37 research outputs found
Effects of long term E2 administration on plasma levels of nitric oxide in postmenopausal women
Effects of short-term transdermal estradiol administration on plasma levels of nitric oxide in postmenopausal women.
Objective: To assess the effects of short-term transdermal E, administration on nitric oxide (NO) plasma levels in postmenopausal women. Design: Randomized, placebo-controlled trial. Setting: Healthy volunteers in an academic research environment.
Patient(s): Twenty-eight healthy postmenopausal women. Intervention(s): Transdermal administration of E, (100 pg/d) or placebo on days 1 and 4 of a l-week treatment regimen. Main Outcome Measure(s): Serum concentrations of E, and plasma concentrations of NO stable oxidation products were assessed on day 1, before placement of the patch, and subsequently on days 2, 3, and 6. Result(s): The mean concentration of NO metabolites on days 2, 3, and 6 was significantly greater in the E, group (40.08 5 15.42 pmol/L, 38.05 _+ 18.82 pmol/L, and 42.03 5 16.81 pmol/L on days 2, 3, and 6, respectively) compared with both baseline levels (23.07 + 5.79 PmolL) and the placebo group (23.51 2 4.06 PmolIL, 21.64 + 4.72 Fmol/L, and 21.81 2 4.46 pmol/L on days 2, 3, and 6, respectively). Conclusion(s): During a l-week treatment regimen with transdermal E,, plasma levels of NO in postmenopausal women were significantly higher than baseline levels on days 2, 3, and 6. This suggests that the effect of estrogens on NO synthesis is rapid and that it is maintained with repeated administration. (Fertil SteriP 1998;69:58-61. 01998 by American Society for Reproductive Medicine.
Variation in nitric oxide production induced by HRT
.Cagliari (Forte Village, Santa Margherita di Pula)
Acute effects of transdermal estradiol administration on plasma levels of NO in postmenopausal women
Objective: To investigate the acute effects of transdermal E2 administration on nitric oxide {NO} plasma levels in postmenopausal women.
Design: Randomized, placebo-controlled trial. Setting: Normal human volunteers in an academic research environment. Patient(s): Twenty healthy postmenopausal women. Intervention(s): Transdermal administration of 100 pg/d E2 or placebo. Main Outcome Measure(s): Plasma concentrations of NO stable oxidation products and
serum concentrations of E._,were assessed before and 24 hours after the administration. Result(s): In the group treated with E2 mean concentration of NO metabolites 24 hours after patch application (37.31 +_7.62 pmol/L) resulted significantly higher than baseline (21.04 ___5.71 pmol/L) and the control group/23.50 _+4.03 pmol/L). The correlation between the mean percent
increase in NO metabolites and absolute E., concentrations 24 hours after the E.~administration was statistically significant.
Conclusion(s): Transderma] administration of E2 to healthy postmenopausal women in- creases the plasma levels of NO and this supports the hypothesis that a NO-related mechanism may contribute to the cardiovascular protective effect of estrogens in postmenopause
Nasal spray bromocriptine: Effects on serum prolactin in puerperal women
Abstract
BACKGROUND:
The objective of this study was to investigate the effectiveness of a single nasal spray administration of 0.8 mg bromocriptine in reducing PRL serum levels.
METHODS:
Eighteen physiologically hyperprolactemic women in the early days of puerperium were randomized to receive nasal bromocriptine or placebo; PRL serum levels were measured by RIA at 45, 30 and 15 minutes before the administration and after the following times: 15, 30, 45, 60, 120, 180, 240, 300, and 480 minutes.
RESULTS:
After the administration of bromocriptine serum levels of PRL decreased rapidly; the reduction was statistically significant after 45 minutes. Four hours after the administration mean serum levels of PRL resulted in the normal range (< 20 micrograms/l); at the eighth hour the PRL levels were still normal. No one patient complained of any local or systemic side-effects.
CONCLUSION:
Nasal route seems to be an effective and probably safe administration route for bromocriptine