Publications by authors named "Rosa E Galvan"

Background: Adiponectin is an hormone produced exclusively in adipose tissue, that actively acts in carbohydrate and fat regulation processes.

Objective: To determine adiponectin levels in a women's group.

Patients And Method: Transversal study in 22 amenorrheal women with climacteric symptoms, and without estrogen therapy.

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Background: Adiponectin has a direct relationship with cellular sensibility grade to insulin action.

Objective: To determine adiponectin concentrations during the three phases of the menstrual cycle in young women, and to study the relationship with 17-beta estradiol and progesterone levels.

Patient And Methods: Longitudinal and prospective study that included 30 normal menstruating women aged between 19 and 36 years; none had received any hormonal therapy prior to this study.

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Objective: To compare the effect of oral and transdermal estrogen replacement therapy (ET) on circulating interleukin-6 (IL-6) in post-menopausal women.

Patients And Method: Prospective open trial study in 55 healthy hysterectomized postmenopausal women with a mean age of 52 years. Twenty-seven women received oral conjugated equine estrogens (0.

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Hyperglycemia is associated with metabolic disturbances affecting cell redox potential, particularly the NADPH/NADP+ ratio and reduced glutathione levels. Under oxidative stress, the NADPH supply for reduced glutathione regeneration is dependent on glucose-6-phosphate dehydrogenase. We assessed the effect of different hyperglycemic conditions on enzymatic activities involved in glutathione regeneration (glucose-6-phosphate dehydrogenase and glutathione reductase), NADP(H) and reduced glutathione concentrations in order to analyze the relative role of these enzymes in the control of glutathione restoration.

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Aim: To determine the expression of two isoforms of the growth hormone (GH) receptor (GHR), which differ by the presence (GHR3+) or absence (GHR3-) of exon 3, and their correlation with circulating GH and insulin-like growth factor I (IGF-I) in normal subjects and in acromegalic patients.

Methods: The expression of GHR isoforms was determined by reverse-transcriptase polymerase chain reaction in lymphocytes from 12 normal subjects and from 11 patients with acromegaly. The levels of GHR mRNA were normalized to those of beta-actin, and ratios were calculated to assess the relative levels of expression.

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