Accumulation of aluminum in rat brain: does it lead to behavioral and electrophysiological changes?

The present study was undertaken to examine possible aluminum (Al) accumulation in the brain of rats and to investigate whether subchronic exposure to the metal leads to behavioral and neurophysiological changes in both treated and control groups. Each of the groups consisted of 10 animals. Aluminum chloride (AlCl₃) at a low (50 mg/kg/d) or high (200 mg/kg/d) dose was applied to male Wistar rats by gavage for 8 wk. Al-free water by gavage was given to the control group throughout the experiment. Behavioral effects were evaluated by open-field (OF) motor activity and by acoustic startle response (ASR). Electrophysiological examination was done by recording spontaneous activity and sensory-evoked potentials from the visual, somatosensory, as well as auditory cortex. The Al content of each whole brain was determined by electrothermal atomic absorption spectrophotometry. Subchronic Al exposure slightly caused some changes in the evoked potentials and electrocorticograms and in the OF and ASR performance, but these results were not statistically significant. The brain Al levels of the control and the low and high dose of Al-exposed groups were measured as 0.717±0.208 μg/g (wet weight), 0.963±0.491 μg/g (wet weight) and 1.816±1.157 μg/g (wet weight), respectively.     

Differential hydrolysis of homocysteine thiolactone by purified human serum (192)Q and (192)R PON1 isoenzymes

Human serum paraoxonase 1 (PON1) is a HDL-associated enzyme that catalyzes the hydrolysis of a variety of aromatic carboxylic acid esters and several organophosphates. Recently it has been suggested that a physiological substrate of serum PON1 is homocysteine thiolactone which is a putative risk factor in atherosclerosis. In this study, human (192)Q and (192)R PON1 isoenzymes were purified from the respective phenotype human serum, using a protocol consisting of ammonium sulfate precipitation and four chromatography steps: gel filtration, ion-exchange, non-specific affinity, and a second ion-exchange. Using paraoxon as substrate, overall purification fold was found as 742 for (192)R PON1 and 590 for (192)Q PON1. The final purified enzymes were shown as single protein bands close to 45kDa on SDS-PAGE and confirmed by Western blot. Substrate kinetics were studied with phenyl acetate, paraoxon and homocysteine thiolactone. Both PON1 isoenzymes showed mixed type inhibition with phenyl acetate. K(m) values of (192)Q and (192)R PON1 for homocysteine thiolactone were 23.5mM and 22.6mM respectively. For (192)R PON1, the V(max) was 2.5-fold and k(cat)/K(m) was 2.6-fold higher than those for (192)Q PON1 when homocysteine thiolactone is used as substrate. The present data suggest that defining (192)Q and (192)R PON1 isoforms could be a good predictor and prognostic marker in the cardiovascular risk assessment.     

Thiol Peroxidase Deficiency Leads to Increased Mutational Load and Decreased Fitness in Saccharomyces cerevisiae

Thiol peroxidases are critical enzymes in the redox control of cellular processes that function by reducing low levels of hydroperoxides and regulating redox signaling. These proteins were also shown to regulate genome stability, but how their dysfunction affects the actual mutations in the genome is not known. Saccharomyces cerevisiae has eight thiol peroxidases of glutathione peroxidase and peroxiredoxin families, and the mutant lacking all these genes (∆8) is viable. In this study, we employed two independent ∆8 isolates to analyze the genome-wide mutation spectrum that results from deficiency in these enzymes. Deletion of these genes was accompanied by a dramatic increase in point mutations, many of which clustered in close proximity and scattered throughout the genome, suggesting strong mutational bias. We further subjected multiple lines of wild-type and ∆8 cells to long-term mutation accumulation, followed by genome sequencing and phenotypic characterization. ∆8 lines showed a significant increase in nonrecurrent point mutations and indels. The original ∆8 cells exhibited reduced growth rate and decreased life span, which were further reduced in all ∆8 mutation accumulation lines. Although the mutation spectrum of the two independent isolates was different, similar patterns of gene expression were observed, suggesting the direct contribution of thiol peroxidases to the observed phenotypes. Expression of a single thiol peroxidase could partially restore the growth phenotype of ∆8 cells. This study shows how deficiency in nonessential, yet critical and conserved oxidoreductase function, leads to increased mutational load and decreased fitness.     

Fortpflanzungsverhalten der Palmtaube (Streptopelia senegalensis): Paarbildung bis Eiablage

Zusammenfassung Die Fortpflanzungsperiode der Palmtaube (Streptopelia s. senegalensis L.) fängt in Diyarbakir/Türkei (37°55N/40°12E) schon Anfang Februar an und kann bis Mitte November dauern. In diesem Zeitraum kann ein Paar bis zu sieben Bruten beginnen (Tab. 1). Nach der Paarbildung fangen die Kopulationen an, die vor allem in der Woche vor der Eiablage stark zunehmen. Während des Brütens und der ersten Woche der Jungenaufzucht sind sie dagegen nicht zu beobachten. Sie werden vom im allgemeinen mit sog. Flügeltippen bzw. Scheinputzen eingeleitet. Nach der Begattung paradiert das um das , das auf der Stelle verharrt. Vor dem Tretakt fällt das dagegen in infantiles Verhalten und bettelt unter Flügelzittern den Partner um Futter an. Es bekommt auch tatsächlich Futter. Die Palmtauben sind zumindest für eine Fortpflanzungssaison monogam. U. a. spielen wechselseitige Gefiederpflege und Anschlußbruten sowie die Fütterung des durch das eine wichtige Rolle für das Zusammenleben und -bleiben der Partner. Der Nistplatz wird vom gezeigt, aber vom gewählt. Das Nistmaterial wird vom eingetragen und im allgemeinen vom alleine in das Nest eingefügt. Nur während des Brutwechsels bringt auch das hin und wieder Nistmaterial, das aber wahrscheinlich nur für den Partner, nicht für das Nest dient. In den späteren Phasen des Brütens gilt dies wahrscheinlich auch für das . 1–4 Tage nach dem Nestbaubeginn wird gegen Abend das erste Ei gelegt, womit auch das Brüten anfängt. Das zweite Ei folgt dann rund 38 Stunden später.

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On the reproductive behaviour of the Laughing Dove (Streptopelia senegalensis): pair-formation to egg-laying

Summary In Diyarbakr/Turkey, the reproductive season of the Laughing Dove begins in early February and lasts til mid November. One pair may start with breeding up to seven times a year. The frequency of copulations which could be observed only after pair formation increased considerably in the week before incubation starts. During incubation and during the first week of the nestling period no copulations could be observed. Usually copulations are initiated by the male pecking behind its folded wings (displacement-preening). Before mating, the female turns into infantile behaviour begging food from its partner by wing-twitching. Food is then delivered by the male. After mating the female parades around the male which stays motionless. Paired birds stay together at least during one reproductive season. Reinforcement of the pair bond will be achieved by mutual preening, courtship feeding of the female by the male, and successive broods. The male indicates the nest site which is successively chosen by the female. The nest material is brought by the male and usually placed by the female at the nest site. Only during change-overs the female sometimes brings nesting material, too. However, this material probably is for the partner, not actually for the nest. The same may be true for similar behaviour of the male in late stages of incubation. One to four days after nest building has started the first egg is laid, mostly in late afternoon. Incubation starts with the first egg; the second egg is laid about 38 hours later.

     

Glassworts as Possible Anticancer Agents Against Human Colorectal Adenocarcinoma Cells with Their Nutritive,Antioxidant and Phytochemical Profiles

In this study, the possible uses of glassworts as potential food ingredients and their antiproliferative activity against colorectal adenocarcinoma cells together with their antioxidant and phytochemical profiles were investigated for the first time. MeOH extracts of five different taxa collected from different localities were screened for their antioxidant capacities by DPPH (IC₅₀ 2.91 – 5.49 mg/ml) and ABTS (24.4 – 38.5 μmol TE/g extract) assays. Salicornia freitagii exhibited the highest DPPH radical scavenging activity. LC/MS/MS analysis displayed that vanillic acid and p‐coumaric acid were two main phenolic compounds in the extract. Salicornia freitagii extracts also exhibited high antiproliferative activity against HT‐29 (IC₅₀ 1.67 mg/ml) and Caco‐2 (IC₅₀ 3.03 mg/ml) cells for 72 h. Mineral analysis indicated that all the species with different proportions of elemental components contained high amount of cations. These results indicate that investigated glassworts, with their high phenolic and mineral contents and also notable antioxidant and cytotoxic properties, may be utilized as a promising source of therapeutics.     

The relationship between the presence of ADHD and certain candidate gene polymorphisms in a Turkish sample

Due to the high heritability of attention-deficit hyperactivity disorder (ADHD), parents of children with ADHD appear to represent a good sample group for investigating the genetics of the disorder. The aim of this study was to investigate the association between ADHD and six polymorphisms in five candidate genes [5-HT2A (rs6311), NET1 (rs2242447), COMT (rs4818), NTF3 (rs6332), SNAP-25 (rs3746544) and (rs1051312)]. We included 228 parents of children diagnosed with ADHD and 109 healthy parents as the control group. The polymorphisms were genotyped using polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) assays and analyzed using the chi-square test and the multinomial logit model. SNAP-25 (rs3746544) polymorphism was associated with loading for ADHD, while 5-HT2A (rs6311) and NET1 (rs2242447) polymorphisms were associated with ADHD. On the other hand, there was no significant association between the SNAP-25 (rs1051312), NTF3 (rs6332), or COMT (rs4818) gene polymorphisms and ADHD.     

RNAi: an ever-growing puzzle

In recent years, sequence-specific gene silencing has been an area of increasing focus, both because of its interesting biology and because of its power as an experimental tool. A growing understanding of one such phenomenon, RNA interference (RNAi), has provided clues that many homology-dependent gene-silencing mechanisms share a common trigger, double-stranded RNA. Recent findings that RNAi and related pathways are involved not only in the response to exogenous pathogenic and endogenous parasitic nucleic acids but also in basic cellular processes, such as gene regulation and heterochromatin formation, have further fueled interest in this rapidly expanding field.