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Biomedical subjects

J Sevcík

Publications and source records attributed to J Sevcík.

At least 37 records · Page 2Linked to original sources

Is nitric oxide involved in 5-HT3 receptor-mediated neurogenic relaxation of guinea pig proximal colon?

The relaxations mediated by the activation of 5-HT receptors in the guinea pig proximal colon were investigated. Longitudinal strips were cut from the colon segment and placed into the bath. In the presence of atropine (0.2 microM), the relaxations were evoked by adding increasing concentrations of 5-HT (1-100 microM). Noncumulative concentration-response curves were established in the absence and presence of either 5-HT or nitric oxide synthase (NOS) antagonists. Selective 5-HT3 antagonists tropisetron (10 and 100 nM) and ondansetron (1 microM) inhibited the relaxations and shifted the concentration-response curves to the right. Similar effects were observed in the presence of the NOS inhibitor N(G)-nitro-L-arginine (3.2, 10, 32 microM) and partly reversed with L-arginine (100, 320 microM). N(G)-nitro-D-arginine, serving as a negative control, was ineffective. The relaxations were further inhibited in the presence of the soluble guanylate cyclase blocker methylene blue (10 microM) or NO scavenger hemoglobin (32 microM). These results suggest that the 5-HT3 receptor plays a role in neurogenic relaxations of guinea pig proximal colon, which are at least partly mediated via release of NO from nerve endings.

Animals↗

Crystallization and preliminary X-ray analysis of the Saccharomycopsis fibuligera glucoamylase expressed from the GLU1 gene in Escherichia coli.

The active non-glycosylated glucoamylase, overexpressed from the Saccharomycopsis fibuligera GLU1 gene in Escherichia coli BL21(DE3), has been purified from the solubilized inclusion bodies and then renatured in vitro. Crystals of the recombinant glucoamylase were obtained by vapour diffusion using PEG as precipitant. The crystals belong to the orthorhombic space group P2(1)2(1)2(1), with unit-cell dimensions of a = 58.1, b = 87.8 and c = 99.9 A, and diffract to 1.7 A resolution. This is the first report of the crystallization of the full-length glucoamylase corresponding to the mature enzyme.

Journal Article↗

Determination of purine nucleoside phosphorylase activity in human erythrocytes by capillary electrophoresis.

Purine nucleoside phosphorylase (EC 2.4.2.1) activity in human erythrocytes was measured using capillary electrophoresis. Enzyme samples were directly loaded into the capillary without preconcentration or purification. The electrophoretic separations were carried out in an uncoated fused-silica capillary (75 microm internal diameter, effective length of 45 cm, total 72 cm) at an electric field of 415 V/cm at ambient temperature (25 degrees C). UV detection at 200 nm was used. Borate buffer (100 mmol/l, pH 9.5) was used as background electrolyte. The results obtained by CE compared favourably (r=0.989) with those of standard HPLC methods. The method presented is reliable, slightly faster and less expensive than the routinely performed HPLC method.

Electrophoresis, Capillary↗

[Serotonin and treatment of mental disorders. Present status and future perspectives].

Serotoninergic system is involved in the regulation of diverse biological and psychological functions and a variety of serotonin receptor subtypes represent a possible target for a new generation of medications. 5-HT receptors play an important role in both schizophrenia and depression. Modern strategies for treating schizophrenia profit from the existence of interaction between serotonin and dopamine systems. New drugs called serotonin-dopamine antagonists (SDAs) offer wider spectra of activity and lower extrapyramidal side effects liability. The principle of the SDAs is that the drug should be a potent serotonin 5-HT 2A antagonist, with slightly less potent dopamine D2 receptor-blocking properties. New pharmacological agents with great therapeutic potential and fewer side effects were recently developed also for the treatment of depression. Among these new antidepressives the serotonin selective reuptake inhibitors (SSRIs) currently play the most important role.

Depressive Disorder↗

A rapid and simple screening method for detection of orotic aciduria by capillary zone electrophoresis.

A rapid and selective capillary zone electrophoretic method for screening of patients with orotic aciduria is described. The method is based on direct measurement of orotic acid in untreated urine. Total analysis time is 5 min with the limit of quantification of 10 mumol/l. Selectivity of the method is given by the use of a low pH of background electrolyte at which practically no interferences from native urine appeared, as well as by using a fast scanning detector which enables the identification of orotic acid via its characteristic UV spectra. This method can be used for quantitative assessment of orotic acid present in urine at physiological conditions after an ion exchange chromatography-clean up and preconcentration procedure. Urine samples containing orotic acid at pathological concentrations (typically more than 1 mol/mol creatinine) could be successfully analysed. The method described was applied to urine specimens collected from both healthy volunteers and patients with orotic acidurias of various origin.

Acidosis↗

Ca(2+)-activated K+ channel and the activation of Ca2+ influx in vanadate-treated red blood cells.

The mechanism by which K+ inhibits vanadate-induced 45Ca2+ influx by human red blood cells (RBC) was studied using several independent approaches. The following results were found: 1. The inhibitory effect of K+ was absent when RBC were loaded with a Ca(2+)-chelator. This treatment at the same time inhibited the vanadate-induced K+ efflux, and the membrane hyperpolarization induced by Ca2+ in vanadate-treated cells. 2. The potency of K+, Rb+, and Cs+ to inhibit vanadate-induced Ca2+ influx corresponded to their ability to depolarize the RBC membrane via the Ca(2+)-activated K+ channel (K(Ca)). 3. Inhibition of the vanadate-induced 45Ca2+ influx by a protonophore proceeded in parallel with the inhibition of the vanadate-plus-Ca(2+)-induced membrane hyperpolarization. 4. Valinomycin in part released the inhibition of the vanadate-induced Ca2+ influx by known K(Ca) inhibitors (quinine, oligomycin, 4-aminopyridine) but not by inhibitors of the Ca2+ channel (Cu2+, HS-reagents, organic Ca2+ channel blockers). 5. K+ did not inhibit the vanadate-induced Ca2+ influx in dog RBC which have K(Ca) but no transmembrane K+ gradient. The inhibition of the vanadate-induced Ca2+ influx by external K+ appears to be due to the elimination of the electrical component of the Ca(2+)-motive force imposed by opening of the K(Ca). This implies that the Ca2+ carrier mediating the influx of Ca2+ in the presence of vanadate is of uniport type, and that the activity of K(Ca) may serve as a supporting element for Ca2+ influx.

Aminoquinolines↗

Vanadate changes Ca2+ influx pathway properties in human red blood cells.

The properties of the basal Ca2+ influx (measured using cells labelled with 45Ca2+) in intact human red blood cells (RBC) were compared with those of 45Ca2+ influx induced by vanadate. The basal Ca2+ influx was not sensitive to inhibitors of vanadate-induced Ca2+ influx such as the HS-reagent p-chloromercuribenzoate and low concentrations of Cu2+, and also the sensitivity to nifedipine was significantly weaker. High K+ known to suppress vanadate-induced 45Ca2+ influx had no effect on the basal Ca2+ influx. Both processes were saturated with Ca2+ but the latter was saturated at higher Ca2+ concentrations (KM(Ca) 2.1 vs. 0.5 mmol/l). These experiments favour the notion that vanadate changes the properties of the inward-directed Ca(2+)-transport pathway in human RBC membrane. Vanadate-induced 45Ca2+ influx was insensitive to pertussis toxin and cholera toxin, and several non-steroidal antiinflammatory agents did not influence it in a consistent manner. Li+ partly inhibited the 45Ca2+ uptake. Vanadate stimulated the incorporation of 32P(in) into PIP2 in human but not in pig RBC which are known to be defective in the phosphoinositide metabolism and in the vanadate-induced 45Ca2+ uptake. These results suggest that the change in the Ca2+ influx pathway properties induced by vanadate may involve changes in the metabolism of phosphoinositides but not of the arachidonate metabolism nor G-protein activation.

Animals↗

Quantitative structure-chromatographic retention relationship study of six underivatized equine estrogens.

Underivatized estrone (ES), equilin (EQ), equilenin (EQN) and their corresponding 17 alpha-diols 17 alpha-estradiol (ESD), 17 alpha-dihydroequilin (DHEQ) and 17 alpha-dihydroequilenin (DHEQN) were separated by TLC, RP-HPLC and capillary GC. Their dipole moments (mu) and Randić's connectivity indices ((1)chi) were determined as parameters of importance for the separation. The number of H atoms was taken as an additive structural parameter of importance for the quantitative structure-chromatographic retention relationship study (QSRR). Principal component analysis (PCA) was applied in order to find similarities and dissimilarities between 9 TLC and 10 RP-HPLC systems. PCA indicated that proton donor-proton acceptor interactions play the most important role for the TLC and RP-HPLC separation. The two-dimensional non-linear map of PC variables showed that the keto-estrogens (ES, EQ and EQN) and the corresponding diols (ESD, DHEQ and DHEQN) form two separate clusters. The relationship between GC retention of equine estrogens characterized by Kováts indices (KI), their (1)chi and mu was expressed by the equation KI/100 = al(1)chi+ b/mu(2) + c. The biological activity of the estrogens was related to log 1/mu(2).

Animals↗

A fast and simple screening method for detection of 2,8-dihydroxyadenine urolithiasis by capillary zone electrophoresis.

2,8-Dihydroxyadenine urolithiasis is an inherited disorder caused by adenine phosphoribosyltransferase deficiency. A fast, simple, sensitive and selective capillary zone electrophoretic method for diagnosis of 2,8-dihydroxyadenine urolithiasis in adenine phosphoribosyltransferase deficiency is described. The method is based on direct measurement of 2,8-dihydroxyadenine in untreated urine in phosphate buffer at pH 3.0 within 8 min. Under the given separation conditions 2,8-dihydroxyadenine is very well separated from other purine and pyrimidine substances and presents characteristic UV spectra which enable identification in case of doubt. The urine samples containing pathological 2,8-dihydroxyadenine could be successfully analysed in levels approaching those relevant for bioanalytical applications. The reliability of the method presented for screening of patients with adenine phosphoribosyltransferase deficiency is demonstrated on a urine sample of a patient with the defect who was already treated with allopurinol at the time of obtaining the sample. No interfering substances were found in 50 urine samples from healthy infants under the analytical condition described.

Adenine↗

Further evidence on the interaction of muramyl dipeptide with the serotonergic system.

The mode of interaction between muramyl dipeptide (MDP), a compound with immunopharmacological activities, and 5-hydroxtryptamine (5-HT, serotonin) was studied in isolated nerve-smooth muscle preparations of the carp stomach. Application of exogenous 5-HT evoked direct smooth muscle contractions; electric neurogenic stimulation evoked twitches due to release of 5-HT from nerve endings. Contractions evoked by a high concentration of 5-HT (3-30 microM) were resistant to atropine and potentiated in the presence of MDP. Isamoltan (5-HTID antagonist) decreased the amplitude of contractions, whereas ketanserin (5-HT2 antagonist) and MDL 72,222 (5-HT3 antagonist) had no effect. The addition of low concentrations (0.1-1.5 microM) of 5-HT did not contract the preparation but caused a decrease in the amplitude of neurogenic twitches, which might be due to the presynaptic inhibition of serotonin release. This effect of 5-HT was not changed by isamoltan or ketanserin, but it was largely reduced in the presence of 5-HT3 antagonists tropisetron and MDL 72,222. This inhibitory effect of 5-HT on twitch amplitude was potentiated by MDP. The interaction of MDP with the serotonergic system thus involved not only potentiation of the postsynaptic effect of higher 5-HT concentrations, which might have been mediated via the 5-HT1 subsystem, but also presynaptic inhibition. MDP enhancement of 5-HT's inhibitory effect, mediated via 5-HT3 receptors, might represent a new feature in mutual 5-HT-MDP interactions.

Acetylmuramyl-Alanyl-Isoglutamine↗

Capillary electrophoretic enantioseparation of selegiline, methamphetamine and ephedrine using a neutral beta-cyclodextrin epichlorhydrin polymer.

This paper describes the development of a capillary zone electrophoretic method for chiral separation of three basic compounds of the selegiline synthetic pathway: ephedrine, methamphetamine and selegiline. The method developed allows one to separate the studied compounds in one run using a neutral beta-cyclodextrin epichlorhydrin polymer. The effect of various experimental parameters, such as chiral selector concentration, concentration and composition of background electrolyte, pH, temperature, and the addition of some organic solvents, on the resolution and migration time is discussed. For selegiline and methamphetamine, it is possible, under optimal conditions, to quantify less than 0.5% of the minor isomer in an excess of the major one.

Cyclodextrins↗

Which type of 5-hydroxytryptamine receptor mediates relaxation of the longitudinal muscle of guinea pig proximal colon in vitro?

Concentration-dependent 5-hydroxytryptamine (5-HT) relaxations of guinea pig proximal colon were evoked in the presence of atropine (0.2 microM). 5-HT effect was neuronally mediated since it was blocked by tetrodotoxin (TTX) (0.5 microM). The type of 5-HT receptor mediating the relaxations was investigated using both 5-HT agonists and antagonists. Selective 5-HT3 antagonists tropisetron (10, 50, 500 nM) and ondansetron (1 microM) shifted the concentration-response curves for 5-HT to the right. Another 5-HT3 antagonist MDL 72222 (0.5 microM), 5-HT1/5-HT2 antagonists methiothepin (0.1 microM) and metergoline (0.1 microM), 5-HT(1A,B) antagonist propranolol (l microM) and 5-HT1B antagonist isamoltane (10 nM) were ineffective. Specific agonist of 5-HT3 receptors 2-methyl-5-hydroxytryptamine (2-methyl-5-HT) and agonist of 5-HT1 receptors 5-carboxamidotryptamine (5-CT) also relaxed the preparation, although the relaxation was not 5-HT relaxation. Neither was it neurogenic because it persisted in the presence of TTX (0.5 microM). The concentration-response curve for 2-methyl-5-HT was not affected by ondansetron (1 microM) or tropisetron (0.5 microM), but it was shifted to the right in the presence of 5-HT1/5-HT2 receptor antagonists methiothepin (0.1 microM) and metergoline (0.1 microM) and in the presence of 5-HT(1Da)/5-HT2A receptor antagonist ketanserin (1 microM). Methiothepin (0.1 microM) also inhibited the relaxations evoked in the presence of 5-CT. Specific agonist of 5-HT4 receptors 5-methoxytryptamine did not exert any effect on the preparation. It is suggested that there are two different mechanisms of relaxation in the guinea pig proximal colon. One is neurogenic and involves the activation of 5-HT3 receptors located on inhibitory neurons to the muscle; the other is myogenic and might be mediated via yet unclassified 5-HT receptors located on the muscle.

Animals↗

The Ca(2+)-dependent activation by fluoride of human red cell membrane sodium permeability: evidence for a chemically activated tetrodotoxin-sensitive Na+ channel.

Fluoride (NaF) (5-15 mM) activated the 22Na+ uptake by human red blood cells (RBC). The effect was Ca(2+)-dependent. Sr2+, but not Ba2+, Mg2+, Mn2+, substituted Ca2+ in supporting the 22Na+ uptake. The NaF-induced 22Na+ uptake was sensitive to tetrodotoxin (TTX), pertussis toxin but not to amiloride nor valinomycin. The value of the influx was 8.6 +/- 5.0 mmol/l cells. Thus, the TTX-sensitive Na(+)-transport system is present in the RBC membrane in an inactive form which could be activated with NaF by a mechanism involving G-protein(s) but not the depolarization.

Calcium↗

Vanadate and fluoride activate red cell Na+ permeability by different mechanism.

Fluoride and vanadate are known to induce the Ca(2+)-dependent K+ efflux. We found that both agents concomitantly induced the Ca(2+)-dependent 22Na+ influx. The extent of the Ca(2+)-dependent 22Na+ influx induced by vanadate was very small in human red blood cells but clearly visible in guinea-pig red blood cells. The effect of fluoride has been studied in human red blood cells only. The 22Na+ influx induced by vanadate was inhibited by amiloride but was resistant to tetrodotoxin, whereas that induced by fluoride was resistant to amiloride but sensitive to tetrodotoxin. The effects of inhibitors indicate that vanadate activates the Na/H antiporter and that fluoride opens a tetrodotoxin-sensitive Na+ channel in red blood cells in the Ca(2+)-dependent manner. The results also indicate that both agents activate the Ca(2+)-dependent Na+ permeabilities by unknown auxiliary mechanisms.

Amiloride↗

[Total serum cholesterol in children 8-15 years of age].

The authors evaluated the difference in the health status of two groups of boys and girls aged 8-15 years, a total of 1037 children. The larger group, 790 children is from Teplice and the other group, a total of 347 children from Roudnice nad Labem. The authors discuss the total serum cholesterol level in the two groups. They provide information on mean serum cholesterol levels in children of comparable age and the significance of differences in relation to age and sex. The assembled values made it possible to calculate percentile values at the 90th and 95th percentile level for children of both areas and thus to examine and evaluate larger groups of children incl. their relatives and to detect critical total cholesterol levels calling for treatment and intervention.

Adolescent↗