Fonseca Fabricia Viana, Mecawi André Souza, Araujo Iracema Gomes, Almeida-Pereira Gislaine, Magalhães-Nunes Ana Paula, Badauê-Passos Daniel, Reis Luís Carlos
Department of Physiologic Sciences, Institute de Biology, Federal Rural University of Rio de Janeiro, BR465, Km07 23890-000, Seropédica, RJ, Brazil.
Exp Neurol. 2009 Jun;217(2):353-60. doi: 10.1016/j.expneurol.2009.03.015. Epub 2009 Mar 26.
We investigated the possible role of 5-HT(1A) somatodendritic autoreceptors in the dorsal raphe nucleus (DRN) on salt intake response during basal conditions and following natriorexigenic challenge aroused by sodium depletion in rats. Acute systemic administration (76-1520 nmol/kg s.c.) of 8-OH-DPAT, a selective 5-HT(1A) somatodendritic autoreceptor agonist, induced a clear and dose-dependent preference for salt intake through free choice between water and 0.3 M NaCl simultaneously offered under basal conditions. Acute intra-DRN microinjection (7.5 nmol/rat) of 8-OH-DPAT significantly mimicked the acute systemic protocol in sodium-replete rats. Interestingly, microinjection of 8-OH-DPAT into the DRN raised an additional long-lasting increase of 0.3 M NaCl intake in sodium-depleted rats despite a high volume ingested 30 min after central injection. Conversely, chronic systemic treatment (1520 nmol/kg s.c.) with 8-OH-DPAT for 2 and 3 weeks or repeated intra-DRN microinjection (7.5 nmol/rat) evoked a significant long-term decrease in 0.3 M NaCl intake in sodium-depleted rats given only water and a sodium-deficient diet over the course of 24 h after furosemide injection. These results show a clear-cut involvement of the DRN 5-HT(1A) somatodendritic autoreceptors in sodium satiety signaling under basal conditions and during the consummatory phase of salt intake in sodium-depleted rats.
我们研究了大鼠背侧中缝核(DRN)中5-羟色胺(5-HT)(1A)树突体自身受体在基础条件下以及钠耗竭引起的促钠摄食刺激后对盐摄入反应的可能作用。急性全身给药(皮下注射76 - 1520 nmol/kg)选择性5-HT(1A)树突体自身受体激动剂8-OH-DPAT,在基础条件下通过同时提供水和0.3 M NaCl进行自由选择,诱导出对盐摄入的明显且剂量依赖性偏好。在钠充足的大鼠中,急性向DRN内微量注射(7.5 nmol/只大鼠)8-OH-DPAT显著模拟了急性全身给药方案。有趣的是,尽管在中枢注射后30分钟摄入量大,但向钠耗竭大鼠的DRN内微量注射8-OH-DPAT仍使0.3 M NaCl摄入量额外长期增加。相反,用8-OH-DPAT进行2周和3周的慢性全身治疗(皮下注射1520 nmol/kg)或重复向DRN内微量注射(7.5 nmol/只大鼠),在速尿注射后的24小时内,仅给予水和缺钠饮食的钠耗竭大鼠中,0.3 M NaCl摄入量出现显著长期减少。这些结果表明,DRN的5-HT(1A)树突体自身受体在基础条件下以及钠耗竭大鼠盐摄入的进食阶段的钠饱腹感信号传导中明显发挥作用。