Stritch School of Medicine, Loyola University Chicago, Maywood, IL, USA.
Department of Microbiology and Immunology, Loyola University Chicago, Maywood, IL, USA.
J Neuroinflammation. 2024 Jun 5;21(1):151. doi: 10.1186/s12974-024-03140-5.
Mounting evidence links glucose intolerance and diabetes as aspects of metabolic dysregulation that are associated with an increased risk of developing dementia. Inflammation and inflammasome activation have emerged as a potential link between these disparate pathologies. As diet is a key factor in both the development of metabolic disorders and inflammation, we hypothesize that long term changes in dietary factors can influence nervous system function by regulating inflammasome activity and that this phenotype would be sex-dependent, as sex hormones are known to regulate metabolism and immune processes.
5-week-old male and female transgenic mice expressing a caspase-1 bioluminescent reporter underwent cranial window surgeries and were fed control (65% complex carbohydrates, 15% fat), high glycemic index (65% carbohydrates from sucrose, 15% fat), or ketogenic (1% complex carbohydrates, 79% fat) diet from 6 to 26 weeks of age. Glucose regulation was assessed with a glucose tolerance test following a 4-h morning fast. Bioluminescence in the brain was quantified using IVIS in vivo imaging. Blood cytokine levels were measured using cytokine bead array. 16S ribosomal RNA gene amplicon sequencing of mouse feces was performed to assess alterations in the gut microbiome. Behavior associated with these dietary changes was also evaluated.
The ketogenic diet caused weight gain and glucose intolerance in both male and female mice. In male mice, the high glycemic diet led to increased caspase-1 biosensor activation over the course of the study, while in females the ketogenic diet drove an increase in biosensor activation compared to their respective controls. These changes correlated with an increase in inflammatory cytokines present in the serum of test mice and the emergence of anxiety-like behavior. The microbiome composition differed significantly between diets; however no significant link between diet, glucose tolerance, or caspase-1 signal was established.
Our findings suggest that diet composition, specifically the source and quantity of carbohydrates, has sex-specific effects on inflammasome activation in the central nervous system and behavior. This phenotype manifested as increased anxiety in male mice, and future studies are needed to determine if this phenotype is linked to alterations in microbiome composition.
越来越多的证据表明,葡萄糖耐量受损和糖尿病是代谢失调的表现,与痴呆风险增加有关。炎症和炎性小体激活已成为这些不同病理之间的潜在联系。由于饮食是代谢紊乱和炎症发展的关键因素,我们假设饮食因素的长期变化可以通过调节炎性小体活性来影响神经系统功能,并且这种表型是性别依赖性的,因为性激素已知可以调节代谢和免疫过程。
5 周龄的雄性和雌性表达半胱氨酸蛋白酶-1生物发光报告基因的转基因小鼠接受颅窗手术,并在 6 至 26 周龄时接受对照(65%复合碳水化合物,15%脂肪)、高血糖指数(65%碳水化合物来自蔗糖,15%脂肪)或生酮(1%复合碳水化合物,79%脂肪)饮食。禁食 4 小时后进行葡萄糖耐量试验评估葡萄糖调节。使用 IVIS 体内成像定量测量大脑中的生物发光。使用细胞因子珠阵列测量血液细胞因子水平。对小鼠粪便中的 16S 核糖体 RNA 基因扩增子进行测序,以评估肠道微生物组的变化。还评估了与这些饮食变化相关的行为。
生酮饮食导致雄性和雌性小鼠体重增加和葡萄糖耐量受损。在雄性小鼠中,高血糖饮食导致在研究过程中 caspase-1 生物传感器激活增加,而在雌性小鼠中,与各自的对照相比,生酮饮食导致生物传感器激活增加。这些变化与测试小鼠血清中炎症细胞因子的增加以及焦虑样行为的出现相关。饮食之间的微生物组组成有显著差异;然而,饮食、葡萄糖耐量或 caspase-1 信号之间没有建立显著联系。
我们的研究结果表明,饮食成分,特别是碳水化合物的来源和数量,对中枢神经系统中炎性小体的激活和行为具有性别特异性影响。这种表型表现为雄性小鼠焦虑增加,需要进一步研究确定这种表型是否与微生物组组成的改变有关。