Adjustment factors to per capita health-care indicators in countries with expatriate male-majority populations.

From 2000 to 2010, the population in the Gulf Cooperation Council (GCC) countries underwent an increase of 53%, compared with an average global increase of 13%. The rates varied by country, ranging from 23% in Oman to 198% in Qatar. The main driving force for this sharp increase in population was the high demand for immigrant labour. The aim of this study was to adjust the population in the GCC countries in order to ensure that the comparisons of health-care key performance indicators with other countries account for the composition of the populations. The conclusion of the study was that adjusting the population in the GCC is instrumental for determining health spending and health outcomes, and that inaccurate forecasting would result in serious overestimation of the need for GCC countries to invest in the health-care sector. Policy-makers can utilize the population models in this study to accurately plan for health-care delivery.

Adjustment factors to per capita health-care indicators in countries with expatriate male-majority populations

From 2000 to 2010, the population in the Gulf Cooperation Council [GCC] countries underwent an increase of 53%, compared with an average global increase of 13%. The rates varied by country, ranging from 23% in Oman to 198% in Qatar. The main driving force for this sharp increase in population was the high demand for immigrant labour. The aim of this study was to adjust the population in the GCC countries in order to ensure that the comparisons of health-care key performance indicators with other countries account for the composition of the populations. The conclusion of the study was that adjusting the population in the GCC is instrumental for determining health spending and health outcomes, and that inaccurate forecasting would result in serious overestimation of the need for GCC countries to invest in the health-care sector. Policy-makers can utilize the population models in this study to accurately plan for health-care delivery

De 2000 à 2010, la population des pays du Conseil de coopération du Golfe a augmenté de 53 %,par rapport à une augmentation moyenne mondiale de 13 %. Les pourcentages varient d'un pays à l’autre, allant de 23 % à Oman à 198 % au Qatar. L'importante demande en main-d’oeuvre immigrante constituait l'élément moteur principal de cette forte augmentation de la population. La présente étude visait à ajuster les populations dans les pays du Conseil de coopération du Golfe afin de garantir que les comparaisons des indicateurs de performance clés pour les soins de santé avec d'autres pays tiennent compte de la composition des populations. L'étude concluait dans un premier temps que l'ajustement des populations des pays du Conseil de coopération du Golfe était essentiel pour déterminer les dépenses de santé et les résultats sanitaires,et dans un deuxième temps que des prévisions inexactes entraîneraient d'importantes surestimations de la nécessité pour les pays du Conseil de coopération du Golfe d’investir dans le secteur des soins de santé. Les responsables politiques peuvent utiliser les modèles de population de cette étude pour planifier avec exactitude la prestation de soins de santé

Comparison between aerobic and anaerobic co-composting of agricultural residues.

Fertile soil is the most important resource for food production. The agricultural area in Egypt is limited to 6 million faddans. This limited area has derived many farmers to use several types of chemical fertilizers, to enhance the fertility of the land and hence the productivity. Excessive application of chemical fertilizer lead to the build up of these residuals because they are superfluous. This will cause waste of money and also soil pollution. Ultimately, this would adversely affect the ecological system in the soil and surrounding environment, especially water bodies. Composting of organic solid wastes will address some of the problems of solid waste disposal and gives a beneficial product which may replace the expensive chemical fertilizers. Other organic compostable solid wastes could be utilized to produce this compost. Agricultural residues are cheap raw materials for such compost and are available in vast quantities as well. This compost can be used as a soil conditioner to improve soil characteristics and its productivity. Crop residues mixed with manure, may be co-composted to give a soil conditioner. Agricultural residues, about 106 million tons/year, may produce about 55 million tons/year of compost. Three co-composting were carried out at the experimental station of the Faculty of Agriculture in Abis. Two aerobic co-composting of winter and summer crop residues and one anaerobic co-composting inter rop esidue were produced. The development of the co-composting processes controlled by the temperature, moisture content, and chemical composition was studied. The aerobic co-composting of winter crop residues was found to be the best experiment as it complied with the standards of the Ministry of Agriculture Decree No. 100/1967. This co-compost is expected to be free from pathogenic microorganisms as the dominant temperature was almost about 50 degrees C from the 42nd day till the 101st day of the experiment.

Decrease of hepatic catalase level by treatment with diallyl sulfide and garlic homogenates in rats and mice.

Diallyl sulfide (DAS) is a flavor compound derived from garlic and is active in the inhibition of chemically induced cytotoxicity and carcinogenicity in animal models. This study was conducted to examine the effects of the treatment of DAS and garlic homogenates on the activities of catalase, glutathione peroxidase, and superoxide dismutase. Male Sprague-Dawley rats were treated with DAS i.g. at daily doses of 50 or 200 mg/kg for 8 days, causing the hepatic catalase activity to decrease by 55 and 95%, respectively. Such a decrease in hepatic catalase activity was also observed when the DAS treatment was extended to 29 days. Western blot analysis showed that the DAS treatments resulted in corresponding decreases in the liver catalase protein level. No significant change in the catalase activity in the kidney, lung, and brain was observed with the treatments, but a slight decrease in heart catalase activity was observed. These treatments did not cause significant changes in superoxide dismutase and glutathione peroxidase activities in these tissues. Treatment with DAS at a daily dose of 200 mg/kg for 1-7 days resulted in a gradual decrease in the liver catalase activity to 5% of the control level, but it did not decrease the erythrocyte catalase activity. Treatment of rats with fresh garlic homogenates (2 or 4 g/kg, i.g., daily for 7 days) caused a 35% decrease in liver catalase activity. A/J mice treated with DAS and garlic homogenates also showed a decrease in the liver catalase activity. Diallyl sulfone (DASO2), a DAS metabolite, however, did not effectively decrease catalase activity in mice. The catalase activity was not inhibited by either DAS or DASO2 in vitro. The present results demonstrate that treatment with DAS and garlic homogenates decrease the hepatic catalase level in rats and mice.

Caffeine induces cytochrome P4501A2: induction of CYP1A2 by tea in rats.

Previous reports indicated that treatment of rats with green tea or black tea extracts increased CYP1A2 activity, but such an induction was not observed with decaffeinated green tea in our preliminary study. Herein we report a comparative study on the induction of CYP1A2 with different tea preparations and caffeine as an inducer. When green tea (2%) or black tea (2%) was given to male Fischer 344 rats as the sole source of drinking fluid for 21 days, a 2.4- or 2.7-fold induction, respectively, of CYP1A2-dependent O-methoxyresorufin demethylase (MROD) activity in liver microsomes was observed. Treating rats with caffeine (0.04%) also resulted in an 1.9-fold increase in the MROD activity, but decaffeinated green tea (0.8%) did not cause such an induction. Rats treated with green tea (2%) or caffeine (0.055%) as the sole source of drinking fluid for 1, 3, and 7 days also showed comparable induction (from 1.7- to 2.1-fold) of the MROD activity. The induction was also shown by intragastric administration of caffeine (100 mg/kg). The induced MROD activity caused by consumption of green tea, black tea, and caffeine corresponded to the increase in liver microsomal CYP1A2 protein, as determined by immunoblot analysis. The concentrations of tea polyphenols and caffeine in plasma were also measured. Close correlation of the increase in the MROD activity was observed only with the plasma caffeine level (r = 0.736, n = 10, p = 0.015), not with the combined tea polyphenol level (r = 0.058, n = 6, p = 0.913). The present study establishes caffeine as an inducer of CYP1A2 and demonstrates that caffeine, not tea polyphenols, is the component in tea responsible for the induction of this enzyme.

Chloroquine polymeric membrane electrodes: Development and applications.

Three main types of PVC solvent polymeric membrane ion-selective electrodes for chloroquine are described. They are based on three ion-pairing agents namely dipicrylamine (DPA), tetraphenylborate (TPB) or tetrakis(4-chlorophenyl)borate (TCPB) with either dioctylphenyl phosphonate (DOPP) or trioctyl phosphate (TOP) solvent mediator. All electrodes exhibit Nernstian responses, fast dynamic response times and a wide useful pH range. The best all-round electrode is based on TPB and TOP plasticizing solvent mediators with a limit of detection of 7.1 x 10(-6)M and was utilized for the assay of chloroquine in tablets. Direct potentiometric determinations with either the analyte addition method or the normal calibration method gave results comparable to the official method.

The interaction of oral hypoglycaemic drugs with insulin on steroid metabolism in hepatocytes isolated from control and diabetic male rats.

The effects of the oral hypoglycaemic drugs, phenformin and tolbutamide, and insulin, alone and in combination, on steroid metabolism in hepatocytes isolated from control and streptozotocin-diabetic male rats has been studied. Both phenformin and tolbutamide mimic the action of insulin in stimulating hepatic steroid metabolism in a dose-dependent manner in control cells. Unlike insulin, however, both drugs give a similar effect in cells derived from diabetic animals although to a lesser extent. Both drugs can partially restore the effect of insulin in cells derived from diabetic animals. Biguanides and sulphonylureas, therefore, have a direct effect on liver cells to mimic insulin action and can still have an effect under conditions where insulin is inactive. Both types of oral hypoglycaemics can also affect insulin-insensitive cells isolated from diabetic rat liver to restore to a certain extent their response to insulin.

Lack of effect of insulin in hepatocytes isolated from streptozotocin-diabetic male rats.

Diabetes mellitus is known to affect drug and steroid metabolism in the rat liver. Recently we have demonstrated that in-vitro insulin addition to hepatocytes obtained from normal male rats showed a significant dose-related increase in androstenedione metabolism. We have extended our study this time by using 3- and 21-days streptozotocin (STZ) diabetic and insulin-treated STZ-diabetic male rats. Hepatocytes from 3- and 21-days STZ-diabetic rats were resistant to the effect of insulin while insulin-treated diabetic rats indicated partial restoration of insulin effect. Since insulin resistance is a characteristic feature of type II diabetes mellitus, we would like to suggest that STZ-diabetic rats may be a model for type II diabetes mellitus.

The effects of glucagon and TH-glucagon on steroid metabolism in isolated rat hepatocytes.

Glucagon decreases the activity of steroid-metabolising enzymes in isolated rat liver cells at physiological concentrations. Higher concentrations are less effective. TH-glucagon (1-N-alpha-trinitrophenylhistidine-12-homoarginine-glucagon) also reduces enzyme activity but does not lose activity at higher concentrations. The effects of the two hormones mimic closely their reported effects on phosphatidylinositol-4,5-bisphosphate breakdown. It is, thus, likely that the effect of glucagon on steroid metabolism is mediated via breakdown of this phospholipid. The calcium ionophore, A23187, had no effect on steroid metabolism whereas the phorbol ester 4 beta-phorbol-12-myristate-13-acetate (PMA) mimicked the effect of glucagon, showing that activation of protein kinase C but not Ca2+ mobilization may be involved in glucagon's action on hepatic steroid metabolism.

The effect of insulin on steroid metabolism in isolated rat hepatocytes.

Insulin administration has previously been shown to reverse the effects of chemically-induced and spontaneous diabetes on hepatic drug and steroid metabolism in the rat. The complex network of the intact hormonal system of the body and its physiological feedback mechanisms makes it difficult to ascribe the effects seen to any particular hormones. The present study investigated the effect of insulin on hepatic steroid metabolism in the absence of other hormonal influences by using isolated rat liver cells. Insulin (10(-9) M) produced two peaks of increased enzyme activity in the hepatocytes (at 1/2 hr and 24 hr). Dose-response curves at 1/2 hr and 24 hr insulin preincubation suggest that these two peaks are probably generated by different mechanisms. The absence of any significant changes in cytochrome P-450 content after 1/2, 1 and 2 hr of insulin treatment indicates that the increase in steroid metabolizing enzyme activities is not due to an increase in de-novo enzyme synthesis. Our observations provide further evidence for the role played by insulin in the regulation of hepatic steroid and drug metabolism in the rat.