Department of Physiology and Pathology, School of Dentistry, São Paulo State University, Araraquara, SP 14801-903, Brazil.
Neuroscience. 2010 Feb 3;165(3):633-41. doi: 10.1016/j.neuroscience.2009.11.011. Epub 2009 Nov 10.
The lateral parabrachial nucleus (LPBN) and the central nucleus of the amygdala (CeA) are important areas for the control of sodium appetite. In the present study we investigated the effects of bilateral lesions of the CeA on the facilitation of water and 0.3 M NaCl intake produced by the blockade of serotonergic mechanisms or activation of alpha(2)-adrenoceptors with bilateral injections of methysergide or moxonidine, respectively, into the LPBN. Male Holtzman rats (n=5-8) with bilateral sham or electrolytic lesions of the CeA (2 mA; 10 s) and stainless steel cannulas implanted bilaterally in the LPBN were used. In sham rats treated with the diuretic furosemide (10 mg/kg b.w.) combined with the angiotensin converting enzyme inhibitor captopril (5 mg/kg b.w) subcutaneously, bilateral injections of moxonidine (0.5 nmol) or methysergide (4 microg) into the LPBN increased 0.3 M NaCl intake (29.8+/-5.1 and 19.5+/-3.7 ml/2 h, respectively, versus vehicle: 8.3+/-1.4 ml/2 h) and water intake (17.9+/-3.7 and 23.3+/-2.8 ml/2 h, respectively, versus vehicle: 11.5+/-1.6 ml/2 h). Lesions of the CeA (5-18 days) abolished the increase in 0.3 M NaCl and water intake produced by bilateral injections of moxonidine (10.3+/-2.8 and 6.8+/-2.3 ml/2 h, respectively) and reduced the increase produced by methysergide (13.6+/-2.5 and 14.5+/-3.2 ml/2 h, respectively) into the LPBN. The present results show that the increase in water and 0.3 M NaCl intake produced by serotonergic blockade and alpha(2)-adrenergic activation in the LPBN depends on the integrity of the CeA, suggesting that facilitatory mechanisms present in the CeA are essential for the increase of water and hypertonic NaCl intake produced by the blockade of the inhibitory mechanisms of the LPBN.
外侧臂旁核(LPBN)和杏仁中央核(CeA)是控制钠食欲的重要区域。在本研究中,我们研究了 CeA 的双侧损伤对 LPBN 中 5-羟色胺能机制阻断或α 2-肾上腺素能激活分别引起的水和 0.3 M NaCl 摄入增加的影响。使用具有双侧假或电解损伤的 CeA(2 mA;10 s)的雄性霍尔茨曼大鼠(n=5-8)和双侧植入 LPBN 的不锈钢套管进行实验。在接受利尿剂呋塞米(10 mg/kg b.w.)联合血管紧张素转换酶抑制剂卡托普利(5 mg/kg b.w.)皮下治疗的假鼠中,双侧 LPBN 注射莫索尼定(0.5 nmol)或甲麦角林(4 微克)增加了 0.3 M NaCl 摄入(分别为 29.8+/-5.1 和 19.5+/-3.7 ml/2 h,而载体为 8.3+/-1.4 ml/2 h)和水摄入(分别为 17.9+/-3.7 和 23.3+/-2.8 ml/2 h,而载体为 11.5+/-1.6 ml/2 h)。CeA 损伤(5-18 天)消除了双侧 LPBN 注射莫索尼定(分别为 10.3+/-2.8 和 6.8+/-2.3 ml/2 h)引起的 0.3 M NaCl 和水摄入增加,并减少了甲麦角林引起的增加(分别为 13.6+/-2.5 和 14.5+/-3.2 ml/2 h)。本研究结果表明,LPBN 中 5-羟色胺能阻断和α 2-肾上腺素能激活引起的水和 0.3 M NaCl 摄入增加依赖于 CeA 的完整性,提示 CeA 中存在的促进机制对于 LPBN 抑制机制阻断引起的水和高渗 NaCl 摄入增加是必不可少的。