Ruginsk S G, Oliveira F R T, Margatho L O, Vivas L, Elias L L K, Antunes-Rodrigues J
Departamento de Fisiologia, Faculdade de Medicina de Ribeirao Preto, Universidade de São Paulo, Brazil.
Exp Neurol. 2007 Aug;206(2):192-200. doi: 10.1016/j.expneurol.2007.04.012. Epub 2007 May 10.
The present study evaluated the involvement of glucocorticoid in the activation of vasopressinergic and oxytocinergic neurons of hypothalamic nuclei and plasma levels of vasopressin (AVP), oxytocin (OT), atrial natriuretic peptide (ANP) and corticosterone (CORT) in response to both isotonic and hypertonic blood volume expansion (BVE). Rats were subjected to isotonic (0.15 M NaCl, 2 ml/100 g b.w., i.v.) or hypertonic (0.30 M NaCl, 2 ml/100 g b.w., i.v.) BVE with or without pre-treatment with dexamethasone (1 mg/kg, i.p.). Results showed that isotonic BVE increased OT, ANP and CORT, and decreased AVP plasma levels. On the other hand, hypertonic BVE enhanced AVP, ANP, OT, and CORT plasma concentrations. Both hypertonic and isotonic BVE induced an increase in the number of Fos-OT double-labeled magnocellular neurons in the PVN and SON. Pre-treatment with dexamethasone reduced OT secretion, as well as Fos-OT immunoreactive neurons in response to both isotonic and hypertonic BVE. We also observed that dexamethasone pre-treatment had no effect on AVP secretion in response to hypertonic BVE, although this effect was associated with a blockade of Fos expression in the vasopressinergic magnocellular neurons in the PVN and SON. In conclusion, these data suggest that, not only the rapid OT release from storages, but also the oxytocinergic cellular activation induced by BVE are modulated by glucocorticoids. However, this pattern of response was not observed for AVP cells, suggesting that dexamethasone is not likely to influence rapid release of AVP but seems to modulate the activation of these neurons in response to hypertonic BVE.
本研究评估了糖皮质激素在下丘脑核团中血管加压素能和催产素能神经元激活过程中的作用,以及在等渗和高渗性血容量扩张(BVE)时血管加压素(AVP)、催产素(OT)、心房利钠肽(ANP)和皮质酮(CORT)的血浆水平。对大鼠进行等渗(0.15 M NaCl,2 ml/100 g体重,静脉注射)或高渗(0.30 M NaCl,2 ml/100 g体重,静脉注射)BVE,同时给予或不给予地塞米松预处理(1 mg/kg,腹腔注射)。结果显示,等渗BVE使OT、ANP和CORT升高,AVP血浆水平降低。另一方面,高渗BVE使AVP、ANP、OT和CORT血浆浓度升高。高渗和等渗BVE均诱导室旁核(PVN)和视上核(SON)中Fos-OT双标大细胞神经元数量增加。地塞米松预处理可降低等渗和高渗BVE时的OT分泌以及Fos-OT免疫反应性神经元数量。我们还观察到,地塞米松预处理对高渗BVE时的AVP分泌无影响,尽管这种作用与PVN和SON中血管加压素能大细胞神经元Fos表达的阻断有关。总之,这些数据表明,糖皮质激素不仅调节OT从储存部位的快速释放,还调节BVE诱导的催产素能细胞激活。然而,AVP细胞未观察到这种反应模式,这表明地塞米松不太可能影响AVP的快速释放,但似乎调节这些神经元对高渗BVE的激活。