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1.
Article de Anglais | WPRIM | ID: wpr-982401

RÉSUMÉ

Wax apple (Syzygium samarangense) has received growing research interest for its high nutritional and medicinal value due to its constituents such as polysaccharide, organic acids, flavonoids, minerals, and other substances. In this study, wax apple polysaccharide (WAP) was isolated from this plant and its protective effect against ethyl carbamate (EC)‍-induced oxidative damage was evaluated in human hepatocytes (L02 cells). Firstly, a series of analyses such as high-performance liquid chromatography (HPLC), high-performance gel permeation chromatography (HPGPC), Fourier transform infrared spectroscopy (FT-IR), gas chromatography/mass spectrometry (GC/MS), and 1H and 13C nuclear magnetic resonance (NMR) were conducted to identify the structure of WAP. Thereafter, in vitro cell experiments were performed to verify the protective effects of WAP against EC-induced cytotoxicity, genotoxicity, and oxidative damage in L02 cells. Our results revealed that WAP is composed of mannose, rhamnose, glucuronic acid, galacturonic acid, glucose, galactose, arabinose, and fucose in a molar ratio of 2.20:‍3.94:‍4.45:‍8.56:‍8.86:‍30.82:‍39.78:‍1.48. Using a combination of methylation and NMR spectroscopic analysis, the primary structure of WAP was identified as Araf-(1→, Glcp-(1→, →2)‍-Araf-(1→, →3)‍-Galp-(1→, →3)‍-Araf-‍(1→, and →6)‍-Galp-‍(1→. Cell experiments indicated that WAP exhibited significant protective effects on EC-treated L02 cells via suppressing cytotoxicity and genotoxicity, reducing reactive oxygen species (ROS) and O2•- formation, as well as improving mitochondrial membrane potential (MMP) and glutathione (GSH). In a nutshell, WAP has the potential as an important therapeutic agent or supplement for hepatic oxidative damage. Meanwhile, further studies are needed to prove the above effects in vivo at the biological and clinical levels.


Sujet(s)
Humains , Syzygium/composition chimique , Uréthane/pharmacologie , Spectroscopie infrarouge à transformée de Fourier , Stress oxydatif , Glutathion/pharmacologie , Hépatocytes , Polyosides/pharmacologie
2.
Int. braz. j. urol ; 42(5): 1018-1027, Sept.-Oct. 2016. tab, graf
Article de Anglais | LILACS | ID: lil-796875

RÉSUMÉ

ABSTRACT Objective: To evaluate the effect of neuronal nitric oxide synthase on the striated urethral sphincter and the urinary bladder. Materials and Methods: A coaxial catheter was implanted in the proximal urethra and another one in the bladder of female rats, which were anesthetized with subcutaneous injection of urethane. The urethral pressure with saline continuous infusion and bladder isovolumetric pressure were simultaneously recorded. Two groups of rats were formed. In group I, an intrathecal catheter was implanted on the day of the experiment at the L6-S1 level of the spinal cord; in group II, an intracerebroventricular cannula was placed 5-6 days before the experiment. Results: It was verified that the group treated with S-methyl-L-thio-citrulline, via intrathecal pathway, showed complete or partial inhibition of the urethral sphincter relaxation and total inhibition of the micturition reflexes. The urethral sphincter and the detrusor functions were recovered after L-Arginine administration. When S-methyl-L-thio-citrulline was administered via intracerebroventricular injection, there was a significant increase of urethral sphincter tonus while preserving the sphincter relaxation and the detrusor contractions, at similar levels as before the use of the drugs. Nevertheless there was normalization of the urethral tonus when L-Arginine was applied. Conclusions: The results indicate that, in female rats anaesthetized with urethane, the nNOS inhibitor administrated through the intrathecal route inhibits urethral sphincter relaxation, while intracerebroventricular injection increases the sphincter tonus, without changing bladder function. These changes were reverted by L-Arginine administration. These findings suggest that the urethral sphincter and detrusor muscle function is modulated by nitric oxide.


Sujet(s)
Animaux , Femelle , Thiourée/analogues et dérivés , Urètre/effets des médicaments et des substances chimiques , Miction/effets des médicaments et des substances chimiques , Vessie urinaire/effets des médicaments et des substances chimiques , Citrulline/analogues et dérivés , Antienzymes/pharmacologie , Nitric oxide synthase type I/pharmacologie , Arginine/pharmacologie , Pression , Valeurs de référence , Thiourée/pharmacologie , Facteurs temps , Uréthane/pharmacologie , Urètre/physiologie , Miction/physiologie , Vessie urinaire/physiologie , Injections rachidiennes , Citrulline/pharmacologie , Rat Wistar , Anesthésiques intraveineux , Contraction musculaire/effets des médicaments et des substances chimiques , Contraction musculaire/physiologie
3.
Rev. cuba. invest. bioméd ; 16(1): 50-4, ene.-jun. 1997. tab
Article de Espagnol | LILACS | ID: lil-205314

RÉSUMÉ

Se caracterizó el patrón respiratorio dle conejo bajo la acción de 3 anestésicos. Se registraron el flujo y el volumen respiratorios mediante un neumotacógrafo, la presión intraesofágica y el electrocardiograma, en animales que respiraban espontáneamente en condiciones basales, agrupados y anestesiados como sigue: grupo 1: pentobarbital EV, 30 mg/kg; grupo 2: mezcla de uretano EV, 400 mg/kg y cloralosa EV, 60-80 mg/kg y grupo 3: uretano IP, 1,5 g/kg. Se analizaron las variables frecuencia respiratoria, volumen corriente, volumen minuto, flujo inspiratorio medio, relación entre tiempo de inspiración y tiempo total de la respiración (tiempo útil), resistencia pulmonar, complianza dinámica y frecuencia cardíaca. En el grupo 3 las variables indicadoras de la ventilación difirieron significativamente respecto a los grupos 1 y 2, que no mostraron diferencias entre sí. El tiempo útil fue diferente en los 3 grupos. En las demás variables no hubo diferencias significativas. Se valora que el uretano pueda ejercer una acción estimulante sobre la respiración


Sujet(s)
Animaux , Lapins , Chloralose/pharmacologie , Pentobarbital/pharmacologie , Lapins/physiologie , Spirométrie , Uréthane/pharmacologie , Ventilation pulmonaire , Ventilation pulmonaire/physiologie , Volume courant , Volume courant/physiologie , Tests de la fonction respiratoire
4.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;26(10): 1091-5, Oct. 1993. graf
Article de Anglais | LILACS | ID: lil-148786

RÉSUMÉ

The present study was carried out to evaluate the effect of anesthetics on reperfusion arrhythmias. Male Wistar rats (200-300 g) were injected ip with heparin (200 IU), followed by anesthesia with thiopental (40 mg/kg), pentobarbital (30 mg/kg), urethane (1.2 g/kg), either, or halothane and sacrificed by decapitation. The isolated heart (5 to 8 per group) was perfused with Locke solution by the Langendorff method and the left coronary artery was ligated for 10 min. The incidence of reperfusion arrhythmias (100 per cent ) was similar in hearts of control and previously anesthetized rats, but the duration of the arrhythmias was significantly increased by anesthesia (5-fold with thiopental, 15-fold with pentobarbital, ether and halothane, and 30-fold with urethane). In hearts taken from unanesthetized rats and perfused with Locke solution containing anesthetics (5-7 per group), the duration of reperfusion arrhythmias decreased with thiopental (0.23 +/- 0.15 min), did not change with pentobarbital (1.14 +/- 0.26 min) and increased with urethane (16.10 +/- 5.60 min). Our results show that anesthetics alter the duration of reperfusion arrhythmias in the isolated rat heart


Sujet(s)
Animaux , Mâle , Rats , Anesthésiques/pharmacologie , Troubles du rythme cardiaque/étiologie , Reperfusion myocardique , Anesthésiques/administration et posologie , Pentobarbital/pharmacologie , Rat Wistar , Thiopental/pharmacologie , Uréthane/pharmacologie
5.
Article de Anglais | WPRIM | ID: wpr-30961

RÉSUMÉ

A wide-spectrum initiation model was investigated in mice. Sequential treatments with diethylnitrosamine, urethane and N-methylnitrosourea, with or without a promoter, phenobarbital, resulted in tumor formation in the lungs in 85-90% of animals, but did not produce any tumorous lesions in other organs. The lung tumors were adenomas and the mean number of adenomas was 2.2-2.6 per mouse. Phenobarbital combination had no additive effect on lung tumor incidence and multiplicity. Splenic NK cell activity showed inconsistent increment in the carcinogen plus phenobarbital-treated group during the experiment (P less than 0.05).


Sujet(s)
Animaux , Femelle , Souris , Adénomes/induit chimiquement , N-Éthyl-N-nitroso-éthanamine/pharmacologie , Cellules tueuses naturelles/effets des médicaments et des substances chimiques , Tumeurs du poumon/induit chimiquement , 1-Méthyl-1-nitroso-urée/pharmacologie , Phénobarbital/pharmacologie , Répartition aléatoire , Uréthane/pharmacologie
6.
Säo Paulo; s.n; jan. 1990. 12 p. tab.(Publicaçäo IPEN, 287).
Monographie de Portugais | LILACS | ID: lil-126883

RÉSUMÉ

Fêz-se um estudo comparativo entre os anestésicos éter etílico e uretana, em ratos (Wistar). Observou-se uma variaçäo significativa nos resultados apresentados, quando investigados radiofármacos para vias renais. Com uretana, a captaçäo renal aumenta progressivamente em virtude da inibiçäo da filtraçäo renal e esta começa a ser restabelecida com a eliminaçäo do efeito da anestesia. Utilizando-se éter etílico observa-se que o radiofármaco é eliminado rapidamente dos rins (filtraçäo tubular ou glomerular), evidenciando a preservaçäo da funçäo renal


Sujet(s)
Animaux , Rats , Uréthane/pharmacologie , Rein/effets des médicaments et des substances chimiques , Oxyde de diéthyle/pharmacologie , Anesthésiques/pharmacologie , Marqueurs biologiques , Lignées consanguines de rats
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