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1.
Article in English | IMSEAR | ID: sea-135763

ABSTRACT

Background & objectives: Hyperprolactinaemia affects testicular functions by influencing hypothalamo-pituitary-testicular (HPT) axis at various levels. Available literature on the level of defect, time course of improvement of gonadal functions and its relation with decline in prolactin levels is scanty. We carried out this study to evaluate the HPT axis in patients with macroprolactinomas, before and six months after cabergoline therapy. Methods: Fifteen men with macroprolactinomas underwent gonadotropin and testosterone response to their respective stimuli before and after six months of cabergoline therapy. Results: Serum prolactin levels decreased after six months of therapy. Pretreatment, mean lutenizing and follicle stimulating hormones (LH and FSH) levels were 2.0 ± 0.4 and 1.4 ± 0.2 IU/l, respectively. However, LH and FSH responses to GnRH were preserved in majority of the patients and LH peaked to 12.1 ± 2.3 IU/l (P<0.01), while FSH to 2.9 ± 0.4 IU/l suggesting the influence of hyperprolactinaemia at the level of hypothalamus with preserved gonadotrope reserve. After cabergoline therapy, there was an increase in basal as well as stimulated LH and FSH levels, though these were not statistically significant when compared to respective pretherapy levels. Basal testosterone (T) levels significantly improved after therapy, but peak T response to hCG was similar at both pre- and post treatment. A significant correlation was observed between peak LH and peak T at baseline (r=0.53, P<0.01) and it further strengthened after therapy (r=0.70, P<0.01). After cabergoline therapy, there was significant improvement in seminal volume, sperm count and motility and sperm count correlated with peak FSH response (r=0.53, P<0.05). Interpretation & conclusions: Hyperprolactinaemia affects testicular functions probably by influencing at the level of hypothalamus resulting in subnormal basal secretion of gonadotropins required for optimal testicular functions.


Subject(s)
Analysis of Variance , Enzyme-Linked Immunosorbent Assay , Ergolines/pharmacology , Ergolines/therapeutic use , Follicle Stimulating Hormone/blood , Gonadotropin-Releasing Hormone/pharmacology , Humans , Hypothalamo-Hypophyseal System/metabolism , Luteinizing Hormone/blood , Magnetic Resonance Imaging , Male , Pituitary Neoplasms/drug therapy , Pituitary Neoplasms/pathology , Prolactin/blood , Prolactinoma/drug therapy , Prolactinoma/pathology , Radioimmunoassay , Sperm Count , Sperm Motility/drug effects , Testis/metabolism , Testosterone/blood , Time Factors
2.
Indian J Exp Biol ; 1990 May; 28(5): 409-16
Article in English | IMSEAR | ID: sea-62930

ABSTRACT

Present study evaluates the chemopreventive actions of tamoxifen (10 mg/kg), retinyl acetate (50 mg/kg), tocopherol (200 mg/kg), aminoglutethimide (1 mg/kg), ergocryptine (5 mg/kg), and sodium selenite (1 mg/kg) when given singly/in combinations on the initiation of mammary carcinogenesis induced by 20 mg of DMBA in virgin female rats. DMBA was given when rats were 50 days old and the modulators were given in diet 10 days before and 10 days after carcinogen treatment and experiments were terminated 6 months later. DMBA alone yielded tumors in 62% rats. When modulators were given singly and in combinations of two, tumor incidences were not altered significantly. The range of tumor incidences was between 30% and 13% when the agents were given in combinations of 3, 4 and 5. Finally when all 6 modulators were given together the tumor incidence dropped down to 8.3%.


Subject(s)
9,10-Dimethyl-1,2-benzanthracene , Aminoglutethimide/pharmacology , Animals , Drug Interactions , Ergolines/pharmacology , Female , Mammary Neoplasms, Experimental/prevention & control , Rats , Selenium/pharmacology , Tamoxifen/pharmacology , Vitamin A/analogs & derivatives , Vitamin E/pharmacology
3.
Cir. pediátr ; 3(2): 28-31, jun.-sept. 1984. ilus
Article in Spanish | LILACS | ID: lil-123210

ABSTRACT

Hemos evaluado en un estudio clínico con grupo control, los efectos de la Nicergolina en 2 grupos de niños, uno con retardo psicomotriz por Hipoxia neonatal y otro con disfunción cerebral mínima. Se evaluaron las variaciones en el EEG, y se efectuaron evaluaciones psicológicas, antes y después del tratamiento. Encontramos que todos los niños que recibieron el tratamiento presentaron una mejoría significativa, aunque durante el estudio, no se realizó estimulación temprana ni fisioterapia. Las pruebas estadísticas revelan una significación importante en los resultados; después de 30-45 días de tratamiento a una dosis de 15-30 mg/24 horas


Subject(s)
Humans , Male , Female , Child, Preschool , Adolescent , Nicergoline/pharmacology , Attention Deficit Disorder with Hyperactivity/diagnosis , Attention Deficit Disorder with Hyperactivity/psychology , Ergolines/pharmacology , Ergolines/therapeutic use , Psychomotor Disorders/diagnosis , Psychomotor Disorders/psychology , Psychomotor Disorders/therapy
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