Laboratory of Biomedicine Translational, Extreme South of Santa Catarina University, Criciúma 88806-000, SC, Brazil.
Department of Pharmacology, Santa Catarina Federal University, Florianópolis 88040-900, SC, Brazil.
Nutrients. 2022 Jul 15;14(14):2906. doi: 10.3390/nu14142906.
Obesity induces insulin resistance, chronic inflammation, oxidative stress, and neurocognitive impairment. Avocado oil (AO) has antioxidants and anti-inflammatory effects. This study evaluated the effect of AO supplementation on obese mice in the adipose tissue, muscle, liver, and hippocampus. Male C57BL/6J mice received a standard and high-fat diet (20 weeks) and then were supplemented with AO (4 mL/kg of body weight, 90 days) and divided into the following groups: control (control), control + avocado oil (control + AO), diet-induced obesity (DIO), and diet-induced obesity + avocado oil (DIO + AO) ( = 10/group). AO supplementation was found to improve insulin sensitivity and decrease hepatic fat accumulation and serum triglyceride levels in DIO mice. AO improved cognitive performance and did not affect mood parameters. Oxidative marker levels were decreased in DIO + AO mice in all the tissues and were concomitant with increased catalase and superoxide dismutase activities in the epididymal adipose tissue and quadriceps, as well as increased catalase activity in the liver. AO in obese animals further induced reductions in TNF-α and IL-1β expressions in the epididymal adipose tissue and quadriceps. These results suggest that AO supplementation has the potential to be an effective strategy for combating the effects of obesity in rats, and human studies are needed to confirm these findings.
肥胖会导致胰岛素抵抗、慢性炎症、氧化应激和神经认知障碍。鳄梨油(AO)具有抗氧化和抗炎作用。本研究评估了 AO 补充剂对肥胖小鼠脂肪组织、肌肉、肝脏和海马中的影响。雄性 C57BL/6J 小鼠接受标准和高脂肪饮食(20 周),然后补充 AO(4 毫升/公斤体重,90 天),并分为以下几组:对照组(control)、对照组+鳄梨油(control + AO)、饮食诱导肥胖组(diet-induced obesity,DIO)和饮食诱导肥胖+鳄梨油组(diet-induced obesity + avocado oil,DIO + AO)(每组 10 只)。结果发现,AO 补充剂可改善 DIO 小鼠的胰岛素敏感性,减少肝脂肪堆积和血清甘油三酯水平。AO 改善了认知表现,对情绪参数没有影响。在 DIO + AO 小鼠的所有组织中,氧化标志物水平降低,同时附睾脂肪组织和四头肌中的过氧化氢酶和超氧化物歧化酶活性增加,肝脏中的过氧化氢酶活性增加。在肥胖动物中,AO 进一步降低了附睾脂肪组织和四头肌中 TNF-α 和 IL-1β 的表达。这些结果表明,AO 补充剂有可能成为对抗肥胖大鼠影响的有效策略,需要进行人体研究来证实这些发现。