RESUMEN
In isolated rings of the pig coronary arteries mechanical damage of endothelium led to a considerable reduction of coronary spastic responses to histamine due to the H1-receptors damage after the denudation of endothelium. The tachyphylaxis to histamine was eliminated after de-endothelialization. The drugs blocking H1-receptors such as dimedrol, were effective for preventing the histamine coronary vasospasm.
Asunto(s)
Vasos Coronarios/efectos de los fármacos , Endotelio Vascular/efectos de los fármacos , Histamina/farmacología , Resistencia Vascular/efectos de los fármacos , Animales , Vasoespasmo Coronario/inducido químicamente , Vasoespasmo Coronario/fisiopatología , Vasos Coronarios/fisiología , Difenhidramina/farmacología , Interacciones Farmacológicas , Endotelio Vascular/fisiología , Técnicas In Vitro , Porcinos , Resistencia Vascular/fisiologíaRESUMEN
The molecular mechanisms of sex hormones (testosterone, progesterone, 17 beta-estradiol) binding with human serum albumin and gamma-globulins were studied. According to the data of equilibrium dialysis, all the sex hormones under study bind with the blood plasma proteins, mainly with the serum albumin. In interaction of the sex hormones with serum albumin and gamma globulins, conformation changes of the proteins occur increasing their molecular affinity.
Asunto(s)
Estradiol/sangre , Progesterona/sangre , Albúmina Sérica/metabolismo , Testosterona/sangre , gammaglobulinas/metabolismo , Diálisis , Interacciones Farmacológicas , Humanos , Unión Proteica , Espectrometría de FluorescenciaRESUMEN
The effect of sex hormones on lipid peroxidation (LPO) in the wall of the aorta of male rats was studied in vivo and in vitro. Female sex hormones (17 beta-estradiol and progesterone) inhibited LPO in the aorta: 17 beta-estradiol caused a maximum antioxidant effect at the beginning of its action, progester one during prolonged action. Testosterone had a marked prooxidant effect, activating lipid LPO in the aorta both in vivo and in vitro whatever its concentration and duration of incubation.
Asunto(s)
Estradiol/farmacología , Peroxidación de Lípido/efectos de los fármacos , Músculo Liso Vascular/efectos de los fármacos , Progesterona/farmacología , Testosterona/farmacología , Animales , Aorta Abdominal/efectos de los fármacos , Aorta Abdominal/metabolismo , Aorta Torácica/efectos de los fármacos , Aorta Torácica/metabolismo , Masculino , Músculo Liso Vascular/metabolismo , RatasRESUMEN
The effect of 17 beta-estradiol on the regions of ischemia and necrosis in experimental myocardial infarction was studied in the experiments on rats. The ability of the hormone to decrease the damaged area due to anti-ischemic and antinecrotic effects is found.
Asunto(s)
Fármacos Cardiovasculares/uso terapéutico , Estradiol/uso terapéutico , Infarto del Miocardio/tratamiento farmacológico , Animales , Evaluación Preclínica de Medicamentos , Femenino , Masculino , Infarto del Miocardio/patología , Miocardio/patología , Necrosis , Ratas , Factores de TiempoRESUMEN
In concentrations of > or = 10(-5) mol/liter nistranol (11 beta-nitroxy-9 alpha-hydroxy-ethynylestradiol-diacetate) demonstrated cardiac and vascular activity in vitro. It caused concentration-dependent and reversible increase of the contractile parameters of an isolated atrial appendage of rats. A three-phase effect of nistranol on a isolated rat thoracic aorta was encountered: vasodilatation-vasoconstriction-vasodilatation. Anti-ischemic and antinecrotic effects of nistranol were noted in experimental myocardial infarction.
Asunto(s)
Cardiotónicos/farmacología , Sistema Cardiovascular/efectos de los fármacos , Congéneres del Estradiol/farmacología , Etinilestradiol/análogos & derivados , Animales , Cardiotónicos/uso terapéutico , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Congéneres del Estradiol/uso terapéutico , Etinilestradiol/farmacología , Técnicas In Vitro , Masculino , Infarto del Miocardio/tratamiento farmacológico , Isquemia Miocárdica/tratamiento farmacológico , RatasRESUMEN
The action of peripheral cholinergic and adrenergic receptor systems on the histamine coronary vasospastic effects are investigated in the experiments on the isolated ring-shaped strips of coronary arteries of pigs with the aid of specific agonists and antagonists. It has been demonstrated that neuromediator systems play a significant role in the regulation of contractile activity of the coronary spasm pathogenesis. When medicines are prescribed to patients with ischemic heart disease it is necessary to take into account the character of the preparations interaction which affect the peripheral neuromediator processes such as histaminergic, cholinergic, adrenergic and others.
Asunto(s)
Vasoespasmo Coronario/etiología , Vasos Coronarios/fisiología , Histamina/fisiología , Receptores Adrenérgicos/fisiología , Receptores Colinérgicos/fisiología , Animales , Vasoespasmo Coronario/inducido químicamente , Vasos Coronarios/efectos de los fármacos , Femenino , Histamina/farmacología , Técnicas In Vitro , Masculino , Receptores Adrenérgicos/efectos de los fármacos , Receptores Colinérgicos/efectos de los fármacos , PorcinosRESUMEN
Menopause, being the end of the reproductive period of a woman's life, is characterized by changes in the endocrine balance in the body, significantly affecting health, quality of life and general life prognosis. These changes can be more significant and even take on a fatal character with "forced", artificial (surgical) menopause.