脑源性神经营养因子通过中枢神经系统调节肥胖糖尿病小鼠的能量消耗。

T Nonomura, A Tsuchida, M Ono-Kishino, T Nakagawa, M Taiji, H Noguchi
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引用次数: 1

摘要

先前已经证明脑源性神经营养因子(BDNF)调节啮齿动物糖尿病模型(如C57BL/KsJ-lepr(db)/lepr(db) (db/db)小鼠)的葡萄糖代谢和能量消耗。BDNF中枢给药可以降低小鼠的血糖,这表明BDNF通过中枢神经系统起作用。在本研究中,我们扩展了这些研究,以探索中枢给药BDNF对能量代谢的影响。脑室内给药BDNF降低了db/db小鼠的血糖,并增加了配对给药的db/db小鼠的胰腺胰岛素含量。在这种配对喂养条件下,给药的db/db小鼠由于食物供应受限,体温下降,而BDNF处理显著缓解了体温下降,提示产热能力增强。BDNF增强去甲肾上腺素的转换,增加肩胛间棕色脂肪组织解偶联蛋白-1 mRNA的表达。我们的证据表明,BDNF通过中枢神经系统激活交感神经系统,调节肥胖糖尿病动物的能量消耗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brain-derived neurotrophic factor regulates energy expenditure through the central nervous system in obese diabetic mice.

It has been previously demonstrated that brain-derived neurotrophic factor (BDNF) regulates glucose metabolism and energy expenditure in rodent diabetic models such as C57BL/KsJ-lepr(db)/lepr(db) (db/db) mice. Central administration of BDNF has been found to reduce blood glucose in db/db mice, suggesting that BDNF acts through the central nervous system. In the present study we have expanded these investigations to explore the effect of central administration of BDNF on energy metabolism. Intracerebroventricular administration of BDNF lowered blood glucose and increased pancreatic insulin content of db/db mice compared with vehicle-treated pellet pair-fed db/db mice. While body temperatures of the pellet pair-fed db/db mice given vehicle were reduced because of restricted food supply in this pair-feeding condition, BDNF treatment remarkably alleviated the reduction of body temperature suggesting the enhancement of thermogenesis. BDNF enhanced norepinephrine turnover and increased uncoupling protein-1 mRNA expression in the interscapular brown adipose tissue. Our evidence indicates that BDNF activates the sympathetic nervous system via the central nervous system and regulates energy expenditure in obese diabetic animals.

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