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The effects of various concentrations of thapsigargin, a specific inhibitor of Ca2+ -ATPase in the endoplasmic reticulum (ER) membrane, on calcium homeostasis in lymphoidal T cells (Jurkat) were investigated. Preincubation of these cells suspended in nominally calcium-free medium with 0.1 UM thapsigargin resulted in a complete release of Ca2+ from intracellular calcium stores. When the medium was supplemented with 3 mM CaCl2 the cells maintained constantly elevated level of cytosolic Ca2+ . However, tha­psigargin applied at lower concentration produced only a partial depletion of the stores. For example, in the cells pretreated with 1 nM thapsigargin and suspended in calcium-free medium approximately 75% of the calcium content was released from the intracellular stores. The addition of 3 mM CaCl2 to such cell suspension led to a transient increase in cytosolic calcium concentration, followed by a return to a lower steady-state. This phenomenon, related to the refilling of the ER by Ca2+ , allowed to estimate the half-time for the process of cell recovery after activation of store-operated calcium channels. By this ap­proach we have found that carbonyl cyanide m-chlorophenylhydrazone, which has been documented to inhibit calcium entry into Jurkat cells, does not influence the stability of the intracellular signal involved in the activation of store-operated calcium channels.
In the present paper, we have presented a theoretical discussion of specific biophysical mechanisms per taining to the regulation (by means of internal factors) of physiological water ex change with the water medium by the cells of the Nitella translucens. The investigation has demonstrated that these cells have a capacity for water ex change regulation through changes in the values of transport parameters of the cell membrane (i.e. the filtration coefficient Lp and the reflection coefficient σ), as well as changes in the concentration Csi (in side the cells) of the osmotically active solute.
It has been hypothesized that developmental stability is increased at higher levels of genetic variability (heterozygosity) in animals. However, the existence of this relationship is questionable for homeotherms in general and mammals in particular. The difference between the sides of a bilateral character in an individual is a measure of fluctuating asymmetry that can be used as a measure of the developmental stability of mammals. Increased developmental stability should result in a greater degree of similarity between the right and left side of the body even though environmental variability would tend to increase the differences between right and left sides of the body. It is necessary to separate the effects of the three types of asymmetry so that an accurate estimate of the variance attributable to fluctuating asymmetry can be made. In addition, many early studies of asymmetry in poikilotherms used meristic characters (such as scale counts), and these types of characters are not easily studied in mammals. Mammals, because of their precise regulation of body temperature show little phenotypic effect of environmental variability, and thus may exhibit low absolute levels of asymmetry. Mammals may also be able to reduce the level of asymmetry during their prolonged intrauterine development and juvenile growth period. The literature is reviewed relative to relationships between genetic variation and asymmetry in mammals. Hypotheses are reviewed as they relate to the relationship between fluctuating asymmetry and heterozygosity observed in previous studies. Finally, recommendations are put forth regarding the design and interpretation of future research into the relationship between developmental homeostasis and genetic variability.
Histochemical studies on the activity of some neuropeptides (PGP, CT, NPY, SP and βE) and enzymes (AP, A1P, SDH and MAO) were performed on guinea pig parathyroid glands after injections of histamine, histamine receptor blockers and muscarinic receptor blocker. Under conditions of histamine shock, the immunoreactivity of CT and the reactivity of SDH and MAO were found to decrease together with an increase in the activity of βE and AP. The reactions for SP, NPY, PGP and A1P did not change in any of the groups.
The effect of sphingosine, sphingosylphosphorylcholine and sphingosine 1-phosphate on L-[U-14C]serine incorporation into phosphatidylserine and phosphatidylserine-derived phosphatidylethanolamine was investigated in intact glioma C6 cells. Sphingosine, sphingosylphosphorylcholine and sphingosine 1-phosphate are potent signalling molecules which, due to their physicochemical features, may function as amphiphilic compounds. It has been found that sphingosine and sphingosylphosphorylcholine (amphiphilic cations) significantly increase [14C]phosphatidylserine synthesis and decrease the amount of 14C-labeled phosphatidylethanolamine. Sphingosine 1-phosphate (an amphiphilic anion) was without effect on phosphatidylserine synthesis but, similarly as sphingosine and sphingosylphosphorylcholine, reduced the conversion of phosphatidylserine to phosphatidylethanolamine. These results strongly suggest that sphingosine, sphingosylphosphorylcholine and sphingosine 1-phosphate can modulate cellular phospholipid homeostasis by stimulation of phosphatidylserine synthesis and an interference with phosphatidylserine decarboxylase.
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