Department of Anatomy, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico.
Laboratory of Molecular Neurophysiology, National Institute of Psychiatry Ramón de la Fuente, Mexico City 14370, Mexico.
Int J Mol Sci. 2024 Oct 18;25(20):11218. doi: 10.3390/ijms252011218.
The associations among increased pain sensitivity, obesity, and systemic inflammation have not been described as related to BBB dysfunctions. To analyze the metabolic, behavioral, and inflammatory effects of a high-fat diet (HFD) and ultrastructural modifications in brain regions, we used an in vivo experimental model. Adult male Wistar rats were randomly assigned to one of two conditions, an ad libitum control group or an HFD (60%)-fed group, for eight weeks. At the end of the protocol, glucose and insulin tolerance tests were performed. Additionally, we analyzed the response to a normally innocuous mechanical stimulus and changes in motor coordination. At the end of the protocol, HFD-fed rats presented increased HOMA-IR and metabolic syndrome (MetS) prevalence. HFD-fed rats also developed an increased nociceptive response to mechanical stimuli and neurological injury, resulting in impaired motor function. Hypothalamus and cerebellum neurons from HFD-fed rats presented with nuclear swelling, an absence of nucleoli, and karyolysis. These results reveal that HFD consumption affects vital brain structures such as the cerebellum, hippocampus, and hypothalamus. This, in turn, could be producing neuronal damage, impairing cellular communication, and consequently altering motricity and pain sensitivity. Although direct evidence of a causal link between BBB dysfunction and sensory-motor changes was not observed, understanding the association uncovered in this study could lead to targeted therapeutic strategies.
肥胖症与全身炎症与疼痛敏感性增加有关,但其与 BBB 功能障碍的关系尚未得到描述。为了分析高脂肪饮食(HFD)的代谢、行为和炎症影响以及大脑区域的超微结构改变,我们使用了体内实验模型。成年雄性 Wistar 大鼠被随机分为两组,自由进食对照组或 HFD(60%)喂养组,持续 8 周。在方案结束时,进行了葡萄糖和胰岛素耐量测试。此外,我们还分析了对正常无害机械刺激的反应以及运动协调能力的变化。在方案结束时,HFD 喂养的大鼠表现出更高的 HOMA-IR 和代谢综合征(MetS)患病率。HFD 喂养的大鼠还表现出对机械刺激的痛觉反应增加和神经损伤,导致运动功能受损。HFD 喂养的大鼠下丘脑和小脑神经元出现核肿胀、核仁缺失和核溶解。这些结果表明,HFD 的摄入会影响重要的大脑结构,如小脑、海马体和下丘脑。这反过来又可能导致神经元损伤,破坏细胞通讯,并最终改变运动能力和疼痛敏感性。尽管没有观察到 BBB 功能障碍与感觉运动变化之间存在因果关系的直接证据,但理解本研究中发现的关联可能会导致针对特定靶点的治疗策略。