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多胺对分离的大鼠脂肪细胞抗脂解作用的表征

Characterization of antilipolytic action of polyamines in isolated rat adipocytes.

作者信息

Richelsen B, Pedersen S B, Hougaard D M

机构信息

University Clinic of Internal Medicin, Division of Endocrinology and Metabolism, Aarhus C, Denmark.

出版信息

Biochem J. 1989 Jul 15;261(2):661-5. doi: 10.1042/bj2610661.

Abstract

The interactions of polyamines with the lipolytic system were studied in isolated rat adipocytes. Spermine, spermidine and putrescine significantly inhibited adenosine deaminase-stimulated lipolysis. An antilipolytic effect of spermine was detectable at a concentration of 0.25 mM (P less than 0.05). At a concentration of 10 mM all three polyamines inhibited the stimulated lipolysis by 50-60% (P less than 0.001). In addition, spermine enhanced the antilipolytic sensitivity of insulin. Spermine (1 mM) decreased the half-maximal inhibitory concentration of insulin from 320 +/- 70 pM to 56 +/- 20 pM (P less than 0.01). The antilipolytic effects and the cyclic-AMP-lowering effects of the polyamines were almost completely prevented in the presence of different phosphodiesterase (PDE) inhibitors (3-isobutyl-1-methylxanthine and RO 20-1724) and, in addition, polyamines had no effect on lipolysis stimulated by dibutyryl cyclic AMP, indicating that polyamines may inhibit lipolysis by activating the PDE enzyme. This latter suggestion was confirmed by demonstrating that spermine (5 mM) significantly enhanced the low-Km PDE enzyme activity (P less than 0.01). Finally, the amounts of polyamines present in isolated adipocytes were measured, and the estimated cytoplasmic concentrations were 0.02 mM (putrescine), 0.86 mM (spermidine), and 1.0 mM (spermine). It is concluded that polyamines may possibly be involved in the physiological regulation of triacylglycerol mobilization in adipocytes.

摘要

在分离的大鼠脂肪细胞中研究了多胺与脂解系统的相互作用。精胺、亚精胺和腐胺显著抑制腺苷脱氨酶刺激的脂解作用。在浓度为0.25 mM时可检测到精胺的抗脂解作用(P<0.05)。在浓度为10 mM时,所有三种多胺均使刺激的脂解作用抑制50 - 60%(P<0.001)。此外,精胺增强了胰岛素的抗脂解敏感性。精胺(1 mM)使胰岛素的半数最大抑制浓度从320±70 pM降至56±20 pM(P<0.01)。在存在不同的磷酸二酯酶(PDE)抑制剂(3 - 异丁基 - 1 - 甲基黄嘌呤和RO 20 - 1724)的情况下,多胺的抗脂解作用和降低环磷酸腺苷的作用几乎完全被阻断,此外,多胺对二丁酰环磷酸腺苷刺激的脂解作用无影响,这表明多胺可能通过激活PDE酶来抑制脂解。通过证明精胺(5 mM)显著增强低Km PDE酶活性(P<0.01)证实了后一种推测。最后,测量了分离的脂肪细胞中多胺的含量,估计的细胞质浓度分别为0.02 mM(腐胺)、0.86 mM(亚精胺)和1.0 mM(精胺)。得出的结论是,多胺可能参与脂肪细胞中三酰甘油动员的生理调节。

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