Correlation of Lower Concentrations of Hydrogen Sulfide with Activation of Protein Kinase CβII in Uremic Accelerated Atherosclerosis Patients

被引:12
|
作者
Wang, Wei [1 ]
Feng, Su-Juan [1 ,2 ]
Li, Han [1 ,2 ]
Zhang, Xiao-Dong [1 ]
Wang, Shi-Xiang [1 ,2 ]
机构
[1] Capital Med Univ, Inst Uronephrol, Beijing Chao Yang Hosp, Beijing 100020, Peoples R China
[2] Capital Med Univ, Nephrol Fac, Beijing Chao Yang Hosp, Dept Blood Purificat, Beijing 100020, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Hemodialysis; Hydrogen Sulfide; Protein Kinase C beta II; Uremic Accelerated Atherosclerosis; CHRONIC KIDNEY-DISEASE; HEMODIALYSIS-PATIENTS; ENDOTHELIAL FUNCTION; HEART-FAILURE; RISK-FACTORS; INHIBITION; MUSCLE; H2S; INJURY;
D O I
10.4103/0366-6999.157653
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Hydrogen sulfide (H2S) plays a protective role in chronic hemodialysis (CHD) patients. In this study, we further investigate the relationship between H-2 S and conventional protein kinase C beta II (cPKC beta II) in CHD patients with uremic accelerated atherosclerosis (UAAS). Methods: A total of 30 healthy people, 30 CHD patients without AS and 30 CHD patients with AS (CHD + AS) were studied. Plasma H2S was measured with a sulfide sensitive electrode, and cPKC beta II membrane translocation was detected by Western blotting. Results: Plasma H2S in CHD + AS group was significantly lower than that in CHD patients. cPKC beta II membrane translocation in CHD + AS group increased significantly compared with CHD group. Plasma H2S concentration was negatively correlated with cPKC beta II membrane translocation in CHD + AS patients. Conclusions: These findings suggest a possible linkage between H2S metabolism and cPKC beta II activation, which may contribute to the development of UAAS in CHD patients.
引用
收藏
页码:1465 / 1470
页数:6
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