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中枢环加氧酶/脂加氧酶在脑室注射 nesfatin-1 诱发大鼠心血管效应中的中介作用。

The intermediary role of the central cyclooxygenase / lipoxygenase enzymes in intracerebroventricular injected nesfatin-1-evoked cardiovascular effects in rats.

机构信息

Department of Physiology, Faculty of Veterinary Medicine, Bursa Uludag University, Bursa, 16059, Turkey.

Department of Physiology, Faculty of Veterinary Medicine, Bursa Uludag University, Bursa, 16059, Turkey.

出版信息

Neurosci Lett. 2021 Jun 21;756:135961. doi: 10.1016/j.neulet.2021.135961. Epub 2021 May 19.

Abstract

That nesfatin-1 is a neuromodulatory peptide for the cardiovascular system is well documented. Several central receptors have been shown to mediate the cardiovascular effects of nesfatin-1. Immunohistochemistry and Western blot studies showed that nesfatin-1 activated the expression of the central cyclooxygenase (COX) -1, -2 and lipoxygenase (LOX). In addition, microdialysis study showed that nesfatin-1 increased the release of total prostaglandins and leukotrienes from the hypothalamus. The present study investigated whether the central COX and LOX enzymes have a direct mediating role in the MAP and HR responses of nesfatin-1. Intracerebroventricularly administered nesfatin-1 produced dose-dependent pressor and phasic HR responses in normotensive conscious rats Sprague Dawley. Central pretreatment with a COX1/2 inhibitor, ibuprofen, completely blocked the nesfatin-1-induced responses. However, central pretreatment with a nonselective LOX inhibitor, nordihydroguaiaretic acid, partially attenuated the cardiovascular responses induced by nesfatin-1. The results suggest that centrally administered nesfatin-1 activates the central enzymes COX and LOX, which may be involved in the cardiovascular responses as a novel central mechanism for nesfatin-1.

摘要

内脂素-1 是心血管系统的神经调节肽,这一点已有充分的文献记载。有几项研究已经表明,内脂素-1 的心血管效应是通过几种中枢受体介导的。免疫组织化学和 Western blot 研究表明,内脂素-1 激活了中枢环氧化酶(COX)-1、-2 和脂氧合酶(LOX)的表达。此外,微透析研究表明,内脂素-1 增加了下丘脑总前列腺素和白三烯的释放。本研究探讨了中枢 COX 和 LOX 酶是否在内脂素-1 引起的平均动脉压(MAP)和心率(HR)反应中具有直接介导作用。向正常血压清醒的 Sprague Dawley 大鼠的侧脑室给予内脂素-1,可产生剂量依赖性升压和相位性 HR 反应。中枢给予 COX1/2 抑制剂布洛芬预处理完全阻断了内脂素-1 引起的反应。然而,中枢给予非选择性 LOX 抑制剂 nordihydroguaiaretic acid 预处理部分减弱了内脂素-1 引起的心血管反应。结果表明,中枢给予内脂素-1 激活了中枢酶 COX 和 LOX,这可能是内脂素-1 作为一种新的中枢机制引起心血管反应的原因。

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