Rodrigues Fernanda da Silva, Jantsch Jeferson, Fraga Gabriel de Farias, Dias Victor Silva, Eller Sarah, De Oliveira Tiago Franco, Giovenardi Márcia, Guedes Renata Padilha
Graduate Program in Biosciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande do Sul, Brazil.
Undergraduate Program in Biomedical Sciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande do Sul, Brazil.
Front Nutr. 2023 Mar 9;10:1150189. doi: 10.3389/fnut.2023.1150189. eCollection 2023.
The implications of maternal overnutrition on offspring metabolic and neuroimmune development are well-known. Increasing evidence now suggests that maternal obesity and poor dietary habits during pregnancy and lactation can increase the risk of central and peripheral metabolic dysregulation in the offspring, but the mechanisms are not sufficiently established. Furthermore, despite many studies addressing preventive measures targeted at the mother, very few propose practical approaches to treat the damages when they are already installed.
Here we investigated the potential of cannabidiol (CBD) treatment to attenuate the effects of maternal obesity induced by a cafeteria diet on hypothalamic inflammation and the peripheral metabolic profile of the offspring in Wistar rats.
We have observed that maternal obesity induced a range of metabolic imbalances in the offspring in a sex-dependant manner, with higher deposition of visceral white adipose tissue, increased plasma fasting glucose and lipopolysaccharides (LPS) levels in both sexes, but the increase in serum cholesterol and triglycerides only occurred in females, while the increase in plasma insulin and the homeostatic model assessment index (HOMA-IR) was only observed in male offspring. We also found an overexpression of the pro-inflammatory cytokines tumor necrosis factor-alpha (TNFα), interleukin (IL) 6, and interleukin (IL) 1β in the hypothalamus, a trademark of neuroinflammation. Interestingly, the expression of GFAP, a marker for astrogliosis, was reduced in the offspring of obese mothers, indicating an adaptive mechanism to neuroinflammation. Treatment with 50 mg/kg CBD oil by oral gavage was able to reduce white adipose tissue and revert insulin resistance in males, reduce plasma triglycerides in females, and attenuate plasma LPS levels and overexpression of TNFα and IL6 in the hypothalamus of both sexes.
Together, these results indicate an intricate interplay between peripheral and central counterparts in both the pathogenicity of maternal obesity and the therapeutic effects of CBD. In this context, the impairment of internal hypothalamic circuitry caused by neuroinflammation runs in tandem with the disruptions of important metabolic processes, which can be attenuated by CBD treatment in both ends.
母体营养过剩对后代代谢和神经免疫发育的影响已广为人知。现在越来越多的证据表明,孕期和哺乳期的母体肥胖及不良饮食习惯会增加后代中枢和外周代谢失调的风险,但其机制尚未完全明确。此外,尽管有许多研究针对母亲提出了预防措施,但很少有人提出在损害已经发生时进行治疗的实用方法。
在此,我们研究了大麻二酚(CBD)治疗减轻由自助餐饮食诱导的母体肥胖对Wistar大鼠后代下丘脑炎症和外周代谢谱影响的潜力。
我们观察到,母体肥胖以性别依赖的方式在后代中引发了一系列代谢失衡,包括两性内脏白色脂肪组织沉积增加、空腹血糖和血浆脂多糖(LPS)水平升高,但血清胆固醇和甘油三酯的升高仅发生在雌性后代中,而血浆胰岛素和稳态模型评估指数(HOMA-IR)的升高仅在雄性后代中观察到。我们还发现下丘脑促炎细胞因子肿瘤坏死因子-α(TNFα)、白细胞介素(IL)6和白细胞介素(IL)1β的过度表达,这是神经炎症的标志。有趣的是,肥胖母亲后代中星形胶质细胞增生的标志物胶质纤维酸性蛋白(GFAP)的表达降低,表明存在对神经炎症的适应性机制。通过口服灌胃给予50 mg/kg CBD油治疗能够减少雄性后代的白色脂肪组织并逆转胰岛素抵抗,降低雌性后代的血浆甘油三酯水平,并减轻两性下丘脑的血浆LPS水平以及TNFα和IL6的过度表达。
总之,这些结果表明在母体肥胖的发病机制和CBD的治疗效果方面,外周和中枢之间存在复杂的相互作用。在这种情况下,神经炎症引起的下丘脑内部神经回路损伤与重要代谢过程的破坏同时发生,而CBD治疗可以在两端减轻这种损伤。