Publications by authors named "Ia F Zverev"

Histochrome is the medicinal form of echinochrome (2,3,5,6,8-pentahydroxy-7-ethyl-1,4-naphthoquinone). The drug pharmacodynamics and its relationship with metabolism, which was revealed in previous investigations, predetermined the aim of this work: to study excretion of echinochrome and its possible metabolites in urine of rats. Histochrome was introduced to Wistar rats (n = 10) subcutaneously in a dose of 10 mg/kg.

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Experiments performed on 23 male rats, were divided into 2 groups. Animals in the control received group 1% solution of ethylene glycol (EG) as a drink during 6 weeks. In the test group, EG was also introduced for 6 weeks, and meloxicam was administered in a dose of 2.

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We studied effects of water regimens on crystallization efficacy in experimental nephrolithiasis on 3 groups of Wistar male rats with initial experimental nephrolithiasis (ethylene glycol model). The animals were on free, limited and supernormal liquid intake regimen. For 3 weeks each 3-4 days we estimated 24-h diuresis, urine concentration of calcium, phosphate and oxalate ions.

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The authors propose a technique for the determination of urinary oxalate ions by high performance liquid chromatography, which may be used for clinical and scientific purposes.

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Long-term administration of furosemide in rats (single daily dose, 20 mg/kg for 7 days) was accompanied by a decrease in the diuretic, natriuretic, and kaliuretic effects, which was related to a decrease in the rate of renal metabolism and excretion. It was found that more than 85% of the daily excretion of sodium takes place within the first 6 h after furosemide administration (on the background of comparable excretion of the drug), while the elimination of potassium and water during one day is more uniform. It is established that the long-term administration of furosemide leads to a decrease in the drug excretion during the first 6-h period, followed by a growth in the subsequent 18-h period of time.

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The effect of leaf decoctions of three plants of the Pyrolaceae family, namely, umbrella wintergreen, one-side ortilia, and round-leaf Pyrola was studied in rat experiments. All plants under study were found to contain approximately equal amounts of tannins and arbutin glycoside. Their concentration was comparable though rather lower than in common bearberry, a well-known plant with diuretic and antiseptic activity.

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The mechanism of the diuretic effect of the new drug polyosm, polyethylene oxide 400 solution, was studied in experiments on anesthetized cats. Intravenous polyosm infusion was attended with a marked diuretic and natriuretic effect developing due to reduced reabsorption of water and natrium and increased glomerular filtration.

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The calcium antagonists verapamil and nifedipine were shown to attenuate the development of carrageenin-induced rat paw inflammatory edema. Oral nifedipine exerted more pronounced antiedematous dose-dependent effects.

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Dichlothiazide and butadione were shown to attenuate equally the development of the rat paw inflammatory edema induced by subplantar dextran administration. Ethacrynic acid produced more pronounced antiedematous effect. Also, ethacrynic acid reduced to the highest degree the damp and dry mass of the inflammatory granuloma.

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It is shown that ethacrynic acid and dichlothiazide in 50 mg/kg dose reduce the dextran-induced increase of rat skin vascular permeability. Besides, durable administration of furosemide, dichlothiazide and ethacrynic acid in 50-80 mg/kg doses decreases the dry mass of inflammatory granuloma. This fact shows the ability of diuretics to suppress the development of proliferative inflammation.

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Experiments on rats have shown that administration of furosemide, dichlothiazide and etacrinic acid (50 mg/kg intraperitoneally) reduced the development of experimental inflammatory edema caused by subplantar administration of 0.1 ml of 6% dextran or 10% ovalbumin. The antiedematous effect of the diuretics was preserved under the conditions of bilateral nephrectomy, which points to the presence of extrarenal mechanisms in the action of the drugs in experimental inflammation.

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Following a protracted introduction of dichlothiazide to rats (20 mg/kg) and to dogs (5 mg/kg) there occurs a marked increase in the tubular secretion of the cardiotrast and passage of urates with urine. A single and long-term administration of the drug to dogs did not have any substantial effect on the maximal reabsorption of glucose.

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The influence of furosemide on the maximal glucose reabsorption, cardiotrast secretion and urate excretion was studied in chronic experiment. Single injection of furosemide increased the maximal glucose reabsorption in dogs. Thesere was no alteration in the secretory cardiotrast transport in response to the drug administration.

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Interaction of renal cardiotrast, glucose and urate transport was investigated in dogs in chronic experiments. There was no alteration in the maximum secretion of cardiotrast and in the malximum glucose reabsorption during simultaneous injection of cardiotrast and glucose. It was also shown that with the maximum saturation of the renal secretory and reabsorption transport there was no significant change in the urate excretion.

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