Chu Shufang, Wang Hongli, Liu Deliang, Zhao Hengxia, Li Juntong, Liu Xuemei, Li Huilin
Department of Endocrinology, Shenzhen Traditional Chinese Medicine Hospital, No.1, Futian District, Shenzhen, Guangdong, 518033, China.
The Fourth Clinical Medicine College of Guangzhou University of Chinese Medicine, Shenzhen, 518033, China.
BMC Cardiovasc Disord. 2025 Aug 18;25(1):610. doi: 10.1186/s12872-025-05012-z.
Heqi San has shown therapeutic potential in the treatment of diabetes. This study aimed to explore the mechanism underlying the effects of Heqi San in treating rats with diabetic atherosclerosis (AS).
We established a model of atherosclerosis in diabetic rats and treated them with Heqi San. Body weight, food intake, and water intake were measured every two weeks. Subsequently, we examined the effects of Heqi San on serum biochemical markers, aortic structure, fat accumulation, and serum levels of inflammatory factors. The levels of p-AMPK and AMPK in thoracic aorta tissue were evaluated by western blotting. Mass spectrometry was used to identify differential serum metabolites after Heqi San treatment.
Intragastric administration of Heqi San enhanced food intake and reduced the excessive water intake caused by diabetic atherosclerosis. Both low and high doses of Heqi San decreased elevated levels of TG, TC, LDL, GLU, and insulin, while increasing HDL levels. Additionally, the AS group showed increased expression of CD68 and CCL-2 in thoracic aorta tissue, along with elevated serum levels of IL-6, IL-1β, and TNF-α. Treatment with Heqi San reduced these inflammatory markers. Heqi San also increased p-AMPK expression in thoracic aorta tissue. Mass spectrometry analysis revealed that the AS group had significantly elevated serum levels of L-NIL, Gln_Cys_Asp, and Geshoidin, whereas high-dose Heqi San treatment decreased the levels of these metabolites.
Heqi San could alleviate atherosclerosis in diabetic rats, and this effect may be associated with changes in serum metabolites such as L-NIL, Gln_Cys_Asp, and Geshoidin.
和剂散在糖尿病治疗中已显示出治疗潜力。本研究旨在探讨和剂散治疗糖尿病动脉粥样硬化(AS)大鼠的作用机制。
我们建立了糖尿病大鼠动脉粥样硬化模型并用和剂散对其进行治疗。每两周测量体重、食物摄入量和饮水量。随后,我们检测了和剂散对血清生化标志物、主动脉结构、脂肪堆积及炎症因子血清水平的影响。通过蛋白质免疫印迹法评估胸主动脉组织中p-AMPK和AMPK的水平。采用质谱法鉴定和剂散治疗后血清差异代谢物。
灌胃给予和剂散可增加食物摄入量,并减少糖尿病动脉粥样硬化所致的过度饮水。低剂量和高剂量的和剂散均降低了升高的甘油三酯(TG)、总胆固醇(TC)、低密度脂蛋白(LDL)、血糖(GLU)和胰岛素水平,同时提高了高密度脂蛋白(HDL)水平。此外,AS组胸主动脉组织中CD68和CCL-2的表达增加,同时血清白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)水平升高。和剂散治疗降低了这些炎症标志物。和剂散还增加了胸主动脉组织中p-AMPK的表达。质谱分析显示,AS组血清L-NIL、Gln_Cys_Asp和Geshoidin水平显著升高,而高剂量和剂散治疗降低了这些代谢物的水平。
和剂散可减轻糖尿病大鼠的动脉粥样硬化,这种作用可能与血清代谢物如L-NIL、Gln_Cys_Asp和Geshoidin的变化有关。