首页> 外文期刊>Hypertension research: Official journal of the Japanese Society of Hypertension >Brain perivascular macrophages contribute to the development of hypertension in stroke-prone spontaneously hypertensive rats via sympathetic activation
【24h】

Brain perivascular macrophages contribute to the development of hypertension in stroke-prone spontaneously hypertensive rats via sympathetic activation

机译:脑血管内巨噬细胞通过交感神经激活促进脑卒中易患高血压大鼠的高血压的发展

获取原文
获取原文并翻译 | 示例
           

摘要

Hypertension is associated with systemic inflammation. The activation of the sympathetic nervous system is critically involved in the pathogenesis of hypertension. Brain perivascular macrophages (PVMs) can be affected by circulating inflammatory cytokines, and the contribution of brain PVMs to sympathoexcitation has been demonstrated in a heart failure model. We thus investigated whether brain PVMs contribute to the development of hypertension through sympathoexcitation. Stroke-prone spontaneously hypertensive rats (SHRSP) developed hypertension over an 8-week period from 4 to 12 weeks of age. The number of brain PVMs and plasma interleukin-1 beta levels significantly increased at the ages of 8 and 12 weeks in SHRSP compared with normotensive Wistar-Kyoto rats (WKY). To determine the contribution of brain PVMs to blood pressure elevation, we intracerebroventricularly injected liposome-encapsulated clodronate, which eliminates macrophages by inducing apoptosis, into 8-week-old rats; we then assessed its effects in 10-week-old rats. Clodronate treatment attenuated the increase in mean blood pressure in SHRSP but not in WKY. Clodronate treatment reduced the depressor effect of hexamethonium, an index of sympathetic activity; it also reduced neuronal activity in sympathetic regulatory nuclei such as the hypothalamic paraventricular nucleus and rostral ventrolateral medulla and reduced the expression of cyclooxygenase-2 and prostaglandin E2, a downstream pathway in activated macrophages, in SHRSP but not in WKY. Furthermore, clodronate treatment attenuated the increase in blood pressure and renal sympathetic nerve activity in response to an acute intravenous injection of interleukin-1 beta in WKY. In conclusion, brain PVMs contribute to the development of hypertension via sympathetic activation. PVMs may be activated by increased levels of circulating interleukin-1 beta.
机译:高血压与全身炎症有关。激活同情神经系统批判性地参与高血压的发病机制。脑血管巨噬细胞(PVM)可以受到循环炎症细胞因子的影响,并且在心力衰竭模型中已经证明了脑PVMS对同情的贡献。因此,我们研究了脑PVMS是否通过同情泌言促进了高血压的发展。中风易于自发性高血压大鼠(SHRSP)在4至12周龄的8周期间发育高血压。与标准沉变的Wistar-kyoto大鼠(WKY)相比,SHRSP的脑PVMS和血浆白细胞介素-1ββ1β水平显着增加。为了确定脑PVM对血压升高的贡献,我们通过诱导细胞凋亡,进入8周龄大鼠来消除巨噬细胞的脂质体积包装的脂质体封装的脂质体。然后,我们在10周龄大鼠中评估了它的影响。克莱膦酸盐治疗减弱了SHRSP中平均血压的增加,但不含WKY。克莱膦酸盐治疗降低了六淀粉的减压效果,是交感神经活动指标;它还降低了同情调节核中的神经元活性,例如下丘脑椎间盘核和泌喷仑腹膜外髓质,并降低了活性巨噬细胞中的环氧化酶-2和前列腺素E2的表达,在SHRSP中,但不含WKY。此外,Clodronate治疗抑制了患有WKY中的急性静脉内注射白细胞介素-1β的血压和肾交感神经活动的增加。总之,脑PVM通过交感神经激活促进高血压的发展。可以通过增加的白细胞介素-1ββ水平激活PVM。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号