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啮齿动物棕色脂肪组织中苯二氮䓬结合位点的药理学和生理学特性。

Pharmacological and physiological properties of benzodiazepine binding sites in rodent brown adipose tissue.

作者信息

Hirsch J D

出版信息

Comp Biochem Physiol C Comp Pharmacol Toxicol. 1984;77(2):339-43. doi: 10.1016/0742-8413(84)90025-2.

Abstract

[3H]Diazepam and [3H] Ro5 -4864 were used as ligands to identify and characterize peripheral-type benzodiazepine binding sites in mouse and rat brown adipose tissue (BAT) membranes. [3H]Diazepam and [3H] Ro5 -4864 binding sites in BAT are pharmacologically similar to peripheral-type benzodiazepine binding sites in other tissues. Stimulators of central-type benzodiazepine receptors had no effect on or inhibited ligand binding to BAT membranes. Brown adipose tissue benzodiazepine binding sites are highly localized to mitochondria-containing subcellular fractions. These binding sites decrease with age in BAT from Fischer 344 rats. Stimulation of BAT thermogenesis in mice with 1-norepinephrine led to a decrease in [3H] Ro5 -4864 binding in the tissue.

摘要

[3H]地西泮和[3H]Ro5-4864被用作配体,以鉴定和表征小鼠和大鼠棕色脂肪组织(BAT)膜中的外周型苯二氮䓬结合位点。BAT中的[3H]地西泮和[3H]Ro5-4864结合位点在药理学上与其他组织中的外周型苯二氮䓬结合位点相似。中枢型苯二氮䓬受体的刺激剂对BAT膜的配体结合没有影响或抑制其结合。棕色脂肪组织苯二氮䓬结合位点高度定位于含线粒体的亚细胞组分。在Fischer 344大鼠的BAT中,这些结合位点随年龄增长而减少。用1-去甲肾上腺素刺激小鼠的BAT产热导致组织中[3H]Ro5-4864结合减少。

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