Fleas of the Moiynkum Desert and their epizootic significance

The species composition of fleas in the Moiynkum Desert (Chu-Talas interfluve) and indices of their domination on different hosts was established on the basis of long-term observations (1973–2000). The most significant and prolonged changes in the population density of mass flea species (Xenopsylla gerbilli minax and Coptopsylla lamellifer, parasites of the great gerbil) occur in association with changes of the population density of rodents. Changes in the population density of rodents are usually observed year after similar changes in the population density of hosts. The leading role in the transmission of the plague vector belongs to the flea X. gerbilli minax.     

A Ca2+-Binding Protein that Regulates the Lifetime of the Transducin Active State

Biophysics - Abstract—It has been previously shown in the study of the kinetic behavior of cGMP-specific phosphodiesterase in preparations of the outer segments of bovine retinal rods, which...     

Taxonomic Status of the Okhotsk Lumpsucker Eumicrotremus ochotonensis (Cyclopteridae,Cottoidei) with Redescription of E. derjugini

Journal of Ichthyology - The species status is justified for the Okhotsk lumpsucker Eumicrotremus ochotonensis based on the morphological characters. The differences from the closely related...     

Inter- and Intra-Species Relationships of Greenland Halibut Reinhardtius hippoglossoides (Pleuronectidae) Based on the Analysis of Nuclear and Mitochondrial Genetic Markers

Journal of Ichthyology - Samples of Greenland halibut Reinhardtius hippoglossoides (Jordan and Snyder, 1901) from the Atlantic, Arctic, and Pacific Oceans were compared using eight microsatellite...     

Actin depolymerizing factor stabilizes an existing state of F-actin and can change the tilt of F-actin subunits

Proteins in the actin depolymerizing factor (ADF)/cofilin family are essential for rapid F-actin turnover, and most depolymerize actin in a pH-dependent manner. Complexes of human and plant ADF with F-actin at different pH were examined using electron microscopy and a novel method of image analysis for helical filaments. Although ADF changes the mean twist of actin, we show that it does this by stabilizing a preexisting F-actin angular conformation. In addition, ADF induces a large ( approximately 12 degrees ) tilt of actin subunits at high pH where filaments are readily disrupted. A second ADF molecule binds to a site on the opposite side of F-actin from that of the previously described ADF binding site, and this second site is only largely occupied at high pH. All of these states display a high degree of cooperativity that appears to be an integral part of F-actin.     

A noninvasive approach to studying fetal cells for prenatal diagnosis of chromosomal aneuploidies

Fetal cells isolated from maternal peripheral blood during the second trimester of pregnancy were analyzed. Blood samples were centrifuged in a Ficoll-Paque gradient, the mononuclear cell fraction was isolated and stained with fluorescent monoclonal antibodies against glycophorine A (GPA + PE), transferrin (CD71 + FITC), and Hoechst 33342. Fluorescence-activated cell sorting (FACS) was conducted on a Vantage flow cytofluorimeter (Becton Dickinson). Fluorescence in situ hybridization (FISH) with Y chromosome-specific DNA probe revealed fetal cells that exhibited Y signal in all 20 blood samples obtained from women pregnant with healthy male fetuses. The concentration of these fetal cells averaged about 1.34% and ranged from 0.1 to 4.2% in different blood samples. In six cases, blood samples were obtained from pregnant women, in which prenatal cytogenetic analysis revealed various fetal aneuploidies. Using FISH with DNA probes specific for chromosomes X, 18, and 13/21, Fetal cells with chromosomal aberrations were detected in these six maternal blood samples at a concentration from 1.5 to 5.6% (on average 3.7%). These results indicate the possibility of a new noninvasive approach, which is safe for both mother and fetus when used for isolation of fetal cells from pregnant women's blood samples and prenatal diagnosis of a broad spectrum of fetal cell chromosomal aberrations.     

The neurochemical mechanisms of the formation and consolidation of haloperidol-induced catalepsy

In rat brain cortex, haloperidol initiates the long-term potentiation of K(+)-induced Ca(2+)-dependent noradrenaline (NA) and dopamine (DA) secretion in vitro and in vivo. In both cases, the long-term potentiation is caused by the long-term increase in catecholamine content in the NA and DA terminals, as it has been shown in cortical tangential slices. Acute intraperitoneal haloperidol injection (2.5 mg/kg) evokes catalepsy and increases the content of NA and DA in the brain structures with localization of catecholamine receptors on terminals. This increase appears to be caused, predominantly, by modification of the terminal DA receptors, since only a trend to catecholamine increase is observed in the brain structures with a mixed type of NA and DA receptor localization (on somata and terminals). It is suggested that the long-term and diffuse action of haloperidol after its acute administration consists in the anxiogenic reaction and consolidation of catalepsy without an additional procedure of training and in the absence of unconditioned stimulus.     

Effect of L-lysine-alpha-oxidase on skin carcinoma induced by methylcholanthrene in mice]

Effect of enzyme L-lisyne-a-oxidase in complex with gel (Sakap) on carcinoma of the skin of mice induced by methylcholantrene was studied. Gel application once daily during 3 weeks decreased carcinoma dimensions on 40 per cent.     

Role of NO-synthase in stimulation of opiate receptors and kidney oxidative stress resistance

It was established that dalarginum injection before ARI (acute renal insufficiency) formation prevented an increases of proteolysis, decrease of SOD (superoxide dismutase), increase of NO2-/NO3- content in kidney tissue. Antioxidant effect of opiate receptor agonist was completely abolished by preliminary injection of OR antagonist--naloxone. Aminoguanidine nitrate (inducible NO-synthase inhibitor) injection removed positive effect of OR stimulation too. Thus OR stimulation increases kidney oxidative stress resistance due to NO-synthase and SOD activation.