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1.
Andrologia ; 48(3): 347-54, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-26174043

RESUMEN

Although Lepidium meyenii (maca), a plant growing in Peru's central Andes, has been traditionally used for enhancing fertility and reproductive performance in domestic animals and human beings, effects of maca on reproductive organs are still unclear. This study examined whether feeding the hydroalcoholic extract powder of maca for 6 weeks affects weight of the reproductive organs, serum concentrations of testosterone and luteinising hormone (LH), number and cytoplasmic area of immunohistochemically stained Leydig cells, and steroidogenesis of cultured Leydig cells in 8-week-old male rats. Feeding the extract powder increased weight of seminal vesicles, serum testosterone level and cytoplasmic area of Leydig cells when compared with controls. Weight of prostate gland, serum LH concentration and number of Leydig cells were not affected by the maca treatment. The testosterone production by Leydig cells significantly increased when cultured with 22R-hydroxycholesterol or pregnenolone and tended to increase when cultured with hCG by feeding the extract powder. The results show that feeding the hydroalcoholic extract powder of maca for 6 weeks increases serum testosterone concentration associated with seminal vesicle stimulation in male rats, and this increase in testosterone level may be related to the enhanced ability of testosterone production by Leydig cells especially in the metabolic process following cholesterol.


Asunto(s)
Lepidium , Células Intersticiales del Testículo/efectos de los fármacos , Extractos Vegetales/farmacología , Testosterona/sangre , Animales , Células Cultivadas , Estradiol/sangre , Células Intersticiales del Testículo/citología , Células Intersticiales del Testículo/metabolismo , Hormona Luteinizante/sangre , Masculino , Tamaño de los Órganos/efectos de los fármacos , Próstata/efectos de los fármacos , Ratas , Ratas Wistar , Testosterona/biosíntesis
2.
Phytomedicine ; 9(3): 239-44, 2002 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12046865

RESUMEN

Free radical scavenging action of Limonium wrightii O. kunthe was examined in vitro and in vivo by using electron spin resonance spectrometer and chemiluminescence analyzer. A water extract of L. wrightii showed a strong scavenging action for the 1,1-diphenyl-2-picrylhydrazyl, or superoxide anion and moderate for hydroxyl radical. The extract also depressed production of reactive oxygen species from polymorphonuclear leukocytes stimulated by phorbor-12-mysistate acetate and inhibited lipid peroxidation in rat liver microsomes. When the extract was given intraperitoneally to mice prior to carbon tetrachloride (CCl4) treatment, CCl4-induced liver toxicity, as seen by an elevation of serum aspartate aminotransferase and alanine aminotransferase activities, was significantly reduced. Gallic acid was identified as the active component of L. wrightii with a strong free radical scavenging action. Our results demonstrate the free radical scavenging action of L. wrightii and that gallic acid contributes to these actions.


Asunto(s)
Antioxidantes/farmacología , Enfermedad Hepática Inducida por Sustancias y Drogas/prevención & control , Depuradores de Radicales Libres/farmacología , Peroxidación de Lípido/efectos de los fármacos , Fitoterapia , Extractos Vegetales/farmacología , Plumbaginaceae , Alanina Transaminasa/sangre , Animales , Antioxidantes/administración & dosificación , Antioxidantes/uso terapéutico , Aspartato Aminotransferasas/sangre , Tetracloruro de Carbono , Enfermedad Hepática Inducida por Sustancias y Drogas/etiología , Depuradores de Radicales Libres/administración & dosificación , Depuradores de Radicales Libres/uso terapéutico , Inyecciones Intraperitoneales , Leucocitos Mononucleares/efectos de los fármacos , Masculino , Ratones , Microsomas Hepáticos/efectos de los fármacos , Extractos Vegetales/administración & dosificación , Extractos Vegetales/uso terapéutico , Ratas , Ratas Sprague-Dawley
3.
Am J Chin Med ; 28(1): 35-40, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-10794115

RESUMEN

Preterm labor (PTL) is one of the main causes of fetal mortality and morbidity in obstetrical medicine. Current methods of treatment are not very effective and often have significant side effects. For this reason new methods of preventing PTL are currently being sought. In Western medicine the newest development is oxytocin antagonists. In Oriental medicine acupuncture and moxibustion are being utilized for the purpose of stopping PTL. The goals of this study were to determine if acupuncture in pregnant rats can suppress oxytocin induced uterine contractions and to compare these results with those inhibited by an oxytocin antagonist. Uterine contractions were induced by continuous infusion of exogenous oxytocin. The first fetus in one uterine horn near the ovarian end was removed and distilled water-filled catheter was inserted into that vacated amniotic sac to measure uterine contractions as intrauterine pressure changes. Two acupoints of Ho-Ku (LI-4) and San-Yin-Chiao (Sp-6) were selected for acupuncture and Kuan-Yüan (Co-4) was used for moxibustion. The oxytocin-induced uterine contractions were significantly suppressed by acupuncture on the LI-4 (p < 0.05), but not by Sp-6. Stimulation of Co-4 by moxibustion had no significant (p > 0.05) tocolytic effect. The administration of oxytocin antagonist eliminated all the uterine contractions induced by oxytocin. The application of acupuncture to re-stimulate the activity that was suppressed by the oxytocin antagonist did not produce any positive results. However, prostaglandins did cause the uterus to contract. In conclusion, acupuncture on LI-4 was found to suppress uterine contractions induced by oxytocin in the pregnant rat. If acupuncture is similarly effective in counteracting the effects of oxytocin in women, then this may an alternative medical treatment for women in preterm labor.


Asunto(s)
Terapia por Acupuntura/estadística & datos numéricos , Miometrio/fisiología , Preñez , Contracción Uterina , Animales , Femenino , Miometrio/efectos de los fármacos , Oxitocina/administración & dosificación , Oxitocina/antagonistas & inhibidores , Embarazo , Ratas , Ratas Sprague-Dawley , Contracción Uterina/efectos de los fármacos
7.
Gan ; 70(6): 731-6, 1979 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-535684

RESUMEN

Pyridine N-oxides having 1-(2-chloroethyl)-1-nitrosoureidoalkyl or 1-methyl-1-nitrosoureidoalkyl groups were evaluated for their antitumor activity against AH13 hepatoma and L1210 leukemia. Among them, 1-(2-chloroethyl)-1-nitroso-3-(2-pyridylmethyl)urea N-oxide (1), its tosylate (2), 1-(2-chloroethyl)-1-nitroso-3-(2-pyridylethyl)urea N-oxide (4), and 1-(2-chloroethyl)-1-nitroso-3-(3-pyridylmethyl)urea N-oxide (6) were highly active against both tumors in ip-ip system. These compounds were also active in ip-iv and ip-po systems of L1210. On the other hand, pyridine N-oxides having 1-methyl-1-nitrosoureidoalkyl group were all inactive against AH13 and weakly active against L1210. Effect on blood cells in Donryu rats bearing EDEN-5 erythroblastic leukemia cells was tested with these 1-(2-chloroethyl)-1-nitrosoureidoalkylureas. These compounds caused leucopenia and compound (4) was only slightly effective against EDEN-5.


Asunto(s)
Antineoplásicos/uso terapéutico , Óxidos N-Cíclicos/uso terapéutico , Compuestos de Mostaza Nitrogenada/uso terapéutico , Compuestos de Nitrosourea/uso terapéutico , Piridinas/uso terapéutico , Animales , Fenómenos Químicos , Química , Evaluación Preclínica de Medicamentos , Leucemia L1210/tratamiento farmacológico , Neoplasias Hepáticas Experimentales/tratamiento farmacológico , Metilnitrosourea/uso terapéutico , Ratones , Ratas , Solubilidad , Factores de Tiempo
11.
Folia Psychiatr Neurol Jpn ; 29(1): 77-82, 1975.
Artículo en Inglés | MEDLINE | ID: mdl-1158318

RESUMEN

Changes in urea cycle enzymatic activities in the liver induced by intracerebral electrical stimulation in rabbits with chronically implanted electrodes in the hypothalamus, the thalamus, and the limbic area were studied in comparison with these activities in non-stimulated controls. In stimulating the ventromedial nucleus of the hypothalamus, the two-hour sessions were followed by significantly reduced activity in arginase and the arginine synthetase system in the liver, but the six-hour stimulation sessions were followed by normal range activity in these enzymes. In stimulating the lateral hypothalamic area, the two-hour sessions were followed by only slightly reduced activity in the arginine synthetase system in the liver. Stimulation of the center median nucleus of the thalamus, the medial area of the amygdala and the dorsal hippocampus produced no significant changes in urea cycle enzymatic activities in the liver. The possibility that ammonia metabolism in the liver may be modified through some functional linkage between the brain and the liver was suggested.


Asunto(s)
Encéfalo/fisiología , Hipotálamo/fisiología , Hígado/enzimología , Urea/metabolismo , Amígdala del Cerebelo/fisiología , Animales , Arginasa/metabolismo , Argininosuccinatoliasa/metabolismo , Argininosuccinato Sintasa/metabolismo , Estimulación Eléctrica , Hipocampo/fisiología , Masculino , Actividad Motora/efectos de los fármacos , Complejos Multienzimáticos/metabolismo , Ornitina Carbamoiltransferasa/metabolismo , Conejos , Núcleos Talámicos/fisiología
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