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1.
Amino Acids ; 35(2): 403-10, 2008 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-18163178

RESUMEN

Endotoxin decreases mesenteric blood flow and inflicts organ injury via free radicals. We investigated whether taurine, an endogenous antioxidant and vasodilator, could attenuate the deleterious effects of endotoxin in a mouse model of sepsis. Swiss albino mice were allocated into four groups and treated either with taurine (150 mg/kg, i.p. at 0(th), 8(th), 16(th) h) or its solvent sterile saline (NaCl 0.9%, w/v) while E. coli endotoxin (20 mg/kg, i.p.) or its solvent saline were also given at 8(th) h. At 24(th) h the animals were anaesthetized and the mesenteric blood flow was measured by using perivascular ultrasonic Doppler-flowmeter. The animals were then exsanguinated, the spleen, liver, and kidneys were isolated for histopathological examination. Thiobarbituric acid-reacting substances (TBARS), glutathione, and myeloperoxidase activity were determined in the liver samples. Endotoxin significantly decreased the mesenteric blood flow and glutathione levels in liver while TBARS and myeloperoxidase activity were increased. However, taurine did not block the deleterious effects of endotoxin nor it did attenuate the histopathological injury. Therefore, we concluded that endotoxin-induced organ injury via free radicals is resistant to blockade by taurine.


Asunto(s)
Velocidad del Flujo Sanguíneo/efectos de los fármacos , Mesenterio/efectos de los fármacos , Insuficiencia Multiorgánica/fisiopatología , Sepsis/fisiopatología , Taurina/farmacología , Animales , Modelos Animales de Enfermedad , Endotoxinas/antagonistas & inhibidores , Endotoxinas/toxicidad , Radicales Libres/metabolismo , Glutatión/análisis , Inyecciones Intraperitoneales , Mesenterio/irrigación sanguínea , Ratones , Insuficiencia Multiorgánica/patología , Peroxidasa/análisis , Peroxidasa/metabolismo , Sepsis/tratamiento farmacológico , Sepsis/patología , Sustancias Reactivas al Ácido Tiobarbitúrico/metabolismo , Factores de Tiempo
2.
Arch Physiol Biochem ; 109(4): 383-7, 2001 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11935378

RESUMEN

Stress is a factor found to be involved in the etiology of many diseases. Gender and menstrual cycle phases are other factors affecting the predisposition of individuals for certain diseases. Results from animal and human studies suggest that the distribution of immune system cells may change at different phases of the menstrual cycle. Acute mental stress in humans alters immune variables, too. The increase in the number of natural killer (NK) cells is the most consistent finding among the immune variables, though there are controversies for the other lymphocyte groups. Nitric oxide (NO) as an immune mediator has an unsettled role whether it causes the redistribution of the immune cells, or is an end product of lymphocyte activation. This study was planned to investigate the effect of mental stress on lymphocyte subtypes and the role of NO, for men and women at different phases of the cycle. For this purpose, healthy men (n = 10) and women (n = 10), during the follicular and luteal phases underwent Stroop colour-word interference and cold pressor tests. The immune system responses before and after the tests were determined by cell counts with the flowcytometer. Menstrual cycle phase was ascertained by plasma estrogen and progesterone measurements. Stress response was evaluated by blood pressure (BP) and heart rate (HR) measurements throughout the tests and plasma cortisol and urinary metanephrine and vanillylmandelic acid (VMA) measurements before and after the tests. Plasma and urinary NO determinations were performed before and after the test was completed. All the results were analysed with the appropriate statistical methods. The luteal phase differed from the other groups due to the presence of suppressed immune response to acute stress, including decreased CD4/CD8 ratio and NK cell percentage. On the other hand, acute stress caused a shift from cellular to humoral immunity in men. As indicated by these results, individual reaction towards stress is affected by gender and menstrual cycle phase. NO appears to be a possible effector molecule for these differences.


Asunto(s)
Sistema Inmunológico/fisiología , Ciclo Menstrual/fisiología , Óxido Nítrico/metabolismo , Caracteres Sexuales , Estrés Fisiológico , Adulto , Femenino , Humanos , Hidrocortisona/sangre , Subgrupos Linfocitarios/metabolismo , Masculino , Metanefrina/sangre , Ácido Vanilmandélico/sangre
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