RESUMEN
Data on the therapeutic effectiveness of intravenous injections of immunoglobulins in high doses in patients with bronchial asthma are analyzed. Some possible mechanisms of this therapeutic effect are considered, which are related to of immunoglobulin fragments capable of interacting with cytochrome P-450 and NO-synthase systems of the liver.
Asunto(s)
Asma/tratamiento farmacológico , Sistema Enzimático del Citocromo P-450/metabolismo , Inmunoglobulinas/uso terapéutico , Hígado/enzimología , Óxido Nítrico Sintasa/metabolismo , Asma/enzimología , HumanosRESUMEN
The effects of carnosine and its combination with essentiale on the processes of lipid peroxidation (LPO) and on the work capacity have been studied in mice. The administration of camosine, essentiale, and vitamin E, increased the work capacity of laboratory mice to a different extent, the effect being most pronounced for a mixture of carnosine and essentiale. Carnosine in the dose range studied exhibited a pronounced antioxidant effect with respect to LPO and optimized the potential of the organism in the course of intensive physical activity. This drug is not a doping and can be recommended as a means of improvement of the physical capacity.
Asunto(s)
Antioxidantes/farmacología , Carnosina/farmacología , Peroxidación de Lípido/efectos de los fármacos , Actividad Motora/efectos de los fármacos , Fosfatidilcolinas/farmacología , Animales , Ratones , Ratones Endogámicos , NataciónAsunto(s)
Diabetes Mellitus Tipo 1/sangre , Diabetes Mellitus Tipo 1/tratamiento farmacológico , Insulina/administración & dosificación , Insulina/sangre , Sustancias Macromoleculares/sangre , Análisis Espectral/métodos , Adolescente , Niño , Preescolar , Humanos , Insulina/uso terapéutico , Rayos LáserAsunto(s)
Sistema Enzimático del Citocromo P-450/metabolismo , Hígado/enzimología , Xenobióticos/farmacología , Animales , Benzo(a)pireno/metabolismo , Cuervos , Hígado/efectos de los fármacos , Hígado/metabolismo , Ratones , Microsomas Hepáticos/efectos de los fármacos , Microsomas Hepáticos/metabolismo , Conejos , Ratas , Especificidad de la Especie , Factores de TiempoAsunto(s)
Adamantano/análogos & derivados , Adamantano/uso terapéutico , Sistema Enzimático del Citocromo P-450/metabolismo , Extremidad Inferior/irrigación sanguínea , Tromboangitis Obliterante/tratamiento farmacológico , Adamantano/metabolismo , Adamantano/farmacología , Viscosidad Sanguínea/efectos de los fármacos , Enfermedad Crónica , Humanos , Oxidación-Reducción/efectos de los fármacos , Tromboangitis Obliterante/sangre , Tromboangitis Obliterante/patología , Ultrasonografía DopplerAsunto(s)
ADN/sangre , Diabetes Mellitus Tipo 1/sangre , Análisis Espectral/métodos , Niño , Diabetes Mellitus Tipo 1/diagnóstico , Diabetes Mellitus Tipo 1/tratamiento farmacológico , Progresión de la Enfermedad , Humanos , Insulina/uso terapéutico , Rayos Láser , Sustancias Macromoleculares , Tamaño de la Partícula , Distribuciones EstadísticasAsunto(s)
Adyuvantes Inmunológicos/farmacología , Arginina/química , Sistema Enzimático del Citocromo P-450/efectos de los fármacos , Inmunoglobulinas/farmacología , Óxido Nítrico/farmacología , Fragmentos de Péptidos/farmacología , Adyuvantes Inmunológicos/química , Animales , Sistema Enzimático del Citocromo P-450/metabolismo , Inmunoglobulinas/química , Masculino , Ratones , Peso Molecular , Fragmentos de Péptidos/químicaAsunto(s)
Adamantano/análogos & derivados , Adamantano/farmacología , Adyuvantes Inmunológicos/farmacología , Fármacos Anti-VIH/farmacología , Sistema Enzimático del Citocromo P-450/metabolismo , Oxidación-Reducción/efectos de los fármacos , Adamantano/química , Relación Dosis-Respuesta a Droga , Cinética , Modelos Químicos , NADP/metabolismo , Oxígeno/metabolismo , Consumo de Oxígeno , Espectrofotometría , TermodinámicaRESUMEN
We performed an analysis of the biological activity of dyes possessing certain redox potential. This provided a theoretical basis for the development of a new trend in pharmacology. We demonstrate the wide potential associated with the use of this group of substances to regulate various biochemical processes in the immunity system.
Asunto(s)
Adyuvantes Inmunológicos/farmacología , Antioxidantes/farmacología , Colorantes/farmacología , Adyuvantes Inmunológicos/química , Adyuvantes Inmunológicos/uso terapéutico , Animales , Antioxidantes/química , Antioxidantes/uso terapéutico , Asma/tratamiento farmacológico , Colorantes/química , Colorantes/uso terapéutico , Diseño de Fármacos , Humanos , Concentración de Iones de Hidrógeno , Linfocitos/efectos de los fármacos , Azul de Metileno/uso terapéutico , Oxidación-ReducciónRESUMEN
For the first time the dynamics of metabolic and immune responses to xenobiotics were analyzed in their long-term effect on the organism. It was shown that the organism gradually lost the capacity to respond to xenobiotics with the induction of hepatic cytochrome P450 and immune response. Possible mechanisms of this phenomenon are under consideration.
Asunto(s)
Adaptación Fisiológica/inmunología , Salud Ambiental , Xenobióticos/efectos adversos , Adaptación Fisiológica/efectos de los fármacos , Animales , Biotransformación , Sistema Enzimático del Citocromo P-450/efectos de los fármacos , Sistema Enzimático del Citocromo P-450/inmunología , Humanos , Tolerancia Inmunológica/efectos de los fármacos , Tolerancia Inmunológica/inmunología , Inmunoquímica , Hígado/efectos de los fármacos , Hígado/enzimología , Hígado/inmunología , Xenobióticos/farmacocinéticaRESUMEN
The long-term administration of xenobiotics carcinogens o-aminoazotoluene (o-AAT) and benz(a)pyrene (BP) to rats was found to cause induction of the liver cytochrome P-450 system which gradually decreases in spite of continued administration of the agents. Induction of microsomal oxygenases under these conditions is followed by induction of the immune response to o-AAT and BP. The data obtained correspond to the conception of the immunochemical functional system of homeostasis implying that the cytochrome-450 system and the immunity system are functionally linked and are elements of the common functional adaptive system of the organism.
Asunto(s)
Reacciones Antígeno-Anticuerpo/efectos de los fármacos , Sistema Enzimático del Citocromo P-450/biosíntesis , Xenobióticos/farmacología , Animales , Reacciones Antígeno-Anticuerpo/inmunología , Benzo(a)pireno/farmacología , Sistema Enzimático del Citocromo P-450/análisis , Inducción Enzimática/efectos de los fármacos , Femenino , Linfocitos/efectos de los fármacos , Linfocitos/inmunología , Microsomas Hepáticos/efectos de los fármacos , Microsomas Hepáticos/enzimología , Microsomas Hepáticos/inmunología , Ratas , Factores de Tiempo , o-Aminoazotolueno/farmacologíaAsunto(s)
Síndrome de Inmunodeficiencia Adquirida/diagnóstico , Antivirales , Antígenos CD4/antagonistas & inhibidores , Linfocitos T CD4-Positivos/efectos de los fármacos , Proteína gp120 de Envoltorio del VIH/antagonistas & inhibidores , Receptores del VIH/efectos de los fármacos , Síndrome de Inmunodeficiencia Adquirida/tratamiento farmacológico , Síndrome de Inmunodeficiencia Adquirida/metabolismo , Antivirales/uso terapéutico , Linfocitos T CD4-Positivos/metabolismo , Humanos , Ligandos , Peso Molecular , Unión Proteica/efectos de los fármacos , Receptores del VIH/metabolismo , SolubilidadRESUMEN
The feasibility of obtaining a conjugated benz(a)pyrene-protein antigen in the liver cytochrome P-450 system was studied. Covalent binding of benz(a)pyrene (BP) to albumin was performed with the use of liver microsomal fractions of 3-methylcholanthrene-induced rabbits. It was demonstrated that BP oxidation in liver microsomes is accompanied by covalent binding of [14C]BP to exogenous rabbit albumin. Immunization of rabbits with the obtained conjugate results in the development of a specific immune response to BP, and the appearance of specific antibodies and lymphocytes specifically binding [14C]BP in the blood.
Asunto(s)
Albúminas/inmunología , Benzo(a)pireno/toxicidad , Sistema Enzimático del Citocromo P-450/metabolismo , Inmunización , Microsomas Hepáticos/enzimología , Albúminas/metabolismo , Animales , Benzo(a)pireno/metabolismo , Linfocitos/metabolismo , Masculino , ConejosRESUMEN
Conjugates morphine-protein which are formed in the systems of cytochrome P-450 and horse-radish peroxidase can induce in rabbits synthesis of the specific antibodies to morphine. In the blood of animals immunized with the above mentioned conjugates there are antimorphine-antibodies being constituents on immunochemical complexes with endogenous ligands. Administration to rabbits of the conjugated antigen morphine-microsomes of the rabbit liver causes the development of the reaction of hypersensitivity of delayed type to morphine.
Asunto(s)
Antígenos/inmunología , Sistema Enzimático del Citocromo P-450/metabolismo , Morfina/inmunología , Animales , Peroxidasa de Rábano Silvestre/metabolismo , Hipersensibilidad Tardía/inmunología , Inmunización , Inmunoquímica , Microsomas Hepáticos/enzimología , Morfina/metabolismo , Oxidación-Reducción , ConejosRESUMEN
Male guinea pigs, intact and orally sensitized with chick ovalbumin (OVA), having initial bw 250-300 g, received glycine intraperitoneally or orally in a single dose of 100 or 200 mg/kg/day, during 3 days. The specific volume of cytochromes P450 and b5 in the microsomal fraction of the liver, activity of aminopyrine N-demethylase and aniline-p-hydroxylase, severity of food anaphylaxis to OVA and the animals' sensitivity to intravenous histamine LD50 were studied. The inducing effect of glycine on the cytochrome P450 system in the liver was more pronounced in the presensitized animals, that was attended by a decreased severity of food anaphylaxis and by a protective action in respect to histamine LD50. Possible mechanisms of glycine action are considered regarding its participation in metabolic processes.
Asunto(s)
Anafilaxia/prevención & control , Sistema Enzimático del Citocromo P-450/biosíntesis , Hipersensibilidad a los Alimentos/prevención & control , Glicina/uso terapéutico , Hígado/enzimología , Anafilaxia/enzimología , Animales , Hipersensibilidad a los Alimentos/enzimología , Cobayas , Hígado/efectos de los fármacos , MasculinoRESUMEN
Gamma-aminobutyric acid (GABA) was shown to exert the immunodepressive effect. The use of GABA under induction of cytochrome P-450 of the liver by phenobarbital or rifampicin was not followed by immunodepression. The obtained data indicate the dependence of GABA pharmacological activity from the function of cytochrome P-450-dependent monooxygenase system of the liver.
Asunto(s)
Sistema Enzimático del Citocromo P-450/biosíntesis , Inmunosupresores , Hígado/efectos de los fármacos , Ácido gamma-Aminobutírico/farmacología , Animales , Inducción Enzimática/efectos de los fármacos , Eritrocitos/inmunología , Hexobarbital/farmacología , Inmunización , Hígado/enzimología , Masculino , Ratones , Fenobarbital/farmacología , Rifampin/farmacología , Sueño/efectos de los fármacosRESUMEN
The principles of coding in the organism of the information about an unlimited scope of substances and the formation of peptide analogues of the original nonpeptide chemical structures are first formulated on the basis of the conception of the immunochemical functional system of homeostasis and the data on the pharmacological activity of antibodies to low molecular organic compounds and the corresponding anti-antibodies.
Asunto(s)
Psiconeuroinmunología/tendencias , Animales , Anticuerpos/inmunología , Cibernética , Homeostasis , Humanos , Sistema Inmunológico/inmunología , Inmunidad , Inmunoquímica , Sistema Nervioso/inmunología , Teoría de SistemasRESUMEN
There was studied the possibility of covalent binding to proteins of a carcinogenic compound benzo(a)pyrene in the system of cytochrome P-450 of the liver and the possibility of the development of the immune reaction to administration of the conjugated antigens obtained in such a way to animals. It was shown that under experimental conditions modelling the processes of microsomal oxidation of benzo(a)pyrene in the organism there occurs irreversible binding of 14C-benzo(a)pyrene both to microsomes and the added albumin. Immunization of rabbits by conjugates benzo(a)pyrene-albumin and benzo(a)pyrene-microsomes leads to the development of the immune response to the original carcinogen. The antibodies and lymphocytes specifically binding 14C-benzo(a)pyrene appear in the blood.