated content of acidic mucin constituents with alterations in the carbohydrate and amino acid composition. In a parallel study with specified pathogen free rats (SPF), the additional influence of the microflora on mucin secreting cells and isolated mucins was determined. An increased number of mucin secreting cells predominantly was observed in rats given the standard diet. Due to bacterial degradation, significantly less mucin was isolated from both dietary groups. The increase of acidic mucin constituents was less pronounced than in GF rat mucin, coinciding with losses of terminally linked monosaccharides. Alterations of the core protein, accompanying the presence of the microflora, were not detected.
Subject(s)
Dietary Fiber/administration & dosage , Intestinal Mucosa/metabolism , Mucins/metabolism , Rats/metabolism , Amino Acids/analysis , Animals , Carbohydrates/analysis , Germ-Free Life , Intestinal Mucosa/anatomy & histology , Male , Mucins/chemistry , Specific Pathogen-Free OrganismsABSTRACT
In order to determine the influence of bacterial colonization on amount and composition of colonic mucins, germfree male AS/Ztm rats were colonized with a rat specific intestinal flora for different times (2, 7, 14, 21, 28, 35, 120 days). The amount of colonic mucins was determined by gel filtration on Sepharose CL-4B; the relative amount of acidic mucins was calculated after ion exchange chromatography. In addition, cecal weight and dry matter of feces were monitored. While germfree and SPF rats revealed similar amounts of colonic mucins (7.0 vs. 7.2 mg mucin/300 g body weight), the initial phase of association was characterized by considerably decreasing values. After four weeks of association, the total amount of colonic mucins had almost equalized in the two groups. The amount of acidic mucins, having decreased during the first three weeks of colonization, rendered values comparable to the SPF mucins after four months of adaptation. Cecomegaly in germfree rats disappeared within the first two days, while solidification of the intestinal content occurred within four months. Mucin losses during initial phase of association are attributed 1. to the disappearance of the cecal mucin pool, and 2. to the mucin degrading activity of some bacterial strains known to be present in the intestinal flora. Further development is conducted by a stimulation of mucin secretion, described to follow the colonization. The initially increased secretion of neutral mucins is attributed to a pronounced release of immature mucin glycoproteins, while the shift to more acidic mucins is considered to result from stimulated secretion as well as from a selective bacterial degradation of neutral mucin components.