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1.
Obstet Gynecol ; 88(4 Pt 1): 517-20, 1996 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-8841209

RESUMO

OBJECTIVE: To compare oxytocin infusion alone and with intravenous (i.v.) propranolol in the management of dysfunctional labor. METHODS: Ninety-six parturients with abnormalities of the active phase of labor were randomly assigned to either propranolol 2 mg IV or an identical placebo, in addition to continuous infusion of oxytocin. Administration of propranolol or placebo was repeated in 1 hour if there was no change in cervical dilation. Patients not responding to this second administration of propranolol or placebo were delivered by cesarean. RESULTS: Among 96 subjects enrolled, 49 were allocated to the propranolol group and 47 to the placebo group; 13 (26.5%) of the former were delivered by cesarean, compared with 24 (51.1%) of the latter (relative risk 0.58, 95% confidence interval 0.35-0.93; P = .02). Between the two groups, no differences were observed in low Apgar scores, cord arterial pH, or incidence of admissions to the neonatal intensive care nursery. Maternal morbidity was similar in both groups. After logistic regression analysis controlling for nulliparity, birth weight, and epidural anesthetic use, the significant reduction in the cesarean rate associated with use of propranolol persisted. Propranolol administration was associated with a markedly reduced cesarean rate among patients with inadequate uterine contractility. CONCLUSION: Low-dose administration of IV propranolol in patients with dysfunctional labor augmented with oxytocin safely reduced the need for cesarean delivery, particularly among patients with inadequate uterine contractility.


Assuntos
Antagonistas Adrenérgicos beta/administração & dosagem , Distocia/tratamento farmacológico , Ocitocina/administração & dosagem , Propranolol/administração & dosagem , Adulto , Cesárea , Parto Obstétrico , Método Duplo-Cego , Quimioterapia Combinada , Distocia/fisiopatologia , Feminino , Humanos , Infusões Intravenosas , Modelos Logísticos , Gravidez , Contração Uterina/efeitos dos fármacos
4.
J Cell Biol ; 101(6): 2345-54, 1985 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-4066762

RESUMO

We report here new characteristics of cell surface tubulin from a human leukemia cell line. These cells (CEM cells) possess tubulin that is readily iodinated on the surface of living cells, turns over at a rate identical to that of other surface proteins, and is present throughout the cell cycle. When removed with trypsin, it rapidly returns to the surface. Peptide mapping of iodinated surface tubulin indicates that it possesses a similar, but not identical, primary structure to total CEM and rat brain tubulin. Living CEM cells are able to bind specifically a subfraction of CEM tubulin from metabolically labeled high speed supernatants of lysed CEM cells. Surface tubulin is more basic than the total tubulin pool. The binding, which is saturable, is inhibited by unlabeled CEM high speed supernatants but not by excess thrice-cycled rat or bovine brain tubulin. Surface tubulin is also shown to bind to living nontransformed normal rat kidney cells but not to normal, circulating, mononuclear white cells. Activated lymphocytes produce a tubulin that binds to CEM cells. Since CEM tubulin was detected in the media of 6-h cultures of CEM cells, we must conclude that at least some of the surface tubulin comes from the media. We further conclude that these leukemic cells produce an unusual tubulin that may bind specifically to any membrane. The presence of iodinatable surface tubulin, however, appears to require both the production of a unique tubulin and the presence of a "receptor-like" surface binding component.


Assuntos
Membrana Celular/metabolismo , Leucemia/patologia , Tubulina (Proteína)/metabolismo , Animais , Ligação Competitiva , Ciclo Celular , Linhagem Celular , Humanos , Ponto Isoelétrico , Leucemia/metabolismo , Leucemia L1210/metabolismo , Camundongos , Ligação Proteica
5.
J Behav Ther Exp Psychiatry ; 13(2): 123-30, 1982 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-6890074

RESUMO

An adaptation of Anxiety Management Training was evaluated as a means of teaching women to use relaxation in order to control menstrual pain and discomfort. After reporting their menstrual symptoms for two successive baseline periods, spasmodic and congestive dysmenorrheic subjects received four individual sessions of pain management training. Following treatment, these subjects reported significant reductions in pain, discomfort, interference, and time loss due to dysmenorrheic symptoms relative to their own baselines and to an untreated control group. These effects were still in evidence 18 months after treatment and appeared to have generalized to behavioral, attentional and autonomic symptoms that might be considered secondary sequelae of dysmenorrhea. With one minor exception, there was no differential response to treatment by spasmodic as opposed to congestive subjects.


Assuntos
Terapia Comportamental/métodos , Dismenorreia/terapia , Adulto , Dismenorreia/psicologia , Feminino , Seguimentos , Humanos , Síndrome Pré-Menstrual/psicologia , Síndrome Pré-Menstrual/terapia
6.
Cancer Res ; 42(4): 1384-9, 1982 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-6949640

RESUMO

Surface-exposed proteins of vinblastine-sensitive human lymphoid cell line of leukemic origin (CCRF-CEM) were examined by the lactoperoxidase-catalyzed iodination and two-dimensional polyacrylamide gel electrophoresis methods. Spots which comigrate with bovine brain tubulin and rabbit muscle actin were prominently labeled in the whole membrane but not in the high-speed supernatant fraction of the disrupted cells. Mild trypsinization of labeled cells removed the iodinated tubulin and actin without significantly affecting the protein staining pattern. Iodination of normal human lymphocytes resulted in no labeling of the tubulin or actin. The presence of surface-exposed tubulin in this leukemic cell line suggests a possible mechanism for their enhanced sensitivity to the cytotoxic action of vinblastine.


Assuntos
Leucemia Linfoide/análise , Proteínas de Membrana/análise , Tubulina (Proteína)/análise , Linhagem Celular , Humanos , Tripsina/farmacologia
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