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2.
Gynecol Endocrinol ; 20(1): 6-12, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15969240

RESUMO

The present study was undertaken to elucidate whether estriol (E3) affects the proliferative activity and the expression of insulin-like growth factor-I (IGF-I) mRNA and IGF-I receptor (IGF-IR) mRNA in cultured human osteoblast-like osteosarcoma cells (HOS TE85). In this study, the effects of E3 on cultured HOS TE85 cells were compared with those of 17 beta-estradiol (E2). HOS TE85 cells were subcultured in phenol red-free Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum for 72 h and then stepped down to serum-free conditions for an additional 72 h in the absence or presence of E3 (3.52 x 10(-9), 3.52 x 10(-8), 3.52 x 10(-7) mol/l) or E2 (3.67 x 10(-8) mol/l). Treatment with either E3 (3.52 x 10(-8), 3.52 x 10(-7) mol/l) or E2 (3.67 x 10(-8) mol/l) resulted in an increase in the number of cultured HOS TE85 cells and their uptake of bromodeoxyuridine. Northern blot hybridization with a IGF-I cDNA probe revealed that RNA prepared from cultured HOS TE85 cells contained IGF-I mRNA transcripts of 1.8, 4.4 and 7.5 kb. Treatment with either E3 (3.52 x 10(-9), 3.52 x 10(-8), 3.52 x 10(-7) mol/l) or E2 (3.67 x 10(-8) mol/l) resulted in increased expression of the three mRNA transcripts relative tot hose in untreated control cultures. Semi-quantitative, reverse transcription polymerase chain reaction analysis showed that the 440-bp IGF-IR mRNA transcript was present in HOS TE85 cells and that treatment with either E3 or E2 did not affect the IGF-IRmRNA expression in these cells. These results demonstrate that E3 (3.52 x 10(-9), 3.52 x 10(-8), 3.52 x 10(-7) mol/l) exerts profound effects on the proliferative potential of cultured HOS TE85 cells, compatible with that of E2 (3.67 x 10(-8) mol/l), through the induction of IGF-I mRNA expression without affecting IGF-IR mRNA expression in these cells.


Assuntos
Proliferação de Células/efeitos dos fármacos , Estriol/farmacologia , Fator de Crescimento Insulin-Like I/efeitos dos fármacos , Osteossarcoma/fisiopatologia , Receptor IGF Tipo 1/efeitos dos fármacos , Bromodesoxiuridina/metabolismo , Estradiol/farmacologia , Humanos , Fator de Crescimento Insulin-Like I/biossíntese , Osteoblastos/efeitos dos fármacos , Osteoblastos/fisiologia , RNA Mensageiro/biossíntese , RNA Mensageiro/efeitos dos fármacos , Receptor IGF Tipo 1/biossíntese , Células Tumorais Cultivadas
3.
Gynecol Obstet Invest ; 59(2): 67-9, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15542934

RESUMO

BACKGROUND: Several studies show that 17beta-estradiol (E2) has protective effects on atherosclerosis in the arterial wall in postmenopausal women. Little information is, however, available regarding the effect of estriol (E3) on atherosclerosis. This study was conducted to investigate the effects of E3 alone and combined E3/pravastatin therapy on intima-media thickness (IMT) of common carotid artery in postmenopausal women. METHODS: Thirty-three postmenopausal women were allocated to four groups: daily treatment with E3 (2 mg) alone (E3 group, n = 10), pravastatin (10 mg) alone (pravastatin group, n = 6), combined treatment with E3 (2 mg) and pravastatin (10 mg; E3/pravastatin group, n = 7) and untreated control group (n = 10). All women attended the Kobe University Hospital once a year for routine gynecological and ultrasonographic examinations for the evaluation of atherosclerosis. RESULTS: A significant decrease in IMT was noted in the E3/pravastatin group compared with that in the untreated control group (p < 0.05), whereas there was no significant difference in the reduction rate of IMT in the pravastatin group, E3 group and untreated control group. CONCLUSIONS: The combined E3/pravastatin therapy appeared to retard the progression of atherosclerosis in postmenopausal women.


Assuntos
Arteriosclerose/tratamento farmacológico , Arteriosclerose/prevenção & controle , Artéria Carótida Primitiva/efeitos dos fármacos , Estriol/administração & dosagem , Pós-Menopausa , Pravastatina/administração & dosagem , Artéria Carótida Primitiva/diagnóstico por imagem , Progressão da Doença , Quimioterapia Combinada , Feminino , Humanos , Inibidores de Hidroximetilglutaril-CoA Redutases/administração & dosagem , Resultado do Tratamento , Túnica Íntima/efeitos dos fármacos , Túnica Média/efeitos dos fármacos , Ultrassonografia
4.
Fetal Diagn Ther ; 18(6): 447-53, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-14564118

RESUMO

OBJECTIVES: To evaluate prenatal MRI in the diagnosis of fetal thoracic abnormalities and to determine whether MRI provides useful information in addition to that of ultrasonography (US). METHODS: Ultrafast MR scanning was performed in 7 pregnant women in whom US was suspicious of fetal congenital anomalies of the thorax [3 cases of congenital diaphragmatic hernia (CDH), 3 cases of chylothorax and 1 case of congenital cystic adenomatoid malformation (CCAM) type III]. The presence, position, size and characteristics of the congenital lesions were determined and compared with postnatal diagnoses. RESULTS: The MRI diagnoses were 3 cases of CDH, 2 of chylothorax and one each of esophageal atresia and CCAM type III. The results of MRI were in agreement with those of US in 6 cases and in disagreement in 1 case of esophageal atresia. Final diagnoses were confirmed at surgery or autopsy in all fetuses. Combined use of MR and US imaging enabled a correct diagnosis in 5 cases and led to an error in the diagnosis of 1 fetus with bronchial stenosis, which had been diagnosed as CCAM type III by US and MRI. MRI led to a correct diagnosis in 1 fetus with esophageal atresia, in whom US had been equivocal in the prenatal diagnosis. CONCLUSION: MRI helped further characterize the fetal thoracic lesions and confirmed or changed the prenatal diagnosis based on US. MRI seems to be powerful in the prenatal diagnosis of thoracic lesions that are atypical or complicated by multiple abnormalities.


Assuntos
Imageamento por Ressonância Magnética/métodos , Tórax/anormalidades , Tórax/diagnóstico por imagem , Ultrassonografia Pré-Natal/métodos , Adulto , Quilotórax/diagnóstico , Quilotórax/diagnóstico por imagem , Atresia Esofágica/diagnóstico , Atresia Esofágica/diagnóstico por imagem , Feminino , Hérnia Diafragmática/diagnóstico , Hérnia Diafragmática/diagnóstico por imagem , Humanos , Gravidez , Estudos Prospectivos , Tórax/patologia
6.
J Perinat Med ; 30(3): 273-5, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12122912

RESUMO

Diabetes insipidus during pregnancy is an uncommon medical problem, and its cause is not entirely clear. We present a woman with twin pregnancy associated with HELLP syndrome, who developed diabetes insipidus during postpartum period. A hypertonic saline infusion study with measurement of plasma arginine vasopressin concentrations confirmed the diagnosis. She had mild response to 1-desamino-8-d-arginine-vasopressin (dDAVP) during the immediate postpartum period. On the 3rd postpartum day two doses of 100 microliters of dDAVP were administered, and her urinary volume gradually decreased. We could stop dDAVP on the 30th postpartum day. This exacerbation may result from increased vasopressinase activity caused by the excessive production in the placenta due to twin pregnancy, together with the insufficient degradation in the liver due to HELLP syndrome.


Assuntos
Diabetes Insípido/diagnóstico , Síndrome HELLP/complicações , Transtornos Puerperais , Gêmeos , Adulto , Cesárea , Desamino Arginina Vasopressina/uso terapêutico , Diabetes Insípido/tratamento farmacológico , Feminino , Idade Gestacional , Síndrome HELLP/diagnóstico , Síndrome HELLP/terapia , Humanos , Gravidez
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