Kang Yu-Ming, Zhang Zhi-Hua, Johnson Ralph F, Yu Yang, Beltz Terry, Johnson Alan Kim, Weiss Robert M, Felder Robert B
Department of Internal Medicine, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Circ Res. 2006 Sep 29;99(7):758-66. doi: 10.1161/01.RES.0000244092.95152.86. Epub 2006 Sep 7.
Blocking brain mineralocorticoid receptors (MRs) reduces the high circulating levels of tumor necrosis factor (TNF)-alpha in heart failure (HF) rats. TNF-alpha and other proinflammatory cytokines activate neurons in the paraventricular nucleus (PVN) of hypothalamus, including corticotropin-releasing hormone (CRH) neurons, by inducing cyclooxygenase (COX)-2 activity and synthesis of prostaglandin E2 by perivascular cells of the cerebral vasculature. We tested the hypothesis that systemic treatment with a MR antagonist would reduce hypothalamic COX-2 expression and PVN neuronal activation in HF rats. Rats underwent coronary ligation to induce HF, confirmed by echocardiography, or sham surgery, followed by 6 weeks treatment with eplerenone (30 mg/kg per day, orally) or vehicle (drinking water). Eplerenone-treated HF rats had lower plasma TNF-alpha, interleukin (IL)-1beta and IL-6, less COX-2 staining of small blood vessels penetrating PVN, fewer PVN neurons expressing Fra-like activity (indicating chronic neuronal activation), and fewer PVN neurons staining for TNF-alpha, IL-1beta, and CRH than vehicle-treated HF rats. COX-2 and CRH protein expression in hypothalamus were 1.7- and 1.9-fold higher, respectively, in HF+vehicle versus sham+vehicle rats; these increases were attenuated (26% and 25%, respectively) in HF+eplerenone rats. Eplerenone-treated HF rats had less prostaglandin E2 in cerebrospinal fluid, lower plasma norepinephrine levels, lower left ventricular end-diastolic pressure, and lower right ventricle/body weight and lung/body weight ratios, but no improvement in left ventricular function. Treatment of HF rats with anticytokine agents, etanercept or pentoxifylline, produced very similar results. This study reveals a previously unrecognized effect of MR antagonism to minimize cytokine-induced central neural excitation in rats with HF.
阻断脑盐皮质激素受体(MRs)可降低心力衰竭(HF)大鼠体内肿瘤坏死因子(TNF)-α的高循环水平。TNF-α和其他促炎细胞因子通过诱导脑循环血管周围细胞的环氧化酶(COX)-2活性和前列腺素E2的合成,激活下丘脑室旁核(PVN)中的神经元,包括促肾上腺皮质激素释放激素(CRH)神经元。我们检验了以下假设:用MR拮抗剂进行全身治疗会降低HF大鼠下丘脑COX-2的表达和PVN神经元的激活。大鼠接受冠状动脉结扎以诱导HF(通过超声心动图确认)或假手术,随后用依普利酮(每天30 mg/kg,口服)或赋形剂(饮用水)进行6周治疗。与赋形剂治疗的HF大鼠相比,依普利酮治疗的HF大鼠血浆TNF-α、白细胞介素(IL)-1β和IL-6水平更低,穿透PVN的小血管的COX-2染色更少,表达Fra样活性(表明慢性神经元激活)的PVN神经元更少,且TNF-α、IL-1β和CRH染色的PVN神经元更少。与假手术+赋形剂组大鼠相比,HF+赋形剂组大鼠下丘脑COX-2和CRH蛋白表达分别高出1.7倍和1.9倍;在HF+依普利酮组大鼠中,这些增加有所减弱(分别为26%和25%)。依普利酮治疗的HF大鼠脑脊液中的前列腺素E2含量更低,血浆去甲肾上腺素水平更低,左心室舒张末期压力更低,右心室/体重和肺/体重比值更低,但左心室功能没有改善。用抗细胞因子药物、依那西普或己酮可可碱治疗HF大鼠产生了非常相似的结果。这项研究揭示了MR拮抗作用在使HF大鼠细胞因子诱导的中枢神经兴奋最小化方面的一种先前未被认识到的作用。