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中枢毒蕈碱和 LPBN 机制对钠摄入的影响。

Central muscarinic and LPBN mechanisms on sodium intake.

机构信息

Department of Physiology and Pathology, School of Dentistry, São Paulo State University - UNESP, Araraquara, SP, Brazil.

Department of Physiology and Pathology, School of Dentistry, São Paulo State University - UNESP, Araraquara, SP, Brazil.

出版信息

Brain Res Bull. 2019 Jan;144:14-20. doi: 10.1016/j.brainresbull.2018.10.011. Epub 2018 Nov 2.

Abstract

Central cholinergic activation stimulates water intake, but also NaCl intake when the inhibitory mechanisms are blocked with injections of moxonidine (α adrenergic/imidazoline agonist) into the lateral parabrachial nucleus (LPBN). In the present study, we investigated the involvement of central M and M muscarinic receptors on NaCl intake induced by pilocarpine (non-selective muscarinic agonist) intraperitoneally combined with moxonidine into the LPBN or by muscimol (GABA agonist) into the LPBN. Male Holtzman rats with stainless steel cannulas implanted bilaterally in the LPBN and in the lateral ventricle were used. Pirenzepine (M muscarinic antagonist, 1 nmol/1 μl) or methoctramine (M muscarinic antagonist, 50 nmol/1 μL) injected intracerebroventricularly (i.c.v.) reduced 0.3 M NaCl and water intake in rats treated with pilocarpine (0.1 mg/100 g of body weight) injected intraperitoneally combined with moxonidine (0.5 nmol/0.2 μL) into the LPBN. In rats treated with muscimol (0.5 nmol/0.2 μL) into the LPBN, methoctramine i.c.v. also reduced 0.3 M NaCl and water intake, however, pirenzepine produced no effect. The results suggest that M and M muscarinic receptors activate central pathways involved in the control of water and sodium intake that are under the influence of the LPBN inhibitory mechanisms.

摘要

中枢胆碱能激活会刺激水的摄入,而当用可乐定(α肾上腺素能/咪唑啉激动剂)注射到外侧臂旁核(LPBN)阻断抑制机制时,也会刺激氯化钠的摄入。在本研究中,我们研究了中央 M 和 M 毒蕈碱受体在毛果芸香碱(非选择性毒蕈碱激动剂)腹腔内注射与 LPBN 中的可乐定联合或 LPBN 中的 muscimol(GABA 激动剂)联合引起的氯化钠摄入中的作用。使用双侧植入 LPBN 和侧脑室不锈钢套管的雄性霍尔茨曼大鼠。脑室注射哌仑西平(M 毒蕈碱拮抗剂,1 nmol/1 μl)或甲硫氧嘧啶(M 毒蕈碱拮抗剂,50 nmol/1 μL)可减少腹腔注射毛果芸香碱(0.1 mg/100 g 体重)与 LPBN 中可乐定(0.5 nmol/0.2 μL)联合治疗大鼠的 0.3 M NaCl 和水摄入。在接受 LPBN 中 muscimol(0.5 nmol/0.2 μL)治疗的大鼠中,甲硫氧嘧啶脑室注射也减少了 0.3 M NaCl 和水的摄入,然而,哌仑西平没有产生影响。结果表明,M 和 M 毒蕈碱受体激活了中枢途径,这些途径参与了水和钠摄入的控制,而这些途径受 LPBN 抑制机制的影响。

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