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1.
Scand J Gastroenterol Suppl ; 169: 70-80, 1989.
Article in English | MEDLINE | ID: mdl-2694347

ABSTRACT

Furazolidone is a synthetic nitrofuran with a broad spectrum of antimicrobial action and has been widely used in the treatment of gastrointestinal infections. This article reviews the adverse reactions to furazolidone reported in the world literature. Of 10,443 adults and children who were treated with the drug, approximately 8.3% (864) experienced such reactions. Because some of these patients had more than 1 adverse reaction, 1178 reactions were reported in these studies. Nausea with vomiting, the commonest adverse reaction, was reported by 51% of the 864 patients who experienced adverse reactions. The authors compare the adverse reactions to furazolidone with those reported for other antimicrobial and antiprotozoal drugs that are frequently used to treat gastrointestinal infections.


Subject(s)
Furazolidone/adverse effects , Adult , Anti-Infective Agents/adverse effects , Antiprotozoal Agents/adverse effects , Child , Humans , Nausea/chemically induced , Vomiting/chemically induced
3.
Arch. invest. méd ; 13(4): 219-24, 1982.
Article in Spanish | LILACS | ID: lil-7771

ABSTRACT

El efecto relajante de las dosis efectivas 50 de androgenos y progestinas sobre las contracciones in vitro del utero de la rata fue prevenido por la administracion previa de Ca2+ o antagonizada por la adicion posterior de este ion. En todos los casos el Ca2+ fue efectivo para antagonizar el efecto inhibitorio de los esteroides. Sin embargo, con la pregnanolona el calcio fue un poco menos potente para revertir la relajacion, a pesar de que la concentracion del esteroide en este caso fue la menor. El analisis matematico usando la ecuacion de Hanes-Woolf para el estudio cinetico de la interacion entre el ion y las hormonas. Los resultados apoyan la idea de que los esteroides podrian ejercer su efecto relajante sobre la contractilidad uterina disminuyendo la permeabilidad de la membrana al ion calcio


Subject(s)
Animals , Rats , Calcium , In Vitro Techniques , Uterine Contraction , Androgens , Progestins
4.
Steroids ; 35(6): 633-41, 1980 Jun.
Article in English | MEDLINE | ID: mdl-6447389

ABSTRACT

The effectiveness of ring A reduced (5 alpha and 5 beta) testosterone (T) derivatives upon the rat uterus spontaneous contractility was tested in vitro. Compounds with the 3 alpha-hydroxy-5 alpha reduced configuration, such as androsterone and androstanediol, and one 5 beta reduced (5 beta-dihydrotestosterone) elicited a remarkable inhibitory effect upon the myometrial activity. Although steroids with 5 beta reduction were less potent than 3 alpha-hydroxy-5 alpha reduced compounds for depressing the myometrial activity, they were somewhat more potent than T, DHEA, androstenedione and the remaining 5 alpha reduced compounds tested. Therefore, T could act as a "prehormone", accounting for the maintenance of the physiological myometrial activity through its 5-reduced derivatives.


Subject(s)
Androgens/pharmacology , Uterine Contraction/drug effects , Androstane-3,17-diol/pharmacology , Androsterone/pharmacology , Animals , Dehydroepiandrosterone/pharmacology , Dihydrotestosterone/pharmacology , Dose-Response Relationship, Drug , Female , In Vitro Techniques , Rats , Stereoisomerism , Structure-Activity Relationship , Testosterone/pharmacology
5.
Steroids ; 34(6 Spec no): 609-17, 1979.
Article in English | MEDLINE | ID: mdl-575442

ABSTRACT

Ten natural progestins were evaluated for their capacity to inhibit the in vitro motility of rat's uterus. Progestins with their ring A reduced in the 5 beta position were significantly more potent than delta 4-3 keto and 5 alpha reduced progestins. These last progestins were ineffective to inhibit uterine motility excepting 3 alpha-hydroxy-5 alpha-pregnan-20-one which was slightly less effective than progesterone. The potency of the progestins to inhibit uterine motility was related to their capacity to induce membrane stabilization. The data indicates that 5 beta, but not 5 alpha reduction of progesterone, may be important for regulating myometrial activity.


Subject(s)
Pregnanes/pharmacology , Progestins/pharmacology , Uterine Contraction/drug effects , 20-alpha-Dihydroprogesterone/pharmacology , Animals , Diestrus , Dose-Response Relationship, Drug , Female , Isomerism , Pregnancy , Pregnanediol/pharmacology , Pregnanediones/pharmacology , Pregnanolone/pharmacology , Progesterone/pharmacology , Rats , Stereoisomerism , Structure-Activity Relationship
6.
Arch Invest Med (Mex) ; 8(2): 145-54, 1977.
Article in Spanish | MEDLINE | ID: mdl-334096

ABSTRACT

The hypnotic properties of leaves and seed of Casimiroa edulis (zapote blanco) a tropical fruit, are well known. In the present investigation, pharmacological studies on aqueous and alcoholic extracts were carried out in dogs, cats, rabbits and guinea pigs, using different experimental models. The action of the extracts upon blood pressure, cardiac activity, respiration rate, muscular tone, electroencephalographic activity, sleep and other parameters were studied too. In addition to, studies upon isolated human, cat, rabbit and guinea pig tissues gave information about the extracts effect on smooth muscle activity. It was found that both aqueous and alcoholic extract of the seed of zapote blanco produced marked hypotension in all animal species, which was followed by a sleep-like stage. Also a definitive oxitocic effect in vivo and in vitro was demonstrated suggesting the presence of a potent uterus constricting substance.


Subject(s)
Fruit , Plant Extracts/pharmacology , Animals , Blood Pressure/drug effects , Brain/drug effects , Cats , Dogs , Ethanol/analysis , Guinea Pigs , Heart Rate/drug effects , History, 16th Century , Pharmacology/history , Rabbits , Water/analysis
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