Analysis of the interactions between growth hormone and metaproterenol on lipid mobilization.

Revista espanola de fisiologia Pub Date : 1995-09-01
M P Portillo, A S del Barrio, J A Martínez
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Abstract

The possible modification of the in vitro lipolytic action of rat growth hormone (rGH) or a mixed beta-adrenergic agonist (metaproterenol) on rat adipose tissue after a previous acute treatment with these compounds was assessed by measuring glycerol release from adipocytes. The involvement of adenosine deaminase (ADA) and dexamethasone, was also considered. The results showed that the previous acute treatment with rGH or the beta-adrenergic agonist did not alter the in vitro rGH or metaproterenol lipolytic response. The presence of ADA at a non-lipolytic concentration per se (0.02 U/ml) potentiated the lipolytic response of both compounds. Also, the addition of non-lipolytic concentrations of dexamethasone (0.5 microM) or beta-adrenergic agonist (10(-7)M) to the incubation medium potentiated the rGH lipolytic response, while the metaproterenol-induced glycerol release was not affected by the simultaneous addition of a rGH concentration (2 x 10(-7) M) which had no lipolytic effect per se.

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生长激素与甲肾上腺素对脂质动员的相互作用分析。
大鼠生长激素(rGH)或混合β -肾上腺素能激动剂(甲丙肾上腺素)对大鼠脂肪组织进行急性治疗后,体外溶脂作用的可能改变是通过测量脂肪细胞的甘油释放来评估的。还考虑了腺苷脱氨酶(ADA)和地塞米松的作用。结果表明,以前的急性治疗与rGH或β肾上腺素激动剂没有改变体外rGH或甲肾上腺素的溶脂反应。ADA在非脂溶性浓度下(0.02 U/ml)的存在增强了两种化合物的脂溶性反应。此外,在培养液中加入非脂溶性浓度的地塞米松(0.5 μ M)或β -肾上腺素能激动剂(10(-7)M)可以增强rGH的脂溶反应,而同时加入浓度为2 × 10(-7)M的rGH本身没有脂溶作用,因此甲丙肾上腺素诱导的甘油释放不受影响。
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