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首页> 外文期刊>American Journal of Physiology >Serotonergic mechanisms of the lateral parabrachial nucleus in renal and hormonal responses to isotonic blood volume expansion.
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Serotonergic mechanisms of the lateral parabrachial nucleus in renal and hormonal responses to isotonic blood volume expansion.

机译:肱臂外侧旁核对等渗血容量扩大的血清素能机制。

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This study investigated the involvement of serotonergic mechanisms of the lateral parabrachial nucleus (LPBN) in the control of sodium (Na+) excretion, potassium (K+) excretion, and urinary volume in unanesthetized rats subjected to acute isotonic blood volume expansion (0.15 M NaCl, 2 ml/100 g of body wt over 1 min) or control rats. Plasma oxytocin (OT), vasopressin (VP), and atrial natriuretic peptide (ANP) levels were also determined in the same protocol. Male Wistar rats with stainless steel cannulas implanted bilaterally into the LPBN were used. In rats treated with vehicle in the LPBN, blood volume expansion increased urinary volume, Na+ and K+ excretion, and also plasma ANP and OT. Bilateral injections of serotonergic receptor antagonist methysergide (1 or 4 microg/200 etal) into the LPBN reduced the effects of blood volume expansion on increased Na+ and K+ excretion and urinary volume, while LPBN injections of serotonergic 5-HT(2a)/HT(2c) receptor agonist, 2.5-dimetoxi-4-iodoamphetamine hydrobromide (DOI; 1 or 5 microg/200 etal) enhanced the effects of blood volume expansion on Na+ and K+ excretion and urinary volume. Methysergide (4 microg) into the LPBN decreased the effects of blood volume expansion on plasma ANP and OT, while DOI (5 microg) increased them. The present results suggest the involvement of LPBN serotonergic mechanisms in the regulation of urinary sodium, potassium and water excretion, and hormonal responses to acute isotonic blood volume expansion.
机译:这项研究调查了未麻醉大鼠在急性等张性血容量扩张(0.15 M NaCl,0.15 mg NaCl, 1分钟内2毫升/ 100克体重)或对照组。血浆催产素(OT),血管加压素(VP)和心房利钠肽(ANP)的水平也以相同的方案确定。使用双侧向LPBN植入不锈钢插管的雄性Wistar大鼠。在LPBN中接受媒介物治疗的大鼠中,血容量增加会增加尿量,Na +和K +排泄,以及血浆ANP和OT。向LPBN双边注射5-羟色胺受体拮抗剂美塞麦肽(1或4 microg / 200 etal)减少了血容量扩张对增加的Na +和K +排泄和尿量的影响,而LPBN注射5-羟色胺5-HT(2a)/ HT( 2c)受体激动剂2.5-二甲毒素-4-碘苯丙胺氢溴酸盐(DOI; 1或5 microg / 200 etal)增强了血容量扩展对Na +和K +排泄及尿量的影响。进入LPBN的美塞麦肽(4微克)降低了血容量膨胀对血浆ANP和OT的影响,而DOI(5微克)则增加了血浆ANP和OT。目前的结果表明,LPBN血清素能机制参与尿钠,钾和水排泄的调节,以及激素对急性等渗血容量膨胀的反应。

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