Home About us Contact
|
Home About us Contact | ||
|
|
||
Membrane Stability (membrane + stability)
Selected AbstractsReduction of intramembranous particles in the periacrosomal plasma membrane of boar spermatozoa during in vitro capacitation: A statistical studyDEVELOPMENT GROWTH & DIFFERENTIATION, Issue 3 2000Fumie Suzuki-Toyota Membrane remodeling in the periacrosomal plasma membrane (PAPM) of boar spermatozoa during incubation in capacitation medium was examined by the freeze-fracture technique. In the preservation medium (PM) group, the major small (about 8 nm) intramembranous particles (IMP) and the minor large (> 10 nm) IMP were distributed evenly in the PAPM. The IMP-free area increased during capacitation. To correct the IMP-free area, arithmetically redistributed (ARD)-IMP density was used for statistical analysis. In the PM group, the mean density ± SD of large IMP was 379 ± 64 and 266 ± 58/,m2, and that of small IMP was 1450 ± 155 and 672 ± 252/,m2 in protoplasmic (P) and external (E) faces, respectively. During capacitation, the significant (P < 0.01) reduction of large IMP density was encountered only in the E face of a few incubation groups, while that of the small IMP density occurred in the P face by 2 h. Consequently, reduction of the total IMP density of both faces was not significant in the large IMP, but it was significant (P < 0.01) in the small IMP. One-fifth of the total small IMP density reduced by 2 h. Filipin-sterol complexes (FSC) were numerous in the PAPM, and FSC-free areas also increased during capacitation. The mechanism of IMP-free area formation and the behavior of the small IMP in the PAPM during capacitation were discussed in relation to membrane stability. [source] Wheat Cellular Membrane Thermotolerance Under Heat StressJOURNAL OF AGRONOMY AND CROP SCIENCE, Issue 2 2010A. S. Dias Abstract Four genotypes of Triticum aestivum L. and Triticum turgidum subsp. durum chosen according to their genetic background diversity were subjected to heat stress after anthesis. Membrane permeability, lipid peroxidation and fatty acids (C14:0, C16:0, C16:1c, C16:1t, C18:0, C18:1, C18:2 and C18:3) were quantified. The estimation of the quantum yield of non-cyclic photosynthetic electron transport was used as well as a test system to further evaluate the implications on thylakoid functioning. It was found differences within bread and durum wheat species concerning the capability to cope with high temperatures at the stage of grain filling. The genotype Sever showed high thermal sensitivity concerning membrane lipid peroxidation and membrane permeability, as evaluated by the increased production of ethylene and MDA, as well as by the impact on TFA (at the middle term of grain filling). In the durum wheat genotypes, differences were also found, with TE 9306 displaying high membrane stability, with no increases on membrane permeability, MDA and ethylene content. In this way, the observed changes on TFA in this genotype might have constituted a mechanism to allow qualitative lipid changes, reflected in lower unsaturation level of membrane FAs which is a positive trait under high temperatures. [source] Indices of Drought Tolerance in Wheat Genotypes at Early Stages of Plant GrowthJOURNAL OF AGRONOMY AND CROP SCIENCE, Issue 1 2004S. S. Dhanda Abstract Thirty diverse genotypes of bread wheat were evaluated for seed vigour index, germination percentage, root length, shoot length, root-to-shoot length ratio, coleoptile length and osmotic membrane stability under laboratory conditions. Considerable variation was observed for all the characters. Discrimination among the genotypes on the basis of mean values was better under normal than under moisture stress conditions, indicating suppression of variability under moisture stress conditions. Comparison of mean performance under normal and osmotic stress conditions indicated that the seed vigour index was the most sensitive trait, followed by shoot length, germination percentage and root length. The root-to-shoot length ratio, however, increased under osmotic stress. The magnitude of genetic components of variance and heritability were, in general, lower under osmotic stress than under normal conditions. All the characters except germination percentage, shoot length and coleoptile length showed considerable genetic variability. Heritability in the broad sense was also moderate to high for all the characters under both environments. Due to high heritability and genetic advance great benefit from selection can be expected for the osmotic membrane stability of leaf segments and root-to-shoot length ratio. Moderate progress can be expected from root length and seed vigour index. Correlation studies indicated that the osmotic membrane stability of the leaf segment was the most important trait, followed by root-to-shoot ratio and root length on the basis of their relationships with other traits. [source] Physiological and Biochemical Responses of Hexaploid and Tetraploid Wheat to Drought StressJOURNAL OF AGRONOMY AND CROP SCIENCE, Issue 4 2000V. Chandrasekar An experiment was conducted to investigate the physiological and biochemical responses of two hexaploids viz., C 306 (water stress tolerant) and Hira (water stress susceptible), and two tetraploids, HW 24 (Triticum dicoccum) and A 9-30-1 (Triticum durum) wheat genotypes to water stress under pot culture condition. Water stress was imposed for a uniform period of 10 days at 50, 60 and 70 days after sowing (DAS) and observations were recorded at 60, 70 and 80 DAS. Total dry matter and plant height were recorded at harvest. Water stress caused a decline in relative water content (RWC), chlorophyll and carotenoid content, membrane stability and nitrate reductase activity and increased accumulation of proline at all stages and abscisic acid (ABA) at 80 DAS in all the genotypes. Both the tetraploids showed a lower reduction in RWC and highest ABA accumulation under water stress. Among the hexaploids Hira showed the most decline in RWC and the lowest ABA accumulation. The tetraploids also showed comparatively higher carotenoid content and membrane stability, closely followed by C 306, while Hira showed the minimum response under water stress. Nitrate reductase activity and chlorophyll content under irrigated conditions were highest in Hira but under water stress the lowest per cent decline was observed in C 306, followed by HW 24, A 9-30-1, and Hira. Proline accumulation under water stress conditions was highest in hexaploids C 306 and Hira and lowest in tetraploids HW 24 and A 9-30-1. Tetraploids HW 24, followed by A 9-30-1 maintained higher plant height and total dry matter (TDM) under water stress and also showed a lower per cent decline under stress than hexaploids C 306 and Hira. From the results it is clear that proline accumulation did not contribute to better drought tolerance of tetraploids than hexaploids. It is also apparent that water stress tolerance is the result of the cumulative action of various physiological processes, and all the parameters/processes may not be positively associated with the drought tolerance of a particular tolerant genotype. [source] Diffusional properties of chitosan hydrogel membranesJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 6 2001Barbara Krajewska Abstract Chitosan membranes were prepared by a solvent evaporation technique, followed by crosslinking with glutaraldehyde and coating with BSA. The effects of crosslinking and BSA coating on the pore structure of such prepared hydrogel chitosan membranes were determined. The diffusion rates of 12 non-electrolytes ranging in molecular radius between 2.5 and 14,Å through the membranes were measured, and the results were interpreted in terms of the capillary pore model and free volume model of solute diffusional transport through hydrogel membranes. Glutaraldehyde crosslinking was found to reduce the membrane water content and consequently the membrane pore size and surface porosity, whereas further BSA coating brought about the opposite effect. The latter effect lessened with an increase in glutaraldehyde pretreatment of the membranes. The optimal chitosan membrane preparation, compromising between the solute flux and membrane stability and durability was obtained when the membranes were crosslinked with glutaraldehyde at concentrations between 0.01 and 0.1% (w/w). The knowledge of transport properties and of physical strength of the membranes is of importance for the development of chitosan-based controlled release systems. © 2001 Society of Chemical Industry [source] Lipid peroxide formation in relation to membrane stability of fresh and frozen thawed stallion spermatozoaMOLECULAR REPRODUCTION & DEVELOPMENT, Issue 2 2005D.M. Neild Abstract In this study we used a new method to detect reactive oxygen species (ROS) induced damage at the level of the sperm plasma membrane in fresh and frozen-thawed stallion sperm. Lipid peroxidation (LPO) in sperm cells was assessed by a fluorescent assay involving the labeling of stallion sperm with the LPO reporter probe C11-BODIPY581/591. The peroxidation dependent spectral emission shift of this membrane probe could be localized using inverted spectral confocal microscopy and quantified on living and deteriorated sperm cells using flow cytometry. Mass spectrometric analysis of the main endogenous lipid class, phosphatidylcholine (PC), was carried out to determine the formation of hydroxy- and hydroperoxyphosphatidylcholine in fresh sperm cells. Peroxidation as reported by the fluorescent probe corresponded with the presence of hydroxy- and hydroperoxyphosphatidylcholine in the sperm membranes, which are early stage products of LPO. This allowed us to correlate endogenous LPO with localization of this process in the living sperm cells. In absence of peroxidation inducers, only relatively little peroxidation was noted in fresh sperm cells whereas some mid-piece specific probe oxidation was noted for frozen-thawed sperm cells. After induction of peroxidation in fresh and frozen-thawed sperm cells with the 0.1 mM of lipid soluble ROS tert -butylhydrogen peroxide (t -BUT) intense probe oxidation was produced in the mid-piece, whereas the probe remained intact in the sperm head, demonstrating antioxidant activity in the head of fresh sperm cells. At higher levels of t -BUT, probe peroxidation was also noted for the sperm head followed by a loss of membranes there. Frozen-thawed sperm were more vulnerable to t -BUT than fresh sperm. The potential importance of the new assays for sperm assessments is discussed. © 2005 Wiley-Liss, Inc. [source] Membrane stabilization by abscisic acid under cold aids proline in alleviating chilling injury in maize (Zea mays L.) cultured cellsPLANT CELL & ENVIRONMENT, Issue 8 2002W. P. Chen Abstract Previous studies of maize suspension-cultured cells showed that abscisic acid (ABA) treatment at warm temperatures improved the tolerance of cells to subsequent chilling. In the present study, it is shown that both ABA-treated and untreated maize cells accumulated proline in response to chilling. However, ABA-treated cells displayed less lipid peroxidation during chilling, and thus, unlike untreated cells, were able to retain the accumulated proline intracellularly. Proline application experiments indicate that an intracellular proline level higher than 2 µmole (g FW),1 prior to chilling was needed to meaningfully reduce chilling-enhanced lipid peroxidation and significantly improve chilling tolerance. The results suggest that total proline accumulation in ABA-treated as well as untreated cells during chilling was enough to potentially improve chilling tolerance, but proline leakage rendered the control cells unable to benefit from the endogenous synthesis of proline in relation to the alleviation of chilling injury. Proline participated in chilling tolerance improvement in ABA-treated maize cells, as evidenced by: (1) the inhibition of proline accumulation by l -methionine- d, l -sulphoximine (MSO), an inhibitor of glutamine synthetase, reduced ABA-improved chilling tolerance, and (2) the addition of glutamine into the medium prevented the MSO-induced reduction in chilling tolerance. The revised relationship between proline accumulation and membrane stability at cold is discussed in the light of these current findings. [source] Action Mechanisms of the Secondary Metabolite Euplotin C: Signaling and Functional Role in EuplotesTHE JOURNAL OF EUKARYOTIC MICROBIOLOGY, Issue 5 2008FRANCESCA TRIELLI ABSTRACT. Among secondary metabolites, the acetylated hemiacetal sesquiterpene euplotin C has been isolated from the marine, ciliated protist Euplotes crassus, and provides an effective mechanism for reducing populations of potential competitors through its cytotoxic properties. However, intracellular signaling mechanisms and their functional correlates mediating the ecological role of euplotin C are largely unknown. We report here that, in E. vannus (an Euplotes morphospecies that does not produce euplotin C and shares with E. crasssus the same interstitial habitat), euplotin C rapidly increases the intracellular concentration of both Ca2+ and Na+, suggesting a generalized effect of this metabolite on cation transport systems. In addition, euplotin C does not induce oxidative stress, but modulates the electrical properties of E. vannus through an increase of the amplitude of graded action potentials. These events parallel the disassembling of the ciliary structures, the inhibition of cell motility, the occurrence of aberrant cytoplasmic vacuoles, and the rapid inhibition of phagocytic activity. Euplotin C also increases lysosomal pH and decreases lysosomal membrane stability of E. vannus. These results suggest that euplotin C exerts a marked disruption of those homeostatic mechanisms whose efficiency represents the essential prerequisite to face the challenges of the interstitial environment. [source] Effects of Xenobiotic Compounds on Cell Activities in Euplotes crassusTHE JOURNAL OF EUKARYOTIC MICROBIOLOGY, Issue 2 2005FRANCESCA TRIELLI It is now widely accepted that Protists are relevant bioassays to be exploited for the study of environmental modifications due to the presence of xenobiotic compounds. In this work, we evaluated the possibility of utilizing Euplotes crassus, an interstitial marine ciliate, for the pre-chemical screening of environmental sites, such as estuarine and coastal sediments. With this aim, we tested the sensitivity of E. crassus to exposure to three classes of pollutants: an organophosphate neurotoxic drug, basudin, largely used for pest control in agricultural sites, a toxic heavy metal, mercury (HgCl2), and an aromatic polycyclic hydrocarbon, benzopyrene (BP). We found a dose-dependent effect of these compounds on cell viability at concentrations ranging from 1/102 v/v to 1/107 v/v for basudin, from 5 ,M to 0.1 ,M for HgCl2, and from 50 ,M to 1 ,M for BP. In particular, 100% mortality was caused by a 1-h exposure to 1/105 v/v basudin, or 2 ,M HgCl2, or 25 ,M BP, and by a 24-h exposure to 1/106 v/v basudin, 0.5 ,M HgCl2, or 5 ,M BP. A significant decrease in the daily mean fission rate (P<0.001) was found after exposure to 1/107 v/v basudin, or 0.25 ,M HgCl2, or 1 ,M BP. Moreover, as it is well known that the inhibition of acetylcholinesterase (AChE) activity represents a specific biomarker for neurotoxic drugs, we first detected this enzyme activity in E. crassus, using cytochemical, spectrophotometric, and electrophoretic methods; then, AChE activity was characterized by its sensitivity to specific AChE inhibitors and to variations in pH and temperature. Like AChE present in higher organisms, the AChE activity detected in E. crassus was inhibited by exposure to basudin. Conversely, exposure to HgCl2, or PB did not inhibit AChE activity, but caused a significant reduction in lysosomal membrane stability. [source] Effects of air exposure on the lysosomal membrane stability of haemocytes in blacklip abalone, Haliotis rubra (Leach)AQUACULTURE RESEARCH, Issue 3 2007Liang Song Abstract The neutral red retention (NRR) assay was used to evaluate the effects of air exposure on lysosomal membrane integrity in the haemolymph of blacklip abalone, Haliotis rubra, and its subsequent recovery in water. After acclimation in 16°C water for 7 days, abalone were exposed to an air temperature of 7, 16 or 23°C for 12 h in the air exposure experiment or to these three air temperatures, e.g., for 12, 24 or 36 h, followed by re-immersion in 16°C water in the lysosomal membrane stability recovery experiment. Statistical analyses of the air exposure experiment showed that when abalone were exposed to different air temperatures (7, 16 or 23°C), the lysosomal membrane stability was significantly affected by the air temperature, the exposure duration and their interaction. Air temperature similar to the acclimation temperature had a significantly lower impact on the lysosomal membrane stability within the initial 4.5 h in comparison with the other two temperatures in the same period. The lysosomal membrane stability recovery experiment showed that after air exposure durations of 12, 24 or 36 h, the re-stabilization of the lysosomal membrane was faster in the animals exposed to lower temperatures than those exposed to higher temperatures. The recovery of the lysosomal membrane stability in abalone exposed to lower 7°C air temperature was not significantly affected (F2, 66=0.251, P=0.779) by the exposure durations (12, 24 and 36 h) used in this study. Alternatively, the lysosomal membrane stability in abalone exposed to higher air temperatures of 16 or 23°C recovered at a faster rate when subjected to shorter durations of air exposure (F2, 66=3.663, P=0.031 and F1, 44=17.057, P<0.001 for 16 and 23°C respectively). [source] | |||||||||||||