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1.
J Phys Condens Matter ; 25(45): 454205, 2013 Nov 13.
Article in English | MEDLINE | ID: mdl-24141005

ABSTRACT

The nature of the dynamic ionic disorder within the high-temperature superionic phase of strontium bromide, ß-SrBr2, has been investigated using reverse Monte Carlo (RMC) modelling of neutron powder diffraction data and complementary ab initio molecular dynamics (MD) simulations. The RMC and MD results are in good agreement and indicate the presence of extensive dynamic disorder within the Br(-) sublattice of the cubic fluorite structure. Rapid anion diffusion predominantly occurs as hops between nearest neighbour sites in the 〈100〉 directions, though the trajectories are markedly curved and pass through the peripheries of the octahedral voids in the cation sublattice. In addition, there are extensive correlations between the motions of individual Br(-), often leading to the formation of a short-lived square antiprism co-ordination environment around the Sr(2+). Such polyhedra are observed within the (ambient temperature) ordered tetragonal crystal structure of α-SrBr2. The nature of the ionic disorder in SrBr2 is of particular interest because it is the only known example of a Br(-)-ion superionic. Owing to the large size of this anion, a comparison with the behaviour of other superionic phases gives an insight into the role of ionic size on the conducting properties within these materials.


Subject(s)
Bromides/chemistry , Molecular Dynamics Simulation , Neutron Diffraction , Strontium/chemistry , Diffusion , Molecular Conformation , Monte Carlo Method
3.
Am Rev Respir Dis ; 141(4 Pt 1): 884-8, 1990 Apr.
Article in English | MEDLINE | ID: mdl-2327651

ABSTRACT

Heterozygous alpha 1-antichymotrypsin (ACT) deficiency is inherited in an autosomal dominant mode independently of alpha 1-antitrypsin with a gene frequency (q) of 0.003. In a previous study, a high prevalence of enlarged residual volumes in subjects with the trait were noted. Neutrophil cathepsin G, the target proteinase of ACT, enhances the elastolytic action of elastase. Thus, hypothetically, subjects with the trait may have increased risk for developing pulmonary emphysema. To test whether heterozygous ACT deficiency predisposes to lung disease, plasma ACT concentrations were determined in a cohort of 1,872 middle-aged women. Women with subnormal levels were studied with respect to heredity, airway symptoms, and lung function. Twelve women (0.64% of the cohort) were classified as heterozygotes after family studies and were compared with control subjects, matched for age, weight, sex, and smoking status. There were no significant differences in airway symptoms between heterozygotes and control subjects. However, the prevalence of ex-smokers was significantly higher among heterozygotes than among the screened population as a whole (prevalence ratio, 2.18; 95% confidence interval, 1.004-4.72). There were no differences between the heterozygotes and the control subjects in the basal spirometry. However, after bronchodilation, five of the 12 heterozygotes manifested residual volumes greater than 2.5 standard deviations above normal mean compared with one of 24 control subjects (p = 0.012). The present investigation thus confirms our previous findings of an increased prevalence of enlarged residual volumes in heterozygous ACT deficiency.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Respiratory Tract Diseases/genetics , alpha 1-Antichymotrypsin/deficiency , Cohort Studies , Cough/genetics , Female , Heterozygote , Humans , Middle Aged , Pneumonia/genetics , Prevalence , Respiratory Function Tests , Respiratory Hypersensitivity/genetics , Respiratory Tract Diseases/epidemiology
4.
Tokai J Exp Clin Med ; 13(6): 365-71, 1988 Dec.
Article in English | MEDLINE | ID: mdl-2483770

ABSTRACT

alpha 1-Antitrypsin, alpha 1-antichymotrypsin and angiotensinogen are three genetically homologous acute phase reactants which belong to the super family of serine proteinase inhibitors (serpins). In this report the dissociate expression of these respective genes in various liver diseases or after exposure to estrogen is emphasized. In addition, the influence of abnormal genetic variants on plasma levels of these proteins and on liver cell function is discussed.


Subject(s)
Acute-Phase Proteins/metabolism , Liver Diseases/blood , Serpins/blood , Angiotensinogen/blood , Humans , alpha 1-Antichymotrypsin/blood , alpha 1-Antichymotrypsin/deficiency , alpha 1-Antitrypsin/metabolism , alpha 1-Antitrypsin Deficiency
5.
Clin Chim Acta ; 152(3): 261-9, 1985 Nov 15.
Article in English | MEDLINE | ID: mdl-3877579

ABSTRACT

We studied 229 patients with biopsy verified liver disease and compared the plasma levels of alpha 1-antichymotrypsin and alpha 1-antitrypsin. We found a significant overall correlation between alpha 1-antichymotrypsin and alpha 1-antitrypsin levels (r = 0.50, p less than 0.001). The strongest correlations were found in patients with chronic active hepatitis (r = 0.76, p less than 0.0001) and alcohol hepatitis (r = 0.60, p less than 0.001). Several clinical subgroups lacked correlation. Unexpectedly high alpha 1-antichymotrypsin values were found in patients with venous congestion. We also used the alpha 1-antichymotrypsin/alpha 1-antitrypsin ratio as a tool to identify PiZ carriers (intermediate alpha 1-antitrypsin-deficiency, PiZ). The sensitivity and predictive values were low and did not exceed that obtained by the simple use of an isolated alpha 1-antitrypsin determination. A small subgroup with low alpha 1-antichymotrypsin/alpha 1-antitrypsin ratio included patients with chronic active hepatitis of unknown etiology. Hypo-alpha 1-antichymotrypsinemia may be secondary to the liver disease per se or be an expression of an abnormal genetic trait.


Subject(s)
Chymotrypsin/antagonists & inhibitors , Liver Diseases/blood , Adolescent , Adult , Aged , Chymotrypsin/blood , Chymotrypsin/deficiency , Female , Genetic Carrier Screening , Hepatitis, Alcoholic/blood , Hepatitis, Chronic/blood , Humans , Liver Diseases/genetics , Liver Diseases, Alcoholic/blood , Male , Middle Aged , Phenotype , alpha 1-Antichymotrypsin , alpha 1-Antitrypsin/blood , alpha 1-Antitrypsin Deficiency
7.
Scand J Gastroenterol ; 19(7): 977-82, 1984 Oct.
Article in English | MEDLINE | ID: mdl-6531667

ABSTRACT

To study the postulated relationship between prior cholecystectomy and occurrence of subsequent colorectal cancer, we examined the prevalence of cholecystectomy in all patients with histologically confirmed colorectal cancer registered during 1966-75 in the city of Malmö. In addition, we studied the frequency of colon cancer in all females autopsied in 1978-79 with a previous cholecystectomy. Of all 1061 cases of colon cancer diagnosed during the 1966-75 period, 94 (8.9%) had undergone cholecystectomy, as compared with 106 (10.0%) in the age-matched controls. In the female subgroup (n = 503) the corresponding figure for cholecystectomy was 58 (11.5%), as compared with 70 (13.9%) in the controls. The incidence of right-sided colon cancer among the 58 females with previous cholecystectomy did not differ from that of age-matched controls (28.6 and 28.1%, respectively). The incidence of colon cancer among 305 females with a prior cholecystectomy autopsied during 1978-79 was 24 (7 right-sided), as compared with 22 (8 right-sided) in age-matched controls without gallbladder disease. Gastric cancer was more frequent (p less than 0.01) in cholecystectomized women than in controls. These results refute the suggested relationship between cholecystectomy and development of colon cancer in any location.


Subject(s)
Cholecystectomy , Colonic Neoplasms/etiology , Gallbladder Diseases/complications , Rectal Neoplasms/etiology , Autopsy , Colonic Neoplasms/pathology , Female , Gallbladder Diseases/surgery , Humans , Male , Rectal Neoplasms/pathology
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