The study investigated the effects of different CaCl2 concentrations (2, 5, and 10 mM) on photosynthetic enzymatic activities, photosynthesis, and chlorophyll fluorescence of tung tree seedlings under drought conditions. Plants were sprayed with either CaCl2 or distilled water until run-off. Irrigation was then withheld to induce drought stress. The strength of drought stress was evaluated by relative leaf water content and soil water content, which was 27.3 and 9.5% on day 0 and day 12, respectively. Drought stress decreased activities of ribulose-1,5-bisphosphate carboxylase/oxygenase and phosphoenolpyruvate carboxylase, chlorophyll (a+b) content, net photosynthetic rate, stomatal conductance, transpiration rate, electron transport rate, the maximal quantum yield of PSII photochemistry, and effective quantum yield of PSII in tung tree seedlings. The CaCl2 pretreatments alleviated the negative effect of drought stress to some degree on all the parameters mentioned above., Z. Li, X. F. Tan, K. Lu, Z. M. Liu, L. L. Wu., and Obsahuje bibliografii
The increase of radical forms of mitochondrial respiratory chain compounds (MRCC) is an indicator of an increased risk of the formation of oxygen radicals. Using electron paramagnetic resonance (EPR), we found an increase of signals corresponding to ubisemichinone radical (·QH) and ironsulfur proteins radical forms (·FeS) of these respiratory chain compounds during ischemia in the isolated perfused rat heart (·QH increased from 1.51 to 3.08, ·FeS1 from 1.14 to 2.65 arbitrary units). During the 5-min reperfusion, the signals returned to normoxic levels. In isolated mitochondria exposed to anoxia and reoxygenation the radical forms of ·QH and ·FeS2 changed in a similar manner as in the intact heart. A combination of in vivo captopril treatment and in vitro L-arginine administration significantly decreased the levels of MRCC radicals in the isolated myocardium (·QH from 2.61 to 1.72 and ·FeS1 from 1.82 to 0.46 under normoxia; ·QH from 4.35 to 2.66 and ·FeS1 from 1.93 to 1.35 during ischemia). This decrease in MRCC radical forms was associated with increased NO levels in the perfusate, determined as NO2-/ NO3-, as well as tissue NO levels determined using EPR as the dinitrosyl iron complex (DNIC). These results provide new information about the cardioprotective effects of ACE inhibitors and L-arginine., H. Vavřínková, M. Tutterová, P. Stopka, J. Divišová, L. Kazdová, Z. Drahota., and Obsahuje bibliografii
The aim of this paper is to investigate the influence of COM (Cellular Organic Matter) produced by Microcystis aeruginosa on the process of water purification by destabilisation and subsequent aggregation of the impurity particles. The research was carried out with a raw water into which COM was added. The removal efficiency of the most significant components of COM, i.e. polysaccharides and proteins, was investigated. It was found that the removal efficiency of polysaccharides and proteins was dependent on the reaction conditions (pH, type of destabilisation reagent and its dosage). The removal efficiency of COM was relatively low. It was about 46% and 41% using ferric sulphate and aluminium sulphate aggregation, respectively. In comparison to the other organic components of COM, mainly polysaccharides, the proteins are removed with a higher efficiency. The GPC analyses of the residual COM showed that the proteins of higher molecular weight were aggregated with a higher efficiency. and Cílem práce je opis vlivu buněčných organických látek (COM) produkovaných sinicí Microcystis aeruginosa na proces úpravy vody pomocí destabilizace a následné agregace znečišťujících příměsí. Výzkum byl uskutečňován se syntetickou surovou vodou, do které byly přidány COM získané laboratorní kultivací M. aeruginosa. V průběhu laboratorních testů byla sledována především účinnost odstranění dvou základních složek COM, tj. polysacharidů a proteinů. Bylo zjištěno, že tato účinnost závisí především na reakčních podmínkách (typu a dávce destabilizačního činidla a pH). Účinnost odstranění COM byla poměrně nízká, maximální dosažená účinnost byla 46% při destabilizaci pomocí síranu železitého a 41% při použití síranu hlinitého. Bylo zjištěno, že s vyšší účinností jsou odstraňovány proteiny, obzvláště pak proteiny s vyšší molekulovou hmotností.
Chemical modification of purifíed phosphoenolpyravate carboxylase (PEPC) from the crassulacean acid metabolism plant Crassula argentea Thunb. with the histidyl reagent diethylpyrocarbonate (DEPC) resulted in a transient increase in activity followed by a decrease of activity with time. This biphasic response was observed when the modifíed enzyme was assayed at both low (sub-K,^ and saturating substráte (phosphoenolpyruvate, PEP) concentrations. There was an approximate 25- fold difference in the apparent rate constants for the activation and inhibition phases. This is in contrast to what we háve observed under similar conditions for the C4 enzyme from Zea mays L. for which only inhibition of activity occurs. Spectral studies indicated that up to 7 of the potential 20 histidine residues per subunit were modifíed, at least 3 of which were necessary for activity. The biphasic response of the Crassula enzyme was dependent on the concentration of DEPC. Progressively less inactivation was observed when modifying the enzyme with lower concentrations of DEPC. Chemical modification of PEPC with 75 pM DEPC resulted in a form of the enzyme with a lower K^, and higher This was concomitant with the modification of 4 histidines per subímit. Changes in the response of the enzyme to allosteric effectors were also observed; with modification the enzyme was desensitized to malate inhibition and glucose-6-phosphate activation. The Kj of the modifíed enzyme for malate increased over 15-fold. This was consistent with fluorescence binding studies using the extrinsic conformationalprobe S-anilino-l-naphthalenesulfonate which indicated the elimination of binding of malate and increased binding of the substráte to PEPC. Protection studies showed that malate desensitization was delayed by the presence of malate during modification. Malate also slowed the initial rate of histidine modifícation as measured spectrophotometrically. Thus histidine plays a role in the malate site of Crassula PEPC.
Alcohol use has been identified as a risk factor for the development of osteoporosis. Eight male Wistar rats at two months of age were alcoho-fed (7.6 g 95 % ethanol/kg b.w. per day) to evaluate the effects of long-term administration (three months) of alcohol in drinking water. We have used a dose which is considered to be comparable to a dose of 1 liter of wine or 2.5 liters of 12° beer used in male adults daily. The bones were tested mechanically by a three-point bending test in a Mini Bionix (MTS) testing system. The bones from alcohol-fed rats were characterized by a reduction in bone density as well as in ash, calcium and phosphate content. In alcohol-fed rats the reduction in bone mineral density (10 %) was reflected by about 12 % reduction of mechanical strength of femur (158±5.5 vs. 178±3.2 N/mm2). Alcohol significantly altered femoral cortical thickness. In our experiment alcohol itself did not exert any antiandrogenic effect and it did not produce changes in the weight of seminal vesicles. Liver function test (GGT, ALP, AST) did not differ between alcohol-fed rats and control rats. Alcohol-induced bone loss is associated with increased bone resorption and decreased bone formation. These results document the efficacy of alcohol at the dose of 7.6 g 95 % ethanol/kg b.w. to cause bone loss and loss of bone mechanical strength in intact rats. The results of the present study may be interpreted as supporting the hypothesis of alcohol as a risk factor for osteoporosis., P. D. Broulík ... [et al.]., and Obsahuje bibliografii a bibliografické odkazy
The study has been designed to characterize protein systems involved in the responses of rat hearts to chronic doxorubicin (DOX) treatment. We investigated the influence of DOX on cardiac function, mitogen-activated protein kinases (MAPKs) and heat stress proteins (HSPs). Doxorubicin was administered to rats by intraperitoneal injections over a period of 6 weeks. In control and DOX-treated hearts exposed to 20 min global ischemia and 40 min reperfusion the recovery of contractile function after ischemia/reperfusion (I/R) was determined. The levels and phosphorylation state of proteins in tissue samples were analyzed using specific antibodies. We found an activation of extracellular signal-regulated kinases (ERKs) in rat hearts exposed to DOX treatment and better recovery of contractile function after I/R. Analysis of HSPs showed that DOX induced up-regulation of the levels of HSP60 and down-regulation of HSP70 levels. The levels and/or specific phosphorylation of other studied proteins (p38-MAPK, HSP27, HSP90) were not in fluenced by DOX. The results point to the possible role of ERKs and some HSPs in mechanisms underlying the response of rat hearts to chronic DOX treatment., P. Šimončíková, T. Ravingerová, M. Barančík., and Obsahuje bibliografii a bibliografické odkazy
The circadian rhythms of many behavioral and physiological functions are regulated by the major circadian pacemaker in the suprachiasmatic nucleus. Long-term opiate addiction and drug withdrawal may affect circad ian rhythmicity of various hormones or the sleep/activity pattern of many experimental subjects; however, limited research has been done on the long -term effects of sustained opiate administration on the intrinsic rhythmicity in the suprachiasmatic nucleus and pineal gland. Here we compared the effects of repeated daily treatment of rats with morphine or methadone and subsequent naloxone-precipitated withdrawal on the expression of the Per1, Per2, and Avp mRNAs in the suprachiasmatic nucleus and on arylalky lamine N-acetyltransferase activity in the pineal gland. We revealed that 10-day administration and withdrawal of both these drugs failed to affect clock genes and Avp expression in the SCN. Our results indicate that opioid-induced changes in behavioral a nd physiological rhythms originate in brain structures downstream of the suprachiasmatic nucleus regulatory output pathway. Furthermore, we observed that acute withdrawal from methadone markedly extended the period of high night AA -NAT activity in the pine al gland. This suggests that withdrawal from methadone, a widely used drug for the treatment of opioid dependence, may have stronger impact on melatonin synthesis than withdrawal from morphine., D. Pačesová, J. Novotný, Z. Bendová., and Obsahuje bibliografii
To find the effects of CO2 enrichment on plant development and photosynthetic capacity of nodulated (line A62-1) and non-nodulated (line A62-2) isogenic lines of soybean (Glycine max Merr.), we examined the interactions among two CO2 treatments (36±3 Pa = AC and 70±5 Pa = EC), and two nitrogen concentrations [0 g(N) m-2(land area) = 0N; 30 g(N) m-2(land area) = 30N]. Nodules were found in both CO2 treatments in 0N of A62-1 where the number and dry mass of nodules increased from AC to EC. While the allocation of dry mass to root and shoot and the amount of N in each organ did not differ between the growth CO2 concentrations, there was larger N allocation to roots in 0N than in 30N for A62-2. The CO2-dependence of net photosynthetic rate
(PN) for A62-1 was unaffected by both CO2 and N treatments. In contrast, the CO2-dependence of PN was lower in 0N than in 30N for A62-2, but it was independent of CO2 treatment. PN per unit N content was unaffected by CO2 concentrations. The leaf area of both soybean lines grown in 30N increased in EC. But in 0N, only the nodulated A62-1 showed an increase in leaf area in EC. Nitrogen use efficiency of plants, NUE [(total dry mass of the plant)/(amount of N accumulated in the plant)] in 30N was unaffected by CO2 treatments. In 0N, NUE in EC was lower than in AC in A62-1, and was higher than that at AC in A62-2. Hence, the larger amount and/or rate of N fixation with the increase of the sink-size of symbiotic microorganisms supplied adequate N to the plant under EC. In EC, N deficiency caused the down-regulation of the soybean plant. and T. Nakamura ... [et al.].
The treatment of hypercholesterolemia with bile acid (BA)
sequestrants results in upregulation of BA synthesis through the
classical pathway initiated by cholesterol 7α-hydroxylase (CYP7A1). To characterize the detailed dynamics of serum lipid and BA concentrations and the BA synthesis rate in response to treatment with BA sequestrants and to determine whether the -203A/C promoter polymorphism of the CYP7A1 encoding gene (CYP7A1) affects such a response, this pilot study was carried out in healthy men (8
h omozygous for the -203A allele and 8 homozygous for the -203C allele of CYP7A1). The subjects were treated for 28 days with colesevelam
and blood was drawn for analysis before and on days 1, 3, 7, 14 and 28 of treatment. The response of lipids, BA, fibroblast growth factor-19 (FGF19) and 7α-hydroxy-4-cholesten-3-one (C4) to colesevelam did not differ between carriers of -203A and -203C alleles; their data were then aggregated for further analysis. Colesevelam treatment caused immediate suppression of FGF19 concentration and a fivefold increase in CYP7A1 activity, as assessed from C4 concentration, followed by a 17% decrease in LDL-cholesterol. Although total plasma BA concentrations were not affected, the ratio of cholic acid/total BA rose from 0.25±0.10 to 0.44±0.16 during treatment at the expense of decreases in chenodeoxycholic and deoxycholic acid.
Glucose tolerance, insulin secretion and in vitro insulin action were examined in streptozotocin-induced diabetic rats following pancreatic islet allotransplantation treated with combination of oral cyclosporine A (10 mg/kg) and hydrocortisone (1.5 mg/kg) intramuscularly. 1400 pure islets from multiple donors were implanted either into the portal vein (n = 10) or under the renal capsule (n=ll). Ten sham-operated non-diabetic animals receiving the same immunosuppressive therapy, 8 healthy animals without any treatment and 10 diabetic animals without immunosuppression following islet transplantation were used as controls. In all transplanted animals blood glucose was normalized by day 3 after transplantation with lower levels in those transplanted intraportally (p<0.05). Non-immunosuppressed animals rejected the graft after 6.5±1.2 days after transplantation, lmmunosuppressed animals in both groups remained normoglycaemic till the end of the experiment on day 28. Oral glucose tolerance tests and insulin levels on days 10 and 28 improved dramatically. No differences in glucose and insulin levels between intraportal and subcapsular groups were found. Post-load glucose levels in immunosuppressed non-transplanted animals were higher on day 28 than before treatment and were also higher than in the healthy non-treated group (p<0.05). In vitro insulin action determined by the incorporation of labelled glucose into adipose tissue was impaired only in animals in which islets were transplanted into the liver (p<0.05 vs other groups). In conclusion, therapy with cyclosporine A and hydrocortisone prevents allogeneic islet rejection in rats during a short-term experiment. Although glucose tolerance is not completely normalized following transplantation, slight impairment is also demonstrable in healthy animals on the same drug therapy.