Araújo Almeida N A, Antunes V R, Abrão Saad W, de Arruda Camargo L A
Department of Physiology, School of Dentistry, Paulista State University, UNESP, Araraquara, Brazil.
Brain Res Bull. 1999 Mar 15;48(5):521-5. doi: 10.1016/s0361-9230(99)00032-5.
The subfornical organ (SFO) and the lateral hypothalamus (LH) have been shown to be important for the central action of angiotensin II (ANG II) on water and salt regulation. Several anatomical findings have demonstrated neural connections between the SFO and the LH. The present experiments were conducted to investigate the role of the alpha-adrenergic antagonists and agonists injected into the LH on the water and salt intake elicited by injections of ANG II into the SFO. Prazosin (an alpha1-adrenergic antagonist) injected into the LH increased the salt ingestion, whereas yohimbine (an alpha2-adrenergic antagonist) and propranolol (a beta-adrenergic antagonist) antagonized the salt ingestion induced by administration of ANG II into the SFO. Previous administration of clonidine (an alpha2-adrenergic agonist) or noradrenaline into the LH increased, whereas pretreatment with phenylephrine decreased the sodium intake induced by injection of ANG II into the SFO. Previous treatment with prazosin and propranolol reduced the water intake induced by ANG II. Phenylephrine increased the dipsogenic responses produced by ANG II, whereas previous treatment with clonidine injected into the LH reduced the water intake induced by ANG II administration into the SFO. The LH involvement with SFO on the excitatory and inhibitory mechanisms related to water and sodium intake is suggested.
穹窿下器(SFO)和下丘脑外侧区(LH)已被证明对于血管紧张素II(ANG II)在水盐调节方面的中枢作用很重要。多项解剖学研究结果表明SFO和LH之间存在神经连接。本实验旨在研究向LH注射α-肾上腺素能拮抗剂和激动剂对向SFO注射ANG II所引发的水盐摄入的作用。向LH注射哌唑嗪(一种α1-肾上腺素能拮抗剂)会增加盐摄入量,而育亨宾(一种α2-肾上腺素能拮抗剂)和普萘洛尔(一种β-肾上腺素能拮抗剂)则会拮抗向SFO注射ANG II所诱导的盐摄入。先前向LH注射可乐定(一种α2-肾上腺素能激动剂)或去甲肾上腺素会增加盐摄入量,而预先用去氧肾上腺素处理则会减少向SFO注射ANG II所诱导的钠摄入量。先前用哌唑嗪和普萘洛尔处理会减少ANG II所诱导的水摄入量。去氧肾上腺素会增加ANG II所产生的饮水反应,而先前向LH注射可乐定处理则会减少向SFO注射ANG II所诱导的水摄入量。提示LH参与了SFO在与水和钠摄入相关的兴奋和抑制机制中所起的作用。