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低热量饮食联合或不联合右旋芬氟拉明治疗对男性肥胖患者生长激素释放因子刺激后生长激素释放的影响。

The effect of hypocaloric diet with and without D-fenfluramine treatment on growth hormone release after growth hormone-releasing factor stimulation in patients with android obesity.

作者信息

Medeiros-Neto G, Lima N, Perozim L, Pedrinola F, Wajchenberg B L

机构信息

Division of Endocrinology, Hospital das Clinicas, University of São Paulo Medical School, Brazil.

出版信息

Metabolism. 1994 Aug;43(8):969-73. doi: 10.1016/0026-0495(94)90176-7.

Abstract

Basal and stimulated growth hormone (GH) secretions are impaired in obesity, and partial restoration of the GH response to various stimuli is observed after weight loss. The aim of the present study was to investigate whether D-fenfluramine, a serotoninergic agent, would increase the GH response to growth hormone-releasing factor (GRF) as compared with placebo in obese android patients. The subjects were 17 patients with android obesity (four men and 13 women) aged 21 to 58 years with a body mass index (BMI) ranging from 32.0 to 52.2 kg/m2 and an abdominal-gluteal ratio greater than 1.0. The following four GRF (1-44) tests were performed: T-30 (control), T0 (after 30 days of a hypocaloric diet), T1 (after 30 days of either placebo or D-fenfluramine 15 mg twice daily), and T2 (after 30 additional days of placebo or D-fenfluramine). The hypocaloric diet was maintained during the T1 and T2 periods. At each test, the serum GH response to GRF was measured at frequent intervals, and the peak GH response and the GH area under the curve were calculated. Serum insulin concentrations were also assayed before GRF stimulation, and the insulin to GH ratio was obtained. The D-fenfluramine-treated group had a mean +/- SEM GH peak level after GRF significantly higher at T1 (43.3 +/- 8.2 micrograms/L) and T2 (50.9 +/- 9.2 micrograms/L) compared with the placebo group. Likewise, the mean integrated areas of GH response were significantly higher for the D-fenfluramine-treated group as compared with the placebo group at both T1 and T2 of therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

肥胖症患者基础及刺激状态下的生长激素(GH)分泌均受损,体重减轻后可观察到GH对各种刺激的反应部分恢复。本研究旨在调查在肥胖男性化患者中,5-羟色胺能药物右芬氟拉明与安慰剂相比,是否能增强GH对生长激素释放因子(GRF)的反应。研究对象为17例男性化肥胖患者(4例男性和13例女性),年龄21至58岁,体重指数(BMI)为32.0至52.2kg/m2,腹臀比大于1.0。进行了以下四项GRF(1-44)试验:T-30(对照)、T0(低热量饮食30天后)、T1(安慰剂或右芬氟拉明15mg每日两次服用30天后)和T2(安慰剂或右芬氟拉明再服用30天后)。在T1和T2阶段维持低热量饮食。每次试验时,频繁测量血清GH对GRF的反应,并计算GH反应峰值和曲线下面积。在GRF刺激前还测定血清胰岛素浓度,并计算胰岛素与GH比值。与安慰剂组相比,右芬氟拉明治疗组在T1(43.3±8.2μg/L)和T2(50.9±9.2μg/L)时GRF后的平均±SEM GH峰值水平显著更高。同样,与安慰剂组相比,右芬氟拉明治疗组在治疗的T1和T2阶段GH反应的平均积分面积均显著更高。(摘要截短于250字)

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