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类固醇激素对大鼠脂肪组织中瘦素的调节作用。

Regulation of leptin by steroid hormones in rat adipose tissue.

作者信息

Kristensen K, Pedersen S B, Richelsen B

机构信息

Department of Endocrinology and Metabolism, Aarhus University Hospital, Aarhus Amtssygehus, Aarhus C., DK-8000, Denmark.

出版信息

Biochem Biophys Res Commun. 1999 Jun 16;259(3):624-30. doi: 10.1006/bbrc.1999.0842.

Abstract

We investigated if steroid hormones regulate the secretion and the expression of leptin in female and male rat adipose tissue fragments in vitro. Dexamethasone time and dose-dependently increased the secretion and mRNA expression of leptin with a half-maximal stimulation of approximately 1 nM. A time-course revealed a maximal stimulatory effect of 17 beta-estradiol after 24 hours. In male adipose tissue 17 beta-estradiol increased leptin secretion (32% by 50 nM 17 beta-estradiol, P = 0.07 and 34% by 500 nM 17 beta-estradiol, P < 1780.05) after 24 hours. An additional effect of estrogen was seen in the dexamethasone (50 nM) stimulated cells (38% with 50 nM 17 beta-estradiol, P < 0.05 and 48% by 500 nM 17 beta-estradiol, P < 0.05). Basal secretion of leptin was equal in female and male adipose tissue, whereas the effects of 17 beta-estradiol (50 nM) and dexamethasone were significantly increased in female as compared with male adipose tissue. Progesterone, testosterone, dihydrotestosterone and dehydroepiandrostendione-sulfate neither affected leptin secretion in male nor female adipose tissue in vitro. Furthermore, to investigate the effect of estrogen female rats were ovariectomized (OVX) and the adipose tissue was incubated in vitro and compared with adipose tissue leptin secretion from sham operated rats (SHAM), and with ovariectomized rats treated with 17 beta-estradiol (EST). A decreased basal and dexamethasone-stimulated leptin secretion from OVX rats compared with SHAM rats was found (P < 0.005) whereas 17 beta-estradiol treatment of ovariectomized rats maintained a normal leptin secretion. However, the dexamethasone stimulation was equally increased above basal levels in SHAM, OVX and EST rats (3.7 +/- 1.2, 2.9 +/- 0.8, 4.2 +/- 1.4, NS, ANOVA) respectively.

摘要

我们研究了类固醇激素是否在体外调节雌性和雄性大鼠脂肪组织碎片中瘦素的分泌和表达。地塞米松在时间和剂量上均呈依赖性地增加瘦素的分泌和mRNA表达,半最大刺激浓度约为1 nM。时间进程显示,24小时后17β-雌二醇具有最大刺激作用。在雄性脂肪组织中,24小时后17β-雌二醇增加了瘦素分泌(50 nM 17β-雌二醇增加32%,P = 0.07;500 nM 17β-雌二醇增加34%,P < 0.05)。在经地塞米松(50 nM)刺激的细胞中观察到雌激素的额外作用(50 nM 17β-雌二醇增加38%,P < 0.05;500 nM 17β-雌二醇增加48%,P < 0.05)。雌性和雄性脂肪组织中瘦素的基础分泌相等,然而,与雄性脂肪组织相比,17β-雌二醇(50 nM)和地塞米松对雌性脂肪组织的作用显著增强。孕酮、睾酮、二氢睾酮和硫酸脱氢表雄酮在体外对雄性和雌性脂肪组织中的瘦素分泌均无影响。此外,为了研究雌激素的作用,对雌性大鼠进行卵巢切除术(OVX),并将脂肪组织进行体外培养,与假手术大鼠(SHAM)的脂肪组织瘦素分泌以及接受17β-雌二醇(EST)治疗的卵巢切除大鼠进行比较。发现与SHAM大鼠相比,OVX大鼠的基础和地塞米松刺激的瘦素分泌减少(P < 0.005),而对卵巢切除大鼠进行17β-雌二醇治疗可维持正常的瘦素分泌。然而,地塞米松刺激在SHAM、OVX和EST大鼠中分别比基础水平同等程度增加(3.7±1.2、2.9±0.8、4.2±1.4,无显著性差异,方差分析)。

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