首页|维生素K2对2型糖尿病大鼠模型血管钙化的影响及机制研究

维生素K2对2型糖尿病大鼠模型血管钙化的影响及机制研究

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目的:探讨维生素K2对2型糖尿病大鼠模型血管钙化的影响及其机制.方法:6周龄Wistar雄性大鼠30只,适应性喂养7 d后,随机抽取10只作为阴性对照组,喂饲普通饲料,注射等量的柠檬酸缓冲液;其余大鼠在高脂高糖饲料持续喂养4周后通过腹腔注射链脲佐菌素诱导糖尿病大鼠模型,糖尿病模型诱导成功后依据分层随机分组原则将大鼠分为糖尿病组和糖尿病+维生素K2组,分别喂饲高脂饲料和含维生素K2的高脂饲料,阴性对照组继续喂饲普通饲料.喂养13周后,处死大鼠,取样,测量血糖及血管中钙浓度;采用Von Kossa染色法进行组织病理学检测;采用qRT-PCR和Western blot法分别测定低氧诱导因子-1α(hypoxia inducible factor-1α,HIF-1α)、丙酮酸脱氢酶激酶4(pyruvate dehydrogenase kinase 4,PDK4)、基质Gla蛋白(matrix Gla protein,MGP)和骨形态发生蛋白-2(bone morphogenetic protein-2,BMP-2)的mRNA和蛋白的相对表达量.结果:与阴性对照组比较,糖尿病组和糖尿病+维生素K2 组大鼠血糖值均显著升高(P<0.01),2组比较差异无统计学意义(P>0.05);3组血管钙浓度比较差异无统计学意义(P>0.05).Von Kossa染色显示阴性对照组大鼠呈现正常大鼠血管结构,糖尿病组大鼠血管中膜弹性纤维间可见大量棕黑色钙化斑,糖尿病+维生素K2组则无钙化斑或只有少量的棕黑色钙化斑.糖尿病组PDK4、MGP和BMP-2的mRNA和蛋白相对表达量均高于阴性对照组(P<0.05),HIF-1α的mRNA和蛋白相对表达量比较差异无统计学意义;糖尿病+维生素K2组仅PDK4蛋白相对表达量与阴性对照组比较差异有统计学意义(P<0.05);糖尿病组与糖尿病+维生素K2组上述指标比较差异均无统计学意义(P>0.05).结论:2型糖尿病可能通过增加PDK4表达引起BMP-2、MGP表达增加,引起血管钙化,维生素K2能抑制糖尿病引起的血管钙化.
Effect and mechanism of vitamin K2 on vascular calcification in type 2 diabetic rats
Objective:To investigate the effect and mechanism of vitamin K2 on vascular calcification in a type 2 diabetes rat model.Methods:Thirty male Wistar rats,6 weeks old,were acclimatized for 7 days.Ten rats were randomly selected as the negative control group,fed a normal diet,and injected with an equal amount of citrate buffer.The remaining rats were fed a high-fat and high-sugar diet for 4 weeks,and then type 2 diabetes was induced by intraperitoneal injection of streptozotocin.After successful induction of the diabetes model,the diabetic rats were numbered by body weight and divided into the diabetes group and the diabetes+vitamin K2 group according to the principle of stratified random grouping.These two groups were fed a high-fat diet and a high-fat diet containing vitamin K2,respectively,while the control group continued to be fed a normal diet.After 13 weeks of feeding,the rats were sacrificed for sample collection,and blood glucose and vascular calcium concentration were measured.Von Kossa staining was used for histopathological detection.The relative expression levels of hypoxia-inducible factor-1α(HIF-1α),pyruvate dehydrogenase kinase 4(PDK4),matrix Gla protein(MGP),and bone morphogenetic protein-2(BMP-2)mRNA and proteins were measured by qRT-PCR and Western blot,respectively.Results:Compared with the control group,blood glucose levels in the diabetes group and diabetes+vitamin K2 group were significantly elevated(P<0.01),but there was no significant difference between the two groups.There was no significant difference in vascular calcium concentration among the three groups(P>0.05).Von Kossa staining showed that the control group exhibited normal vascular structures,while the diabetes group showed a large number of brown-black calcification plaques between elastic fibers in the vascular media.The diabetes+vitamin K2 group had either no calcification plaques or only a few brown-black calcification plaques.Compared with the control group,the expression levels of PDK4,MGP,and BMP-2 mRNA and proteins were higher in the diabetes group(P<0.05),but there was no significant difference in the expression level of HIF-1α.Only the expression level of PKD4 protein had significance between the control group and diabetes+vitamin K2 group(P<0.05).There was no significant difference in the above indexes between the diabetic group and diabetic+vitamin K2 group(P>0.05).Conclusions:Type 2 diabetes mellitus may cause vascular calcification by increasing the expression of PDK4,which in turn leads to increased expression of BMP-2 and MGP.Vitamin K2 can inhibit vascular calcification in diabetes.

diabetesvascular calcificationvitamin K2MGPHIF-1αPDK4BMP-2

邓丽丽、李明慧、于叶、吴杰、杨晨、裴秀丛、郭连莹

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沈阳医学院公共卫生学院,辽宁 沈阳 110034

糖尿病 血管钙化 维生素K2 MGP HIF-1α PDK4 BMP-2

2024

沈阳医学院学报
沈阳医学院

沈阳医学院学报

影响因子:0.591
ISSN:1008-2344
年,卷(期):2024.26(5)