...
首页> 外文期刊>American Journal of Physiology >Renal sympathetic nerve activity modulates afferent renal nerve activity by PGE2-dependent activation of alpha1- and alpha2-adrenoceptors on renal sensory nerve fibers.
【24h】

Renal sympathetic nerve activity modulates afferent renal nerve activity by PGE2-dependent activation of alpha1- and alpha2-adrenoceptors on renal sensory nerve fibers.

机译:肾交感神经活动通过肾感觉神经纤维上的PGE2依赖的α1和α2肾上腺素能受体的激活来调节肾传入神经活动。

获取原文
获取原文并翻译 | 示例
           

摘要

Increasing efferent renal sympathetic nerve activity (ERSNA) increases afferent renal nerve activity (ARNA). To test whether the ERSNA-induced increases in ARNA involved norepinephrine activating alpha-adrenoceptors on the renal sensory nerves, we examined the effects of renal pelvic administration of the alpha(1)- and alpha(2)-adrenoceptor antagonists prazosin and rauwolscine on the ARNA responses to reflex increases in ERSNA (placing the rat's tail in 49 degrees C water) and renal pelvic perfusion with norepinephrine in anesthetized rats. Hot tail increased ERSNA and ARNA, 6,930 +/- 900 and 4,870 +/- 670%.s (area under the curve ARNA vs. time). Renal pelvic perfusion with norepinephrine increased ARNA 1,870 +/- 210%.s. Immunohistochemical studies showed that the sympathetic and sensory nerves were closely related in the pelvic wall. Renal pelvic perfusion with prazosin blocked and rauwolscine enhanced the ARNA responses to reflex increases in ERSNA and norepinephrine. Studies in a denervated renal pelvic wall preparation showed that norepinephrine increased substance P release, from 8 +/- 1 to 16 +/- 1 pg/min, and PGE(2) release, from 77 +/- 11 to 161 +/- 23 pg/min, suggesting a role for PGE(2) in the norepinephrine-induced activation of renal sensory nerves. Prazosin and indomethacin reduced and rauwolscine enhanced the norepinephrine-induced increases in substance P and PGE(2). PGE(2) enhanced the norepinephrine-induced activation of renal sensory nerves by stimulation of EP4 receptors. Interaction between ERSNA and ARNA is modulated by norepinephrine, which increases and decreases the activation of the renal sensory nerves by stimulating alpha(1)- and alpha(2)-adrenoceptors, respectively, on the renal pelvic sensory nerve fibers. Norepinephrine-induced activation of the sensory nerves is dependent on renal pelvic synthesis/release of PGE(2).
机译:传出肾交感神经活性(ERSNA)增加会增加传出肾神经活性(ARNA)。为了测试ERSNA诱导的ARNA的增加是否涉及去甲肾上腺素激活的肾感觉神经上的去甲肾上腺素,我们检查了肾盂施用α(1)-和α(2)-肾上腺素能受体拮抗剂prazosin和rauwolscine对肾上腺素的影响在麻醉的大鼠中,ARNA对ERSNA反射增加的反应(将大鼠的尾巴放在49摄氏度的水中)和肾上腺素与去甲肾上腺素的灌注有关。热尾增加了ERSNA和ARNA,分别为6,930 +/- 900和4,870 +/- 670%.s(ARNA与时间曲线下的面积)。肾上腺素肾上腺素灌注增加ARNA 1,870 +/- 210%.s。免疫组织化学研究表明,交感神经和感觉神经在骨盆壁密切相关。肾盂灌注与哌唑嗪阻断,劳劳素增强了对ERSNA和去甲肾上腺素反射增加的ARNA反应。在去神经化的肾盂壁准备中的研究表明,去甲肾上腺素将P物质的释放从8 +/- 1 pg / min增加到16 +/- 1 pg / min,PGE(2)的释放从77 +/- 11到161 +/- 23 pg / min,表明PGE(2)在去甲肾上腺素诱导的肾感觉神经激活中的作用。吡唑嗪和吲哚美辛减少,劳伍素增强去甲肾上腺素引起的P和PGE物质增加(2)。 PGE(2)通过刺激EP4受体增强了去甲肾上腺素诱导的肾感觉神经的激活。去甲肾上腺素调节ERSNA与ARNA之间的相互作用,去甲肾上腺素通过分别刺激肾盂感觉神经纤维上的alpha(1)-和alpha(2)-肾上腺素受体来增加和减少肾感觉神经的激活。去甲肾上腺素诱导的感觉神经激活取决于肾盂合成/释放PGE(2)。

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