Protein Kinase D was involved in vascular remodeling in spontaneously hypertensive rats

被引:5
作者
Geng, Jing [1 ]
Zhao, Zhuo [2 ]
Yang, Le [1 ]
Zhang, Mingwei [1 ]
Liu, Xiangjuan [3 ,4 ]
机构
[1] Shandong Univ, Shandong Prov Hosp, Jinan, Shandong, Peoples R China
[2] Jinan Cent Hosp, Dept Cardiol, Jinan, Shandong, Peoples R China
[3] Shandong Univ, Qilu Hosp, Key Lab Cardiovasc Remodeling & Funct Res, Chinese Minist Educ, Jinan, Shandong, Peoples R China
[4] Shandong Univ, Qilu Hosp, Key Lab Cardiovasc Remodeling & Funct Res, Chinese Minist Hlth, Jinan, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Protein Kinase D; vascular remodeling; hypertension; OXIDATIVE STRESS; ENDOTHELIAL FUNCTION; D ACTIVATION; VEGF; INFLAMMATION; PHOSPHORYLATION; VULNERABILITY; ANGIOGENESIS; ALDOSTERONE; CONTRIBUTES;
D O I
10.1080/10641963.2018.1469647
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study was designed to determine the role of PKD in vascular remodeling (VR) in Spontaneously hypertensive rats (SHRs). Increased SBP, VR and PKD activation were prominent in SHRs. The SBP has a positive correlation with the activation of PKD in SHRs. The ratio of media to lumen (MT/LD), volume fraction of collagen (VFC), hydroxyproline, IL-6, TNF-alpha and nitrotyrosine content were significantly related to the activated PKD. It may be concluded that PKD plays a central role in VR, and the mechanism may be related to its regulation of hypertrophy, fibrosis, inflammation and oxidative stress.
引用
收藏
页码:299 / 306
页数:8
相关论文
共 36 条
[21]   Inflammation and vascular remodeling in the ventral hippocampus contributes to vulnerability to stress [J].
Pearson-Leary, J. ;
Eacret, D. ;
Chen, R. ;
Takano, H. ;
Nicholas, B. ;
Bhatnagar, S. .
TRANSLATIONAL PSYCHIATRY, 2017, 7 :e1160-e1160
[22]  
Protein Kinase RE, 2011, PHYSIOLOGY BETHESDA, V26, P23
[23]   Angiotensin II-mediated protein kinase D activation stimulates aldosterone and cortisol secretion in H295R human adrenocortical cells [J].
Romero, Damian G. ;
Welsh, Bronwyn L. ;
Gomez-Sanchez, Elise P. ;
Yanes, Licy L. ;
Rilli, Silvia ;
Gomez-Sanchez, Celso E. .
ENDOCRINOLOGY, 2006, 147 (12) :6046-6055
[24]   Protein kinase D signaling [J].
Rozengurt, E ;
Rey, O ;
Waldron, RT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (14) :13205-13208
[25]  
Shimizu Fumitaka, 2013, Brain Nerve, V65, P165
[26]   PKD prevents H2O2-induced apoptosis via NF-κB and p38 MAPK in RIE-1 cells [J].
Song, Jun ;
Li, Jing ;
Qiao, Jingbo ;
Jain, Sunil ;
Evers, B. Mark ;
Chung, Dai H. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 378 (03) :610-614
[27]   Regulation of PKD by the MAPK p38δ in Insulin Secretion and Glucose Homeostasis [J].
Sumara, Grzegorz ;
Formentini, Ivan ;
Collins, Stephan ;
Sumara, Izabela ;
Windak, Renata ;
Bodenmiller, Bernd ;
Ramracheya, Reshma ;
Caille, Dorothee ;
Jiang, Huiping ;
Platt, Kenneth A. ;
Meda, Paolo ;
Aebersold, Rudolf ;
Rorsman, Patrik ;
Ricci, Romeo .
CELL, 2009, 136 (02) :235-248
[28]   DETERMINATION OF HYDROXYPROLINE IN TISSUE [J].
SWITZER, BR .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1991, 2 (04) :229-231
[29]   Oxidative stress-induced signal transduction pathways in cardiac myocytes: Involvement of ROS in heart diseases [J].
Takano, H ;
Zou, YZ ;
Hasegawa, H ;
Akazawa, H ;
Nagai, T ;
Komuro, I .
ANTIOXIDANTS & REDOX SIGNALING, 2003, 5 (06) :789-794
[30]   Redox control of endothelial function and dysfunction: Molecular mechanisms and therapeutic opportunities [J].
Thomas, Shane R. ;
Witting, Paul K. ;
Drummond, Grant R. .
ANTIOXIDANTS & REDOX SIGNALING, 2008, 10 (10) :1713-1765