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对重度肥胖受试者分离出的脂肪组织细胞进行的体外观察。

In-vitro observations on isolated adipose tissue cells from hyperobese subjects.

作者信息

Burns T W, Terry B E, Langley P E, Robison G A

出版信息

Diabetes. 1977 Jul;26(7):657-62. doi: 10.2337/diab.26.7.657.

Abstract

Isolated adipose tissue cells were prepared from subcutaneous samples obtained from nine morbidly obese subjects weighing from 187 to 306% of ideal body weight. The responsiveness of these adipocytes to a number of test substances was determined by measuring cellular cyclic AMP concentration at one-half hour and glycerol release at four hours. Theophylline (10(-3) M) and epinephrine (10(-5) M) stimulated lipolysis; theophylline stimulated an increase in cyclic AMP, while epinephrine failed to prompt a significant change in the nucleotide. Neither the alpha blocker, phentolamine (10(-5) M), nor the beta blocker, propranolol (3 X 10(-5) M), affected lipolysis or cyclic AMP; when these agents were incubated in combination with epinephrine, changes occurred indicative of the presence of both alpha and beta adrenergic receptor sites. Insulin significantly reduced both basal and stimulated lipolysis but failed to affect cyclic AMP. With minor exceptions, adipocytes from hyperobese subjects behaved similarly to cells from unselected donors; at the concentration used, there was no evidence of resistance to insulin.

摘要

从9名病态肥胖受试者的皮下样本中制备了分离的脂肪组织细胞,这些受试者的体重为理想体重的187%至306%。通过在半小时时测量细胞内环磷酸腺苷(cAMP)浓度和在4小时时测量甘油释放量,来确定这些脂肪细胞对多种测试物质的反应性。茶碱(10⁻³ M)和肾上腺素(10⁻⁵ M)刺激脂肪分解;茶碱刺激cAMP增加,而肾上腺素未能促使该核苷酸发生显著变化。α受体阻滞剂酚妥拉明(10⁻⁵ M)和β受体阻滞剂普萘洛尔(3×10⁻⁵ M)均未影响脂肪分解或cAMP;当这些药物与肾上腺素一起孵育时,出现了表明同时存在α和β肾上腺素能受体位点的变化。胰岛素显著降低了基础和刺激状态下的脂肪分解,但未影响cAMP。除了少数例外情况,极度肥胖受试者的脂肪细胞与未选择的供体的细胞表现相似;在所使用的浓度下,没有证据表明对胰岛素有抵抗。

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