RESUMO
A pot experiment under open air conditions was carried out to investigate the uptake, accumulation and toxicity effects of fluoride in olive trees (Olea europaea L.) grown in a soil spiked with inorganic sodium fluoride (NaF). Six different levels (0, 20, 40, 60, 80 and 100mM NaF) of soil spiking were applied through NaF to irrigation water. At the end of the experiment, total fluoride content in soil was 20 and 1770mgFkg(-1) soil in control and 100mM NaF treatments, respectively. The comparative distribution of fluoride partitioning among the different olive tree parts showed that the roots accumulated the most fluoride and olive fruits were minimally affected by soil NaF spiking as they had the lowest fluoride content. In fact, total fluoride concentration varied between 12 and 1070µgFg(-1) in roots, between 9 and 570µgFg(-1) in shoots, between 12 and 290µgFg(-1) in leaves, and between 10 and 29µgFg(-1) in fruits, respectively for control and 100mM NaF treatments. Indeed, the fluoride accumulation pattern showed the following distribution: roots>shoots>leaves>fruits. On the other hand, fluoride toxicity symptoms such as leaf necrosis and leaf drop appeared only in highly spiked soils (60, 80 and 100mM NaF).
Assuntos
Fluoretos/toxicidade , Olea/efeitos dos fármacos , Poluentes do Solo/toxicidade , Biomassa , Fluoretos/análise , Frutas/metabolismo , Olea/crescimento & desenvolvimento , Olea/metabolismo , Folhas de Planta/metabolismo , Raízes de Plantas/metabolismo , Solo/químicaRESUMO
OBJECTIVE: Early diagnosis and prompt effective therapy are crucial to fight against tuberculosis (TB), particularly in regions with a high prevalence. We aimed to evaluate TB diagnostic delays and identify the associated risk factors. METHODS: We conducted a survey in various health facilities in Tunisia between March 24th and October 30th, 2014. We included all patients aged ≥ 18 years who presented with pulmonary TB (PTB) and who had been initiated on an anti-TB treatment. We evaluated the time between respiratory symptom onset and treatment initiation. Treatment delays were divided into three categories: delays due to the patient, to the healthcare system, and overall delays. RESULTS: We included 352 patients in the study (242 men and 110 women). The mean age was 42.2 years±17.7. The median time from symptom onset to treatment initiation was 52.56 days. Patient delays were longer for men, for patients presenting with alcohol dependence, and for patients who already knew they were sick. Healthcare system delays were associated with older age, female patients, patients consulting a private physician, and outpatients. CONCLUSION: TB symptoms should be better explained to the population and healthcare professionals should be better trained to both reduce such delays and initiate treatment as early as possible.
Assuntos
Diagnóstico Tardio/estatística & dados numéricos , Tuberculose Pulmonar/diagnóstico , Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fatores de Risco , Tunísia , Adulto JovemRESUMO
Ten typical cases of sideropenic dysphagia over four years reported and clinical, biological, endoscopic and radiological signs are studied. The authors stress the value of oesophagal opacification for diagnosis. The particularities of our study are the relative high frequency of the disease in Tunisia and the unusual attack in two black patients.
Assuntos
Transtornos de Deglutição/diagnóstico , Síndrome de Plummer-Vinson/diagnóstico , Adulto , Esofagoscopia , Etnicidade , Feminino , Tecnologia de Fibra Óptica , Seguimentos , Humanos , Pessoa de Meia-Idade , Síndrome de Plummer-Vinson/diagnóstico por imagem , Síndrome de Plummer-Vinson/epidemiologia , Radiografia , Tunísia/epidemiologiaRESUMO
We have studied the configuration of genes encoding for the heavy and light chains in the tumoral cells of 6 patients affected by alpha heavy chain disease (alpha HCD). The results showed the presence of rearrangement of the alpha heavy chain as well as the kappa light chain genes whereas the lambda genes were in germinal configuration. Thus, these results suggest the presence of a monoclonal compound in the tumoral cells in the alpha HCD.
Assuntos
Rearranjo Gênico/genética , Genes de Imunoglobulinas/genética , Doença Imunoproliferativa do Intestino Delgado/genética , Adulto , Southern Blotting , HumanosAssuntos
Doença de Hodgkin/diagnóstico , Neoplasias Intestinais/diagnóstico , Jejuno/diagnóstico por imagem , Transtornos da Alimentação e da Ingestão de Alimentos/etiologia , Doença de Hodgkin/diagnóstico por imagem , Doença de Hodgkin/patologia , Doença de Hodgkin/cirurgia , Humanos , Neoplasias Intestinais/diagnóstico por imagem , Neoplasias Intestinais/patologia , Neoplasias Intestinais/cirurgia , Masculino , Pessoa de Meia-Idade , RadiografiaAssuntos
Cateterismo , Colangiografia , Ductos Pancreáticos/diagnóstico por imagem , Ampola Hepatopancreática/diagnóstico por imagem , Doenças Biliares/diagnóstico por imagem , Colelitíase/diagnóstico por imagem , Duodenopatias/diagnóstico por imagem , Endoscopia , Tecnologia de Fibra Óptica , Humanos , Radioisótopos do Iodo , Métodos , Pancreatopatias/diagnóstico por imagemAssuntos
Úlcera Duodenal/sangue , Gastrinas/sangue , Adolescente , Adulto , Idoso , Úlcera Duodenal/cirurgia , Feminino , Humanos , Masculino , Pessoa de Meia-IdadeRESUMO
Human alpha heavy chain disease is characterized by the production of abnormally short alpha IgH chains. In previously published cases it has been found that the malignant cells produce abnormal alpha mRNA, lacking VH and CH1 sequences and composed of a leader sequence peptide, sequences of variable length (69 to 84 bp) and of unknown origin, followed by normal CH2 and CH3 sequences. In this study we established the nucleotide sequence of alpha mRNA for six cases of alpha heavy chain disease. We observed that all six alpha mRNA lack the VH and CH1 sequences as do those previously described. They also contain in-frame inserts of unknown origin between the leader peptide and the normal CH2 and CH3 coding sequences. These inserts are of variable length (42 to 105 bp) and they are unrelated. These results suggest the existence of a common mechanism defect leading to deletions/insertions in alpha heavy chain disease rather than a specific interaction between alpha 1 IgH gene with a unique defined molecular species.