Cedraz-Mercez P L, Mecawi A S, Lepletier A, Araújo I G, Costa-e-Sousa R H, Rocha F F, Olivares E L, Medeiros M A, Reis L C
Department of Physiological Sciences, Biology Institute, Federal Rural University of Rio de Janeiro, BR465, Km 7, 23890-000, Seropédica, RJ, Brazil.
Exp Physiol. 2007 Sep;92(5):923-31. doi: 10.1113/expphysiol.2007.037317. Epub 2007 Jun 25.
The present study was carried out to assess the influence of noradrenergic stimulation of the midbrain dorsal (DRN) and median raphe nuclei (MRN) on urinary volume and electrolyte excretion in hydrated rats. Wistar rats were implanted with a guide cannula into the MRN or DRN and then submitted to two intragastric administrations of water in order to attain an increased diuresis. The following treatments were performed. (1) Intra-DRN microinjections of saline (0.2 microl), alpha(1)-adrenergic agonist phenylephrine (PHE, 0.49 and 4.9 nmol in 0.2 microl), alpha(2)-adrenergic antagonist idazoxan (IDZ, 0.42 and 4.2 nmol in 0.2 microl) or the alpha(1)-adrenergic antagonist prazosin (PRZ, 0.24 and 2.4 nmol in 0.2 microl). (2) Intra-MRN microinjections of saline, IDZ (4.2 nmol in 0.2 microl), PHE (4.9 nmol in 0.2 microl) or PRZ (2.4 nmol in 0.2 microl). Urine samples were subsequently collected over 120 min at 20 min intervals for photometric measurement of sodium and potassium. Intra-DRN administration of PHE and IDZ significantly increased the urinary volume, natriuresis and kaliuresis. Intra-DRN microinjection of a higher dose of PRZ reduced the urinary volume and both sodium and potassium excretion. Intra-MRN microinjections of PHE, IDZ or PRZ did not induce any significant effect on urinary volume or electrolyte excretion. These data suggest that the increase of tonic excitatory noradrenergic input conveyed to DRN influences the hydroelectrolyte homeostasis, possibly through 5-HTergic circuitry.
本研究旨在评估中脑背侧缝际核(DRN)和中缝正中核(MRN)的去甲肾上腺素能刺激对水合大鼠尿量和电解质排泄的影响。将Wistar大鼠植入引导套管至MRN或DRN,然后进行两次胃内给水以增加利尿。进行了以下处理。(1)向DRN内微量注射生理盐水(0.2微升)、α(1)-肾上腺素能激动剂去氧肾上腺素(PHE,0.2微升中含0.49和4.9纳摩尔)、α(2)-肾上腺素能拮抗剂咪唑克生(IDZ,0.2微升中含0.42和4.2纳摩尔)或α(1)-肾上腺素能拮抗剂哌唑嗪(PRZ,0.2微升中含0.24和2.4纳摩尔)。(2)向MRN内微量注射生理盐水、IDZ(0.2微升中含4.2纳摩尔)、PHE(0.2微升中含4.9纳摩尔)或PRZ(0.2微升中含2.4纳摩尔)。随后每隔20分钟收集120分钟的尿液样本,用于钠和钾的光度测量。向DRN内注射PHE和IDZ显著增加了尿量、尿钠排泄和尿钾排泄。向DRN内微量注射较高剂量的PRZ减少了尿量以及钠和钾的排泄。向MRN内微量注射PHE、IDZ或PRZ对尿量或电解质排泄未产生任何显著影响。这些数据表明,传递至DRN的紧张性兴奋性去甲肾上腺素能输入的增加可能通过5-羟色胺能神经回路影响水电解质稳态。