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We investigated L-kynurenine distribution and metabolism in rats with experimental chronic renal failure of various severity, induced by unilateral nephrectomy and partial removal of contralateral kidney cortex. In animals with renal insufficiency the plasma concentration and the content of L-tryptophan in homogenates of kidney, liver, lung, intestine and spleen were significantly decreased. These changes were accompanied by increase activity of liver tryptophan 2,3-dioxygenase, the rate-limiting enzyme of kynurenine pathway in rats, while indoleamine 2,3-dioxygenase activity was unchanged. Conversely, the plasma concentration and tissue content of L-kynurenine, 3-hydroxykynurenine, and anthranilic, kynurenic, xanthurenic and quinolinic acids in the kidney, liver, lung, intestine, spleen and muscles were increased. The accumulation of L-kynurenine and the products of its degradation was proportional to the severity of renal failure and correlated with the concentration of renal insufficiency marker, creatinine. Kynurenine aminotransferase, kynureninase and 3-hydroxyanthranilate-3,4-dioxygenase activity was diminished or unchanged, while the activity of kynurenine 3-hydroxylase was significantly increased. We conclude that chronic renal failure is associated with the accumulation of L-kynurenine metabolites, which may be involved in the pathogenesis of certain uremic syndromes.
This study investigated the kynurenine metabolism in rats treated with cadmium. We used an animal model at the levels of Cd corresponding to human environmental and occupational exposure to this metal which allows the assessment of its early effect on the structure and function of kidneys. We observed significant decrease in the serum concentration of tryptophan (TRP) and its metabolites: kynurenine (KYN), kynurenic acid (KYNA), and 3-hydroxykynurenine (3-HKYN), which was accompanied by a decrease in KYN derivatives in kidney and liver tissues. This effect was dependent on the level of Cd exposure. Regression analysis showed negative correlations between blood concentrations of Cd and TRP derivatives in serum, kidney and liver tissues. Conversely, the urinary concentration of KYN and KYNA increased. Changes in product degradation of TRP after Cd treatment were proportional to the severity of renal damage and correlated with the concentration of proximal tubular injury marker — urinary isoenzyme B of N-acetyl-D-glucosaminidase (NAG-B). Our results seem to indicate that intoxication with Cd induced significant disturbances in the peripheral kynurenine pathway.
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Kynurenine and its metabolites in the rat with experimental renal insufficiency

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In uremia a great number of the endogenous metabolites that are ordinarily excreted in urine accumulate in the blood. Among these are the products of KYN degradation. In the present study we evaluated the peripheral KYN metabolism in the various stages of the rat experimental chronic renal insufficiency. Our results showed significant disturbances in peripheral kynurenic pathway, which resulted in the significant decrease of TRP plasma level and augmentation of concentration of its metabolites. The high concentrations of 3-hydroxykynurenine, xanthurenic acid, kynurenic acid, anthranilic acid and quinolinic acid positively correlated with degree of the renal insufficiency. Talking into account the biological properties of KYN metabolites, their accumulation in the blood, may be at least partially, responsible for severity of uremia as well as for uremic symptoms such as neuropathy, increased susceptibility to infections, hypertension, lipid disturbances and anemia.
Badania owocników gąsówki nagiej Lepista nuda przeprowadzone za pomocą metod chromatograficznych i spektralnych wykazały obecność kwasowych pochodnych tryptofanu: kwasów 3-indolooctowego (IAA) i 3-indolopropionowego (IPrA) oraz produktów biochemicznej degradacji tryptofanu: kynureniny i 3-hydroksykynureniny. Dwa ostatnie produkty nie byty obecne w hodowli mycelialnej tego gatunku, która zawierała głównie kwas 3-indolooctowy i tryptofan.
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