VA Puget Sound Health Care System, Office of Research and Development Medical Research Service, Department of Veterans Affairs Medical Center, Seattle, WA, United States.
Division of Cardiology, Department of Medicine, University of Washington School of Medicine, Seattle, WA, United States.
Front Endocrinol (Lausanne). 2024 Jul 31;15:1440070. doi: 10.3389/fendo.2024.1440070. eCollection 2024.
Previous studies indicate that CNS administration of oxytocin (OT) reduces body weight in high fat diet-induced obese (DIO) rodents by reducing food intake and increasing energy expenditure (EE). We recently demonstrated that hindbrain (fourth ventricular [4V]) administration of OT elicits weight loss and elevates interscapular brown adipose tissue temperature (T, a surrogate measure of increased EE) in DIO mice. What remains unclear is whether OT-elicited weight loss requires increased sympathetic nervous system (SNS) outflow to IBAT. We hypothesized that OT-induced stimulation of SNS outflow to IBAT contributes to its ability to activate BAT and elicit weight loss in DIO mice. To test this hypothesis, we determined the effect of disrupting SNS activation of IBAT on the ability of 4V OT administration to increase T and elicit weight loss in DIO mice. We first determined whether bilateral surgical SNS denervation to IBAT was successful as noted by ≥ 60% reduction in IBAT norepinephrine (NE) content in DIO mice. NE content was selectively reduced in IBAT at 1-, 6- and 7-weeks post-denervation by 95.9 ± 2.0, 77.4 ± 12.7 and 93.6 ± 4.6% (<0.05), respectively and was unchanged in inguinal white adipose tissue, pancreas or liver. We subsequently measured the effects of acute 4V OT (1, 5 µg ≈ 0.99, 4.96 nmol) on T in DIO mice following sham or bilateral surgical SNS denervation to IBAT. We found that the high dose of 4V OT (5 µg ≈ 4.96 nmol) elevated T similarly in sham mice as in denervated mice. We subsequently measured the effects of chronic 4V OT (16 nmol/day over 29 days) or vehicle infusions on body weight, adiposity and food intake in DIO mice following sham or bilateral surgical denervation of IBAT. Chronic 4V OT reduced body weight by 5.7 ± 2.23% and 6.6 ± 1.4% in sham and denervated mice (<0.05), respectively, and this effect was similar between groups (=NS). OT produced corresponding reductions in whole body fat mass (<0.05). Together, these findings support the hypothesis that sympathetic innervation of IBAT is not necessary for OT-elicited increases in BAT thermogenesis and reductions of body weight and adiposity in male DIO mice.
先前的研究表明,通过减少食物摄入和增加能量消耗(EE),中枢神经系统(CNS)给予催产素(OT)可减轻高脂肪饮食诱导肥胖(DIO)啮齿动物的体重。我们最近证明,后脑(第四脑室[4V])给予 OT 可引起 DIO 小鼠体重减轻,并升高肩胛间棕色脂肪组织温度(T,EE 增加的替代测量)。目前尚不清楚 OT 引起的体重减轻是否需要增加交感神经系统(SNS)对 IBAT 的输出。我们假设,OT 诱导的 SNS 对 IBAT 输出的刺激有助于其激活 BAT 的能力,并在 DIO 小鼠中引起体重减轻。为了验证这一假设,我们确定了破坏 IBAT 的 SNS 激活对 4V OT 给药增加 T 和引起 DIO 小鼠体重减轻的能力的影响。我们首先确定双侧 SNS 到 IBAT 的手术去神经支配是否成功,DIO 小鼠的 IBAT 去甲肾上腺素(NE)含量降低了≥60%。去神经支配后 1、6 和 7 周,IBAT 中的 NE 含量分别选择性降低了 95.9±2.0%、77.4±12.7%和 93.6±4.6%(<0.05),而腹股沟白色脂肪组织、胰腺或肝脏中的 NE 含量不变。随后,我们测量了急性 4V OT(1、5μg≈0.99、4.96nmol)对 sham 或双侧手术 SNS 去神经支配到 IBAT 的 DIO 小鼠 T 的影响。我们发现,高剂量的 4V OT(5μg≈4.96nmol)在 sham 小鼠和去神经支配的小鼠中同样升高了 T。随后,我们测量了慢性 4V OT(16nmol/天,持续 29 天)或载体输注对 sham 或双侧手术 IBAT 去神经支配的 DIO 小鼠体重、肥胖和食物摄入的影响。慢性 4V OT 使 sham 组和去神经支配组的体重分别降低了 5.7±2.23%和 6.6±1.4%(<0.05),两组之间的效果相似(=NS)。OT 还相应减少了全身脂肪量(<0.05)。总之,这些发现支持这样的假设,即 IBAT 的交感神经支配对于 OT 引起的 BAT 产热增加以及雄性 DIO 小鼠体重和肥胖的减轻不是必需的。