Inhibition of TNF-α in hypothalamic paraventricular nucleus attenuates hypertension and cardiac hypertrophy by inhibiting neurohormonal excitation in spontaneously hypertensive rats

被引:57
作者
Song, Xin-Ai [1 ]
Jia, Lin-Lin [1 ]
Cui, Wei [3 ]
Zhang, Meng [1 ]
Chen, Wensheng [4 ]
Yuan, Zu-Yi [5 ]
Guo, Jing [1 ]
Li, Hui-Hua [6 ]
Zhu, Guo-Qing [7 ]
Liu, Hao [2 ]
Kang, Yu-Ming [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Med, Cardiovasc Res Ctr, Dept Physiol & Pathophysiol, Xian 710061, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 1, Dept Neurosurg, Xian 710061, Peoples R China
[3] Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 1, Dept Endocrinol & Metab, Xian 710061, Peoples R China
[4] Fourth Mil Med Univ, Xing Hosp, Dept Cardiovasc Med, Xian 710032, Peoples R China
[5] Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 1, Dept Cardiovasc Med, Xian 710061, Peoples R China
[6] Capital Med Univ, Sch Basic Med Sci, Dept Pathol, Key Lab Remodeling Related Cardiovasc Dis, Beijing 100069, Peoples R China
[7] Nanjing Med Univ, Dept Physiol, Key Lab Cardiovasc Dis & Mol Intervent, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Hypertension; Hypothalamic paraventricular nucleus; Tumor necrosis factor-alpha; Neurohormonal excitation; Cardiac hypertrophy; FACTOR-KAPPA-B; II-INDUCED HYPERTENSION; NECROSIS-FACTOR-ALPHA; HEART-FAILURE; ANGIOTENSIN-II; MYOCARDIAL-INFARCTION; SYMPATHETIC OUTFLOW; OXIDATIVE STRESS; CROSS-TALK; BRAIN;
D O I
10.1016/j.taap.2014.09.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We hypothesized that chronic inhibition of tumor necrosis factor-alpha (TNF-alpha) in the hypothalamic paraventricular nucleus (PVN) delays the progression of hypertension and attenuates cardiac hypertrophy by up-regulating anti-inflammatory cytokines, reducing pro-inflammatory cytokines (PICs), decreasing nuclear factor-kappa B (NF-kappa B) p65 and NAD(P)H oxidase activities, as well as restoring the neurotransmitters balance in the PVN of spontaneously hypertensive rats (SHR). Adult normotensive Wistar-Kyoto (WRY) and SHR rats received bilateral PVN infusion of a TNF-alpha blacker (pentoxifylline or etanercept) or vehicle for 4 weeks. SHR rats showed higher mean arterial pressure and cardiac hypertrophy compared with WRY rats, as indicated by increased whole heart weight/body weight ratio, whole heart weight/tibia length ratio, left ventricular weight/tibia length ratio, and cardiac atrial natriuretic peptide (ANP) and beta-myosin heavy chain (beta-MHC) mRNA expressions. Compared with WKY rats, SHR rats had higher PVN levels of tyrosine hydroxylase, PICs, the chemokine monocyte chemoattractant protein-1 (MCP-1), NF-kappa B p65 activity, mRNA expressions of NOX-2 and NOX-4, and lower PVN levels of IL-10 and 67-kDa isoform of glutamate decarboxylase (GAD67), and higher plasma norepinephrine. PVN infusion of pentoxifylline or etanercept attenuated all these changes in SHR rats. These findings suggest that SHR rats have an imbalance between excitatory and inhibitory neurotransmitters, as well as an imbalance between pro- and anti-inflammatory cytokines in the PVN; and chronic inhibition of TNF-alpha in the PVN delays the progression of hypertension by restoring the balances of neurotransmitters and cytokines in the PVN, and attenuating PVN NF-kappa B p65 activity and oxidative stress, thereby attenuating hypertension-induced sympathetic hyperactivity and cardiac hypertrophy. (C) 2014 Elsevier Inc All rights reserved.
引用
收藏
页码:101 / 108
页数:8
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