Studies have shown that uridine concentration in plasma may be an indicator of uric acid production in patients with gout. It has been also postulated that uridine takes part in blood pressure regulation. Since physical exercise is an effective tool in treatment and prevention of cardio-vascular diseases that are often accompanied by hyperuricemia and hypertension, it seemed advisable to attempt to evaluate the relationship between oxypurine concentrations (Hyp, Xan and UA) and that of Urd and BP after physical exercise in healthy subjects. Sixty healthy men (17.2±1.71 years, BMI 23.2±2.31 kg m-2, VO2max 54.7±6.48 ml kg-1 min-1) took part in the study. The subjects performed a single maximal physical exercise on a bicycle ergometer. Blood for analyses was sampled three times: immediately before exercise, immediately after exercise, and in the 30th min of rest. Concentrations of uridine and hypoxanthine, xanthine and uric acid were determined in whole blood using high-performance liquid chromatography. We have shown in this study that the maximal exercise-induced increase of uridine concentration correlates with the post-exercise increase of uric acid concentration and systolic blood pressure. The results of our study show a relationship between uridine concentration in blood and uric acid concentration and blood pressure. We have been the first to demonstrate that a maximal exercise-induced increase in uridine concentration is correlated with the post-exercise and recovery-continued increase of uric acid concentration in healthy subjects. Thus, it appears that uridine may be an indicator of post-exercise hyperuricemia and blood pressure., W. Dudzinska, A. Lubkowska, B. Dolegowska, M. Suska, M. Janiak., and Obsahuje bibliografii
The presence of large amounts of proteins in mammal urine is usually associated with a pathological condition and indicates serious renal lesions. However, there are few species with obligate proteinuria indicating that they must derive some benefit from this condition. Urinary proteins have been most extensively studied in the house mouse and the rat, and findings to date indicate that their function in intraspecific communication is complex and not yet fully understood. Other proteins of the same protein family as MUPs have been also found in urine of some other rodent species, and still less is known about these. In this study we demonstrate the existence of urinary lipocalins in Mastomys coucha for the first time. Our results support the hypothesis that urinary proteins may play an important role in chemical communication, and level of polymorphism of these proteins in different rodents may help us to understand their specific function.
The hyperinsulinemic euglycemic clamp (HEC) combined with indirect calorimetry (IC) is used for estimation of insulin-stimulated substrate utilization. Calculations are based on urinary urea nitrogen excretion (UE), which is influenced by correct urine collection. The aims of our study were to improve the timing of urine collection during the clamp and to test the effect of insulin on UE in patients with type 1 diabetes (DM1; n=11) and healthy subjects (C; n=11). Urine samples were collected (a) over 24 h divided into 3-h periods and (b) before and during two-step clamp (1 and 10 mIU.kg-1.min-1; period 1 and period 2) combined with IC. The UE during the clamp was corrected for changes in urea pool size (UEc). There were no significant differences in 24-h UE between C and DM1 and no circadian variation in UE in either group. During the clamp, serum urea decreased significantly in both groups (p<0.01). Therefore, UEc was significantly lower as compared to UE not adjusted for changes in urea pool size both in C (p<0.001) and DM1 (p<0.001). While UE did not change during the clamp, UEc decreased significantly in both groups (p<0.01). UEc during the clamp was significantly higher in DM1 compared to C both in period 1 (p<0.05) and period 2 (p<0.01). The UE over 24 h and UEc during the clamp were statistically different in both C and DM1. We conclude that urine collection performed during the clamp with UE adjusted for changes in urea pool size is the most suitable technique for measuring substrate utilization during the clamp both in DM1 and C. Urine collections during the clamp cannot be replaced either by 24-h sampling (periods I-VII) or by a single 24-h urine collection. Attenuated insulin-induced decrease in UEc in DM1 implicates the impaired insulin effect on proteolysis. and Obsahuje bibliografii a bibliografické odkazy
In this study, a loop-mediated isothermal amplification (LAMP) assay was established to detect Toxoplasma gondii DNA in mice infected with T. gondii PRU strain. This LAMP assay was based on the sequence of highly repetitive B1 gene. The detection limit of T. gondii LAMP assay was 1 pg of T. gondii DNA, which was evaluated using 10-fold serially diluted DNA of cultured parasites. The LAMP assay was also highly specific for T. gondii and able to detect T. gondii DNA in urine of mice treated with dexamethasone at 90 day post infection (p.i.), although this assay could not detect the DNA in mice urine 2-6 days p.i. These results demonstrated that LAMP is effective for evaluation of therapy effectiveness for T. gondii infection. The established LAMP assay may represent a useful and practical tool for the routine diagnosis and therapeutic evaluation of human toxoplasmosis.
Endogenous regulators, such as angiotensin-II (AngII), endothelin-1 (ET-1) and urotensin-II (U-II) are released from various cell types and their plasma levels are elevated in several cardiovascular diseases. The present study evaluated a potential crosstalk between these systems by investigating if the myocardial effects of U-II are modulated by AngII or ET-1. Effects of U-II (10-8 , 10 -7 , 10 -6 M) were tested in rabbit papillary muscles in the absence and in the presence of losartan (selective AT1 receptor antagonist), PD-145065 ( nonselective ET-1 receptors antagonist), losartan plus PD-145065, AngII or ET-1. U-II promoted concentration-dependent negative inotropic and lusitropic effects that were abolished in all experimental conditions. Also, U-II increased resting muscle length up to 1.008±0.002 L/Lmax. Correcting it to its initial value resulted in a 19.5±3.5 % decrease of resting tension, indicating increased muscle distensibility. This effect on muscle length was completely abolished in the presence of losartan and significantly attenuated by PD-145065 or losartan plus PD-145065. This effect was increased in the presence of AngII, resulting in a 27.5±3.9 % decrease of resting tension, but was unaffected by the presence of ET-1. This study demonstrated an interaction of the U-II system with the AngII and ET-1 systems in terms of regulation of systolic and diastolic function., A. P. Fontes-Sousa ... [et al.]., and Obsahuje seznam literatury
Erythropoietic protoporphyria (EPP) is an inherited disorder of heme biosynthesis caused by partial ferrochelatase deficiency, resulting in protoporphyrin overproduction which is responsible for painful skin photosensitivity. Chronic liver disease is the most severe complication of EPP, requiring liver transplantation in some patients. Data from a
mouse model suggest that cytotoxic bile formation with high concentrations of bile salts and protoporphyrin may cause biliary fibrosis by damaging bile duct epithelium. In humans, cholestasis is a result of intracellular and canalicular precipitation of protoporphyrin. To limit liver damage two strategies may be considered: the first is to reduce protoporphyrin production and the second is to enhance protoporphyrin excretion. Bile salts are known to increase protoporphyrin excretion via the bile, while heme arginate is used to decrease the production of porphyrins in acute attacks of hepatic porphyrias. The Griseofulvin-induced protoporphyria mouse model has been used to study several aspects of human protoporphyria including the effects of bile salts. However,
the best EPP animal model is an ethylnitrosourea-induced point mutation with fully recessive transmission, named ferrochelatase deficiency (Fech
m1Pas). Here we investigate the effect of early ursodesoxycholic acid (UDCA) administration and heme-arginate injections on the ferrochelatase deficient EPP mouse model. In this model UDCA administration and heme-arginate injections do not improve the protoporphyric condition of
Fechm1Pas/Fechm1Pas mice.
Urychlovače slouží k získávání intenzivních svazků iontů nebo částic s vysokou rychlostí a energií. Kinetické energie dodávané současnými urychlovači jsou v rozsahu od několika stovek keV do několika TeV (1 eV = 1.6 x 10(19) J). V makrosvětě tyto energie nikoho neohromí, ale v mikrosvětě je vše jinak: rychlost protonu s kinetickou energií 200 keV činí 2 % rychlosti světla, u elektronu se stejnou kinetickou eneregií je to dokonce 70 %. Ve světě vysokých energií se slovo urychlovač stává trochu nesmyslným, neboť rychlost částic už skoro neroste (blíží se rychlosti světla), ale roste jejich energie a tudíž i relativistická hmotnost., Zdeněk Doležal., and Obsahuje bibliografii
Using ^^C02, ^^02 and H2O gas exchange as weU as metabolite analysis, net CO2 uptake (P]4) and transpiration rate (£) were measured in the water-stressed plants of Digitalis lanata EHRH. The leaf conductance (gcch). the gross CO2 uptake (Pq), Úie photorespiration (Rp) and reassíinilation (RA) rates were calculated from measuied parameters. The pulse modulated fluorescence was measured duiing the steady statě photosynthesis. After withholding iirigation, the leaf water potential decreased to -2.S MPa, but leaves remained turgid and fully exposed to iiradiance even at a severe water stress. Due to the stress-induced reduction of gcch. and E were drastically reduced, whereas Pq and Rp were less affected. Water use efficiency (WUE), which was higher in 1 000 than 350 cm3(C02) increased as the water stress developed. The stomatal closure induced an increase in the reassimilation (RA) of internally liberated CO2 (Rp). The increased CO2 recycling in relation to the water stress was high in 350 cm^(C02) m-^ and still substantial in 1 000 cm3(C02) and consumed a substantial amount of radiant energy in the form of ATP and reduction equivalents. Consequently, the metabolic demand for radiant energy was reduced by less than 40 %, whereas was diminished by more than 70 % in severely stressed plants at 350 cm3(C02) m*3. Additionally, the quantum efiBciency of photosystem 2 as a measure for the flux of photosynthetically generated electrons was reduced upon the stress. This (and possibly other mechanisms) enabled the stressed plants to avoid overreduction of the photosynthetic electron transport chain.