Correia M L, Morgan D A, Mitchell J L, Sivitz W I, Mark A L, Haynes W G
Specialized Center of Research in Hypertension Genetics, Department of Internal Medicine, University of Iowa, and Veterans Affairs Medical Center, Iowa City, Iowa 52242, USA.
Hypertension. 2001 Sep;38(3):384-8. doi: 10.1161/01.hyp.38.3.384.
Leptin and corticotrophin-releasing factor increase sympathetic nervous activity to interscapular brown adipose tissue, kidneys, and adrenal glands. Leptin is known to increase hypothalamic corticotrophin-releasing factor. In this study, we tested the hypothesis that leptin-dependent increases in sympathetic nervous activity are mediated through increases in central nervous system corticotrophin-releasing factor activity. We examined the effects of intracerebroventricular administration of corticotrophin-releasing factor and intravenous leptin on sympathetic nervous activity to interscapular brown adipose tissue through multifiber neurography in anesthetized Sprague-Dawley rats pretreated with intracerebroventricular alpha-helical corticotrophin-releasing factor(9-41) (corticotrophin-releasing factor receptor antagonist) or vehicle. Centrally administered corticotrophin-releasing factor substantially increased interscapular brown adipose tissue sympathetic nervous activity. The responses to corticotrophin-releasing factor were substantially attenuated in animals pretreated with alpha-helical corticotrophin-releasing factor(9-41). Leptin-dependent increases in interscapular brown adipose tissue sympathetic nervous activity were significantly inhibited by pretreatment with alpha-helical corticotrophin-releasing factor(9-41). Interestingly, leptin also significantly increased arterial pressure over 6 hours, but this pressor action was not attenuated by the corticotrophin-releasing factor receptor antagonist. These results suggest that corticotrophin-releasing factor may mediate the sympathoexcitatory effect of leptin on thermogenic tissue without altering its cardiovascular actions.
瘦素和促肾上腺皮质激素释放因子可增强对肩胛间棕色脂肪组织、肾脏及肾上腺的交感神经活动。已知瘦素可增加下丘脑促肾上腺皮质激素释放因子的含量。在本研究中,我们验证了以下假说:瘦素依赖性交感神经活动增强是通过中枢神经系统促肾上腺皮质激素释放因子活性增加介导的。我们通过多纤维神经电图,在经脑室内注射α-螺旋促肾上腺皮质激素释放因子(9-41)(促肾上腺皮质激素释放因子受体拮抗剂)或溶剂预处理的麻醉Sprague-Dawley大鼠中,研究了脑室内注射促肾上腺皮质激素释放因子和静脉注射瘦素对肩胛间棕色脂肪组织交感神经活动的影响。中枢给予促肾上腺皮质激素释放因子可显著增强肩胛间棕色脂肪组织的交感神经活动。在预先注射α-螺旋促肾上腺皮质激素释放因子(9-41)的动物中,对促肾上腺皮质激素释放因子的反应显著减弱。预先注射α-螺旋促肾上腺皮质激素释放因子(9-41)可显著抑制瘦素依赖性肩胛间棕色脂肪组织交感神经活动增强。有趣的是,瘦素在6小时内也显著升高动脉血压,但这种升压作用并未被促肾上腺皮质激素释放因子受体拮抗剂减弱。这些结果表明,促肾上腺皮质激素释放因子可能介导瘦素对产热组织的交感兴奋作用,而不改变其心血管作用。