Environmental impact of combustion of ethanolic biodiesel/diesel blends from several feedstocks on the gas emission levels in the atmosphere.

The aim of this work was to evaluate simultaneously the effect of produced ethanolic biodiesel from several feedstocks (soybean, crambe, macaw, sunflower, and waste cooking oil) and engine operational conditions (low and high engine speed) during combustion of biodiesel/diesel blends on the N2O, NOx, NO, CO2, and CO emission levels in the atmosphere. The biodiesel samples were prepared in one and/or two reaction steps, according to the acid index of each raw material, by esterification using H2SO4 and/or chemical transesterification using sodium ethoxide, both, through ethanolic route. The quality of the produced biodiesels was confirmed by ASTM/EN specifications. Then, biodiesel/diesel blends were prepared according to the following proportions: 10% (B10), 15% (B15), 25% (B25), and 50% (B50). In general way, all raw materials under combustion at low and high engine speed contributed to the formation of NOx and this effect was more drastically increased as the biodiesel concentration in the blends increases. N2O presented a similar behavior except for blends containing crambe and macaw biodiesel whose emissions were slightly reduced as a function of biodiesel content in these blends. Then, Principal component analysis (PCA) was applied to discriminate the effect of engine operating conditions, biodiesel kind, and biodiesel content in the blends during their combustion on the exhaust emissions. The attained results point to crambe and macaw as more environmentally sustainable feedstocks for biodiesel production because they generate less greenhouse gas emissions. These results are particularly attractive considering that, both, crambe and macaw are non-edible feedstocks with great potential for biodiesel production.

Cloning, expression, purification, and kinetic characterization of mitochondrial thioredoxin (TsTrx2), cytosolic thioredoxin (TsTrx1), and glutaredoxin (TsGrx1) from Taenia solium.

We report the complete coding sequences of mitochondrial thioredoxin (TsTrx2) and glutaredoxin (TsGrx1) from the cysticerci of T. solium. The full-length DNA of the TsTrx2 gene shows two introns of 88 and 77 bp and three exons. The TsTrx2 gene contains a single ORF of 423 bp, encoding 140 amino acid residues with an estimated molecular weight of 15,560 Da. A conserved C64NPC67 active site and a 30-amino acid extension at its N-terminus were identified. An insulin reduction reaction was used to determine whether it was a functional recombinant protein. The full-length DNA of the TsGrx1 gene shows one intron of 39 bp and a single ORF of 315 bp, encoding 105 amino acid residues with an estimated molecular weight of 12,582 Da. Sequence analysis revealed a conserved dithiol C34PYC37 active site, GSH-binding motifs (CXXC, Lys and Gln/Arg, TVP, and CXD), and a conserved Gly-Gly motif. The r-TsGrx1 kinetic constants for glutathione (GSH) and 2-hydroxyethyl disulfide (HED) were determined. In addition, cytosolic thioredoxin (TsTrx1), as reported by (Jiménez et al., Biomed Res Int 2015:453469, 2015), was cloned and expressed, and its catalytic constants were obtained along with those of the other two reductases. Rabbit-specific antibodies showed immune cross-reactions between TsTrx1 and TsTrx2 but not with TsGrx1. Both TsTGRs as reported by (Plancarte and Nava, Exp Parasitol 149:65-73, 2015) were biochemically purified to obtain and compare the catalytic constants for their natural substrates, r-TsTrx1, and r-TsTrx2, compared to those for Trx-S2E. coli. In addition, we determined the catalytic differences between the glutaredoxin activity of the TsTGRs compared with r-TsGrx1. These data increase the knowledge of the thioredoxin and GSH systems in T. solium, which is relevant for detoxification and immune evasion.

New evidence for refinement of anesthetic choice in procedures preceding the forced swimming test and the elevated plus-maze.

Previous studies indicated that some general anesthetics induce long-term antidepressant and/or anxiolytic-like effects. This raises the concern about the use of anesthesia in surgeries that precede psychopharmacological tests, since it may be a potential bias on results depending on the experimental design used. Thus, we evaluated whether general anesthetics used in surgeries preceding psychopharmacological tests would affect rats behavior in tests predictive of antidepressant or anxiolytic-like effects. We tested if a single exposure to sub-anesthetic or anesthetic doses of tribromoethanol, chloral hydrate, thiopental or isoflurane would change rats behavior in the forced swimming test (FST) or in the elevated plus-maze (EPM) test, at 2 h or 7 days after their administration. We also evaluated whether prior anesthesia would interfere in the detection of the antidepressant-like effect of imipramine or the anxiolytic-like effect of diazepam. Previous anesthesia with the aforementioned anesthetics did not change rats behaviors in FST per se nor it changed the antidepressant-like effect induced by imipramine treatment. Rats previously anesthetized with tribromoethanol or chloral hydrate exhibited, respectively, anxiogenic-like and anxiolytic-like behaviors in the EPM. Prior anesthesia with thiopental or isoflurane did not produce any per se effect in rats behaviors in the EPM nor disturbed the anxiolytic-like effect of diazepam. Our results suggest that, in our experimental conditions, tribromoethanol and chloral hydrate are improper anesthetics for surgeries that precede behavioral analysis in the EPM. Isoflurane or thiopental may be suitable for anesthesia before evaluation in the EPM or in the FST.

The facilitating effect of unfavorable lactation on the potentiation of electrocorticogram after spreading depression in awake and anesthetized adult rats.

OBJECTIVES: Cortical spreading depression (CSD) is a brain excitability-related phenomenon that can be affected by unfavorable conditions of lactation and by anesthetic agents. We have previously demonstrated that after CSD the electrocorticogram (ECoG) amplitude increases significantly (ECoG potentiation). Here, we investigated this potentiation in awake and anesthetized adult rats that were previously suckled among different lactation conditions. METHODS: Newborn rats were suckled in litters with 6 pups or 12 pups (L6 or L12 condition, respectively). At adulthood, we evaluated the ECoG potentiation after CSD at two cortical points (one point near, and another remote to the CSD-eliciting site). The amplitude of the ECoG waves was averaged with the support of an algorithm implemented in Matlab™ software. In both L6 and L12 condition, awake animals were compared with anesthetized groups that received either tribromoethanol- or urethane + chloralose-anesthesia. RESULTS: L12 rats presented significantly lower body- and brain weights than L6 rats (P < 0.01), indicating a nutritional deficiency. The anesthetized L6 groups presented with ECoG potentiation (P < 0.05) only in the near cortical recording point (28.0% and 32.6% increase for the tribromoethanol and urethane + chloralose groups, respectively), whereas the L12 groups displayed ECoG potentiation in both near (67.0% and 55.0%) and remote points (37.0% and 20.0%), in comparison with the baseline values (before CSD). DISCUSSION: The results suggest a facilitating effect of unfavorable lactation on the potentiation of ECoG after spreading depression in anesthetized adult rats. The potential implications for the human neurological health remain to be investigated.

Production, characterization, and evaluation of the stability of biodiesel obtained from greasy agroindustrial waste during storage.

Greasy agroindustrial waste from the process of cooking hog meat was used to produce biodiesel (fatty acid methyl esters and fatty acid ethyl esters) under a specific storage condition. The operating conditions necessary to achieve the optimal relationship between quality and productivity were assessed. Next, batches of methyl and ethyl biodiesels were produced, generating 2 L of each product to evaluate their stability during 150 days of storage. The following study indicates that, for methyl route, the molar ratio (1:5) and catalyst (0.5%) yielded the best result of 90.77% (w/v) and quality parameters within the international standards. The ethyl route also showed the highest yield (77.09% w/v) and better quality parameters with a molar ratio (1:5) and catalyst (0.5%). No significant differences were observed in the methyl biodiesel obtained from the batch process for up to 45 days, while the ethyl biodiesel degraded in 30 days of storage.

Anesthetic agents modulate ECoG potentiation after spreading depression, and insulin-induced hypoglycemia does not modify this effect.

Cortical spreading depression (CSD) is characterized by reversible reduction of spontaneous and evoked electrical activity of the cerebral cortex. Experimental evidence suggests that CSD may modulate neural excitability and synaptic activity, with possible implications for long-term potentiation. Systemic factors like anesthetics and insulin-induced hypoglycemia can influence CSD propagation. In this study, we examined whether the post-CSD ECoG potentiation can be modulated by anesthetics and insulin-induced hypoglycemia. We found that awake adult rats displayed increased ECoG potentiation after CSD, as compared with rats under urethane+chloralose anesthesia or tribromoethanol anesthesia. In anesthetized rats, insulin-induced hypoglycemia did not modulate ECoG potentiation. Comparison of two cortical recording regions in awake rats revealed a similarly significant (p<0.05) potentiation effect in both regions, whereas in the anesthetized groups the potentiation was significant only in the recording region nearer to the stimulating point. Our data suggest that urethane+chloralose and tribromoethanol anesthesia modulate the post-CSD potentiation of spontaneous electrical activity in the adult rat cortex, and insulin-induced hypoglycemia does not modify this effect. Data may help to gain a better understanding of excitability-dependent mechanisms underlying CSD-related neurological diseases.

Antinociceptive effect of stimulating the occipital or retrosplenial cortex in rats.

UNLABELLED: A role for the occipital or retrosplenial cortex in nociceptive processing has not been demonstrated yet, but connections from these cortices to brain structures involved in descending pain-inhibitory mechanisms were already demonstrated. This study demonstrated that the electrical stimulation of the occipital or retrosplenial cortex produces antinociception in the rat tail-flick and formalin tests. Bilateral lesions of the dorsolateral funiculus abolished the effect of cortical stimulation in the tail-flick test. Injection of glutamate into the same targets was also antinociceptive in the tail-flick test. No rats stimulated in the occipital or retrosplenial cortex showed any change in motor performance on the Rota-rod test, or had epileptiform changes in the EEG recording during or up to 3 hours after stimulation. The antinociception induced by occipital cortex stimulation persisted after neural block of the retrosplenial cortex. The effect of retrosplenial cortex stimulation also persisted after neural block of the occipital cortex. We conclude that stimulation of the occipital or retrosplenial cortex in rats leads to antinociception activating distinct descending pain-inhibitory mechanisms, and this is unlikely to result from a reduced motor performance or a postictal phenomenon. PERSPECTIVE: This study presents evidence that stimulation of the retrosplenial or occipital cortex produces antinociception in rat models of acute pain. These findings enhance our understanding of the role of the cerebral cortex in control of pain.

Preparation and characterisation of ethylcellulose microparticles containing propolis

Ethylcellulose microparticles containing propolis ethanolic extract (PE) were prepared by the emulsification and solvent evaporation method. Three ratios of ethylcellulose to PE dry residue value (DR) weretested (1:0.25, 1:4 and 1:10). Moreover, polysorbate 80 was used as emulsifier in the external phase (1.0 or 1.5% w/w). Regular particle morphology without amorphous and/or sticking characteristics was achieved only when an ethylcellulose: DR ratio of 1:0.25 and 1.0% polysorbate 80 were used. Microparticles had a mean diameter of 85.83 mium. The entrapment efficiency forpropolis of the microparticles was 62.99 more or less 0.52%. These ethylcellulose microparticles containing propolis would be useful for developing propolis aqueous dosage forms without the strong and unpleasant taste, aromatic odour and high ethanol concentration of PE.

A method to study preovulatory surges of gonadotropins.

The aim of this study was to describe and validate a method to evaluate the preovulatory surges of gonadotropins in rats submitted to anesthesia and implantation of a jugular vein cannula in the morning of proestrus and to withdrawal of serial blood samples in the afternoon of the same day. In experiment I, to choose an adequate anesthetic, cycling female rats were anesthetized in the morning of proestrus (10:00-11:00 h) with tribromoethanol, ketamine/xylazine or tiletamine/zolazepam and a Silastic cannula was implanted into the jugular vein. Blood samples (0.6 ml) were withdrawn hourly between 12:00 and 18:00 h of the same day and, on estrus morning, the rats were decapitated and the number of ova was counted. The preovulatory gonadotropin surges as well as ovulation occurred in rats anesthetized with tribromoethanol, while they were prevented by ketamine/xylazine or tiletamine/zolazepam. To investigate if the jugular cannulation under tribromoethanol anesthesia and serial blood sampling performed in experiment I altered the magnitude of the gonadotropin surges and the number of ova, intact rats (control) or rats anesthetized with tribromoethanol followed or not by jugular vein cannulation were decapitated at 16:00 h of proestrus and in the morning of estrus. The magnitude of preovulatory gonadotropin surges and the number of ova were not different among groups. Thus, since neither tribromoethanol nor surgical procedures or serial blood sampling altered the preovulatory gonadotropin surges or the ovulation process, this method seems to be suitable for this sort of study in rats.