Smith James A, Ramirez-Perez Francisco I, Burr Katherine, Gonzalez-Vallejo Juan D, Morales-Quinones Mariana, McMillan Neil J, Ferreira-Santos Larissa, Sharma Neekun, Foote Christopher A, Martinez-Lemus Luis A, Padilla Jaume, Manrique-Acevedo Camila
Department of Nutrition and Exercise Physiology, University of Missouri, Columbia, Missouri, United States.
NextGen Precision Health, University of Missouri, Columbia, Missouri, United States.
J Appl Physiol (1985). 2024 Dec 1;137(6):1592-1603. doi: 10.1152/japplphysiol.00651.2024. Epub 2024 Oct 31.
Degradation of the endothelial glycocalyx in type 2 diabetes (T2D) is thought to contribute to impaired shear stress mechanotransduction, leading to endothelial dysfunction and the development of cardiovascular disease. Herein, we tested the hypothesis that restoration of the endothelial glycocalyx with dietary supplementation of glycocalyx precursors (DSGPs, containing glucosamine sulfate, fucoidan, superoxide dismutase, and high-molecular weight hyaluronan) improves endothelial function and other indices of vascular function in T2D. First, in db/db mice, we showed that treatment with DSGP (100 mg/kg/day) for 4 wk restored endothelial glycocalyx length, as assessed via atomic force microscopy in aortic explants. Restoration of the glycocalyx with DSGP was accompanied by improved flow-mediated dilation (FMD) and reduced arterial stiffness in isolated mesenteric arteries. Further corroborating these findings, the treatment of cultured endothelial cells with that same mixture of glycocalyx precursors promoted glycocalyx growth. Next, as an initial step to investigate the translatability of these findings, we conducted a pilot ( = 22) double-blinded randomized placebo-controlled clinical trial to assess the effects of DSGP (3,712.5 mg/day) for 8 wk on endothelial glycocalyx integrity and indices of vascular function, including FMD, in Veterans with T2D. Contrary to the hypothesis, DSGP neither enhanced endothelial glycocalyx integrity nor improved vascular function indices relative to placebo. Together, these findings conceptually support the notion that restoration of the endothelial glycocalyx can lead to improvements in vascular function in a mouse model of T2D; however, DSGP as a therapeutic strategy to enhance vascular function in individuals with T2D does not appear to be efficacious. Endothelial glycocalyx degradation in type 2 diabetes (T2D) is thought to contribute to impaired shear stress mechanotransduction, leading to vascular dysfunction. The findings of this study support the notion that restoration of the endothelial glycocalyx using a dietary supplementation of glycocalyx precursors can lead to improvements in vascular function in diabetic mice. However, the utilized dietary supplement as a therapeutic strategy to enhance vascular function in individuals with T2D is not efficacious.
2型糖尿病(T2D)中内皮糖萼的降解被认为会导致剪切应力机械转导受损,进而导致内皮功能障碍和心血管疾病的发生。在此,我们检验了以下假设:通过饮食补充糖萼前体(DSGP,含有硫酸葡萄糖胺、岩藻多糖、超氧化物歧化酶和高分子量透明质酸)来恢复内皮糖萼,可改善T2D患者的内皮功能和其他血管功能指标。首先,在db/db小鼠中,我们发现用DSGP(100毫克/千克/天)治疗4周可恢复内皮糖萼长度,这是通过原子力显微镜在主动脉外植体中评估得出的。DSGP恢复糖萼的同时,还改善了离体肠系膜动脉的血流介导的舒张功能(FMD)并降低了动脉僵硬度。用相同的糖萼前体混合物处理培养的内皮细胞进一步证实了这些发现,促进了糖萼生长。接下来,作为研究这些发现可转化性的第一步,我们进行了一项初步的(n = 22)双盲随机安慰剂对照临床试验,以评估DSGP(3712.5毫克/天)治疗8周对T2D退伍军人内皮糖萼完整性和血管功能指标(包括FMD)的影响。与假设相反,相对于安慰剂,DSGP既未增强内皮糖萼完整性,也未改善血管功能指标。总之,这些发现从概念上支持了以下观点:恢复内皮糖萼可导致T2D小鼠模型的血管功能改善;然而,DSGP作为增强T2D个体血管功能的治疗策略似乎并不有效。2型糖尿病(T2D)中内皮糖萼的降解被认为会导致剪切应力机械转导受损,进而导致血管功能障碍。本研究结果支持以下观点:通过饮食补充糖萼前体来恢复内皮糖萼可改善糖尿病小鼠的血管功能。然而,所使用的饮食补充剂作为增强T2D个体血管功能的治疗策略并不有效。