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1.
JEMDSA (Online) ; 24(2): 46-49, 2019. ilus
Article in English | AIM (Africa) | ID: biblio-1263766

ABSTRACT

Introduction: Non-communicable diseases, especially cardiovascular diseases (CVD), have become more prevalent across the world, more so in developing countries. Novel methods in the management of CVD risks in patients with diabetes mellitus, type 2 (DM2) requires constant attention and an ever-evolving approach. The role of magnesium supplementation in the management of CVD has been described, but the relationship between serum magnesium (Mg) and the lipid subsets have had conflicting results in different population groups. Methods: A cross-sectional study was performed by collecting data on patients with DM2 from a specialised diabetes clinic at Edendale Hospital, Pietermaritzburg, KwaZulu-Natal, South Africa, between July 1, 2015 and June 30, 2016. Lipid subsets (total cholesterol [TC], high-density lipoprotein cholesterol [HDL], low-density lipoprotein cholesterol [LDL] and triglycerides [TG]), age, sex and Mg were recorded for analysis. Results: A total of 495 clinical data sheets were analysed. The majority of participants were female (73.45%) with a mean age of 56.97 years. A statistically significant, positive, linear relationship was found between Mg and TC (R= 0.11;p= 0.01) as well as Mg and LDL R= 0.14;p= 0.001), but not between Mg and HDL (R= 0.02;p= 0.66) and Mg and TG (R= 0.01;p= 0.82). Discussion: The results of this study are similar to findings by a group of researchers in China and differ when compared with studies observing Caucasian patients. It is plausible that intrinsic ethnic differences in lipid metabolism and the various ways in which magnesium requiring enzymatic processes are utilised may be responsible for the results found in the present study population versus those found in Caucasian study participants in other countries. More research is required to determine the effect of magnesium supplementation and CVD outcomes in the present study population


Subject(s)
Cardiovascular Diseases , Cholesterol , Developing Countries , Diabetes Mellitus , Lipids , South Africa
2.
Epidemiol Infect ; 115(1): 193-205, 1995 Aug.
Article in English | MEDLINE | ID: mdl-7543860

ABSTRACT

This paper compares strains of foot-and-mouth disease (FMD) serotype SAT (South African Territories) 2 viruses isolated from Zimbabwe and other African countries using monoclonal antibodies (MAb). A sandwich-ELISA was used to examine the relative binding of anti-SAT 2 MAb to the various viruses. The MAb-binding profiles of viruses isolated from field samples were compared using hierarchical cluster analysis. Viruses were obtained from game animals, mainly African buffalo (Syncerus caffer) which is the natural host and reservoir for SAT serotypes in Africa, and from cattle showing clinical signs of FMD, as well as from animals suspected of carrying the virus subclinically. Some isolates have been adapted for use as vaccine strains. The results showed that most of the Zimbabwe isolates collected between 1989 and 1992 were an antigenically closely-related group. Although differences were observed between Zimbabwe isolates collected between 1989 and 1992 and those collected in 1987, there was no correlation with the different MAb binding patterns within the 1987 group and the epidemiological information received from the field. Similar profiles were observed for many SAT 2 viruses, including viruses isolated over a 50-year period and from geographically distant areas. This indicates an inherent stability in antigenic profiles of SAT 2 viruses. The MAb panel was capable of assessing antigenic variation, since very different profiles were obtained for some isolates. The work also allowed comparison and characterization of anti-type SAT 2 MAb from different laboratories. The findings are discussed with reference to selection of vaccine strains.


Subject(s)
Antibodies, Monoclonal/metabolism , Aphthovirus/classification , Cattle Diseases/virology , Disease Outbreaks/veterinary , Foot-and-Mouth Disease/virology , Animals , Aphthovirus/metabolism , Buffaloes , Cattle , Cattle Diseases/epidemiology , Cattle Diseases/immunology , Cluster Analysis , Enzyme-Linked Immunosorbent Assay , Epitopes , Foot-and-Mouth Disease/epidemiology , Foot-and-Mouth Disease/immunology , Serotyping , Zimbabwe
3.
Circ Shock ; 38(4): 253-63, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1292889

ABSTRACT

The purpose of our study was to set up a baboon hyperdynamic sepsis model with live bacteria administration, which produces within 8 hr an organ failure comparable to human pathological conditions. Twelve adult male baboons were instrumented and studied for 8 hr under pentobarbital (2-3 mg/kg BW/hr) anesthesia breathing spontaneously. The animals were divided into two groups: 1) Live Escherichia coli were infused intravenously at a dose of 1.0-2.0 x 10(10) CFU/kg BW over 8 hr; 2) Live E. coli were infused i.v. at a dose of 5 x 10(8) CFU/kg BW over 2 hr. Organ damage was monitored by a newly developed scoring system. Organ damage was clearly dependent on the concentration of the bacterial challenge. Bacterial challenge at a dosage of 5.0 x 10(8) produces insignificant hemodynamic effects, while the 1.0-2.0 x 10(10) animals demonstrated massive hemodynamic alterations and needed much higher fluid support. The higher E. coli dosage was associated with an overwhelming organ damage seen, e.g., from the lung weight (12 g/kg BW vs. 9.6 g/kg BW with the lower dosage) or from the organ failure score, which is based on macroscopic pathology, histological data and organ weight. The percentage of animals with one, two, or three organ failures (organ failure score > or = 2) was higher in baboons with the higher dosage/kg BW. Therefore, we believe that the less severe organ damage in the acute phase after 8 hr with live bacteria 5 x 10(8) CFU/kg BW infusion over 2 hr is better to monitor the efficacy of newly developed therapeutic regimens, since in another set of experiments this model still produces lethal organ damage (80%) in a subchronic setting over 72 hr.


Subject(s)
Injury Severity Score , Kidney/pathology , Liver/pathology , Lung/pathology , Sepsis/pathology , Adrenal Glands/pathology , Animals , Disease Models, Animal , Escherichia coli/pathogenicity , Intestines/pathology , Male , Myocardium/pathology , Organ Size , Papio
4.
S Afr Med J ; 78(5): 258-9, 1990 Sep 01.
Article in English | MEDLINE | ID: mdl-2118277

ABSTRACT

The suggested use of tobramycin in selective decontamination of the digestive tract led to the investigation of the part played clinically by ribosomal resistance in Pseudomonas aeruginosa. Examination of 32 tobramycin-resistant isolates, both enzyme and non-enzyme producing, suggests that ribosomal resistance is clinically important.


Subject(s)
Pseudomonas aeruginosa/drug effects , Ribosomes/drug effects , Tobramycin/pharmacology , Animals , Drug Resistance, Microbial , Evaluation Studies as Topic , Microbial Sensitivity Tests
5.
Int J Biochem ; 14(10): 899-904, 1982.
Article in English | MEDLINE | ID: mdl-7128907

ABSTRACT

1. The influence of 60Co gamma-radiation on the sedimentation behaviour of human lymphocyte nucleoids in neutral sucrose gradients was studied with the aid of a modified fluorescent monitor system consisting of the DNA-binding dye, Hoechst 33258 and a vertical centrifuge rotor. 2. A combined method employing the sedimentation procedure and the incorporation of tritiated nucleosides was utilized to evaluate the repair of gamma-radiated DNA.


Subject(s)
DNA Repair , DNA/radiation effects , Lymphocytes/radiation effects , Centrifugation, Density Gradient , Gamma Rays , Humans , Hydrogen-Ion Concentration , In Vitro Techniques , Lymphocytes/metabolism
6.
Contrib Microbiol Immunol ; 5: 324-8, 1979.
Article in English | MEDLINE | ID: mdl-394919

ABSTRACT

Of nine Y. enterocolitica serotypes examined by us, only type 3 was shown to be enteropathogenic. 3 of 16 strains recovered from clinical material, produced a heat-stable toxin similar to that reported in E. coli. A fourth isolate produced histological changes resembling those associated with salmonellae. The mechanism whereby the majority of Y. enterocolitica strains produce diarrhoea is uncertain. Our isolates may have lost a plasmid essential for enteropathogenicity, or they may resemble the 'classical' enteropathogenic strains of E. coli for which no satisfactory experimental model exists. Further studies on freshly isolated strains are in progress in order to determine the prevalence of enterotoxigenic Y. enterocolitica.


Subject(s)
Gastroenteritis/etiology , Yersinia Infections/etiology , Adhesiveness , Animals , Bacteriological Techniques , Child , Cricetinae , Enterotoxins/biosynthesis , Gastroenteritis/microbiology , Humans , Ileum/microbiology , Infant , Intestinal Mucosa/microbiology , Mice , Rabbits , Species Specificity , Yersinia/isolation & purification , Yersinia/metabolism , Yersinia/physiology , Yersinia Infections/microbiology
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