EFFECTS OF MILK PRESERVATION USING THE LACTOPEROXIDASE SYSTEM ON PROCESSED YOGURT AND CHEESE QUALITY

ABSTRACT The lactoperoxidase system (LP-system) is an acceptable chemical method for raw milk preservation, especially in rural areas where refrigeration facilities are absent to farmers. Milk production in most African countries is dominated by small-scale traditional production systems using low yielding local breeds. Therefore, processors who operate in such situations must rely on small volumes of milk from many farmers. Application of the LP-system prolongs the shelf life of raw milk and also encourages grouping of farmers hence facilitating milk collection by processors. The application of the LP-system is a recent preservation method for milk in Cameroon whose efficiency has been proven. Therefore, need arose for further studies on the influence of this method on milk processing as well as the quality dairy products. The LP-system was activated by adding 10 ppm sodium thiocyanate and 8.5 ppm sodium percarbonate to fresh milk. Yoghurt and Bambui cheese were processed separately from treated and untreated (control) milk samples. Yogurt was produced from both the treated and the control milk samples at 2%, 3%, 4% and 5% (v/v) culture levels. Yogurt samples were analysed for acidity, protein content and dry matter content while cheese was analysed for butterfat and moisture content. Statistical tests were conducted by Analysis of Variance using the Fisher's test. Simple organoleptic assessments were conducted to compare yogurt and cheese from the treated and the control milk. Activation of the LP-system delayed lactic acid formation in yogurt during incubation and storage leading to increased energy consumption during processing and an improved keeping quality during storage. LPsystem treatment reduced the overall organoleptic quality of yogurt while it improved on that of Bambui cheese. Dry matter content and fat content of yogurt were not significantly affected by LP-system treatment (P<0.05). LP-system treatment did not also affect the moisture and fat content of cheese but slightly improved on its yield

Effets de l’amprolin-300 Ws sur quelques paramètres de croissance et de reproduction chez le lapin mâle (Oryctolagus cuniculus)

Objectif : L’objectif de la présente étude a été de rechercher les effets de l’Amprolin-300, un anticoccidien largement utilisé en médecine vétérinaire, sur quelques paramètres de croissance et de reproduction chez le lapin mâle de race locale. Méthodologie et résultats : Vingt-quatre (24) lapins âgés de 5 mois environ et pesant entre 2,01 et 2,78 kg ont été répartis en 4 lots comparables de 6 lapins chacun. Ils ont été traités pendant 60 jours avec différentes doses d’Amprolin-300 ws via l’eau de boisson : 0 ; 30 ; 60 et 110 mg/kg de poids corporel. Les résultats obtenus ont révélé que la consommation d’eau a significativement (p<0,05) diminué chez les lapins traités aux doses 60 et 110 mg/kg de poids corporel par rapport aux témoins. Le gain de poids et le gain moyen quotidien ont diminué de manière significative (p<0,05) chez les animaux traités aux doses 30 et 60 mg/kg de poids corporel par rapport aux animaux du lot témoin. Par contre, l’indice de consommation a diminué de façon significative (p<0,05) chez les animaux témoins et chez ceux qui ont ingéré la plus forte dose d’Amprolin-300 ws (110 mg/kg de poids corporel) comparé aux lapins traités avec les doses 30 et 60 mg/kg respectivement. Le pH de la semence a significativement (p<0,05) augmenté chez les mâles traités aux doses 30 et 60 mg/kg de poids corporel par rapport Aux mâles du lot témoin. La motilité individuelle et la concentration des spermatozoïdes ont diminué de manière significative (p<0,05) chez les lapins qui ont ingéré la plus forte dose d’anticoccidien par rapport aux lapins témoins. Conclusion et application des résultats : Ainsi, à la dose de 110 mg/kg de poids corporel, l’Amprolin-300 ws a réduit la consommation alimentaire, le gain de poids, le gain moyen quotidien, le poids spécifique et le pH de la semence. Cette dose a également inhibé la spermatogenèse et réduit le pourcentage de spermatozoïdes mobiles. Son usage devrait donc être règlementé.Mots clés : Amprolin-300 ws, lapin mâle, production et fertilité.Objective: In this study, the effects of Amprolin-300 ws, an anticoccidiostat abundantly used in veterinary medicine, on some growth and reproductive parameters in male rabbits were investigated. Methodology and results: Twenty four (24) rabbits aged 5 months and weighing between 2.01 and 2.78 kg were divided into 4 comparable groups of six rabbits each and treated for 60 days with different doses of Amprolin-300 ws from drinking water: 0, 30, 60 and 110 g/kg of body weight. The results showed that water consumption was significantly (p<0.05) decreased in rabbits treated with 60 and 110 mg/kg of body weight of Amprolin-300 compared to control rabbits. Body weight gain and average daily gain decreased significantly (p<0.05) in animals treated with 30 and 60 mg/kg of body weight compared to control rabbits. On the other hand, feed efficiency decreased significantly (p<0.05) in control animals and those who ingested the highest dose (110 mg/kg of body weight) compared to rabbits treated with 30 and 60 mg/kg of body weight respectively. The pH of semen increased significantly (p<0.05) in animals treated with 30 and 60 mg/kg of body weight compared to control animals. Individual motility and sperm concentration decreased significantly (p<0.05) in rabbits who received the highest dose of Amprolin-300 compared to control rabbits. Conclusion and application of results: Thus, at the dose of 110 mg/kg body weight, Amprolinws-300 reduced in male rabbit, food consumption, body and average daily weight gain, specific weight and pH of semen. It inhibited spermatogenesis and reduced sperm mobility. Therefore its use should be regulated

In vitro reactivation of latent HIV-1 by cytostatic bis (thiosemicarbazonate) gold(III) complexes

BACKGROUND : A number of cytostatic agents have been investigated for the ability to reactivate latent viral reservoirs, which is a major prerequisite for the eradication of HIV-1 infection. Two cytostatic bis(thiosemicarbazonate) gold(III) complexes (designated 1 and 2) were tested for this potential in the U1 latency model of HIV-1 infection. METHODS : Cell viability in the presence or absence of 1 and 2 was determined using a tetrazolium dye and evidence of reactivation was assessed by p24 antigen capture following exposure to a latency stimulant, phorbol myristate acetate (PMA) and or test compounds. The latency reactivation mechanism was explored by determining the effect of the complexes on protein kinase C (PKC), histone deacetylases (HDAC) and proinflammatory cytokine production. RESULTS : The CC50 of the complexes in U1 cells were 0.53 ± 0.12 μM for 1 and 1.0 ± 0.4 μM for 2. In the absence of PMA and at non toxic concentrations of 0.2 and 0.5 μM, 1 and 2 significantly (p ≤ 0.02) reactivated virus in U1 cells by 2.7 and 2.3 fold respectively. In comparison, a 2.6 fold increase (p = 0.03) in viral reactivation was observed for hydroxyurea (HU), which was used as a cytostatic and latent HIV reactivation control. Viral reactivation was absent for the complexes during co-stimulation with PMA indicating the lack of an additive effect between the chemicals as well as an absence of inhibition of PMA induced HIV reactivation but for HU inhibition of the stimulant’s activity was observed (p = 0.01). Complex 1 and 2 activated PKC activity by up to 32% (p < 0.05) but no significant inhibition of HDAC was observed. Increases in TNF-α levels suggested that the reactivation of virus by the complexes may have been due to contributions from the latter and the activation of PKC. CONCLUSION : The ethyl group structural difference between 1 and 2 seems to influence bioactivity with lower active concentrations of 1, suggesting that further structural modifications should improve specificity. The cytostatic effect of 1 and 2 and now HIV reactivation from a U1 latency model is consistent with that of the cytostatic agent, HU. These findings suggest that the complexes have a potential dual (cytostatic and reactivation) role in viral “activation/elimination”.AuTEK Biomed (Mintek and Harmony Gold),Technology Innovation Agency (TIA) and the University of Pretoria.http://www.biomedcentral.com/bmcinfectdis/hb201

A gold-containing drug against parasitic polyamine metabolism: the X-ray structure of trypanothione reductase from Leishmania infantum in complex with auranofin reveals a dual mechanism of enzyme inhibition

Auranofin is a gold(I)-containing drug in clinical use as an antiarthritic agent. Recent studies showed that auranofin manifests interesting antiparasitic actions very likely arising from inhibition of parasitic enzymes involved in the control of the redox metabolism. Trypanothione reductase is a key enzyme of Leishmania infantum polyamine-dependent redox metabolism, and a validated target for antileishmanial drugs. As trypanothione reductase contains a dithiol motif at its active site and gold(I) compounds are known to be highly thiophilic, we explored whether auranofin might behave as an effective enzyme inhibitor and as a potential antileishmanial agent. Notably, enzymatic assays revealed that auranofin causes indeed a pronounced enzyme inhibition. To gain a deeper insight into the molecular basis of enzyme inhibition, crystals of the auranofin-bound enzyme, in the presence of NADPH, were prepared, and the X-ray crystal structure of the auranofin–trypanothione reductase–NADPH complex was solved at 3.5 Å resolution. In spite of the rather low resolution, these data were of sufficient quality as to identify the presence of the gold center and of the thiosugar of auranofin, and to locate them within the overall protein structure. Gold binds to the two active site cysteine residues of TR, i.e. Cys52 and Cys57, while the thiosugar moiety of auranofin binds to the trypanothione binding site; thus auranofin appears to inhibit TR through a dual mechanism. Auranofin kills the promastigote stage of L. infantum at micromolar concentration; these findings will contribute to the design of new drugs against leishmaniasis

The morphology and biochemistry of nanostructures provide evidence for synthesis and signaling functions in human cerebrospinal fluid

<p>Abstract</p> <p>Background</p> <p>Cerebrospinal fluid (CSF) contacts many brain regions and may mediate humoral signaling distinct from synaptic neurotransmission. However, synthesis and transport mechanisms for such signaling are not defined. The purpose of this study was to investigate whether human CSF contains discrete structures that may enable the regulation of humoral transmission.</p> <p>Methods</p> <p>Lumbar CSF was collected prospectively from 17 participants: with no neurological or psychiatric disease, with Alzheimer's disease, multiple sclerosis, or migraine; and ventricular CSF from two cognitively healthy participants with long-standing shunts for congenital hydrocephalus. Cell-free CSF was subjected to ultracentrifugation to yield supernatants and pellets that were examined by transmission electron microscopy, shotgun protein sequencing, electrophoresis, western blotting, lipid analysis, enzymatic activity assay, and immuno-electron microscopy.</p> <p>Results</p> <p>Over 3,600 CSF proteins were identified from repeated shotgun sequencing of cell-free CSF from two individuals with Alzheimer's disease: 25% of these proteins are normally present in membranes. Abundant nanometer-scaled structures were observed in ultracentrifuged pellets of CSF from all 16 participants examined. The most common structures included synaptic vesicle and exosome components in 30-200 nm spheres and irregular blobs. Much less abundant nanostructures were present that derived from cellular debris. Nanostructure fractions had a unique composition compared to CSF supernatant, richer in omega-3 and phosphoinositide lipids, active prostanoid enzymes, and fibronectin.</p> <p>Conclusion</p> <p>Unique morphology and biochemistry features of abundant and discrete membrane-bound CSF nanostructures are described. Prostaglandin H synthase activity, essential for prostanoid production and previously unknown in CSF, is localized to nanospheres. Considering CSF bulk flow and its circulatory dynamics, we propose that these nanostructures provide signaling mechanisms <it>via </it>volume transmission within the nervous system that are for slower, more diffuse, and of longer duration than synaptic transmission.</p

Multiplicity of cerebrospinal fluid functions: New challenges in health and disease

This review integrates eight aspects of cerebrospinal fluid (CSF) circulatory dynamics: formation rate, pressure, flow, volume, turnover rate, composition, recycling and reabsorption. Novel ways to modulate CSF formation emanate from recent analyses of choroid plexus transcription factors (E2F5), ion transporters (NaHCO3 cotransport), transport enzymes (isoforms of carbonic anhydrase), aquaporin 1 regulation, and plasticity of receptors for fluid-regulating neuropeptides. A greater appreciation of CSF pressure (CSFP) is being generated by fresh insights on peptidergic regulatory servomechanisms, the role of dysfunctional ependyma and circumventricular organs in causing congenital hydrocephalus, and the clinical use of algorithms to delineate CSFP waveforms for diagnostic and prognostic utility. Increasing attention focuses on CSF flow: how it impacts cerebral metabolism and hemodynamics, neural stem cell progression in the subventricular zone, and catabolite/peptide clearance from the CNS. The pathophysiological significance of changes in CSF volume is assessed from the respective viewpoints of hemodynamics (choroid plexus blood flow and pulsatility), hydrodynamics (choroidal hypo- and hypersecretion) and neuroendocrine factors (i.e., coordinated regulation by atrial natriuretic peptide, arginine vasopressin and basic fibroblast growth factor). In aging, normal pressure hydrocephalus and Alzheimer's disease, the expanding CSF space reduces the CSF turnover rate, thus compromising the CSF sink action to clear harmful metabolites (e.g., amyloid) from the CNS. Dwindling CSF dynamics greatly harms the interstitial environment of neurons. Accordingly the altered CSF composition in neurodegenerative diseases and senescence, because of adverse effects on neural processes and cognition, needs more effective clinical management. CSF recycling between subarachnoid space, brain and ventricles promotes interstitial fluid (ISF) convection with both trophic and excretory benefits. Finally, CSF reabsorption via multiple pathways (olfactory and spinal arachnoidal bulk flow) is likely complemented by fluid clearance across capillary walls (aquaporin 4) and arachnoid villi when CSFP and fluid retention are markedly elevated. A model is presented that links CSF and ISF homeostasis to coordinated fluxes of water and solutes at both the blood-CSF and blood-brain transport interfaces