Baigiamajame darbe išnagrinėta adaptacijos ir kultūrinio šoko sampratos, aptarta pagrindiniai adaptacijos bruožai lietuvių emigrantų Ispanijoje ir Airijoje. Pagrindinis tyrimo tikslas – nustatyti lietuvių emigrantų adapacijos pobūdį, išsiaiškinti kokios priežastys lemia sėkmingą / nesėkmingą adaptaciją, kas lemia norą / nenorą grįžti į Lietuvą. Įvairūs tyrimai rodo, kad Lietuvos migracijos potencialas labai didelis:40 – 60 % Lietuvos gyventojų norėtų išvykti gyventi/ dirbti į užsienį; ypač yra daug norinčių išvykti tarp 15 – 24 metų jaunimo – 70 – 90 %; tarp aukštajį išsilavinimą turinčių norėtų išvykti 60 – 75 %. Tačiau tik nedaugelis norėtų išvykti visam laikui. Lietuva visų pirma praranda jaunimą, todėl ateityje tai paveiks tiek kitus demografinius procesus (santuoką, gimstamumą, šeimos raidą) tiek ir darbo išteklius, kuriuos gali tekti importuoti iš trečiųjų šalių. Emigrantus būtų galima suskirstyti į dvi grupes – jaunimą, kurie neįvertinti kaip jauni specialistai baigia aukštuosius mokslus užsienyje arba dėl nebaigto aukštojo mokslo ar nepaklausios specialybės jiems yra itin sunku susirasti poreikius atitinkantį darbą Lietuvoje, ir vidutinio amžiaus žmones, kurie praranda darbą Lietuvoje ir dėl savo amžiaus, ribotų galimybių persikvalifikuoti išvyksta. Norint mažinti emigracijos mastus būtina sudaryti šioms gyventojų grupėms geresnes įsidarbinimo/persikvalifikavimo Lietuvoje galimybes. / The thesis analyses the concepts of adaptation and culture shock and deals with the main issues of adaptation of Lithuanian emigrants in Spain and Ireland. The main aim of the research was to define the nature of the adaptation of Lithuanian emigrants; to find out the causes of either successful adaptation or failure to do so; as well as to identify the factors that influence emigrants’ willingness or unwillingness to return to Lithuania. Different investigations show that the potential of Lithuanian migration is very big – 40 to 60 percent of Lithuanian inhabitants would like to go abroad to live or work; the rate is especially high among young people between 15 and 24 years of age – 70 to 90 percent; 60 to 75 percent of inhabitants with higher education would like to leave the country. However, not many people would like to emigrate forever. Mainly, Lithuania is abandoned by young people, which in future will affect other demographic processes (marriages, births, family development), as well as labour resources that Lithuania might need to import from third countries. The emigrants may be divided into two groups: young people who, having been underestimated as young professionals, finish their studies to obtain higher education in foreign countries, or those who have not acquired higher education or have non-demanded professions and therefore have difficulty finding jobs which would meet their needs; and middle-aged people who leave the country under... [to full text]

Sodium arsenite and cadmium chloride are two widespread environmental toxicants which have deleterious effects on living organisms. At the cellular level, sodium arsenite and cadmium chloride cause oxidative stress, dysregulation of gene expression, apoptosis, and the unfolding of protein. Furthermore, both chemical stressors individually have the ability to induce heat shock protein (HSP) accumulation. HSPs are molecular chaperones that aid in protein folding, translocation and in preventing stress-induced protein aggregation. Previously, our laboratory demonstrated that treatment of A6 kidney epithelial cells of the frog Xenopus laevis, with either cadmium chloride or sodium arsenite plus a concurrent mild heat shock resulted in an enhanced accumulation of HSPs that was greater than found with the sum of the individual stressors. To the best of our knowledge, no information is available to date on the effect that these two chemical stressors have in combination on HSP accumulation in aquatic organisms. The present study examined the effect of simultaneous sodium arsenite and cadmium chloride treatment on the pattern of HSP30 and HSP70 accumulation in Xenopus A6 cells. Immunoblot analysis revealed that the relative levels of HSP30 and HSP70 accumulation in A6 cells treated concurrently with sodium arsenite and cadmium chloride for 12 h were significantly higher than the sum of HSP30 or HSP70 accumulation from cells subjected to the treatments individually. For instance, the combined 10 µM sodium arsenite plus 100 µM cadmium chloride treatment resulted in a 3.5 fold increase in HSP30 accumulation and a 2.5 fold increase in HSP70 accumulation compared to the sum of the stressors individually. This finding suggested a synergistic action between the two stressors. Pretreatment of cells with KNK437, an HSF1 inhibitor, inhibited the combined sodium arsenite- and cadmium chloride-induced accumulation of HSP30 and HSP70 suggesting that this accumulation of HSPs may be regulated, at least in part, at the level of transcription. Immunocytochemical analysis employing the use of laser scanning confocal microscopy (LSCM) revealed that simultaneous treatment of cells with the two stressors induced HSP30 accumulation primarily in the cytoplasm in a punctate pattern with some dysregulation of F-actin structure. Increased ubiquitinated protein accumulation was observed with combined 10 µM sodium arsenite and 10, 50 or 100 µM cadmium chloride treatment compared to individual stressors suggesting an impairment of the ubiquitin-proteasome degradation system. Finally, while incubation of A6 cells with 1 µM sodium arsenite plus 10 µM cadmium chloride did not induce a detectable accumulation of HSPs, the addition of a 30 °C mild heat shock resulted in a strong accumulation of HSP30 and HSP70. This study has demonstrated that concurrent sodium arsenite and cadmium chloride treatment can enhance HSP accumulation. Since HSP accumulation is triggered by proteotoxic stress, these findings are relevant given the fact that aquatic amphibians in their natural habitat may be exposed to multiple chemical stressors simultaneously.

There are sex differences in degenerative disease prevalence in humans. Most models of degenerative disease use male animals. Examining female and male responses to stress may give insight into disease prevalence. Heat shock proteins are chaperones linked to damaged proteins in degenerative diseases and may be expressed differentially in females and males. My goal was to characterize the induced expression of Hsp70 and Hsp27 in the brain and heart of female and male rats. Rats were heat shocked, brains and hearts were removed 24 hours after, and western analyses were done to quantify the expression of these proteins. Immunofluorescence was used to localize Hsp70 and Hsp27 in the hippocampus. Overall, male rats have significantly greater induced expression of both Hsp70 and Hsp27 in the brain. In the hippocampus, Hsp70 was localized in blood vessels and microglia, and Hsp27 was localized in astrocytes, following heat shock.

Gene expression at the level of mRNA translation is critical for cells to respond to external signals; it allows changes in protein synthesis without triggering transcription of a new set of genes. Control of mRNA translation and stability is important in several cellular processes including cell growth and differentiation. Thus regulation of the cellular machinery involved in mRNA translation is crucial. Poly (A) binding protein (PABP1), eukaryotic elongation factor 1A (eEF1A) and ribosomal protein S6 (RPS6) are important members of the cellular mRNA translation machinery, the mRNAs that encode these proteins belong to the terminal oligo pyrimidine tract (TOP) containing family. Translation of the TOP mRNAs is regulated by growth signals and usually codes for several proteins involved in mRNA translation. Our laboratory has previously reported up regulation of PABP1 mRNA translation during recovery from heat shock. It was also shown that the terminal oligopyrmidine tract (TOP) cis-element of PABP1 mRNA is responsible for the preferential increase of PABP1 mRNA translation; however the mechanism for achieving this is unknown. In the studies reported here, we showed that translation of eEF1A and RPS6 expression was similarly enhanced during recovery from heat shock. Analyses of samples of in vivo cross linked RNA– protein complexes, immunoprecipitated by ZNF9 antibody, for the presence of specific mRNAs showed that the cellular nucleic acid binding protein ZNF9 binds not only to TOP mRNAs but also mRNA that lack the TOP element such as to β-actin mRNA. To elucidate the mechanism of activation of TOP mRNA translation, as a candidate trans acting factor, siRNA was used to deplete the cellular level of ZNF9 from heat shocked HeLa cells to examine its potential role in stimulation of TOP mRNA translation during recovery from heat shock. Results show that the knock down of ZNF9 disallowed the preferred stimulation of PABP1, eEF1A and RPS6 expression during recovery from heat shock. There was no detectable effect on the constitutive expression of either β-actin or PABP1, eEF1A and RPS6 in exponentially growing HeLa cells. These results suggest that binding of ZNF9 to TOP mRNAs per se does not inhibit translation, but more likely it acts as a general facilitator of mRNA translation. It is possible that modification of the interaction between ZNF9 with other unknown protein factors is responsible for its preferred effect on all three TOP mRNAs studied here. Additionally, results also suggest that a different TOP sequences amongst the observed TOP mRNAs responds similarly to ZNF9.

Processing information in the nervous system is energetically expensive, constraining the ability of the system to survive disturbances caused by stress. While some organisms compensate for extreme changes in the abiotic features of their environment, the mechanisms underlying this are poorly understood. We used the locust Descending Contralateral Movement Detector (DCMD) neuron to study how the propagation characteristics of action potentials (APs) change following an acute energy stress in control and heat shock (HS) pre-treated animals. We also attempted to determine if Ca2+ is involved in the DCMD AP and the possible changes indicated above. Conduction velocity decreased over an hour of recording in all groups, except those with minimal dissections, and we observed an increase in AP half-width and a decrease in the slope of the rising phase of the AP over time. After HS pre-treatment the response to a standard looming stimulus was delayed, showed significantly fewer APs and a lower peak frequency compared to controls. Brief application of sodium azide (NaN3) as an acute metabolic inhibitor did not subsequently affect DCMD’s conduction velocity or ability to fire at high frequencies during the recording period. There were no significant differences from control animals with extracellular Ca2+ manipulations; however we cannot conclude that Ca2+ does not contribute to DCMD’s AP because Na+ could have flowed through Ca2+ channels in the absence of extracellular Ca2+. Furthermore, examination of possible performance impairments with decreased Ca2+ currents, to indicate if Ca2+ current manipulation may account for the performance impairment, could not be conducted because no differences in AP characteristics were observed with Ca2+ manipulations. We suggest that the slowing of propagation in all groups represents a response to energetic stress and that HS modifies neuronal properties in ways that can be interpreted as saving energy in case of future stressors. / Thesis (Master, Neuroscience Studies) -- Queen's University, 2009-08-11 08:36:26.571

The present study deals with the development of a single-stage implosion-driven hypervelocity launcher. A thin-walled tube filled with helium surrounded by explosives acts as a driver for the launcher. Implosion of the tube drives a strong shock that reflects back and forth between the projectile and the implosion pinch, generating very high temperatures and pressures. Simple analytic models were used to approximate the performance of the pump tube and its use as a driver for a launcher. Experiments to evaluate the implosion dynamics and performance of the pump tube were carried out, and implosion-driven launcher experiments demonstrated muzzle velocities above 4 km/s with 5-mm-diameter aluminum projectiles. Projectile integrity was verified by high-speed photography. Disagreement of experimental data with the analytical models of performance is mostly due to failure to seal the chamber of the launcher, resulting in loss of driver gas, and pump tube expansion, which weakens the precursor shock.

The mechanism and subsequent patterns of Heat shock protein (Hsp) expression in skeletal muscle specific to contraction type was determined. Rat tibialis anterior (TA) muscle was forcibly lengthened (LC) or shortened (SC) in 5 sets of 20 repetitions before being removed at 2, 8, 24, 48, 72, or 168 hours and analyzed for muscle damage and Hsp25 and Hsp72 expression. Isometric peak torque was reduced to 63% and 33% (P<0.001) at 3-minutes after SC and LC, respectively. Muscle fibre damage appeared at 8h and beyond following LCs, but no damage was observed after SCs. Hsp25 content in LC muscle increased by 3.1±0.53 fold (P<0.01) at 48h and remained elevated. Hsp72 content increased by 3.8±0.66 fold at 24h and remained elevated. Neither Hsp25 nor Hsp72 content was elevated following SCs. Muscle damage associated with LCs results in a greater Hsp accumulation than SCs and 100 SCs do not result in increased Hsp content.

The mechanism and subsequent patterns of Heat shock protein (Hsp) expression in skeletal muscle specific to contraction type was determined. Rat tibialis anterior (TA) muscle was forcibly lengthened (LC) or shortened (SC) in 5 sets of 20 repetitions before being removed at 2, 8, 24, 48, 72, or 168 hours and analyzed for muscle damage and Hsp25 and Hsp72 expression. Isometric peak torque was reduced to 63% and 33% (P<0.001) at 3-minutes after SC and LC, respectively. Muscle fibre damage appeared at 8h and beyond following LCs, but no damage was observed after SCs. Hsp25 content in LC muscle increased by 3.1±0.53 fold (P<0.01) at 48h and remained elevated. Hsp72 content increased by 3.8±0.66 fold at 24h and remained elevated. Neither Hsp25 nor Hsp72 content was elevated following SCs. Muscle damage associated with LCs results in a greater Hsp accumulation than SCs and 100 SCs do not result in increased Hsp content.

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