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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.
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页码:1465 / 1470
页数:6
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