1.The intensive insulin therapy and different enteral nutrition in critically ill patients
Liquan HUANG ; Lincong WANG ; Ronglin JIANG
Parenteral & Enteral Nutrition 1997;0(04):-
0.05).The amount of insulin in ZL group was significantly lower than that in the control group(P
2.Experimental study of calvarial critical size defect in rats with type 2 diabetes mellitus
Lifeng WANG ; Kaixiu FANG ; Xiaoru XU ; Shuai REN ; Naiwen TAN ; Zhen LI ; Lincong QIU ; Wei MA ; Dehua LI ; Yingliang SONG
Journal of Practical Stomatology 2015;(2):157-161
Objective:To explore the calvarial critical size defect (CSD)in rats with type 2 diabetes mellitus(T2DM).Methods:T2DM model of SD rats(weighted 300-320 g)was induced by high fat and high sugar diet and low dose intraperitoneal streptozotocin (STZ)injection.The rats with T2DMand the normal controls were divided into 4 groups(n=3)respectively.Defects with the diame-ter(mm)of 2,3,4 and 5 were made on the central calvaria of each rat.General observation,X-ray examination and histological study were performed 8 weeks postoperatively.Results:In the T2DM group,only the defects of 2 mm diameter were healed completely,X-ray resistance and new bone formation were observed;the defects of 3,4 and 5 mm diameter were unhealed,X-ray transmission was observed and newly formed bone was insufficient.In the control group,the defects of 2,3 and 4 mm diameter were healed completely, X-ray resistance and new bone formation were observed;the defects of 5 mm diameter were unhealed,X-ray transmission was ob-served,newly formed bone was insufficient.Conclusion:The calvarial CSD of T2DM rat model can be defined as the defect with the diameter of 3 mm.
3.Research progress on the protective mechanism of proprotein convertase subtilisin/kexin type 9 inhibitors on vascular endothelium
Yan FENG ; Wengping LUO ; Mingming ZHANG ; Lincong SHE ; Jiaxin WANG ; Yongxin SUN ; Haoqing CHEN ; Wei ZHANG
Journal of Clinical Medicine in Practice 2024;28(15):142-148
Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors not only have good lipid-lowering effects, but also have pleiotropic effects such as improving cardiovascular outcomes, relieving anti-inflammation, relieving oxidative stress and improving vascular endothelium. In recent years, the continuous development of PCSK9 inhibitors provides new ideas for the treatment of cardiovascular diseases. This article reviewed the pleiotropic mechanisms of PCSK9 inhibitors, especially on vascular endothelial function.